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Author Details

Marylyn D Ritchie
Center for Systems Genomics, Pennsylvania State University, University Park
2001
409
75
PMIDPaper TitleJournal TitlePublished Year
37519237Penn Healthy Diet survey: pilot validation and scoring.Br J Nutr2024
37519237Penn Healthy Diet survey: pilot validation and scoring.Br J Nutr2024
36350094How to Run the Pharmacogenomics Clinical Annotation Tool (PharmCAT).Clin Pharmacol Ther2023
36350094How to Run the Pharmacogenomics Clinical Annotation Tool (PharmCAT).Clin Pharmacol Ther2023
37757824Frequencies of pharmacogenomic alleles across biogeographic groups in a large-scale biobank.Am J Hum Genet2023
37986758Cross-phenotype associations between Alzheimer's Disease and its comorbidities may provide clues to progression.medRxiv2023
37898691Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection.Sci Rep2023
37968452Author Correction: Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection.Sci Rep2023
37873439Discovery of Ancestry-specific Variants Associated with Clopidogrel Response among Caribbean Hispanics.medRxiv2023
37689782Projecting genetic associations through gene expression patterns highlights disease etiology and drug mechanisms.Nat Commun2023
36656851Gene burden analysis identifies genes associated with increased risk and severity of adult-onset hearing loss in a diverse hospital-based cohort.PLoS Genet2023
37474378Opportunities and challenges for biomarker discovery using electronic health record data.Trends Mol Med2023
37028392Evidence of epistasis in regions of long-range linkage disequilibrium across five complex diseases in the UK Biobank and eMERGE datasets.Am J Hum Genet2023
37147389Psychosis brain subtypes validated in first-episode cohorts and related to illness remission: results from the PHENOM consortium.Mol Psychiatry2023
37333190The Genetic Architecture of Multimodal Human Brain Age.bioRxiv2023
37196359Gene Interactions in Human Disease Studies-Evidence Is Mounting.Annu Rev Biomed Data Sci2023
37194596Prevalence of Pathogenic Variants in Dilated Cardiomyopathy-Associated Genes in Patients Evaluated for Cardiac Sarcoidosis.Circ Genom Precis Med2023
36802703Multiancestry Genome-Wide Association Study of Aortic Stenosis Identifies Multiple Novel Loci in the Million Veteran Program.Circulation2023
37308786Genome-wide association study of thoracic aortic aneurysm and dissection in the Million Veteran Program.Nat Genet2023
36540998Quantifying factors that affect polygenic risk score performance across diverse ancestries and age groups for body mass index.Pac Symp Biocomput2023
36540980Leveraging Multi-Ancestry Polygenic Risk Scores for Body Mass Index to Predict Antiretroviral Therapy-Induced Weight Gain.Pac Symp Biocomput2023
37350896Exploring Automated Machine Learning for Cognitive Outcome Prediction from Multimodal Brain Imaging using STREAMLINE.AMIA Jt Summits Transl Sci Proc2023
37350880Comparing Amyloid Imaging Normalization Strategies for Alzheimer's Disease Classification using an Automated Machine Learning Pipeline.AMIA Jt Summits Transl Sci Proc2023
37224457Beyond the symptom: the biology of fatigue.Sleep2023
37099271Pharmacogenetics of tenofovir renal toxicity in HIV-positive Southern Africans.Pharmacogenet Genomics2023
37098852Pharmacogenetics of tenofovir clearance among Southern Africans living with HIV.Pharmacogenet Genomics2023
37034649Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.medRxiv2023
36846987Inference of Causal Relationships Between Genetic Risk Factors for Cardiometabolic Phenotypes and Female-Specific Health Conditions.J Am Heart Assoc2023
37757824Frequencies of pharmacogenomic alleles across biogeographic groups in a large-scale biobank.Am J Hum Genet2023
37898691Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection.Sci Rep2023
37986758Cross-phenotype associations between Alzheimer's Disease and its comorbidities may provide clues to progression.medRxiv2023
37689782Projecting genetic associations through gene expression patterns highlights disease etiology and drug mechanisms.Nat Commun2023
37873439Discovery of Ancestry-specific Variants Associated with Clopidogrel Response among Caribbean Hispanics.medRxiv2023
37968452Author Correction: Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection.Sci Rep2023
37350896Exploring Automated Machine Learning for Cognitive Outcome Prediction from Multimodal Brain Imaging using STREAMLINE.AMIA Jt Summits Transl Sci Proc2023
37350880Comparing Amyloid Imaging Normalization Strategies for Alzheimer's Disease Classification using an Automated Machine Learning Pipeline.AMIA Jt Summits Transl Sci Proc2023
37147389Psychosis brain subtypes validated in first-episode cohorts and related to illness remission: results from the PHENOM consortium.Mol Psychiatry2023
37308786Genome-wide association study of thoracic aortic aneurysm and dissection in the Million Veteran Program.Nat Genet2023
37034649Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.medRxiv2023
37474378Opportunities and challenges for biomarker discovery using electronic health record data.Trends Mol Med2023
37333190The Genetic Architecture of Multimodal Human Brain Age.bioRxiv2023
37099271Pharmacogenetics of tenofovir renal toxicity in HIV-positive Southern Africans.Pharmacogenet Genomics2023
37098852Pharmacogenetics of tenofovir clearance among Southern Africans living with HIV.Pharmacogenet Genomics2023
37196359Gene Interactions in Human Disease Studies-Evidence Is Mounting.Annu Rev Biomed Data Sci2023
37224457Beyond the symptom: the biology of fatigue.Sleep2023
37194596Prevalence of Pathogenic Variants in Dilated Cardiomyopathy-Associated Genes in Patients Evaluated for Cardiac Sarcoidosis.Circ Genom Precis Med2023
37028392Evidence of epistasis in regions of long-range linkage disequilibrium across five complex diseases in the UK Biobank and eMERGE datasets.Am J Hum Genet2023
36656851Gene burden analysis identifies genes associated with increased risk and severity of adult-onset hearing loss in a diverse hospital-based cohort.PLoS Genet2023
36846987Inference of Causal Relationships Between Genetic Risk Factors for Cardiometabolic Phenotypes and Female-Specific Health Conditions.J Am Heart Assoc2023
36540998Quantifying factors that affect polygenic risk score performance across diverse ancestries and age groups for body mass index.Pac Symp Biocomput2023
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Mariza de Andrade
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William S Bush
Cleveland Institute for Computational Biology, Case Western Reserve University
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Jennifer A Pacheco
University of Pennsylvania
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Rex L Chisholm
Center for Genetic Medicine, Feinberg School of Medicine, Northwestern University
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Murray H Brilliant
Marshfield Clinic Research Institute
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Hakon Hakonarson
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Melissa A Basford
Vanderbilt University
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Scott M Damrauer
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Release 1.2