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Genomewide association for schizophrenia in the CATIE study: results of stage 1

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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·2008·Molecular Psychiatry

DOI 10.1038/mp.2008.25

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Diagnostic and Statistical Manual of Mental Disorders
Williams, J. B. W., & First, M. (2013) · Encyclopedia of Social Work · doi:10.1093/acrefore/9780199975839.013.104 · Cited by 109,519
Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing
Benjamini, Y., & Hochberg, Y. (1995) · Journal of the Royal Statistical Society Series B: Statistical Methodology · doi:10.1111/j.2517-6161.1995.tb02031.x · Cited by 109,482
PLINK: a tool set for whole-genome association and population-based linkage analyses.
Purcell, S., Neale, B., Todd-Brown, K., Thomas, L., Ferreira, M. A. R., Bender, D., Maller, J., Sklar, P., de Bakker, P. I. W., Daly, M. J., et al. (2007) · The American Journal of Human Genetics · doi:10.1086/519795 · Cited by 34,089
Introduction to Quantitative Genetics.
Edwards, A. W. F., & Falconer, D. S. (1982) · Biometrics · doi:10.2307/2529912 · Cited by 21,447
The Positive and Negative Syndrome Scale (PANSS) for schizophrenia.
Kay, S. R., Fiszbein, A., & Opler, L. A. (1987) · Schizophrenia Bulletin · doi:10.1093/schbul/13.2.261 · Cited by 21,378
Haploview: analysis and visualization of LD and haplotype maps
Barrett, J. C., Fry, B., Maller, J., & Daly, M. J. (2005) · Bioinformatics · doi:10.1093/bioinformatics/bth457 · Cited by 14,525
Database resources of the National Center for Biotechnology Information: update
Wheeler, D. L. (2004) · Nucleic Acids Research · doi:10.1093/nar/gkh073 · Cited by 10,641
Principal components analysis corrects for stratification in genome-wide association studies
Price, A. L., Patterson, N. J., Plenge, R. M., Weinblatt, M. E., Shadick, N. A., & Reich, D. (2006) · Nature Genetics · doi:10.1038/ng1847 · Cited by 10,248
Statistical significance for genomewide studies
Storey, J. D., & Tibshirani, R. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1530509100 · Cited by 9,692
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
The Wellcome Trust Case Control Consortium, Management Committee, Burton, P. R., Clayton, D. G., Cardon, L. R., Craddock, N., Deloukas, P., Duncanson, A., Kwiatkowski, D. P., McCarthy, M. I., et al. (2007) · Nature · doi:10.1038/nature05911 · Cited by 9,442
Genetics of Food Intake Self-Regulation in Childhood: Literature Review and Research Opportunities
Faith, M. S., Carnell, S., & Kral, T. V. E. (2013) · Human Heredity · doi:10.1159/000353879 · Cited by 7,601
Impact of Informing Overweight Individuals about the Role of Genetics in Obesity: An Online Experimental Study
Lippa, N. C., & Sanderson, S. C. (2013) · Human Heredity · doi:10.1159/000353712 · Cited by 6,078
Effectiveness of Antipsychotic Drugs in Patients with Chronic Schizophrenia
Lieberman, J. A., Stroup, T. S., McEvoy, J. P., Swartz, M. S., Rosenheck, R. A., Perkins, D. O., Keefe, R. S. E., Davis, S. M., Davis, C. E., Lebowitz, B. D., et al. (2005) · New England Journal of Medicine · doi:10.1056/nejmoa051688 · Cited by 5,892
Self-citation
The Structure of Haplotype Blocks in the Human Genome
Gabriel, S. B., Schaffner, S. F., Nguyen, H., Moore, J. M., Roy, J., Blumenstiel, B., Higgins, J., DeFelice, M., Lochner, A., Faggart, M., et al. (2002) · Science · doi:10.1126/science.1069424 · Cited by 5,863
A haplotype map of the human genome
