Matthew P. Conomos

University of Maryland, Baltimore — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

44h-index11.3kcitations133works5.02yr avg
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Research Topics

Genetic Associations and Epidemiology(63), Genomics and Rare Diseases(21), Genetic Mapping and Diversity in Plants and Animals(18), Epigenetics and DNA Methylation(13), Bioinformatics and Genomic Networks(10)

Publications114 total

Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencing
UNC Libraries·2025Open Access
TOP-LD: A tool to explore linkage disequilibrium with TOPMed whole-genome sequence data
UNC Libraries·2025Open Access
Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program
UNC Libraries·2025Open Access
Whole-genome sequencing uncovers two loci for coronary artery calcification and identifies ARSE as a regulator of vascular calcification
UNC Libraries·2025Open Access
African Ancestry–Specific Alleles and Kidney Disease Risk in Hispanics/Latinos
UNC Libraries·2025Open Access
Data sharing in the PRIMED Consortium: Design, implementation, and recommendations for future policymaking
The American Journal of Human Genetics·2025· 2 citedOpen Access
A data model for population descriptors in genomic research
The American Journal of Human Genetics·2025
Independent Versus Joint Effects of Polygenic or Family-Based Schizophrenia Risk in Diverse Ancestry Youth in the ABCD Study
2025Open Access
Whole genome sequencing analysis of body mass index identifies novel African ancestry-specific risk allele
Nature Communications·2025· 3 citedOpen Access
Independent versus joint effects of polygenic or family-based schizophrenia risk in diverse ancestry youth in the ABCD study
Psychological Medicine·2025· 1 citedOpen Access
The PRIMED Consortium: Reducing disparities in polygenic risk assessment
UNC Libraries·2024Open Access
The PRIMED Consortium: Reducing disparities in polygenic risk assessment
The American Journal of Human Genetics·2024· 29 citedOpen Access
Validation of human telomere length multi-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as human telomere length regulation genes
UNC Libraries·2024Open Access
Fetal Gene Regulatory Gene Deletions are Associated with Poor Cognition in Schizophrenia and Community-Based Samples
2024Open Access
Validation of human telomere length multi-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as human telomere length regulation genes
Nature Communications·2024· 6 citedOpen Access
Admix-kit: an integrated toolkit and pipeline for genetic analyses of admixed populations
Bioinformatics·2024· 15 citedOpen Access
The power of representation: Statistical analysis of diversity in US Alzheimer's disease genetics data
Alzheimer s & Dementia Translational Research & Clinical Interventions·2024· 9 citedOpen Access
A multitrait genetic study of hemostatic factors and hemorrhagic transformation after stroke treatment
Journal of Thrombosis and Haemostasis·2023· 6 citedOpen Access
Whole-genome sequencing uncovers two loci for coronary artery calcification and identifies ARSE as a regulator of vascular calcification
Nature Cardiovascular Research·2023· 17 citedOpen Access
Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencing
Nature Genetics·2023· 23 citedOpen Access
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Frequent Co-authors

Timothy A. Thornton(21), Cathy C. Laurie(20), Jerome I. Rotter(20), Adrienne M. Stilp(16), Kent D. Taylor(16), Stephanie M. Gogarten(15), Jennifer A. Brody(15), Eric Boerwinkle(15), Kenneth Rice(14), Tamar Sofer(14), Paul L. Auer(13), John Blangero(12), Xiuqing Guo(12), Laura M. Raffield(12), Charles Kooperberg(11), Cecelia Laurie(11), Stephen S. Rich(11), Joshua C. Bis(11), Thomas W. Blackwell(10), Brian E. Cade(10)