Gail P Jarvik

发表

Approaches to carrier testing and results disclosure in translational genomics research: The clinical sequencing exploratory research consortium experience

Yaping Yang, Katrina A B Goddard, Kathryn M Porter, 2018, Molecular genetics & genomic medicine.

The Genomic Medicine Integrative Research Framework: A Conceptual Framework for Conducting Genomic Medicine Research.

Josh Peterson, Katrina A B Goddard, Carol R Horowitz, 2019, American journal of human genetics.

ePhenotyping for Abdominal Aortic Aneurysm in the Electronic Medical Records and Genomics (eMERGE) Network: Algorithm Development and Konstanz Information Miner Workflow

Jyotishman Pathak, Joshua C Denny, Peggy L Peissig, 2015, International journal of biomedical data mining.

Summary report: Missing data and pedigree and genotyping errors

Duncan C Thomas, Gail P Jarvik, Michael D Badzioch, 2003, Genetic epidemiology.

Atlas-CNV: a validated approach to call single-exon CNVs in the eMERGESeq gene panel

Alexander Fedotov, Simon White, Eric Boerwinkle, 2018, Genetics in Medicine.

Pitfalls of merging GWAS data: lessons learned in the eMERGE network and quality control procedures to maintain high data quality

Dana C Crawford, Yuki Bradford, Mariza de Andrade, 2011, Genetic epidemiology.

Complement receptor 1 gene variants are associated with erythrocyte sedimentation rate.

Christopher G Chute, Joshua C Denny, Khader Shameer, 2011, American journal of human genetics.

Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

Eden R Martin, Seth Love, Brian Lawlor, 2019, Nature Genetics.

Multiple genome-wide analyses of smoking behavior in the Framingham Heart Study

Gail P Jarvik, Ellen L Goode, Karen L Edwards, 2003, BMC Genetics.

Biology-Driven Gene-Gene Interaction Analysis of Age-Related Cataract in the eMERGE Network

Gerard Tromp, Dana C Crawford, Helena Kuivaniemi, 2015, Genetic epidemiology.

Performance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research Consortium.

Matthew S. Lebo, Aleksandar Milosavljevic, Heidi L Rehm, 2016, American journal of human genetics.

National Institutes of Health State-of-the-Science Conference Statement: Family History and Improving Health.

Robert A Hiatt, Gail P Jarvik, John J Mulvihill, 2009, Annals of internal medicine.

Return of results: Ethical and legal distinctions between research and clinical care

Gail P Jarvik, Wylie Burke, Barbara J Evans, 2014, American journal of medical genetics. Part C, Seminars in medical genetics.

Follow-up of carriers of BRCA1 and BRCA2 variants of unknown significance: Variant reclassification and surgical decisions

Gail P Jarvik, G. Jarvik, Felecia Cerrato, 2011, Genetics in Medicine.

Next-Generation Sequencing Panels for the Diagnosis of Colorectal Cancer and Polyposis Syndromes: A Cost-Effectiveness Analysis.

Colin C Pritchard, Laura M Amendola, Gail P Jarvik, 2015, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci.

Christian Gieger, Xiaofeng Zhu, Tom R. Gaunt, 2014, American journal of human genetics.

Development of clinical decision support alerts for pharmacogenomic incidental findings from exome sequencing

Peter Tarczy-Hornoch, Laura M Amendola, Gail P Jarvik, 2015, Genetics in Medicine.

Characterizing genetic variants for clinical action

Kensaku Kawamoto, Nazneen Rahman, Elaine Lyon, 2014, American journal of medical genetics. Part C, Seminars in medical genetics.

Presence of Intraplaque Hemorrhage Stimulates Progression of Carotid Atherosclerotic Plaques: A High-Resolution Magnetic Resonance Imaging Study

Chun Yuan, Gail P Jarvik, Baocheng Chu, 2005, Circulation.

Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.

Nikhil Wagle, Peter Tarczy-Hornoch, Richard M Myers, 2016, American journal of human genetics.

Refining the structure and content of clinical genomic reports

Peter Tarczy-Hornoch, Laura M Amendola, Gail P Jarvik, 2014, American journal of medical genetics. Part C, Seminars in medical genetics.

