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Thomas Meitinger

Showing results (401-410 of 508) with videos related to

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The New England Journal of Medicine|June 19, 2014
Loss-of-function mutations in APOC3, triglycerides, and coronary disease, Jacy Crosby, Gina M Peloso, et al.
Hepatology (Baltimore, Md.)|November 17, 2023
Genetic landscape of pediatric acute liver failure of indeterminate originDominic Lenz, Lea D Schlieben, Masaru Shimura, et al.
Human Molecular Genetics|July 20, 2010
Genome-wide association analysis identifies multiple loci related to resting heart rateMark Eijgelsheim, Christopher Newton-Cheh, Nona Sotoodehnia, et al.
European Journal of Human Genetics : EJHG|May 5, 2016
Genetic variants in RBFOX3 are associated with sleep latencyNajaf Amin, Karla V Allebrandt, Ashley van der Spek, et al.
Circulation Research|December 10, 2021
Common Genetic Variants Contribute to Risk of Transposition of the Great ArteriesDoris Škorić-Milosavljević, Rafik Tadros, Fernanda M Bosada, et al.
Nature Genetics|July 26, 2016
NEK1 variants confer susceptibility to amyotrophic lateral sclerosisKevin P Kenna, Perry T C van Doormaal, Annelot M Dekker, et al.
Nature Genetics|December 6, 2022
Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participantsKrishna G Aragam, Tao Jiang, Anuj Goel, et al.
Nature Genetics|May 1, 2012
Meta-analysis identifies six new susceptibility loci for atrial fibrillationPatrick T Ellinor, Kathryn L Lunetta, Christine M Albert, et al.
Human Genetics|November 5, 2014
Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortiumQing Li, Robert Wojciechowski, Claire L Simpson, et al.
American Journal of Human Genetics|October 9, 2021
Bi-allelic variants in SPATA5L1 lead to intellectual disability, spastic-dystonic cerebral palsy, epilepsy, and hearing lossElodie M Richard, Somayeh Bakhtiari, Ashley P L Marsh, et al.
Pageof 51

Showing results (401-410 of 508) with videos related to

Sort By:
Pageof 51
The New England Journal of Medicine|June 19, 2014
Loss-of-function mutations in APOC3, triglycerides, and coronary disease, Jacy Crosby, Gina M Peloso, et al.
Hepatology (Baltimore, Md.)|November 17, 2023
Genetic landscape of pediatric acute liver failure of indeterminate originDominic Lenz, Lea D Schlieben, Masaru Shimura, et al.
Human Molecular Genetics|July 20, 2010
Genome-wide association analysis identifies multiple loci related to resting heart rateMark Eijgelsheim, Christopher Newton-Cheh, Nona Sotoodehnia, et al.
European Journal of Human Genetics : EJHG|May 5, 2016
Genetic variants in RBFOX3 are associated with sleep latencyNajaf Amin, Karla V Allebrandt, Ashley van der Spek, et al.
Circulation Research|December 10, 2021
Common Genetic Variants Contribute to Risk of Transposition of the Great ArteriesDoris Škorić-Milosavljević, Rafik Tadros, Fernanda M Bosada, et al.
Nature Genetics|July 26, 2016
NEK1 variants confer susceptibility to amyotrophic lateral sclerosisKevin P Kenna, Perry T C van Doormaal, Annelot M Dekker, et al.
Nature Genetics|December 6, 2022
Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participantsKrishna G Aragam, Tao Jiang, Anuj Goel, et al.
Nature Genetics|May 1, 2012
Meta-analysis identifies six new susceptibility loci for atrial fibrillationPatrick T Ellinor, Kathryn L Lunetta, Christine M Albert, et al.
Human Genetics|November 5, 2014
Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortiumQing Li, Robert Wojciechowski, Claire L Simpson, et al.
American Journal of Human Genetics|October 9, 2021
Bi-allelic variants in SPATA5L1 lead to intellectual disability, spastic-dystonic cerebral palsy, epilepsy, and hearing lossElodie M Richard, Somayeh Bakhtiari, Ashley P L Marsh, et al.
Pageof 51