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Thomas Meitinger

Showing results (331-340 of 508) with videos related to

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Circulation. Cardiovascular Genetics|June 10, 2010
Genetic regulation of serum phytosterol levels and risk of coronary artery diseaseDaniel Teupser, Ronny Baber, Uta Ceglarek, et al.
Plos Genetics|May 1, 2007
The association of a SNP upstream of INSIG2 with body mass index is reproduced in several but not all cohortsHelen N Lyon, Valur Emilsson, Anke Hinney, et al.
Circulation|October 25, 2021
Sequential Defects in Cardiac Lineage Commitment and Maturation Cause Hypoplastic Left Heart SyndromeMarkus Krane, Martina Dreßen, Gianluca Santamaria, et al.
American Journal of Human Genetics|January 31, 2017
Biallelic Mutations in DNAJC12 Cause Hyperphenylalaninemia, Dystonia, and Intellectual DisabilityYair Anikster, Tobias B Haack, Thierry Vilboux, et al.
American Journal of Human Genetics|December 1, 2014
Compound heterozygosity of low-frequency promoter deletions and rare loss-of-function mutations in TXNL4A causes Burn-McKeown syndromeDagmar Wieczorek, William G Newman, Thomas Wieland, et al.
The Lancet. Respiratory Medicine|December 24, 2014
Genome-wide association study of survival from sepsis due to pneumonia: an observational cohort studyAnna Rautanen, Tara C Mills, Anthony C Gordon, et al.
Nature|November 12, 2013
Dysfunctional nitric oxide signalling increases risk of myocardial infarctionJeanette Erdmann, Klaus Stark, Ulrike B Esslinger, et al.
Nature Genetics|February 10, 2009
Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery diseaseDavid-Alexandre Trégouët, Inke R König, Jeanette Erdmann, et al.
Plos Genetics|August 12, 2010
Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levelsTamra E Meyer, Germaine C Verwoert, Shih-Jen Hwang, et al.
Circulation. Cardiovascular Genetics|November 22, 2011
A large candidate gene survey identifies the KCNE1 D85N polymorphism as a possible modulator of drug-induced torsades de pointesStefan Kääb, Dana C Crawford, Moritz F Sinner, et al.
Pageof 51

Showing results (331-340 of 508) with videos related to

Sort By:
Pageof 51
Circulation. Cardiovascular Genetics|June 10, 2010
Genetic regulation of serum phytosterol levels and risk of coronary artery diseaseDaniel Teupser, Ronny Baber, Uta Ceglarek, et al.
Plos Genetics|May 1, 2007
The association of a SNP upstream of INSIG2 with body mass index is reproduced in several but not all cohortsHelen N Lyon, Valur Emilsson, Anke Hinney, et al.
Circulation|October 25, 2021
Sequential Defects in Cardiac Lineage Commitment and Maturation Cause Hypoplastic Left Heart SyndromeMarkus Krane, Martina Dreßen, Gianluca Santamaria, et al.
American Journal of Human Genetics|January 31, 2017
Biallelic Mutations in DNAJC12 Cause Hyperphenylalaninemia, Dystonia, and Intellectual DisabilityYair Anikster, Tobias B Haack, Thierry Vilboux, et al.
American Journal of Human Genetics|December 1, 2014
Compound heterozygosity of low-frequency promoter deletions and rare loss-of-function mutations in TXNL4A causes Burn-McKeown syndromeDagmar Wieczorek, William G Newman, Thomas Wieland, et al.
The Lancet. Respiratory Medicine|December 24, 2014
Genome-wide association study of survival from sepsis due to pneumonia: an observational cohort studyAnna Rautanen, Tara C Mills, Anthony C Gordon, et al.
Nature|November 12, 2013
Dysfunctional nitric oxide signalling increases risk of myocardial infarctionJeanette Erdmann, Klaus Stark, Ulrike B Esslinger, et al.
Nature Genetics|February 10, 2009
Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery diseaseDavid-Alexandre Trégouët, Inke R König, Jeanette Erdmann, et al.
Plos Genetics|August 12, 2010
Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levelsTamra E Meyer, Germaine C Verwoert, Shih-Jen Hwang, et al.
Circulation. Cardiovascular Genetics|November 22, 2011
A large candidate gene survey identifies the KCNE1 D85N polymorphism as a possible modulator of drug-induced torsades de pointesStefan Kääb, Dana C Crawford, Moritz F Sinner, et al.
Pageof 51