Matthew DeFelice

Broad Institute

Full Professor(heuristic)

Cancer Genomics and Diagnostics · Cancer Research

h-index15

i10-index16

Publications86

Citations17,565

Grants

No NSF/NIH grants on record.

Lab Funding Health

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In-Field Influence

0.0024

PageRank within Cancer Research co-authorship network

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Admission Signals

New paper: Single-Molecule Real-Time Sequencing for MUC1 Variable Number of Tandem Repeat Variation to Improve Autosomal Dominant Tubulointerstitial Kidney Disease Diagnosis (Journal of the American Society of Nephrology)2026-04-10
New preprint: Long-Read Sequencing of the <i>MUC1</i> VNTR: Genomic Variation, Mutational Landscape, and Its Impact on ADTKD Diagnosis and Progression2025-09-15

Data Freshness

Publications as of 2026-07-01
Grants as of 2026-06-30

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ORCID: 0009-0007-2481-8842

Career Trajectory

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Recent Publications

Last 2 years · showing 4 of 4

Single-Molecule Real-Time Sequencing for MUC1 Variable Number of Tandem Repeat Variation to Improve Autosomal Dominant Tubulointerstitial Kidney Disease Diagnosis
Journal of the American Society of Nephrology · 2026-04-10 · 2 citations
Sickle cell disease is associated with early-onset clonal hematopoiesis involving DNA damage response pathway mutations
Blood · 2025-11-03 · 4 citations
Long-Read Sequencing of the <i>MUC1</i> VNTR: Genomic Variation, Mutational Landscape, and Its Impact on ADTKD Diagnosis and ProgressionPreprint
bioRxiv (Cold Spring Harbor Laboratory) · 2025-09-15 · 3 citations
A blended genome and exome sequencing method captures genetic variation in an unbiased, high-quality, and cost-effective mannerPreprint
bioRxiv (Cold Spring Harbor Laboratory) · 2024-09-09 · 13 citations

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