Michael J Bamshad

65PUBLICATIONS
551CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)NeurogeneticsData qualityComputing education
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Publications (65)

|Sep 24, 2026
AlphaGenome Atlas: in silico mutagenesis of the entire human genome improves prioritization and interpretation of non-coding variants.

|Sep 24, 2026
Genomic Research as a Critical Pathway to Diagnosis for Individuals with Rare Disease.

|Jul 01, 2026
Harmonizing standards and resources for the medical genome.

|Jun 22, 2026
Long-term Penetrance of Disease Variants in Genes Prioritized for Genomic Newborn Screening: Evidence from Adult Biobanks.

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

|Sep 05, 2025
ClinGen Variant Curation Interface Workshops: Training Variant Scientists on an International Platform.

D I Ritter, M Mandell, C Preston

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Frequent Collaborators

14 joint publications

Anne O'Donnell-Luria

9 joint publications

Steven M Harrison

7 joint publications

Mark J Daly

6 joint publications

Benjamin M Neale