-
1
-
-
77950231051
-
Medicine. The future of psychiatric research: genomes and neural circuits
-
Akil H., Brenner S., Kandel E., Kendler K.S., King M.C., Scolnick E., Watson J.D., Zoghbi H.Y. Medicine. The future of psychiatric research: genomes and neural circuits. Science 2010, 327:1580-1581.
-
(2010)
Science
, vol.327
, pp. 1580-1581
-
-
Akil, H.1
Brenner, S.2
Kandel, E.3
Kendler, K.S.4
King, M.C.5
Scolnick, E.6
Watson, J.D.7
Zoghbi, H.Y.8
-
2
-
-
70349556543
-
Personalized copy number and segmental duplication maps using next-generation sequencing
-
Alkan C., Kidd J.M., Marques-Bonet T., Aksay G., Antonacci F., Hormozdiari F., Kitzman J.O., Baker C., Malig M., Mutlu O., Sahinalp S.C., Gibbs R.A., Eichler E.E. Personalized copy number and segmental duplication maps using next-generation sequencing. Nat. Genet. 2009, 41:1061-1067.
-
(2009)
Nat. Genet.
, vol.41
, pp. 1061-1067
-
-
Alkan, C.1
Kidd, J.M.2
Marques-Bonet, T.3
Aksay, G.4
Antonacci, F.5
Hormozdiari, F.6
Kitzman, J.O.7
Baker, C.8
Malig, M.9
Mutlu, O.10
Sahinalp, S.C.11
Gibbs, R.A.12
Eichler, E.E.13
-
3
-
-
0032503887
-
22q11 deletion syndrome in adults with schizophrenia
-
Bassett A.S., Hodgkinson K., Chow E.W., Correia S., Scutt L.E., Weksberg R. 22q11 deletion syndrome in adults with schizophrenia. Am. J. Med. Genet. 1998, 81:328-337.
-
(1998)
Am. J. Med. Genet.
, vol.81
, pp. 328-337
-
-
Bassett, A.S.1
Hodgkinson, K.2
Chow, E.W.3
Correia, S.4
Scutt, L.E.5
Weksberg, R.6
-
4
-
-
69749108657
-
The ClinSeq Project: piloting large-scale genome sequencing for research in genomic medicine
-
Biesecker L.G., Mullikin J.C., Facio F.M., Turner C., Cherukuri P.F., Blakesley R.W., Bouffard G.G., Chines P.S., Cruz P., Hansen N.F., Teer J.K., Maskeri B., Young A.C., Manolio T.A., Wilson A.F., Finkel T., Hwang P., Arai A., Remaley A.T., Sachdev V., Shamburek R., Cannon R.O., Green E.D. The ClinSeq Project: piloting large-scale genome sequencing for research in genomic medicine. Genome Res. 2009, 19:1665-1674.
-
(2009)
Genome Res.
, vol.19
, pp. 1665-1674
-
-
Biesecker, L.G.1
Mullikin, J.C.2
Facio, F.M.3
Turner, C.4
Cherukuri, P.F.5
Blakesley, R.W.6
Bouffard, G.G.7
Chines, P.S.8
Cruz, P.9
Hansen, N.F.10
Teer, J.K.11
Maskeri, B.12
Young, A.C.13
Manolio, T.A.14
Wilson, A.F.15
Finkel, T.16
Hwang, P.17
Arai, A.18
Remaley, A.T.19
Sachdev, V.20
Shamburek, R.21
Cannon, R.O.22
Green, E.D.23
more..
-
5
-
-
34250305146
-
Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project
-
Birney E., Stamatoyannopoulos J.A., Dutta A., Guigo R., Gingeras T.R., Margulies E.H., Weng Z., Snyder M., Dermitzakis E.T., Thurman R.E., Kuehn M.S., Taylor C.M., Neph S., Koch C.M., Asthana S., Malhotra A., Adzhubei I., Greenbaum J.A., Andrews R.M., Flicek P., Boyle P.J., Cao H., Carter N.P., Clelland G.K., Davis S., Day N., Dhami P., Dillon S.C., Dorschner M.O., Fiegler H., Giresi P.G., Goldy J., Hawrylycz M., Haydock A., Humbert R., James K.D., Johnson B.E., Johnson E.M., Frum T.T., Rosenzweig E.R., Karnani N., Lee K., Lefebvre G.C., Navas P.A., Neri F., Parker S.C., Sabo P.J., Sandstrom R., Shafer A., Vetrie D., Weaver M., Wilcox S., Yu M., Collins F.S., Dekker J., Lieb J.D., Tullius T.D., Crawford G.E., Sunyaev S., Noble W.S., Dunham I., Denoeud F., Reymond A., Kapranov P., Rozowsky J., Zheng D., Castelo R., Frankish A., Harrow J., Ghosh S., Sandelin A., Hofacker I.L., Baertsch R., Keefe D., Dike S., Cheng J., Hirsch H.A., Sekinger E.A., Lagarde J., Abril J.F., Shahab A., Flamm C., Fried C., Hackermuller J., Hertel J., Lindemeyer M., Missal K., Tanzer A., Washietl S., Korbel J., Emanuelsson O., Pedersen J.S., Holroyd N., Taylor R., Swarbreck D., Matthews N., Dickson M.C., Thomas D.J., Weirauch M.T., Gilbert J., Drenkow J., Bell I., Zhao X., Srinivasan K.G., Sung W.K., Ooi H.S., Chiu K.P., Foissac S., Alioto T., Brent M., Pachter L., Tress M.L., Valencia A., Choo S.W., Choo C.Y., Ucla C., Manzano C., Wyss C., Cheung E., Clark T.G., Brown J.B., Ganesh M., Patel S., Tammana H., Chrast J., Henrichsen C.N., Kai C., Kawai J., Nagalakshmi U., Wu J., Lian Z., Lian J., Newburger P., Zhang X., Bickel P., Mattick J.S., Carninci P., Hayashizaki Y., Weissman S., Hubbard T., Myers R.M., Rogers J., Stadler P.F., Lowe T.M., Wei C.L., Ruan Y., Struhl K., Gerstein M., Antonarakis S.E., Fu Y., Green E.D., Karaoz U., Siepel A., Taylor J., Liefer L.A., Wetterstrand K.A., Good P.J., Feingold E.A., Guyer M.S., Cooper G.M., Asimenos G., Dewey C.N., Hou M., Nikolaev S., Montoya-Burgos J.I., Loytynoja A., Whelan S., Pardi F., Massingham T., Huang H., Zhang N.R., Holmes I., Mullikin J.C., Ureta-Vidal A., Paten B., Seringhaus M., Church D., Rosenbloom K., Kent W.J., Stone E.A., Batzoglou S., Goldman N., Hardison R.C., Haussler D., Miller W., Sidow A., Trinklein N.D., Zhang Z.D., Barrera L., Stuart R., King D.C., Ameur A., Enroth S., Bieda M.C., Kim J., Bhinge A.A., Jiang N., Liu J., Yao F., Vega V.B., Lee C.W., Ng P., Yang A., Moqtaderi Z., Zhu Z., Xu X., Squazzo S., Oberley M.J., Inman D., Singer M.A., Richmond T.A., Munn K.J., Rada-Iglesias A., Wallerman O., Komorowski J., Fowler J.C., Couttet P., Bruce A.W., Dovey O.M., Ellis P.D., Langford C.F., Nix D.A., Euskirchen G., Hartman S., Urban A.E., Kraus P., Van Calcar S., Heintzman N., Kim T.H., Wang K., Qu C., Hon G., Luna R., Glass C.K., Rosenfeld M.G., Aldred S.F., Cooper S.J., Halees A., Lin J.M., Shulha H.P., Xu M., Haidar J.N., Yu Y., Iyer V.R., Green R.D., Wadelius C., Farnham P.J., Ren B., Harte R.A., Hinrichs A.S., Trumbower H., Clawson H., Hillman-Jackson J., Zweig A.S., Smith K., Thakkapallayil A., Barber G., Kuhn R.M., Karolchik D., Armengol L., Bird C.P., de Bakker P.I., Kern A.D., Lopez-Bigas N., Martin J.D., Stranger B.E., Woodroffe A., Davydov E., Dimas A., Eyras E., Hallgrimsdottir I.B., Huppert J., Zody M.C., Abecasis G.R., Estivill X., Bouffard G.G., Guan X., Hansen N.F., Idol J.R., Maduro V.V., Maskeri B., McDowell J.C., Park M., Thomas P.J., Young A.C., Blakesley R.W., Muzny D.M., Sodergren E., Wheeler D.A., Worley K.C., Jiang H., Weinstock G.M., Gibbs R.A., Graves T., Fulton R., Mardis E.R., Wilson R.K., Clamp M., Cuff J., Gnerre S., Jaffe D.B., Chang J.L., Lindblad-Toh K., Lander E.S., Koriabine M., Nefedov M., Osoegawa K., Yoshinaga Y., Zhu B., de Jong P.J. Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project. Nature 2007, 447:799-816.
-
(2007)
Nature
, vol.447
, pp. 799-816
-
-
Birney, E.1
Stamatoyannopoulos, J.A.2
Dutta, A.3
Guigo, R.4
Gingeras, T.R.5
Margulies, E.H.6
Weng, Z.7
Snyder, M.8
Dermitzakis, E.T.9
Thurman, R.E.10
Kuehn, M.S.11
Taylor, C.M.12
Neph, S.13
Koch, C.M.14
Asthana, S.15
Malhotra, A.16
Adzhubei, I.17
Greenbaum, J.A.18
Andrews, R.M.19
Flicek, P.20
Boyle, P.J.21
Cao, H.22
Carter, N.P.23
Clelland, G.K.24
Davis, S.25
Day, N.26
Dhami, P.27
Dillon, S.C.28
Dorschner, M.O.29
Fiegler, H.30
Giresi, P.G.31
Goldy, J.32
Hawrylycz, M.33
Haydock, A.34
Humbert, R.35
James, K.D.36
Johnson, B.E.37
Johnson, E.M.38
Frum, T.T.39
Rosenzweig, E.R.40
Karnani, N.41
Lee, K.42
Lefebvre, G.C.43
Navas, P.A.44
Neri, F.45
Parker, S.C.46
Sabo, P.J.47
Sandstrom, R.48
Shafer, A.49
Vetrie, D.50
Weaver, M.51
Wilcox, S.52
Yu, M.53
Collins, F.S.54
Dekker, J.55
Lieb, J.D.56
Tullius, T.D.57
Crawford, G.E.58
Sunyaev, S.59
Noble, W.S.60
Dunham, I.61
Denoeud, F.62
Reymond, A.63
Kapranov, P.64
Rozowsky, J.65
Zheng, D.66
Castelo, R.67
Frankish, A.68
Harrow, J.69
Ghosh, S.70
Sandelin, A.71
Hofacker, I.L.72
Baertsch, R.73
Keefe, D.74
Dike, S.75
Cheng, J.76
Hirsch, H.A.77
Sekinger, E.A.78
Lagarde, J.79
Abril, J.F.80
Shahab, A.81
Flamm, C.82
Fried, C.83
Hackermuller, J.84
Hertel, J.85
Lindemeyer, M.86
Missal, K.87
Tanzer, A.88
Washietl, S.89
Korbel, J.90
Emanuelsson, O.91
Pedersen, J.S.92
Holroyd, N.93
Taylor, R.94
Swarbreck, D.95
Matthews, N.96
Dickson, M.C.97
Thomas, D.J.98
Weirauch, M.T.99
more..
-
6
-
-
34447305469
-
Severe mental retardation with breathing abnormalities (Pitt-Hopkins syndrome) is caused by haploinsufficiency of the neuronal bHLH transcription factor TCF4
-
Brockschmidt A., Todt U., Ryu S., Hoischen A., Landwehr C., Birnbaum S., Frenck W., Radlwimmer B., Lichter P., Engels H., Driever W., Kubisch C., Weber R.G. Severe mental retardation with breathing abnormalities (Pitt-Hopkins syndrome) is caused by haploinsufficiency of the neuronal bHLH transcription factor TCF4. Hum. Mol. Genet. 2007, 16:1488-1494.
-
(2007)
Hum. Mol. Genet.
, vol.16
, pp. 1488-1494
-
-
Brockschmidt, A.1
Todt, U.2
Ryu, S.3
Hoischen, A.4
Landwehr, C.5
Birnbaum, S.6
Frenck, W.7
Radlwimmer, B.8
Lichter, P.9
Engels, H.10
Driever, W.11
Kubisch, C.12
Weber, R.G.13
-
7
-
-
56749154242
-
Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities
-
Brunetti-Pierri N., Berg J.S., Scaglia F., Belmont J., Bacino C.A., Sahoo T., Lalani S.R., Graham B., Lee B., Shinawi M., Shen J., Kang S.H., Pursley A., Lotze T., Kennedy G., Lansky-Shafer S., Weaver C., Roeder E.R., Grebe T.A., Arnold G.L., Hutchison T., Reimschisel T., Amato S., Geragthy M.T., Innis J.W., Obersztyn E., Nowakowska B., Rosengren S.S., Bader P.I., Grange D.K., Naqvi S., Garnica A.D., Bernes S.M., Fong C.T., Summers A., Walters W.D., Lupski J.R., Stankiewicz P., Cheung S.W., Patel A. Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities. Nat. Genet. 2008, 40:1466-1471.
-
(2008)
Nat. Genet.
, vol.40
, pp. 1466-1471
-
-
Brunetti-Pierri, N.1
Berg, J.S.2
Scaglia, F.3
Belmont, J.4
Bacino, C.A.5
Sahoo, T.6
Lalani, S.R.7
Graham, B.8
Lee, B.9
Shinawi, M.10
Shen, J.11
Kang, S.H.12
Pursley, A.13
Lotze, T.14
Kennedy, G.15
Lansky-Shafer, S.16
Weaver, C.17
Roeder, E.R.18
Grebe, T.A.19
Arnold, G.L.20
Hutchison, T.21
Reimschisel, T.22
Amato, S.23
Geragthy, M.T.24
Innis, J.W.25
Obersztyn, E.26
Nowakowska, B.27
Rosengren, S.S.28
Bader, P.I.29
Grange, D.K.30
Naqvi, S.31
Garnica, A.D.32
Bernes, S.M.33
Fong, C.T.34
Summers, A.35
Walters, W.D.36
Lupski, J.R.37
Stankiewicz, P.38
Cheung, S.W.39
Patel, A.40
more..
-
8
-
-
19544391975
-
A synonymous SNP of the corneodesmosin gene leads to increased mRNA stability and demonstrates association with psoriasis across diverse ethnic groups
-
Capon F., Allen M.H., Ameen M., Burden A.D., Tillman D., Barker J.N., Trembath R.C. A synonymous SNP of the corneodesmosin gene leads to increased mRNA stability and demonstrates association with psoriasis across diverse ethnic groups. Hum. Mol. Genet. 2004, 13:2361-2368.
-
(2004)
Hum. Mol. Genet.
, vol.13
, pp. 2361-2368
-
-
Capon, F.1
Allen, M.H.2
Ameen, M.3
Burden, A.D.4
Tillman, D.5
Barker, J.N.6
Trembath, R.C.7
-
9
-
-
31144465926
-
Hearing silence: non-neutral evolution at synonymous sites in mammals
-
Chamary J.V., Parmley J.L., Hurst L.D. Hearing silence: non-neutral evolution at synonymous sites in mammals. Nat. Rev. Genet. 2006, 7:98-108.
-
(2006)
Nat. Rev. Genet.
, vol.7
, pp. 98-108
-
-
Chamary, J.V.1
Parmley, J.L.2
Hurst, L.D.3
-
10
-
-
49349106191
-
Rhesus monkey tryptophan hydroxylase-2 coding region haplotypes affect mRNA stability
-
Chen G.L., Miller G.M. Rhesus monkey tryptophan hydroxylase-2 coding region haplotypes affect mRNA stability. Neuroscience 2008, 155:485-491.
-
(2008)
Neuroscience
, vol.155
, pp. 485-491
-
-
Chen, G.L.1
Miller, G.M.2
-
11
-
-
44349186162
-
Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder
-
Christian S.L., Brune C.W., Sudi J., Kumar R.A., Liu S., Karamohamed S., Badner J.A., Matsui S., Conroy J., McQuaid D., Gergel J., Hatchwell E., Gilliam T.C., Gershon E.S., Nowak N.J., Dobyns W.B., Cook E.H. Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder. Biol. Psychiatry 2008, 63:1111-1117.
-
(2008)
Biol. Psychiatry
, vol.63
, pp. 1111-1117
-
-
Christian, S.L.1
Brune, C.W.2
Sudi, J.3
Kumar, R.A.4
Liu, S.5
Karamohamed, S.6
Badner, J.A.7
Matsui, S.8
Conroy, J.9
McQuaid, D.10
Gergel, J.11
Hatchwell, E.12
Gilliam, T.C.13
Gershon, E.S.14
Nowak, N.J.15
Dobyns, W.B.16
Cook, E.H.17
-
12
-
-
66149185456
-
Genomewide association studies: history, rationale, and prospects for psychiatric disorders
-
Cichon S., Craddock N., Daly M., Faraone S.V., Gejman P.V., Kelsoe J., Lehner T., Levinson D.F., Moran A., Sklar P., Sullivan P.F. Genomewide association studies: history, rationale, and prospects for psychiatric disorders. Am. J. Psychiatry 2009, 166:540-556.
-
(2009)
Am. J. Psychiatry
, vol.166
, pp. 540-556
-
-
Cichon, S.1
Craddock, N.2
Daly, M.3
Faraone, S.V.4
Gejman, P.V.5
Kelsoe, J.6
Lehner, T.7
Levinson, D.F.8
Moran, A.9
Sklar, P.10
Sullivan, P.F.11
-
13
-
-
60349092402
-
Mapping complex disease traits with global gene expression
-
Cookson W., Liang L., Abecasis G., Moffatt M., Lathrop M. Mapping complex disease traits with global gene expression. Nat. Rev. Genet. 2009, 10:184-194.
-
(2009)
Nat. Rev. Genet.
, vol.10
, pp. 184-194
-
-
Cookson, W.1
Liang, L.2
Abecasis, G.3
Moffatt, M.4
Lathrop, M.5
-
14
-
-
52949093111
-
Systematic assessment of copy number variant detection via genome-wide SNP genotyping
-
Cooper G.M., Zerr T., Kidd J.M., Eichler E.E., Nickerson D.A. Systematic assessment of copy number variant detection via genome-wide SNP genotyping. Nat. Genet. 2008, 40:1199-1203.
