-
1
-
-
70350048798
-
The genetics of inbreeding depression
-
doi: 10.1038/nrg2664
-
Charlesworth D, Willis JH. 2009. The genetics of inbreeding depression. Nat Rev Genet 10(11):783-796. doi: 10.1038/nrg2664
-
(2009)
Nat Rev Genet
, vol.10
, Issue.11
, pp. 783-796
-
-
Charlesworth, D.1
Willis, J.H.2
-
2
-
-
0034916018
-
Genome-wide distribution of linkage disequilibrium in the population of Palau and its implications for gene flow in Remote Oceania
-
Devlin B, Roeder K, Otto C, Tiobech S, Byerley W. 2001. Genome-wide distribution of linkage disequilibrium in the population of Palau and its implications for gene flow in Remote Oceania. Hum Genet 108(6):521-528.
-
(2001)
Hum Genet
, vol.108
, Issue.6
, pp. 521-528
-
-
Devlin, B.1
Roeder, K.2
Otto, C.3
Tiobech, S.4
Byerley, W.5
-
3
-
-
4344707182
-
Mutation frequencies for glycogen storage disease Ia in the Ashkenazi Jewish population
-
doi: 10.1002/ajmg.a.30232
-
Ekstein J, Rubin BY, Anderson SL, Weinstein DA, Bach G, Abeliovich D, Webb M, Risch N. 2004. Mutation frequencies for glycogen storage disease Ia in the Ashkenazi Jewish population. Am J Med Genet Part A 129A(2):162-164. doi: 10.1002/ajmg.a.30232
-
(2004)
Am J Med Genet Part A
, vol.129 A
, Issue.2
, pp. 162-164
-
-
Ekstein, J.1
Rubin, B.Y.2
Anderson, S.L.3
Weinstein, D.A.4
Bach, G.5
Abeliovich, D.6
Webb, M.7
Risch, N.8
-
4
-
-
0018119373
-
A diagnostic interview: The schedule for affective disorders and schizophrenia
-
Endicott J, Spitzer RL. 1978. A diagnostic interview: The schedule for affective disorders and schizophrenia. Arch Gen Psychiatry 35(7):837-844.
-
(1978)
Arch Gen Psychiatry
, vol.35
, Issue.7
, pp. 837-844
-
-
Endicott, J.1
Spitzer, R.L.2
-
5
-
-
41149144099
-
Carrier frequency of autosomal-recessive disorders in the Ashkenazi Jewish population: Should the rationale for mutation choice for screening be reevaluated
-
doi: 10.1002/pd.1943
-
Fares F, Badarneh K, Abosaleh M, Harari-Shaham A, Diukman R, David M. 2008. Carrier frequency of autosomal-recessive disorders in the Ashkenazi Jewish population: Should the rationale for mutation choice for screening be reevaluated? Prenat Diagn 28(3):236-241. doi: 10.1002/pd.1943
-
(2008)
Prenat Diagn
, vol.28
, Issue.3
, pp. 236-241
-
-
Fares, F.1
Badarneh, K.2
Abosaleh, M.3
Harari-Shaham, A.4
Diukman, R.5
David, M.6
-
6
-
-
84880252779
-
Intellectual disability is associated with increased runs-of-homozygosity in simplex autism
-
Gamsiz ED, Viscidi EW, Frederick AM, Nagpal S, Sanders SJ, Murtha MT, Schmidt M, Triche EW, Geschwind DH, State MW, Istrail S, Cook EH, Devlin B, Morrow EM. 2013. Intellectual disability is associated with increased runs-of-homozygosity in simplex autism. Am J Hum Genet 93(1):103-109.
-
(2013)
Am J Hum Genet
, vol.93
, Issue.1
, pp. 103-109
-
-
Gamsiz, E.D.1
Viscidi, E.W.2
Frederick, A.M.3
Nagpal, S.4
Sanders, S.J.5
Murtha, M.T.6
Schmidt, M.7
Triche, E.W.8
Geschwind, D.H.9
State, M.W.10
Istrail, S.11
Cook, E.H.12
Devlin, B.13
Morrow, E.M.14
-
7
-
-
33144460067
-
Extended tracts of homozygosity in outbred human populations
-
doi: 10.1093/hmg/ddi493
-
Gibson J, Morton NE, Collins A. 2006. Extended tracts of homozygosity in outbred human populations. Hum Mol Genet 15(5):789-795. doi: 10.1093/hmg/ddi493
-
(2006)
Hum Mol Genet
, vol.15
, Issue.5
, pp. 789-795
-
-
Gibson, J.1
Morton, N.E.2
Collins, A.3
-
8
-
-
77955067694
-
Population genetic structure of the people of Qatar
-
doi: 10.1016/j.ajhg.2010.05.018
-
Hunter-Zinck H, Musharoff S, Salit J, Al-Ali KA, Chouchane L, Gohar A, Matthews R, Butler MW, Fuller J, Hackett NR, Crystal RG, Clark AG. 2010. Population genetic structure of the people of Qatar. Am J Hum Genet 87(1):17-25. doi: 10.1016/j.ajhg.2010.05.018
-
(2010)
Am J Hum Genet
, vol.87
, Issue.1
, pp. 17-25
-
-
Hunter-Zinck, H.1
Musharoff, S.2
Salit, J.3
Al-Ali, K.A.4
Chouchane, L.5
Gohar, A.6
Matthews, R.7
Butler, M.W.8
Fuller, J.9
Hackett, N.R.10
Crystal, R.G.11
Clark, A.G.12
-
9
-
-
0034529505
-
Epidemiology of schizophrenia: The global burden of disease and disability
-
Jablensky A. 2000. Epidemiology of schizophrenia: The global burden of disease and disability. Eur Arch Psychiatry Clin Neurosci 250(6):274-285.
