Marylyn D Ritchie


Ontology type: schema:Person     


Person Info

NAME

Marylyn D

SURNAME

Ritchie

Publications in SciGraph latest 50 shown

  • 2019-04 Integration of genetic and functional genomics data to uncover chemotherapeutic induced cytotoxicity in THE PHARMACOGENOMICS JOURNAL
  • 2018-12 Collective feature selection to identify crucial epistatic variants in BIODATA MINING
  • 2018-12 Rare variants in drug target genes contributing to complex diseases, phenome-wide in SCIENTIFIC REPORTS
  • 2018-12 A study paradigm integrating prospective epidemiologic cohorts and electronic health records to identify disease biomarkers in NATURE COMMUNICATIONS
  • 2018-12 A simulation study investigating power estimates in phenome-wide association studies in BMC BIOINFORMATICS
  • 2018-08 Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals in NATURE GENETICS
  • 2018-05 Early cancer diagnoses through BRCA1/2 screening of unselected adult biobank participants in GENETICS IN MEDICINE
  • 2017-12 Current Scope and Challenges in Phenome-Wide Association Studies in CURRENT EPIDEMIOLOGY REPORTS
  • 2017-12 Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individuals in BIODATA MINING
  • 2017-12 PLATO software provides analytic framework for investigating complexity beyond genome-wide association studies in NATURE COMMUNICATIONS
  • 2017-11 Electronic health record phenotype in subjects with genetic variants associated with arrhythmogenic right ventricular cardiomyopathy: a study of 30,716 subjects with exome sequencing in GENETICS IN MEDICINE
  • 2017-06 Trans-ethnic fine-mapping of genetic loci for body mass index in the diverse ancestral populations of the Population Architecture using Genomics and Epidemiology (PAGE) Study reveals evidence for multiple signals at established loci in HUMAN GENETICS
  • 2017-05 Knowledge-driven binning approach for rare variant association analysis: application to neuroimaging biomarkers in Alzheimer’s disease in BMC MEDICAL INFORMATICS AND DECISION MAKING
  • 2017-04 Celebrating parasites in NATURE GENETICS
  • 2017-02 Identifying gene–gene interactions that are highly associated with four quantitative lipid traits across multiple cohorts in HUMAN GENETICS
  • 2016-12 A biologically informed method for detecting rare variant associations in BIODATA MINING
  • 2016-12 Identification of genetic interaction networks via an evolutionary algorithm evolved Bayesian network in BIODATA MINING
  • 2016-08 eMERGE Phenome-Wide Association Study (PheWAS) identifies clinical associations and pleiotropy for stop-gain variants in BMC MEDICAL GENOMICS
  • 2016-02 Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma in NATURE GENETICS
  • 2015-12 Concept and design of a genome-wide association genotyping array tailored for transplantation-specific studies in GENOME MEDICINE
  • 2015-12 Prospective participant selection and ranking to maximize actionable pharmacogenetic variants and discovery in the eMERGE Network in GENOME MEDICINE
  • 2015-06 Identifying gene-gene interactions that are highly associated with Body Mass Index using Quantitative Multifactor Dimensionality Reduction (QMDR) in BIODATA MINING
  • 2015-06 Phenome-Wide Association Studies: Leveraging Comprehensive Phenotypic and Genotypic Data for Discovery in CURRENT GENETIC MEDICINE REPORTS
  • 2015-02 Genetic studies of body mass index yield new insights for obesity biology in NATURE
  • 2015-02 Methods of integrating data to uncover genotype-phenotype interactions in NATURE REVIEWS GENETICS
  • 2015-02 New genetic loci link adipose and insulin biology to body fat distribution in NATURE
  • 2015 Finding the Epistasis Needles in the Genome-Wide Haystack in EPISTASIS
  • 2015-01 Genetic variation in the HLA region is associated with susceptibility to herpes zoster in GENES & IMMUNITY
  • 2014-12 Diverse convergent evidence in the genetic analysis of complex disease: coordinating omic, informatic, and experimental evidence to better identify and validate risk factors in BIODATA MINING
  • 2014-12 Knowledge-driven genomic interactions: an application in ovarian cancer in BIODATA MINING
  • 2014-12 Validation of PhenX measures in the personalized medicine research project for use in gene/environment studies in BMC MEDICAL GENOMICS
  • 2014-11 Defining the role of common variation in the genomic and biological architecture of adult human height in NATURE GENETICS
  • 2014-08 Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization in NATURE GENETICS
  • 2014-08 Polygenic inheritance of paclitaxel-induced sensory peripheral neuropathy driven by axon outgrowth gene sets in CALGB 40101 (Alliance) in THE PHARMACOGENOMICS JOURNAL
  • 2014-01 A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects in HUMAN GENETICS
  • 2014 Evaluation of Parameter Contribution to Neural Network Size and Fitness in ATHENA for Genetic Analysis in GENETIC PROGRAMMING THEORY AND PRACTICE XI
  • 2014 Replication of SCN5A Associations with Electrocardiographic Traits in African Americans from Clinical and Epidemiologic Studies in APPLICATIONS OF EVOLUTIONARY COMPUTATION
  • 2013-12 Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data in NATURE BIOTECHNOLOGY
  • 2013-12 Visualizing genomic information across chromosomes with PhenoGram in BIODATA MINING
  • 2013-12 The central role of biological data mining in connecting diverse disciplines in BIODATA MINING
  • 2013-12 Genomic analyses with biofilter 2.0: knowledge driven filtering, annotation, and model development in BIODATA MINING
  • 2013-12 Erratum to: The success of pharmacogenomics in moving genetic association studies from bench to bedside: study design and implementation of precision medicine in the post-GWAS era in HUMAN GENETICS
  • 2013-12 ATHENA: Identifying interactions between different levels of genomic data associated with cancer clinical outcomes using grammatical evolution neural network in BIODATA MINING
  • 2013-12 Effects of smoking on the genetic risk of obesity: the population architecture using genomics and epidemiology study in BMC MEDICAL GENETICS
  • 2013-10 The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future in GENETICS IN MEDICINE
  • 2013-05 BioBin: a bioinformatics tool for automating the binning of rare variants using publicly available biological knowledge in BMC MEDICAL GENOMICS
  • 2013 Meta-Dimensional Analysis of Phenotypes Using the Analysis Tool for Heritable and Environmental Network Associations (ATHENA): Challenges with Building Large Networks in GENETIC PROGRAMMING THEORY AND PRACTICE X
  • 2013 A Graph-Based Integration of Multimodal Brain Imaging Data for the Detection of Early Mild Cognitive Impairment (E-MCI) in MULTIMODAL BRAIN IMAGE ANALYSIS
  • 2012-12 Visually integrating and exploring high throughput Phenome-Wide Association Study (PheWAS) results using PheWAS-View in BIODATA MINING
  • 2012-12 Mitochondrial DNA variation and HIV-associated sensory neuropathy in CHARTER in JOURNAL OF NEUROVIROLOGY
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