The International HapMap Consortium (2005) · Nature · doi:10.1038/nature04226 · Cited by 5,858
Population Structure and Eigenanalysis
Patterson, N., Price, A. L., & Reich, D. (2006) · PLoS Genetics · doi:10.1371/journal.pgen.0020190 · Cited by 5,280
A Common Variant in the FTO Gene Is Associated with Body Mass Index and Predisposes to Childhood and Adult Obesity
Frayling, T. M., Timpson, N. J., Weedon, M. N., Zeggini, E., Freathy, R. M., Lindgren, C. M., Perry, J. R. B., Elliott, K. S., Lango, H., Rayner, N. W., et al. (2007) · Science · doi:10.1126/science.1141634 · Cited by 4,531
Complement factor H polymorphism in age-related macular degeneration
Klein, R. J., Zeiss, C., Chew, E. Y., Tsai, J.-Y., Sackler, R. S., Haynes, C., Henning, A. K., SanGiovanni, J. P., Mane, S. M., Mayne, S. T., et al. (2005) · Science · doi:10.1126/science.1109557 · Cited by 4,492
Genomic Control for Association Studies
Devlin, B., & Roeder, K. (1999) · Biometrics · doi:10.1111/j.0006-341x.1999.00997.x · Cited by 3,162 · cited 1×
“At least five major methods for population stratification control have been described – genomic control (42), structured association (43), principal components (44), multi-dimensional scaling (36), and partial least squares relating phenotype to ancestry-informative markers (45, 46).”
Background
A Genome-Wide Association Study Identifies IL23R as an Inflammatory Bowel Disease Gene
Duerr, R. H., Taylor, K. D., Brant, S. R., Rioux, J. D., Silverberg, M. S., Daly, M. J., Steinhart, A. H., Abraham, C., Regueiro, M., Griffiths, A., et al. (2006) · Science · doi:10.1126/science.1135245 · Cited by 3,039
A genome-wide association study identifies novel risk loci for type 2 diabetes
Sladek, R., Rocheleau, G., Rung, J., Dina, C., Shen, L., Serre, D., Boutin, P., Vincent, D., Belisle, A., Hadjadj, S., et al. (2007) · Nature · doi:10.1038/nature05616 · Cited by 2,993
Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels
Saxena, R., Voight, B. F., Lyssenko, V., Burtt, N. P., de Bakker, P. I. W., Chen, H., Roix, J. J., Kathiresan, S., Hirschhorn, J. N., Daly, M. J., et al. (2007) · Science · doi:10.1126/science.1142358 · Cited by 2,843
A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants
Scott, L. J., Mohlke, K. L., Bonnycastle, L. L., Willer, C. J., Li, Y., Duren, W. L., Erdos, M. R., Stringham, H. M., Chines, P. S., Jackson, A. U., et al. (2007) · Science · doi:10.1126/science.1142382 · Cited by 2,753
Schizophrenia as a Complex Trait: Evidence From a Meta-analysis of Twin Studies
Sullivan, P. F., Kendler, K. S., & Neale, M. C. (2003) · Archives of General Psychiatry · doi:10.1001/archpsyc.60.12.1187 · Cited by 2,356
Self-citation
The positive false discovery rate: a Bayesian interpretation and the q-value
Storey, J. D. (2003) · The Annals of Statistics · doi:10.1214/aos/1074290335 · Cited by 2,204
Replication of Genome-Wide Association Signals in UK Samples Reveals Risk Loci for Type 2 Diabetes
Zeggini, E., Weedon, M. N., Lindgren, C. M., Frayling, T. M., Elliott, K. S., Lango, H., Timpson, N. J., Perry, J. R. B., Rayner, N. W., Freathy, R. M., et al. (2007) · Science · doi:10.1126/science.1142364 · Cited by 2,194
A Systematic Review of the Prevalence of Schizophrenia
Saha, S., Chant, D., Welham, J., & McGrath, J. (2005) · PLoS Medicine · doi:10.1371/journal.pmed.0020141 · Cited by 2,168
Association Mapping in Structured Populations
Pritchard, J. K., Stephens, M., Rosenberg, N. A., & Donnelly, P. (2000) · The American Journal of Human Genetics · doi:10.1086/302959 · Cited by 2,051
Introduction to Quantitative Genetics.
