-
1
-
-
42349095075
-
Advances in autism genetics: On the threshold of a new neurobiology
-
Abrahams B.S. & Geschwind D.H. (2008). Advances in autism genetics: on the threshold of a new neurobiology. Nature Review. Genetics 9, 341-355.
-
(2008)
Nature Review. Genetics
, vol.9
, pp. 341-355
-
-
Abrahams, B.S.1
Geschwind, D.H.2
-
2
-
-
17344364477
-
Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21
-
Blouin J.L., Dombroski B.A., Nath S.K., Lasseter V.K., Wolyniec P.S., Nestadt G., Thornquist M., Ullrich G., McGrath J., Kasch L., Lamacz M., Thomas M.G., Gehrig C., Radhakrishna U., Snyder S.E., Balk K.G., Neufeld K., Swartz K.L., DeMarchi N., Papadimitriou G.N., Dikeos D.G., Stefanis C.N., Chakravarti A., Childs B., Housman D.E., Kazazian H.H., Antonarakis S. & Pulver A.E. (1998). Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21. Nature Genetics 20, 70-73.
-
(1998)
Nature Genetics
, vol.20
, pp. 70-73
-
-
Blouin, J.L.1
Dombroski, B.A.2
Nath, S.K.3
Lasseter, V.K.4
Wolyniec, P.S.5
Nestadt, G.6
Thornquist, M.7
Ullrich, G.8
McGrath, J.9
Kasch, L.10
Lamacz, M.11
Thomas, M.G.12
Gehrig, C.13
Radhakrishna, U.14
Snyder, S.E.15
Balk, K.G.16
Neufeld, K.17
Swartz, K.L.18
Demarchi, N.19
Papadimitriou, G.N.20
Dikeos, D.G.21
Stefanis, C.N.22
Chakravarti, A.23
Childs, B.24
Housman, D.E.25
Kazazian, H.H.26
Antonarakis, S.27
Pulver, A.E.28
more..
-
3
-
-
56749154242
-
Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities
-
Epub 2008 Nov.
-
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. (2008). Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities. Nature Genetics Epub 2008 Nov.
-
(2008)
Nature Genetics
-
-
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..
-
4
-
-
0034724924
-
Location of a major susceptibility locus for familial schizophrenia on chromosome 1q21-q22
-
Brzustowicz L.M., Hodgkinson K.A., Chow E.W., Honer W.G. & Bassett A.S. (2000). Location of a major susceptibility locus for familial schizophrenia on chromosome 1q21-q22. Science 288(5466), 678-682.
-
(2000)
Science
, vol.288
, Issue.5466
, pp. 678-682
-
-
Brzustowicz, L.M.1
Hodgkinson, K.A.2
Chow, E.W.3
Honer, W.G.4
Bassett, A.S.5
-
5
-
-
54049144653
-
Copy-number variations associated with neuropsychiatric conditions
-
Cook E.H., Jr. & Scherer S.W. (2008). Copy-number variations associated with neuropsychiatric conditions. Nature 455(7215), 919-923.
-
(2008)
Nature
, vol.455
, Issue.7215
, pp. 919-923
-
-
Cook Jr., E.H.1
Scherer, S.W.2
-
6
-
-
25444432040
-
Diagnostic genome profiling in mental retardation
-
de Vries B.B., Pfundt R., Leisink M., Koolen D.A., Vissers L.E., Janssen I.M., Reijmersdal S., Nillesen W.M., Huys E.H., Leeuw N., Smeets D., Sistermans E.A., Feuth T., Ravenswaaij-Arts C.M., van Kessel A.G., Schoenmakers E.F., Brunner H.G. &Veltman J.A. (2005). Diagnostic genome profiling in mental retardation. American Journal of Human Genetics 77, 606-616.
