-
1
-
-
46249104490
-
Systematic meta-analyses and field synopsis of genetic association studies in schizophrenia: The SzGene database
-
DOI 10.1038/ng.171, PII NG171
-
Allen NC, Bagade S, McQueen MB, Ioannidis JP, Kavvoura FK, Khoury MJ, Tanzi RE, Bertram L (2008). Systematic meta-analyses and field synopsis of genetic association studies in schizophrenia : the SzGene database. Nature Genetics 40, 827-834. (Pubitemid 351913655)
-
(2008)
Nature Genetics
, vol.40
, Issue.7
, pp. 827-834
-
-
Allen, N.C.1
Bagade, S.2
McQueen, M.B.3
Ioannidis, J.P.A.4
Kavvoura, F.K.5
Khoury, M.J.6
Tanzi, R.E.7
Bertram, L.8
-
2
-
-
77955426959
-
Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohort
-
Athanasiu L, Mattingsdal M, Kahler AK, Brown A, Gustafsson O, Agartz I, Giegling I, Muglia P, Cichon S, Rietschel M, Pietilainen OP, Peltonen L, Bramon E, Collier D, Clair DS, Sigurdsson E, Petursson H, Rujescu D, Melle I, Steen VM, Djurovic S, Andreassen OA (2010). Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohort. Journal of Psychiatric Research 44, 748-753.
-
(2010)
Journal of Psychiatric Research
, vol.44
, pp. 748-753
-
-
Athanasiu, L.1
Mattingsdal, M.2
Kahler, A.K.3
Brown, A.4
Gustafsson, O.5
Agartz, I.6
Giegling, I.7
Muglia, P.8
Cichon, S.9
Rietschel, M.10
Pietilainen, O.P.11
Peltonen, L.12
Bramon, E.13
Collier, D.14
Clair, D.S.15
Sigurdsson, E.16
Petursson, H.17
Rujescu, D.18
Melle, I.19
Steen, V.M.20
Djurovic, S.21
Andreassen, O.A.22
more..
-
3
-
-
39649124023
-
Array-based DNA diagnostics: Let the revolution begin
-
DOI 10.1146/annurev.med.59.012907.101800
-
Beaudet AL, Belmont JW (2008). Array-based DNA diagnostics : let the revolution begin. Annual Review of Medicine 59, 113-129. (Pubitemid 351287927)
-
(2008)
Annual Review of Medicine
, vol.59
, pp. 113-129
-
-
Beaudet, A.L.1
Belmont, J.W.2
-
4
-
-
0034082294
-
Repeat sizes at CAG/CTG loci CTG18.1, ERDA1 and TGC13-7a in schizophrenia
-
Bowen T, Guy CA, Cardno AG, Vincent JB, Kennedy JL, Jones LA, Gray M, Sanders RD, McCarthy G, Murphy KC, Owen MJ, O'Donovan MC (2000). Repeat sizes at CAG/CTG loci CTG18.1, ERDA1 and TGC13-7a in schizophrenia. Psychiatric Genetics 10, 33-37. (Pubitemid 30345190)
-
(2000)
Psychiatric Genetics
, vol.10
, Issue.1
, pp. 33-37
-
-
Bowen, T.1
Guy, C.A.2
Cardno, A.G.3
Vincent, J.B.4
Kennedy, J.L.5
Jones, L.A.6
Gray, M.7
Sanders, R.D.8
McCarthy, G.9
Murphy, K.C.10
Owen, M.J.11
O'Donovan, M.C.12
-
5
-
-
62649155943
-
A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals
-
Browning BL, Browning SR (2009). A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals. American Journal of Human Genetics 84, 210-223.
