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Thomas Meitinger

Showing results (291-300 of 508) with videos related to

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American Journal of Human Genetics|August 1, 2017
Biallelic Mutations in LIPT2 Cause a Mitochondrial Lipoylation Defect Associated with Severe Neonatal EncephalopathyFlorence Habarou, Yamina Hamel, Tobias B Haack, et al.
American Journal of Human Genetics|October 15, 2013
Macrocytic anemia and mitochondriopathy resulting from a defect in sideroflexin 4Gordon J Hildick-Smith, Jeffrey D Cooney, Caterina Garone, et al.
American Journal of Human Genetics|November 27, 2012
Exome sequencing reveals de novo WDR45 mutations causing a phenotypically distinct, X-linked dominant form of NBIATobias B Haack, Penelope Hogarth, Michael C Kruer, et al.
BMC Medical Genomics|October 17, 2015
Extensive alterations of the whole-blood transcriptome are associated with body mass index: results of an mRNA profiling study involving two large population-based cohortsGeorg Homuth, Simone Wahl, Christian Müller, et al.
Plos One|August 21, 2008
Lifelong reduction of LDL-cholesterol related to a common variant in the LDL-receptor gene decreases the risk of coronary artery disease--a Mendelian Randomisation studyPatrick Linsel-Nitschke, Anika Götz, Jeanette Erdmann, et al.
European Heart Journal|January 15, 2009
Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillationStefan Kääb, Dawood Darbar, Charlotte van Noord, et al.
BMC Medical Genetics|March 13, 2010
A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2 with serum creatinine levelCristian Pattaro, Alessandro De Grandi, Veronique Vitart, et al.
Cardiovascular Research|April 20, 2021
Cis-epistasis at the LPA locus and risk of cardiovascular diseasesLingyao Zeng, Sylvain Moser, Nazanin Mirza-Schreiber, et al.
Nature|September 3, 2011
Human metabolic individuality in biomedical and pharmaceutical researchKarsten Suhre, So-Youn Shin, Ann-Kristin Petersen, et al.
Genome Research|March 20, 2014
Restless legs syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalonDerek Spieler, Maria Kaffe, Franziska Knauf, et al.
Pageof 51

Showing results (291-300 of 508) with videos related to

Sort By:
Pageof 51
American Journal of Human Genetics|August 1, 2017
Biallelic Mutations in LIPT2 Cause a Mitochondrial Lipoylation Defect Associated with Severe Neonatal EncephalopathyFlorence Habarou, Yamina Hamel, Tobias B Haack, et al.
American Journal of Human Genetics|October 15, 2013
Macrocytic anemia and mitochondriopathy resulting from a defect in sideroflexin 4Gordon J Hildick-Smith, Jeffrey D Cooney, Caterina Garone, et al.
American Journal of Human Genetics|November 27, 2012
Exome sequencing reveals de novo WDR45 mutations causing a phenotypically distinct, X-linked dominant form of NBIATobias B Haack, Penelope Hogarth, Michael C Kruer, et al.
BMC Medical Genomics|October 17, 2015
Extensive alterations of the whole-blood transcriptome are associated with body mass index: results of an mRNA profiling study involving two large population-based cohortsGeorg Homuth, Simone Wahl, Christian Müller, et al.
Plos One|August 21, 2008
Lifelong reduction of LDL-cholesterol related to a common variant in the LDL-receptor gene decreases the risk of coronary artery disease--a Mendelian Randomisation studyPatrick Linsel-Nitschke, Anika Götz, Jeanette Erdmann, et al.
European Heart Journal|January 15, 2009
Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillationStefan Kääb, Dawood Darbar, Charlotte van Noord, et al.
BMC Medical Genetics|March 13, 2010
A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2 with serum creatinine levelCristian Pattaro, Alessandro De Grandi, Veronique Vitart, et al.
Cardiovascular Research|April 20, 2021
Cis-epistasis at the LPA locus and risk of cardiovascular diseasesLingyao Zeng, Sylvain Moser, Nazanin Mirza-Schreiber, et al.
Nature|September 3, 2011
Human metabolic individuality in biomedical and pharmaceutical researchKarsten Suhre, So-Youn Shin, Ann-Kristin Petersen, et al.
Genome Research|March 20, 2014
Restless legs syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalonDerek Spieler, Maria Kaffe, Franziska Knauf, et al.
Pageof 51