-
(2008)
Nat. Genet.
, vol.40
, pp. 1199-1203
-
-
Cooper, G.M.1
Zerr, T.2
Kidd, J.M.3
Eichler, E.E.4
Nickerson, D.A.5
-
15
-
-
33745210614
-
Association of estrogen receptor alpha (ESR1) PvuII and XbaI polymorphisms with sporadic Alzheimer's disease and their effect on apolipoprotein E concentrations
-
Corbo R.M., Gambina G., Ruggeri M., Scacchi R. Association of estrogen receptor alpha (ESR1) PvuII and XbaI polymorphisms with sporadic Alzheimer's disease and their effect on apolipoprotein E concentrations. Dement. Geriatr. Cogn. Disord. 2006, 22:67-72.
-
(2006)
Dement. Geriatr. Cogn. Disord.
, vol.22
, pp. 67-72
-
-
Corbo, R.M.1
Gambina, G.2
Ruggeri, M.3
Scacchi, R.4
-
16
-
-
44449090109
-
Parental psychiatric disorders associated with autism spectrum disorders in the offspring
-
Daniels J.L., Forssen U., Hultman C.M., Cnattingius S., Savitz D.A., Feychting M., Sparen P. Parental psychiatric disorders associated with autism spectrum disorders in the offspring. Pediatrics 2008, 121:e1357-1362.
-
(2008)
Pediatrics
, vol.121
-
-
Daniels, J.L.1
Forssen, U.2
Hultman, C.M.3
Cnattingius, S.4
Savitz, D.A.5
Feychting, M.6
Sparen, P.7
-
17
-
-
74249088463
-
Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies
-
de Kovel C.G., Trucks H., Helbig I., Mefford H.C., Baker C., Leu C., Kluck C., Muhle H., von Spiczak S., Ostertag P., Obermeier T., Kleefuss-Lie A.A., Hallmann K., Steffens M., Gaus V., Klein K.M., Hamer H.M., Rosenow F., Brilstra E.H., Trenite D.K., Swinkels M.E., Weber Y.G., Unterberger I., Zimprich F., Urak L., Feucht M., Fuchs K., Moller R.S., Hjalgrim H., De Jonghe P., Suls A., Ruckert I.M., Wichmann H.E., Franke A., Schreiber S., Nurnberg P., Elger C.E., Lerche H., Stephani U., Koeleman B.P., Lindhout D., Eichler E.E., Sander T. Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies. Brain 2010, 133:23-32.
-
(2010)
Brain
, vol.133
, pp. 23-32
-
-
de Kovel, C.G.1
Trucks, H.2
Helbig, I.3
Mefford, H.C.4
Baker, C.5
Leu, C.6
Kluck, C.7
Muhle, H.8
von Spiczak, S.9
Ostertag, P.10
Obermeier, T.11
Kleefuss-Lie, A.A.12
Hallmann, K.13
Steffens, M.14
Gaus, V.15
Klein, K.M.16
Hamer, H.M.17
Rosenow, F.18
Brilstra, E.H.19
Trenite, D.K.20
Swinkels, M.E.21
Weber, Y.G.22
Unterberger, I.23
Zimprich, F.24
Urak, L.25
Feucht, M.26
Fuchs, K.27
Moller, R.S.28
Hjalgrim, H.29
De Jonghe, P.30
Suls, A.31
Ruckert, I.M.32
Wichmann, H.E.33
Franke, A.34
Schreiber, S.35
Nurnberg, P.36
Elger, C.E.37
Lerche, H.38
Stephani, U.39
Koeleman, B.P.40
Lindhout, D.41
Eichler, E.E.42
Sander, T.43
more..
-
18
-
-
70350774172
-
Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance
-
Dibbens L.M., Mullen S., Helbig I., Mefford H.C., Bayly M.A., Bellows S., Leu C., Trucks H., Obermeier T., Wittig M., Franke A., Caglayan H., Yapici Z., Sander T., Eichler E.E., Scheffer I.E., Mulley J.C., Berkovic S.F. Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance. Hum. Mol. Genet. 2009, 18:3626-3631.
-
(2009)
Hum. Mol. Genet.
, vol.18
, pp. 3626-3631
-
-
Dibbens, L.M.1
Mullen, S.2
Helbig, I.3
Mefford, H.C.4
Bayly, M.A.5
Bellows, S.6
Leu, C.7
Trucks, H.8
Obermeier, T.9
Wittig, M.10
Franke, A.11
Caglayan, H.12
Yapici, Z.13
Sander, T.14
Eichler, E.E.15
Scheffer, I.E.16
Mulley, J.C.17
Berkovic, S.F.18
-
19
-
-
77249134594
-
-
Rare variants create synthetic genome-wide associations, PLoS Biol. 8 e1000294.
-
S.P. Dickson, K. Wang, I. Krantz, H. Hakonarson, D.B. Goldstein, Rare variants create synthetic genome-wide associations, PLoS Biol. 8 e1000294.
-
-
-
Dickson, S.P.1
Wang, K.2
Krantz, I.3
Hakonarson, H.4
Goldstein, D.B.5
-
20
-
-
0037320652
-
Synonymous mutations in the human dopamine receptor D2 (DRD2) affect mRNA stability and synthesis of the receptor
-
Duan J., Wainwright M.S., Comeron J.M., Saitou N., Sanders A.R., Gelernter J., Gejman P.V. Synonymous mutations in the human dopamine receptor D2 (DRD2) affect mRNA stability and synthesis of the receptor. Hum. Mol. Genet. 2003, 12:205-216.
-
(2003)
Hum. Mol. Genet.
, vol.12
, pp. 205-216
-
-
Duan, J.1
Wainwright, M.S.2
Comeron, J.M.3
Saitou, N.4
Sanders, A.R.5
Gelernter, J.6
Gejman, P.V.7
-
21
-
-
77950243833
-
Multiple common variants for celiac disease influencing immune gene expression
-
Dubois P.C., Trynka G., Franke L., Hunt K.A., Romanos J., Curtotti A., Zhernakova A., Heap G.A., Adany R., Aromaa A., Bardella M.T., van den Berg L.H., Bockett N.A., de la Concha E.G., Dema B., Fehrmann R.S., Fernandez-Arquero M., Fiatal S., Grandone E., Green P.M., Groen H.J., Gwilliam R., Houwen R.H., Hunt S.E., Kaukinen K., Kelleher D., Korponay-Szabo I., Kurppa K., MacMathuna P., Maki M., Mazzilli M.C., McCann O.T., Mearin M.L., Mein C.A., Mirza M.M., Mistry V., Mora B., Morley K.I., Mulder C.J., Murray J.A., Nunez C., Oosterom E., Ophoff R.A., Polanco I., Peltonen L., Platteel M., Rybak A., Salomaa V., Schweizer J.J., Sperandeo M.P., Tack G.J., Turner G., Veldink J.H., Verbeek W.H., Weersma R.K., Wolters V.M., Urcelay E., Cukrowska B., Greco L., Neuhausen S.L., McManus R., Barisani D., Deloukas P., Barrett J.C., Saavalainen P., Wijmenga C., van Heel D.A. Multiple common variants for celiac disease influencing immune gene expression. Nat. Genet. 2010, 42:295-302.
-
(2010)
Nat. Genet.
, vol.42
, pp. 295-302
-
-
Dubois, P.C.1
Trynka, G.2
Franke, L.3
Hunt, K.A.4
Romanos, J.5
Curtotti, A.6
Zhernakova, A.7
Heap, G.A.8
Adany, R.9
Aromaa, A.10
Bardella, M.T.11
van den Berg, L.H.12
Bockett, N.A.13
de la Concha, E.G.14
Dema, B.15
Fehrmann, R.S.16
Fernandez-Arquero, M.17
Fiatal, S.18
Grandone, E.19
Green, P.M.20
Groen, H.J.21
Gwilliam, R.22
Houwen, R.H.23
Hunt, S.E.24
Kaukinen, K.25
Kelleher, D.26
Korponay-Szabo, I.27
Kurppa, K.28
MacMathuna, P.29
Maki, M.30
Mazzilli, M.C.31
McCann, O.T.32
Mearin, M.L.33
Mein, C.A.34
Mirza, M.M.35
Mistry, V.36
Mora, B.37
Morley, K.I.38
Mulder, C.J.39
Murray, J.A.40
Nunez, C.41
Oosterom, E.42
Ophoff, R.A.43
Polanco, I.44
Peltonen, L.45
Platteel, M.46
Rybak, A.47
Salomaa, V.48
Schweizer, J.J.49
Sperandeo, M.P.50
Tack, G.J.51
Turner, G.52
Veldink, J.H.53
Verbeek, W.H.54
Weersma, R.K.55
Wolters, V.M.56
Urcelay, E.57
Cukrowska, B.58
Greco, L.59
Neuhausen, S.L.60
McManus, R.61
Barisani, D.62
Deloukas, P.63
Barrett, J.C.64
Saavalainen, P.65
Wijmenga, C.66
van Heel, D.A.67
more..
-
22
-
-
42249087793
-
Estimation of significance thresholds for genomewide association scans
-
Dudbridge F., Gusnanto A. Estimation of significance thresholds for genomewide association scans. Genet. Epidemiol. 2008, 32:227-234.
-
(2008)
Genet. Epidemiol.
, vol.32
, pp. 227-234
-
-
Dudbridge, F.1
Gusnanto, A.2
-
23
-
-
0036957751
-
Transvection effects in Drosophila
-
Duncan I.W. Transvection effects in Drosophila. Annu. Rev. Genet. 2002, 36:521-556.
-
(2002)
Annu. Rev. Genet.
, vol.36
, pp. 521-556
-
-
Duncan, I.W.1
-
24
-
-
33645907194
-
Association of schizophrenia and autoimmune diseases: linkage of Danish national registers
-
Eaton W.W., Byrne M., Ewald H., Mors O., Chen C.Y., Agerbo E., Mortensen P.B. Association of schizophrenia and autoimmune diseases: linkage of Danish national registers. Am. J. Psychiatry 2006, 163:521-528.
-
(2006)
Am. J. Psychiatry
, vol.163
, pp. 521-528
-
-
Eaton, W.W.1
Byrne, M.2
Ewald, H.3
Mors, O.4
Chen, C.Y.5
Agerbo, E.6
Mortensen, P.B.7
-
25
-
-
65549147665
-
Neural mechanisms of a genome-wide supported psychosis variant
-
Esslinger C., Walter H., Kirsch P., Erk S., Schnell K., Arnold C., Haddad L., Mier D., Opitz von Boberfeld C., Raab K., Witt S.H., Rietschel M., Cichon S., Meyer-Lindenberg A. Neural mechanisms of a genome-wide supported psychosis variant. Science 2009, 324:605.
-
(2009)
Science
, vol.324
, pp. 605
-
-
Esslinger, C.1
Walter, H.2
Kirsch, P.3
Erk, S.4
Schnell, K.5
Arnold, C.6
Haddad, L.7
Mier, D.8
Opitz von Boberfeld, C.9
Raab, K.10
Witt, S.H.11
Rietschel, M.12
Cichon, S.13
Meyer-Lindenberg, A.14
-
26
-
-
77949718910
-
Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder
-
Fernandez B.A., Roberts W., Chung B., Weksberg R., Meyn S., Szatmari P., Joseph-George A.M., Mackay S., Whitten K., Noble B., Vardy C., Crosbie V., Luscombe S., Tucker E., Turner L., Marshall C.R., Scherer S.W. Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder. J. Med. Genet. 2010, 47:195-203.
-
(2010)
J. Med. Genet.
, vol.47
, pp. 195-203
-
-
Fernandez, B.A.1
Roberts, W.2
Chung, B.3
Weksberg, R.4
Meyn, S.5
Szatmari, P.6
Joseph-George, A.M.7
Mackay, S.8
Whitten, K.9
Noble, B.10
Vardy, C.11
Crosbie, V.12
Luscombe, S.13
Tucker, E.14
Turner, L.15
Marshall, C.R.16
Scherer, S.W.17
-
27
-
-
34848860827
-
The E-protein Tcf4 interacts with Math1 to regulate differentiation of a specific subset of neuronal progenitors
-
Flora A., Garcia J.J., Thaller C., Zoghbi H.Y. The E-protein Tcf4 interacts with Math1 to regulate differentiation of a specific subset of neuronal progenitors. Proc. Natl. Acad. Sci. U.S.A. 2007, 104:15382-15387.
-
(2007)
Proc. Natl. Acad. Sci. U.S.A.
, vol.104
, pp. 15382-15387
-
-
Flora, A.1
Garcia, J.J.2
Thaller, C.3
Zoghbi, H.Y.4
-
28
-
-
0021832252
-
Quinolinic acid phosphoribosyltransferase in human and rat brain: activity in Huntington's disease and in quinolinate-lesioned rat striatum
-
Foster A.C., Whetsell W.O., Bird E.D., Schwarcz R. Quinolinic acid phosphoribosyltransferase in human and rat brain: activity in Huntington's disease and in quinolinate-lesioned rat striatum. Brain Res. 1985, 336:207-214.
-
(1985)
Brain Res.
, vol.336
, pp. 207-214
-
-
Foster, A.C.1
Whetsell, W.O.2
Bird, E.D.3
Schwarcz, R.4
-
29
-
-
43249120160
-
Genetic variability in the SNCA gene influences alpha-synuclein levels in the blood and brain
-
Fuchs J., Tichopad A., Golub Y., Munz M., Schweitzer K.J., Wolf B., Berg D., Mueller J.C., Gasser T. Genetic variability in the SNCA gene influences alpha-synuclein levels in the blood and brain. FASEB J. 2008, 22:1327-1334.
-
(2008)
FASEB J.
, vol.22
, pp. 1327-1334
-
-
Fuchs, J.1
Tichopad, A.2
Golub, Y.3
Munz, M.4
Schweitzer, K.J.5
Wolf, B.6
Berg, D.7
Mueller, J.C.8
Gasser, T.9
-
30
-
-
77649252269
-
Visualization of omics data for systems biology
-
Gehlenborg N., O'Donoghue S.I., Baliga N.S., Goesmann A., Hibbs M.A., Kitano H., Kohlbacher O., Neuweger H., Schneider R., Tenenbaum D., Gavin A.C. Visualization of omics data for systems biology. Nat. Methods 2010, 7:S56-S68.
-
(2010)
Nat. Methods
, vol.7
-
-
Gehlenborg, N.1
O'Donoghue, S.I.2
Baliga, N.S.3
Goesmann, A.4
Hibbs, M.A.5
Kitano, H.6
Kohlbacher, O.7
Neuweger, H.8
Schneider, R.9
Tenenbaum, D.10
Gavin, A.C.11
-
31
-
-
0023875083
-
A controlled family study of chronic psychoses Schizophrenia and schizoaffective disorder
-
Gershon E.S., DeLisi L.E., Hamovit J., Nurnberger J.I., Maxwell M.E., Schreiber J., Dauphinais D., Dingman C.W., Guroff J.J. A controlled family study of chronic psychoses Schizophrenia and schizoaffective disorder. Arch. Gen. Psychiatry 1988, 45:328-336.
-
(1988)
Arch. Gen. Psychiatry
, vol.45
, pp. 328-336
-
-
Gershon, E.S.1
DeLisi, L.E.2
Hamovit, J.3
Nurnberger, J.I.4
Maxwell, M.E.5
Schreiber, J.6
Dauphinais, D.7
Dingman, C.W.8
Guroff, J.J.9
-
32
-
-
77649122250
-
A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay
-
Girirajan S., Rosenfeld J.A., Cooper G.M., Antonacci F., Siswara P., Itsara A., Vives L., Walsh T., McCarthy S.E., Baker C., Mefford H.C., Kidd J.M., Browning S.R., Browning B.L., Dickel D.E., Levy D.L., Ballif B.C., Platky K., Farber D.M., Gowans G.C., Wetherbee J.J., Asamoah A., Weaver D.D., Mark P.R., Dickerson J., Garg B.P., Ellingwood S.A., Smith R., Banks V.C., Smith W., McDonald M.T., Hoo J.J., French B.N., Hudson C., Johnson J.P., Ozmore J.R., Moeschler J.B., Surti U., Escobar L.F., El-Khechen D., Gorski J.L., Kussmann J., Salbert B., Lacassie Y., Biser A., McDonald-McGinn D.M., Zackai E.H., Deardorff M.A., Shaikh T.H., Haan E., Friend K.L., Fichera M., Romano C., Gecz J., DeLisi L.E., Sebat J., King M.C., Shaffer L.G., Eichler E.E. A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay. Nat. Genet. 2010, 42:203-209.
-
(2010)
Nat. Genet.
, vol.42
, pp. 203-209
-
-
Girirajan, S.1
Rosenfeld, J.A.2
Cooper, G.M.3
Antonacci, F.4
Siswara, P.5
Itsara, A.6
Vives, L.7
Walsh, T.8
McCarthy, S.E.9
Baker, C.10
Mefford, H.C.11
Kidd, J.M.12
Browning, S.R.13
Browning, B.L.14
Dickel, D.E.15
Levy, D.L.16
Ballif, B.C.17
Platky, K.18
Farber, D.M.19
Gowans, G.C.20
Wetherbee, J.J.21
Asamoah, A.22
Weaver, D.D.23
Mark, P.R.24
Dickerson, J.25
Garg, B.P.26
Ellingwood, S.A.27
Smith, R.28
Banks, V.C.29
Smith, W.30
McDonald, M.T.31
Hoo, J.J.32
French, B.N.33
Hudson, C.34
Johnson, J.P.35
Ozmore, J.R.36
Moeschler, J.B.37
Surti, U.38
Escobar, L.F.39
El-Khechen, D.40
Gorski, J.L.41
Kussmann, J.42
Salbert, B.43
Lacassie, Y.44
Biser, A.45
McDonald-McGinn, D.M.46
Zackai, E.H.47
Deardorff, M.A.48
Shaikh, T.H.49
Haan, E.50
Friend, K.L.51
Fichera, M.52
Romano, C.53
Gecz, J.54
DeLisi, L.E.55
Sebat, J.56
King, M.C.57
Shaffer, L.G.58
Eichler, E.E.59
more..