Edwards, J. H., & Falconer, D. S. (1960) · Journal of the Royal Statistical Society. Series A (General) · doi:10.2307/2342481 · Cited by 1,784
Score Tests for Association between Traits and Haplotypes when Linkage Phase Is Ambiguous
Schaid, D. J., Rowland, C. M., Tines, D. E., Jacobson, R. M., & Poland, G. A. (2002) · The American Journal of Human Genetics · doi:10.1086/338688 · Cited by 1,783
Neuregulin 1 and Susceptibility to Schizophrenia
Stefansson, H., Petursson, H., Sigurdsson, E., Steinthorsdottir, V., Bjornsdottir, S., Sigmundsson, T., Ghosh, S., Brynjolfsson, J., Gunnarsdottir, S., Ivarsson, O., et al. (2002) · The American Journal of Human Genetics · doi:10.1086/342734 · Cited by 1,683
The UCSC Genome Browser Database: update 2006
Hinrichs, A. S. (2006) · Nucleic Acids Research · doi:10.1093/nar/gkj144 · Cited by 1,646
Introduction to quantitative genetics (4th edn)
Frankham, R. (1996) · Trends in Genetics · doi:10.1016/0168-9525(96)81458-2 · Cited by 1,449
A Note on Exact Tests of Hardy-Weinberg Equilibrium
Wigginton, J. E., Cutler, D. J., & Abecasis, G. R. (2005) · The American Journal of Human Genetics · doi:10.1086/429864 · Cited by 1,446
Replicating genotype–phenotype associations
NCI-NHGRI Working Group on Replication in Association Studies, Chanock, S. J., Manolio, T., Boehnke, M., Boerwinkle, E., Hunter, D. J., Thomas, G., Hirschhorn, J. N., Abecasis, G., Altshuler, D., et al. (2007) · Nature · doi:10.1038/447655a · Cited by 1,352
A tutorial on statistical methods for population association studies
Balding, D. J. (2006) · Nature Reviews Genetics · doi:10.1038/nrg1916 · Cited by 1,335
Linkage strategies for genetically complex traits. I. Multilocus models.
RISCH, N. J. (1990) · PubMed · Cited by 1,309
Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studies
Skol, A. D., Scott, L. J., Abecasis, G. R., & Boehnke, M. (2006) · Nature Genetics · doi:10.1038/ng1706 · Cited by 1,286
Disruption of two novel genes by a translocation co-segregating with schizophrenia
Millar, J. K. (2000) · Human Molecular Genetics · doi:10.1093/hmg/9.9.1415 · Cited by 1,254
Whole-Genome Patterns of Common DNA Variation in Three Human Populations
Hinds, D. A., Stuve, L. L., Nilsen, G. B., Halperin, E., Eskin, E., Ballinger, D. G., Frazer, K. A., & Cox, D. R. (2005) · Science · doi:10.1126/science.1105436 · Cited by 1,170
Schizophrenia: The epigenetic puzzle
Haier, R. J. (1982) · Psychiatry Research · doi:10.1016/0165-1781(92)90099-o · Cited by 1,167
A variant in CDKAL1 influences insulin response and risk of type 2 diabetes
Steinthorsdottir, V., Thorleifsson, G., Reynisdottir, I., Benediktsson, R., Jonsdottir, T., Walters, G. B., Styrkarsdottir, U., Gretarsdottir, S., Emilsson, V., Ghosh, S., et al. (2007) · Nature Genetics · doi:10.1038/ng2043 · Cited by 1,072
The effects of human population structure on large genetic association studies
Marchini, J., Cardon, L. R., Phillips, M. S., & Donnelly, P. (2004) · Nature Genetics · doi:10.1038/ng1337 · Cited by 869
