Sample-size considerations and strategies for linkage analysis in autosomal recessive disorders.

gan Wong, F L, Cantor, R M, Rotter, J I
Cyhoeddwyd 1986

Sandhoff disease heterozygote detection: a component of population screening for Tay-Sachs disease carriers. II. Sandhoff disease gene frequencies in American Jewish and non-Jewish...

gan Cantor, R M, Roy, C, Lim, J S, Kaback, M M
Cyhoeddwyd 1987

Sandhoff disease heterozygote detection: a component of population screening for Tay-Sachs disease carriers. I. Statistical methods.

gan Cantor, R M, Lim, J S, Roy, C, Kaback, M M
Cyhoeddwyd 1985

Complex genetic contribution of the Apo AI-CIII-AIV gene cluster to familial combined hyperlipidemia. Identification of different susceptibility haplotypes.

gan Dallinga-Thie, G M, van Linde-Sibenius Trip, M, Rotter, J I, Cantor, R M, Bu, X, Lusis, A J, de Bruin, T W
Cyhoeddwyd 1997

Linkage analysis of Norrie disease with an X-chromosomal ornithine aminotransferase locus.

gan Bateman, J B, Kojis, T L, Cantor, R M, Heinzmann, C, Ngo, J T, Spence, M A, Inana, G, Kivlin, J D, Curtis, D, Sparkes, R S
Cyhoeddwyd 1993

The Tay-Sachs disease gene in North American Jewish populations: geographic variations and origin.

gan Petersen, G M, Rotter, J I, Cantor, R M, Field, L L, Greenwald, S, Lim, J S, Roy, C, Schoenfeld, V, Lowden, J A, Kaback, M M
Cyhoeddwyd 1983

Multilocus genetic determinants of LDL particle size in coronary artery disease families.

gan Rotter, J. I., Bu, X., Cantor, R. M., Warden, C. H., Brown, J., Gray, R. J., Blanche, P. J., Krauss, R. M., Lusis, A. J.
Cyhoeddwyd 1996

Families with familial combined hyperlipidemia and families enriched for coronary artery disease share genetic determinants for the atherogenic lipoprotein phenotype.

gan Allayee, H, Aouizerat, B E, Cantor, R M, Dallinga-Thie, G M, Krauss, R M, Lanning, C D, Rotter, J I, Lusis, A J, de Bruin, T W
Cyhoeddwyd 1998

PCR-based screening for cystic fibrosis carrier mutations in an ethnically diverse pregnant population.

gan Grody, W W, Dunkel-Schetter, C, Tatsugawa, Z H, Fox, M A, Fang, C Y, Cantor, R M, Novak, J M, Bass, H N, Crandall, B F
Cyhoeddwyd 1997

Obesity and obesogenic growth are both highly heritable and modified by diet in a nonhuman primate model, the African green monkey (Chlorocebus aethiops sabaeus)

gan Schmitt, C A, Service, S K, Jasinska, A J, Dyer, T D, Jorgensen, M J, Cantor, R M, Weinstock, G M, Blangero, J, Kaplan, J R, Freimer, N B
Cyhoeddwyd yn Int J Obes (Lond) (2018)

A genome scan for familial combined hyperlipidemia reveals evidence of linkage with a locus on chromosome 11.

gan Aouizerat, B E, Allayee, H, Cantor, R M, Davis, R C, Lanning, C D, Wen, P Z, Dallinga-Thie, G M, de Bruin, T W, Rotter, J I, Lusis, A J
Cyhoeddwyd 1999

Evidence for linkage of a candidate chromosome 1 region to human systemic lupus erythematosus.

gan Tsao, B P, Cantor, R M, Kalunian, K C, Chen, C J, Badsha, H, Singh, R, Wallace, D J, Kitridou, R C, Chen, S L, Shen, N, Song, Y W, Isenberg, D A, Yu, C L, Hahn, B H, Rotter, J I
Cyhoeddwyd 1997

Seasonal variation of serotonin turnover in human cerebrospinal fluid, depressive symptoms and the role of the 5-HTTLPR

gan Luykx, J J, Bakker, S C, van Geloven, N, Eijkemans, M J C, Horvath, S, Lentjes, E, Boks, M P M, Strengman, E, DeYoung, J, Buizer-Voskamp, J E, Cantor, R M, Lu, A, van Dongen, E P A, Borgdorff, P, Bruins, P, Kahn, R S, Ophoff, R A
Cyhoeddwyd 2013

Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis

gan Gallagher, C. S., Mäkinen, N., Harris, H. R., Rahmioglu, N., Uimari, O., Cook, J. P., Shigesi, N., Ferreira, T., Velez-Edwards, D. R., Edwards, T. L., Mortlock, S., Ruhioglu, Z., Day, F., Becker, C. M., Karhunen, V., Martikainen, H., Järvelin, M.-R., Cantor, R. M., Ridker, P. M., Terry, K. L., Buring, J. E., Gordon, S. D., Medland, S. E., Montgomery, G. W., Nyholt, D. R., Hinds, D. A., Tung, J. Y., Perry, J. R. B., Lind, P. A., Painter, J. N., Martin, N. G., Morris, A. P., Chasman, D. I., Missmer, S. A., Zondervan, K. T., Morton, C. C.
Cyhoeddwyd yn Nat Commun (2019)