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926 results
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Evidence for recessive and against dominant inheritance at the HLA-"linked" locus in coeliac disease.
Greenberg DA, Hodge SE, Rotter JI. Greenberg DA, et al. Among authors: rotter ji. Am J Hum Genet. 1982 Mar;34(2):263-77. Am J Hum Genet. 1982. PMID: 6951410 Free PMC article.
HLA class II haplotype associations with inflammatory bowel disease in Jewish (Ashkenazi) and non-Jewish caucasian populations.
Trachtenberg EA, Yang H, Hayes E, Vinson M, Lin C, Targan SR, Tyan D, Erlich H, Rotter JI. Trachtenberg EA, et al. Among authors: rotter ji. Hum Immunol. 2000 Mar;61(3):326-33. doi: 10.1016/s0198-8859(99)00134-2. Hum Immunol. 2000. PMID: 10689124 Free PMC article.
Multilocus genetic determinants of LDL particle size in coronary artery disease families.
Rotter JI, Bu X, Cantor RM, Warden CH, Brown J, Gray RJ, Blanche PJ, Krauss RM, Lusis AJ. Rotter JI, et al. Am J Hum Genet. 1996 Mar;58(3):585-94. Am J Hum Genet. 1996. PMID: 8644718 Free PMC article.
Genetic variation in lipoprotein (a) levels in families enriched for coronary artery disease is determined almost entirely by the apolipoprotein (a) gene locus.
DeMeester CA, Bu X, Gray RJ, Lusis AJ, Rotter JI. DeMeester CA, et al. Among authors: rotter ji. Am J Hum Genet. 1995 Jan;56(1):287-93. Am J Hum Genet. 1995. PMID: 7825589 Free PMC article.
Additional evidence of linkage between Crohn's disease and a putative locus on chromosome 12.
Yang H, Ohmen JD, Ma Y, Bentley LG, Targan SR, Fischel-Ghodsian N, Rotter JI. Yang H, et al. Among authors: rotter ji. Genet Med. 1999 Jul-Aug;1(5):194-8. doi: 10.1097/00125817-199907000-00005. Genet Med. 1999. PMID: 11256672
Leber hereditary optic neuropathy: estimation of number of embryonic precursor cells and disease threshold in heterozygous affected females at the X-linked locus.
Bu X, Rotter JI. Bu X, et al. Among authors: rotter ji. Clin Genet. 1992 Sep;42(3):143-8. doi: 10.1111/j.1399-0004.1992.tb03226.x. Clin Genet. 1992. PMID: 1395084
Identification of TNFRSF1B as a novel modifier gene in familial combined hyperlipidemia.
Geurts JM, Janssen RG, van Greevenbroek MM, van der Kallen CJ, Cantor RM, Bu X, Aouizerat BE, Allayee H, Rotter JI, de Bruin TW. Geurts JM, et al. Among authors: rotter ji. Hum Mol Genet. 2000 Sep 1;9(14):2067-74. doi: 10.1093/hmg/9.14.2067. Hum Mol Genet. 2000. PMID: 10958645
A genome scan for familial combined hyperlipidemia reveals evidence of linkage with a locus on chromosome 11.
Aouizerat BE, Allayee H, Cantor RM, Davis RC, Lanning CD, Wen PZ, Dallinga-Thie GM, de Bruin TW, Rotter JI, Lusis AJ. Aouizerat BE, et al. Among authors: rotter ji. Am J Hum Genet. 1999 Aug;65(2):397-412. doi: 10.1086/302490. Am J Hum Genet. 1999. PMID: 10417282 Free PMC article.
Families with familial combined hyperlipidemia and families enriched for coronary artery disease share genetic determinants for the atherogenic lipoprotein phenotype.
Allayee H, Aouizerat BE, Cantor RM, Dallinga-Thie GM, Krauss RM, Lanning CD, Rotter JI, Lusis AJ, de Bruin TW. Allayee H, et al. Among authors: rotter ji. Am J Hum Genet. 1998 Aug;63(2):577-85. doi: 10.1086/301983. Am J Hum Genet. 1998. PMID: 9683614 Free PMC article.
Cost-effective sib-pair designs in the mapping of quantitative-trait loci.
Zhao H, Zhang H, Rotter JI. Zhao H, et al. Among authors: rotter ji. Am J Hum Genet. 1997 May;60(5):1211-21. Am J Hum Genet. 1997. PMID: 9150169 Free PMC article.
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