Kaitlin E Samocha

15PUBLICATIONS
89CO-AUTHORS
Evolutionary computationGene expression (incl. microarray and other genome-wide approaches)Neurology and neuromuscular diseasesArtificial life and complex adaptive systemsNeurogenetics
Featured researcher

Get your video featured.

JoVEPublish with JoVE
Journal

Publications (15)

|Jun 24, 2026
Automated reanalysis of genomic data for rare disease diagnostics at scale.

|Jun 22, 2026
Inference of elevated mutation rates and variant effects using 700k exomes.

|May 18, 2026
NeuroDev: etiology and experience of neurodevelopmental disorders in Kenya and South Africa.

|Nov 12, 2025
GREGoR: accelerating genomics for rare diseases.

Moez Dawood, Ben Heavner, Marsha M Wheeler

|Jul 15, 2025
Scalable automated reanalysis of genomic data in research and clinical rare disease cohorts.

Matthew J Welland, K D Ahlquist, Paul De Fazio

|Nov 20, 2024
Examining the role of common variants in rare neurodevelopmental conditions.

Qin Qin Huang, Emilie M Wigdor, Daniel S Malawsky

Pageof 3

Frequent Collaborators

8 joint publications

Anne O'Donnell-Luria

5 joint publications

Konrad J Karczewski

5 joint publications

Matthew E Hurles

5 joint publications

Daniel G MacArthur