Author

A. Jeremy Willsey

Rutgers, The State University of New Jersey

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Benjamin M. NealeiD· 2 shared Aaron R. QuinlaniD· 1 shared Alden Y. Huang· 1 shared Alden Yen-Wen Huang· 1 shared Andrea DietrichiD· 1 shared Andreas HartmanniD· 1 shared Andrew FarrelliD· 1 shared Anke HinneyiD· 1 shared

Activity by Year

2019-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Benjamin M. NealeORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Synaptic processes and immune-related pathways implicated in Tourette Syndrome

Fotis Tsetsos, Dongmei Yu, Jae Hoon Sul, Alden Y. Huang, Cornelia Illmann, Lisa Osiecki, Sabrina Michelle Darrow, Matthew E. Hirschtritt, Erica Greenberg, Kirsten Müller‐Vahl, Manfred Stuhrmann, Yves Dion, Guy Armand Rouleau, Harald N. Aschauer, Mara Stamenkovic, , Harald Aschauer

This study identifies gene sets associated with Tourette Syndrome using genome-wide data, highlighting synaptic and immune-related pathways.

Translational Psychiatry · Jan 18, 2021Peer-reviewedGenetic & Genomic Medicine

Limited contribution of rare, noncoding variation to autism spectrum disorder from sequencing of 2,076 genomes in quartet families

Donna M. Werling, Harrison Brand, Joon‐Yong An, Matthew R. Stone, Joseph Glessner, Lingxue Zhu, Ryan L. Collins, Shan Dong, Ryan M. Layer, Eirene Markenscoff-Papadimitriou, Andrew Farrell, Grace Schwartz, Benjamin Currall, Jeanselle Dea, Clif Duhn, , Stephan Sanders

This study examines the role of noncoding variation in autism spectrum disorder using whole genome sequencing of 2,076 genomes, finding no significant association after correction for multiple testing.

European Neuropsychopharmacology · Jan 1, 2019Peer-reviewedGenomics