Author

Seulgi Jung

Icahn School of Medicine at Mount SinaiORCID 0000-0002-7264-4310Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 4

Signature Assays, Organisms & Methods

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Organism:human· 4 Approach:statistical model· 4 Research Focus:differential expression· 2 Research Focus:gene regulatory network inference· 2 Research Focus:GWAS / association mapping· 2 Assay:whole-exome sequencing· 2 Assay:GWAS summary statistics· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Behrang MahjaniiD· 3 shared Bernie DevliniD· 2 shared Joseph D. BuxbaumiD· 2 shared Kathryn RoederiD· 2 shared Marina Natividad AvilaiD· 2 shared Ábel FóthiiD· 1 shared Adrianna P. KępińskaiD· 1 shared Ahmad Seif KanaaniD· 1 shared

Activity by Year

2024-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Behrang MahjaniORCID

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4 papers

Recent·Most cited

Genetic & Genomic MedicineMolecular PsychiatryPeer-reviewedMay 14, 2026

Genetic Architecture of Postpartum Psychosis: From Common to Rare Genetic Variation

Seulgi Jung, Madison Caballero, Adrianna P. Kępińska…·Behrang Mahjani

The paper estimates heritability of postpartum psychosis using genomic data and identifies potential risk genes, showing overlaps with psychiatric and autoimmune disorders.

3 citationstop 3%

humanwhole-genome sequencing

Genetic & Genomic MedicinemedRxivPreprintApr 13, 2026

Genome-Wide Association Analysis of Tic Disorders Reveals 6 Independent Risk Loci and Highlights Tic-Associated Cell Types and Brain Circuitry

Dongmei Yu, Nora I. Strom, Zachary F. Gerring…·Pablo Mir

This study identifies six genome-wide significant risk loci for tic disorders and links genetic risk to specific brain cell types and circuits.

2 citations

humanGWAS summary statistics

Genetic & Genomic MedicinemedRxivPreprintDec 23, 2025

Rare coding variation in OCD implicates shared genes with other psychiatric disorders

Seulgi Jung, Matthew Delayne Halvorson, Nancy Pedersen…·Dorothy E. Grice

This study identifies rare coding variants contributing to OCD risk and shows genetic overlap with CTD and neurodevelopmental disorders, while showing minimal overlap with bipolar disorder and schizophrenia.

3 citations

humanwhole-exome sequencing

Genetic & Genomic MedicinemedRxivPreprintDec 27, 2024

Deleterious coding variation associated with autism is consistent across populations, as exemplified by admixed Latin American populations

Marina Natividad Avila, Seulgi Jung, F. Kyle Satterstrom…·Joseph D. Buxbaum

This paper identifies 35 genome-wide significant ASD risk genes in admixed Latin American populations, showing consistency with European cohorts and supporting the universality of ASD biology.

3 citations

humanwhole-exome sequencing