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., et al. (2002) · The American Journal of Human Genetics · doi:10.1086/341750 · Cited by 856
A Highly Significant Association between a COMT Haplotype and Schizophrenia
Shifman, S., Bronstein, M., Sternfeld, M., Pisanté-Shalom, A., Lev-Lehman, E., Weizman, A., Reznik, I., Spivak, B., Grisaru, N., Karp, L., et al. (2002) · The American Journal of Human Genetics · doi:10.1086/344514 · Cited by 691
Sample size requirements for matched case‐control studies of gene–environment interaction
Gauderman, W. J. (2002) · Statistics in Medicine · doi:10.1002/sim.973 · Cited by 643
The National Institute of Mental Health Clinical Antipsychotic Trials of Intervention Effectiveness (CATIE) Project: Schizophrenia Trial Design and Protocol Development
Stroup, T. S., McEvoy, J. P., Swartz, M. S., Byerly, M. J., Glick, I. D., Canive, J. M., McGee, M. F., Simpson, G. M., Stevens, M. C., & Lieberman, J. A. (2003) · Schizophrenia Bulletin · doi:10.1093/oxfordjournals.schbul.a006986 · Cited by 636
Self-citation
Novel genes identified in a high-density genome wide association study for nicotine dependence
Bierut, L. J., Madden, P. A. F., Breslau, N., Johnson, E. O., Hatsukami, D., Pomerleau, O. F., Swan, G. E., Rutter, J., Bertelsen, S., Fox, L., et al. (2007) · Human Molecular Genetics · doi:10.1093/hmg/ddl441 · Cited by 622
Sample Size Requirements for Association Studies of Gene-Gene Interaction
Gauderman, W. J. (2002) · American Journal of Epidemiology · doi:10.1093/aje/155.5.478 · Cited by 614
Genome–wide association studies provide new insights into type 2 diabetes aetiology
Frayling, T. M. (2007) · Nature Reviews Genetics · doi:10.1038/nrg2178 · Cited by 594
The UCSC Known Genes
Hsu, F., Kent, W. J., Clawson, H., Kuhn, R. M., Diekhans, M., & Haussler, D. (2006) · Bioinformatics · doi:10.1093/bioinformatics/btl048 · Cited by 502
Baseline Neurocognitive Deficits in the CATIE Schizophrenia Trial
Keefe, R. S. E., Bilder, R. M., Harvey, P. D., Davis, S. M., Palmer, B. W., Gold, J. M., Meltzer, H. Y., Green, M. F., Miller, D. D., Canive, J. M., et al. (2006) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301072 · Cited by 472
Self-citation
Rational Inferences about Departures from Hardy-Weinberg Equilibrium
Wittke-Thompson, J. K., Pluzhnikov, A., & Cox, N. J. (2005) · The American Journal of Human Genetics · doi:10.1086/430507 · Cited by 421
Evaluating coverage of genome-wide association studies
Barrett, J. C., & Cardon, L. R. (2006) · Nature Genetics · doi:10.1038/ng1801 · Cited by 415
Neuregulin 1 transcripts are differentially expressed in schizophrenia and regulated by 5′ SNPs associated with the disease
Law, A. J., Lipska, B. K., Weickert, C. S., Hyde, T. M., Straub, R. E., Hashimoto, R., Harrison, P. J., Kleinman, J. E., & Weinberger, D. R. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0602002103 · Cited by 402
Database resources of the National Center for Biotechnology Information
Wheeler, D. L. (2006) · Nucleic Acids Research · doi:10.1093/nar/gkj158 · Cited by 370