-
(2005)
American Journal of Human Genetics
, vol.77
, pp. 606-616
-
-
De Vries, B.B.1
Pfundt, R.2
Leisink, M.3
Koolen, D.A.4
Vissers, L.E.5
Janssen, I.M.6
Reijmersdal, S.7
Nillesen, W.M.8
Huys, E.H.9
Leeuw, N.10
Smeets, D.11
Sistermans, E.A.12
Feuth, T.13
Ravenswaaij-Arts, C.M.14
Van Kessel, A.G.15
Schoenmakers, E.F.16
Brunner, H.G.17
Veltman, J.A.18
-
7
-
-
0024385396
-
Exclusion of linkage to 5q11-13 in families with schizophrenia and other psychiatric disorders
-
Detera-Wadleigh S.D., Goldin L.R., Sherrington R., Encio I., de Miguel C., Berrettini W., Gurling H. & Gershon E.S. (1989). Exclusion of linkage to 5q11-13 in families with schizophrenia and other psychiatric disorders. Nature 340(6232), 391-393.
-
(1989)
Nature
, vol.340
, Issue.6232
, pp. 391-393
-
-
Detera-Wadleigh, S.D.1
Goldin, L.R.2
Sherrington, R.3
Encio, I.4
De Miguel, C.5
Berrettini, W.6
Gurling, H.7
Gershon, E.S.8
-
8
-
-
17444448778
-
Genome scan of European-American schizophrenia pedigrees: Results of the NIMH Genetics Initiative and Millennium Consortium
-
Faraone S.V., Matise T., Svrakic D., Pepple J., Malaspina D., Suarez B., Hampe C., Zambuto C.T., Schmitt K., Meyer J., Markel P., Lee H., Harkavy Friedman J., Kaufmann C., Cloninger C.R. & Tsuang M.T. (1998). Genome scan of European-American schizophrenia pedigrees: results of the NIMH Genetics Initiative and Millennium Consortium. American Journal of Medical Genetics 10, 81, 290-295.
-
(1998)
American Journal of Medical Genetics
, vol.10
, Issue.81
, pp. 290-295
-
-
Faraone, S.V.1
Matise, T.2
Svrakic, D.3
Pepple, J.4
Malaspina, D.5
Suarez, B.6
Hampe, C.7
Zambuto, C.T.8
Schmitt, K.9
Meyer, J.10
Markel, P.11
Lee, H.12
Harkavy Friedman, J.13
Kaufmann, C.14
Cloninger, C.R.15
Tsuang, M.T.16
-
9
-
-
0029874880
-
A combined analysis of D22S278 marker alleles in affected sib-pairs: Support for a susceptibility locus for schizophrenia at chromosome 22q12. Schizophrenia Collaborative Linkage Group (Chromosome 22)
-
Gill M., Vallada H., Collier D., Sham P., Holmans P., Murray R., McGuffin P., Nanko S., Owen M., Antonarakis S., Housman D., Kazazian H., Nestadt G., Pulver A.E., Straub R.E., MacLean C.J., Walsh D., Kendler K.S., DeLisi L., Polymeropoulos M., Coon H., Byerley W., Lofthouse R., Gershon E., Read C.M. et al. (1996). A combined analysis of D22S278 marker alleles in affected sib-pairs: support for a susceptibility locus for schizophrenia at chromosome 22q12. Schizophrenia Collaborative Linkage Group (Chromosome 22). American Journal of Medical Genetics 16, 67, 40-45.
-
(1996)
American Journal of Medical Genetics
, vol.16
, Issue.67
, pp. 40-45
-
-
Gill, M.1
Vallada, H.2
Collier, D.3
Sham, P.4
Holmans, P.5
Murray, R.6
McGuffin, P.7
Nanko, S.8
Owen, M.9
Antonarakis, S.10
Housman, D.11
Kazazian, H.12
Nestadt, G.13
Pulver, A.E.14
Straub, R.E.15
MacLean, C.J.16
Walsh, D.17
Kendler, K.S.18
Delisi, L.19
Polymeropoulos, M.20
Coon, H.21
Byerley, W.22
Lofthouse, R.23
Gershon, E.24
Read, C.M.25
more..
-
10
-
-
51649107017
-
Rare chromosomal deletions and duplications increase risk of schizophrenia
-
International Schizophrenia Consortium
-
International Schizophrenia Consortium (2008). Rare chromosomal deletions and duplications increase risk of schizophrenia. Nature. 455(7210), 237-241.
-
(2008)
Nature.
, vol.455
, Issue.7210
, pp. 237-241
-
-
-
11
-
-
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. (2008). Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia. Human Molecular Genetics 17, 458-465.