-
(2009)
American Journal of Human Genetics
, vol.84
, pp. 210-223
-
-
Browning, B.L.1
Browning, S.R.2
-
6
-
-
35348817330
-
Rapid and accurate haplotype phasing and missing-data inference for whole-genome association studies by use of localized haplotype clustering
-
DOI 10.1086/521987
-
Browning SR, Browning BL (2007). Rapid and accurate haplotype phasing and missing-data inference for whole-genome association studies by use of localized haplotype clustering. American Journal of Human Genetics 81, 1084-1097. (Pubitemid 47580259)
-
(2007)
American Journal of Human Genetics
, vol.81
, Issue.5
, pp. 1084-1097
-
-
Browning, S.R.1
Browning, B.L.2
-
7
-
-
34249997024
-
Replicating genotype-phenotype associations
-
DOI 10.1038/447655a, PII 447655A
-
Chanock SJ, Manolio T, Boehnke M, Boerwinkle E, Hunter DJ, Thomas G, Hirschhorn JN, Abecasis G, Altshuler D, Bailey-Wilson JE, Brooks LD, Cardon LR, Daly M, Donnelly P, Fraumeni Jr. JF, Freimer NB, Gerhard DS, Gunter C, Guttmacher AE, Guyer MS, Harris EL, Hoh J, Hoover R, Kong CA, Merikangas KR, Morton CC, Palmer LJ, Phimister EG, Rice JP, Roberts J, Rotimi C, Tucker MA, Vogan KJ, Wacholder S, Wijsman EM, Winn DM, Collins FS (2007). Replicating genotype-phenotype associations. Nature 447, 655-660. (Pubitemid 46889722)
-
(2007)
Nature
, vol.447
, Issue.7145
, pp. 655-660
-
-
Chanock, S.J.1
Manolio, T.2
Boehnke, M.3
Boerwinkle, E.4
Hunter, D.J.5
Thomas, G.6
Hirschhorn, J.N.7
Abecasis, G.8
Altshuler, D.9
Bailey-Wilson, J.E.10
Brooks, L.D.11
Cardon, L.R.12
Daly, M.13
Donnelly, P.14
Fraumeni Jr., J.F.15
Freimer, N.B.16
Gerhard, D.S.17
Gunter, C.18
Guttmacher, A.E.19
Guyer, M.S.20
Harris, E.L.21
Hoh, J.22
Hoover, R.23
Kong, C.A.24
Merikangas, K.R.25
Morton, C.C.26
Palmer, L.J.27
Phimister, E.G.28
Rice, J.P.29
Roberts, J.30
Rotimi, C.31
Tucker, M.A.32
Vogan, K.J.33
Wacholder, S.34
Wijsman, E.M.35
Winn, D.M.36
Collins, F.S.37
more..
-
8
-
-
66149185456
-
Genomewide association studies : History, rationale, and prospects for psychiatric disorders
-
Cichon S, Craddock N, Daly M, Faraone SV, Gejman PV, Kelsoe J, Lehner T, Levinson DF, Moran A, Sklar P, Sullivan PF (2009). Genomewide association studies : history, rationale, and prospects for psychiatric disorders. American Journal of Psychiatry 166, 540-556.
-
(2009)
American Journal of 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
-
9
-
-
0038005018
-
DAVID: Database for annotation, visualization, and integrated discovery
-
Dennis Jr. G, Sherman BT, Hosack DA, Yang J, Gao W, Lane HC, Lempicki RA (2003). DAVID: Database for Annotation, Visualization, and Integrated Discovery. Genome Biology 4, P3.
-
(2003)
Genome Biology
, vol.4
-
-
Dennis Jr., G.1
Sherman, B.T.2
Hosack, D.A.3
Yang, J.4
Gao, W.5
Lane, H.C.6
Lempicki, R.A.7
-
11
-
-
0037080655
-
Sample size requirements for matched case-control studies of gene-environment interaction
-
DOI 10.1002/sim.973
-
Gauderman WJ (2002). Sample size requirements for matched case-control studies of gene-environment interaction. Statistics in Medicine 21, 35-50. (Pubitemid 34065703)
-
(2002)
Statistics in Medicine
, vol.21
, Issue.1
, pp. 35-50
-
-
Gauderman, W.J.1
-
12
-
-
0346801873
-
The gene oncology (GO) database and informatics resource
-