Structured clinical interview for DSM-IV axis I disorders : SCID-I: clinical version : administration booklet
First, M. B., Spitzer, R. L., Gibbon, M., & Williams, J. B. W. (1997) · Medical Entomology and Zoology · Cited by 367
Association of DISC1/TRAX Haplotypes With Schizophrenia, Reduced Prefrontal Gray Matter, and Impaired Short- and Long-term Memory
Cannon, T. D., Hennah, W., van Erp, T. G. M., Thompson, P. M., Lonnqvist, J., Huttunen, M., Gasperoni, T., Tuulio-Henriksson, A., Pirkola, T., Toga, A. W., et al. (2005) · Archives of General Psychiatry · doi:10.1001/archpsyc.62.11.1205 · Cited by 337
Spurious Genetic Associations
Sullivan, P. F. (2007) · Biological Psychiatry · doi:10.1016/j.biopsych.2006.11.010 · Cited by 335
Self-citation
Haplotype transmission analysis provides evidence of association for DISC1 to schizophrenia and suggests sex-dependent effects
Hennah, W. (2003) · Human Molecular Genetics · doi:10.1093/hmg/ddg341 · Cited by 325
The Genetics of Schizophrenia
Sullivan, P. F. (2005) · PLoS Medicine · doi:10.1371/journal.pmed.0020212 · Cited by 321
Self-citation
New models of collaboration in genome-wide association studies: the Genetic Association Information Network
The GAIN Collaborative Research Group (2007) · Nature Genetics · doi:10.1038/ng2127 · Cited by 318
Schizophrenia: a common disease caused by multiple rare alleles
McClellan, J. M., Susser, E., & King, M.-C. (2007) · British Journal of Psychiatry · doi:10.1192/bjp.bp.106.025585 · Cited by 296
Meta-analysis shows strong positive association of the neuregulin 1 ( NRG1 ) gene with schizophrenia
Li, D., Collier, D. A., & He, L. (2006) · Human Molecular Genetics · doi:10.1093/hmg/ddl122 · Cited by 295
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. (2007) · Molecular Psychiatry · doi:10.1038/sj.mp.4001983 · Cited by 278
Genetic model testing and statistical power in population‐based association studies of quantitative traits
Lettre, G., Lange, C., & Hirschhorn, J. N. (2007) · Genetic Epidemiology · doi:10.1002/gepi.20217 · Cited by 247
A neuregulin 1 variant associated with abnormal cortical function and psychotic symptoms
Hall, J., Whalley, H. C., Job, D. E., Baig, B. J., McIntosh, A. M., Evans, K. L., Thomson, P. A., Porteous, D. J., Cunningham-Owens, D. G., Johnstone, E. C., et al. (2006) · Nature Neuroscience · doi:10.1038/nn1795 · Cited by 241
Estimating the proportion of false null hypotheses among a large number of independently tested hypotheses
Meinshausen, N., & Rice, J. (2006) · The Annals of Statistics · doi:10.1214/009053605000000741 · Cited by 204
Recurrence risks for schizophrenia in a Swedish National Cohort
LICHTENSTEIN, P., BJÖRK, C., HULTMAN, C. M., SCOLNICK, E., SKLAR, P., & SULLIVAN, P. F. (2006) · Psychological Medicine · doi:10.1017/s0033291706008385 · Cited by 197
Self-citation
The use of race variables in genetic studies of complex traits and the goal of reducing health disparities: A transdisciplinary perspective.
