Concepedia

Elliott H. Sherr

EH

Statistics

Publications

6

Citations

482

H-Index

6

Active since

1993

Affiliations

University of California, San Francisco(Current)

Boston Children's Hospital

Harvard University

University of Washington

Stanford University

Elliott H. Sherr is an author at University of California, San Francisco specializing in genetics, life sciences, and neurogenetics.

Publications per year

1993–2022

6

Publications

6

Mutations in PIEZO2 Cause Gordon Syndrome, Marden-Walker Syndrome, and Distal Arthrogryposis Type 5

Margaret J. McMillin, Anita E. Beck, Jessica X. Chong et al. · The American Journal of Human Genetics · 2014 · 218 citations · Full text

, , +4

Mammalian myosin I alpha, I beta, and I gamma: new widely expressed genes of the myosin I family.

Elliott H. Sherr, M. Patricia Joyce, Lloyd A. Greene · The Journal of Cell Biology · 1993 · 74 citations · Full text

, , +13

Infantile Spasms of Unknown Cause: Predictors of Outcome and Genotype-Phenotype Correlation

Christopher J. Yuskaitis, Maura Ruzhnikov, Katherine B. Howell et al. · Pediatric Neurology · 2018 · 70 citations · Full text

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De Novo Pathogenic Variants in N-cadherin Cause a Syndromic Neurodevelopmental Disorder with Corpus Callosum, Axon, Cardiac, Ocular, and Genital Defects

Andrea Accogli, Sara Calabretta, Judith St‐Onge et al. · The American Journal of Human Genetics · 2019 · 51 citations · Full text

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Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humans

Thomas Gstrein, Andrew Edwards, Anna Přistoupilová et al. · Nature Neuroscience · 2018 · 47 citations · Full text

, , +14

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