ColoSeq provides comprehensive lynch and polyposis syndrome mutational analysis using massively parallel sequencing.

Colin C Pritchard, Stephen J Salipante, Gail P Jarvik, 2012, The Journal of molecular diagnostics : JMD.

Genetic Variation in LPAL2, LPA, and PLG Predicts Plasma Lipoprotein(a) Level and Carotid Artery Disease Risk

Gail P Jarvik, Patrick Heagerty, Thomas Hatsukami, 2011, Stroke.

Reporting genetic results in research studies: Summary and recommendations of an NHLBI working group

Gail P Jarvik, John H Eckfeldt, Greg Koski, 2006, American journal of medical genetics. Part A.

The FDA and genomic tests--getting regulation right.

Gail P Jarvik, Wylie Burke, Barbara J Evans, 2015, The New England journal of medicine.

Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci.

Tom R. Gaunt, Fotios Drenos, Meena Kumari, 2012, American journal of human genetics.

Patient characteristics are important determinants of neurodevelopmental outcome at one year of age after neonatal and infant cardiac surgery.

Gil Wernovsky, Gail P Jarvik, Elaine Zackai, 2007, The Journal of thoracic and cardiovascular surgery.

Periventricular leukomalacia is common after neonatal cardiac surgery.

Gil Wernovsky, Gail P Jarvik, R. Zimmerman, 2004, The Journal of thoracic and cardiovascular surgery.

Performance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research Consortium.

Matthew S. Lebo, Aleksandar Milosavljevic, Heidi L Rehm, 2016, American journal of human genetics.

Actionable exomic incidental findings in 6503 participants: challenges of variant classification

Avni Santani, Steven Joffe, Michael J Bamshad, 2015, Genome research.

Rare and Coding Region Genetic Variants Associated With Risk of Ischemic Stroke: The NHLBI Exome Sequence Project.

Sudha Seshadri, Deborah A Nickerson, Wei-Min Chen, 2015, JAMA neurology.

The cost-effectiveness of returning incidental findings from next-generation genomic sequencing

Gail P Jarvik, David L Veenstra, Wylie Burke, 2014, Genetics in Medicine.

Return of genomic results to research participants: the floor, the ceiling, and the choices in between.

Heidi L Rehm, Susan M Wolf, Laura M Amendola, 2014, American journal of human genetics.

Loss-of-function mutations in APOC3, triglycerides, and coronary disease.

He Zhang, Thomas Meitinger, Raimund Erbel, 2014, The New England journal of medicine.

Association of Arrhythmia-Related Genetic Variants With Phenotypes Documented in Electronic Medical Records.

Michael J Ackerman, Joshua C Denny, Dan M Roden, 2016, JAMA.

National Institutes of Health State-of-the-Science Conference Statement: Family History and Improving Health: August 24-26, 2009.

Robert A Hiatt, Gail P Jarvik, John J Mulvihill, 2009, NIH consensus and state-of-the-science statements.

Predictors of carotid atherosclerotic plaque progression as measured by noninvasive magnetic resonance imaging.

Chun Yuan, Gail P Jarvik, Jianming Cai, 2007, Atherosclerosis.

An examination of the genotyping error detection function of SIMWALK2

Gail P Jarvik, Hawkins B DeFrance, G. Jarvik, 2003, BMC Genetics.

Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci.

Christian Gieger, Ingo Ruczinski, Tom R. Gaunt, 2012, American journal of human genetics.

TagSNP analyses of the PON gene cluster: effects on PON1 activity, LDL oxidative susceptibility, and vascular disease Published, JLR Papers in Press, February 11, 2006.

Patrick J Heagerty, Gail P Jarvik, Deborah Nickerson, 2006, Journal of Lipid Research.

Comparative effectiveness of next generation genomic sequencing for disease diagnosis: design of a randomized controlled trial in patients with colorectal cancer/polyposis syndromes.

Peter Tarczy-Hornoch, Deborah A Nickerson, Laura M Amendola, 2014, Contemporary clinical trials.