-
(2008)
Human Molecular Genetics
, 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
-
12
-
-
0033842462
-
Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: Schizophrenia linkage collaborative group III
-
Levinson D.F., Holmans P., Straub R.E., Owen M.J., Wildenauer D.B., Gejman P.V., Pulver A.E., Laurent C., Kendler K.S., Walsh D., Norton N., Williams N.M., Schwab S.G., Lerer B., Mowry B.J., Sanders A.R., Antonarakis S.E., Blouin J.L., DeLeuze J.F. & Mallet J. (2000). Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: schizophrenia linkage collaborative group III. American Journal of Medical Genetics 67, 652-663.
-
(2000)
American Journal of Medical Genetics
, vol.67
, pp. 652-663
-
-
Levinson, D.F.1
Holmans, P.2
Straub, R.E.3
Owen, M.J.4
Wildenauer, D.B.5
Gejman, P.V.6
Pulver, A.E.7
Laurent, C.8
Kendler, K.S.9
Walsh, D.10
Norton, N.11
Williams, N.M.12
Schwab, S.G.13
Lerer, B.14
Mowry, B.J.15
Sanders, A.R.16
Antonarakis, S.E.17
Blouin, J.L.18
Deleuze, J.F.19
Mallet, J.20
more..
-
13
-
-
0038003196
-
Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia
-
Lewis C.M., Levinson D.F., Wise L.H., DeLisi L.E., Straub R.E., Hovatta I., Williams N.M., Schwab S.G., Pulver A.E., Faraone S.V., Brzustowicz L.M., Kaufmann C.A., Garver D.L., Gurling H.M., Lindholm E., Coon H., Moises H.W., Byerley W., Shaw S.H., Mesen A., Sherrington R., O'Neill F.A., Walsh D., Kendler K.S., Ekelund J., Paunio T., Lonnqvist J., Peltonen L., O'Donovan M.C., Owen M.J., Wildenauer D.B., Maier W., Nestadt G., Blouin J.L., Antonarakis S.E., Mowry B.J., Silverman J.M., Crowe R.R., Cloninger C.R., Tsuang M.T., Malaspina D., Harkavy-Friedman J.M., Svrakic D.M., Bassett A.S., Holcomb J., Kalsi G., McQuillin A., Brynjolfson J., Sigmundsson T., Petursson H., Jazin E., Zoega T. & Helgason T. (2003). Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia. American Journal of Medical Genetics 73, 34-48.
-
(2003)
American Journal of Medical Genetics
, vol.73
, pp. 34-48
-
-
Lewis, C.M.1
Levinson, D.F.2
Wise, L.H.3
Delisi, L.E.4
Straub, R.E.5
Hovatta, I.6
Williams, N.M.7
Schwab, S.G.8
Pulver, A.E.9
Faraone, S.V.10
Brzustowicz, L.M.11
Kaufmann, C.A.12
Garver, D.L.13
Gurling, H.M.14
Lindholm, E.15
Coon, H.16
Moises, H.W.17
Byerley, W.18
Shaw, S.H.19
Mesen, A.20
Sherrington, R.21
O'Neill, F.A.22
Walsh, D.23
Kendler, K.S.24
Ekelund, J.25
Paunio, T.26
Lonnqvist, J.27
Peltonen, L.28
O'Donovan, M.C.29
Owen, M.J.30
Wildenauer, D.B.31
Maier, W.32
Nestadt, G.33
Blouin, J.L.34
Antonarakis, S.E.35
Mowry, B.J.36
Silverman, J.M.37
Crowe, R.R.38
Cloninger, C.R.39
Tsuang, M.T.40
Malaspina, D.41
Harkavy-Friedman, J.M.42
Svrakic, D.M.43
Bassett, A.S.44
Holcomb, J.45
Kalsi, G.46
McQuillin, A.47
Brynjolfson, J.48
Sigmundsson, T.49
Petursson, H.50
Jazin, E.51
Zoega, T.52
Helgason, T.53
more..
-
14
-
-
0029565202
-
Suggestive evidence for linkage of schizophrenia to markers on chromosome 13q14.1-q32
-
Lin M.W., Curtis D., Williams N., Arranz M., Nanko S., Collier D., McGuffin P., Murray R., Owen M., Gill M., et al. (1995). Suggestive evidence for linkage of schizophrenia to markers on chromosome 13q14.1-q32. Psychiatric Genetics 5(3), 117-26.
