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Thomas Meitinger

Showing results (311-320 of 508) with videos related to

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Nature Genetics|December 22, 2009
Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palateElisabeth Mangold, Kerstin U Ludwig, Stefanie Birnbaum, et al.
Brain : a Journal of Neurology|January 18, 2018
Hot-spot KIF5A mutations cause familial ALSDavid Brenner, Rüstem Yilmaz, Kathrin Müller, et al.
American Journal of Human Genetics|May 15, 2018
Mutations in PPCS, Encoding Phosphopantothenoylcysteine Synthetase, Cause Autosomal-Recessive Dilated CardiomyopathyArcangela Iuso, Marit Wiersma, Hans-Joachim Schüller, et al.
European Journal of Epidemiology|March 19, 2015
Prevalence of refractive error in Europe: the European Eye Epidemiology (E(3)) ConsortiumKatie M Williams, Virginie J M Verhoeven, Phillippa Cumberland, et al.
Molecular Psychiatry|July 26, 2023
Circulating metabolites modulated by diet are associated with depressionAshley van der Spek, Isobel D Stewart, Brigitte Kühnel, et al.
American Journal of Human Genetics|January 20, 2015
CLPB mutations cause 3-methylglutaconic aciduria, progressive brain atrophy, intellectual disability, congenital neutropenia, cataracts, movement disorderSaskia B Wortmann, Szymon Ziętkiewicz, Maria Kousi, et al.
Cephalalgia : an International Journal of Headache|September 3, 2014
Concordance of genetic risk across migraine subgroups: Impact on current and future genetic association studiesDale R Nyholt, , Verneri Anttila, et al.
American Journal of Human Genetics|September 26, 2017
Biallelic C1QBP Mutations Cause Severe Neonatal-, Childhood-, or Later-Onset Cardiomyopathy Associated with Combined Respiratory-Chain DeficienciesRené G Feichtinger, Monika Oláhová, Yoshihito Kishita, et al.
Human Mutation|June 16, 2016
Mutation Update for Kabuki Syndrome Genes KMT2D and KDM6A and Further Delineation of X-Linked Kabuki Syndrome Subtype 2Nina Bögershausen, Vincent Gatinois, Vera Riehmer, et al.
Annals of the Rheumatic Diseases|September 13, 2015
Dense genotyping of immune-related loci in idiopathic inflammatory myopathies confirms HLA alleles as the strongest genetic risk factor and suggests different genetic background for major clinical subgroupsSimon Rothwell, Robert G Cooper, Ingrid E Lundberg, et al.
Pageof 51

Showing results (311-320 of 508) with videos related to

Sort By:
Pageof 51
Nature Genetics|December 22, 2009
Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palateElisabeth Mangold, Kerstin U Ludwig, Stefanie Birnbaum, et al.
Brain : a Journal of Neurology|January 18, 2018
Hot-spot KIF5A mutations cause familial ALSDavid Brenner, Rüstem Yilmaz, Kathrin Müller, et al.
American Journal of Human Genetics|May 15, 2018
Mutations in PPCS, Encoding Phosphopantothenoylcysteine Synthetase, Cause Autosomal-Recessive Dilated CardiomyopathyArcangela Iuso, Marit Wiersma, Hans-Joachim Schüller, et al.
European Journal of Epidemiology|March 19, 2015
Prevalence of refractive error in Europe: the European Eye Epidemiology (E(3)) ConsortiumKatie M Williams, Virginie J M Verhoeven, Phillippa Cumberland, et al.
Molecular Psychiatry|July 26, 2023
Circulating metabolites modulated by diet are associated with depressionAshley van der Spek, Isobel D Stewart, Brigitte Kühnel, et al.
American Journal of Human Genetics|January 20, 2015
CLPB mutations cause 3-methylglutaconic aciduria, progressive brain atrophy, intellectual disability, congenital neutropenia, cataracts, movement disorderSaskia B Wortmann, Szymon Ziętkiewicz, Maria Kousi, et al.
Cephalalgia : an International Journal of Headache|September 3, 2014
Concordance of genetic risk across migraine subgroups: Impact on current and future genetic association studiesDale R Nyholt, , Verneri Anttila, et al.
American Journal of Human Genetics|September 26, 2017
Biallelic C1QBP Mutations Cause Severe Neonatal-, Childhood-, or Later-Onset Cardiomyopathy Associated with Combined Respiratory-Chain DeficienciesRené G Feichtinger, Monika Oláhová, Yoshihito Kishita, et al.
Human Mutation|June 16, 2016
Mutation Update for Kabuki Syndrome Genes KMT2D and KDM6A and Further Delineation of X-Linked Kabuki Syndrome Subtype 2Nina Bögershausen, Vincent Gatinois, Vera Riehmer, et al.
Annals of the Rheumatic Diseases|September 13, 2015
Dense genotyping of immune-related loci in idiopathic inflammatory myopathies confirms HLA alleles as the strongest genetic risk factor and suggests different genetic background for major clinical subgroupsSimon Rothwell, Robert G Cooper, Ingrid E Lundberg, et al.
Pageof 51