Bidirectional Mendelian randomization to explore the causal relationships between body mass index and polycystic ovary syndrome von Brower, M A, Hai, Y, Jones, M R, Guo, X, Chen, Y -D I, Rotter, J I, Krauss, R M, Legro, R S, Azziz, R, Goodarzi, M O

Volltext

Insulin clearance: confirmation as a highly heritable trait, and genome-wide linkage analysis von Guo, X., Cui, J., Jones, M. R., Haritunians, T., Xiang, A. H., Chen, Y.-D. I., Taylor, K. D., Buchanan, T. A., Davis, R. C., Hsueh, W. A., Raffel, L. J., Rotter, J. I., Goodarzi, M. O.

Volltext

Systematic evaluation of validated type 2 diabetes and glycaemic trait loci for association with insulin clearance von Goodarzi, M. O., Guo, X., Cui, J., Jones, M. R., Haritunians, T., Xiang, A. H., Chen, Y.-D. I., Taylor, K. D., Buchanan, T. A., Hsueh, W. A., Raffel, L. J., Rotter, J. I.

Volltext

Common genetic variants differentially influence the transition from clinically defined states of fasting glucose metabolism von Walford, G. A., Green, T., Neale, B., Isakova, T., Rotter, J. I., Grant, S. F. A., Fox, C. S., Pankow, J. S., Wilson, J. G., Meigs, J. B., Siscovick, D. S., Bowden, D. W., Daly, M. J., Florez, J. C.

Volltext

Characterization of Statin Dose Response in Electronic Medical Records von Wei, W-Q, Feng, Q, Jiang, L, Waitara, M S, Iwuchukwu, O F, Roden, D M, Jiang, M, Xu, H, Krauss, R M, Rotter, J I, Nickerson, D A, Davis, R L, Berg, R L, Peissig, P L, McCarty, C A, Wilke, R A, Denny, J C

Volltext

The role of the Toll receptor pathway in susceptibility to inflammatory bowel diseases von De Jager, P L, Franchimont, D, Waliszewska, A, Bitton, A, Cohen, A, Langelier, D, Belaiche, J, Vermeire, S, Farwell, L, Goris, A, Libioulle, C, Jani, N, Dassopoulos, T, Bromfield, G P, Dubois, B, Cho, J H, Brant, S R, Duerr, R H, Yang, H, Rotter, J I, Silverberg, M S, Steinhart, A H, Daly, M J, Podolsky, D K, Louis, E, Hafler, D A, Rioux, J D

Volltext

genome-wide association scan for acute insulin response to glucose in Hispanic-Americans: the Insulin Resistance Atherosclerosis Family Study (IRAS FS) von Rich, S. S, Goodarzi, M. O, Palmer, N. D, Langefeld, C. D, Ziegler, J, Haffner, S. M, Bryer-Ash, M, Norris, J. M, Taylor, K. D, Haritunians, T, Rotter, J. I, Chen, Y.-D. I, Wagenknecht, L. E, Bowden, D. W, Bergman, R. N

Volltext

Candidate loci for insulin sensitivity and disposition index from a genome-wide association analysis of Hispanic participants in the Insulin Resistance Atherosclerosis (IRAS) Famil... von Palmer, N. D, Langefeld, C. D, Ziegler, J. T, Hsu, F, Haffner, S. M, Fingerlin, T, Norris, J. M, Chen, Y. I, Rich, S. S, Haritunians, T, Taylor, K. D, Bergman, R. N, Rotter, J. I, Bowden, D. W

Volltext

Familial expression of anti-Saccharomyces cerevisiae mannan antibodies in affected and unaffected relatives of patients with Crohn's disease von Sutton, C L, Yang, H, Li, Z, Rotter, J I, Targan, S R, Braun, J

