Gail P Jarvik


Ontology type: schema:Person     


Person Info

NAME

Gail P

SURNAME

Jarvik

Publications in SciGraph latest 50 shown

  • 2019-01-22 Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study in GENETICS IN MEDICINE
  • 2018-12 A study paradigm integrating prospective epidemiologic cohorts and electronic health records to identify disease biomarkers in NATURE COMMUNICATIONS
  • 2018-11-21 Unfolding of hidden white blood cell count phenotypes for gene discovery using latent class mixed modeling in GENES & IMMUNITY
  • 2018-10-05 Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study in GENETICS IN MEDICINE
  • 2018-10 Anticipated responses of early adopter genetic specialists and nongenetic specialists to unsolicited genomic secondary findings in GENETICS IN MEDICINE
  • 2018-10 Rare loss of function variants in candidate genes and risk of colorectal cancer in HUMAN GENETICS
  • 2018-09 Patient preferences for massively parallel sequencing genetic testing of colorectal cancer risk: a discrete choice experiment in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2018-09-01 The Feelings About genomiC Testing Results (FACToR) Questionnaire: Development and Preliminary Validation in JOURNAL OF GENETIC COUNSELING
  • 2018-05 Impact of HIPAA’s minimum necessary standard on genomic data sharing in GENETICS IN MEDICINE
  • 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
  • 2018-05 Arno G. Motulsky, MD (1923–2018): Holocaust survivor who cofounded the field of medical genetics in GENETICS IN MEDICINE
  • 2018-05 Navigating the research–clinical interface in genomic medicine: analysis from the CSER Consortium in GENETICS IN MEDICINE
  • 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 Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individuals in BIODATA MINING
  • 2017-12 ClinGen Pathogenicity Calculator: a configurable system for assessing pathogenicity of genetic variants in GENOME MEDICINE
  • 2017-12 Molecular outcomes, clinical consequences, and genetic diagnosis of Oculocutaneous Albinism in Pakistani population in SCIENTIFIC REPORTS
  • 2017-09 Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease in NATURE GENETICS
  • 2017-07 Genome sequencing and carrier testing: decisions on categorization and whether to disclose results of carrier testing in GENETICS IN MEDICINE
  • 2017-05 A survey of current practices for genomic sequencing test interpretation and reporting processes in US laboratories in GENETICS IN MEDICINE
  • 2017-05 Mastering genomic terminology in GENETICS IN MEDICINE
  • 2017-02-01 Rare and low-frequency coding variants alter human adult height in NATURE
  • 2017-02 Is “incidental finding” the best term?: a study of patients’ preferences in GENETICS IN MEDICINE
  • 2017-02 Identifying gene–gene interactions that are highly associated with four quantitative lipid traits across multiple cohorts in HUMAN GENETICS
  • 2016-12 Conducting a large, multi-site survey about patients’ views on broad consent: challenges and solutions in BMC MEDICAL RESEARCH METHODOLOGY
  • 2016-11 Recommendations for the integration of genomics into clinical practice in GENETICS IN MEDICINE
  • 2016-06 A genome-wide association study identifies variants in KCNIP4 associated with ACE inhibitor-induced cough in THE PHARMACOGENOMICS JOURNAL
  • 2016-06 Next Generation Sequencing in the Clinic: a Patterns of Care Study in a Retrospective Cohort of Subjects Referred to a Genetic Medicine Clinic for Suspected Lynch Syndrome in JOURNAL OF GENETIC COUNSELING
  • 2016-01 A novel Alzheimer disease locus located near the gene encoding tau protein in MOLECULAR PSYCHIATRY
  • 2015-12 Prospective participant selection and ranking to maximize actionable pharmacogenetic variants and discovery in the eMERGE Network in GENOME MEDICINE
  • 2015-11 Development of clinical decision support alerts for pharmacogenomic incidental findings from exome sequencing in GENETICS IN MEDICINE
  • 2015-11 A Robust e-Epidemiology Tool in Phenotyping Heart Failure with Differentiation for Preserved and Reduced Ejection Fraction: the Electronic Medical Records and Genomics (eMERGE) Network in JOURNAL OF CARDIOVASCULAR TRANSLATIONAL RESEARCH
  • 2015-07 The cost-effectiveness of returning incidental findings from next-generation genomic sequencing in GENETICS IN MEDICINE
  • 2015-06 Identifying gene-gene interactions that are highly associated with Body Mass Index using Quantitative Multifactor Dimensionality Reduction (QMDR) in BIODATA MINING
  • 2015-04 Response to Phillips et al. in GENETICS IN MEDICINE
  • 2015-01 Genetic variation in the HLA region is associated with susceptibility to herpes zoster in GENES & IMMUNITY
  • 2014-12 Effects of dietary components on high-density lipoprotein measures in a cohort of 1,566 participants in NUTRITION & METABOLISM
  • 2014-11 Regulatory changes raise troubling questions for genomic testing in GENETICS IN MEDICINE
  • 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
  • 2014-07 Large numbers of individuals are required to classify and define risk for rare variants in known cancer risk genes in GENETICS IN MEDICINE
  • 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 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 Dietary fatty acid intake is associated with paraoxonase 1 activity in a cohort-based analysis of 1,548 subjects in LIPIDS IN HEALTH AND DISEASE
  • 2013-11 Processes and preliminary outputs for identification of actionable genes as incidental findings in genomic sequence data in the Clinical Sequencing Exploratory Research Consortium in GENETICS IN MEDICINE
  • 2013-11 Return of incidental findings in genomic medicine: measuring what patients value—development of an instrument to measure preferences for information from next-generation testing (IMPRINT) in GENETICS IN MEDICINE
  • 2013-11 Recommendations for returning genomic incidental findings? We need to talk! in GENETICS IN MEDICINE
  • 2013-10 A survey of informatics approaches to whole-exome and whole-genome clinical reporting in the electronic health record in GENETICS IN MEDICINE
  • 2013-10 The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future in GENETICS IN MEDICINE
  • 2013-04 Leveraging the electronic health record to implement genomic medicine in GENETICS IN MEDICINE
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