-
(1995)
Psychiatric Genetics
, vol.5
, Issue.3
, pp. 117-126
-
-
Lin, M.W.1
Curtis, D.2
Williams, N.3
Arranz, M.4
Nanko, S.5
Collier, D.6
McGuffin, P.7
Murray, R.8
Owen, M.9
Gill, M.10
-
15
-
-
77951565141
-
-
Erratum in: Spring
-
Erratum in: Psychiatric Genetics 1996 Spring 6(1), 37.
-
(1996)
Psychiatric Genetics
, vol.6
, Issue.1
, pp. 37
-
-
-
18
-
-
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 G.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. (2008) .Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes. New England Journal of Medicine 359, 1685-1699.
-
(2008)
New England Journal of Medicine
, 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, G.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..
-
19
-
-
33846669291
-
Detection of a novel familial deletion of four genes between BP1 and BP2 of the Prader-Willi/Angelman syndrome critical region by oligo-array CGH in a child with neurological disorder and speech impairment
-
Murthy S.K., Nygren A.O., El Shakankiry H.M., Schouten J.P., Al Khayat A.I., Ridha A. & Al Ali M.T. (2007). Detection of a novel familial deletion of four genes between BP1 and BP2 of the Prader-Willi/Angelman syndrome critical region by oligo-array CGH in a child with neurological disorder and speech impairment. Cytogenetic and Genome Research 116, 135-140.
-
(2007)
Cytogenetic and Genome Research
, vol.116
, pp. 135-140
-
-
Murthy, S.K.1
Nygren, A.O.2
El Shakankiry, H.M.3
Schouten, J.P.4
Al Khayat, A.I.5
Ridha, A.6
Al Ali, M.T.7
-
21
-
-
56749179965
-
Phenotypic variations on the theme of CNVs
-
O'Donovan M.C., Kirov G. & Owen M.J. (2008a). Phenotypic variations on the theme of CNVs. Nature Genetics 40, 1392-1393.
-
(2008)
Nature Genetics
, vol.40
, pp. 1392-1393
-
-
O'Donovan, M.C.1
Kirov, G.2
Owen, M.J.3
-
22
-
-
50449100461
-
Identification of loci associated with schizophrenia by genome-wide association and follow-up
-
Molecular Genetics of Schizophrenia Collaboration
-
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., Möller 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., Nöthen 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. & Molecular Genetics of Schizophrenia Collaboration (2008b). Identification of loci associated with schizophrenia by genome-wide association and follow-up. Nature Genetics 40, 1053-1055.
-
(2008)
Nature Genetics
, 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
Möller, 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
Nöthen, 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..
-
23
-
-
25144488980
-
Genomic approaches to schizophrenia
-
Owen M.J. (2005) .Genomic approaches to schizophrenia. Clinical Therapy 27, Suppl. A, S2-7.
-
(2005)
Clinical Therapy
, vol.27
, Issue.SUPPL. A
-
-
Owen, M.J.1
-
25
-
-
54049106103
-
Failure of neuronal homeostasis results in common neuropsychiatric phenotypes
-
Ramocki M.B. & Zoghbi H.Y. (2008). Failure of neuronal homeostasis results in common neuropsychiatric phenotypes. Nature 455(7215), 912-918.
-
(2008)
Nature
, vol.455
, Issue.7215
, pp. 912-918
-
-
Ramocki, M.B.1
Zoghbi, H.Y.2
-
26
-
-
58849158696
-
Disruption of the neurexin 1 gene is associated with schizophrenia
-
Epub 2008 Oct.
-
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., Hoffmann P., Crombie C., Fraser G., Walker N., Lonnqvist J., Suvisaari J., Tuulio-Henriksson A., Andreassen O.A., Djurovic S., Hansen T., Werge T., Melle I., Kiemeney L.A., Franke B., Buizer-Voskamp J.E., Ophoff R.A., Rietschel M., Nothen M.M., Stefansson K., Peltonen L., St Clair D., Stefansson H. & Collier D.A. (2008). Disruption of the neurexin 1 gene is associated with schizophrenia. Human Molecular Genetics, Epub 2008 Oct.