-
(2000)
Eur Arch Psychiatry Clin Neurosci
, vol.250
, Issue.6
, pp. 274-285
-
-
Jablensky, A.1
-
10
-
-
0026436979
-
Schizophrenia: Manifestations, incidence and course in different cultures. A World Health Organization ten-country study
-
Jablensky A, Sartorius N, Ernberg G, Anker M, Korten A, Cooper JE, Day R, Bertelsen A. 1992. Schizophrenia: Manifestations, incidence and course in different cultures. A World Health Organization ten-country study. Psychol Med Monogr Suppl 20:1-97.
-
(1992)
Psychol Med Monogr Suppl
, vol.20
, pp. 1-97
-
-
Jablensky, A.1
Sartorius, N.2
Ernberg, G.3
Anker, M.4
Korten, A.5
Cooper, J.E.6
Day, R.7
Bertelsen, A.8
-
11
-
-
64549083234
-
Use of a genetic isolate to identify rare disease variants: C7 on 5p associated with MS
-
doi: 10.1093/hmg/ddp073
-
Kallio SP, Jakkula E, Purcell S, Suvela M, Koivisto K, Tienari PJ, Elovaara I, Pirttila T, Reunanen M, Bronnikov D, Viander M, Meri S, Hillert J, Lundmark F, Harbo HF, Lorentzen AR, De Jager PL, Daly MJ, Hafler DA, Palotie A, Peltonen L, Saarela J. 2009. Use of a genetic isolate to identify rare disease variants: C7 on 5p associated with MS. Hum Mol Genet 18(9):1670-1683. doi: 10.1093/hmg/ddp073
-
(2009)
Hum Mol Genet
, vol.18
, Issue.9
, pp. 1670-1683
-
-
Kallio, S.P.1
Jakkula, E.2
Purcell, S.3
Suvela, M.4
Koivisto, K.5
Tienari, P.J.6
Elovaara, I.7
Pirttila, T.8
Reunanen, M.9
Bronnikov, D.10
Viander, M.11
Meri, S.12
Hillert, J.13
Lundmark, F.14
Harbo, H.F.15
Lorentzen, A.R.16
De Jager, P.L.17
Daly, M.J.18
Hafler, D.A.19
Palotie, A.20
Peltonen, L.21
Saarela, J.22
more..
-
12
-
-
84860559560
-
Runs of homozygosity implicate autozygosity as a schizophrenia risk factor
-
doi: 10.1371/journal.pgen.1002656
-
Keller MC, Simonson MA, Ripke S, Neale BM, Gejman PV, Howrigan DP, Lee SH, Lencz T, Levinson DF, Sullivan PF. 2012. Runs of homozygosity implicate autozygosity as a schizophrenia risk factor. PLoS Genet 8(4):e1002656. doi: 10.1371/journal.pgen.1002656
-
(2012)
PLoS Genet
, vol.8
, Issue.4
-
-
Keller, M.C.1
Simonson, M.A.2
Ripke, S.3
Neale, B.M.4
Gejman, P.V.5
Howrigan, D.P.6
Lee, S.H.7
Lencz, T.8
Levinson, D.F.9
Sullivan, P.F.10
-
13
-
-
78649730822
-
Genomic runs of homozygosity record population history and consanguinity
-
doi: 10.1371/journal.pone.0013996
-
Kirin M, McQuillan R, Franklin CS, Campbell H, McKeigue PM, Wilson JF. 2010. Genomic runs of homozygosity record population history and consanguinity. PLoS ONE 5(11):e13996. doi: 10.1371/journal.pone.0013996
-
(2010)
PLoS ONE
, vol.5
, Issue.11
-
-
Kirin, M.1
McQuillan, R.2
Franklin, C.S.3
Campbell, H.4
McKeigue, P.M.5
Wilson, J.F.6
-
14
-
-
23944524611
-
Linkage analysis of a completely ascertained sample of familial schizophrenics and bipolars from Palau, Micronesia
-
doi: 10.1007/s00439-005-1320-1
-