-
33
-
-
52149086547
-
Trends in large-scale mouse mutagenesis: from genetics to functional genomics
-
Gondo Y. Trends in large-scale mouse mutagenesis: from genetics to functional genomics. Nat. Rev. Genet. 2008, 9:803-810.
-
(2008)
Nat. Rev. Genet.
, vol.9
, pp. 803-810
-
-
Gondo, Y.1
-
35
-
-
0038823525
-
The endophenotype concept in psychiatry: etymology and strategic intentions
-
Gottesman I.I., Gould T.D. The endophenotype concept in psychiatry: etymology and strategic intentions. Am. J. Psychiatry 2003, 160:636-645.
-
(2003)
Am. J. Psychiatry
, vol.160
, pp. 636-645
-
-
Gottesman, I.I.1
Gould, T.D.2
-
36
-
-
77957172596
-
The bipolar disorder risk allele at CACNA1C also confers risk of recurrent major depression and of schizophrenia
-
Green E.K., Grozeva D., Jones I., Jones L., Kirov G., Caesar S., Gordon-Smith K., Fraser C., Forty L., Russell E., Hamshere M.L., Moskvina V., Nikolov I., Farmer A., McGuffin P., Holmans P.A., Owen M.J., O'Donovan M.C., Craddock N. The bipolar disorder risk allele at CACNA1C also confers risk of recurrent major depression and of schizophrenia. Mol. Psychiatry 2009.
-
(2009)
Mol. Psychiatry
-
-
Green, E.K.1
Grozeva, D.2
Jones, I.3
Jones, L.4
Kirov, G.5
Caesar, S.6
Gordon-Smith, K.7
Fraser, C.8
Forty, L.9
Russell, E.10
Hamshere, M.L.11
Moskvina, V.12
Nikolov, I.13
Farmer, A.14
McGuffin, P.15
Holmans, P.A.16
Owen, M.J.17
O'Donovan, M.C.18
Craddock, N.19
-
37
-
-
33645861074
-
DOC2A and DOC2B are sensors for neuronal activity with unique calcium-dependent and kinetic properties
-
Groffen A.J., Friedrich R., Brian E.C., Ashery U., Verhage M. DOC2A and DOC2B are sensors for neuronal activity with unique calcium-dependent and kinetic properties. J. Neurochem. 2006, 97:818-833.
-
(2006)
J. Neurochem.
, vol.97
, pp. 818-833
-
-
Groffen, A.J.1
Friedrich, R.2
Brian, E.C.3
Ashery, U.4
Verhage, M.5
-
38
-
-
0037303824
-
Induced gene expression in human brain after the split from chimpanzee
-
Gu J., Gu X. Induced gene expression in human brain after the split from chimpanzee. Trends Genet. 2003, 19:63-65.
-
(2003)
Trends Genet.
, vol.19
, pp. 63-65
-
-
Gu, J.1
Gu, X.2
-
39
-
-
56749098073
-
Beta-catenin-mediated Wnt signaling regulates neurogenesis in the ventral telencephalon
-
Gulacsi A.A., Anderson S.A. Beta-catenin-mediated Wnt signaling regulates neurogenesis in the ventral telencephalon. Nat. Neurosci. 2008, 11:1383-1391.
-
(2008)
Nat. Neurosci.
, vol.11
, pp. 1383-1391
-
-
Gulacsi, A.A.1
Anderson, S.A.2
-
40
-
-
36048946374
-
Sez-6 proteins affect dendritic arborization patterns and excitability of cortical pyramidal neurons
-
Gunnersen J.M., Kim M.H., Fuller S.J., De Silva M., Britto J.M., Hammond V.E., Davies P.J., Petrou S., Faber E.S., Sah P., Tan S.S. Sez-6 proteins affect dendritic arborization patterns and excitability of cortical pyramidal neurons. Neuron 2007, 56:621-639.
-
(2007)
Neuron
, vol.56
, pp. 621-639
-
-
Gunnersen, J.M.1
Kim, M.H.2
Fuller, S.J.3
De Silva, M.4
Britto, J.M.5
Hammond, V.E.6
Davies, P.J.7
Petrou, S.8
Faber, E.S.9
Sah, P.10
Tan, S.S.11
-
41
-
-
64349091037
-
SNP imputation in association studies
-
Halperin E., Stephan D.A. SNP imputation in association studies. Nat. Biotechnol. 2009, 27:349-351.
-
(2009)
Nat. Biotechnol.
, vol.27
, pp. 349-351
-
-
Halperin, E.1
Stephan, D.A.2
-
42
-
-
0014044677
-
Schizophrenia as an immunologic disorder I. Demonstration of antibrain globulins by fluorescent antibody techniques
-
Heath R.G., Krupp I.M. Schizophrenia as an immunologic disorder I. Demonstration of antibrain globulins by fluorescent antibody techniques. Arch. Gen. Psychiatry 1967, 16:1-9.
-
(1967)
Arch. Gen. Psychiatry
, vol.16
, pp. 1-9
-
-
Heath, R.G.1
Krupp, I.M.2
-
43
-
-
59149096726
-
15q13.3 microdeletions increase risk of idiopathic generalized epilepsy
-
Helbig I., Mefford H.C., Sharp A.J., Guipponi M., Fichera M., Franke A., Muhle H., de Kovel C., Baker C., von Spiczak S., Kron K.L., Steinich I., Kleefuss-Lie A.A., Leu C., Gaus V., Schmitz B., Klein K.M., Reif P.S., Rosenow F., Weber Y., Lerche H., Zimprich F., Urak L., Fuchs K., Feucht M., Genton P., Thomas P., Visscher F., de Haan G.J., Moller R.S., Hjalgrim H., Luciano D., Wittig M., Nothnagel M., Elger C.E., Nurnberg P., Romano C., Malafosse A., Koeleman B.P., Lindhout D., Stephani U., Schreiber S., Eichler E.E., Sander T. 15q13.3 microdeletions increase risk of idiopathic generalized epilepsy. Nat. Genet. 2009, 41:160-162.
-
(2009)
Nat. Genet.
, vol.41
, pp. 160-162
-
-
Helbig, I.1
Mefford, H.C.2
Sharp, A.J.3
Guipponi, M.4
Fichera, M.5
Franke, A.6
Muhle, H.7
de Kovel, C.8
Baker, C.9
von Spiczak, S.10
Kron, K.L.11
Steinich, I.12
Kleefuss-Lie, A.A.13
Leu, C.14
Gaus, V.15
Schmitz, B.16
Klein, K.M.17
Reif, P.S.18
Rosenow, F.19
Weber, Y.20
Lerche, H.21
Zimprich, F.22
Urak, L.23
Fuchs, K.24
Feucht, M.25
Genton, P.26
Thomas, P.27
Visscher, F.28
de Haan, G.J.29
Moller, R.S.30
Hjalgrim, H.31
Luciano, D.32
Wittig, M.33
Nothnagel, M.34
Elger, C.E.35
Nurnberg, P.36
Romano, C.37
Malafosse, A.38
Koeleman, B.P.39
Lindhout, D.40
Stephani, U.41
Schreiber, S.42
Eichler, E.E.43
Sander, T.44
more..
-
44
-
-
63449117467
-
Segmental copy number variation shapes tissue transcriptomes
-
Henrichsen C.N., Vinckenbosch N., Zollner S., Chaignat E., Pradervand S., Schutz F., Ruedi M., Kaessmann H., Reymond A. Segmental copy number variation shapes tissue transcriptomes. Nat. Genet. 2009, 41:424-429.
-
(2009)
Nat. Genet.
, vol.41
, pp. 424-429
-
-
Henrichsen, C.N.1
Vinckenbosch, N.2
Zollner, S.3
Chaignat, E.4
Pradervand, S.5
Schutz, F.6
Ruedi, M.7
Kaessmann, H.8
Reymond, A.9
-
45
-
-
67249117049
-
Potential etiologic and functional implications of genome-wide association loci for human diseases and traits
-
Hindorff L.A., Sethupathy P., Junkins H.A., Ramos E.M., Mehta J.P., Collins F.S., Manolio T.A. Potential etiologic and functional implications of genome-wide association loci for human diseases and traits. Proc. Natl. Acad. Sci. U.S.A. 2009, 106:9362-9367.
-
(2009)
Proc. Natl. Acad. Sci. U.S.A.
, vol.106
, pp. 9362-9367
-
-
Hindorff, L.A.1
Sethupathy, P.2
Junkins, H.A.3
Ramos, E.M.4
Mehta, J.P.5
Collins, F.S.6
Manolio, T.A.7
-
46
-
-
30044449524
-
A 200-kb region of human chromosome 22q11.2 confers antipsychotic-responsive behavioral abnormalities in mice
-
Hiroi N., Zhu H., Lee M., Funke B., Arai M., Itokawa M., Kucherlapati R., Morrow B., Sawamura T., Agatsuma S. A 200-kb region of human chromosome 22q11.2 confers antipsychotic-responsive behavioral abnormalities in mice. Proc. Natl. Acad. Sci. U.S.A. 2005, 102:19132-19137.
-
(2005)
Proc. Natl. Acad. Sci. U.S.A.
, vol.102
, pp. 19132-19137
-
-
Hiroi, N.1
Zhu, H.2
Lee, M.3
Funke, B.4
Arai, M.5
Itokawa, M.6
Kucherlapati, R.7
Morrow, B.8
Sawamura, T.9
Agatsuma, S.10
-
47
-
-
48949116172
-
Verbal working memory impairments in individuals with schizophrenia and their first-degree relatives: findings from the Consortium on the Genetics of Schizophrenia
-
Horan W.P., Braff D.L., Nuechterlein K.H., Sugar C.A., Cadenhead K.S., Calkins M.E., Dobie D.J., Freedman R., Greenwood T.A., Gur R.E., Gur R.C., Light G.A., Mintz J., Olincy A., Radant A.D., Schork N.J., Seidman L.J., Siever L.J., Silverman J.M., Stone W.S., Swerdlow N.R., Tsuang D.W., Tsuang M.T., Turetsky B.I., Green M.F. Verbal working memory impairments in individuals with schizophrenia and their first-degree relatives: findings from the Consortium on the Genetics of Schizophrenia. Schizophr. Res. 2008, 103:218-228.
-
(2008)
Schizophr. Res.
, vol.103
, pp. 218-228
-
-
Horan, W.P.1
Braff, D.L.2
Nuechterlein, K.H.3
Sugar, C.A.4
Cadenhead, K.S.5
Calkins, M.E.6
Dobie, D.J.7
Freedman, R.8
Greenwood, T.A.9
Gur, R.E.10
Gur, R.C.11
Light, G.A.12
Mintz, J.13
Olincy, A.14
Radant, A.D.15
Schork, N.J.16
Seidman, L.J.17
Siever, L.J.18
Silverman, J.M.19
Stone, W.S.20
Swerdlow, N.R.21
Tsuang, D.W.22
Tsuang, M.T.23
Turetsky, B.I.24
Green, M.F.25
more..
-
48
-
-
0033198239
-
Presynaptic mechanism for phorbol ester-induced synaptic potentiation
-
Hori T., Takai Y., Takahashi T. Presynaptic mechanism for phorbol ester-induced synaptic potentiation. J. Neurosci. 1999, 19:7262-7267.
-
(1999)
J. Neurosci.
, vol.19
, pp. 7262-7267
-
-
Hori, T.1
Takai, Y.2
Takahashi, T.3
-
49
-
-
4444291843
-
Detection of large-scale variation in the human genome
-
Iafrate A.J., Feuk L., Rivera M.N., Listewnik M.L., Donahoe P.K., Qi Y., Scherer S.W., Lee C. Detection of large-scale variation in the human genome. Nat. Genet. 2004, 36:949-951.
-
(2004)
Nat. Genet.
, vol.36
, pp. 949-951
-
-
Iafrate, A.J.1
Feuk, L.2
Rivera, M.N.3
Listewnik, M.L.4
Donahoe, P.K.5
Qi, Y.6
Scherer, S.W.7
Lee, C.8
-
50
-
-
62549134121
-
Genome-wide analysis in vivo of translation with nucleotide resolution using ribosome profiling
-
Ingolia N.T., Ghaemmaghami S., Newman J.R., Weissman J.S. Genome-wide analysis in vivo of translation with nucleotide resolution using ribosome profiling. Science 2009, 324:218-223.
-
(2009)
Science
, vol.324
, pp. 218-223
-
-
Ingolia, N.T.1
Ghaemmaghami, S.2
Newman, J.R.3
Weissman, J.S.4
-
51
-
-
72449180352
-
Mice with genetically altered glutamate receptors as models of schizophrenia: a comprehensive review
-
Inta D., Monyer H., Sprengel R., Meyer-Lindenberg A., Gass P. Mice with genetically altered glutamate receptors as models of schizophrenia: a comprehensive review. Neurosci. Biobehav. Rev. 2010, 34:285-294.
-
(2010)
Neurosci. Biobehav. Rev.
, vol.34
, pp. 285-294
-
-
Inta, D.1
Monyer, H.2
Sprengel, R.3
Meyer-Lindenberg, A.4
Gass, P.5
-
52
-
-
51649107017
-
Rare chromosomal deletions and duplications increase risk of schizophrenia
-
ISC
-
ISC Rare chromosomal deletions and duplications increase risk of schizophrenia. Nature 2008, 455:237-241.
-
(2008)
Nature
, vol.455
, pp. 237-241
-
-
-
53
-
-
33748052338
-
Subtyping schizophrenia: implications for genetic research
-
Jablensky A. Subtyping schizophrenia: implications for genetic research. Mol. Psychiatry 2006, 11:815-836.
-
(2006)
Mol. Psychiatry
, vol.11
, pp. 815-836
-
-
Jablensky, A.1
-
54
-
-
49449094620
-
Disruption of the TCF4 gene in a girl with mental retardation but without the classical Pitt-Hopkins syndrome
-
Kalscheuer V.M., Feenstra I., Van Ravenswaaij-Arts C.M., Smeets D.F., Menzel C., Ullmann R., Musante L., Ropers H.H. Disruption of the TCF4 gene in a girl with mental retardation but without the classical Pitt-Hopkins syndrome. Am. J. Med. Genet. A 2008, 146A:2053-2059.
-
(2008)
Am. J. Med. Genet. A
, vol.146 A
, pp. 2053-2059
-
-
Kalscheuer, V.M.1
Feenstra, I.2
Van Ravenswaaij-Arts, C.M.3
Smeets, D.F.4
Menzel, C.5
Ullmann, R.6
Musante, L.7
Ropers, H.H.8
-
55
-
-
0029102665
-
Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11
-
Karayiorgou M., Morris M.A., Morrow B., Shprintzen R.J., Goldberg R., Borrow J., Gos A., Nestadt G., Wolyniec P.S., Lasseter V.K., et al. Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11. Proc. Natl. Acad. Sci.U.S.A. 1995, 92:7612-7616.
-
(1995)
Proc. Natl. Acad. Sci.U.S.A.
, vol.92
, pp. 7612-7616
-
-
Karayiorgou, M.1
Morris, M.A.2
Morrow, B.3
Shprintzen, R.J.4
Goldberg, R.5
Borrow, J.6
Gos, A.7
Nestadt, G.8
Wolyniec, P.S.9
Lasseter, V.K.10
-
56
-
-
0027272195
-
The Roscommon Family Study I. Methods, diagnosis of probands, and risk of schizophrenia in relatives
-
Kendler K.S., McGuire M., Gruenberg A.M., O'Hare A., Spellman M., Walsh D. The Roscommon Family Study I. Methods, diagnosis of probands, and risk of schizophrenia in relatives. Arch. Gen. Psychiatry 1993, 50:527-540.
-
(1993)
Arch. Gen. Psychiatry
, vol.50
, pp. 527-540
-
-
Kendler, K.S.1
McGuire, M.2
Gruenberg, A.M.3
O'Hare, A.4
Spellman, M.5
Walsh, D.6
-
57
-
-
9444279547
-
Alpha-synuclein induces apoptosis by altered expression in human peripheral lymphocyte in Parkinson's disease
-
Kim S., Jeon B.S., Heo C., Im P.S., Ahn T.B., Seo J.H., Kim H.S., Park C.H., Choi S.H., Cho S.H., Lee W.J., Suh Y.H. Alpha-synuclein induces apoptosis by altered expression in human peripheral lymphocyte in Parkinson's disease. FASEB J. 2004, 18:1615-1617.
-
(2004)
FASEB J.
, vol.18
, pp. 1615-1617
-
-
Kim, S.1
Jeon, B.S.2
Heo, C.3
Im, P.S.4
Ahn, T.B.5
Seo, J.H.6
Kim, H.S.7
Park, C.H.8
Choi, S.H.9
Cho, S.H.10
Lee, W.J.11
Suh, Y.H.12
-
58
-
-
77952367798
-
-
Widespread transcription at neuronal activity-regulated enhancers, Nature [Epub ahead of print].
-
T.K. Kim, M. Hemberg, J.M. Gray, A.M. Costa, D.M. Bear, J. Wu, D.A. Harmin, M. Laptewicz, K. Barbara-Haley, S. Kuersten, E. Markenscoff-Papadimitriou, D. Kuhl, H. Bito, P.F. Worley, G. Kreiman, M.E. Greenberg, Widespread transcription at neuronal activity-regulated enhancers, Nature (2010) [Epub ahead of print].
-
(2010)
-
-
Kim, T.K.1
Hemberg, M.2
Gray, J.M.3
Costa, A.M.4
Bear, D.M.5
Wu, J.6
Harmin, D.A.7
Laptewicz, M.8
Barbara-Haley, K.9
Kuersten, S.10
Markenscoff-Papadimitriou, E.11
Kuhl, D.12
Bito, H.13
Worley, P.F.14
Kreiman, G.15
Greenberg, M.E.16
-
59
-
-
72049114493
-
Induced pluripotent stem (iPS) cells and their future in psychiatry
-
Kim K.S. Induced pluripotent stem (iPS) cells and their future in psychiatry. Neuropsychopharmacology 2010, 35:346-348.
-
(2010)
Neuropsychopharmacology
, vol.35
, pp. 346-348
-
-
Kim, K.S.1
-
60
-
-
0016669094
-
Evolution at two levels in humans and chimpanzees
-
King M.C., Wilson A.C. Evolution at two levels in humans and chimpanzees. Science 1975, 188:107-116.
