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Thomas Meitinger

Showing results (301-310 of 508) with videos related to

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Human Molecular Genetics|October 28, 2008
Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysisAsa Johansson, Fabio Marroni, Caroline Hayward, et al.
Lancet (London, England)|October 2, 2012
Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing studyAnita Rauch, Dagmar Wieczorek, Elisabeth Graf, et al.
The New England Journal of Medicine|July 20, 2007
Genomewide association analysis of coronary artery diseaseNilesh J Samani, Jeanette Erdmann, Alistair S Hall, et al.
American Journal of Human Genetics|August 16, 2016
Sudden Cardiac Death Due to Deficiency of the Mitochondrial Inorganic Pyrophosphatase PPA2Hannah Kennedy, Tobias B Haack, Verity Hartill, et al.
Circulation. Cardiovascular Genetics|June 12, 2014
Novel calmodulin mutations associated with congenital arrhythmia susceptibilityNaomasa Makita, Nobue Yagihara, Lia Crotti, et al.
Nature Genetics|November 27, 2004
Polymorphisms in FKBP5 are associated with increased recurrence of depressive episodes and rapid response to antidepressant treatmentElisabeth B Binder, Daria Salyakina, Peter Lichtner, et al.
European Journal of Human Genetics : EJHG|December 20, 2012
Genetic characterization of northeastern Italian population isolates in the context of broader European genetic diversityTõnu Esko, Massimo Mezzavilla, Mari Nelis, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|January 14, 2017
Immune-Array Analysis in Sporadic Inclusion Body Myositis Reveals HLA-DRB1 Amino Acid Heterogeneity Across the Myositis SpectrumSimon Rothwell, Robert G Cooper, Ingrid E Lundberg, et al.
Plos Genetics|October 27, 2010
Genetic association study identifies HSPB7 as a risk gene for idiopathic dilated cardiomyopathyKlaus Stark, Ulrike B Esslinger, Wibke Reinhard, et al.
American Journal of Human Genetics|November 8, 2018
Bi-allelic ADPRHL2 Mutations Cause Neurodegeneration with Developmental Delay, Ataxia, and Axonal NeuropathyKatharina Danhauser, Bader Alhaddad, Christine Makowski, et al.
Pageof 51

Showing results (301-310 of 508) with videos related to

Sort By:
Pageof 51
Human Molecular Genetics|October 28, 2008
Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysisAsa Johansson, Fabio Marroni, Caroline Hayward, et al.
Lancet (London, England)|October 2, 2012
Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing studyAnita Rauch, Dagmar Wieczorek, Elisabeth Graf, et al.
The New England Journal of Medicine|July 20, 2007
Genomewide association analysis of coronary artery diseaseNilesh J Samani, Jeanette Erdmann, Alistair S Hall, et al.
American Journal of Human Genetics|August 16, 2016
Sudden Cardiac Death Due to Deficiency of the Mitochondrial Inorganic Pyrophosphatase PPA2Hannah Kennedy, Tobias B Haack, Verity Hartill, et al.
Circulation. Cardiovascular Genetics|June 12, 2014
Novel calmodulin mutations associated with congenital arrhythmia susceptibilityNaomasa Makita, Nobue Yagihara, Lia Crotti, et al.
Nature Genetics|November 27, 2004
Polymorphisms in FKBP5 are associated with increased recurrence of depressive episodes and rapid response to antidepressant treatmentElisabeth B Binder, Daria Salyakina, Peter Lichtner, et al.
European Journal of Human Genetics : EJHG|December 20, 2012
Genetic characterization of northeastern Italian population isolates in the context of broader European genetic diversityTõnu Esko, Massimo Mezzavilla, Mari Nelis, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|January 14, 2017
Immune-Array Analysis in Sporadic Inclusion Body Myositis Reveals HLA-DRB1 Amino Acid Heterogeneity Across the Myositis SpectrumSimon Rothwell, Robert G Cooper, Ingrid E Lundberg, et al.
Plos Genetics|October 27, 2010
Genetic association study identifies HSPB7 as a risk gene for idiopathic dilated cardiomyopathyKlaus Stark, Ulrike B Esslinger, Wibke Reinhard, et al.
American Journal of Human Genetics|November 8, 2018
Bi-allelic ADPRHL2 Mutations Cause Neurodegeneration with Developmental Delay, Ataxia, and Axonal NeuropathyKatharina Danhauser, Bader Alhaddad, Christine Makowski, et al.
Pageof 51