Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Thomas Meitinger

Showing results (341-350 of 508) with videos related to

Pageof 51
Sort By:
Plos Genetics|March 19, 2015
A meta-analysis of gene expression signatures of blood pressure and hypertensionTianxiao Huan, Tõnu Esko, Marjolein J Peters, et al.
Plos Genetics|October 3, 2009
Genetic determinants of circulating sphingolipid concentrations in European populationsAndrew A Hicks, Peter P Pramstaller, Asa Johansson, et al.
Annals of Clinical and Translational Neurology|May 23, 2015
Deficiency of ECHS1 causes mitochondrial encephalopathy with cardiac involvementTobias B Haack, Christopher B Jackson, Kei Murayama, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 4, 2023
De novo variants in RNF213 are associated with a clinical spectrum ranging from Leigh syndrome to early-onset strokeTheresa Brunet, Benedikt Zott, Victoria Lieftüchter, et al.
Heart Rhythm|June 12, 2012
A meta-analysis of genome-wide association studies of the electrocardiographic early repolarization patternMoritz F Sinner, Kimmo Porthan, Peter A Noseworthy, et al.
Journal of the American Society of Nephrology : JASN|June 19, 2010
Common genetic variants associate with serum phosphorus concentrationBryan Kestenbaum, Nicole L Glazer, Anna Köttgen, et al.
American Journal of Human Genetics|July 25, 2020
Bi-allelic HPDL Variants Cause a Neurodegenerative Disease Ranging from Neonatal Encephalopathy to Adolescent-Onset Spastic ParaplegiaRalf A Husain, Mona Grimmel, Matias Wagner, et al.
American Journal of Human Genetics|June 4, 2016
Riboflavin-Responsive and -Non-responsive Mutations in FAD Synthase Cause Multiple Acyl-CoA Dehydrogenase and Combined Respiratory-Chain DeficiencyRikke K J Olsen, Eliška Koňaříková, Teresa A Giancaspero, et al.
American Journal of Human Genetics|January 10, 2017
Mutations in ATP6V1E1 or ATP6V1A Cause Autosomal-Recessive Cutis LaxaTim Van Damme, Thatjana Gardeitchik, Miski Mohamed, et al.
Nature Genetics|June 12, 2012
Genome-wide association analysis identifies susceptibility loci for migraine without auraTobias Freilinger, Verneri Anttila, Boukje de Vries, et al.
Pageof 51

Showing results (341-350 of 508) with videos related to

Sort By:
Pageof 51
Plos Genetics|March 19, 2015
A meta-analysis of gene expression signatures of blood pressure and hypertensionTianxiao Huan, Tõnu Esko, Marjolein J Peters, et al.
Plos Genetics|October 3, 2009
Genetic determinants of circulating sphingolipid concentrations in European populationsAndrew A Hicks, Peter P Pramstaller, Asa Johansson, et al.
Annals of Clinical and Translational Neurology|May 23, 2015
Deficiency of ECHS1 causes mitochondrial encephalopathy with cardiac involvementTobias B Haack, Christopher B Jackson, Kei Murayama, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 4, 2023
De novo variants in RNF213 are associated with a clinical spectrum ranging from Leigh syndrome to early-onset strokeTheresa Brunet, Benedikt Zott, Victoria Lieftüchter, et al.
Heart Rhythm|June 12, 2012
A meta-analysis of genome-wide association studies of the electrocardiographic early repolarization patternMoritz F Sinner, Kimmo Porthan, Peter A Noseworthy, et al.
Journal of the American Society of Nephrology : JASN|June 19, 2010
Common genetic variants associate with serum phosphorus concentrationBryan Kestenbaum, Nicole L Glazer, Anna Köttgen, et al.
American Journal of Human Genetics|July 25, 2020
Bi-allelic HPDL Variants Cause a Neurodegenerative Disease Ranging from Neonatal Encephalopathy to Adolescent-Onset Spastic ParaplegiaRalf A Husain, Mona Grimmel, Matias Wagner, et al.
American Journal of Human Genetics|June 4, 2016
Riboflavin-Responsive and -Non-responsive Mutations in FAD Synthase Cause Multiple Acyl-CoA Dehydrogenase and Combined Respiratory-Chain DeficiencyRikke K J Olsen, Eliška Koňaříková, Teresa A Giancaspero, et al.
American Journal of Human Genetics|January 10, 2017
Mutations in ATP6V1E1 or ATP6V1A Cause Autosomal-Recessive Cutis LaxaTim Van Damme, Thatjana Gardeitchik, Miski Mohamed, et al.
Nature Genetics|June 12, 2012
Genome-wide association analysis identifies susceptibility loci for migraine without auraTobias Freilinger, Verneri Anttila, Boukje de Vries, et al.
Pageof 51