Marylyn Ritchie
0000-0002-1208-1720
12 papers found
Refreshing results…
Psychosis brain subtypes validated in first-episode cohorts and related to illness remission: results from the PHENOM consortium
Inference of Causal Relationships Between Genetic Risk Factors for Cardiometabolic Phenotypes and Female‐Specific Health Conditions
Epigenomic and transcriptomic analyses define core cell types, genes and targetable mechanisms for kidney disease
A unified framework identifies new links between plasma lipids and diseases from electronic medical records across large-scale cohorts
Medical records-based chronic kidney disease phenotype for clinical care and “big data” observational and genetic studies
Disrupting upstream translation in mRNAs is associated with human disease
Kidney disease genetic risk variants alter lysosomal beta-mannosidase (MANBA) expression and disease severity
Exome-wide evaluation of rare coding variants using electronic health records identifies new gene–phenotype associations
PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity
PLATO software provides analytic framework for investigating complexity beyond genome-wide association studies
Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization
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