Patrick f. Sullivan - Genetic Mutations

Author Information

Patrick F. Sullivan is affiliated with the Department of Genetics at the University of North Carolina, Chapel Hill, NC, USA. He is a prominent researcher with a substantial body of work in the field of genetics, particularly in psychiatric disorders.

Research Contributions

Patrick F. Sullivan has made significant contributions to the field of genetics, with a particular focus on psychiatric disorders such as schizophrenia and depression. His recent research includes studies on postpartum depression, structural variants in schizophrenia, and the impact of rare coding variants on schizophrenia risk. Additionally, he has worked on developing powerful association analysis methods for twin studies and polygenic risk scoring to estimate the association of common genetic variants with treatment resistance in schizophrenia.

Aliases

Patrick F. Sullivan is also known by the aliases Patrick Sullivan and Patrick f. Sullivan.

Publication and Citation Metrics

Metric	Value
Citation Count	13,446
H-Index	52
Paper Count	160

Publications:

Transcriptome-wide association study for postpartum depression implicates altered B-cell activation and insulin resistance

DOI: 10.1038/s41380-022-01525-7

Year: 2022

Author Correction: Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia

DOI: 10.1038/s41467-021-27826-z

Year: 2022

TwinEQTL: Ultra Fast and Powerful Association Analysis for eQTL and GWAS in Twin Studies

DOI: 10.1101/2022.04.08.487703

Year: 2022

Rare coding variants in ten genes confer substantial risk for schizophrenia.

DOI: 10.1038/s41586-022-04556-w

Year: 2022

Mapping genomic loci implicates genes and synaptic biology in schizophrenia.

DOI: 10.1038/s41586-022-04434-5

Year: 2022

Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia

DOI: 10.1001/jamapsychiatry.2021.3799

Year: 2022

contribution to risk and recurrent , isoform-specific NRXN 1 disruptions 2

DOI:

Year: 2021

A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts

DOI: 10.1016/j.biopsych.2021.04.018

Year: 2021

Classical Human Leukocyte Antigen Alleles and C4 Haplotypes Are Not Significantly Associated With Depression

DOI: 10.1016/j.biopsych.2019.06.031

Year: 2020

SA82 HLA-DQB1 6672G>C INFLUENCES THE RISK OF CLOZAPINE-INDUCED AGRANULOCYTOSIS IN INDIVIDUALS OF EUROPEAN ANCESTRY

DOI: 10.1016/j.euroneuro.2017.08.154

Year: 2019

How are CNVs Detected?

How Are Transversions Detected and Analyzed?

What Causes the Mutation in HbS?

How Do Errors Occur During Meiosis?

How do Genetic Mutations Lead to Cancer?

Are There Examples of Genetic Mutations Providing Resistance to Infectious Diseases?

What Ethical Considerations Are Involved?

How is Biotechnology Applied in Medicine?

What are the types of inherited mutations?

Can Genetic Testing Help Diagnose Fertility Issues?

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