-
(1975)
Science
, vol.188
, pp. 107-116
-
-
King, M.C.1
Wilson, A.C.2
-
61
-
-
64549147485
-
Support for the involvement of large copy number variants in the pathogenesis of schizophrenia
-
Kirov G., Grozeva D., Norton N., Ivanov D., Mantripragada K.K., Holmans P., Craddock N., Owen M.J., O'Donovan M.C. Support for the involvement of large copy number variants in the pathogenesis of schizophrenia. Hum. Mol. Genet. 2009, 18:1497-1503.
-
(2009)
Hum. Mol. Genet.
, vol.18
, pp. 1497-1503
-
-
Kirov, G.1
Grozeva, D.2
Norton, N.3
Ivanov, D.4
Mantripragada, K.K.5
Holmans, P.6
Craddock, N.7
Owen, M.J.8
O'Donovan, M.C.9
-
62
-
-
38349106160
-
Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia
-
Kirov G., Gumus D., Chen W., Norton N., Georgieva L., Sari M., O'Donovan M.C., Erdogan F., Owen M.J., Ropers H.H., Ullmann R. Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia. Hum. Mol. Genet. 2008, 17:458-465.
-
(2008)
Hum. Mol. Genet.
, vol.17
, pp. 458-465
-
-
Kirov, G.1
Gumus, D.2
Chen, W.3
Norton, N.4
Georgieva, L.5
Sari, M.6
O'Donovan, M.C.7
Erdogan, F.8
Owen, M.J.9
Ropers, H.H.10
Ullmann, R.11
-
63
-
-
11144339384
-
Long-range control of gene expression: emerging mechanisms and disruption in disease
-
Kleinjan D.A., van Heyningen V. Long-range control of gene expression: emerging mechanisms and disruption in disease. Am. J. Hum. Genet. 2005, 76:8-32.
-
(2005)
Am. J. Hum. Genet.
, vol.76
, pp. 8-32
-
-
Kleinjan, D.A.1
van Heyningen, V.2
-
64
-
-
52949085789
-
Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs
-
Korn J.M., Kuruvilla F.G., McCarroll S.A., Wysoker A., Nemesh J., Cawley S., Hubbell E., Veitch J., Collins P.J., Darvishi K., Lee C., Nizzari M.M., Gabriel S.B., Purcell S., Daly M.J., Altshuler D. Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs. Nat. Genet. 2008, 40:1253-1260.
-
(2008)
Nat. Genet.
, vol.40
, pp. 1253-1260
-
-
Korn, J.M.1
Kuruvilla, F.G.2
McCarroll, S.A.3
Wysoker, A.4
Nemesh, J.5
Cawley, S.6
Hubbell, E.7
Veitch, J.8
Collins, P.J.9
Darvishi, K.10
Lee, C.11
Nizzari, M.M.12
Gabriel, S.B.13
Purcell, S.14
Daly, M.J.15
Altshuler, D.16
-
65
-
-
38849126088
-
Recurrent 16p11.2 microdeletions in autism
-
Kumar R.A., KaraMohamed S., Sudi J., Conrad D.F., Brune C., Badner J.A., Gilliam T.C., Nowak N.J., Cook E.H., Dobyns W.B., Christian S.L. Recurrent 16p11.2 microdeletions in autism. Hum. Mol. Genet. 2008, 17:628-638.
-
(2008)
Hum. Mol. Genet.
, vol.17
, pp. 628-638
-
-
Kumar, R.A.1
KaraMohamed, S.2
Sudi, J.3
Conrad, D.F.4
Brune, C.5
Badner, J.A.6
Gilliam, T.C.7
Nowak, N.J.8
Cook, E.H.9
Dobyns, W.B.10
Christian, S.L.11
-
66
-
-
21444461559
-
Is there a relation between APOE expression and brain amyloid load in Alzheimer's disease?
-
Lambert J.C., Mann D., Richard F., Tian J., Shi J., Thaker U., Merrot S., Harris J., Frigard B., Iwatsubo T., Lendon C., Amouyel P. Is there a relation between APOE expression and brain amyloid load in Alzheimer's disease?. J. Neurol. Neurosurg. Psychiatry 2005, 76:928-933.
-
(2005)
J. Neurol. Neurosurg. Psychiatry
, vol.76
, pp. 928-933
-
-
Lambert, J.C.1
Mann, D.2
Richard, F.3
Tian, J.4
Shi, J.5
Thaker, U.6
Merrot, S.7
Harris, J.8
Frigard, B.9
Iwatsubo, T.10
Lendon, C.11
Amouyel, P.12
-
67
-
-
18544369453
-
Risk factors for autism: perinatal factors, parental psychiatric history, and socioeconomic status
-
916-925; discussion 926-918
-
Larsson H.J., Eaton W.W., Madsen K.M., Vestergaard M., Olesen A.V., Agerbo E., Schendel D., Thorsen P., Mortensen P.B. Risk factors for autism: perinatal factors, parental psychiatric history, and socioeconomic status. Am. J. Epidemiol. 2005, 161. 916-925; discussion 926-918.
-
(2005)
Am. J. Epidemiol.
, vol.161
-
-
Larsson, H.J.1
Eaton, W.W.2
Madsen, K.M.3
Vestergaard, M.4
Olesen, A.V.5
Agerbo, E.6
Schendel, D.7
Thorsen, P.8
Mortensen, P.B.9
-
68
-
-
34249332776
-
Converging evidence for a pseudoautosomal cytokine receptor gene locus in schizophrenia
-
Lencz T., Morgan T.V., Athanasiou M., Dain B., Reed C.R., Kane J.M., Kucherlapati R., Malhotra A.K. Converging evidence for a pseudoautosomal cytokine receptor gene locus in schizophrenia. Mol. Psychiatry 2007, 12:572-580.
-
(2007)
Mol. Psychiatry
, vol.12
, pp. 572-580
-
-
Lencz, T.1
Morgan, T.V.2
Athanasiou, M.3
Dain, B.4
Reed, C.R.5
Kane, J.M.6
Kucherlapati, R.7
Malhotra, A.K.8
-
69
-
-
11844278458
-
Conserved seed pairing, often flanked by adenosines, indicates that thousands of human genes are microRNA targets
-
Lewis B.P., Burge C.B., Bartel D.P. Conserved seed pairing, often flanked by adenosines, indicates that thousands of human genes are microRNA targets. Cell 2005, 120:15-20.
-
(2005)
Cell
, vol.120
, pp. 15-20
-
-
Lewis, B.P.1
Burge, C.B.2
Bartel, D.P.3
-
70
-
-
42649111672
-
Evaluation of coverage variation of SNP chips for genome-wide association studies
-
Li M., Li C., Guan W. Evaluation of coverage variation of SNP chips for genome-wide association studies. Eur. J. Hum. Genet. 2008, 16:635-643.
-
(2008)
Eur. J. Hum. Genet.
, vol.16
, pp. 635-643
-
-
Li, M.1
Li, C.2
Guan, W.3
-
71
-
-
50949095168
-
Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data
-
Li B., Leal S.M. Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data. Am. J. Hum. Genet. 2008, 83:311-321.
-
(2008)
Am. J. Hum. Genet.
, vol.83
, pp. 311-321
-
-
Li, B.1
Leal, S.M.2
-
72
-
-
58149464318
-
Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study
-
Lichtenstein P., Yip B.H., Bjork C., Pawitan Y., Cannon T.D., Sullivan P.F., Hultman C.M. Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study. Lancet 2009, 373:234-239.
-
(2009)
Lancet
, vol.373
, pp. 234-239
-
-
Lichtenstein, P.1
Yip, B.H.2
Bjork, C.3
Pawitan, Y.4
Cannon, T.D.5
Sullivan, P.F.6
Hultman, C.M.7
-
73
-
-
34547664096
-
Genomic disorders: molecular mechanisms for rearrangements and conveyed phenotypes
-
Lupski J.R., Stankiewicz P. Genomic disorders: molecular mechanisms for rearrangements and conveyed phenotypes. PLoS Genet. 2005, 1:e49.
-
(2005)
PLoS Genet.
, vol.1
-
-
Lupski, J.R.1
Stankiewicz, P.2
-
74
-
-
67651108806
-
The genetics of quantitative traits: challenges and prospects
-
Mackay T.F., Stone E.A., Ayroles J.F. The genetics of quantitative traits: challenges and prospects. Nat. Rev. Genet. 2009, 10:565-577.
-
(2009)
Nat. Rev. Genet.
, vol.10
, pp. 565-577
-
-
Mackay, T.F.1
Stone, E.A.2
Ayroles, J.F.3
-
75
-
-
0027432603
-
Continuity and discontinuity of affective disorders and schizophrenia. Results of a controlled family study
-
Maier W., Lichtermann D., Minges J., Hallmayer J., Heun R., Benkert O., Levinson D.F. Continuity and discontinuity of affective disorders and schizophrenia. Results of a controlled family study. Arch. Gen. Psychiatry 1993, 50:871-883.
-
(1993)
Arch. Gen. Psychiatry
, vol.50
, pp. 871-883
-
-
Maier, W.1
Lichtermann, D.2
Minges, J.3
Hallmayer, J.4
Heun, R.5
Benkert, O.6
Levinson, D.F.7
-
76
-
-
0036774854
-
The dichotomy of schizophrenia and affective disorders in extended pedigrees
-
Maier W., Lichtermann D., Franke P., Heun R., Falkai P., Rietschel M. The dichotomy of schizophrenia and affective disorders in extended pedigrees. Schizophr. Res. 2002, 57:259-266.
-
(2002)
Schizophr. Res.
, vol.57
, pp. 259-266
-
-
Maier, W.1
Lichtermann, D.2
Franke, P.3
Heun, R.4
Falkai, P.5
Rietschel, M.6
-
77
-
-
70349956433
-
Finding the missing heritability of complex diseases
-
Manolio T.A., Collins F.S., Cox N.J., Goldstein D.B., Hindorff L.A., Hunter D.J., McCarthy M.I., Ramos E.M., Cardon L.R., Chakravarti A., Cho J.H., Guttmacher A.E., Kong A., Kruglyak L., Mardis E., Rotimi C.N., Slatkin M., Valle D., Whittemore A.S., Boehnke M., Clark A.G., Eichler E.E., Gibson G., Haines J.L., Mackay T.F., McCarroll S.A., Visscher P.M. Finding the missing heritability of complex diseases. Nature 2009, 461:747-753.
-
(2009)
Nature
, vol.461
, pp. 747-753
-
-
Manolio, T.A.1
Collins, F.S.2
Cox, N.J.3
Goldstein, D.B.4
Hindorff, L.A.5
Hunter, D.J.6
McCarthy, M.I.7
Ramos, E.M.8
Cardon, L.R.9
Chakravarti, A.10
Cho, J.H.11
Guttmacher, A.E.12
Kong, A.13
Kruglyak, L.14
Mardis, E.15
Rotimi, C.N.16
Slatkin, M.17
Valle, D.18
Whittemore, A.S.19
Boehnke, M.20
Clark, A.G.21
Eichler, E.E.22
Gibson, G.23
Haines, J.L.24
Mackay, T.F.25
McCarroll, S.A.26
Visscher, P.M.27
more..
-
78
-
-
75549091892
-
New strategies and emerging technologies for massively parallel sequencing: applications in medical research
-
Mardis E.R. New strategies and emerging technologies for massively parallel sequencing: applications in medical research. Genome Med. 2009, 1:40.
-
(2009)
Genome Med.
, vol.1
, pp. 40
-
-
Mardis, E.R.1
-
79
-
-
40749089626
-
Structural variation of chromosomes in autism spectrum disorder
-
Marshall C.R., Noor A., Vincent J.B., Lionel A.C., Feuk L., Skaug J., Shago M., Moessner R., Pinto D., Ren Y., Thiruvahindrapduram B., Fiebig A., Schreiber S., Friedman J., Ketelaars C.E., Vos Y.J., Ficicioglu C., Kirkpatrick S., Nicolson R., Sloman L., Summers A., Gibbons C.A., Teebi A., Chitayat D., Weksberg R., Thompson A., Vardy C., Crosbie V., Luscombe S., Baatjes R., Zwaigenbaum L., Roberts W., Fernandez B., Szatmari P., Scherer S.W. Structural variation of chromosomes in autism spectrum disorder. Am. J. Hum. Genet. 2008, 82:477-488.
-
(2008)
Am. J. Hum. Genet.
, vol.82
, pp. 477-488
-
-
Marshall, C.R.1
Noor, A.2
Vincent, J.B.3
Lionel, A.C.4
Feuk, L.5
Skaug, J.6
Shago, M.7
Moessner, R.8
Pinto, D.9
Ren, Y.10
Thiruvahindrapduram, B.11
Fiebig, A.12
Schreiber, S.13
Friedman, J.14
Ketelaars, C.E.15
Vos, Y.J.16
Ficicioglu, C.17
Kirkpatrick, S.18
Nicolson, R.19
Sloman, L.20
Summers, A.21
Gibbons, C.A.22
Teebi, A.23
Chitayat, D.24
Weksberg, R.25
Thompson, A.26
Vardy, C.27
Crosbie, V.28
Luscombe, S.29
Baatjes, R.30
Zwaigenbaum, L.31
Roberts, W.32
Fernandez, B.33
Szatmari, P.34
Scherer, S.W.35
more..
-
80
-
-
18444381728
-
Knockout of ERK1 MAP kinase enhances synaptic plasticity in the striatum and facilitates striatal-mediated learning and memory
-
Mazzucchelli C., Vantaggiato C., Ciamei A., Fasano S., Pakhotin P., Krezel W., Welzl H., Wolfer D.P., Pages G., Valverde O., Marowsky A., Porrazzo A., Orban P.C., Maldonado R., Ehrengruber M.U., Cestari V., Lipp H.P., Chapman P.F., Pouyssegur J., Brambilla R. Knockout of ERK1 MAP kinase enhances synaptic plasticity in the striatum and facilitates striatal-mediated learning and memory. Neuron 2002, 34:807-820.
-
(2002)
Neuron
, vol.34
, pp. 807-820
-
-
Mazzucchelli, C.1
Vantaggiato, C.2
Ciamei, A.3
Fasano, S.4
Pakhotin, P.5
Krezel, W.6
Welzl, H.7
Wolfer, D.P.8
Pages, G.9
Valverde, O.10
Marowsky, A.11
Porrazzo, A.12
Orban, P.C.13
Maldonado, R.14
Ehrengruber, M.U.15
Cestari, V.16
Lipp, H.P.17
Chapman, P.F.18
Pouyssegur, J.19
Brambilla, R.20
more..
-
81
-
-
52949141845
-
Integrated detection and population-genetic analysis of SNPs and copy number variation
-
McCarroll S.A., Kuruvilla F.G., Korn J.M., Cawley S., Nemesh J., Wysoker A., Shapero M.H., de Bakker P.I., Maller J.B., Kirby A., Elliott A.L., Parkin M., Hubbell E., Webster T., Mei R., Veitch J., Collins P.J., Handsaker R., Lincoln S., Nizzari M., Blume J., Jones K.W., Rava R., Daly M.J., Gabriel S.B., Altshuler D. Integrated detection and population-genetic analysis of SNPs and copy number variation. Nat. Genet. 2008, 40:1166-1174.
-
(2008)
Nat. Genet.
, vol.40
, pp. 1166-1174
-
-
McCarroll, S.A.1
Kuruvilla, F.G.2
Korn, J.M.3
Cawley, S.4
Nemesh, J.5
Wysoker, A.6
Shapero, M.H.7
de Bakker, P.I.8
Maller, J.B.9
Kirby, A.10
Elliott, A.L.11
Parkin, M.12
Hubbell, E.13
Webster, T.14
Mei, R.15
Veitch, J.16
Collins, P.J.17
Handsaker, R.18
Lincoln, S.19
Nizzari, M.20
Blume, J.21
Jones, K.W.22
Rava, R.23
Daly, M.J.24
Gabriel, S.B.25
Altshuler, D.26
more..
-
82
-
-
70350626873
-
Microduplications of 16p11.2 are associated with schizophrenia
-
McCarthy S.E., Makarov V., Kirov G., Addington A.M., McClellan J., Yoon S., Perkins D.O., Dickel D.E., Kusenda M., Krastoshevsky O., Krause V., Kumar R.A., Grozeva D., Malhotra D., Walsh T., Zackai E.H., Kaplan P., Ganesh J., Krantz I.D., Spinner N.B., Roccanova P., Bhandari A., Pavon K., Lakshmi B., Leotta A., Kendall J., Lee Y.H., Vacic V., Gary S., Iakoucheva L.M., Crow T.J., Christian S.L., Lieberman J.A., Stroup T.S., Lehtimaki T., Puura K., Haldeman-Englert C., Pearl J., Goodell M., Willour V.L., Derosse P., Steele J., Kassem L., Wolff J., Chitkara N., McMahon F.J., Malhotra A.K., Potash J.B., Schulze T.G., Nothen M.M., Cichon S., Rietschel M., Leibenluft E., Kustanovich V., Lajonchere C.M., Sutcliffe J.S., Skuse D., Gill M., Gallagher L., Mendell N.R., Craddock N., Owen M.J., O'Donovan M.C., Shaikh T.H., Susser E., Delisi L.E., Sullivan P.F., Deutsch C.K., Rapoport J., Levy D.L., King M.C., Sebat J. Microduplications of 16p11.2 are associated with schizophrenia. Nat. Genet. 2009, 41:1223-1227.
-
(2009)
Nat. Genet.
, vol.41
, pp. 1223-1227
-
-
McCarthy, S.E.1
Makarov, V.2
Kirov, G.3
Addington, A.M.4
McClellan, J.5
Yoon, S.6
Perkins, D.O.7
Dickel, D.E.8
Kusenda, M.9
Krastoshevsky, O.10
Krause, V.11
Kumar, R.A.12
Grozeva, D.13
Malhotra, D.14
Walsh, T.15
Zackai, E.H.16
Kaplan, P.17
Ganesh, J.18
Krantz, I.D.19
Spinner, N.B.20
Roccanova, P.21
Bhandari, A.22
Pavon, K.23
Lakshmi, B.24
Leotta, A.25
Kendall, J.26
Lee, Y.H.27
Vacic, V.28
Gary, S.29
Iakoucheva, L.M.30
Crow, T.J.31
Christian, S.L.32
Lieberman, J.A.33
Stroup, T.S.34
Lehtimaki, T.35
Puura, K.36
Haldeman-Englert, C.37
Pearl, J.38
Goodell, M.39
Willour, V.L.40
Derosse, P.41
Steele, J.42
Kassem, L.43
Wolff, J.44
Chitkara, N.45
McMahon, F.J.46
Malhotra, A.K.47
Potash, J.B.48
Schulze, T.G.49
Nothen, M.M.50
Cichon, S.51
Rietschel, M.52
Leibenluft, E.53
Kustanovich, V.54
Lajonchere, C.M.55
Sutcliffe, J.S.56
Skuse, D.57
Gill, M.58
Gallagher, L.59
Mendell, N.R.60
Craddock, N.61
Owen, M.J.62
O'Donovan, M.C.63
Shaikh, T.H.64
Susser, E.65
Delisi, L.E.66
Sullivan, P.F.67
Deutsch, C.K.68
Rapoport, J.69
Levy, D.L.70
King, M.C.71
Sebat, J.72
more..