Shields, A. E., Fortun, M., Hammonds, E. M., King, P. A., Lerman, C., Rapp, R., & Sullivan, P. F. (2005) · American Psychologist · doi:10.1037/0003-066x.60.1.77 · Cited by 179
Self-citation
False Discovery Rate in Linkage and Association Genome Screens for Complex Disorders
Sabatti, C., Service, S., & Freimer, N. (2003) · Genetics · doi:10.1093/genetics/164.2.829 · Cited by 171
Controlling the Proportion of False Positives in Multiple Dependent Tests
Fernando, R. L., Nettleton, D., Southey, B. R., Dekkers, J. C. M., Rothschild, M. F., & Soller, M. (2004) · Genetics · doi:10.1534/genetics.166.1.611 · Cited by 165
Clinical correlates of tardive dyskinesia in schizophrenia: Baseline data from the CATIE schizophrenia trial
Miller, D. D., McEvoy, J. P., Davis, S. M., Caroff, S. N., Saltz, B. L., Chakos, M. H., Swartz, M. S., Keefe, R. S. E., Rosenheck, R. A., Stroup, T. S., et al. (2005) · Schizophrenia Research · doi:10.1016/j.schres.2005.07.034 · Cited by 158
Self-citation
Identification of the semaphorin receptor PLXNA2 as a candidate for susceptibility to schizophrenia
Mah, S. P., Nelson, M. R., DeLisi, L. E., Reneland, R., Markward, N., James, M. R., Nyholt, D. R., Hayward, N. K., Handoko, H. Y., Mowry, B. J., et al. (2006) · Molecular Psychiatry · doi:10.1038/sj.mp.4001785 · Cited by 157
False discoveries and models for gene discovery
van den Oord, E. J. C. G., & Sullivan, P. F. (2003) · Trends in Genetics · doi:10.1016/j.tig.2003.08.003 · Cited by 149
Self-citation
Estimation of False Discovery Rates in Multiple Testing: Application to Gene Microarray Data
Tsai, C., Hsueh, H., & Chen, J. J. (2003) · Biometrics · doi:10.1111/j.0006-341x.2003.00123.x · Cited by 149
A Simple and Improved Correction for Population Stratification in Case-Control Studies
Epstein, M. P., Allen, A. S., & Satten, G. A. (2007) · The American Journal of Human Genetics · doi:10.1086/516842 · Cited by 146
The pseudoautosomal regions, SHOX and disease
Blaschke, R. J., & Rappold, G. (2006) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2006.04.004 · Cited by 137
Effects of Age, Sex, and Ethnicity on the Association Between Apolipoprotein E Genotype and Alzheimer Disease: A Meta-analysis
Farrer, L. A. (1997) · JAMA · doi:10.1001/jama.1997.03550160069041 · Cited by 124
Analysis of High-Resolution HapMap of DTNBP1 (Dysbindin) Suggests No Consistency between Reported Common Variant Associations and Schizophrenia
Mutsuddi, M., Morris, D. W., Waggoner, S. G., Daly, M. J., Scolnick, E. M., & Sklar, P. B. (2006) · The American Journal of Human Genetics · doi:10.1086/508942 · Cited by 119
Methods correcting for multiple testing: operating characteristics
Brown, B. W., & Russell, K. E. (1997) · Statistics in Medicine · Cited by 118
NCAM1 and Neurocognition in Schizophrenia
Sullivan, P. F., Keefe, R. S. E., Lange, L. A., Lange, E. M., Stroup, T. S., Lieberman, J. A., & Maness, P. F. (2006) · Biological Psychiatry · doi:10.1016/j.biopsych.2006.07.036 · Cited by 94
Self-citation
Comparative Effectiveness of Antipsychotic Drugs
Lieberman, J. A. (2006) · Archives of General Psychiatry · doi:10.1001/archpsyc.63.10.1069 · Cited by 88
Self-citation
Controlling false discoveries in genetic studies
van den Oord, E. J. C. G. (2007) · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · doi:10.1002/ajmg.b.30650 · Cited by 84
TAMAL: an integrated approach to choosing SNPs for genetic studies of human complex traits
Hemminger, B. M., Saelim, B., & Sullivan, P. F. (2006) · Bioinformatics · doi:10.1093/bioinformatics/btk025 · Cited by 65
Self-citation
Flavin monooxygenase 3 (FMO3) polymorphism in a white population: Allele frequencies, mutation linkage, and functional effects on clozapine and caffeine metabolism*1