Klei L, Bacanu SA, Myles-Worsley M, Galke B, Xie W, Tiobech J, Otto C, Roeder K, Devlin B, Byerley W. 2005. Linkage analysis of a completely ascertained sample of familial schizophrenics and bipolars from Palau, Micronesia. Hum Genet 117(4):349-356. doi: 10.1007/s00439-005-1320-1
-
(2005)
Hum Genet
, vol.117
, Issue.4
, pp. 349-356
-
-
Klei, L.1
Bacanu, S.A.2
Myles-Worsley, M.3
Galke, B.4
Xie, W.5
Tiobech, J.6
Otto, C.7
Roeder, K.8
Devlin, B.9
Byerley, W.10
-
15
-
-
44449116152
-
Homozygosity mapping in a family presenting with schizophrenia, epilepsy and hearing impairment
-
doi: 10.1038/ejhg.2008.11
-
Knight HM, Maclean A, Irfan M, Naeem F, Cass S, Pickard BS, Muir WJ, Blackwood DH, Ayub M. 2008. Homozygosity mapping in a family presenting with schizophrenia, epilepsy and hearing impairment. Eur J Hum Genet 16(6):750-758. doi: 10.1038/ejhg.2008.11
-
(2008)
Eur J Hum Genet
, vol.16
, Issue.6
, pp. 750-758
-
-
Knight, H.M.1
Maclean, A.2
Irfan, M.3
Naeem, F.4
Cass, S.5
Pickard, B.S.6
Muir, W.J.7
Blackwood, D.H.8
Ayub, M.9
-
16
-
-
52949085789
-
Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs
-
doi: 10.1038/ng.237
-
Korn JM, Kuruvilla FG, McCarroll SA, Wysoker A, Nemesh J, Cawley S, Hubbell E, Veitch J, Collins PJ, Darvishi K, Lee C, Nizzari MM, Gabriel SB, Purcell S, Daly MJ, Altshuler D. 2008. Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs. Nat Genet 40(10):1253-1260. doi: 10.1038/ng.237
-
(2008)
Nat Genet
, vol.40
, Issue.10
, 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
-
17
-
-
38049164192
-
Runs of homozygosity reveal highly penetrant recessive loci in schizophrenia
-
doi: 10.1073/pnas.0710021104
-
Lencz T, Lambert C, DeRosse P, Burdick KE, Morgan TV, Kane JM, Kucherlapati R, Malhotra AK. 2007. Runs of homozygosity reveal highly penetrant recessive loci in schizophrenia. Proc Natl Acad Sci USA 104(50):19942-19947. doi: 10.1073/pnas.0710021104
-
(2007)
Proc Natl Acad Sci USA
, vol.104
, Issue.50
, pp. 19942-19947
-
-
Lencz, T.1
Lambert, C.2
DeRosse, P.3
Burdick, K.E.4
Morgan, T.V.5
Kane, J.M.6
Kucherlapati, R.7
Malhotra, A.K.8
-
18
-
-
33750911214
-
Long contiguous stretches of homozygosity in the human genome
-
doi: 10.1002/humu.20399
-
Li LH, Ho SF, Chen CH, Wei CY, Wong WC, Li LY, Hung SI, Chung WH, Pan WH, Lee MT, Tsai FJ, Chang CF, Wu JY, Chen YT. 2006. Long contiguous stretches of homozygosity in the human genome. Hum Mutat 27(11):1115-1121. doi: 10.1002/humu.20399
-
(2006)
Hum Mutat
, vol.27
, Issue.11
, pp. 1115-1121
-
-
Li, L.H.1
Ho, S.F.2
Chen, C.H.3
Wei, C.Y.4
Wong, W.C.5
Li, L.Y.6
Hung, S.I.7
Chung, W.H.8
Pan, W.H.9
Lee, M.T.10
Tsai, F.J.11
Chang, C.F.12
Wu, J.Y.13
Chen, Y.T.14
-
19
-
-
84872722295
-
Rare complete knockouts in humans: Population distribution and significant role in autism spectrum disorders
-
doi: 10.1016/j.neuron.2012.12.029
-
