JeromeI. Rotter

发表

J. Holton, G. Rook, J. Grange, 1994, The Lancet.

M. Silverberg, A. Steinhart, D. Rubin, 2009, The Lancet.

Genome scan for adiposity in Dutch dyslipidemic families reveals novel quantitative trait loci for leptin, body mass index and soluble tumor necrosis factor receptor superfamily 1A

R. Cantor, A. Lusis, H. Allayee, 2000, International Journal of Obesity.

Candidate locus for a nuclear modifier gene for maternally inherited deafness.

X. Estivill, Huiying Yang, J. Rotter, 2000, American journal of human genetics.

Geographic origins of Jewish patients with inflammatory bowel disease.

J. Rotter, G. Petersen, M. Roth, 1989, Gastroenterology.

Familial empirical risks for inflammatory bowel disease: differences between Jews and non-Jews.

S. Targan, Huiying Yang, J. Rotter, 1993, Gut.

Common genetic variants differentially influence the transition from clinically defined states of fasting glucose metabolism

J. Pankow, M. Daly, S. Grant, 2012, Diabetologia.

Susceptibility locus for inflammatory bowel disease on chromosome 16 has a role in Crohn's disease, but not in ulcerative colitis.

S. Targan, Huiying Yang, J. Rotter, 1996, Human molecular genetics.

Quantitative trait locus mapping of human blood pressure to a genetic region at or near the lipoprotein lipase gene locus on chromosome 8p22.

W. Sheu, J. Rotter, T. Katsuya, 1996, The Journal of clinical investigation.

Relative predispositional effects of HLA class II DRB1-DQB1 haplotypes and genotypes on type 1 diabetes: a meta-analysis.

P. Bingley, J. Ilonen, Å. Lernmark, 2007, Tissue antigens.

ANCA pattern and LTA haplotype relationship to clinical responses to anti-TNF antibody treatment in Crohn's disease.

S. Targan, K. Taylor, Huiying Yang, 2001, Gastroenterology.

GWAS for executive function and processing speed suggests involvement of the CADM2 gene

Blair H. Smith, J. Bressler, M. Fornage, 2016, Molecular Psychiatry.

Familial expression of anti-Saccharomyces cerevisiae mannan antibodies in affected and unaffected relatives of patients with Crohn's disease

S. Targan, Huiying Yang, J. Rotter, 2000, Gut.

Familial visceral neuropathy with autosomal dominant transmission.

J. Rotter, E. Mayer, M. D. Schuffler, 1986, Gastroenterology.

Linkage of a candidate gene locus to familial combined hyperlipidemia: lecithin:cholesterol acyltransferase on 16q.

J. Rotter, A. Lusis, H. Allayee, 1999, Arteriosclerosis, thrombosis, and vascular biology.

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

R. Krauss, J. Rotter, A. Lusis, 1998, American journal of human genetics.

Perinuclear antineutrophil cytoplasmic antibodies in patients with Crohn's disease define a clinical subgroup.

S. Targan, E. Vasiliauskas, Huiying Yang, 1996, Gastroenterology.

HLA class II haplotype associations with inflammatory bowel disease in Jewish (Ashkenazi) and non-Jewish caucasian populations.

S. Targan, Huiying Yang, J. Rotter, 2000, Human immunology.

An SNP linkage scan identifies significant Crohn's disease loci on chromosomes 13q13.3 and, in Jewish families, on 1p35.2 and 3q29

J. Rioux, M. Silverberg, A. Cohen, 2008, Genes and Immunity.

Tumor necrosis factor microsatellites define a Crohn's disease-associated haplotype on chromosome 6.

S. Targan, Huiying Yang, J. Rotter, 1996, Gastroenterology.

A genome-wide search identifies potential new susceptibility loci for Crohn's disease

S. Targan, Huiying Yang, J. Rotter, 1999 .

Neutrophil autoantibodies in ulcerative colitis: familial aggregation and genetic heterogeneity.

S. Targan, R. Duerr, Huiying Yang, 1992, Gastroenterology.

Functional and ethnic association of allele 2 of the interleukin-1 receptor antagonist gene in ulcerative colitis.

Huiying Yang, J. Rotter, F. Cominelli, 1999, Gastroenterology.

Intercellular adhesion molecule 1 gene associations with immunologic subsets of inflammatory bowel disease.

A. Beaudet, S. Targan, Huiying Yang, 1995, Gastroenterology.

Familial empiric risk estimates of inflammatory bowel disease in Ashkenazi Jews.

J. Rotter, G. Petersen, J. Panish, 1989, Gastroenterology.

Contribution of the hepatic lipase gene to the atherogenic lipoprotein phenotype in familial combined hyperlipidemia.

R. Cantor, R. Krauss, J. Rotter, 2000, Journal of lipid research.

A genome-wide search identifies potential new susceptibility loci for Crohn's disease.

S. Targan, Huiying Yang, J. Rotter, 1999, Inflammatory bowel diseases.

Hermansky-Pudlak syndrome: an immunologic assessment of 15 cases.

S. Targan, L. Randolph, F. Shanahan, 1988, The American journal of medicine.

Linkage of Crohn’s disease to the major histocompatibility complex region is detected by multiple non-parametric analyses

S. Targan, K. Taylor, Huiying Yang, 1999, Gut.