Harris MA, Clark J, Ireland A, Lomax J, Ashburner M, Foulger R, Eilbeck K, Lewis S, Marshall B, Mungall C, Richter J, Rubin GM, Blake JA, Bult C, Dolan M, Drabkin H, Eppig JT, Hill DP, Ni L, Ringwald M, Balakrishnan R, Cherry JM, Christie KR, Costanzo MC, Dwight SS, Engel S, Fisk DG, Hirschman JE, Hong EL, Nash RS, Sethuraman A, Theesfeld CL, Botstein D, Dolinski K, Feierbach B, Berardini T, Mundodi S, Rhee SY, Apweiler R, Barrell D, Camon E, Dimmer E, Lee V, Chisholm R, Gaudet P, Kibbe W, Kishore R, Schwarz EM, Sternberg P, Gwinn M, Hannick L, Wortman J, Berriman M, Wood V, de la Cruz N, Tonellato P, Jaiswal P, Seigfried T, White R; Gene Ontology Consortium (2004). The Gene Ontology (GO) database and informatics resource. Nucleic Acids Research 32, D258-D261. (Pubitemid 38081651)
-
(2004)
Nucleic Acids Research
, vol.32
, Issue.DATABASE ISSUE
-
-
Harris, M.A.1
Clark, J.2
Ireland, A.3
Lomax, J.4
Ashburner, M.5
Foulger, R.6
Eilbeck, K.7
Lewis, S.8
Marshall, B.9
Mungall, C.10
Richter, J.11
Rubin, G.M.12
Blake, J.A.13
Bult, C.14
Dolan, M.15
Drabkin, H.16
Eppig, J.T.17
Hill, D.P.18
Ni, L.19
Ringwald, M.20
Balakrishnan, R.21
Cherry, J.M.22
Christie, K.R.23
Costanzo, M.C.24
Dwight, S.S.25
Engel, S.26
Fisk, D.G.27
Hirschman, J.E.28
Hong, E.L.29
Nash, R.S.30
Sethuraman, A.31
Theesfeld, C.L.32
Botstein, D.33
Dolinski, K.34
Feierbach, B.35
Berardini, T.36
Mundodi, S.37
Rhee, S.Y.38
Apweiler, R.39
Barrell, D.40
Camon, E.41
Dimmer, E.42
Lee, V.43
Chisholm, R.44
Gaudet, P.45
Kibbe, W.46
Kishore, R.47
Schwarz, E.M.48
Sternberg, P.49
Gwinn, M.50
Hannick, L.51
Wortman, J.52
Berriman, M.53
Wood, V.54
De La Cruz, N.55
Tonellato, P.56
Jaiswal, P.57
Seigfried, T.58
White, R.59
more..
-
13
-
-
67249117049
-
Potential etiologic and functional implications of genome-wide association loci for human diseases and traits
-
Hindorff LA, Sethupathy P, Junkins HA, Ramos EM, Mehta JP, Collins FS, Manolio TA (2009). Potential etiologic and functional implications of genome-wide association loci for human diseases and traits. Proceedings of the National Academy of Sciences USA 106, 9362-9367.
-
(2009)
Proceedings of the National Academy of Sciences USA
, 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
-
14
-
-
67649584052
-
Gene ontology analysis of GWA study data sets provides insights into the biology of bipolar disorder
-
Holmans P, Green EK, Pahwa JS, Ferreira MA, Purcell SM, Sklar P, Owen MJ, O'Donovan MC, Craddock N (2009). Gene ontology analysis of GWA study data sets provides insights into the biology of bipolar disorder. American Journal of Human Genetics 85, 13-24.
-
(2009)
American Journal of Human Genetics
, vol.85
, pp. 13-24
-
-
Holmans, P.1
Green, E.K.2
Pahwa, J.S.3
Ferreira, M.A.4
Purcell, S.M.5
Sklar, P.6
Owen, M.J.7
O'Donovan, M.C.8
Craddock, N.9
-
15
-
-
61449172037
-
Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources
-
Huang DW, Sherman BT, Lempicki RA (2009). Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources. Nature Protocols 4, 44-57.
-
(2009)
Nature Protocols
, vol.4
, pp. 44-57
-
-
Huang, D.W.1
Sherman, B.T.2
Lempicki, R.A.3
-
16
-
-
79959524146
-
A haplotype map of the human genome
-
International HapMap Consortium (2005). A haplotype map of the human genome. Nature 437, 1299-1320.
-
(2005)
Nature
, vol.437
, pp. 1299-1320
-
-
Hapmap Consortium, I.1
-
17
-
-
51649107017
-
Rare chromosomal deletions and duplications increase risk of schizophrenia
-
International Schizophrenia Consortium (2008). Rare chromosomal deletions and duplications increase risk of schizophrenia. Nature 455, 237-241.
