Patrick F. Sullivan

Biochemistry, Genetics and Molecular Biology · Life Sciences

159h-index141.0kcitations1.1kworks7.92yr avg
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Research Topics

Genetic Associations and Epidemiology(364), Genomics and Rare Diseases(134), Genetics and Neurodevelopmental Disorders(116), Genomic variations and chromosomal abnormalities(112), Eating Disorders and Behaviors(81)

Publications1.0k total

cdg2020-bip-mdd
Figshare·2026Open Access
Genome-wide association analyses identify distinct genetic architectures for early-onset and late-onset depression
Nature Genetics·2025· 3 citedOpen Access
80. Association Between Clinical Factors and Post-Transplant Psychiatric Diagnoses: Promises and Pitfalls of EHR-Based Analyses
Journal of the Academy of Consultation-Liaison Psychiatry·2025
The X chromosome’s influences on the human brain
UNC Libraries·2025Open Access
Identification and validation of postpartum depression subtypes: a population-based cohort study
EClinicalMedicine·2025Open Access
69. GENOME-WIDE ASSOCIATION STUDY USING NORDIC BIOBANK AND LONGITUDINAL HEALTH REGISTRY REVEALS DIFFERENT GENETIC ARCHITECTURE BETWEEN EARLY- AND LATE-ONSET DEPRESSION
European Neuropsychopharmacology·2025
Associations of polygenic risk scores for major depression and depression severity: an investigation of 105 623 individuals with 16 years follow-up
Molecular Psychiatry·2025Open Access
Editors’ Notes
New Directions for Community Colleges·2025
Gender, care-seeking behavior, and adverse mental health during the first year of the COVID-19 pandemic in Sweden: an exploratory study
UNC Libraries·2025Open Access
Medical Multimorbidity in Patients With Treatment‐Resistant Psychosis and Rare Copy Number Variants: A Retrospective Case Series of 24 Patients
American Journal of Medical Genetics Part A·2025
Delineating lifetime multimorbidity associated with 16p13.11 duplication: A literature review, meta-analysis, and case study
Progress in Neuro-Psychopharmacology and Biological Psychiatry·2025
Correction: Common-variant associations with fragile X syndrome
UNC Libraries·2025Open Access
Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk
UNC Libraries·2025Open Access
Gene expression imputation across multiple brain regions provides insights into schizophrenia risk
Utrecht University Repository (Utrecht University)·2025Open Access
The Psychiatric Genomics Consortium: discoveries and directions
The Lancet Psychiatry·2025· 12 citedOpen Access
Genome-wide association meta-analysis and rare copy number variant analysis of treatment-resistant depression
Molecular Psychiatry·2025· 3 citedOpen Access
Risk factors, impact, and healthcare use related to initial suicide attempts: comprehensive analysis of Swedish population
BMJ Medicine·2025· 1 citedOpen Access
Clinical, genetic, and sociodemographic predictors of symptom severity after internet-delivered cognitive behavioural therapy for depression and anxiety
BMC Psychiatry·2025Open Access
The Eating Disorders Genetics Initiative 2 (EDGI2): study protocol
BMC Psychiatry·2025· 1 citedOpen Access
Medical Multimorbidity in Patients with Treatment-Resistant Psychosis and Rare Copy Number Variants: A Retrospective Case Series of 24 Patients
2025Open Access
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Frequent Co-authors

Michael O’Donovan(13), Shaun Purcell(12), Pamela Sklar(12), Steven A. McCarroll(10), Benjamin M. Neale(10), Stephan Ripke(10), Menachem Fromer(9), Christina M. Hultman(9), Jennifer L. Moran(9), Douglas M. Ruderfer(8), Mark J. Daly(8), Kimberly Chambert(7), Daniëlle Posthuma(7), Daniel H. Geschwind(7), Peter Holmans(6), Nick Craddock(6), Christiaan de Leeuw(6), Christina M. Hultman(5), Naomi R. Wray(5), Paul Lichtenstein(5)