Lim ET, Raychaudhuri S, Sanders SJ, Stevens C, Sabo A, Macarthur DG, Neale BM, Kirby A, Ruderfer DM, Fromer M, Lek M, Liu L, Flannick J, Ripke S, Nagaswamy U, Muzny D, Reid JG, Hawes A, Newsham I, Wu Y, Lewis L, Dinh H, Gross S, Wang LS, Lin CF, Valladares O, Gabriel SB, Depristo M, Altshuler DM, Purcell SM, State MW, Boerwinkle E, Buxbaum JD, Cook EH, Gibbs RA, Schellenberg GD, Sutcliffe JS, Devlin B, Roeder K, Daly MJ. 2013. Rare complete knockouts in humans: Population distribution and significant role in autism spectrum disorders. Neuron 77(2):235-242. doi: 10.1016/j.neuron.2012.12.029
-
(2013)
Neuron
, vol.77
, Issue.2
, pp. 235-242
-
-
Lim, E.T.1
Raychaudhuri, S.2
Sanders, S.J.3
Stevens, C.4
Sabo, A.5
Macarthur, D.G.6
Neale, B.M.7
Kirby, A.8
Ruderfer, D.M.9
Fromer, M.10
Lek, M.11
Liu, L.12
Flannick, J.13
Ripke, S.14
Nagaswamy, U.15
Muzny, D.16
Reid, J.G.17
Hawes, A.18
Newsham, I.19
Wu, Y.20
Lewis, L.21
Dinh, H.22
Gross, S.23
Wang, L.S.24
Lin, C.F.25
Valladares, O.26
Gabriel, S.B.27
Depristo, M.28
Altshuler, D.M.29
Purcell, S.M.30
State, M.W.31
Boerwinkle, E.32
Buxbaum, J.D.33
Cook, E.H.34
Gibbs, R.A.35
Schellenberg, G.D.36
Sutcliffe, J.S.37
Devlin, B.38
Roeder, K.39
Daly, M.J.40
more..
-
20
-
-
77954144873
-
Consanguinity and increased risk for schizophrenia in Egypt
-
doi: 10.1016/j.schres.2010.03.026
-
Mansour H, Fathi W, Klei L, Wood J, Chowdari K, Watson A, Eissa A, Elassy M, Ali I, Salah H, Yassin A, Tobar S, El-Boraie H, Gaafar H, Ibrahim NE, Kandil K, El-Bahaei W, El-Boraie O, Alatrouny M, El-Chennawi F, Devlin B, Nimgaonkar VL. 2010. Consanguinity and increased risk for schizophrenia in Egypt. Schizophr Res 120(1-3):108-112. doi: 10.1016/j.schres.2010.03.026
-
(2010)
Schizophr Res
, vol.120
, Issue.1-3
, pp. 108-112
-
-
Mansour, H.1
Fathi, W.2
Klei, L.3
Wood, J.4
Chowdari, K.5
Watson, A.6
Eissa, A.7
Elassy, M.8
Ali, I.9
Salah, H.10
Yassin, A.11
Tobar, S.12
El-Boraie, H.13
Gaafar, H.14
Ibrahim, N.E.15
Kandil, K.16
El-Bahaei, W.17
El-Boraie, O.18
Alatrouny, M.19
El-Chennawi, F.20
Devlin, B.21
Nimgaonkar, V.L.22
more..
-
21
-
-
50949106932
-
Runs of homozygosity in European populations
-
doi: 10.1016/j.ajhg.2008.08.007
-
McQuillan R, Leutenegger AL, Abdel-Rahman R, Franklin CS, Pericic M, Barac-Lauc L, Smolej-Narancic N, Janicijevic B, Polasek O, Tenesa A, Macleod AK, Farrington SM, Rudan P, Hayward C, Vitart V, Rudan I, Wild SH, Dunlop MG, Wright AF, Campbell H, Wilson JF. 2008. Runs of homozygosity in European populations. Am J Hum Genet 83(3):359-372. doi: 10.1016/j.ajhg.2008.08.007
-
(2008)
Am J Hum Genet
, vol.83
, Issue.3
, pp. 359-372
-
-
McQuillan, R.1
Leutenegger, A.L.2
Abdel-Rahman, R.3
Franklin, C.S.4
Pericic, M.5
Barac-Lauc, L.6
Smolej-Narancic, N.7
Janicijevic, B.8
Polasek, O.9
Tenesa, A.10
Macleod, A.K.11
Farrington, S.M.12
Rudan, P.13
Hayward, C.14
Vitart, V.15
Rudan, I.16
Wild, S.H.17
Dunlop, M.G.18
Wright, A.F.19
Campbell, H.20
Wilson, J.F.21
more..