-
(2008)
Nature
, vol.455
, pp. 237-241
-
-
-
18
-
-
0035179971
-
Replication validity of genetic association studies
-
DOI 10.1038/ng749
-
Ioannidis JP, Ntzani EE, Trikalinos TA, Contopoulos-Ioannidis DG (2001). Replication validity of genetic association studies. Nature Genetics 29, 306-309. (Pubitemid 33096456)
-
(2001)
Nature Genetics
, vol.29
, Issue.3
, pp. 306-309
-
-
Ioannidis, J.P.A.1
Ntzani, E.E.2
Trikalinos, T.A.3
Contopoulos-Ioannidis, D.G.4
-
19
-
-
67651180973
-
A genome-wide association study in 574 schizophrenia trios using DNA pooling
-
Kirov G, Zaharieva I, Georgieva L, Moskvina V, Nikolov I, Cichon S, Hillmer A, Toncheva D, Owen MJ, O'Donovan MC (2009). A genome-wide association study in 574 schizophrenia trios using DNA pooling. Molecular Psychiatry 14, 796-803.
-
(2009)
Molecular Psychiatry
, vol.14
, pp. 796-803
-
-
Kirov, G.1
Zaharieva, I.2
Georgieva, L.3
Moskvina, V.4
Nikolov, I.5
Cichon, S.6
Hillmer, A.7
Toncheva, D.8
Owen, M.J.9
O'Donovan, M.C.10
-
20
-
-
77954366969
-
No association of the serotonin transporter polymorphisms 5-HTTLPR and rs2553 with schizophrenia or neurocognition
-
Konneker TI, Crowley JJ, Quackenbush CR, Keefe RS, Perkins DO, Stroup TS, Lieberman JA, van den Oord E, Sullivan PF (2010). No association of the serotonin transporter polymorphisms 5-HTTLPR and rs2553 with schizophrenia or neurocognition. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics 153B, 1115-1117.
-
(2010)
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics
, vol.153 B
, pp. 1115-1117
-
-
Konneker, T.I.1
Crowley, J.J.2
Quackenbush, C.R.3
Keefe, R.S.4
Perkins, D.O.5
Stroup, T.S.6
Lieberman, J.A.7
Van Den Oord, E.8
Sullivan, P.F.9
-
21
-
-
52949085789
-
Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs
-
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. Nature Genetics 40, 1253-1260.
-
(2008)
Nature Genetics
, 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
-
23
-
-
34249332776
-
Converging evidence for a pseudoautosomal cytokine receptor gene locus in schizophrenia
-
DOI 10.1038/sj.mp.4001983, PII 4001983
-
Lencz T, Morgan TV, Athanasiou M, Dain B, Reed CR, Kane JM, Kucherlapati R, Malhotra AK (2007). Converging evidence for a pseudoautosomal cytokine receptor gene locus in schizophrenia. Molecular Psychiatry 12, 572-580. (Pubitemid 46816774)
-
(2007)
Molecular Psychiatry
, vol.12
, Issue.6
, 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
-
24
-
-
0033949096
-
Allelic distribution of CTG18.1 in Caucasian populations: Association studies in bipolar disorder, schizophrenia, and ataxia
-
McInnis MG, Swift-Scanlanl T, Mahoney AT, Vincent J, Verheyen G, Lan TH, Oruc L, Riess O, Van Broeckhoven C, Chen H, Kennedy JL, MacKinnon DF, Margolis RL, Simpson SG, McMahon FJ, Gershon E, Nurnberger J, Reich T, DePaulo JR, Ross CA (2000). Allelic distribution of CTG18.1 in Caucasian populations : association studies in bipolar disorder, schizophrenia, and ataxia. Molecular Psychiatry 5, 439-442. (Pubitemid 30455959)
-
(2000)
Molecular Psychiatry
, vol.5
, Issue.4
, pp. 439-442
-
-
McInnis, M.G.1
Swift-Scanlanl, T.2
Mahoney, A.T.3
Vincent, J.4
Verheyen, G.5
Hung Lan, T.6
Oruc, L.7
Riess, O.8
Van Broeckhoven, C.9
Chen, H.10
Kennedy, J.L.11
MacKinnon, D.F.12
Margolis, R.L.13
Simpson, S.G.14
McMahon, F.J.15
Gershon, E.16
Nurnberger, J.17
Reich, T.18
Depaulo, J.R.19
Ross, C.A.20
more..
