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Stacey Gabriel

Showing results (71-80 of 195) with videos related to

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Circulation|October 7, 2017
Phenotypic Consequences of a Genetic Predisposition to Enhanced Nitric Oxide SignalingConnor A Emdin, Amit V Khera, Derek Klarin, et al.
Circulation|December 28, 2018
Whole-Genome Sequencing to Characterize Monogenic and Polygenic Contributions in Patients Hospitalized With Early-Onset Myocardial InfarctionAmit V Khera, Mark Chaffin, Seyedeh M Zekavat, et al.
Diabetes|November 4, 2018
DNA Sequence Variation in <i>ACVR1C</i> Encoding the Activin Receptor-Like Kinase 7 Influences Body Fat Distribution and Protects Against Type 2 DiabetesConnor A Emdin, Amit V Khera, Krishna Aragam, et al.
Nature Genetics|December 9, 2008
Genome-wide association analysis of metabolic traits in a birth cohort from a founder populationChiara Sabatti, Susan K Service, Anna-Liisa Hartikainen, et al.
Circulation. Genomic and Precision Medicine|September 1, 2020
Heterozygous <i>ABCG5</i> Gene Deficiency and Risk of Coronary Artery DiseaseAkihiro Nomura, Connor A Emdin, Hong Hee Won, et al.
Science (New York, N.Y.)|September 8, 2012
Mutations in BCKD-kinase lead to a potentially treatable form of autism with epilepsyGaia Novarino, Paul El-Fishawy, Hulya Kayserili, et al.
European Journal of Human Genetics : EJHG|February 7, 2013
Phenotypic spectrum and prevalence of INPP5E mutations in Joubert syndrome and related disordersLorena Travaglini, Francesco Brancati, Jennifer Silhavy, et al.
Cell|February 19, 2013
Evolution and impact of subclonal mutations in chronic lymphocytic leukemiaDan A Landau, Scott L Carter, Petar Stojanov, et al.
HGG Advances|June 1, 2022
Accounting for population structure in genetic studies of cystic fibrosisHanley Kingston, Adrienne M Stilp, William Gordon, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 17, 2008
Drug-sensitive FGFR2 mutations in endometrial carcinomaAmit Dutt, Helga B Salvesen, Tzu-Hsiu Chen, et al.
Pageof 20

Showing results (71-80 of 195) with videos related to

Sort By:
Pageof 20
Circulation|October 7, 2017
Phenotypic Consequences of a Genetic Predisposition to Enhanced Nitric Oxide SignalingConnor A Emdin, Amit V Khera, Derek Klarin, et al.
Circulation|December 28, 2018
Whole-Genome Sequencing to Characterize Monogenic and Polygenic Contributions in Patients Hospitalized With Early-Onset Myocardial InfarctionAmit V Khera, Mark Chaffin, Seyedeh M Zekavat, et al.
Diabetes|November 4, 2018
DNA Sequence Variation in <i>ACVR1C</i> Encoding the Activin Receptor-Like Kinase 7 Influences Body Fat Distribution and Protects Against Type 2 DiabetesConnor A Emdin, Amit V Khera, Krishna Aragam, et al.
Nature Genetics|December 9, 2008
Genome-wide association analysis of metabolic traits in a birth cohort from a founder populationChiara Sabatti, Susan K Service, Anna-Liisa Hartikainen, et al.
Circulation. Genomic and Precision Medicine|September 1, 2020
Heterozygous <i>ABCG5</i> Gene Deficiency and Risk of Coronary Artery DiseaseAkihiro Nomura, Connor A Emdin, Hong Hee Won, et al.
Science (New York, N.Y.)|September 8, 2012
Mutations in BCKD-kinase lead to a potentially treatable form of autism with epilepsyGaia Novarino, Paul El-Fishawy, Hulya Kayserili, et al.
European Journal of Human Genetics : EJHG|February 7, 2013
Phenotypic spectrum and prevalence of INPP5E mutations in Joubert syndrome and related disordersLorena Travaglini, Francesco Brancati, Jennifer Silhavy, et al.
Cell|February 19, 2013
Evolution and impact of subclonal mutations in chronic lymphocytic leukemiaDan A Landau, Scott L Carter, Petar Stojanov, et al.
HGG Advances|June 1, 2022
Accounting for population structure in genetic studies of cystic fibrosisHanley Kingston, Adrienne M Stilp, William Gordon, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 17, 2008
Drug-sensitive FGFR2 mutations in endometrial carcinomaAmit Dutt, Helga B Salvesen, Tzu-Hsiu Chen, et al.
Pageof 20