-
83
-
-
55249091422
-
Schizophrenia: a concise overview of incidence, prevalence, and mortality
-
McGrath J., Saha S., Chant D., Welham J. Schizophrenia: a concise overview of incidence, prevalence, and mortality. Epidemiol. Rev. 2008, 30:67-76.
-
(2008)
Epidemiol. Rev.
, vol.30
, pp. 67-76
-
-
McGrath, J.1
Saha, S.2
Chant, D.3
Welham, J.4
-
84
-
-
54049094444
-
Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes
-
Mefford H.C., Sharp A.J., Baker C., Itsara A., Jiang Z., Buysse K., Huang S., Maloney V.K., Crolla J.A., Baralle D., Collins A., Mercer C., Norga K., de Ravel T., Devriendt K., Bongers E.M., de Leeuw N., Reardon W., Gimelli S., Bena F., Hennekam R.C., Male A., Gaunt L., Clayton-Smith J., Simonic I., Park S.M., Mehta S.G., Nik-Zainal S., Woods C.G., Firth H.V., Parkin G., Fichera M., Reitano S., Lo Giudice M., Li K.E., Casuga I., Broomer A., Conrad B., Schwerzmann M., Raber L., Gallati S., Striano P., Coppola A., Tolmie J.L., Tobias E.S., Lilley C., Armengol L., Spysschaert Y., Verloo P., De Coene A., Goossens L., Mortier G., Speleman F., van Binsbergen E., Nelen M.R., Hochstenbach R., Poot M., Gallagher L., Gill M., McClellan J., King M.C., Regan R., Skinner C., Stevenson R.E., Antonarakis S.E., Chen C., Estivill X., Menten B., Gimelli G., Gribble S., Schwartz S., Sutcliffe J.S., Walsh T., Knight S.J., Sebat J., Romano C., Schwartz C.E., Veltman J.A., de Vries B.B., Vermeesch J.R., Barber J.C., Willatt L., Tassabehji M., Eichler E.E. Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes. N. Engl. J. Med. 2008, 359:1685-1699.
-
(2008)
N. Engl. J. Med.
, vol.359
, pp. 1685-1699
-
-
Mefford, H.C.1
Sharp, A.J.2
Baker, C.3
Itsara, A.4
Jiang, Z.5
Buysse, K.6
Huang, S.7
Maloney, V.K.8
Crolla, J.A.9
Baralle, D.10
Collins, A.11
Mercer, C.12
Norga, K.13
de Ravel, T.14
Devriendt, K.15
Bongers, E.M.16
de Leeuw, N.17
Reardon, W.18
Gimelli, S.19
Bena, F.20
Hennekam, R.C.21
Male, A.22
Gaunt, L.23
Clayton-Smith, J.24
Simonic, I.25
Park, S.M.26
Mehta, S.G.27
Nik-Zainal, S.28
Woods, C.G.29
Firth, H.V.30
Parkin, G.31
Fichera, M.32
Reitano, S.33
Lo Giudice, M.34
Li, K.E.35
Casuga, I.36
Broomer, A.37
Conrad, B.38
Schwerzmann, M.39
Raber, L.40
Gallati, S.41
Striano, P.42
Coppola, A.43
Tolmie, J.L.44
Tobias, E.S.45
Lilley, C.46
Armengol, L.47
Spysschaert, Y.48
Verloo, P.49
De Coene, A.50
Goossens, L.51
Mortier, G.52
Speleman, F.53
van Binsbergen, E.54
Nelen, M.R.55
Hochstenbach, R.56
Poot, M.57
Gallagher, L.58
Gill, M.59
McClellan, J.60
King, M.C.61
Regan, R.62
Skinner, C.63
Stevenson, R.E.64
Antonarakis, S.E.65
Chen, C.66
Estivill, X.67
Menten, B.68
Gimelli, G.69
Gribble, S.70
Schwartz, S.71
Sutcliffe, J.S.72
Walsh, T.73
Knight, S.J.74
Sebat, J.75
Romano, C.76
Schwartz, C.E.77
Veltman, J.A.78
de Vries, B.B.79
Vermeesch, J.R.80
Barber, J.C.81
Willatt, L.82
Tassabehji, M.83
Eichler, E.E.84
more..
-
85
-
-
75149113273
-
An integrative modular approach to systematically predict gene-phenotype associations
-
Mehan M.R., Nunez-Iglesias J., Dai C., Waterman M.S., Zhou X.J. An integrative modular approach to systematically predict gene-phenotype associations. BMC Bioinformatics 2010, 11(Suppl. 1):S62.
-
(2010)
BMC Bioinformatics
, vol.11
, Issue.SUPPL. 1
-
-
Mehan, M.R.1
Nunez-Iglesias, J.2
Dai, C.3
Waterman, M.S.4
Zhou, X.J.5
-
86
-
-
0032530085
-
Role of the Doc2 alpha-Munc13-1 interaction in the neurotransmitter release process
-
Mochida S., Orita S., Sakaguchi G., Sasaki T., Takai Y. Role of the Doc2 alpha-Munc13-1 interaction in the neurotransmitter release process. Proc. Natl. Acad. Sci. U.S.A. 1998, 95:11418-11422.
-
(1998)
Proc. Natl. Acad. Sci. U.S.A.
, vol.95
, pp. 11418-11422
-
-
Mochida, S.1
Orita, S.2
Sakaguchi, G.3
Sasaki, T.4
Takai, Y.5
-
87
-
-
34547216747
-
Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma
-
Moffatt M.F., Kabesch M., Liang L., Dixon A.L., Strachan D., Heath S., Depner M., von Berg A., Bufe A., Rietschel E., Heinzmann A., Simma B., Frischer T., Willis-Owen S.A., Wong K.C., Illig T., Vogelberg C., Weiland S.K., von Mutius E., Abecasis G.R., Farrall M., Gut I.G., Lathrop G.M., Cookson W.O. Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma. Nature 2007, 448:470-473.
-
(2007)
Nature
, vol.448
, pp. 470-473
-
-
Moffatt, M.F.1
Kabesch, M.2
Liang, L.3
Dixon, A.L.4
Strachan, D.5
Heath, S.6
Depner, M.7
von Berg, A.8
Bufe, A.9
Rietschel, E.10
Heinzmann, A.11
Simma, B.12
Frischer, T.13
Willis-Owen, S.A.14
Wong, K.C.15
Illig, T.16
Vogelberg, C.17
Weiland, S.K.18
von Mutius, E.19
Abecasis, G.R.20
Farrall, M.21
Gut, I.G.22
Lathrop, G.M.23
Cookson, W.O.24
more..
-
88
-
-
77950458649
-
Transcriptome genetics using second generation sequencing in a Caucasian population
-
Montgomery S.B., Sammeth M., Gutierrez-Arcelus M., Lach R.P., Ingle C., Nisbett J., Guigo R., Dermitzakis E.T. Transcriptome genetics using second generation sequencing in a Caucasian population. Nature 2010, 464:773-777.
-
(2010)
Nature
, vol.464
, pp. 773-777
-
-
Montgomery, S.B.1
Sammeth, M.2
Gutierrez-Arcelus, M.3
Lach, R.P.4
Ingle, C.5
Nisbett, J.6
Guigo, R.7
Dermitzakis, E.T.8
-
89
-
-
77956649235
-
An evaluation of statistical approaches to rare variant analysis in genetic association studies
-
Morris A.P., Zeggini E. An evaluation of statistical approaches to rare variant analysis in genetic association studies. Genet. Epidemiol. 2009.
-
(2009)
Genet. Epidemiol.
-
-
Morris, A.P.1
Zeggini, E.2
-
90
-
-
54949150182
-
Palmitoylation-dependent neurodevelopmental deficits in a mouse model of 22q11 microdeletion
-
Mukai J., Dhilla A., Drew L.J., Stark K.L., Cao L., MacDermott A.B., Karayiorgou M., Gogos J.A. Palmitoylation-dependent neurodevelopmental deficits in a mouse model of 22q11 microdeletion. Nat. Neurosci. 2008, 11:1302-1310.
-
(2008)
Nat. Neurosci.
, vol.11
, pp. 1302-1310
-
-
Mukai, J.1
Dhilla, A.2
Drew, L.J.3
Stark, K.L.4
Cao, L.5
MacDermott, A.B.6
Karayiorgou, M.7
Gogos, J.A.8
-
91
-
-
0032882849
-
High rates of schizophrenia in adults with velo-cardio-facial syndrome
-
Murphy K.C., Jones L.A., Owen M.J. High rates of schizophrenia in adults with velo-cardio-facial syndrome. Arch. Gen. Psychiatry 1999, 56:940-945.
-
(1999)
Arch. Gen. Psychiatry
, vol.56
, pp. 940-945
-
-
Murphy, K.C.1
Jones, L.A.2
Owen, M.J.3
-
92
-
-
33845899137
-
Human catechol-O-methyltransferase haplotypes modulate protein expression by altering mRNA secondary structure
-
Nackley A.G., Shabalina S.A., Tchivileva I.E., Satterfield K., Korchynskyi O., Makarov S.S., Maixner W., Diatchenko L. Human catechol-O-methyltransferase haplotypes modulate protein expression by altering mRNA secondary structure. Science 2006, 314:1930-1933.
-
(2006)
Science
, vol.314
, pp. 1930-1933
-
-
Nackley, A.G.1
Shabalina, S.A.2
Tchivileva, I.E.3
Satterfield, K.4
Korchynskyi, O.5
Makarov, S.S.6
Maixner, W.7
Diatchenko, L.8
-
93
-
-
61449229353
-
A genome-wide investigation of SNPs and CNVs in schizophrenia
-
Need A.C., Ge D., Weale M.E., Maia J., Feng S., Heinzen E.L., Shianna K.V., Yoon W., Kasperaviciute D., Gennarelli M., Strittmatter W.J., Bonvicini C., Rossi G., Jayathilake K., Cola P.A., McEvoy J.P., Keefe R.S., Fisher E.M., St Jean P.L., Giegling I., Hartmann A.M., Moller H.J., Ruppert A., Fraser G., Crombie C., Middleton L.T., St Clair D., Roses A.D., Muglia P., Francks C., Rujescu D., Meltzer H.Y., Goldstein D.B. A genome-wide investigation of SNPs and CNVs in schizophrenia. PLoS Genet. 2009, 5:e1000373.
-
(2009)
PLoS Genet.
, vol.5
-
-
Need, A.C.1
Ge, D.2
Weale, M.E.3
Maia, J.4
Feng, S.5
Heinzen, E.L.6
Shianna, K.V.7
Yoon, W.8
Kasperaviciute, D.9
Gennarelli, M.10
Strittmatter, W.J.11
Bonvicini, C.12
Rossi, G.13
Jayathilake, K.14
Cola, P.A.15
McEvoy, J.P.16
Keefe, R.S.17
Fisher, E.M.18
St Jean, P.L.19
Giegling, I.20
Hartmann, A.M.21
Moller, H.J.22
Ruppert, A.23
Fraser, G.24
Crombie, C.25
Middleton, L.T.26
St Clair, D.27
Roses, A.D.28
Muglia, P.29
Francks, C.30
Rujescu, D.31
Meltzer, H.Y.32
Goldstein, D.B.33
more..
-
94
-
-
0043122919
-
SIFT: predicting amino acid changes that affect protein function
-
Ng P.C., Henikoff S. SIFT: predicting amino acid changes that affect protein function. Nucleic Acids Res. 2003, 31:3812-3814.
-
(2003)
Nucleic Acids Res.
, vol.31
, pp. 3812-3814
-
-
Ng, P.C.1
Henikoff, S.2
-
95
-
-
77951439152
-
Trait-associated SNPs are more likely to be eQTLs: annotation to enhance discovery from GWAS
-
Nicolae D.L., Gamazon E., Zhang W., Duan S., Dolan M.E., Cox N.J. Trait-associated SNPs are more likely to be eQTLs: annotation to enhance discovery from GWAS. PLoS Genet. 2010, 6:e1000888.
-
(2010)
PLoS Genet.
, vol.6
-
-
Nicolae, D.L.1
Gamazon, E.2
Zhang, W.3
Duan, S.4
Dolan, M.E.5
Cox, N.J.6
-
96
-
-
60549116311
-
A comprehensive evaluation of SNP genotype imputation
-
Nothnagel M., Ellinghaus D., Schreiber S., Krawczak M., Franke A. A comprehensive evaluation of SNP genotype imputation. Hum. Genet. 2009, 125:163-171.
-
(2009)
Hum. Genet.
, vol.125
, pp. 163-171
-
-
Nothnagel, M.1
Ellinghaus, D.2
Schreiber, S.3
Krawczak, M.4
Franke, A.5
-
97
-
-
50449100461
-
Identification of loci associated with schizophrenia by genome-wide association and follow-up
-
O'Donovan M.C., Craddock N., Norton N., Williams H., Peirce T., Moskvina V., Nikolov I., Hamshere M., Carroll L., Georgieva L., Dwyer S., Holmans P., Marchini J.L., Spencer C.C., Howie B., Leung H.T., Hartmann A.M., Moller H.J., Morris D.W., Shi Y., Feng G., Hoffmann P., Propping P., Vasilescu C., Maier W., Rietschel M., Zammit S., Schumacher J., Quinn E.M., Schulze T.G., Williams N.M., Giegling I., Iwata N., Ikeda M., Darvasi A., Shifman S., He L., Duan J., Sanders A.R., Levinson D.F., Gejman P.V., Cichon S., Nothen M.M., Gill M., Corvin A., Rujescu D., Kirov G., Owen M.J., Buccola N.G., Mowry B.J., Freedman R., Amin F., Black D.W., Silverman J.M., Byerley W.F., Cloninger C.R. Identification of loci associated with schizophrenia by genome-wide association and follow-up. Nat. Genet. 2008, 40:1053-1055.
-
(2008)
Nat. Genet.
, vol.40
, pp. 1053-1055
-
-
O'Donovan, M.C.1
Craddock, N.2
Norton, N.3
Williams, H.4
Peirce, T.5
Moskvina, V.6
Nikolov, I.7
Hamshere, M.8
Carroll, L.9
Georgieva, L.10
Dwyer, S.11
Holmans, P.12
Marchini, J.L.13
Spencer, C.C.14
Howie, B.15
Leung, H.T.16
Hartmann, A.M.17
Moller, H.J.18
Morris, D.W.19
Shi, Y.20
Feng, G.21
Hoffmann, P.22
Propping, P.23
Vasilescu, C.24
Maier, W.25
Rietschel, M.26
Zammit, S.27
Schumacher, J.28
Quinn, E.M.29
Schulze, T.G.30
Williams, N.M.31
Giegling, I.32
Iwata, N.33
Ikeda, M.34
Darvasi, A.35
Shifman, S.36
He, L.37
Duan, J.38
Sanders, A.R.39
Levinson, D.F.40
Gejman, P.V.41
Cichon, S.42
Nothen, M.M.43
Gill, M.44
Corvin, A.45
Rujescu, D.46
Kirov, G.47
Owen, M.J.48
Buccola, N.G.49
Mowry, B.J.50
Freedman, R.51
Amin, F.52
Black, D.W.53
Silverman, J.M.54
Byerley, W.F.55
Cloninger, C.R.56
more..
-
98
-
-
0037112088
-
Effect of the ubiquitous transcription factors SP1 and MAZ, on NMDA receptor subunit type 1 (NR1) expression during neuronal differentiation
-
Okamoto S., Sherman K., Bai G., Lipton S.A. Effect of the ubiquitous transcription factors SP1 and MAZ, on NMDA receptor subunit type 1 (NR1) expression during neuronal differentiation. Brain Res. Mol. Brain Res. 2002, 107:89-96.
-
(2002)
Brain Res. Mol. Brain Res.
, vol.107
, pp. 89-96
-
-
Okamoto, S.1
Sherman, K.2
Bai, G.3
Lipton, S.A.4
-
99
-
-
45549092100
-
The genetics of multiple sclerosis: SNPs to pathways to pathogenesis
-
Oksenberg J.R., Baranzini S.E., Sawcer S., Hauser S.L. The genetics of multiple sclerosis: SNPs to pathways to pathogenesis. Nat. Rev. Genet. 2008, 9:516-526.
-
(2008)
Nat. Rev. Genet.
, vol.9
, pp. 516-526
-
-
Oksenberg, J.R.1
Baranzini, S.E.2
Sawcer, S.3
Hauser, S.L.4
-
100
-
-
77953694663
-
-
Optimizing copy number variation analysis using genome-wide short sequence oligonucleotide arrays, Nucleic Acids Res. [Epub ahead of print].
-
D.A. Oldridge, S. Banerjee, S.R. Setlur, A. Sboner, F. Demichelis, Optimizing copy number variation analysis using genome-wide short sequence oligonucleotide arrays, Nucleic Acids Res. (2010) [Epub ahead of print].
-
(2010)
-
-
Oldridge, D.A.1
Banerjee, S.2
Setlur, S.R.3
Sboner, A.4
Demichelis, F.5
-
101
-
-
56749098074
-
Deep surveying of alternative splicing complexity in the human transcriptome by high-throughput sequencing
-
Pan Q., Shai O., Lee L.J., Frey B.J., Blencowe B.J. Deep surveying of alternative splicing complexity in the human transcriptome by high-throughput sequencing. Nat. Genet. 2008, 40:1413-1415.
-
(2008)
Nat. Genet.
