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Adam S Gordon

Showing results (1-10 of 45) with videos related to

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Circulation. Genomic and Precision Medicine|September 11, 2025
Age-Dependent Contributions of Rare and Common Genetic Variation in Atrial FibrillationZhanlin Chen, Peter F Aziz, Philip Greenland, et al.
Pharmacogenetics and Genomics|January 7, 2016
PGRNseq: a targeted capture sequencing panel for pharmacogenetic research and implementationAdam S Gordon, Robert S Fulton, Xiang Qin, et al.
Plos Genetics|February 20, 2008
Adaptations to climate in candidate genes for common metabolic disordersAngela M Hancock, David B Witonsky, Adam S Gordon, et al.
Genetics|April 13, 2021
Multiplexing mutation rate assessment: determining pathogenicity of Msh2 variants in Saccharomyces cerevisiaeAnja R Ollodart, Chiann-Ling C Yeh, Aaron W Miller, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Response to McGurk et alMichael H Gollob, Ray E Hershberger, Adam S Gordon, et al.
Clinical Pharmacology and Therapeutics|June 21, 2021
Genome-Wide Approach to Measure Variant-Based Heritability of Drug Outcome PhenotypesAyesha Muhammad, Ida T Aka, Kelly A Birdwell, et al.
Journal of Clinical and Translational Science|February 1, 2023
Anti-racist strategies for clinical and translational research: Design, implementation, and lessons learned from a new courseNia J Heard-Garris, Jen F Brown, Uchenna C Ewulonu, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|March 12, 2014
Refining the structure and content of clinical genomic reportsMichael O Dorschner, Laura M Amendola, Brian H Shirts, et al.
Molecular Genetics & Genomic Medicine|April 1, 2017
Building a family network from genetic testingKathleen A Leppig, Heidi A Thiese, David Carrel, et al.
Anesthesiology|September 10, 2013
Exome sequencing reveals novel rare variants in the ryanodine receptor and calcium channel genes in malignant hyperthermia familiesJerry H Kim, Gail P Jarvik, Brian L Browning, et al.
Pageof 5

Showing results (1-10 of 45) with videos related to

Sort By:
Pageof 5
Circulation. Genomic and Precision Medicine|September 11, 2025
Age-Dependent Contributions of Rare and Common Genetic Variation in Atrial FibrillationZhanlin Chen, Peter F Aziz, Philip Greenland, et al.
Pharmacogenetics and Genomics|January 7, 2016
PGRNseq: a targeted capture sequencing panel for pharmacogenetic research and implementationAdam S Gordon, Robert S Fulton, Xiang Qin, et al.
Plos Genetics|February 20, 2008
Adaptations to climate in candidate genes for common metabolic disordersAngela M Hancock, David B Witonsky, Adam S Gordon, et al.
Genetics|April 13, 2021
Multiplexing mutation rate assessment: determining pathogenicity of Msh2 variants in Saccharomyces cerevisiaeAnja R Ollodart, Chiann-Ling C Yeh, Aaron W Miller, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Response to McGurk et alMichael H Gollob, Ray E Hershberger, Adam S Gordon, et al.
Clinical Pharmacology and Therapeutics|June 21, 2021
Genome-Wide Approach to Measure Variant-Based Heritability of Drug Outcome PhenotypesAyesha Muhammad, Ida T Aka, Kelly A Birdwell, et al.
Journal of Clinical and Translational Science|February 1, 2023
Anti-racist strategies for clinical and translational research: Design, implementation, and lessons learned from a new courseNia J Heard-Garris, Jen F Brown, Uchenna C Ewulonu, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|March 12, 2014
Refining the structure and content of clinical genomic reportsMichael O Dorschner, Laura M Amendola, Brian H Shirts, et al.
Molecular Genetics & Genomic Medicine|April 1, 2017
Building a family network from genetic testingKathleen A Leppig, Heidi A Thiese, David Carrel, et al.
Anesthesiology|September 10, 2013
Exome sequencing reveals novel rare variants in the ryanodine receptor and calcium channel genes in malignant hyperthermia familiesJerry H Kim, Gail P Jarvik, Brian L Browning, et al.
Pageof 5