-
(2008)
Human Molecular Genetics
-
-
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.27
Hoffmann, P.28
Crombie, C.29
Fraser, G.30
Walker, N.31
Lonnqvist, J.32
Suvisaari, J.33
Tuulio-Henriksson, A.34
Andreassen, O.A.35
Djurovic, S.36
Hansen, T.37
Werge, T.38
Melle, I.39
Kiemeney, L.A.40
Franke, B.41
Buizer-Voskamp, J.E.42
Ophoff, R.A.43
Rietschel, M.44
Nothen, M.M.45
Stefansson, K.46
Peltonen, L.47
St Clair, D.48
Stefansson, H.49
Collier, D.A.50
more..
-
27
-
-
43349097737
-
No significant association of 14 candidate genes with schizophrenia in a large European ancestry sample: Implications for psychiatric genetics
-
Erratum in: American Journal of Psychiatry 165, 1359.
-
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. (2008). No significant association of 14 candidate genes with schizophrenia in a large European ancestry sample: implications for psychiatric genetics. American Journal of Psychiatry 165, 497-506. Erratum in: American Journal of Psychiatry 165, 1359.
-
(2008)
American Journal of Psychiatry
, vol.165
, pp. 497-506
-
-
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..
-
28
-
-
0029845435
-
Additional support for schizophrenia linkage on chromosomes 6 and 8: A multicenter study. Schizophrenia linkage collaborative group for chromosomes 3, 6 and 8
-
Schizophrenia linkage collaborative group
-
Schizophrenia linkage collaborative group (1996). Additional support for schizophrenia linkage on chromosomes 6 and 8: a multicenter study. Schizophrenia Linkage Collaborative Group for Chromosomes 3, 6 and 8. American Journal of Medical Genetics 22;67, 580-594.
-
(1996)
American Journal of Medical Genetics
, vol.22
, Issue.67
, pp. 580-594
-
-
-
29
-
-
8244226000
-
Evidence suggestive of a locus on chromosome 5q31 contributing to susceptibility for schizophrenia in German and Israeli families by multipoint affected sib-pair linkage analysis
-
Schwab S.G., Eckstein G.N., Hallmayer J., Lerer B., Albus M., Borrmann M., Lichtermann D., Ertl M.A., Maier W. & Wildenauer D.B. (1997). Evidence suggestive of a locus on chromosome 5q31 contributing to susceptibility for schizophrenia in German and Israeli families by multipoint affected sib-pair linkage analysis. Molecular Psychiatry 2, 156-160.
-
(1997)
Molecular Psychiatry
, vol.2
, pp. 156-160
-
-
Schwab, S.G.1
Eckstein, G.N.2
Hallmayer, J.3
Lerer, B.4
Albus, M.5
Borrmann, M.6
Lichtermann, D.7
Ertl, M.A.8
Maier, W.9
Wildenauer, D.B.10
-
30
-
-
0037222276
-
Support for association of schizophrenia with genetic variation in the 6p22.3 gene, dysbindin, in sib-pair families with linkage and in an additional sample of triad families
-
Schwab S.G., Knapp M., Mondabon S., Hallmayer J., Borrmann-Hassenbach M., Albus M., Lerer B., Rietschel M., Trixler M., Maier W. & Wildenauer D.B. (2003). Support for association of schizophrenia with genetic variation in the 6p22.3 gene, dysbindin, in sib-pair families with linkage and in an additional sample of triad families. American Journal of Human Genetics 72, 185-190.
-
(2003)
American Journal of Human Genetics
, vol.72
, pp. 185-190
-
-
Schwab, S.G.1
Knapp, M.2
Mondabon, S.3
Hallmayer, J.4
Borrmann-Hassenbach, M.5
Albus, M.6
Lerer, B.7
Rietschel, M.8
Trixler, M.9
Maier, W.10
Wildenauer, D.B.11
-
31
-
-
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. (2007). Strong association of de novo copy number mutations with autism. Science 316(5823), 445-449.
-
(2007)
Science
, vol.316
, Issue.5823
, 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..
-
32
-
-
33748333194
-
Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome
-
Sharp A.J., Hansen S., Selzer R.R., Cheng Z., Regan R., Hurst J.A., Stewart H., Price S.M., Blair E., Hennekam R.C., Fitzpatrick C.A., Segraves R., Richmond T.A., Guiver C., Albertson D.G., Pinkel D., Eis P.S., Schwartz S., Knight S.J. & Eichler E.E. (2006). Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome. Nature Genetics 38,1038-1042.
