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Adam S Gordon

Showing results (21-30 of 45) with videos related to

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Arthritis & Rheumatology (Hoboken, N.J.)|April 21, 2020
Pleiotropy in the Genetic Predisposition to Rheumatoid Arthritis: A Phenome-Wide Association Study and Inverse Variance-Weighted Meta-AnalysisVivian K Kawai, Mingjian Shi, Qiping Feng, et al.
Journal of Lipid Research|April 9, 2014
Rare coding variation in paraoxonase-1 is associated with ischemic stroke in the NHLBI Exome Sequencing ProjectDaniel Seung Kim, David R Crosslin, Paul L Auer, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 20, 2021
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2021 update: a policy statement of the American College of Medical Genetics and Genomics (ACMG)David T Miller, Kristy Lee, Adam S Gordon, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 4, 2021
Correction to: ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG)David T Miller, Kristy Lee, Wendy K Chung, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 20, 2021
ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG)David T Miller, Kristy Lee, Wendy K Chung, et al.
Circulation. Heart Failure|May 6, 2021
Practice Patterns After Return of Rare Variants Associated With Cardiomyopathy in the Electronic Medical Records and Genomics NetworkSadiya S Khan, Christin Hoell, Lisa M Castillo, et al.
Genome Medicine|July 30, 2015
Prospective participant selection and ranking to maximize actionable pharmacogenetic variants and discovery in the eMERGE NetworkDavid R Crosslin, Peggy D Robertson, David S Carrell, et al.
The Journal of Molecular Diagnostics : JMD|May 16, 2017
Concordance between Research Sequencing and Clinical Pharmacogenetic Genotyping in the eMERGE-PGx StudyLaura J Rasmussen-Torvik, Berta Almoguera, Kimberly F Doheny, et al.
BMC Medical Genomics|January 7, 2021
Association between triglycerides, known risk SNVs and conserved rare variation in SLC25A40 in a multi-ancestry cohortElisabeth A Rosenthal, David R Crosslin, Adam S Gordon, et al.
Human Molecular Genetics|November 28, 2013
Quantifying rare, deleterious variation in 12 human cytochrome P450 drug-metabolism genes in a large-scale exome datasetAdam S Gordon, Holly K Tabor, Andrew D Johnson, et al.
Pageof 5

Showing results (21-30 of 45) with videos related to

Sort By:
Pageof 5
Arthritis & Rheumatology (Hoboken, N.J.)|April 21, 2020
Pleiotropy in the Genetic Predisposition to Rheumatoid Arthritis: A Phenome-Wide Association Study and Inverse Variance-Weighted Meta-AnalysisVivian K Kawai, Mingjian Shi, Qiping Feng, et al.
Journal of Lipid Research|April 9, 2014
Rare coding variation in paraoxonase-1 is associated with ischemic stroke in the NHLBI Exome Sequencing ProjectDaniel Seung Kim, David R Crosslin, Paul L Auer, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 20, 2021
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2021 update: a policy statement of the American College of Medical Genetics and Genomics (ACMG)David T Miller, Kristy Lee, Adam S Gordon, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 4, 2021
Correction to: ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG)David T Miller, Kristy Lee, Wendy K Chung, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 20, 2021
ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG)David T Miller, Kristy Lee, Wendy K Chung, et al.
Circulation. Heart Failure|May 6, 2021
Practice Patterns After Return of Rare Variants Associated With Cardiomyopathy in the Electronic Medical Records and Genomics NetworkSadiya S Khan, Christin Hoell, Lisa M Castillo, et al.
Genome Medicine|July 30, 2015
Prospective participant selection and ranking to maximize actionable pharmacogenetic variants and discovery in the eMERGE NetworkDavid R Crosslin, Peggy D Robertson, David S Carrell, et al.
The Journal of Molecular Diagnostics : JMD|May 16, 2017
Concordance between Research Sequencing and Clinical Pharmacogenetic Genotyping in the eMERGE-PGx StudyLaura J Rasmussen-Torvik, Berta Almoguera, Kimberly F Doheny, et al.
BMC Medical Genomics|January 7, 2021
Association between triglycerides, known risk SNVs and conserved rare variation in SLC25A40 in a multi-ancestry cohortElisabeth A Rosenthal, David R Crosslin, Adam S Gordon, et al.
Human Molecular Genetics|November 28, 2013
Quantifying rare, deleterious variation in 12 human cytochrome P450 drug-metabolism genes in a large-scale exome datasetAdam S Gordon, Holly K Tabor, Andrew D Johnson, et al.
Pageof 5