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Mark Lathrop

Showing results (51-60 of 443) with videos related to

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Diabetes|March 28, 2002
Molecular analysis of Berardinelli-Seip congenital lipodystrophy in Oman: evidence for multiple lociKirsten 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 cancersPatrick 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-p13.13Philippe 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 levelsMaria 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 DataBenjamin J Cairns, Sean Coffey, Ruth C Travis, et al.
Epigenomics|December 22, 2020
Estimating cell-type-specific DNA methylation effects in heterogeneous cellular populationsYen-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 projectTiphaine 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 DeathMahsa Tahmasebivand, Sepideh Mehvari, Fatemeh Ghodratpour, et al.
Pageof 45

Showing results (51-60 of 443) with videos related to

Sort By:
Pageof 45
Diabetes|March 28, 2002
Molecular analysis of Berardinelli-Seip congenital lipodystrophy in Oman: evidence for multiple lociKirsten 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 cancersPatrick 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-p13.13Philippe 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 levelsMaria 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 DataBenjamin J Cairns, Sean Coffey, Ruth C Travis, et al.
Epigenomics|December 22, 2020
Estimating cell-type-specific DNA methylation effects in heterogeneous cellular populationsYen-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 projectTiphaine 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 DeathMahsa Tahmasebivand, Sepideh Mehvari, Fatemeh Ghodratpour, et al.
Pageof 45