-
22
-
-
81855182144
-
Copy number variants for schizophrenia and related psychotic disorders in Oceanic Palau: Risk and transmission in extended pedigrees
-
doi: 10.1016/j.biopsych.2011.08.009
-
Melhem N, Middleton F, McFadden K, Klei L, Faraone SV, Vinogradov S, Tiobech J, Yano V, Kuartei S, Roeder K, Byerley W, Devlin B, Myles-Worsley M. 2011. Copy number variants for schizophrenia and related psychotic disorders in Oceanic Palau: Risk and transmission in extended pedigrees. Biol Psychiatry 70(12):1115-1121. doi: 10.1016/j.biopsych.2011.08.009
-
(2011)
Biol Psychiatry
, vol.70
, Issue.12
, pp. 1115-1121
-
-
Melhem, N.1
Middleton, F.2
McFadden, K.3
Klei, L.4
Faraone, S.V.5
Vinogradov, S.6
Tiobech, J.7
Yano, V.8
Kuartei, S.9
Roeder, K.10
Byerley, W.11
Devlin, B.12
Myles-Worsley, M.13
-
23
-
-
0033525171
-
Genetic epidemiological study of schizophrenia in Palau, Micronesia: Prevalence and familiality
-
Myles-Worsley M, Coon H, Tiobech J, Collier J, Dale P, Wender P, Reimherr F, Polloi A, Byerley W. 1999. Genetic epidemiological study of schizophrenia in Palau, Micronesia: Prevalence and familiality. Am J Med Genet 88(1):4-10.
-
(1999)
Am J Med Genet
, vol.88
, Issue.1
, pp. 4-10
-
-
Myles-Worsley, M.1
Coon, H.2
Tiobech, J.3
Collier, J.4
Dale, P.5
Wender, P.6
Reimherr, F.7
Polloi, A.8
Byerley, W.9
-
24
-
-
79952594457
-
Familial transmission of schizophrenia in Palau: A 20-year genetic epidemiological study in three generations
-
doi: 10.1002/ajmg.b.31171
-
Myles-Worsley M, Tiobech J, Blailes F, Middleton FA, Vinogradov S, Byerley W, Faraone SV. 2011. Familial transmission of schizophrenia in Palau: A 20-year genetic epidemiological study in three generations. Am J Med Genet Part B 156B(3):247-254. doi: 10.1002/ajmg.b.31171
-
(2011)
Am J Med Genet Part B
, vol.156 B
, Issue.3
, pp. 247-254
-
-
Myles-Worsley, M.1
Tiobech, J.2
Blailes, F.3
Middleton, F.A.4
Vinogradov, S.5
Byerley, W.6
Faraone, S.V.7
-
25
-
-
84874161631
-
Deletion at the SLC1A1 glutamate transporter gene co-segregates with schizophrenia and bipolar schizoaffective disorder in a 5-generation family
-
doi: 10.1002/ajmg.b.32125
-
Myles-Worsley M, Tiobech J, Browning SR, Korn J, Goodman S, Gentile K, Melhem N, Byerley W, Faraone SV, Middleton FA. 2013. Deletion at the SLC1A1 glutamate transporter gene co-segregates with schizophrenia and bipolar schizoaffective disorder in a 5-generation family. Am J Med Genet Part B 162B(2):87-95. doi: 10.1002/ajmg.b.32125
-
(2013)
Am J Med Genet Part B
, vol.162 B
, Issue.2
, pp. 87-95
-
-
Myles-Worsley, M.1
Tiobech, J.2
Browning, S.R.3
Korn, J.4
Goodman, S.5
Gentile, K.6
Melhem, N.7
Byerley, W.8
Faraone, S.V.9
Middleton, F.A.10
-
26
-
-
79952005563
-
Parental consanguineous marriages and age at onset of schizophrenia
-
doi: 10.1016/j.schres.2010.11.029
-
Nafissi S, Ansari-Lari M, Saadat M. 2011. Parental consanguineous marriages and age at onset of schizophrenia. Schizophr Res 126(1-3):298-299. doi: 10.1016/j.schres.2010.11.029
-
(2011)
Schizophr Res
, vol.126
, Issue.1-3
, pp. 298-299
-
-
Nafissi, S.1
Ansari-Lari, M.2
Saadat, M.3
-
27
-
-
12244264435
-
Genetic power calculator: Design of linkage and association genetic mapping studies of complex traits
-
Purcell S, Cherny SS, Sham PC. 2003. Genetic power calculator: Design of linkage and association genetic mapping studies of complex traits. Bioinformatics 19(1):149-150.
