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Author Details
Full Name
Douglas F Levinson
Affiliation
Stanford University School of Medicine
ORCID
Career Start Year
1979
Papers
191
H Index
65
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36934603
Reductions in synaptic marker SV2A in early-course Schizophrenia.
J Psychiatr Res
2023
37777856
GWAS Meta-Analysis of Suicide Attempt: Identification of 12 Genome-Wide Significant Loci and Implication of Genetic Risks for Specific Health Factors.
Am J Psychiatry
2023
37461564
Genetic structure of major depression symptoms across clinical and community cohorts.
medRxiv
2023
37379808
Evaluation of C4 Gene Copy Number in Pediatric Acute Neuropsychiatric Syndrome.
Dev Neurosci
2023
36934603
Reductions in synaptic marker SV2A in early-course Schizophrenia.
J Psychiatr Res
2023
37777856
GWAS Meta-Analysis of Suicide Attempt: Identification of 12 Genome-Wide Significant Loci and Implication of Genetic Risks for Specific Health Factors.
Am J Psychiatry
2023
37379808
Evaluation of C4 Gene Copy Number in Pediatric Acute Neuropsychiatric Syndrome.
Dev Neurosci
2023
37461564
Genetic structure of major depression symptoms across clinical and community cohorts.
medRxiv
2023
34099189
Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders.
Biol Psychiatry
2022
35396580
Mapping genomic loci implicates genes and synaptic biology in schizophrenia.
Nature
2022
35990050
Corrigendum: Potential genetic overlap between insomnia and sleep symptoms in major depressive disorder: A polygenic risk score analysis.
Front Psychiatry
2022
34099189
Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders.
Biol Psychiatry
2022
35396580
Mapping genomic loci implicates genes and synaptic biology in schizophrenia.
Nature
2022
35990050
Corrigendum: Potential genetic overlap between insomnia and sleep symptoms in major depressive disorder: A polygenic risk score analysis.
Front Psychiatry
2022
34035170
Cross-platform validation of neurotransmitter release impairments in schizophrenia patient-derived <i>NRXN1</i>-mutant neurons.
Proc Natl Acad Sci U S A
2021
33691233
Genome-wide analyses of smoking behaviors in schizophrenia: Findings from the Psychiatric Genomics Consortium.
J Psychiatr Res
2021
33779983
Narcolepsy and psychosis: A systematic review.
Acta Psychiatr Scand
2021
33721783
The association between genetically determined ABO blood types and major depressive disorder.
Psychiatry Res
2021
34035170
Cross-platform validation of neurotransmitter release impairments in schizophrenia patient-derived <i>NRXN1</i>-mutant neurons.
Proc Natl Acad Sci U S A
2021
34925085
Potential Genetic Overlap Between Insomnia and Sleep Symptoms in Major Depressive Disorder: A Polygenic Risk Score Analysis.
Front Psychiatry
2021
34632698
Polygenic burden could explain high rates of affective disorders in a community with restricted founder population.
Am J Med Genet B Neuropsychiatr Genet
2021
34552056
Increased activation product of complement 4 protein in plasma of individuals with schizophrenia.
Transl Psychiatry
2021
34588609
Transcriptome-based polygenic score links depression-related corticolimbic gene expression changes to sex-specific brain morphology and depression risk.
Neuropsychopharmacology
2021
33779983
Narcolepsy and psychosis: A systematic review.
Acta Psychiatr Scand
2021
33691233
Genome-wide analyses of smoking behaviors in schizophrenia: Findings from the Psychiatric Genomics Consortium.
J Psychiatr Res
2021
33721783
The association between genetically determined ABO blood types and major depressive disorder.
Psychiatry Res
2021
34925085
Potential Genetic Overlap Between Insomnia and Sleep Symptoms in Major Depressive Disorder: A Polygenic Risk Score Analysis.
Front Psychiatry
2021
34588609
Transcriptome-based polygenic score links depression-related corticolimbic gene expression changes to sex-specific brain morphology and depression risk.
Neuropsychopharmacology
2021
34552056
Increased activation product of complement 4 protein in plasma of individuals with schizophrenia.
Transl Psychiatry
2021
34632698
Polygenic burden could explain high rates of affective disorders in a community with restricted founder population.
Am J Med Genet B Neuropsychiatr Genet
2021
32231276
Minimal phenotyping yields genome-wide association signals of low specificity for major depression.
Nat Genet
2020
32231276
Minimal phenotyping yields genome-wide association signals of low specificity for major depression.
Nat Genet
2020
31874744
Developmental and symptom profiles in early-onset psychosis.
Schizophr Res
2020
32461290
Cohort profile: the Australian genetics of depression study.
BMJ Open
2020
31874744
Developmental and symptom profiles in early-onset psychosis.
Schizophr Res
2020
32461290
Cohort profile: the Australian genetics of depression study.
BMJ Open
2020
31164008
GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores.
Am J Psychiatry
2019
31164008
GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores.
Am J Psychiatry
2019
31003785
Genome-wide Burden of Rare Short Deletions Is Enriched in Major Depressive Disorder in Four Cohorts.
Biol Psychiatry
2019
30708398
Quantifying between-cohort and between-sex genetic heterogeneity in major depressive disorder.
Am J Med Genet B Neuropsychiatr Genet
2019
30708398
Quantifying between-cohort and between-sex genetic heterogeneity in major depressive disorder.
Am J Med Genet B Neuropsychiatr Genet
2019
31003785
Genome-wide Burden of Rare Short Deletions Is Enriched in Major Depressive Disorder in Four Cohorts.
Biol Psychiatry
2019
28526280
An overview of medical risk factors for childhood psychosis: Implications for research and treatment.
Schizophr Res
2018
28526280
An overview of medical risk factors for childhood psychosis: Implications for research and treatment.
Schizophr Res
2018
30217971
Genome-wide association study of seasonal affective disorder.
Transl Psychiatry
2018
30155272
1q21.1 microduplication: large verbal-nonverbal performance discrepancy and ddPCR assays of HYDIN/HYDIN2 copy number.
NPJ Genom Med
2018
29960699
Catatonia in Children and Adolescents: AÂ High Rate of Genetic Conditions.
J Am Acad Child Adolesc Psychiatry
2018
29866841
Transdifferentiation of human adult peripheral blood T cells into neurons.
Proc Natl Acad Sci U S A
2018
29129318
Does Childhood Trauma Moderate Polygenic Risk for Depression? A Meta-analysis of 5765 Subjects From the Psychiatric Genomics Consortium.
Biol Psychiatry
2018
29700475
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression.
Nat Genet
2018
1 - 50 of 382
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Patrick F Sullivan
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Naomi R Wray
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Gerome Breen
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Markus M N??then
Institute of Human Genetics, University Hospital Bonn
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Nick Craddock
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Sven Cichon
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