Segregation analysis of serum uric acid in the NHLBI Family Heart Study
Wilk, J.B., Djousse, L., Borecki, I., Atwood, L.D., Hunt, S.C., Rich, S.S., Eckfeldt, J.H., Arnett, D.K., Rao, D.C., Myers, R.H.
Published in Human genetics (30.03.2000)
Published in Human genetics (30.03.2000)
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Journal Article
Haplotypes and gene expression implicate the MAPT region for Parkinson disease: the GenePD Study
Tobin, J E, Latourelle, J C, Lew, M F, Klein, C, Suchowersky, O, Shill, H A, Golbe, L I, Mark, M H, Growdon, J H, Wooten, G F, Racette, B A, Perlmutter, J S, Watts, R, Guttman, M, Baker, K B, Goldwurm, S, Pezzoli, G, Singer, C, Saint-Hilaire, M H, Hendricks, A E, Williamson, S, Nagle, M W, Wilk, J B, Massood, T, Laramie, J M, DeStefano, A L, Litvan, I, Nicholson, G, Corbett, A, Isaacson, S, Burn, D J, Chinnery, P F, Pramstaller, P P, Sherman, S, Al-hinti, J, Drasby, E, Nance, M, Moller, A T, Ostergaard, K, Roxburgh, R, Snow, B, Slevin, J T, Cambi, F, Gusella, J F, Myers, R H
Published in Neurology (01.07.2008)
Published in Neurology (01.07.2008)
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Journal Article
Common Variants in the 5′ Region of the Leptin Gene Are Associated with Body Mass Index in Men from the National Heart, Lung, and Blood Institute Family Heart Study
Jiang, Y., Wilk, J.B., Borecki, I., Williamson, S., DeStefano, A.L., Xu, G., Liu, J., Ellison, R.C., Province, M., Myers, R.H.
Published in American journal of human genetics (01.08.2004)
Published in American journal of human genetics (01.08.2004)
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Journal Article
Predictors of nursing home placement in Huntington disease
Wheelock, V L, Tempkin, T, Marder, K, Nance, M, Myers, R H, Zhao, H, Kayson, E, Orme, C, Shoulson, I
Published in Neurology (25.03.2003)
Published in Neurology (25.03.2003)
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Interaction of normal and expanded CAG repeat sizes influences age at onset of Huntington disease
Djoussé, L., Knowlton, B., Hayden, M., Almqvist, E.W., Brinkman, R., Ross, C., Margolis, R., Rosenblatt, A., Durr, A., Dode, C., Morrison, P.J., Novelletto, A., Frontali, M., Trent, R.J.A., McCusker, E., Gómez-Tortosa, E., Mayo, D., Jones, R., Zanko, A., Nance, M., Abramson, R., Suchowersky, O., Paulsen, J., Harrison, M., Yang, Q., Cupples, L.A., Gusella, J.F., MacDonald, M.E., Myers, R.H.
Published in American journal of medical genetics. Part A (15.06.2003)
Published in American journal of medical genetics. Part A (15.06.2003)
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Journal Article
Environmental, medical, and family history risk factors for Parkinson's disease: a New England-based case control study
Taylor, C A, Saint-Hilaire, M H, Cupples, L A, Thomas, C A, Burchard, A E, Feldman, R G, Myers, R H
Published in American journal of medical genetics (15.12.1999)
Published in American journal of medical genetics (15.12.1999)
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Evidence for the GluR6 gene associated with younger onset age of Huntington's disease
MacDonald, M E, Vonsattel, J P, Shrinidhi, J, Couropmitree, N N, Cupples, L A, Bird, E D, Gusella, J F, Myers, R H
Published in Neurology (12.10.1999)
Published in Neurology (12.10.1999)
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Journal Article
HD Repeat Determines the Rate of Neuropathological Change
Massood, T., Latourelle, J., Srinidhi Mysore, J., Fossale, E., Gillis, T., Gusella, J.F., MacDonald, M.E., Myers, R.H.