-
(2003)
Bioinformatics
, vol.19
, Issue.1
, pp. 149-150
-
-
Purcell, S.1
Cherny, S.S.2
Sham, P.C.3
-
28
-
-
34548292504
-
PLINK: A tool set for whole-genome association and population-based linkage analyses
-
doi: 10.1086/519795
-
Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MA, Bender D, Maller J, Sklar P, de Bakker PI, Daly MJ, Sham PC. 2007. PLINK: A tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet 81(3):559-575. doi: 10.1086/519795
-
(2007)
Am J Hum Genet
, vol.81
, Issue.3
, pp. 559-575
-
-
Purcell, S.1
Neale, B.2
Todd-Brown, K.3
Thomas, L.4
Ferreira, M.A.5
Bender, D.6
Maller, J.7
Sklar, P.8
de Bakker, P.I.9
Daly, M.J.10
Sham, P.C.11
-
29
-
-
84885020424
-
Genome-wide association analysis identifies 13 new risk loci for schizophrenia
-
doi: 10.1038/ng.2742
-
Ripke S, O'Dushlaine C, Chambert K, Moran JL, Kahler AK, Akterin S, Bergen SE, Collins AL, Crowley JJ, Fromer M, Kim Y, Lee SH, Magnusson PK, Sanchez N, Stahl EA, Williams S, Wray NR, Xia K, Bettella F, Borglum AD, Bulik-Sullivan BK, Cormican P, Craddock N, de Leeuw C, Durmishi N, Gill M, Golimbet V, Hamshere ML, Holmans P, Hougaard DM, Kendler KS, Lin K, Morris DW, Mors O, Mortensen PB, Neale BM, O'Neill FA, Owen MJ, Milovancevic MP, Posthuma D, Powell J, Richards AL, Riley BP, Ruderfer D, Rujescu D, Sigurdsson E, Silagadze T, Smit AB, Stefansson H, Steinberg S, Suvisaari J, Tosato S, Verhage M, Walters JT, Levinson DF, Gejman PV, Laurent C, Mowry BJ, O'Donovan MC, Pulver AE, Schwab SG, Wildenauer DB, Dudbridge F, Shi J, Albus M, Alexander M, Campion D, Cohen D, Dikeos D, Duan J, Eichhammer P, Godard S, Hansen M, Lerer FB, Liang KY, Maier W, Mallet J, Nertney DA, Nestadt G, Norton N, Papadimitriou GN, Ribble R, Sanders AR, Silverman JM, Walsh D, Williams NM, Wormley B, Arranz MJ, Bakker S, Bender S, Bramon E, Collier D, Crespo-Facorro B, Hall J, Iyegbe C, Jablensky A, Kahn RS, Kalaydjieva L, Lawrie S, Lewis CM, Linszen DH, Mata I, McIntosh A, Murray RM, Ophoff RA, Van Os J, Walshe M, Weisbrod M, Wiersma D, Donnelly P, Barroso I, Blackwell JM, Brown MA, Casas JP, Corvin AP, Deloukas P, Duncanson A, Jankowski J, Markus HS, Mathew CG, Palmer CN, Plomin R, Rautanen A, Sawcer SJ, Trembath RC, Viswanathan AC, Wood NW, Spencer CC, Band G, Bellenguez C, Freeman C, Hellenthal G, Giannoulatou E, Pirinen M, Pearson RD, Strange A, Su Z, Vukcevic D, Langford C, Hunt SE, Edkins S, Gwilliam R, Blackburn H, Bumpstead SJ, Dronov S, Gillman M, Gray E, Hammond N, Jayakumar A, McCann OT, Liddle J, Potter SC, Ravindrarajah R, Ricketts M, Tashakkori-Ghanbaria A, Waller MJ, Weston P, Widaa S, Whittaker P, McCarthy MI, Stefansson K, Scolnick E, Purcell S, McCarroll SA, Sklar P, Hultman CM, Sullivan PF. 2013. Genome-wide association analysis identifies 13 new risk loci for schizophrenia. Nat Genet 45(10):1150-1159. doi: 10.1038/ng.2742
-
(2013)
Nat Genet
, vol.45
, Issue.10
, pp. 1150-1159
-
-
Ripke, S.1
O'Dushlaine, C.2
Chambert, K.3
Moran, J.L.4
Kahler, A.K.5
Akterin, S.6
Bergen, S.E.7
Collins, A.L.8
Crowley, J.J.9
Fromer, M.10
Kim, Y.11
Lee, S.H.12
Magnusson, P.K.13
Sanchez, N.14
Stahl, E.A.15
Williams, S.16
Wray, N.R.17
Xia, K.18
Bettella, F.19
Borglum, A.D.20
Bulik-Sullivan, B.K.21
Cormican, P.22
Craddock, N.23
de Leeuw, C.24
Durmishi, N.25
Gill, M.26
Golimbet, V.27
Hamshere, M.L.28
Holmans, P.29
Hougaard, D.M.30
Kendler, K.S.31
Lin, K.32
Morris, D.W.33
Mors, O.34
Mortensen, P.B.35
Neale, B.M.36
