Murray H Brilliant


Ontology type: schema:Person     


Person Info

NAME

Murray H

SURNAME

Brilliant

Publications in SciGraph latest 50 shown

  • 2018-12 A study paradigm integrating prospective epidemiologic cohorts and electronic health records to identify disease biomarkers in NATURE COMMUNICATIONS
  • 2018-05 Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity in NATURE GENETICS
  • 2018-05 Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity in NATURE GENETICS
  • 2018-01 Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity in NATURE GENETICS
  • 2017-12 Is Low FMR1 CGG Repeat Length in Males Correlated with Family History of BRCA-Associated Cancers? An Exploratory Analysis of Medical Records in JOURNAL OF GENETIC COUNSELING
  • 2017-12 PLATO software provides analytic framework for investigating complexity beyond genome-wide association studies in NATURE COMMUNICATIONS
  • 2017-11 Genetic correlations between intraocular pressure, blood pressure and primary open-angle glaucoma: a multi-cohort analysis in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2017-02-01 Rare and low-frequency coding variants alter human adult height in NATURE
  • 2016-12 Conducting a large, multi-site survey about patients’ views on broad consent: challenges and solutions in BMC MEDICAL RESEARCH METHODOLOGY
  • 2016-12 Identification of genetic interaction networks via an evolutionary algorithm evolved Bayesian network in BIODATA MINING
  • 2016-06 A genome-wide association study identifies variants in KCNIP4 associated with ACE inhibitor-induced cough in THE PHARMACOGENOMICS JOURNAL
  • 2016-04-25 Identifying genetically driven clinical phenotypes using linear mixed models in NATURE COMMUNICATIONS
  • 2016-02 Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma in NATURE GENETICS
  • 2016-02 A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants in NATURE GENETICS
  • 2016 Personalized Medicine in DRUG DISCOVERY AND EVALUATION: PHARMACOLOGICAL ASSAYS
  • 2015-12 Comparison of RNA-seq and microarray-based models for clinical endpoint prediction in GENOME BIOLOGY
  • 2015-06 A polymorphism in HLA-G modifies statin benefit in asthma in THE PHARMACOGENOMICS JOURNAL
  • 2015-06 Prevalence estimation for monogenic autosomal recessive diseases using population-based genetic data in HUMAN GENETICS
  • 2015-04 Phenome-wide association studies (PheWASs) for functional variants in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2015 Personalized Medicine in DRUG DISCOVERY AND EVALUATION: PHARMACOLOGICAL ASSAYS
  • 2015 The Oral Microbiome and Its Relationship to Genomics and Oral Disease in GENOMICS, PERSONALIZED MEDICINE AND ORAL DISEASE
  • 2014-12 Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process in NATURE COMMUNICATIONS
  • 2014-12 Validation of PhenX measures in the personalized medicine research project for use in gene/environment studies in BMC MEDICAL GENOMICS
  • 2014-10 Design and Anticipated Outcomes of the eMERGE‐PGx Project: A Multicenter Pilot for Preemptive Pharmacogenomics in Electronic Health Record Systems in CLINICAL PHARMACOLOGY & THERAPEUTICS
  • 2014-10 Hypothesis-independent pathway analysis implicates GABA and Acetyl-CoA metabolism in primary open-angle glaucoma and normal-pressure glaucoma in HUMAN GENETICS
  • 2014-06 Vascular tone pathway polymorphisms in relation to primary open-angle glaucoma in EYE
  • 2014 Benefits of Accurate Imputations in GWAS 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
  • 2013-10 Stakeholder engagement: a key component of integrating genomic information into electronic health records in GENETICS IN MEDICINE
  • 2013-10 The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future in GENETICS IN MEDICINE
  • 2013-04 Implementing genomic medicine in the clinic: the future is here in GENETICS IN MEDICINE
  • 2013-04 A PheWAS approach in studying HLA-DRB1*1501 in GENES & IMMUNITY
  • 2005-03 Meningococccal meningitis and complement component 6 deficiency associated with oculocutaneous albinism in EUROPEAN JOURNAL OF PEDIATRICS
  • 2001-06 Meeting Report: 14th International Mouse Genome Conference in MAMMALIAN GENOME
  • 2000-10 Aberrant pH of Melanosomes in Pink-Eyed Dilution (p) Mutant Melanocytes in JOURNAL OF INVESTIGATIVE DERMATOLOGY
  • 2000-10 The Underwhite (uw) Locus Acts Autonomously and Reduces the Production of Melanin in JOURNAL OF INVESTIGATIVE DERMATOLOGY
  • 2000-09-10 One-Dimensional Genome Scanning–Detection of Genomic Changes in Ovarian Carcinoma in OVARIAN CANCER
  • 1997-09 Type 2 oculocutaneous albinism (OCA2) in Zimbabwe and Cameroon: distribution of the 2.7-kb deletion allele of the P gene in HUMAN GENETICS
  • 1997-01 Mouse chromosome 7 in MAMMALIAN GENOME
  • 1993-07 A cluster of three GABAA receptor subunit genes is deleted in a neurological mutant of the mouse p locus in NATURE
  • 1992-04 The mouse pink-eyed dilution locus: a model for aspects of Prader-Willi syndrome, Angelman syndrome, and a form of hypomelanosis of Ito in MAMMALIAN GENOME
  • 1991-03 Thep locus is closely linked to the mouse homolog of a gene from the Prader-Willi chromosomal region in MAMMALIAN GENOME
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