-
25
-
-
61449229353
-
A genome-wide investigation of SNPs and CNVs in schizophrenia
-
Need AC, Ge D, Weale ME, Maia J, Feng S, Heinzen EL, Shianna KV, Yoon W, Kasperaviciute D, Gennarelli M, Strittmatter WJ, Bonvicini C, Rossi G, Jayathilake K, Cola PA, McEvoy JP, Keefe RS, Fisher EM, St Jean PL, Giegling I, Hartmann AM, Moller HJ, Ruppert A, Fraser G, Crombie C, Middleton LT, St Clair D, Roses AD, Muglia P, Francks C, Rujescu D, Meltzer HY, Goldstein DB (2009). A genome-wide investigation of SNPs and CNVs in schizophrenia. PLoS Genetics 5, e1000373.
-
(2009)
PLoS Genetics
, 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..
-
26
-
-
50449100461
-
Identification of loci associated with schizophrenia by genome-wide association and follow-up
-
O'Donovan MC, Craddock N, Norton N, Williams H, Peirce T, Moskvina V, Nikolov I, Hamshere M, Carroll L, Georgieva L, Dwyer S, Holmans P, Marchini JL, Spencer CC, Howie B, Leung HT, Hartmann AM, Moller HJ, Morris DW, Shi Y, Feng G, Hoffmann P, Propping P, Vasilescu C, Maier W, Rietschel M, Zammit S, Schumacher J, Quinn EM, Schulze TG, Williams NM, Giegling I, Iwata N, Ikeda M, Darvasi A, Shifman S, He L, Duan J, Sanders AR, Levinson DF, Gejman PV, Cichon S, Nothen MM, Gill M, Corvin A, Rujescu D, Kirov G, Owen MJ, Buccola NG, Mowry BJ, Freedman R, Amin F, Black DW, Silverman JM, Byerley WF, Cloninger CR (2008). 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
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..
-
27
-
-
40949127393
-
How to interpret a genome-wide association study
-
Pearson TA, Manolio TA (2008). How to interpret a genome-wide association study. Journal of the American Medical Association 299, 1335-1344.
-
(2008)
Journal of the American Medical Association
, vol.299
, pp. 1335-1344
-
-
Pearsonta, M.1
-
28
-
-
13444306641
-
NCBI Reference Sequence (RefSeq): A curated non-redundant sequence database of genomes, transcripts and proteins
-
DOI 10.1093/nar/gki025
-
Pruitt KD, Tatusova T, Maglott DR (2005). NCBI Reference Sequence (RefSeq) : a curated non-redundant sequence database of genomes, transcripts and proteins. Nucleic Acids Research 33, D501-D504. (Pubitemid 40207924)
-
(2005)
Nucleic Acids Research
, vol.33
, Issue.DATABASE ISSUE
-
-
Pruitt, K.D.1
Tatusova, T.2
Maglott, D.R.3
-
29
-
-
68449086236
-
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder
-
Purcell SM, Wray NR, Stone JL, Visscher PM, O'Donovan MC, Sullivan PF, Sklar P (2009). Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. Nature 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
-
30
-
-
0003734175
-
-
SAS Institute Inc SAS Institute, Inc. : Cary, NC
-
SAS Institute Inc (2004). SAS/STAT1 Software : Version 9. SAS Institute, Inc. : Cary, NC.
-
(2004)
SAS/STAT1 Software : Version 9
-
-
-
31
-
-
33845915280
-
-
SAS Institute Inc (Version 6). SAS Institute, Inc. : Cary, NC
-
SAS Institute Inc (2005). JMP User's Guide (Version 6). SAS Institute, Inc. : Cary, NC.
-
(2005)
JMP User's Guide
-
-
-
32
-
-
38049148026
-
DAVID Knowledgebase: A gene-centered database integrating heterogeneous gene annotation resources to facilitate high-throughput gene functional analysis
-
Sherman BT, Huang DW, Tan Q, Guo Y, Bour S, Liu D, Stephens R, Baseler MW, Lane HC, Lempicki RA (2007). DAVID Knowledgebase: a gene-centered database integrating heterogeneous gene annotation resources to facilitate high-throughput gene functional analysis. BMC Bioinformatics 8, 426.