-
(2006)
Nature Genetics
, vol.38
, pp. 1038-1042
-
-
Sharp, A.J.1
Hansen, S.2
Selzer, R.R.3
Cheng, Z.4
Regan, R.5
Hurst, J.A.6
Stewart, H.7
Price, S.M.8
Blair, E.9
Hennekam, R.C.10
Fitzpatrick, C.A.11
Segraves, R.12
Richmond, T.A.13
Guiver, C.14
Albertson, D.G.15
Pinkel, D.16
Eis, P.S.17
Schwartz, S.18
Knight, S.J.19
Eichler, E.E.20
more..
-
33
-
-
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. (2008). A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures. Nature Genetics 40, 322-328.
-
(2008)
Nature Genetics
, 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..
-
34
-
-
0023923609
-
Translocation 5;21 and interstitial deletion of chromosome 7 in a case of chronic myelomonocytic leukemia
-
Sherrington P.D., Nacheva E., Fischer P., Rees J.K., Hoyle C., Dyer M., Harper P., Knight C. & Hayhoe F.G. (1988). Translocation 5;21 and interstitial deletion of chromosome 7 in a case of chronic myelomonocytic leukemia. Cancer Genetics and Cytogenetics 31, 247-252.
-
(1988)
Cancer Genetics and Cytogenetics
, vol.31
, pp. 247-252
-
-
Sherrington, P.D.1
Nacheva, E.2
Fischer, P.3
Rees, J.K.4
Hoyle, C.5
Dyer, M.6
Harper, P.7
Knight, C.8
Hayhoe, F.G.9
-
35
-
-
44249121777
-
Novel microdeletion syndromes detected by chromosome microarrays
-
Slavotinek A.M. (2008). Novel microdeletion syndromes detected by chromosome microarrays. Human Genetics 124, 1-17.
-
(2008)
Human Genetics
, vol.124
, pp. 1-17
-
-
Slavotinek, A.M.1
-
36
-
-
77951518600
-
Copy number variation and schizophrenia
-
Epub 2008 Nov.
-
St Clair D. (2008). Copy number variation and schizophrenia. Schizophrenia Bulletin Epub 2008 Nov.
-
(2008)
Schizophrenia Bulletin
-
-
St Clair, D.1
-
37
-
-
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., 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. (2008). Large recurrent microdeletions associated with schizophrenia. Nature 455(7210), 232-236.
-
(2008)
Nature
, vol.455
, Issue.7210
, 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
Jonasdottir, A.22
Bjornsson, A.23
Mattiasdottir, S.24
Blondal, T.25
Haraldsson, M.26
Magnusdottir, B.B.27
Giegling, I.28
Moller, H.J.29
Hartmann, A.30
Shianna, K.V.31
Ge, D.32
Need, A.C.33
Crombie, C.34
Fraser, G.35
Walker, N.36
Lonnqvist, J.37
Suvisaari, J.38
Tuulio-Henriksson, A.39
Paunio, T.40
Toulopoulou, T.41
Bramon, E.42
Di Forti, M.43
Murray, R.44
Ruggeri, M.45
Vassos, E.46
Tosato, S.47
Walshe, M.48
Li, T.49
Vasilescu, C.50
Muhleisen, T.W.51
Wang, A.G.52
Ullum, H.53
Djurovic, S.54
Melle, I.55
Olesen, J.56
Kiemeney, L.A.57
Franke, B.58
Sabatti, C.59
Freimer, N.B.60
Gulcher, J.R.61
Thorsteinsdottir, U.62
Kong, A.63
Andreassen, O.A.64
Ophoff, R.A.65
Georgi, A.66
Rietschel, M.67
Werge, T.68
Petursson, H.69
Goldstein, D.B.70
Nothen, M.M.71
Peltonen, L.72
Collier, D.A.73
St Clair, D.74
Stefansson, K.75
more..
