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Author Details

Pamela Sklar
1984
191
87
PMIDPaper TitleJournal TitlePublished Year
37777856GWAS Meta-Analysis of Suicide Attempt: Identification of 12 Genome-Wide Significant Loci and Implication of Genetic Risks for Specific Health Factors.Am J Psychiatry2023
35396579Rare coding variants in ten genes confer substantial risk for schizophrenia.Nature2022
33674754Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder.Mol Psychiatry2021
32492425Analysis of Genetically Regulated Gene Expression Identifies a Prefrontal PTSD Gene, SNRNP35, Specific to Military Cohorts.Cell Rep2020
31767120Characterization of Single Gene Copy Number Variants in Schizophrenia.Biol Psychiatry2020
32455122A molecular approach to treating cognition in schizophrenia by calcium channel blockade: An open-label pilot study of the calcium-channel antagonist isradipine.Schizophrenia Research: Cognition2020
31548722Synergistic effects of common schizophrenia risk variants.Nat Genet2019
31740837Comparative genetic architectures of schizophrenia in East Asian and European populations.Nat Genet2019
30478444Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder.Nat Genet2019
29740122Differential activity of transcribed enhancers in the prefrontal cortex of 537 cases with schizophrenia and controls.Mol Psychiatry2019
31086353Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk.Nat Genet2019
30686506Contribution of Rare Copy Number Variants to Bipolar Disorder Risk Is Limited to Schizoaffective Cases.Biol Psychiatry2019
31164008GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores.Am J Psychiatry2019
31160808Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.Nat Genet2019
29805045Landscape of Conditional eQTL in Dorsolateral Prefrontal Cortex and Co-localization with Schizophrenia GWAS.Am J Hum Genet2018
30451900Author Correction: Expression-based drug screening of neural progenitor cells from individuals with schizophrenia.Nat Commun2018
30356048Expression-based drug screening of neural progenitor cells from individuals with schizophrenia.Nat Commun2018
29930110Analysis of shared heritability in common disorders of the brain.Science2018
30297968Integrative transcriptome analyses of the aging brain implicate altered splicing in Alzheimer's disease susceptibility.Nat Genet2018
30087329Evaluation of chromatin accessibility in prefrontal cortex of individuals with schizophrenia.Nat Commun2018
30038276Cell-specific histone modification maps in the human frontal lobe link schizophrenia risk to the neuronal epigenome.Nat Neurosci2018
29666432Genetic validation of bipolar disorder identified by automated phenotyping using electronic health records.Transl Psychiatry2018
29483656Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.Nat Genet2018
29370225Examining the role of common and rare mitochondrial variants in schizophrenia.PLoS One2018
27869829Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.Nat Genet2017
2868685610 Years of GWAS Discovery: Biology, Function, and Translation.Am J Hum Genet2017
28686855Large-Scale Identification of Common Trait and Disease Variants Affecting Gene Expression.Am J Hum Genet2017
28552197Large-Scale Identification of Common Trait and Disease Variants Affecting Gene Expression.Am J Hum Genet2017
28982267Institutional profile: translational pharmacogenomics at the Icahn School of Medicine at Mount Sinai.Pharmacogenomics2017
28851079Genome-wide significant locus for Research Diagnostic Criteria Schizoaffective Disorder Bipolar type.Am J Med Genet B Neuropsychiatr Genet2017
28719003Mutation intolerant genes and targets of FMRP are enriched for nonsynonymous alleles in schizophrenia.Am J Med Genet B Neuropsychiatr Genet2017
28877483Dysregulation of miRNA-9 in a Subset of Schizophrenia Patient-Derived Neural Progenitor Cells.Cell Rep2017
28650482The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability.Nat Genet2017
29263384Transcriptional signatures of schizophrenia in hiPSC-derived NPCs and neurons are concordant with post-mortem adult brains.Nat Commun2017
29262854Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disorders.Genome Med2017
27113501Practical Guidelines for High-Resolution Epigenomic Profiling of Nucleosomal Histones in Postmortem Human Brain Tissue.Biol Psychiatry2017
28072414Evidence for genetic heterogeneity between clinical subtypes of bipolar disorder.Transl Psychiatry2017
27759917Implication of LRRC4C and DPP6 in neurodevelopmental disorders.Am J Med Genet A2017
28194006Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder.Mol Psychiatry2017
27535533Analysis of protein-coding genetic variation in 60,706 humans.Nature2016
25560756Copy number variation in bipolar disorder.Mol Psychiatry2016
27065010Analysis of 589,306 genomes identifies individuals resilient to severe Mendelian childhood diseases.Nat Biotechnol2016
27346079Constance E. Lieber, Theodore R. Stanley, and the Enduring Impact of Philanthropy on Psychiatry Research.Biol Psychiatry2016
26974950Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders.Nat Neurosci2016
26791950Quantifying prion disease penetrance using large population control cohorts.Sci Transl Med2016
26915512Polygenic overlap between schizophrenia risk and antipsychotic response: a genomic medicine approach.Lancet Psychiatry2016
27120077Exome Sequencing of Familial Bipolar Disorder.JAMA Psychiatry2016
27117414Dysregulation of miRNA-9 in a Subset of Schizophrenia Patient-Derived Neural Progenitor Cells.Cell Rep2016
26467098Nicotine dependence and psychosis in Bipolar disorder and Schizoaffective disorder, Bipolar type.Am J Med Genet B Neuropsychiatr Genet2016
26503763Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder.Mol Psychiatry2016
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