-
(2007)
BMC Bioinformatics
, vol.8
, pp. 426
-
-
Sherman, B.T.1
Huang, D.W.2
Tan, Q.3
Guo, Y.4
Bour, S.5
Liu, D.6
Stephens, R.7
Baseler, M.W.8
Lane, H.C.9
Lempicki, R.A.10
-
33
-
-
68449096727
-
Common variants on chromosome 6p22.1 are associated with schizophrenia
-
Shi J, Levinson DF, Duan J, Sanders AR, Zheng Y, Pe'er I, Dudbridge F, Holmans PA, Whittemore AS, Mowry BJ, Olincy A, Amin F, Cloninger CR, Silverman JM, Buccola NG, Byerley WF, Black DW, Crowe RR, Oksenberg JR, Mirel DB, Kendler KS, Freedman R, Gejman PV (2009). Common variants on chromosome 6p22.1 are associated with schizophrenia. Nature 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..
-
34
-
-
40149105889
-
Genome-wide association identifies a common variant in the reelin gene that increases the risk of schizophrenia only in women
-
Shifman S, Johannesson M, Bronstein M, Chen SX, Collier DA, Craddock NJ, Kendler KS, Li T, O'Donovan M, O'Neill FA, Owen MJ, Walsh D, Weinberger DR, Sun C, Flint J, Darvasi A (2008). Genome-wide association identifies a common variant in the reelin gene that increases the risk of schizophrenia only in women. PLoS Genetics 4, e28.
-
(2008)
PLoS Genetics
, vol.4
-
-
Shifman, S.1
Johannesson, M.2
Bronstein, M.3
Chen, S.X.4
Collier, D.A.5
Craddock, N.J.6
Kendler, K.S.7
Li, T.8
O'Donovan, M.9
O'Neill, F.A.10
Owen, M.J.11
Walsh, D.12
Weinberger, D.R.13
Sun, C.14
Flint, J.15
Darvasi, A.16
-
35
-
-
68449090594
-
Common variants conferring risk of schizophrenia
-
Stefansson H, Ophoff RA, Steinberg S, Andreassen OA, Cichon S, Rujescu D, Werge T, Pietilainen OP, Mors O, Mortensen PB, Sigurdsson E, Gustafsson O, Nyegaard M, Tuulio-Henriksson A, Ingason A, Hansen T, Suvisaari J, Lonnqvist J, Paunio T, Borglum AD, Hartmann A, Fink-Jensen A, Nordentoft M, Hougaard D, Norgaard-Pedersen B, Bottcher Y, Olesen J, Breuer R, Moller HJ, Giegling I, Rasmussen HB, Timm S, Mattheisen M, Bitter I, Rethelyi JM, Magnusdottir BB, Sigmundsson T, Olason P, Masson G, Gulcher JR, Haraldsson M, Fossdal R, Thorgeirsson TE, Thorsteinsdottir U, Ruggeri M, Tosato S, Franke B, Strengman E, Kiemeney LA, 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 AC, Ge D, Yoon JL, Shianna KV, Freimer NB, Cantor RM, Murray R, Kong A, Golimbet V, Carracedo A, Arango C, Costas J, Jonsson EG, Terenius L, Agartz I, Petursson H, Nothen MM, Rietschel M, Matthews PM, Muglia P, Peltonen L, St Clair D, Goldstein DB, Stefansson K, Collier DA (2009). Common variants conferring risk of schizophrenia. Nature 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..