O'Neill, F.A.37
Owen, M.J.38
Milovancevic, M.P.39
Posthuma, D.40
Powell, J.41
Richards, A.L.42
Riley, B.P.43
Ruderfer, D.44
Rujescu, D.45
Sigurdsson, E.46
Silagadze, T.47
Smit, A.B.48
Stefansson, H.49
Steinberg, S.50
Suvisaari, J.51
Tosato, S.52
Verhage, M.53
Walters, J.T.54
Levinson, D.F.55
Gejman, P.V.56
Laurent, C.57
Mowry, B.J.58
O'Donovan, M.C.59
Pulver, A.E.60
Schwab, S.G.61
Wildenauer, D.B.62
Dudbridge, F.63
Shi, J.64
Albus, M.65
Alexander, M.66
Campion, D.67
Cohen, D.68
Dikeos, D.69
Duan, J.70
Eichhammer, P.71
Godard, S.72
Hansen, M.73
Lerer, F.B.74
Liang, K.Y.75
Maier, W.76
Mallet, J.77
Nertney, D.A.78
Nestadt, G.79
Norton, N.80
Papadimitriou, G.N.81
Ribble, R.82
Sanders, A.R.83
Silverman, J.M.84
Walsh, D.85
Williams, N.M.86
Wormley, B.87
Arranz, M.J.88
Bakker, S.89
Bender, S.90
Bramon, E.91
Collier, D.92
Crespo-Facorro, B.93
Hall, J.94
Iyegbe, C.95
Jablensky, A.96
Kahn, R.S.97
Kalaydjieva, L.98
Lawrie, S.99
Lewis, C.M.100
Linszen, D.H.101
Mata, I.102
McIntosh, A.103
Murray, R.M.104
Ophoff, R.A.105
Van Os, J.106
Walshe, M.107
Weisbrod, M.108
Wiersma, D.109
Donnelly, P.110
Barroso, I.111
Blackwell, J.M.112
Brown, M.A.113
Casas, J.P.114
Corvin, A.P.115
Deloukas, P.116
Duncanson, A.117
Jankowski, J.118
Markus, H.S.119
Mathew, C.G.120
Palmer, C.N.121
Plomin, R.122
Rautanen, A.123
Sawcer, S.J.124
Trembath, R.C.125
Viswanathan, A.C.126
Wood, N.W.127
Spencer, C.C.128
Band, G.129
Bellenguez, C.130
Freeman, C.131
Hellenthal, G.132
Giannoulatou, E.133
Pirinen, M.134
Pearson, R.D.135
Strange, A.136
Su, Z.137
Vukcevic, D.138
Langford, C.139
Hunt, S.E.140
Edkins, S.141
Gwilliam, R.142
Blackburn, H.143
Bumpstead, S.J.144
Dronov, S.145
Gillman, M.146
Gray, E.147
Hammond, N.148
Jayakumar, A.149
McCann, O.T.150
Liddle, J.151
Potter, S.C.152
Ravindrarajah, R.153
Ricketts, M.154
Tashakkori-Ghanbaria, A.155
Waller, M.J.156
Weston, P.157
Widaa, S.158
Whittaker, P.159
McCarthy, M.I.160
Stefansson, K.161
Scolnick, E.162
Purcell, S.163
McCarroll, S.A.164
Sklar, P.165
Hultman, C.M.166
Sullivan, P.F.167
more..
-
30
-
-
0037385394
-
Geographic distribution of disease mutations in the Ashkenazi Jewish population supports genetic drift over selection
-
doi: 10.1086/373882
-
Risch N, Tang H, Katzenstein H, Ekstein J. 2003. Geographic distribution of disease mutations in the Ashkenazi Jewish population supports genetic drift over selection. Am J Hum Genet 72(4):812-822. doi: 10.1086/373882
-
(2003)
Am J Hum Genet
, vol.72
, Issue.4
, pp. 812-822
-
-
Risch, N.1
Tang, H.2
Katzenstein, H.3
Ekstein, J.4
-
31
-
-
33846531959
-
Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals
-
doi: 10.1093/hmg/ddl436
-
Simon-Sanchez J, Scholz S, Fung HC, Matarin M, Hernandez D, Gibbs JR, Britton A, de Vrieze FW, Peckham E, Gwinn-Hardy K, Crawley A, Keen JC, Nash J, Borgaonkar D, Hardy J, Singleton A. 2007. Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals. Hum Mol Genet 16(1):1-14. doi: 10.1093/hmg/ddl436
-
(2007)
Hum Mol Genet
, vol.16
, Issue.1
, pp. 1-14
-
-
Simon-Sanchez, J.1
Scholz, S.2
Fung, H.C.3
Matarin, M.4
Hernandez, D.5
Gibbs, J.R.6
Britton, A.7
de Vrieze, F.W.8
Peckham, E.9
Gwinn-Hardy, K.10
Crawley, A.11
Keen, J.C.12
Nash, J.13
Borgaonkar, D.14
Hardy, J.15
Singleton, A.16
-
32
-
-
0018082913
-
Research diagnostic criteria: Rationale and reliability
-
Spitzer RL, Endicott J, Robins E. 1978. Research diagnostic criteria: Rationale and reliability. Arch Gen Psychiatry 35(6):773-782.
