Purcell, Shaun

Cross-disorder genomewide analysis of schizophrenia, bipolar disorder, and depression

Huang, J., Perlis, R. H., Lee, P. H., Rush, A. J., Fava, M., Sachs, G. S., Lieberman, J., Hamilton, S. P., Sullivan, P., Sklar, P., et al. (2010) · American Journal of Psychiatry

Schizophrenia research and treatmentGenetic Associations and Epidemiology

Cited by 213

zCall: a rare variant caller for array-based genotyping

Goldstein, J. I., Crenshaw, A., Carey, J., Grant, G. B., Maguire, J., Fromer, M., O’Dushlaine, C., Moran, J. L., Chambert, K., Stevens, C., et al. (2012) · Bioinformatics

Genetic Associations and EpidemiologyGenomics and Rare Diseases

Cited by 196

Synthetic Associations Created by Rare Variants Do Not Explain Most GWAS Results

Wray, N. R., Purcell, S. M., & Visscher, P. M. (2011) · PLoS Biology

Genetic Associations and EpidemiologyGenetic Mapping and Diversity in Plants and Animals

Cited by 176

A Genome-Wide Association Study of Depressive Symptoms

Hek, K., Demirkan, A., Lahti, J., Terracciano, A., Teumer, A., Cornelis, M. C., Amin, N., Bakshis, E., Baumert, J., Ding, J., et al. (2013) · Biological Psychiatry

Genetic Associations and EpidemiologyNeurotransmitter Receptor Influence on Behavior

Cited by 172

Family dysfunction interacts with genes in the causation of antisocial symptoms

Button, T. M. M., Scourfield, J., Martin, N., Purcell, S., & McGuffin, P. (2005) · Behavior Genetics

Child and Adolescent Psychosocial and Emotional DevelopmentPsychopathy, Forensic Psychiatry, Sexual Offending

Cited by 171

Functional gene group analysis identifies synaptic gene groups as risk factor for schizophrenia

the International Schizophrenia Consortium, Lips, E. S., Cornelisse, L. N., Toonen, R. F., Min, J. L., Hultman, C. M., Holmans, P. A., O'Donovan, M. C., Purcell, S. M., Smit, A. B., et al. (2012) · Molecular Psychiatry

Schizophrenia research and treatmentGenetic Associations and Epidemiology

Cited by 167

Sex differences in obstructive sleep apnea phenotypes, the multi-ethnic study of atherosclerosis

Won, C. H. J., Reid, M., Sofer, T., Azarbarzin, A., Purcell, S., White, D., Wellman, A., Sands, S., & Redline, S. (2020) · Sleep

Obstructive Sleep Apnea ResearchSleep and related disorders

Cited by 152

Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study

Voight, B. F., Peloso, G. M., Orho-Melander, M., Frikke-Schmidt, R., Barbalic, M., Jensen, M. K., Hindy, G., Hólm, H., Ding, E. L., Johnson, T., et al. (2012) · The Lancet

Genetic Associations and EpidemiologyLipoproteins and Cardiovascular Health

Cited by 148

Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function

Raychaudhuri, S., Korn, J. M., McCarroll, S. A., The International Schizophrenia Consortium, Altshuler, D., Sklar, P., Purcell, S., & Daly, M. J. (2010) · PLoS Genetics

Genomic variations and chromosomal abnormalitiesSchizophrenia research and treatment

Cited by 131

Schizophrenia susceptibility alleles are enriched for alleles that affect gene expression in adult human brain

Richards, A. L., Jones, L., Moskvina, V, Kirov, G., Gejman, P. V., Levinson, D. F., Sanders, A. R., Molecular Genetics of Schizophrenia Collaboration (MGS), International Schizophrenia Consortium (ISC), Purcell, S., et al. (2012) · Molecular Psychiatry

Genetic Associations and EpidemiologySchizophrenia research and treatment

Cited by 123

Genome-wide association study implicates a novel RNA gene, the lincRNA AC068718.1, as a risk factor for post-traumatic stress disorder in women

Guffanti, G., Galea, S., Yan, L., Roberts, A. L., Solovieff, N., Aiello, A. E., Smoller, J. W., De Vivo, I., Ranu, H., Uddin, M., et al. (2013) · Psychoneuroendocrinology