, vol.40
, pp. 1413-1415
-
-
Pan, Q.1
Shai, O.2
Lee, L.J.3
Frey, B.J.4
Blencowe, B.J.5
-
102
-
-
77951719393
-
Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing
-
Park H., Kim J.I., Ju Y.S., Gokcumen O., Mills R.E., Kim S., Lee S., Suh D., Hong D., Kang H.P., Yoo Y.J., Shin J.Y., Kim H.J., Yavartanoo M., Chang Y.W., Ha J.S., Chong W., Hwang G.R., Darvishi K., Kim H., Yang S.J., Yang K.S., Hurles M.E., Scherer S.W., Carter N.P., Tyler-Smith C., Lee C., Seo J.S. Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing. Nat. Genet. 2010, 42:400-405.
-
(2010)
Nat. Genet.
, vol.42
, pp. 400-405
-
-
Park, H.1
Kim, J.I.2
Ju, Y.S.3
Gokcumen, O.4
Mills, R.E.5
Kim, S.6
Lee, S.7
Suh, D.8
Hong, D.9
Kang, H.P.10
Yoo, Y.J.11
Shin, J.Y.12
Kim, H.J.13
Yavartanoo, M.14
Chang, Y.W.15
Ha, J.S.16
Chong, W.17
Hwang, G.R.18
Darvishi, K.19
Kim, H.20
Yang, S.J.21
Yang, K.S.22
Hurles, M.E.23
Scherer, S.W.24
Carter, N.P.25
Tyler-Smith, C.26
Lee, C.27
Seo, J.S.28
more..
-
103
-
-
67649440746
-
Major vault protein is expressed along the nucleus-neurite axis and associates with mRNAs in cortical neurons
-
Paspalas C.D., Perley C.C., Venkitaramani D.V., Goebel-Goody S.M., Zhang Y., Kurup P., Mattis J.H., Lombroso P.J. Major vault protein is expressed along the nucleus-neurite axis and associates with mRNAs in cortical neurons. Cereb. Cortex 2009, 19:1666-1677.
-
(2009)
Cereb. Cortex
, vol.19
, pp. 1666-1677
-
-
Paspalas, C.D.1
Perley, C.C.2
Venkitaramani, D.V.3
Goebel-Goody, S.M.4
Zhang, Y.5
Kurup, P.6
Mattis, J.H.7
Lombroso, P.J.8
-
104
-
-
27644478443
-
Transcriptional and behavioral interaction between 22q11.2 orthologs modulates schizophrenia-related phenotypes in mice
-
Paterlini M., Zakharenko S.S., Lai W.S., Qin J., Zhang H., Mukai J., Westphal K.G., Olivier B., Sulzer D., Pavlidis P., Siegelbaum S.A., Karayiorgou M., Gogos J.A. Transcriptional and behavioral interaction between 22q11.2 orthologs modulates schizophrenia-related phenotypes in mice. Nat. Neurosci. 2005, 8:1586-1594.
-
(2005)
Nat. Neurosci.
, vol.8
, pp. 1586-1594
-
-
Paterlini, M.1
Zakharenko, S.S.2
Lai, W.S.3
Qin, J.4
Zhang, H.5
Mukai, J.6
Westphal, K.G.7
Olivier, B.8
Sulzer, D.9
Pavlidis, P.10
Siegelbaum, S.A.11
Karayiorgou, M.12
Gogos, J.A.13
-
105
-
-
33646733029
-
Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome
-
Paylor R., Glaser B., Mupo A., Ataliotis P., Spencer C., Sobotka A., Sparks C., Choi C.H., Oghalai J., Curran S., Murphy K.C., Monks S., Williams N., O'Donovan M.C., Owen M.J., Scambler P.J., Lindsay E. Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome. Proc. Natl. Acad. Sci. U.S.A. 2006, 103:7729-7734.
-
(2006)
Proc. Natl. Acad. Sci. U.S.A.
, vol.103
, pp. 7729-7734
-
-
Paylor, R.1
Glaser, B.2
Mupo, A.3
Ataliotis, P.4
Spencer, C.5
Sobotka, A.6
Sparks, C.7
Choi, C.H.8
Oghalai, J.9
Curran, S.10
Murphy, K.C.11
Monks, S.12
Williams, N.13
O'Donovan, M.C.14
Owen, M.J.15
Scambler, P.J.16
Lindsay, E.17
-
106
-
-
77950460661
-
Understanding mechanisms underlying human gene expression variation with RNA sequencing
-
Pickrell J.K., Marioni J.C., Pai A.A., Degner J.F., Engelhardt B.E., Nkadori E., Veyrieras J.B., Stephens M., Gilad Y., Pritchard J.K. Understanding mechanisms underlying human gene expression variation with RNA sequencing. Nature 2010, 464:768-772.
-
(2010)
Nature
, vol.464
, pp. 768-772
-
-
Pickrell, J.K.1
Marioni, J.C.2
Pai, A.A.3
Degner, J.F.4
Engelhardt, B.E.5
Nkadori, E.6
Veyrieras, J.B.7
Stephens, M.8
Gilad, Y.9
Pritchard, J.K.10
-
107
-
-
68449086236
-
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder
-
Purcell S.M., Wray N.R., Stone J.L., Visscher P.M., O'Donovan M.C., Sullivan P.F., Sklar P. Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. Nature 2009, 460:748-752.
-
(2009)
Nature
, vol.460
, pp. 748-752
-
-
Purcell, S.M.1
Wray, N.R.2
Stone, J.L.3
Visscher, P.M.4
O'Donovan, M.C.5
Sullivan, P.F.6
Sklar, P.7
-
108
-
-
70349117273
-
Characterization of small RNAs in aplysia reveals a role for miR-124 in constraining synaptic plasticity through CREB
-
Rajasethupathy P., Fiumara F., Sheridan R., Betel D., Puthanveettil S.V., Russo J.J., Sander C., Tuschl T., Kandel E. Characterization of small RNAs in aplysia reveals a role for miR-124 in constraining synaptic plasticity through CREB. Neuron 2009, 63:803-817.
-
(2009)
Neuron
, vol.63
, pp. 803-817
-
-
Rajasethupathy, P.1
Fiumara, F.2
Sheridan, R.3
Betel, D.4
Puthanveettil, S.V.5
Russo, J.J.6
Sander, C.7
Tuschl, T.8
Kandel, E.9
-
109
-
-
60549106509
-
Disruption of the neurexin 1 gene is associated with schizophrenia
-
Rujescu D., Ingason A., Cichon S., Pietilainen O.P., Barnes M.R., Toulopoulou T., Picchioni M., Vassos E., Ettinger U., Bramon E., Murray R., Ruggeri M., Tosato S., Bonetto C., Steinberg S., Sigurdsson E., Sigmundsson T., Petursson H., Gylfason A., Olason P.I., Hardarsson G., Jonsdottir G.A., Gustafsson O., Fossdal R., Giegling I., Moller H.J., Hartmann A.M., Hoffmann P., Crombie C., Fraser G., Walker N., Lonnqvist J., Suvisaari J., Tuulio-Henriksson A., Djurovic S., Melle I., Andreassen O.A., Hansen T., Werge T., Kiemeney L.A., Franke B., Veltman J., Buizer-Voskamp J.E., Sabatti C., Ophoff R.A., Rietschel M., Nothen M.M., Stefansson K., Peltonen L., St Clair D., Stefansson H., Collier D.A. Disruption of the neurexin 1 gene is associated with schizophrenia. Hum. Mol. Genet. 2009, 18:988-996.
-
(2009)
Hum. Mol. Genet.
, vol.18
, pp. 988-996
-
-
Rujescu, D.1
Ingason, A.2
Cichon, S.3
Pietilainen, O.P.4
Barnes, M.R.5
Toulopoulou, T.6
Picchioni, M.7
Vassos, E.8
Ettinger, U.9
Bramon, E.10
Murray, R.11
Ruggeri, M.12
Tosato, S.13
Bonetto, C.14
Steinberg, S.15
Sigurdsson, E.16
Sigmundsson, T.17
Petursson, H.18
Gylfason, A.19
Olason, P.I.20
Hardarsson, G.21
Jonsdottir, G.A.22
Gustafsson, O.23
Fossdal, R.24
Giegling, I.25
Moller, H.J.26
Hartmann, A.M.27
Hoffmann, P.28
Crombie, C.29
Fraser, G.30
Walker, N.31
Lonnqvist, J.32
Suvisaari, J.33
Tuulio-Henriksson, A.34
Djurovic, S.35
Melle, I.36
Andreassen, O.A.37
Hansen, T.38
Werge, T.39
Kiemeney, L.A.40
Franke, B.41
Veltman, J.42
Buizer-Voskamp, J.E.43
Sabatti, C.44
Ophoff, R.A.45
Rietschel, M.46
Nothen, M.M.47
Stefansson, K.48
Peltonen, L.49
St Clair, D.50
Stefansson, H.51
Collier, D.A.52
more..
-
110
-
-
16844366262
-
Haplotypic association spanning the 22q11.21 genes COMT and ARVCF with schizophrenia
-
Sanders A.R., Rusu I., Duan J., Vander Molen J.E., Hou C., Schwab S.G., Wildenauer D.B., Martinez M., Gejman P.V. Haplotypic association spanning the 22q11.21 genes COMT and ARVCF with schizophrenia. Mol. Psychiatry 2005, 10:353-365.
-
(2005)
Mol. Psychiatry
, vol.10
, pp. 353-365
-
-
Sanders, A.R.1
Rusu, I.2
Duan, J.3
Vander Molen, J.E.4
Hou, C.5
Schwab, S.G.6
Wildenauer, D.B.7
Martinez, M.8
Gejman, P.V.9
-
111
-
-
43349097737
-
No significant association of 14 candidate genes with schizophrenia in a large European ancestry sample: implications for psychiatric genetics
-
Sanders A.R., Duan J., Levinson D.F., Shi J., He D., Hou C., Burrell G.J., Rice J.P., Nertney D.A., Olincy A., Rozic P., Vinogradov S., Buccola N.G., Mowry B.J., Freedman R., Amin F., Black D.W., Silverman J.M., Byerley W.F., Crowe R.R., Cloninger C.R., Martinez M., Gejman P.V. No significant association of 14 candidate genes with schizophrenia in a large European ancestry sample: implications for psychiatric genetics. Am. J. Psychiatry 2008.
-
(2008)
Am. J. Psychiatry
-
-
Sanders, A.R.1
Duan, J.2
Levinson, D.F.3
Shi, J.4
He, D.5
Hou, C.6
Burrell, G.J.7
Rice, J.P.8
Nertney, D.A.9
Olincy, A.10
Rozic, P.11
Vinogradov, S.12
Buccola, N.G.13
Mowry, B.J.14
Freedman, R.15
Amin, F.16
Black, D.W.17
Silverman, J.M.18
Byerley, W.F.19
Crowe, R.R.20
Cloninger, C.R.21
Martinez, M.22
Gejman, P.V.23
more..
-
112
-
-
70549084415
-
Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease
-
Satake W., Nakabayashi Y., Mizuta I., Hirota Y., Ito C., Kubo M., Kawaguchi T., Tsunoda T., Watanabe M., Takeda A., Tomiyama H., Nakashima K., Hasegawa K., Obata F., Yoshikawa T., Kawakami H., Sakoda S., Yamamoto M., Hattori N., Murata M., Nakamura Y., Toda T. Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease. Nat. Genet. 2009, 41:1303-1307.
-
(2009)
Nat. Genet.
, vol.41
, pp. 1303-1307
-
-
Satake, W.1
Nakabayashi, Y.2
Mizuta, I.3
Hirota, Y.4
Ito, C.5
Kubo, M.6
Kawaguchi, T.7
Tsunoda, T.8
Watanabe, M.9
Takeda, A.10
Tomiyama, H.11
Nakashima, K.12
Hasegawa, K.13
Obata, F.14
Yoshikawa, T.15
Kawakami, H.16
Sakoda, S.17
Yamamoto, M.18
Hattori, N.19
Murata, M.20
Nakamura, Y.21
Toda, T.22
more..
-
113
-
-
70249134919
-
Molecular networks as sensors and drivers of common human diseases
-
Schadt E.E. Molecular networks as sensors and drivers of common human diseases. Nature 2009, 461:218-223.
-
(2009)
Nature
, vol.461
, pp. 218-223
-
-
Schadt, E.E.1
-
114
-
-
70450248489
-
MicroRNAs at the synapse
-
Schratt G. microRNAs at the synapse. Nat. Rev. Neurosci. 2009, 10:842-849.
-
(2009)
Nat. Rev. Neurosci.
, vol.10
, pp. 842-849
-
-
Schratt, G.1
-
115
-
-
34247481814
-
Strong association of de novo copy number mutations with autism
-
Sebat J., Lakshmi B., Malhotra D., Troge J., Lese-Martin C., Walsh T., Yamrom B., Yoon S., Krasnitz A., Kendall J., Leotta A., Pai D., Zhang R., Lee Y.H., Hicks J., Spence S.J., Lee A.T., Puura K., Lehtimaki T., Ledbetter D., Gregersen P.K., Bregman J., Sutcliffe J.S., Jobanputra V., Chung W., Warburton D., King M.C., Skuse D., Geschwind D.H., Gilliam T.C., Ye K., Wigler M. Strong association of de novo copy number mutations with autism. Science 2007, 316:445-449.
-
(2007)
Science
, vol.316
, pp. 445-449
-
-
Sebat, J.1
Lakshmi, B.2
Malhotra, D.3
Troge, J.4
Lese-Martin, C.5
Walsh, T.6
Yamrom, B.7
Yoon, S.8
Krasnitz, A.9
Kendall, J.10
Leotta, A.11
Pai, D.12
Zhang, R.13
Lee, Y.H.14
Hicks, J.15
Spence, S.J.16
Lee, A.T.17
Puura, K.18
Lehtimaki, T.19
Ledbetter, D.20
Gregersen, P.K.21
Bregman, J.22
Sutcliffe, J.S.23
Jobanputra, V.24
Chung, W.25
Warburton, D.26
King, M.C.27
Skuse, D.28
Geschwind, D.H.29
Gilliam, T.C.30
Ye, K.31
Wigler, M.32
more..
-
116
-
-
79952817229
-
Do COMT, BDNF and NRG1 polymorphisms influence P50 sensory gating in psychosis?
-
Shaikh M., Hall M.H., Schulze K., Dutt A., Walshe M., Williams I., Constante M., Picchioni M., Toulopoulou T., Collier D., Rijsdijk F., Powell J., Arranz M., Murray R.M., Bramon E. Do COMT, BDNF and NRG1 polymorphisms influence P50 sensory gating in psychosis?. Psychol. Med. 2010, 1-14.
-
(2010)
Psychol. Med.
, pp. 1-14
-
-
Shaikh, M.1
Hall, M.H.2
Schulze, K.3
Dutt, A.4
Walshe, M.5
Williams, I.6
Constante, M.7
Picchioni, M.8
Toulopoulou, T.9
Collier, D.10
Rijsdijk, F.11
Powell, J.12
Arranz, M.13
Murray, R.M.14
Bramon, E.15
-
117
-
-
39749154724
-
A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures
-
Sharp A.J., Mefford H.C., Li K., Baker C., Skinner C., Stevenson R.E., Schroer R.J., Novara F., De Gregori M., Ciccone R., Broomer A., Casuga I., Wang Y., Xiao C., Barbacioru C., Gimelli G., Bernardina B.D., Torniero C., Giorda R., Regan R., Murday V., Mansour S., Fichera M., Castiglia L., Failla P., Ventura M., Jiang Z., Cooper G.M., Knight S.J., Romano C., Zuffardi O., Chen C., Schwartz C.E., Eichler E.E. A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures. Nat. Genet. 2008, 40:322-328.
-
(2008)
Nat. Genet.
, vol.40
, pp. 322-328
-
-
Sharp, A.J.1
Mefford, H.C.2
Li, K.3
Baker, C.4
Skinner, C.5
Stevenson, R.E.6
Schroer, R.J.7
Novara, F.8
De Gregori, M.9
Ciccone, R.10
Broomer, A.11
Casuga, I.12
Wang, Y.13
Xiao, C.14
Barbacioru, C.15
Gimelli, G.16
Bernardina, B.D.17
Torniero, C.18
Giorda, R.19
Regan, R.20
Murday, V.21
Mansour, S.22
Fichera, M.23
Castiglia, L.24
Failla, P.25
Ventura, M.26
Jiang, Z.27
Cooper, G.M.28
Knight, S.J.29
Romano, C.30
Zuffardi, O.31
Chen, C.32
Schwartz, C.E.33
Eichler, E.E.34
more..
-
118
-
-
68449096727
-
Common variants on chromosome 6p22.1 are associated with schizophrenia
-
Shi J., Levinson D.F., Duan J., Sanders A.R., Zheng Y., Pe'er I., Dudbridge F., Holmans P.A., Whittemore A.S., Mowry B.J., Olincy A., Amin F., Cloninger C.R., Silverman J.M., Buccola N.G., Byerley W.F., Black D.W., Crowe R.R., Oksenberg J.R., Mirel D.B., Kendler K.S., Freedman R., Gejman P.V. Common variants on chromosome 6p22.1 are associated with schizophrenia. Nature 2009, 460:753-757.
-
(2009)
Nature
, vol.460
, pp. 753-757
-
-
Shi, J.1
Levinson, D.F.2
Duan, J.3
Sanders, A.R.4
Zheng, Y.5
Pe'er, I.6
Dudbridge, F.7
Holmans, P.A.8
Whittemore, A.S.9
Mowry, B.J.10
Olincy, A.11
Amin, F.12
Cloninger, C.R.13
Silverman, J.M.14
Buccola, N.G.15
Byerley, W.F.16
Black, D.W.17
Crowe, R.R.18
Oksenberg, J.R.19
Mirel, D.B.20
Kendler, K.S.21
Freedman, R.22
Gejman, P.V.23
more..
-
119
-
-
0026511481
-
Late-onset psychosis in the velo-cardio-facial syndrome
-
Shprintzen R.J., Goldberg R., Golding-Kushner K.J., Marion R.W. Late-onset psychosis in the velo-cardio-facial syndrome. Am. J. Med. Genet. 1992, 42:141-142.
-
(1992)
Am. J. Med. Genet.