-
38
-
-
0030980118
-
Support for a possible schizophrenia vulnerability locus in region 5q22-31 in Irish families
-
Straub R.E., MacLean C.J., O'Neill F.A., Walsh D. & Kendler K.S. (1997). Support for a possible schizophrenia vulnerability locus in region 5q22-31 in Irish families. Molecular Psychiatry 2, 148-155.
-
(1997)
Molecular Psychiatry
, vol.2
, pp. 148-155
-
-
Straub, R.E.1
MacLean, C.J.2
O'Neill, F.A.3
Walsh, D.4
Kendler, K.S.5
-
39
-
-
0006739554
-
A schizophrenia locus may be located in region 10p15-p11
-
Straub R.E., MacLean C.J., Martin R.B., Ma Y., Myakishev M.V., Harris-Kerr C., Webb B.T., O'Neill F.A., Walsh D. & Kendler K.S. (1998). A schizophrenia locus may be located in region 10p15-p11. American Journal of Medical Genetics 81, 296-301.
-
(1998)
American Journal of Medical Genetics
, vol.81
, pp. 296-301
-
-
Straub, R.E.1
MacLean, C.J.2
Martin, R.B.3
Ma, Y.4
Myakishev, M.V.5
Harris-Kerr, C.6
Webb, B.T.7
O'Neill, F.A.8
Walsh, D.9
Kendler, K.S.10
-
40
-
-
18444364206
-
Genetic variation in the 6p22.3 gene DTNBP1, the human ortholog of the mouse dysbindin gene, is associated with schizophrenia
-
Straub R.E., Jiang Y., MacLean C.J., Ma Y., Webb B.T., Myakishev M.V., Harris-Kerr C., Wormley B., Sadek H., Kadambi B., Cesare A.J., Gibberman A., Wang X., O'Neill F.A., Walsh D. & Kendler K.S. (2002). Genetic variation in the 6p22.3 gene DTNBP1, the human ortholog of the mouse dysbindin gene, is associated with schizophrenia. American Journal of Human Genetics 71, 337-348.
-
(2002)
American Journal of Human Genetics
, vol.71
, pp. 337-348
-
-
Straub, R.E.1
Jiang, Y.2
MacLean, C.J.3
Ma, Y.4
Webb, B.T.5
Myakishev, M.V.6
Harris-Kerr, C.7
Wormley, B.8
Sadek, H.9
Kadambi, B.10
Cesare, A.J.11
Gibberman, A.12
Wang, X.13
O'Neill, F.A.14
Walsh, D.15
Kendler, K.S.16
-
41
-
-
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. (2008). Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia. Science 320(5875), 539-543.
-
(2008)
Science
, vol.320
, Issue.5875
, 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..
-
42
-
-
25144432238
-
Genetic mechanisms of psychosis: In vivo and postmortem genomics
-
Weinberger D.R. (2005). Genetic mechanisms of psychosis: in vivo and postmortem genomics. Clinical Therapy 27, Suppl A, S8-15.
-
(2005)
Clinical Therapy
, vol.27
, Issue.SUPPL. A
-
-
Weinberger, D.R.1
-
43
-
-
39049163023
-
Association between microdeletion and microduplication at 16p11.2 and autism
-
Weiss L.A., Shen Y., Korn J.M., Arking D.E., Miller D.T., Fossdal R., Saemundsen E., Stefansson H., Ferreira M.A., Green T., Platt O.S., Ruderfer D.M., Walsh C.A., Altshuler D., Chakravarti A., Tanzi R.E., Stefansson K., Santangelo S.L., Gusella J.F., Sklar P., Wu B.L. & Daly M.J. (2008). Association between microdeletion and microduplication at 16p11.2 and autism. New England Journal of Medicine 358, 667-675.
-
(2008)
New England Journal of Medicine
, vol.358
, pp. 667-675
-
-
Weiss, L.A.1
Shen, Y.2
Korn, J.M.3
Arking, D.E.4
Miller, D.T.5
Fossdal, R.6
Saemundsen, E.7
Stefansson, H.8
Ferreira, M.A.9
Green, T.10
Platt, O.S.11
Ruderfer, D.M.12
Walsh, C.A.13
Altshuler, D.14
Chakravarti, A.15
Tanzi, R.E.16
Stefansson, K.17
Santangelo, S.L.18
Gusella, J.F.19
Sklar, P.20
Wu, B.L.21
Daly, M.J.22
more..
|