Author

Emily Schulman

University of Maryland, Baltimore

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

Signature Assays, Organisms & Methods

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Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Amy L. McGuireiD· 1 shared Chad A. ShawiD· 1 shared Donna Marie MuznyiD· 1 shared Emily J. HilliD· 1 shared HarshaVardhan DoddapaneniiD· 1 shared Hiba Saade· 1 shared Jamie C FongiD· 1 shared Jennifer DegeriD· 1 shared

Activity by Year

2022-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Amy L. McGuireORCID

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1 paper

Recent·Most cited

Genome sequencing in the Parkinson disease clinic

Emily J. Hill, Laurie A. Robak, Rami Al‐Ouran, Jennifer Deger, Jamie C Fong, Paul J. Vandeventer, Emily Schulman, Sindhu Rao, Hiba Saade, Joseph M. Savitt, Rainer von Coelln, Neeja Desai, HarshaVardhan Doddapaneni, Sejal Salvi, Shannon Dugan, , Joshua M Shulman

This study performs genome sequencing in Parkinson's disease patients and finds genetic variants in 3.4% for LRRK2 and 10.1% for GBA, with 82% of patients willing to share variants with relatives.

Neurology Genetics · Jun 20, 2022Peer-reviewedGenetic & Genomic Medicine