Professor, Medicine, University of Washington School of Medicine
Medical Genetics
Dr. Gail P. Jarvik, MD
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Gail P. Jarvik, MD practices Medical Genetics. She studied medicine at University of Iowa Carver College of Medicine. University of Iowa Carver College of Medicine is ranked 29 in research and 16 in primary care medicine She received awards:"Regional Top Doctor". Gail Jarvik is also published. She has 66 publications published. The lastest publication: "The phenotypic legacy of admixture between modern humans and Neandertals.'
Publications
- Patients' ratings of genetic conditions validate a taxonomy to simplify decisions about preconception carrier screening via genome sequencing.
- The phenotypic legacy of admixture between modern humans and Neandertals.
- CSER and eMERGE: current and potential state of the display of genetic information in the electronic health record.
- A Robust e-Epidemiology Tool in Phenotyping Heart Failure with Differentiation for Preserved and Reduced Ejection Fraction: the Electronic Medical Records and Genomics...
- Desiderata for computable representations of electronic health records-driven phenotype algorithms.
- Patients' Choices for Return of Exome Sequencing Results to Relatives in the Event of Their Death.
- Next-generation gene discovery for variants of large impact on lipid traits.
- Actionable exomic incidental findings in 6503 participants: challenges of variant classification.
- Development of clinical decision support alerts for pharmacogenomic incidental findings from exome sequencing.
- Societal preferences for the return of incidental findings from clinical genomic sequencing: a discrete-choice experiment.
- Parallel reaction monitoring (PRM) and selected reaction monitoring (SRM) exhibit comparable linearity, dynamic range and precision for targeted quantitative HDL prote...
- Rarity of the Alzheimer Disease-Protective APP A673T Variant in the United States.
- The cost-effectiveness of returning incidental findings from next-generation genomic sequencing.
- Design and Anticipated Outcomes of the eMERGE-PGx Project: A Multicenter Pilot for Preemptive Pharmacogenomics in Electronic Health Record Systems.
- Genetic variation in the HLA region is associated with susceptibility to herpes zoster.
- Regulatory changes raise troubling questions for genomic testing.
- Effects of Multiple Genetic Loci on Age at Onset in Late-Onset Alzheimer Disease: A Genome-Wide Association Study.
- Quantification of HDL Particle Concentration by Calibrated Ion Mobility Analysis.
- Validation of association of the apolipoprotein E ε2 allele with neurodevelopmental dysfunction after cardiac surgery in neonates and infants.
- Comparative effectiveness of next generation genomic sequencing for disease diagnosis: Design of a randomized controlled trial in patients with colorectal cancer/polyp...
- TCIRG1-Associated Congenital Neutropenia.
- HDL-3 is a superior predictor of carotid artery disease in a case-control cohort of 1725 participants.
- Patient Genotypes Impact Survival After Surgery for Isolated Congenital Heart Disease.
- Return of Genomic Results to Research Participants: The Floor, the Ceiling, and the Choices In Between.
- Rare coding variation in paraoxonase-1 is associated with ischemic stroke in the NHLBI Exome Sequencing Project.
- Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol.
- Gene-centric Meta-analysis in 87,736 Individuals of European Ancestry Identifies Multiple Blood-Pressure-Related Loci.
- Large numbers of individuals are required to classify and define risk for rare variants in known cancer risk genes.
- Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data.
- Joint Linkage and Association Analysis with Exome Sequence Data Implicates SLC25A40 in Hypertriglyceridemia.
- Processes and preliminary outputs for identification of actionable genes as incidental findings in genomic sequence data in the Clinical Sequencing Exploratory Researc...
- A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects.
- Pharmacogenetics of paraoxonase activity: elucidating the role of high-density lipoprotein in disease.
- A survey of informatics approaches to whole-exome and whole-genome clinical reporting in the electronic health record.
- Actionable, Pathogenic Incidental Findings in 1,000 Participants' Exomes.
- Recommendations for returning genomic incidental findings? We need to talk!
- Postoperative electroencephalographic seizures are associated with deficits in executive function and social behaviors at 4 years of age following cardiac surgery in i...
- The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future.
- Return of incidental findings in genomic medicine: measuring what patients value-development of an instrument to measure preferences for information from next-generati...
- Return of incidental findings in genomic medicine: measuring what patients value.
- Leveraging the electronic health record to implement genomic medicine.
- WNT1 Mutations in Families Affected by Moderately Severe and Progressive Recessive Osteogenesis Imperfecta.
- Novel gene-by-environment interactions: APOB and NPC1L1 variants affect the relationship between dietary and total plasma cholesterol.
- Genome- and Phenome-Wide Analysis of Cardiac Conduction Identifies Markers of Arrhythmia Risk.
- Loci influencing blood pressure identified using a cardiovascular gene-centric array.
- Genetic variation associated with circulating monocyte count in the eMERGE Network.
- Novel common and rare genetic determinants of paraoxonase activity: FTO, SERPINA12, and ITGAL.
- Dietary cholesterol increases paraoxonase 1 enzyme activity.
- Informed Consent in Genome-Scale Research: What Do Prospective Participants Think?
- Pilot Genome-Wide Association Search Identifies Potential Loci for Risk of Erectile Dysfunction in Type 1 Diabetes Using the DCCT/EDIC Study Cohort.
- Additional Common Polymorphisms in the PON Gene Cluster Predict PON1 Activity but Not Vascular Disease.
- ColoSeq Provides Comprehensive Lynch and Polyposis Syndrome Mutational Analysis Using Massively Parallel Sequencing.
- Return of individual research results from genome-wide association studies: experience of the Electronic Medical Records and Genomics (eMERGE) Network.
- Imputation and quality control steps for combining multiple genome-wide datasets.
- Replication of SCN5A Associations with Electrocardio-graphic Traits in African Americans from Clinical and Epidemiologic Studies.
- Genetic Variants Associated with Serum Thyroid Stimulating Hormone (TSH) Levels in European Americans and African Americans from the eMERGE Network.
- Controlling for population structure and genotyping platform bias in the eMERGE multi-institutional biobank linked to electronic health records.
- Effects of dietary components on high-density lipoprotein measures in a cohort of 1,566 participants.
- Phenome-wide association studies demonstrating pleiotropy of genetic variants within FTO with and without adjustment for body mass index.
- eMERGEing progress in genomics-the first seven years.
- Copy number variation analysis in the context of electronic medical records and large-scale genomics consortium efforts.
- Return of results in the genomic medicine projects of the eMERGE network.
- Mechanistic Phenotypes: An Aggregative Phenotyping Strategy to Identify Disease Mechanisms Using GWAS Data.
- Dietary fatty acid intake is associated with paraoxonase 1 activity in a cohort-based analysis of 1,548 subjects.
- Burden of potentially pathologic copy number variants is higher in children with isolated congenital heart disease and significantly impairs covariate-adjusted transpl...
Schools
University of Ia Roy J amp L Carver Com
Hospital Of The University Of Pennsylvania
University Wash Med Center
Doctors Specialties
- Clinical Genetics
- Internal Medicine
- Medical Genetics
Accepted Insurances
Awards
- Regional Top Doctor
Education
-
University of Pennsylvania Health System -
University of Iowa Carver College of Medicine
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