, vol.42
, pp. 141-142
-
-
Shprintzen, R.J.1
Goldberg, R.2
Golding-Kushner, K.J.3
Marion, R.W.4
-
120
-
-
44149115417
-
Velo-cardio-facial syndrome: 30 years of study
-
Shprintzen R.J. Velo-cardio-facial syndrome: 30 years of study. Dev. Disabil. Res. Rev. 2008, 14:3-10.
-
(2008)
Dev. Disabil. Res. Rev.
, vol.14
, pp. 3-10
-
-
Shprintzen, R.J.1
-
121
-
-
43949118134
-
Whole-genome association study of bipolar disorder
-
Sklar P., Smoller J.W., Fan J., Ferreira M.A., Perlis R.H., Chambert K., Nimgaonkar V.L., McQueen M.B., Faraone S.V., Kirby A., de Bakker P.I., Ogdie M.N., Thase M.E., Sachs G.S., Todd-Brown K., Gabriel S.B., Sougnez C., Gates C., Blumenstiel B., Defelice M., Ardlie K.G., Franklin J., Muir W.J., McGhee K.A., MacIntyre D.J., McLean A., VanBeck M., McQuillin A., Bass N.J., Robinson M., Lawrence J., Anjorin A., Curtis D., Scolnick E.M., Daly M.J., Blackwood D.H., Gurling H.M., Purcell S.M. Whole-genome association study of bipolar disorder. Mol. Psychiatry 2008, 13:558-569.
-
(2008)
Mol. Psychiatry
, vol.13
, pp. 558-569
-
-
Sklar, P.1
Smoller, J.W.2
Fan, J.3
Ferreira, M.A.4
Perlis, R.H.5
Chambert, K.6
Nimgaonkar, V.L.7
McQueen, M.B.8
Faraone, S.V.9
Kirby, A.10
de Bakker, P.I.11
Ogdie, M.N.12
Thase, M.E.13
Sachs, G.S.14
Todd-Brown, K.15
Gabriel, S.B.16
Sougnez, C.17
Gates, C.18
Blumenstiel, B.19
Defelice, M.20
Ardlie, K.G.21
Franklin, J.22
Muir, W.J.23
McGhee, K.A.24
MacIntyre, D.J.25
McLean, A.26
VanBeck, M.27
McQuillin, A.28
Bass, N.J.29
Robinson, M.30
Lawrence, J.31
Anjorin, A.32
Curtis, D.33
Scolnick, E.M.34
Daly, M.J.35
Blackwood, D.H.36
Gurling, H.M.37
Purcell, S.M.38
more..
-
122
-
-
43949124669
-
Altered brain microRNA biogenesis contributes to phenotypic deficits in a 22q11-deletion mouse model
-
Stark K.L., Xu B., Bagchi A., Lai W.S., Liu H., Hsu R., Wan X., Pavlidis P., Mills A.A., Karayiorgou M., Gogos J.A. Altered brain microRNA biogenesis contributes to phenotypic deficits in a 22q11-deletion mouse model. Nat. Genet. 2008, 40:751-760.
-
(2008)
Nat. Genet.
, vol.40
, pp. 751-760
-
-
Stark, K.L.1
Xu, B.2
Bagchi, A.3
Lai, W.S.4
Liu, H.5
Hsu, R.6
Wan, X.7
Pavlidis, P.8
Mills, A.A.9
Karayiorgou, M.10
Gogos, J.A.11
-
123
-
-
49949085933
-
Large recurrent microdeletions associated with schizophrenia
-
Stefansson H., Rujescu D., Cichon S., Pietilainen O.P., Ingason A., Steinberg S., Fossdal R., Sigurdsson E., Sigmundsson T., Buizer-Voskamp J.E., Hansen T., Jakobsen K.D., Muglia P., Francks C., Matthews P.M., Gylfason A., Halldorsson B.V., Gudbjartsson D., Thorgeirsson T.E., Sigurdsson A., Jonasdottir A., Bjornsson A., Mattiasdottir S., Blondal T., Haraldsson M., Magnusdottir B.B., Giegling I., Moller H.J., Hartmann A., Shianna K.V., Ge D., Need A.C., Crombie C., Fraser G., Walker N., Lonnqvist J., Suvisaari J., Tuulio-Henriksson A., Paunio T., Toulopoulou T., Bramon E., Di Forti M., Murray R., Ruggeri M., Vassos E., Tosato S., Walshe M., Li T., Vasilescu C., Muhleisen T.W., Wang A.G., Ullum H., Djurovic S., Melle I., Olesen J., Kiemeney L.A., Franke B., Sabatti C., Freimer N.B., Gulcher J.R., Thorsteinsdottir U., Kong A., Andreassen O.A., Ophoff R.A., Georgi A., Rietschel M., Werge T., Petursson H., Goldstein D.B., Nothen M.M., Peltonen L., Collier D.A., St Clair D., Stefansson K. Large recurrent microdeletions associated with schizophrenia. Nature 2008, 455:232-236.
-
(2008)
Nature
, vol.455
, pp. 232-236
-
-
Stefansson, H.1
Rujescu, D.2
Cichon, S.3
Pietilainen, O.P.4
Ingason, A.5
Steinberg, S.6
Fossdal, R.7
Sigurdsson, E.8
Sigmundsson, T.9
Buizer-Voskamp, J.E.10
Hansen, T.11
Jakobsen, K.D.12
Muglia, P.13
Francks, C.14
Matthews, P.M.15
Gylfason, A.16
Halldorsson, B.V.17
Gudbjartsson, D.18
Thorgeirsson, T.E.19
Sigurdsson, A.20
Jonasdottir, A.21
Bjornsson, A.22
Mattiasdottir, S.23
Blondal, T.24
Haraldsson, M.25
Magnusdottir, B.B.26
Giegling, I.27
Moller, H.J.28
Hartmann, A.29
Shianna, K.V.30
Ge, D.31
Need, A.C.32
Crombie, C.33
Fraser, G.34
Walker, N.35
Lonnqvist, J.36
Suvisaari, J.37
Tuulio-Henriksson, A.38
Paunio, T.39
Toulopoulou, T.40
Bramon, E.41
Di Forti, M.42
Murray, R.43
Ruggeri, M.44
Vassos, E.45
Tosato, S.46
Walshe, M.47
Li, T.48
Vasilescu, C.49
Muhleisen, T.W.50
Wang, A.G.51
Ullum, H.52
Djurovic, S.53
Melle, I.54
Olesen, J.55
Kiemeney, L.A.56
Franke, B.57
Sabatti, C.58
Freimer, N.B.59
Gulcher, J.R.60
Thorsteinsdottir, U.61
Kong, A.62
Andreassen, O.A.63
Ophoff, R.A.64
Georgi, A.65
Rietschel, M.66
Werge, T.67
Petursson, H.68
Goldstein, D.B.69
Nothen, M.M.70
Peltonen, L.71
Collier, D.A.72
St Clair, D.73
Stefansson, K.74
more..
-
124
-
-
68449090594
-
Common variants conferring risk of schizophrenia
-
Stefansson H., Ophoff R.A., Steinberg S., Andreassen O.A., Cichon S., Rujescu D., Werge T., Pietilainen O.P., Mors O., Mortensen P.B., Sigurdsson E., Gustafsson O., Nyegaard M., Tuulio-Henriksson A., Ingason A., Hansen T., Suvisaari J., Lonnqvist J., Paunio T., Borglum A.D., Hartmann A., Fink-Jensen A., Nordentoft M., Hougaard D., Norgaard-Pedersen B., Bottcher Y., Olesen J., Breuer R., Moller H.J., Giegling I., Rasmussen H.B., Timm S., Mattheisen M., Bitter I., Rethelyi J.M., Magnusdottir B.B., Sigmundsson T., Olason P., Masson G., Gulcher J.R., Haraldsson M., Fossdal R., Thorgeirsson T.E., Thorsteinsdottir U., Ruggeri M., Tosato S., Franke B., Strengman E., Kiemeney L.A., Melle I., Djurovic S., Abramova L., Kaleda V., Sanjuan J., de Frutos R., Bramon E., Vassos E., Fraser G., Ettinger U., Picchioni M., Walker N., Toulopoulou T., Need A.C., Ge D., Yoon J.L., Shianna K.V., Freimer N.B., Cantor R.M., Murray R., Kong A., Golimbet V., Carracedo A., Arango C., Costas J., Jonsson E.G., Terenius L., Agartz I., Petursson H., Nothen M.M., Rietschel M., Matthews P.M., Muglia P., Peltonen L., St Clair D., Goldstein D.B., Stefansson K., Collier D.A. Common variants conferring risk of schizophrenia. Nature 2009, 460:744-747.
-
(2009)
Nature
, vol.460
, pp. 744-747
-
-
Stefansson, H.1
Ophoff, R.A.2
Steinberg, S.3
Andreassen, O.A.4
Cichon, S.5
Rujescu, D.6
Werge, T.7
Pietilainen, O.P.8
Mors, O.9
Mortensen, P.B.10
Sigurdsson, E.11
Gustafsson, O.12
Nyegaard, M.13
Tuulio-Henriksson, A.14
Ingason, A.15
Hansen, T.16
Suvisaari, J.17
Lonnqvist, J.18
Paunio, T.19
Borglum, A.D.20
Hartmann, A.21
Fink-Jensen, A.22
Nordentoft, M.23
Hougaard, D.24
Norgaard-Pedersen, B.25
Bottcher, Y.26
Olesen, J.27
Breuer, R.28
Moller, H.J.29
Giegling, I.30
Rasmussen, H.B.31
Timm, S.32
Mattheisen, M.33
Bitter, I.34
Rethelyi, J.M.35
Magnusdottir, B.B.36
Sigmundsson, T.37
Olason, P.38
Masson, G.39
Gulcher, J.R.40
Haraldsson, M.41
Fossdal, R.42
Thorgeirsson, T.E.43
Thorsteinsdottir, U.44
Ruggeri, M.45
Tosato, S.46
Franke, B.47
Strengman, E.48
Kiemeney, L.A.49
Melle, I.50
Djurovic, S.51
Abramova, L.52
Kaleda, V.53
Sanjuan, J.54
de Frutos, R.55
Bramon, E.56
Vassos, E.57
Fraser, G.58
Ettinger, U.59
Picchioni, M.60
Walker, N.61
Toulopoulou, T.62
Need, A.C.63
Ge, D.64
Yoon, J.L.65
Shianna, K.V.66
Freimer, N.B.67
Cantor, R.M.68
Murray, R.69
Kong, A.70
Golimbet, V.71
Carracedo, A.72
Arango, C.73
Costas, J.74
Jonsson, E.G.75
Terenius, L.76
Agartz, I.77
Petursson, H.78
Nothen, M.M.79
Rietschel, M.80
Matthews, P.M.81
Muglia, P.82
Peltonen, L.83
St Clair, D.84
Goldstein, D.B.85
Stefansson, K.86
Collier, D.A.87
more..
-
125
-
-
43949122950
-
Genomewide association for schizophrenia in the CATIE study: results of stage 1
-
Sullivan P.F., Lin D., Tzeng J.Y., van den Oord E., Perkins D., Stroup T.S., Wagner M., Lee S., Wright F.A., Zou F., Liu W., Downing A.M., Lieberman J., Close S.L. Genomewide association for schizophrenia in the CATIE study: results of stage 1. Mol. Psychiatry 2008, 13:570-584.
-
(2008)
Mol. Psychiatry
, vol.13
, pp. 570-584
-
-
Sullivan, P.F.1
Lin, D.2
Tzeng, J.Y.3
van den Oord, E.4
Perkins, D.5
Stroup, T.S.6
Wagner, M.7
Lee, S.8
Wright, F.A.9
Zou, F.10
Liu, W.11
Downing, A.M.12
Lieberman, J.13
Close, S.L.14
-
126
-
-
47649124124
-
A global view of gene activity and alternative splicing by deep sequencing of the human transcriptome
-
Sultan M., Schulz M.H., Richard H., Magen A., Klingenhoff A., Scherf M., Seifert M., Borodina T., Soldatov A., Parkhomchuk D., Schmidt D., O'Keeffe S., Haas S., Vingron M., Lehrach H., Yaspo M.L. A global view of gene activity and alternative splicing by deep sequencing of the human transcriptome. Science 2008, 321:956-960.
-
(2008)
Science
, vol.321
, pp. 956-960
-
-
Sultan, M.1
Schulz, M.H.2
Richard, H.3
Magen, A.4
Klingenhoff, A.5
Scherf, M.6
Seifert, M.7
Borodina, T.8
Soldatov, A.9
Parkhomchuk, D.10
Schmidt, D.11
O'Keeffe, S.12
Haas, S.13
Vingron, M.14
Lehrach, H.15
Yaspo, M.L.16
-
127
-
-
0035869223
-
Prediction of deleterious human alleles
-
Sunyaev S., Ramensky V., Koch I., Lathe W., Kondrashov A.S., Bork P. Prediction of deleterious human alleles. Hum. Mol. Genet. 2001, 10:591-597.
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 591-597
-
-
Sunyaev, S.1
Ramensky, V.2
Koch, I.3
Lathe, W.4
Kondrashov, A.S.5
Bork, P.6
-
128
-
-
39749118602
-
Multiple loci identified in a genome-wide association study of prostate cancer
-
Thomas G., Jacobs K.B., Yeager M., Kraft P., Wacholder S., Orr N., Yu K., Chatterjee N., Welch R., Hutchinson A., Crenshaw A., Cancel-Tassin G., Staats B.J., Wang Z., Gonzalez-Bosquet J., Fang J., Deng X., Berndt S.I., Calle E.E., Feigelson H.S., Thun M.J., Rodriguez C., Albanes D., Virtamo J., Weinstein S., Schumacher F.R., Giovannucci E., Willett W.C., Cussenot O., Valeri A., Andriole G.L., Crawford E.D., Tucker M., Gerhard D.S., Fraumeni J.F., Hoover R., Hayes R.B., Hunter D.J., Chanock S.J. Multiple loci identified in a genome-wide association study of prostate cancer. Nat. Genet. 2008, 40:310-315.
-
(2008)
Nat. Genet.
, vol.40
, pp. 310-315
-
-
Thomas, G.1
Jacobs, K.B.2
Yeager, M.3
Kraft, P.4
Wacholder, S.5
Orr, N.6
Yu, K.7
Chatterjee, N.8
Welch, R.9
Hutchinson, A.10
Crenshaw, A.11
Cancel-Tassin, G.12
Staats, B.J.13
Wang, Z.14
Gonzalez-Bosquet, J.15
Fang, J.16
Deng, X.17
Berndt, S.I.18
Calle, E.E.19
Feigelson, H.S.20
Thun, M.J.21
Rodriguez, C.22
Albanes, D.23
Virtamo, J.24
Weinstein, S.25
Schumacher, F.R.26
Giovannucci, E.27
Willett, W.C.28
Cussenot, O.29
Valeri, A.30
Andriole, G.L.31
Crawford, E.D.32
Tucker, M.33
Gerhard, D.S.34
Fraumeni, J.F.35
Hoover, R.36
Hayes, R.B.37
Hunter, D.J.38
Chanock, S.J.39
more..
-
129
-
-
34548694283
-
Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma
-
Thorleifsson G., Magnusson K.P., Sulem P., Walters G.B., Gudbjartsson D.F., Stefansson H., Jonsson T., Jonasdottir A., Stefansdottir G., Masson G., Hardarson G.A., Petursson H., Arnarsson A., Motallebipour M., Wallerman O., Wadelius C., Gulcher J.R., Thorsteinsdottir U., Kong A., Jonasson F., Stefansson K. Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma. Science 2007, 317:1397-1400.
-
(2007)
Science
, vol.317
, pp. 1397-1400
-
-
Thorleifsson, G.1
Magnusson, K.P.2
Sulem, P.3
Walters, G.B.4
Gudbjartsson, D.F.5
Stefansson, H.6
Jonsson, T.7
Jonasdottir, A.8
Stefansdottir, G.9
Masson, G.10
Hardarson, G.A.11
Petursson, H.12
Arnarsson, A.13
Motallebipour, M.14
Wallerman, O.15
Wadelius, C.16
Gulcher, J.R.17
Thorsteinsdottir, U.18
Kong, A.19
Jonasson, F.20
Stefansson, K.21
more..
-
130
-
-
43549121020
-
Human MHC architecture and evolution: implications for disease association studies
-
Traherne J.A. Human MHC architecture and evolution: implications for disease association studies. Int. J. Immunogenet. 2008, 35:179-192.
-
(2008)
Int. J. Immunogenet.
, vol.35
, pp. 179-192
-
-
Traherne, J.A.1
-
131
-
-
0037043032
-
Heritability and number of quantitative trait loci of neurocognitive functions in families with schizophrenia
-
Tuulio-Henriksson A., Haukka J., Partonen T., Varilo T., Paunio T., Ekelund J., Cannon T.D., Meyer J.M., Lonnqvist J. Heritability and number of quantitative trait loci of neurocognitive functions in families with schizophrenia. Am. J. Med. Genet. 2002, 114:483-490.
-
(2002)
Am. J. Med. Genet.
, vol.114
, pp. 483-490
-
-
Tuulio-Henriksson, A.1
Haukka, J.2
Partonen, T.3
Varilo, T.4
Paunio, T.5
Ekelund, J.6
Cannon, T.D.7
Meyer, J.M.8
Lonnqvist, J.9
-
132
-
-
0034615867
-
Increased morbid risk for schizophrenia in families of in-patients with bipolar illness
-
Valles V., Van Os J., Guillamat R., Gutierrez B., Campillo M., Gento P., Fananas L. Increased morbid risk for schizophrenia in families of in-patients with bipolar illness. Schizophr. Res. 2000, 42:83-90.
-
(2000)
Schizophr. Res.
, vol.42
, pp. 83-90
-
-
Valles, V.1
Van Os, J.2
Guillamat, R.3
Gutierrez, B.4
Campillo, M.5
Gento, P.6
Fananas, L.7
-
134
-
-
70349558418
-
Alzheimer's disease beyond APOE
-
van Es M.A., van den Berg L.H. Alzheimer's disease beyond APOE. Nat. Genet. 2009, 41:1047-1048.
-
(2009)
Nat. Genet.
, vol.41
, pp. 1047-1048
-
-
van Es, M.A.1
van den Berg, L.H.2
-
135
-
-
67650456775
-
Meta-analytic evidence for familial coaggregation of schizophrenia and bipolar disorder
-
Van Snellenberg J.X., de Candia T. Meta-analytic evidence for familial coaggregation of schizophrenia and bipolar disorder. Arch. Gen. Psychiatry 2009, 66:748-755.