Published in Neurotherapeutics (01.04.2008)
Published in Neurotherapeutics (01.04.2008)
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Journal Article
Apolipoprotein E polymorphism modifies the alcohol-HDL association observed in the National Heart, Lung, and Blood Institute Family Heart Study
Djousse, L, Pankow, J.S, Arnett, D.K, Eckfeldt, J.H, Myers, R.H, Ellison, R.C
Published in The American journal of clinical nutrition (01.12.2004)
Published in The American journal of clinical nutrition (01.12.2004)
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Journal Article
Circulating MCP-1 levels shows linkage to chemokine receptor gene cluster on chromosome 3: the NHLBI Family Heart Study follow-up examination
Bielinski, S J, Pankow, J S, Miller, M B, Hopkins, P N, Eckfeldt, J H, Hixson, J, Liu, Y, Register, T, Myers, R H, Arnett, D K
Published in Genes and immunity (01.12.2007)
Published in Genes and immunity (01.12.2007)
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Journal Article
NYD-SP18 is associated with obesity in the NHLBI Family Heart Study
Wilk, J.B, Laramie, J.M, Latourelle, J.C, Williamson, S, Nagle, M.W, Tobin, J.E, Foster, C.L, Eckfeldt, J.H, Province, M.A, Borecki, I.B
Published in International Journal of Obesity (01.06.2008)
Published in International Journal of Obesity (01.06.2008)
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Journal Article
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 study
Karamohamed, Samer, Golbe, L.I., Mark, M.H., Lazzarini, A.M., Suchowersky, O., Labelle, N., Guttman, Mark, Currie, L.J., Wooten, G.F., Stacy, M., Saint-Hilaire, M., Feldman, R.G., Liu, J., Shoemaker, C.M., Wilk, J.B., DeStefano, A.L., Latourelle, J.C., Xu, G., Watts, R., Growdon, J., Lew, M., Waters, C., Vieregge, P., Pramstaller, P.P., Klein, C., Racette, B.A., Perlmutter, J.S., Parsian, A., Singer, Carlos, Montgomery, E., Baker, K., Gusella, J.F., Herbert, A., Myers, R.H.
Published in Movement disorders (01.09.2005)
Published in Movement disorders (01.09.2005)
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Journal Article
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 Gene PD study
Karamohamed, Samer, Golbe, L.I., Mark, M.H., Lazzarini, A.M., Suchowersky, O., Labelle, N., Guttman, Mark, Currie, L.J., Wooten, G.F., Stacy, M., Saint‐Hilaire, M., Feldman, R.G., Liu, J., Shoemaker, C.M., Wilk, J.B., DeStefano, A.L., Latourelle, J.C., Xu, G., Watts, R., Growdon, J., Lew, M., Waters, C., Vieregge, P., Pramstaller, P.P., Klein, C., Racette, B.A., Perlmutter, J.S., Parsian, A., Singer, Carlos, Montgomery, E., Baker, K., Gusella, J.F., Herbert, A., Myers, R.H.
Published in Movement disorders (01.09.2005)
Published in Movement disorders (01.09.2005)
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Journal Article
The Genetic Defect Causing Familial Alzheimer's Disease Maps on Chromosome 21
St George-Hyslop, Peter H., Tanzi, Rudolph E., Polinsky, Ronald J., Haines, Jonathan L., Nee, Linda, Watkins, Paul C., Myers, Richard H., Feldman, Robert G., Pollen, Daniel, Drachman, David, Growdon, John, Bruni, Amalia, Foncin, Jean-Francois, Salmon, Denise, Frommelt, Peter, Amaducci, Luigi, Sorbi, Sandro, Piacentini, Silva, Stewart, Gordon D., Hobbs, Wendy J., Conneally, P. Michael, Gusella, James F.
Published in Science (American Association for the Advancement of Science) (20.02.1987)
Published in Science (American Association for the Advancement of Science) (20.02.1987)
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Journal Article
Incomplete dominance of type III hyperlipoproteinemia is associated with the rare apolipoprotein E2 (Arg136 → Ser) variant in multigenerational pedigree studies
Pocovi, M., Cenarro, A., Civeir, F., Myers, R.H., Casao, E., Esteban, M., Ordovas, J.M.
Published in Atherosclerosis (26.04.1996)
Published in Atherosclerosis (26.04.1996)
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Journal Article
Segregation analysis of serum uric acid in the NHLBI Family Heart Study
WILK, J. B, DJOUSSE, L, BORECKI, I, ATWOOD, L. D, HUNT, S. C, RICH, S. S, ECKFELDT, J. H, ARNETT, D. K, RAO, D. C, MYERS, R. H
Published in Human genetics (01.03.2000)
Published in Human genetics (01.03.2000)
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