Matthew DeFelice
Broad Institute(US)
Publications by Year
Research Areas
Cancer Genomics and Diagnostics, Sarcoma Diagnosis and Treatment, Genetic factors in colorectal cancer, BRCA gene mutations in cancer, Genomics and Rare Diseases
Most-Cited Works
- → The Structure of Haplotype Blocks in the Human Genome(2002)5,889 cited
- → A second generation human haplotype map of over 3.1 million SNPs(2007)4,566 cited
- → Genome-Wide Association Analysis Identifies Loci for Type 2 Diabetes and Triglyceride Levels(2007)2,885 cited
- → Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder(2008)1,246 cited
- → Whole-genome association study of bipolar disorder(2008)704 cited
- → The Genomic Landscape of Pediatric Ewing Sarcoma(2014)567 cited
- → High-Throughput Detection of Actionable Genomic Alterations in Clinical Tumor Samples by Targeted, Massively Parallel Sequencing(2011)537 cited
- → Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing(2013)306 cited
- → Comparative transmissibility of SARS-CoV-2 variants Delta and Alpha in New England, USA(2022)197 cited
- → Sensitive Detection of Minimal Residual Disease in Patients Treated for Early-Stage Breast Cancer(2020)190 cited