QTL-specific genotype-by-smoking interaction and burden of calcified coronary atherosclerosis: The NHLBI Family Heart Study
North, K.E, Carr, J.J, Borecki, I.B, Kraja, A, Province, M, Pankow, J.S, Wilk, J.B, Hixson, J.E, Heiss, G
Published in Atherosclerosis (01.07.2007)
Published in Atherosclerosis (01.07.2007)
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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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TSLP polymorphisms are associated with asthma in a sex‐specific fashion
Hunninghake, G.M, Soto‐Quirós, M.E, Avila, L, Kim, H.P, Lasky‐Su, J, Rafaels, N, Ruczinski, I, Beaty, T.H, Mathias, R.A, Barnes, K.C, Wilk, J.B, O'Connor, G.T, James Gauderman, W, Vora, H, Baurley, J.W, Gilliland, F, Liang, C, Sylvia, J.S, Klanderman, B.J, Sharma, S.S, Himes, B.E, Bossley, C.J, Israel, E, Raby, B.A, Bush, A, Choi, A.M, Weiss, S.T, Celedón, J.C
Published in Allergy (Copenhagen) (01.12.2010)
Published in Allergy (Copenhagen) (01.12.2010)
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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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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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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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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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Segregation analysis of Parkinson disease revealing evidence for a major causative gene
Maher, N E, Currie, L J, Lazzarini, A M, Wilk, J B, Taylor, C A, Saint-Hilaire, M H, Feldman, R G, Golbe, L I, Wooten, G F, Myers, R H
Published in American journal of medical genetics (01.05.2002)
Published in American journal of medical genetics (01.05.2002)
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