-
(1978)
Arch Gen Psychiatry
, vol.35
, Issue.6
, pp. 773-782
-
-
Spitzer, R.L.1
Endicott, J.2
Robins, E.3
-
33
-
-
34547756415
-
Case-control association testing with related individuals: A more powerful quasi-likelihood score test
-
doi: 10.1086/519497
-
Thornton T, McPeek MS. 2007. Case-control association testing with related individuals: A more powerful quasi-likelihood score test. Am J Hum Genet 81(2):321-337. doi: 10.1086/519497
-
(2007)
Am J Hum Genet
, vol.81
, Issue.2
, pp. 321-337
-
-
Thornton, T.1
McPeek, M.S.2
-
34
-
-
84866699724
-
Evidence for an epigenetic role in inbreeding depression
-
doi: 10.1098/rsbl.2012.0494
-
Vergeer P, Wagemaker NC, Ouborg NJ. 2012. Evidence for an epigenetic role in inbreeding depression. Biol Lett 8(5):798-801. doi: 10.1098/rsbl.2012.0494
-
(2012)
Biol Lett
, vol.8
, Issue.5
, pp. 798-801
-
-
Vergeer, P.1
Wagemaker, N.C.2
Ouborg, N.J.3
-
35
-
-
77956661477
-
Population-based study of genetic variation in individuals with autism spectrum disorders from Croatia
-
doi: 10.1186/1471-2350-11-134
-
Wang LS, Hranilovic D, Wang K, Lindquist IE, Yurcaba L, Petkovic ZB, Gidaya N, Jernej B, Hakonarson H, Bucan M. 2010. Population-based study of genetic variation in individuals with autism spectrum disorders from Croatia. BMC Med Genet 11:134. doi: 10.1186/1471-2350-11-134
-
(2010)
BMC Med Genet
, vol.11
, pp. 134
-
-
Wang, L.S.1
Hranilovic, D.2
Wang, K.3
Lindquist, I.E.4
Yurcaba, L.5
Petkovic, Z.B.6
Gidaya, N.7
Jernej, B.8
Hakonarson, H.9
Bucan, M.10
-
36
-
-
84872696957
-
Using Whole-exome sequencing to identify inherited causes of autism
-
doi: 10.1016/j.neuron.2012.11.002
-
Yu TW, Chahrour MH, Coulter ME, Jiralerspong S, Okamura-Ikeda K, Ataman B, Schmitz-Abe K, Harmin DA, Adli M, Malik AN, D'Gama AM, Lim ET, Sanders SJ, Mochida GH, Partlow JN, Sunu CM, Felie JM, Rodriguez J, Nasir RH, Ware J, Joseph RM, Hill RS, Kwan BY, Al-Saffar M, Mukaddes NM, Hashmi A, Balkhy S, Gascon GG, Hisama FM, Leclair E, Poduri A, Oner O, Al-Saad S, Al-Awadi SA, Bastaki L, Ben-Omran T, Teebi AS, Al-Gazali L, Eapen V, Stevens CR, Rappaport L, Gabriel SB, Markianos K, State MW, Greenberg ME, Taniguchi H, Braverman NE, Morrow EM, Walsh CA. 2013. Using Whole-exome sequencing to identify inherited causes of autism. Neuron 77(2):259-273. doi: 10.1016/j.neuron.2012.11.002
-
(2013)
Neuron
, vol.77
, Issue.2
, pp. 259-273
-
-
Yu, T.W.1
Chahrour, M.H.2
Coulter, M.E.3
Jiralerspong, S.4
Okamura-Ikeda, K.5
Ataman, B.6
Schmitz-Abe, K.7
Harmin, D.A.8
Adli, M.9
Malik, A.N.10
D'Gama, A.M.11
Lim, E.T.12
Sanders, S.J.13
Mochida, G.H.14
Partlow, J.N.15
Sunu, C.M.16
Felie, J.M.17
Rodriguez, J.18
Nasir, R.H.19
Ware, J.20
Joseph, R.M.21
Hill, R.S.22
Kwan, B.Y.23
Al-Saffar, M.24
Mukaddes, N.M.25
Hashmi, A.26
Balkhy, S.27
Gascon, G.G.28
Hisama, F.M.29
Leclair, E.30
Poduri, A.31
Oner, O.32
Al-Saad, S.33
Al-Awadi, S.A.34
Bastaki, L.35
Ben-Omran, T.36
Teebi, A.S.37
Al-Gazali, L.38
Eapen, V.39
Stevens, C.R.40
Rappaport, L.41
Gabriel, S.B.42
Markianos, K.43
State, M.W.44
Greenberg, M.E.45
Taniguchi, H.46
Braverman, N.E.47
Morrow, E.M.48
Walsh, C.A.49
more..
|