Marylyn D. Ritchie

University of Pennsylvania — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

99h-index55.1kcitations780works10.42yr avg
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Research Topics

Genetic Associations and Epidemiology(289), Bioinformatics and Genomic Networks(148), Gene expression and cancer classification(84), Genomics and Rare Diseases(67), Genetic Mapping and Diversity in Plants and Animals(59)

Publications734 total

Consent, Concern, and Capacity: Factors Associated With Attitudes Toward Pharmacogenetic Testing Among Patients With Gastrointestinal Cancer
Clinical and Translational Science·2026Open Access
Polygenic Background and Penetrance of Pathogenic Variants in Hypertrophic and Dilated Cardiomyopathies
JAMA Cardiology·2025· 1 citedOpen Access
DRIVE-KG: Enhancing variant-phenotype association discovery in understudied complex diseases using heterogeneous knowledge graphs
2025Open Access
FRONT MATTER
2025
Electronic health records to test influence of race and multimorbidity on plasma biomarkers
Alzheimer s & Dementia·2025Open Access
A random-walk-based learning framework to uncover novel gene candidates for Alzheimer’s disease therapy
2025Open Access
Author Correction: Common-variant and rare-variant genetic architecture of heart failure across the allele-frequency spectrum
Nature Genetics·2025Open Access
Melanocortin-4 Receptor Gene Variants and Weight Change Following Switch to Integrase Inhibitor-Based Antiretroviral Therapy
Open Forum Infectious Diseases·2025Open Access
Integrating polygenic scores with clinical, lifestyle, and social risk factors to improve heart failure risk prediction
2025Open Access
Integrative multi‐omics approaches identify molecular pathways and improve Alzheimer's disease risk prediction
Alzheimer s & Dementia·2025· 3 citedOpen Access
Endophenotype Guided Genome-Wide Association Study to Enhance Genetic Risk Prediction of Primary Open-Angle Glaucoma in African Ancestry Populations
2025Open Access
Multimodal Prediction of Primary Open-Angle Glaucoma Using Polygenic Risk Scores and Clinical Features in a High-Risk African Ancestry Cohort
2025Open Access
A novel computational analysis integrating social determinants information from EHR and literature with Alzheimer’s disease biological knowledge through large language models and knowledge graphs
Innovation in Aging·2025· 1 citedOpen Access
CASTER-DTA: equivariant graph neural networks for predicting drug–target affinity
Briefings in Bioinformatics·2025· 2 citedOpen Access
Ascending Aortic Dimensions and Body Size
JACC. Cardiovascular imaging·2025
DRIVE-KG: Enhancing variant-phenotype association discovery in understudied complex diseases using heterogeneous knowledge graphs
2025Open Access
Integrating Imaging-Derived Clinical Endotypes with Plasma Proteomics and External Polygenic Risk Scores Enhances Coronary Microvascular Disease Risk Prediction <sup>†</sup>
2025Open Access
Enabling Few-Shot Alzheimer's Disease Diagnosis on Biomarker Data with Tabular LLMs
ArXiv.org·2025Open Access
A one-shot, lossless algorithm for cross-cohort learning in mixed-outcomes analysis
Patterns·2025Open Access
Protein risk scores enable precise prediction of cardiovascular events in chronic kidney disease patients
2025Open Access
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Frequent Co-authors

Dan M. Roden(14), Dana C. Crawford(13), Gail P. Jarvik(12), Iftikhar J. Kullo(11), Joshua C. Denny(10), Catherine A. McCarty(9), David J. Carey(9), Jason H. Moore(8), Melissa Basford(8), David R. Crosslin(8), Teri A. Manolio(8), Rex L. Chisholm(8), Jonathan L. Haines(8), Aris Baras(8), Rongling Li(8), David Carrell(7), Sarah A. Pendergrass(7), Christopher G. Chute(7), Omri Gottesman(7), Daniel R. Masys(6)