-
36
-
-
0013375948
-
Neuregulin 1 and susceptibility to schizophrenia
-
Stefansson H, Sigurdsson E, Steinthorsdottir V, Bjornsdottir S, Sigmundsson T, Ghosh S, Brynjolfsson J, Gunnarsdottir S, Ivarsson O, Chou TT, Hjaltason O, Birgisdottir B, Jonsson H, Gudnadottir VG, Gudmundsdottir E, Bjornsson A, Ingvarsson B, Ingason A, Sigfusson S, Hardardottir H, Harvey RP, Lai D, Zhou M, Brunner D, Mutel V, Gonzalo A, Lemke G, Sainz J, Johannesson G, Andresson T, Gudbjartsson D, Manolescu A, Frigge ML, Gurney ME, Kong A, Gulcher JR, Petursson H, Stefansson K (2002). Neuregulin 1 and susceptibility to schizophrenia. American Journal of Human Genetics 71, 877-892. (Pubitemid 135750519)
-
(2002)
American Journal of Human Genetics
, vol.71
, Issue.4
, pp. 877-892
-
-
Stefansson, H.1
Sigurdsson, E.2
Steinthorsdottir, V.3
Bjornsdottir, S.4
Sigmundsson, T.5
Ghosh, S.6
Brynjolfsson, J.7
Gunnarsdottir, S.8
Ivarsson, O.9
Chou, T.T.10
Hjaltason, O.11
Birgisdottir, B.12
Jonsson, H.13
Gudnadottir, V.G.14
Gudmundsdottir, E.15
Bjornsson, A.16
Ingvarsson, B.17
Ingason, A.18
Sigfusson, S.19
Hardardottir, H.20
Harvey, R.P.21
Lai, D.22
Zhou, M.23
Brunner, D.24
Mutel, V.25
Gonzalo, A.26
Lemke, G.27
Sainz, J.28
Johannesson, G.29
Andresson, T.30
Gudbjartsson, D.31
Manolescu, A.32
Frigge, M.L.33
Gurney, M.E.34
Kong, A.35
Gulcher, J.R.36
Petursson, H.37
Stefansson, K.38
more..
-
37
-
-
1542315614
-
Patterns of linkage disequilibrium in the MHC region on human chromosome 6p
-
DOI 10.1007/s00439-003-1075-5
-
Stenzel A, Lu T, Koch WA, Hampe J, Guenther SM, De La Vega FM, Krawczak M, Schreiber S (2004). Patterns of linkage disequilibrium in the MHC region on human chromosome 6p. Human Genetics 114, 377-385. (Pubitemid 38324950)
-
(2004)
Human Genetics
, vol.114
, Issue.4
, pp. 377-385
-
-
Stenzel, A.1
Lu, T.2
Koch, W.A.3
Hampe, J.4
Guenther, S.M.5
De La Vega, F.M.6
Krawczak, M.7
Schreiber, S.8
-
38
-
-
18444364206
-
Genetic variation in the 6p22.3 Gene DTNBP1, the human ortholog of the mouse dysbindin gene, is associated with schizophrenia
-
DOI 10.1086/341750
-
Straub RE, Jiang Y, MacLean CJ, Ma Y, Webb BT, Myakishev MV, Harris-Kerr C, Wormley B, Sadek H, Kadambi B, Cesare AJ, Gibberman A, Wang X, O'Neill FA, Walsh D, Kendler KS (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. (Pubitemid 34800250)
-
(2002)
American Journal of Human Genetics
, vol.71
, Issue.2
, 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
-
39
-
-
43949122950
-
Genomewide association for schizophrenia in the CATIE study: Results of stage 1
-
DOI 10.1038/mp.2008.25, PII MP200825
-
Sullivan PF, Lin D, Tzeng JY, van den Oord E, Perkins D, Stroup TS, Wagner M, Lee S, Wright FA, Zou F, Liu W, Downing AM, Lieberman J, Close SL (2008). Genomewide association for schizophrenia in the CATIE study : results of stage 1. Molecular Psychiatry 13, 570-584. (Pubitemid 351704941)
-
(2008)
Molecular Psychiatry
, vol.13
, Issue.6
, 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
-
40
-
-
0033046558
-
Analysis of genome-wide CAG/CTG repeats, and at SEF2-1B and ERDA1 in schizophrenia and bipolar affective disorder
-
Vincent JB, Petronis A, Strong E, Parikh SV, Meltzer HY, Lieberman J, Kennedy JL (1999). Analysis of genome-wide CAG/CTG repeats, and at SEF2-1B and ERDA1 in schizophrenia and bipolar affective disorder. Molecular Psychiatry 4, 229-234. (Pubitemid 29292172)
-
(1999)
Molecular Psychiatry
, vol.4
, Issue.3
, pp. 229-234
-
-
Vincent, J.B.1
Petronis, A.2
Strong, E.3
Parikh, S.V.4
Meltzer, H.Y.5
Lieberman, J.6
Kennedy, J.L.7
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