| human | Q5 |
| P856 | official website | https://www.broadinstitute.org/bios/shaun-purcell |
| P496 | ORCID iD | 0000-0002-7402-5812 |
| P1416 | affiliation | Broad Institute | Q4971893 |
| P69 | educated at | University of Oxford | Q34433 |
| University of London | Q170027 | ||
| University College London | Q193196 | ||
| King's College London | Q245247 | ||
| P108 | employer | Massachusetts General Hospital | Q126412 |
| Whitehead Institute | Q825987 | ||
| Icahn School of Medicine at Mount Sinai | Q1950740 | ||
| Brigham and Women's Hospital | Q2900977 | ||
| P734 | family name | Purcell | Q16881491 |
| Purcell | Q16881491 | ||
| Purcell | Q16881491 | ||
| P735 | given name | Shaun | Q19819741 |
| Shaun | Q19819741 | ||
| P106 | occupation | researcher | Q1650915 |
| P21 | sex or gender | male | Q6581097 |
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| Q43742579 | A genome wide survey supports the involvement of large copy number variants in schizophrenia with and without intellectual disability. |
| Q28943434 | A genome-wide association study of depressive symptoms |
| Q34632245 | A role for noncoding variation in schizophrenia |
| Q24651939 | A second generation human haplotype map of over 3.1 million SNPs |
| Q40397660 | An Analysis of Two Genome-wide Association Meta-analyses Identifies a New Locus for Broad Depression Phenotype |
| Q33649276 | An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis |
| Q26831376 | Analysis of protein-coding genetic variation in 60,706 humans |
| Q24655630 | Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder |
| Q34561066 | Common variation in three genes, including a noncoding variant in CFH, strongly influences risk of age-related macular degeneration |
| Q39217627 | Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects |
| Q28943274 | Cross-disorder genomewide analysis of schizophrenia, bipolar disorder, and depression |
| Q34555512 | De novo CNVs in bipolar affective disorder and schizophrenia |
| Q34540372 | De novo mutations in schizophrenia implicate synaptic networks |
| Q36451466 | Disruption of a large intergenic noncoding RNA in subjects with neurodevelopmental disabilities |
| Q57699656 | Dysbindin (DTNBP1) and the Biogenesis of Lysosome-Related Organelles Complex 1 (BLOC-1): Main and Epistatic Gene Effects Are Potential Contributors to Schizophrenia Susceptibility |
| Q57400076 | Erratum |
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| Q41882858 | Extremely low-coverage sequencing and imputation increases power for genome-wide association studies |
| Q28263893 | Family-based association study of lithium-related and other candidate genes in bipolar disorder |
| Q63728374 | Gene expression imputation across multiple brain regions provides insights into schizophrenia risk |
| Q33470869 | Gene ontology analysis of GWA study data sets provides insights into the biology of bipolar disorder |
| Q38505803 | Genetic differences between five European populations |
| Q57661758 | Genetic evidence of assortative mating in humans |
| Q28296286 | Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs |
| Q52560096 | Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. |
| Q28297287 | Genome-wide association analysis identifies 13 new risk loci for schizophrenia |
| Q29417107 | Genome-wide association analysis of age at onset and psychotic symptoms in bipolar disorder |
| Q24645076 | Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants |
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| Q34142739 | Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution |
| Q36133352 | Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores |
| Q57760214 | Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores |
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| Q30988023 | New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis |
| Q24677407 | PLINK: a tool set for whole-genome association and population-based linkage analyses |
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| Q92001139 | Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk |
| Q104486646 | Publisher Correction: Macro and micro sleep architecture and cognitive performance in older adults |
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| Q47138654 | Sequence data and association statistics from 12,940 type 2 diabetes cases and controls |
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| Q46293580 | The Genetics of Endophenotypes of Neurofunction to Understand Schizophrenia (GENUS) consortium: A collaborative cognitive and neuroimaging genetics project |
| Q24608580 | The Promises and Pitfalls of Genoeconomics |
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| Q21135294 | The genetic structure of the Swedish population |
| Q28754746 | The genome-wide patterns of variation expose significant substructure in a founder population |
| Q37120830 | Two independent alleles at 6q23 associated with risk of rheumatoid arthritis |
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