R H MYERS - JoVE Visualize

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International Journal of Obesity (2005)|March 5, 2008

NYD-SP18 is associated with obesity in the NHLBI Family Heart StudyJ B Wilk, J M Laramie, J C Latourelle, et al.

The New England Journal of Medicine|April 18, 1996

Absence of association or genetic linkage between the angiotensin-converting-enzyme gene and left ventricular massK Lindpaintner, M Lee, M G Larson, et al.

Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|July 1, 1997

The BsmI vitamin D receptor restriction fragment length polymorphism (bb) influences the effect of calcium intake on bone mineral densityD P Kiel, R H Myers, L A Cupples, et al.

Human Molecular Genetics|May 18, 2000

Evidence for a gene influencing the TG/HDL-C ratio on chromosome 7q32.3-qter: a genome-wide scan in the Framingham studyA M Shearman, J M Ordovas, L A Cupples, et al.

Neurology|March 1, 1996

Apolipoprotein E epsilon4 association with dementia in a population-based study: The Framingham studyR H Myers, E J Schaefer, P W Wilson, et al.

Arteriosclerosis, Thrombosis, and Vascular Biology|April 9, 1999

Increased platelet aggregability associated with platelet GPIIIa PlA2 polymorphism: the Framingham Offspring StudyD Feng, K Lindpaintner, M G Larson, et al.

American Journal of Medical Genetics. Part A|June 5, 2003

Interaction of normal and expanded CAG repeat sizes influences age at onset of Huntington diseaseL Djoussé, B Knowlton, M Hayden, et al.

Neurology|January 10, 2002

Epidemiologic study of 203 sibling pairs with Parkinson's disease: the GenePD studyN E Maher, L I Golbe, A M Lazzarini, et al.

Neurology|September 26, 2001

Genome-wide scan for Parkinson's disease: the GenePD StudyA L DeStefano, L I Golbe, M H Mark, et al.

Movement Disorders : Official Journal of the Movement Disorder Society|June 21, 2005

Absence of previously reported variants in the SCNA (G88C and G209A), NR4A2 (T291D and T245G) and the DJ-1 (T497C) genes in familial Parkinson's disease from the GenePD studySamer Karamohamed, L I Golbe, M H Mark, et al.

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Showing results (111-120 of 126) with videos related to

Sort By:

Pageof 13

International Journal of Obesity (2005)|March 5, 2008

NYD-SP18 is associated with obesity in the NHLBI Family Heart StudyJ B Wilk, J M Laramie, J C Latourelle, et al.

The New England Journal of Medicine|April 18, 1996

Absence of association or genetic linkage between the angiotensin-converting-enzyme gene and left ventricular massK Lindpaintner, M Lee, M G Larson, et al.

Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|July 1, 1997

The BsmI vitamin D receptor restriction fragment length polymorphism (bb) influences the effect of calcium intake on bone mineral densityD P Kiel, R H Myers, L A Cupples, et al.

Human Molecular Genetics|May 18, 2000

Evidence for a gene influencing the TG/HDL-C ratio on chromosome 7q32.3-qter: a genome-wide scan in the Framingham studyA M Shearman, J M Ordovas, L A Cupples, et al.

Neurology|March 1, 1996

Apolipoprotein E epsilon4 association with dementia in a population-based study: The Framingham studyR H Myers, E J Schaefer, P W Wilson, et al.

Arteriosclerosis, Thrombosis, and Vascular Biology|April 9, 1999

Increased platelet aggregability associated with platelet GPIIIa PlA2 polymorphism: the Framingham Offspring StudyD Feng, K Lindpaintner, M G Larson, et al.

American Journal of Medical Genetics. Part A|June 5, 2003

Interaction of normal and expanded CAG repeat sizes influences age at onset of Huntington diseaseL Djoussé, B Knowlton, M Hayden, et al.

Neurology|January 10, 2002

Epidemiologic study of 203 sibling pairs with Parkinson's disease: the GenePD studyN E Maher, L I Golbe, A M Lazzarini, et al.

Neurology|September 26, 2001

Genome-wide scan for Parkinson's disease: the GenePD StudyA L DeStefano, L I Golbe, M H Mark, et al.

Movement Disorders : Official Journal of the Movement Disorder Society|June 21, 2005

Absence of previously reported variants in the SCNA (G88C and G209A), NR4A2 (T291D and T245G) and the DJ-1 (T497C) genes in familial Parkinson's disease from the GenePD studySamer Karamohamed, L I Golbe, M H Mark, et al.

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