Concepedia

Kathryn M. Shively

KM

Statistics

Publications

5

Citations

353

H-Index

5

Active since

2012

Affiliations

University of Washington(Current)

Seattle Children's Hospital

University of California, Irvine

Inserm

Kathryn M. Shively is an author at University of Washington specializing in genetics, medical genetics, and molecular genetics.

Publications per year

2012–2025

5

Publications

5

De Novo Mutations in NALCN Cause a Syndrome Characterized by Congenital Contractures of the Limbs and Face, Hypotonia, and Developmental Delay

Jessica X. Chong, Margaret J. McMillin, Kathryn M. Shively et al. · The American Journal of Human Genetics · 2015 · 157 citations · Full text

, , +14

Mutations in KCTD1 Cause Scalp-Ear-Nipple Syndrome

Alexander G. Marneros, Anita E. Beck, Emily H. Turner et al. · The American Journal of Human Genetics · 2013 · 90 citations · Full text

, , +8

Mutations in ECEL1 Cause Distal Arthrogryposis Type 5D

Margaret J. McMillin, Jennifer E. Below, Kathryn M. Shively et al. · The American Journal of Human Genetics · 2012 · 81 citations · Full text

, , +4

SeqFirst: Building equity access to a precise genetic diagnosis in critically ill newborns

Tara Wenger, Abbey Scott, Lukas Kruidenier et al. · The American Journal of Human Genetics · 2025 · 15 citations · Full text

, , +17

Variants regulating <i>ZBTB4</i> are associated with age‐at‐onset of Alzheimer's disease

Elizabeth Blue, Chang‐En Yu, Timothy A. Thornton et al. · Genes Brain & Behavior · 2017 · 10 citations

, , +17

1–5 of 5