Michael J Bamshad

12PUBLICATIONS
96CO-AUTHORS
Data qualityEpigenetics (incl. genome methylation and epigenomics)Psycholinguistics (incl. speech production and comprehension)Gene expression (incl. microarray and other genome-wide approaches)
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Publications (12)

|Jun 04, 2026
Building an Interoperable Rare Disease Multi-omic Resource: The GREGoR Data Model and Dataset.

|Jun 04, 2025
Cell Modeling and Rescue of a Novel Non-coding Genetic Cause of Glycogen Storage Disease IX.

Apoorva K Iyengar, Xue Zou, Jian Dai

|Jan 02, 2025
CHP2 Modifies Chronic Pseudomonas aeruginosa Airway Infection Risk in Cystic Fibrosis.

Anna V Faino, William W Gordon, Kati Buckingham

|Jun 10, 2024
Bi-allelic variants in MYH3 cause recessively-inherited arthrogryposis.

Burcin Morali, Valancy Miranda, John Raelson

|Apr 18, 2024
CFAP47 is a novel causative gene implicated in X-linked polycystic kidney disease.

Takayasu Mori, Takuya Fujimaru, Chunyu Liu

|Mar 27, 2024
Genetic variation in severe cystic fibrosis liver disease is associated with novel mechanisms for disease pathogenesis.

Jaclyn R Stonebraker, Rhonda G Pace, Paul J Gallins

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Frequent Collaborators

5 joint publications

Jessica X Chong

4 joint publications

Danny E Miller

2 joint publications

Stephanie DiTroia

2 joint publications

Heidi L Rehm