Volltext

Functional and ethnic association of allele 2 of the interleukin-1 receptor antagonist gene in ulcerative colitis von Tountas, Nikolaos A., Casini–Raggi, Vincenzo, Yang, Huiying, Di Giovine, Francesco S., Vecchi, Maurizio, Kam, Lori, Melani, Lorenzo, Pizarro, Theresa T., Rotter, Jerome I., Cominelli, Fabio

Volltext

Perinuclear antineutrophil cytoplasmic antibodies in patients with Crohn's disease define a clinical subgroup von Vasiliauskas, EA, Plevy, SE, Landers, CJ, Binder, SW, Ferguson, DM, Yang, H, Rotter, JI, Vidrich, A, Targan, SR

Volltext

Genetic variants of the NOTCH3 gene in the elderly and magnetic resonance imaging correlates of age-related cerebral small vessel disease von Schmidt, Helena, Zeginigg, Marion, Wiltgen, Marco, Freudenberger, Paul, Petrovic, Katja, Cavalieri, Margherita, Gider, Pierre, Enzinger, Christian, Fornage, Myriam, Debette, Stephanie, Rotter, Jerome I., Ikram, Mohammad A., Launer, Lenore J., Schmidt, Reinhold

Volltext

Familial empirical risks for inflammatory bowel disease: differences between Jews and non-Jews von Yang, H, McElree, C, Roth, M P, Shanahan, F, Targan, S R, Rotter, J I

Volltext

Associations of pentraxin 3 with cardiovascular disease: the Multi‐Ethnic Study of Atherosclerosis von Jenny, N. S., Blumenthal, R. S., Kronmal, R. A., Rotter, J. I., Siscovick, D. S., Psaty, B. M.

Volltext

Linkage of Crohn’s disease to the major histocompatibility complex region is detected by multiple non-parametric analyses von Yang, H, Plevy, S E, Taylor, K, Tyan, D, Fischel-Ghodsian, N, McElree, C, Targan, S R, Rotter, J I

Volltext

Familial Mediterranean Fever: Effects of Genotype and Ethnicity on Inflammatory Attacks and Amyloidosis von Mimouni, Aviva, Magal, Nurit, Stoffman, Nava, Shohat, Tamy, Minasian, Ara, Krasnov, Michael, Halpern, Gabrielle J, Rotter, Jerome I, Fischel-Ghodsian, Nathan, Danon, Yehuda L, Shohat, Mordechai

Volltext

Insulin-IGF2 region on chromosome 11p encodes a gene implicated in HLA-DR4-dependent diabetes susceptibility von Julier, C, Hyer, R. N, Davies, J, Merlin, F, Soularue, P, Briant, L, Cathelineau, G, Deschamps, I, Rotter, J. I, Froguel, P, Boitard, C, Bell, J. I, Lathrop, G. M

Volltext

Genetic mapping of a susceptibility locus for insulin-dependent diabetes mellitus on chromosome llq von Hashimoto, L, Habita, C, Beressi, J. P, Delepine, M, Basse, C, Cambon-Thomsen, A, Deschamps, I, Rotter, J. I, Djoulah, S, James, M. R, Froguel, P, Weissenbach, J, Lathrop, G. M, Julier, C

Volltext

Genetic mapping of a susceptibility locus for insulin-dependent diabetes mellitus on chromosome 11q von HASHIMOTO, L, HABITA, C, FROGUEL, P, WEISSENBACH, J, LATHROP, G. M, JULIER, C, BERESSI, J. P, DELEPINE, M, BESSE, C, CAMBON-THOMSEN, A, DESCHAMPS, I, ROTTER, J. I, DJOUIAH, S, JAMES, M. R

Volltext

Phenotype-genotype correlation in familial Mediterranean fever: evidence for an association between Met694Val and amyloidosis von Shohat, M, Magal, N, Shohat, T, Chen, X, Dagan, T, Mimouni, A, Danon, Y, Lotan, R, Ogur, G, Sirin, A, Schlezinger, M, Halpern, G J, Schwabe, A, Kastner, D, Rotter, J I, Fischel-Ghodsian, N

Volltext