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Diabetes
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March 28, 2002
Molecular analysis of Berardinelli-Seip congenital lipodystrophy in Oman: evidence for multiple loci
Kirsten Heathcote, Anna Rajab, Jocelyne Magré, et al.
International Journal of Epidemiology
|
July 28, 2006
Fibrinogen and coronary heart disease: test of causality by 'Mendelian randomization'
Bernard Keavney, John Danesh, Sarah Parish, et al.
International Journal of Cancer
|
May 2, 2008
Variants in DNA double-strand break repair and DNA damage-response genes and susceptibility to lung and head and neck cancers
Patrick Danoy, Stefan Michiels, Philippe Dessen, et al.
Epilepsia
|
March 20, 2004
Polygenic control of idiopathic generalized epilepsy phenotypes in the genetic absence rats from Strasbourg (GAERS)
Gabrielle Rudolf, Marie Thérèse Bihoreau, Richard F Godfrey, et al.
Circulation
|
July 7, 2005
Mapping of familial thoracic aortic aneurysm/dissection with patent ductus arteriosus to 16p12.2-p13.13
Philippe Khau Van Kien, Flavie Mathieu, Limin Zhu, et al.
Human Genetics
|
June 20, 2008
A genome-wide exploration suggests an oligogenic model of inheritance for the TAFI activity and its antigen levels
Maria Sabater-Lleal, Alfonso Buil, Juan Carlos Souto, et al.
Circulation
|
March 22, 2017
A Replicated, Genome-Wide Significant Association of Aortic Stenosis With a Genetic Variant for Lipoprotein(a): Meta-Analysis of Published and Novel Data
Benjamin J Cairns, Sean Coffey, Ruth C Travis, et al.
Epigenomics
|
December 22, 2020
Estimating cell-type-specific DNA methylation effects in heterogeneous cellular populations
Yen-Chen A Feng, Yichen Guo, Lucile Pain, et al.
British Journal of Haematology
|
March 27, 2012
Genome wide association study for plasma levels of natural anticoagulant inhibitors and protein C anticoagulant pathway: the MARTHA project
Tiphaine Oudot-Mellakh, William Cohen, Marine Germain, et al.
International Journal of Genomics
|
January 9, 2026
Identification of Two Rare Variants in Iranian Families With Familial Sudden Cardiac Death
Mahsa Tahmasebivand, Sepideh Mehvari, Fatemeh Ghodratpour, et al.
Page
of 45
Search research articles
Search
Showing results (51-60 of 443) with videos related to
Sort By:
Page
of 45
Diabetes
|
March 28, 2002
Molecular analysis of Berardinelli-Seip congenital lipodystrophy in Oman: evidence for multiple loci
Kirsten Heathcote, Anna Rajab, Jocelyne Magré, et al.
International Journal of Epidemiology
|
July 28, 2006
Fibrinogen and coronary heart disease: test of causality by 'Mendelian randomization'
Bernard Keavney, John Danesh, Sarah Parish, et al.
International Journal of Cancer
|
May 2, 2008
Variants in DNA double-strand break repair and DNA damage-response genes and susceptibility to lung and head and neck cancers
Patrick Danoy, Stefan Michiels, Philippe Dessen, et al.
Epilepsia
|
March 20, 2004
Polygenic control of idiopathic generalized epilepsy phenotypes in the genetic absence rats from Strasbourg (GAERS)
Gabrielle Rudolf, Marie Thérèse Bihoreau, Richard F Godfrey, et al.
Circulation
|
July 7, 2005
Mapping of familial thoracic aortic aneurysm/dissection with patent ductus arteriosus to 16p12.2-p13.13
Philippe Khau Van Kien, Flavie Mathieu, Limin Zhu, et al.
Human Genetics
|
June 20, 2008
A genome-wide exploration suggests an oligogenic model of inheritance for the TAFI activity and its antigen levels
Maria Sabater-Lleal, Alfonso Buil, Juan Carlos Souto, et al.
Circulation
|
March 22, 2017
A Replicated, Genome-Wide Significant Association of Aortic Stenosis With a Genetic Variant for Lipoprotein(a): Meta-Analysis of Published and Novel Data
Benjamin J Cairns, Sean Coffey, Ruth C Travis, et al.
Epigenomics
|
December 22, 2020
Estimating cell-type-specific DNA methylation effects in heterogeneous cellular populations
Yen-Chen A Feng, Yichen Guo, Lucile Pain, et al.
British Journal of Haematology
|
March 27, 2012
Genome wide association study for plasma levels of natural anticoagulant inhibitors and protein C anticoagulant pathway: the MARTHA project
Tiphaine Oudot-Mellakh, William Cohen, Marine Germain, et al.
International Journal of Genomics
|
January 9, 2026
Identification of Two Rare Variants in Iranian Families With Familial Sudden Cardiac Death
Mahsa Tahmasebivand, Sepideh Mehvari, Fatemeh Ghodratpour, et al.
Page
of 45