Sachse, C. (1999) · Clinical Pharmacology & Therapeutics · doi:10.1053/cp.1999.v66.a102203 · Cited by 56
Statistical Genetics
Neale, B. M., Ferreira, M. A. R., Medland, S. E., et al. (2007) · Taylor & Francis eBooks · doi:10.1201/9780203967201 · Cited by 49
Effect of Population Stratification on Case-Control Association Studies
Gorroochurn, P., Hodge, S. E., Heiman, G. A., & Greenberg, D. A. (2004) · Human Heredity · doi:10.1159/000081455 · Cited by 47
A Framework for Controlling False Discovery Rates and Minimizing the Amount of Genotyping in the Search for Disease Mutations
van den Oord, E. J. C. G., & Sullivan, P. F. (2003) · Human Heredity · doi:10.1159/000076393 · Cited by 47
Self-citation
Statistical Genetics: Gene Mapping Through Linkage and Association
Gibson, G. C. (2008) · Genes Brain & Behavior · doi:10.1111/j.1601-183x.2008.00457.x · Cited by 45
Effect of Population Stratification on Case-Control Association Studies
Heiman, G. A., Hodge, S. E., Gorroochurn, P., Zhang, J., & Greenberg, D. A. (2004) · Human Heredity · doi:10.1159/000081454 · Cited by 45
The neuregulin 1 promoter polymorphism rs6994992 is not associated with chronic schizophrenia or neurocognition
Crowley, J. J., Keefe, R. S. E., Perkins, D. O., Stroup, T. S., Lieberman, J. A., & Sullivan, P. F. (2008) · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · doi:10.1002/ajmg.b.30727 · Cited by 32
Self-citation
Controlling false discoveries in candidate gene studies
van den Oord, E. J. C. G. (2005) · Molecular Psychiatry · doi:10.1038/sj.mp.4001581 · Cited by 29
Comparative Effectiveness of Antipsychotic Drugs
Gupta, S. (2003) · American Journal of Psychiatry · doi:10.1176/appi.ajp.160.3.591 · Cited by 20

A Critical Review of the First 10 Years of Candidate Gene-by-Environment Interaction Research in Psychiatry
Duncan, L. E., & Keller, M. C. (2011) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2011.11020191 · Cited by 1,032
A high-coverage Neandertal genome from Vindija Cave in Croatia
Prüfer, K., de Filippo, C., Grote, S., Mafessoni, F., Korlević, P., Hajdinjak, M., Vernot, B., Skov, L., Hsieh, P., Peyrégne, S., et al. (2017) · Science · doi:10.1126/science.aao1887 · Cited by 719
An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people
Nelson, M. R., Wegmann, D., Ehm, M. G., Kessner, D., St. Jean, P., Verzilli, C., Shen, J., Tang, Z., Bacanu, S.-A., Fraser, D., et al. (2012) · Science · doi:10.1126/science.1217876 · Cited by 647
Sequencing Chromosomal Abnormalities Reveals Neurodevelopmental Loci that Confer Risk across Diagnostic Boundaries
Talkowski, M. E., Rosenfeld, J. A., Blumenthal, I., Pillalamarri, V., Chiang, C., Heilbut, A., Ernst, C., Hanscom, C., Rossin, E., Lindgren, A. M., et al. (2012) · Cell · doi:10.1016/j.cell.2012.03.028 · Cited by 577
Neuregulin-ERBB Signaling in the Nervous System and Neuropsychiatric Diseases
Mei, L., & Nave, K.-A. (2014) · Neuron · doi:10.1016/j.neuron.2014.06.007 · Cited by 592

See all 355

Authors: 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.
Venue: Molecular Psychiatry
Publisher: Springer Science and Business Media LLC
Published: 2008-03-18
Volume: 13
Issue: 6
Pages: 570-584
ISSN: 1359-4184 (ISSN-L)
1476-5578
DOI: 10.1038/mp.2008.25
OpenAlex: W2089843122
Cited by: 355
References: 94
FWCI: 36.56
Type: journal article
Language: en
Open access: green

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Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.

Genomewide association for schizophrenia in the CATIE study: results of stage 1

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