Pathway Modeling of Genomic and Tissue-Specific Transcriptomic Architecture Identifies Personalized Mechanisms of Atrial Fibrillation Risk †
Rasika Venkatesh, Rajat Deo, Thomas P. Cappola, Penn Medicine BioBank et autres
0 citationsmedRxiv
Marylyn D. Ritchie
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784Publications signalées
57595Citations signalées
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Domaines associés
Genetic Associations and EpidemiologyBioinformatics and Genomic NetworksGenomics and Rare DiseasesGene expression and cancer classificationGenetic Mapping and Diversity in Plants and Animals
Publications récentes
A pre-train and fine-tune framework for adaptive boosting of pre-trained polygenic risk scores
Jie Hu, R. Chen, Maxwell Salvatore, Olivia Wu et autres
0 citationsNature Communications
AI-based multimodal integration of genomics and electronic health records
Rasika Venkatesh, Marylyn D. Ritchie
0 citationsNature Reviews Genetics
Protective Effect of the APOL1 p.N264K Variant Against CKD among People with HIV Carrying APOL1 High-Risk Genotypes
Junyu Chen, Jennie Mather, Rachel Hung, Qin Hui et autres
0 citationsJournal of the American Society of Nephrology
Eras of bioinformatics technologies from command-line interfaces to artificial intelligence (AI) chatbots
Van Truong, Marylyn D. Ritchie
1 citationBriefings in Bioinformatics
Proteomic risk score for early prediction of kidney disease progression in individuals with APOL1 high-risk genotypes
Chenyu Li, Shola M. Richards, Ghazal Z. Quinn, Amin Abedini et autres
0 citationsNature Medicine
Age at Natural Menopause and Disease Patterns Across the Lifespan: Phenome-Wide and Genetic Evidence from Multi-Ancestry Biobanks
Stephanie Mohammed, Lindsay Guare, Tess Cherlin, Marylyn D. Ritchie et autres
0 citationsResearch Square
DRIVE-KG: Enhancing variant-phenotype association discovery in understudied complex diseases using heterogeneous knowledge graphs
Ananya S. Rajagopalan, Tram Anh Thi Nguyen, Lindsay Guare, Andre Luis Garao Rico et autres
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FRONT MATTER
Russ B. Altman, Lawrence Hunter, Marylyn D. Ritchie, Tiffany Murray et autres
0 citations
A random-walk-based learning framework to uncover novel gene candidates for Alzheimer’s disease therapy
Alena Orlenko, Binglan Li, Neda Khanjani, Mythreye Venkatesan et autres
1 citation
Author Correction: Common-variant and rare-variant genetic architecture of heart failure across the allele-frequency spectrum
David S.M. Lee, Kathleen M. Cardone, David Zhang, Noah L. Tsao et autres
0 citationsNature Genetics
Melanocortin-4 Receptor Gene Variants and Weight Change Following Switch to Integrase Inhibitor-Based Antiretroviral Therapy
Todd Hulgan, Kristine M. Erlandson, Yuki Bradford, Katherine Tassiopoulos et autres
1 citationOpen Forum Infectious Diseases
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