-
(2009)
Arch. Gen. Psychiatry
, vol.66
, pp. 748-755
-
-
Van Snellenberg, J.X.1
de Candia, T.2
-
136
-
-
73349125417
-
Somatic mutations of the Parkinson's disease-associated gene PARK2 in glioblastoma and other human malignancies
-
Veeriah S., Taylor B.S., Meng S., Fang F., Yilmaz E., Vivanco I., Janakiraman M., Schultz N., Hanrahan A.J., Pao W., Ladanyi M., Sander C., Heguy A., Holland E.C., Paty P.B., Mischel P.S., Liau L., Cloughesy T.F., Mellinghoff I.K., Solit D.B., Chan T.A. Somatic mutations of the Parkinson's disease-associated gene PARK2 in glioblastoma and other human malignancies. Nat. Genet. 2010, 42:77-82.
-
(2010)
Nat. Genet.
, vol.42
, pp. 77-82
-
-
Veeriah, S.1
Taylor, B.S.2
Meng, S.3
Fang, F.4
Yilmaz, E.5
Vivanco, I.6
Janakiraman, M.7
Schultz, N.8
Hanrahan, A.J.9
Pao, W.10
Ladanyi, M.11
Sander, C.12
Heguy, A.13
Holland, E.C.14
Paty, P.B.15
Mischel, P.S.16
Liau, L.17
Cloughesy, T.F.18
Mellinghoff, I.K.19
Solit, D.B.20
Chan, T.A.21
more..
-
137
-
-
77949775636
-
Targeted deletion of the 9p21 non-coding coronary artery disease risk interval in mice
-
Visel A., Zhu Y., May D., Afzal V., Gong E., Attanasio C., Blow M.J., Cohen J.C., Rubin E.M., Pennacchio L.A. Targeted deletion of the 9p21 non-coding coronary artery disease risk interval in mice. Nature 2010, 464:409-412.
-
(2010)
Nature
, vol.464
, pp. 409-412
-
-
Visel, A.1
Zhu, Y.2
May, D.3
Afzal, V.4
Gong, E.5
Attanasio, C.6
Blow, M.J.7
Cohen, J.C.8
Rubin, E.M.9
Pennacchio, L.A.10
-
138
-
-
39749108026
-
Next-generation sequencing: the race is on
-
von Bubnoff A. Next-generation sequencing: the race is on. Cell 2008, 132:721-723.
-
(2008)
Cell
, vol.132
, pp. 721-723
-
-
von Bubnoff, A.1
-
139
-
-
42349088634
-
Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia
-
Walsh T., McClellan J.M., McCarthy S.E., Addington A.M., Pierce S.B., Cooper G.M., Nord A.S., Kusenda M., Malhotra D., Bhandari A., Stray S.M., Rippey C.F., Roccanova P., Makarov V., Lakshmi B., Findling R.L., Sikich L., Stromberg T., Merriman B., Gogtay N., Butler P., Eckstrand K., Noory L., Gochman P., Long R., Chen Z., Davis S., Baker C., Eichler E.E., Meltzer P.S., Nelson S.F., Singleton A.B., Lee M.K., Rapoport J.L., King M.C., Sebat J. Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia. Science 2008, 320:539-543.
-
(2008)
Science
, vol.320
, pp. 539-543
-
-
Walsh, T.1
McClellan, J.M.2
McCarthy, S.E.3
Addington, A.M.4
Pierce, S.B.5
Cooper, G.M.6
Nord, A.S.7
Kusenda, M.8
Malhotra, D.9
Bhandari, A.10
Stray, S.M.11
Rippey, C.F.12
Roccanova, P.13
Makarov, V.14
Lakshmi, B.15
Findling, R.L.16
Sikich, L.17
Stromberg, T.18
Merriman, B.19
Gogtay, N.20
Butler, P.21
Eckstrand, K.22
Noory, L.23
Gochman, P.24
Long, R.25
Chen, Z.26
Davis, S.27
Baker, C.28
Eichler, E.E.29
Meltzer, P.S.30
Nelson, S.F.31
Singleton, A.B.32
Lee, M.K.33
Rapoport, J.L.34
King, M.C.35
Sebat, J.36
more..
-
140
-
-
25144433260
-
Multidrug resistance polypeptide 1 (MDR1, ABCB1) variant 3435C>T affects mRNA stability
-
Wang D., Johnson A.D., Papp A.C., Kroetz D.L., Sadee W. Multidrug resistance polypeptide 1 (MDR1, ABCB1) variant 3435C>T affects mRNA stability. Pharmacogenet. Genomics 2005, 15:693-704.
-
(2005)
Pharmacogenet. Genomics
, vol.15
, pp. 693-704
-
-
Wang, D.1
Johnson, A.D.2
Papp, A.C.3
Kroetz, D.L.4
Sadee, W.5
-
141
-
-
57749195712
-
RNA-Seq: a revolutionary tool for transcriptomics
-
Wang Z., Gerstein M., Snyder M. RNA-Seq: a revolutionary tool for transcriptomics. Nat. Rev. Genet. 2009, 10:57-63.
-
(2009)
Nat. Rev. Genet.
, vol.10
, pp. 57-63
-
-
Wang, Z.1
Gerstein, M.2
Snyder, M.3
-
142
-
-
21444444084
-
Evaluation of the chromosome 2q37.3 gene CENTG2 as an autism susceptibility gene
-
Wassink T.H., Piven J., Vieland V.J., Jenkins L., Frantz R., Bartlett C.W., Goedken R., Childress D., Spence M.A., Smith M., Sheffield V.C. Evaluation of the chromosome 2q37.3 gene CENTG2 as an autism susceptibility gene. Am. J. Med. Genet. B: Neuropsychiatr. Genet. 2005, 136B:36-44.
-
(2005)
Am. J. Med. Genet. B: Neuropsychiatr. Genet.
, vol.136 B
, pp. 36-44
-
-
Wassink, T.H.1
Piven, J.2
Vieland, V.J.3
Jenkins, L.4
Frantz, R.5
Bartlett, C.W.6
Goedken, R.7
Childress, D.8
Spence, M.A.9
Smith, M.10
Sheffield, V.C.11
-
143
-
-
42649139571
-
Genome-wide association analysis identifies 20 loci that influence adult height
-
Weedon M.N., Lango H., Lindgren C.M., Wallace C., Evans D.M., Mangino M., Freathy R.M., Perry J.R., Stevens S., Hall A.S., Samani N.J., Shields B., Prokopenko I., Farrall M., Dominiczak A., Johnson T., Bergmann S., Beckmann J.S., Vollenweider P., Waterworth D.M., Mooser V., Palmer C.N., Morris A.D., Ouwehand W.H., Zhao J.H., Li S., Loos R.J., Barroso I., Deloukas P., Sandhu M.S., Wheeler E., Soranzo N., Inouye M., Wareham N.J., Caulfield M., Munroe P.B., Hattersley A.T., McCarthy M.I., Frayling T.M. Genome-wide association analysis identifies 20 loci that influence adult height. Nat. Genet. 2008, 40:575-583.
-
(2008)
Nat. Genet.
, vol.40
, pp. 575-583
-
-
Weedon, M.N.1
Lango, H.2
Lindgren, C.M.3
Wallace, C.4
Evans, D.M.5
Mangino, M.6
Freathy, R.M.7
Perry, J.R.8
Stevens, S.9
Hall, A.S.10
Samani, N.J.11
Shields, B.12
Prokopenko, I.13
Farrall, M.14
Dominiczak, A.15
Johnson, T.16
Bergmann, S.17
Beckmann, J.S.18
Vollenweider, P.19
Waterworth, D.M.20
Mooser, V.21
Palmer, C.N.22
Morris, A.D.23
Ouwehand, W.H.24
Zhao, J.H.25
Li, S.26
Loos, R.J.27
Barroso, I.28
Deloukas, P.29
Sandhu, M.S.30
Wheeler, E.31
Soranzo, N.32
Inouye, M.33
Wareham, N.J.34
Caulfield, M.35
Munroe, P.B.36
Hattersley, A.T.37
McCarthy, M.I.38
Frayling, T.M.39
more..
-
144
-
-
38849191674
-
Strong evidence that GNB1L is associated with schizophrenia
-
Williams N.M., Glaser B., Norton N., Williams H., Pierce T., Moskvina V., Monks S., Del Favero J., Goossens D., Rujescu D., Giegling I., Kirov G., Craddock N., Murphy K.C., O'Donovan M.C., Owen M.J. Strong evidence that GNB1L is associated with schizophrenia. Hum. Mol. Genet. 2008, 17:555-566.
-
(2008)
Hum. Mol. Genet.
, vol.17
, pp. 555-566
-
-
Williams, N.M.1
Glaser, B.2
Norton, N.3
Williams, H.4
Pierce, T.5
Moskvina, V.6
Monks, S.7
Del Favero, J.8
Goossens, D.9
Rujescu, D.10
Giegling, I.11
Kirov, G.12
Craddock, N.13
Murphy, K.C.14
O'Donovan, M.C.15
Owen, M.J.16
-
146
-
-
77956649798
-
-
Fine mapping of ZNF804A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder, Mol. Psychiatry [Epub ahead of print].
-
H.J. Williams, N. Norton, S. Dwyer, V. Moskvina, I. Nikolov, L. Carroll, L. Georgieva, N.M. Williams, D.W. Morris, E.M. Quinn, I. Giegling, M. Ikeda, J. Wood, T. Lencz, C. Hultman, P. Lichtenstein, D. Thiselton, B.S. Maher, A.K. Malhotra, B. Riley, K.S. Kendler, M. Gill, P. Sullivan, P. Sklar, S. Purcell, V.L. Nimgaonkar, G. Kirov, P. Holmans, A. Corvin, D. Rujescu, N. Craddock, M.J. Owen, M.C. O'Donovan, Fine mapping of ZNF804A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder, Mol. Psychiatry (2010) [Epub ahead of print].
-
(2010)
-
-
Williams, H.J.1
Norton, N.2
Dwyer, S.3
Moskvina, V.4
Nikolov, I.5
Carroll, L.6
Georgieva, L.7
Williams, N.M.8
Morris, D.W.9
Quinn, E.M.10
Giegling, I.11
Ikeda M.Wood, J.12
Lencz T.Hultman, C.13
Lichtenstein, P.14
Thiselton, D.15
Maher, B.S.16
Malhotra, A.K.17
Riley, B.18
Kendler, K.S.19
Gill, M.20
Sullivan, P.21
Sklar, P.22
Purcell, S.23
Nimgaonkar, V.L.24
Kirov, G.25
Holmans, P.26
Corvin, A.27
Rujescu, D.28
Craddock, N.29
Owen, M.J.30
O'Donovan, M.C.31
more..
-
147
-
-
53849120906
-
PRODH variants and risk for schizophrenia
-
Willis A., Bender H.U., Steel G., Valle D. PRODH variants and risk for schizophrenia. Amino Acids 2008, 35:673-679.
-
(2008)
Amino Acids
, vol.35
, pp. 673-679
-
-
Willis, A.1
Bender, H.U.2
Steel, G.3
Valle, D.4
-
148
-
-
84969213492
-
WTCCC Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
-
WTCCC Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature 2007, 447:661-678.
-
(2007)
Nature
, vol.447
, pp. 661-678
-
-
-
149
-
-
77950405093
-
WTCCC Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls
-
WTCCC Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls. Nature 2010, 464:713-720.
-
(2010)
Nature
, vol.464
, pp. 713-720
-
-
-
150
-
-
46249093584
-
Strong association of de novo copy number mutations with sporadic schizophrenia
-
Xu B., Roos J.L., Levy S., van Rensburg E.J., Gogos J.A., Karayiorgou M. Strong association of de novo copy number mutations with sporadic schizophrenia. Nat. Genet. 2008, 40:880-885.
-
(2008)
Nat. Genet.
, vol.40
, pp. 880-885
-
-
Xu, B.1
Roos, J.L.2
Levy, S.3
van Rensburg, E.J.4
Gogos, J.A.5
Karayiorgou, M.6
-
151
-
-
35648973737
-
Activity-induced protocadherin arcadlin regulates dendritic spine number by triggering N-cadherin endocytosis via TAO2beta and p38 MAP kinases
-
Yasuda S., Tanaka H., Sugiura H., Okamura K., Sakaguchi T., Tran U., Takemiya T., Mizoguchi A., Yagita Y., Sakurai T., De Robertis E.M., Yamagata K. Activity-induced protocadherin arcadlin regulates dendritic spine number by triggering N-cadherin endocytosis via TAO2beta and p38 MAP kinases. Neuron 2007, 56:456-471.
-
(2007)
Neuron
, vol.56
, pp. 456-471
-
-
Yasuda, S.1
Tanaka, H.2
Sugiura, H.3
Okamura, K.4
Sakaguchi, T.5
Tran, U.6
Takemiya, T.7
Mizoguchi, A.8
Yagita, Y.9
Sakurai, T.10
De Robertis, E.M.11
Yamagata, K.12
-
152
-
-
69749122557
-
Sensitive and accurate detection of copy number variants using read depth of coverage
-
Yoon S., Xuan Z., Makarov V., Ye K., Sebat J. Sensitive and accurate detection of copy number variants using read depth of coverage. Genome Res. 2009, 19:1586-1592.
-
(2009)
Genome Res.
, vol.19
, pp. 1586-1592
-
-
Yoon, S.1
Xuan, Z.2
Makarov, V.3
Ye, K.4
Sebat, J.5
-
153
-
-
42349106044
-
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes
-
Zeggini E., Scott L.J., Saxena R., Voight B.F., Marchini J.L., Hu T., de Bakker P.I., Abecasis G.R., Almgren P., Andersen G., Ardlie K., Bostrom K.B., Bergman R.N., Bonnycastle L.L., Borch-Johnsen K., Burtt N.P., Chen H., Chines P.S., Daly M.J., Deodhar P., Ding C.J., Doney A.S., Duren W.L., Elliott K.S., Erdos M.R., Frayling T.M., Freathy R.M., Gianniny L., Grallert H., Grarup N., Groves C.J., Guiducci C., Hansen T., Herder C., Hitman G.A., Hughes T.E., Isomaa B., Jackson A.U., Jorgensen T., Kong A., Kubalanza K., Kuruvilla F.G., Kuusisto J., Langenberg C., Lango H., Lauritzen T., Li Y., Lindgren C.M., Lyssenko V., Marvelle A.F., Meisinger C., Midthjell K., Mohlke K.L., Morken M.A., Morris A.D., Narisu N., Nilsson P., Owen K.R., Palmer C.N., Payne F., Perry J.R., Pettersen E., Platou C., Prokopenko I., Qi L., Qin L., Rayner N.W., Rees M., Roix J.J., Sandbaek A., Shields B., Sjogren M., Steinthorsdottir V., Stringham H.M., Swift A.J., Thorleifsson G., Thorsteinsdottir U., Timpson N.J., Tuomi T., Tuomilehto J., Walker M., Watanabe R.M., Weedon M.N., Willer C.J., Illig T., Hveem K., Hu F.B., Laakso M., Stefansson K., Pedersen O., Wareham N.J., Barroso I., Hattersley A.T., Collins F.S., Groop L., McCarthy M.I., Boehnke M., Altshuler D. Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. Nat. Genet. 2008, 40:638-645.
-
(2008)
Nat. Genet.
, vol.40
, pp. 638-645
-
-
Zeggini, E.1
Scott, L.J.2
Saxena, R.3
Voight, B.F.4
Marchini, J.L.5
Hu, T.6
de Bakker, P.I.7
Abecasis, G.R.8
Almgren, P.9
Andersen, G.10
Ardlie, K.11
Bostrom, K.B.12
Bergman, R.N.13
Bonnycastle, L.L.14
Borch-Johnsen, K.15
Burtt, N.P.16
Chen, H.17
Chines, P.S.18
Daly, M.J.19
Deodhar, P.20
Ding, C.J.21
Doney, A.S.22
Duren, W.L.23
Elliott, K.S.24
Erdos, M.R.25
Frayling, T.M.26
Freathy, R.M.27
Gianniny, L.28
Grallert, H.29
Grarup, N.30
Groves, C.J.31
Guiducci, C.32
Hansen, T.33
Herder, C.34
Hitman, G.A.35
Hughes, T.E.36
Isomaa, B.37
Jackson, A.U.38
Jorgensen, T.39
Kong, A.40
Kubalanza, K.41
Kuruvilla, F.G.42
Kuusisto, J.43
Langenberg, C.44
Lango, H.45
Lauritzen, T.46
Li, Y.47
Lindgren, C.M.48
Lyssenko, V.49
Marvelle, A.F.50
Meisinger, C.51
Midthjell, K.52
Mohlke, K.L.53
Morken, M.A.54
Morris, A.D.55
Narisu, N.56
Nilsson, P.57
Owen, K.R.58
Palmer, C.N.59
Payne, F.60
Perry, J.R.61
Pettersen, E.62
Platou, C.63
Prokopenko, I.64
Qi, L.65
Qin, L.66
Rayner, N.W.67
Rees, M.68
Roix, J.J.69
Sandbaek, A.70
Shields, B.71
Sjogren, M.72
Steinthorsdottir, V.73
Stringham, H.M.74
Swift, A.J.75
Thorleifsson, G.76
Thorsteinsdottir, U.77
Timpson, N.J.78
Tuomi, T.79
Tuomilehto, J.80
Walker, M.81
Watanabe, R.M.82
Weedon, M.N.83
Willer, C.J.84
Illig, T.85
Hveem, K.86
Hu, F.B.87
Laakso, M.88
Stefansson, K.89
Pedersen, O.90
Wareham, N.J.91
Barroso, I.92
Hattersley, A.T.93
Collins, F.S.94
Groop, L.95
McCarthy, M.I.96
Boehnke, M.97
Altshuler, D.98
more..
-
154
-
-
70350221909
-
Copy number variation in human health, disease, and evolution
-
Zhang F., Gu W., Hurles M.E., Lupski J.R. Copy number variation in human health, disease, and evolution. Annu. Rev. Genomics Hum. Genet. 2009, 10:451-481.
-
(2009)
Annu. Rev. Genomics Hum. Genet.
, vol.10
, pp. 451-481
-
-
Zhang, F.1
Gu, W.2
Hurles, M.E.3
Lupski, J.R.4
|