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Andreas Ziegler

Showing results (401-410 of 422) with videos related to

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Science Advances|July 8, 2016
Novel multiple sclerosis susceptibility loci implicated in epigenetic regulationTill F M Andlauer, Dorothea Buck, Gisela Antony, et al.
Human Mutation|January 6, 2022
Clinico-radiological features, molecular spectrum, and identification of prognostic factors in developmental and epileptic encephalopathy due to inosine triphosphate pyrophosphatase (ITPase) deficiencyMarcello Scala, Saskia B Wortmann, Namik Kaya, et al.
Circulation. Cardiovascular Genetics|May 25, 2011
A genome-wide association study identifies LIPA as a susceptibility gene for coronary artery diseasePhilipp S Wild, Tanja Zeller, Arne Schillert, et al.
Brain : a Journal of Neurology|September 26, 2020
Defining the clinical, molecular and imaging spectrum of adaptor protein complex 4-associated hereditary spastic paraplegiaDarius Ebrahimi-Fakhari, Julian Teinert, Robert Behne, et al.
The New England Journal of Medicine|August 26, 2023
Global Effect of Modifiable Risk Factors on Cardiovascular Disease and Mortality, Christina Magnussen, Francisco M Ojeda, et al.
Nature Genetics|February 10, 2009
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants, Sekar Kathiresan, Benjamin F Voight, et al.
Nature Genetics|September 13, 2011
Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaqueJoshua C Bis, Maryam Kavousi, Nora Franceschini, 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.
American Journal of Human Genetics|October 2, 2012
Discovery and fine mapping of serum protein loci through transethnic meta-analysisNora Franceschini, Frank J A van Rooij, Bram P Prins, et al.
The Journal of Clinical Investigation|April 11, 2017
Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and functionPhilipp S Wild, Janine F Felix, Arne Schillert, et al.
Pageof 43

Showing results (401-410 of 422) with videos related to

Sort By:
Pageof 43
Science Advances|July 8, 2016
Novel multiple sclerosis susceptibility loci implicated in epigenetic regulationTill F M Andlauer, Dorothea Buck, Gisela Antony, et al.
Human Mutation|January 6, 2022
Clinico-radiological features, molecular spectrum, and identification of prognostic factors in developmental and epileptic encephalopathy due to inosine triphosphate pyrophosphatase (ITPase) deficiencyMarcello Scala, Saskia B Wortmann, Namik Kaya, et al.
Circulation. Cardiovascular Genetics|May 25, 2011
A genome-wide association study identifies LIPA as a susceptibility gene for coronary artery diseasePhilipp S Wild, Tanja Zeller, Arne Schillert, et al.
Brain : a Journal of Neurology|September 26, 2020
Defining the clinical, molecular and imaging spectrum of adaptor protein complex 4-associated hereditary spastic paraplegiaDarius Ebrahimi-Fakhari, Julian Teinert, Robert Behne, et al.
The New England Journal of Medicine|August 26, 2023
Global Effect of Modifiable Risk Factors on Cardiovascular Disease and Mortality, Christina Magnussen, Francisco M Ojeda, et al.
Nature Genetics|February 10, 2009
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants, Sekar Kathiresan, Benjamin F Voight, et al.
Nature Genetics|September 13, 2011
Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaqueJoshua C Bis, Maryam Kavousi, Nora Franceschini, 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.
American Journal of Human Genetics|October 2, 2012
Discovery and fine mapping of serum protein loci through transethnic meta-analysisNora Franceschini, Frank J A van Rooij, Bram P Prins, et al.
The Journal of Clinical Investigation|April 11, 2017
Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and functionPhilipp S Wild, Janine F Felix, Arne Schillert, et al.
Pageof 43