Posttraumatic Stress Disorder ResearchGenetic Associations and Epidemiology

Cited by 120

Admixture mapping identifies novel loci for obstructive sleep apnea in Hispanic/Latino Americans

Wang, H., Cade, B. E., Sofer, T., Sands, S. A., Chen, H., Browning, S. R., Stilp, A. M., Louie, T. L., Thornton, T. A., Johnson, W. C., et al. (2019) · Human Molecular Genetics

Obstructive Sleep Apnea ResearchGenetic Associations and Epidemiology

Cited by 56

Evaluation of an approximation method for assessment of overall significance of multiple‐dependent tests in a genomewide association study

Moskvina, V., O'Dushlaine, C., Purcell, S., Craddock, N., Holmans, P., & O'Donovan, M. C. (2011) · Genetic Epidemiology

Genetic Associations and EpidemiologyBioinformatics and Genomic Networks

Cited by 49

Analysis of genetic deletions and duplications in the University College London bipolar disorder case control sample

McQuillin, A., Bass, N., Anjorin, A., Lawrence, J., Kandaswamy, R., Lydall, G., Moran, J., Sklar, P., Purcell, S., & Gurling, H. (2011) · European Journal of Human Genetics

Genomic variations and chromosomal abnormalitiesBipolar Disorder and Treatment

Cited by 47

Prenatal life and post-natal psychopathology: evidence for negative gene–birth weight interaction

WICHERS, M. C., PURCELL, S., DANCKAERTS, M., DEROM, C., DEROM, R., VLIETINCK, R., & VAN OS, J. (2002) · Psychological Medicine

Maternal Mental Health During Pregnancy and PostpartumBirth, Development, and Health

Cited by 45

An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis

Morris, D. W., Pearson, R. D., Cormican, P., Kenny, E. M., O'Dushlaine, C. T., Perreault, L.-P. L., Giannoulatou, E., Tropea, D., Maher, B. S., Wormley, B., et al. (2014) · Human Molecular Genetics

Schizophrenia research and treatmentGenomic variations and chromosomal abnormalities

Cited by 42

Associations of variants In the hexokinase 1 and interleukin 18 receptor regions with oxyhemoglobin saturation during sleep

Cade, B. E., Chen, H., Stilp, A. M., Louie, T., Ancoli-Israel, S., Arens, R., Barfield, R., Below, J. E., Cai, J., Conomos, M. P., et al. (2019) · PLOS Genetics

Obstructive Sleep Apnea ResearchGenetic Associations and Epidemiology

Cited by 39

Genetic Differences between Five European Populations

Moskvina, V., Smith, M., Ivanov, D., Blackwood, D., StClair, D., Hultman, C., Toncheva, D., Gill, M., Corvin, A., O’Dushlaine, C., et al. (2010) · Human Heredity

Forensic and Genetic ResearchGenetic Associations and Epidemiology

Cited by 38

A family-based study of common polygenic variation and risk of schizophrenia

Ruderfer, D. M., Kirov, G., Chambert, K., Moran, J. L., Owen, M. J., O'Donovan, M. C., Sklar, P., & Purcell, S. M. (2011) · Molecular Psychiatry

Genetic Associations and EpidemiologySchizophrenia research and treatment

Cited by 28

Sequencing Analysis at 8p23 Identifies Multiple Rare Variants in DLC1 Associated with Sleep-Related Oxyhemoglobin Saturation Level

Liang, J., Cade, B. E., He, K. Y., Wang, H., Lee, J., Sofer, T., Williams, S., Li, R., Chen, H., Gottlieb, D. J., et al. (2019) · The American Journal of Human Genetics

Obstructive Sleep Apnea ResearchGenetic Associations and Epidemiology

Cited by 21

Ascertainment through family history of disease often decreases the power of family-based association studies

Ferreira, M. A. R., Sham, P., Daly, M. J., & Purcell, S. (2007) · Behavior Genetics

Genetic Associations and EpidemiologyGenetic Mapping and Diversity in Plants and Animals

Cited by 15