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Hypertension (Dallas, Tex. : 1979)
|
March 13, 2013
Genetic predisposition to higher blood pressure increases coronary artery disease risk
Wolfgang Lieb, Henning Jansen, Christina Loley, et al.
BMC Proceedings
|
March 1, 2012
Identifying rare variants from exome scans: the GAW17 experience
Saurabh Ghosh, Heike Bickeböller, Julia Bailey, et al.
European Journal of Human Genetics : EJHG
|
March 3, 2016
Clinical, neuroradiological and molecular characterization of cerebellar dysplasia with cysts (Poretti-Boltshauser syndrome)
Alessia Micalizzi, Andrea Poretti, Marta Romani, et al.
Plos Genetics
|
August 17, 2013
GUESS-ing polygenic associations with multiple phenotypes using a GPU-based evolutionary stochastic search algorithm
Leonardo Bottolo, Marc Chadeau-Hyam, David I Hastie, et al.
Human Heredity
|
September 28, 2006
SNP-based analysis of genetic substructure in the German population
Michael Steffens, Claudia Lamina, Thomas Illig, et al.
Journal of Molecular Medicine (Berlin, Germany)
|
July 2, 2008
Lack of association of genetic variants in the LRP8 gene with familial and sporadic myocardial infarction
Wolfgang Lieb, Tanja Zeller, Massimo Mangino, et al.
Scientific Reports
|
April 14, 2018
Low-level mitochondrial heteroplasmy modulates DNA replication, glucose metabolism and lifespan in mice
Misa Hirose, Paul Schilf, Yask Gupta, et al.
Circulation. Cardiovascular Genetics
|
September 13, 2015
Molecular Characterization of the NLRC4 Expression in Relation to Interleukin-18 Levels
Tanja Zeller, Tina Haase, Christian Müller, et al.
Plos One
|
December 14, 2012
Analyzing illumina gene expression microarray data from different tissues: methodological aspects of data analysis in the metaxpress consortium
Claudia Schurmann, Katharina Heim, Arne Schillert, et al.
Eclinicalmedicine
|
May 21, 2026
The phenotypic spectrum and genetic determinants of severe spinal muscular atrophy in individuals with a single <i>SMN2</i> copy: an international retrospective observational study
Gianpaolo Cicala, Anna Capasso, Marianna Villa, et al.
Page
of 43
Search research articles
Search
Showing results (351-360 of 422) with videos related to
Sort By:
Page
of 43
Hypertension (Dallas, Tex. : 1979)
|
March 13, 2013
Genetic predisposition to higher blood pressure increases coronary artery disease risk
Wolfgang Lieb, Henning Jansen, Christina Loley, et al.
BMC Proceedings
|
March 1, 2012
Identifying rare variants from exome scans: the GAW17 experience
Saurabh Ghosh, Heike Bickeböller, Julia Bailey, et al.
European Journal of Human Genetics : EJHG
|
March 3, 2016
Clinical, neuroradiological and molecular characterization of cerebellar dysplasia with cysts (Poretti-Boltshauser syndrome)
Alessia Micalizzi, Andrea Poretti, Marta Romani, et al.
Plos Genetics
|
August 17, 2013
GUESS-ing polygenic associations with multiple phenotypes using a GPU-based evolutionary stochastic search algorithm
Leonardo Bottolo, Marc Chadeau-Hyam, David I Hastie, et al.
Human Heredity
|
September 28, 2006
SNP-based analysis of genetic substructure in the German population
Michael Steffens, Claudia Lamina, Thomas Illig, et al.
Journal of Molecular Medicine (Berlin, Germany)
|
July 2, 2008
Lack of association of genetic variants in the LRP8 gene with familial and sporadic myocardial infarction
Wolfgang Lieb, Tanja Zeller, Massimo Mangino, et al.
Scientific Reports
|
April 14, 2018
Low-level mitochondrial heteroplasmy modulates DNA replication, glucose metabolism and lifespan in mice
Misa Hirose, Paul Schilf, Yask Gupta, et al.
Circulation. Cardiovascular Genetics
|
September 13, 2015
Molecular Characterization of the NLRC4 Expression in Relation to Interleukin-18 Levels
Tanja Zeller, Tina Haase, Christian Müller, et al.
Plos One
|
December 14, 2012
Analyzing illumina gene expression microarray data from different tissues: methodological aspects of data analysis in the metaxpress consortium
Claudia Schurmann, Katharina Heim, Arne Schillert, et al.
Eclinicalmedicine
|
May 21, 2026
The phenotypic spectrum and genetic determinants of severe spinal muscular atrophy in individuals with a single <i>SMN2</i> copy: an international retrospective observational study
Gianpaolo Cicala, Anna Capasso, Marianna Villa, et al.
Page
of 43