X chromosome-linked and mitochondrial gene control of Leber hereditary optic neuropathy : evidence from segregation analysis for dependence on X chromosome inactivationXIANGDONG BU; ROTTER, J. I.Proceedings of the National Academy of Sciences of the United States of America. 1991, Vol 88, Num 18, pp 8198-8202, issn 0027-8424Article

The genetic background of inflammatory bowel disease : Inflammatory Bowel DiseaseHUIYING YANG; ROTTER, J. I.Hepato-gastroenterology. 2000, Vol 47, Num 31, pp 5-14, issn 0172-6390Article

Wolfram syndrome : a mitochondrial-mediated disorder ?XIANGDONG BU; ROTTER, J. I.Lancet (British edition). 1993, Vol 342, Num 8871, pp 598-600, issn 0140-6736Article

Leber hereditary optic neuropathy : estimation of number of embryonic precursor cells and disease threshold in heterozygous affected females at the X-linked locusBU, X; ROTTER, J. I.Clinical genetics. 1992, Vol 42, Num 3, pp 143-148, issn 0009-9163Article

Measuring the genetic contribution of a single locus to a multilocus diseaseROTTER, J. I; LANBAW, E. M.Clinical genetics. 1984, Vol 26, Num 6, pp 529-542, issn 0009-9163Article

The use of association data to identify family menbers at high risk for marker-linked diseasesCONTE, W. J; ROTTER, J. I.American journal of human genetics. 1984, Vol 36, Num 1, pp 152-166, issn 0002-9297Article

Genetic epidemiological study of keratoconus : Evidence for major gene determinationWANG, Y; RABINOWITZ, Y. S; ROTTER, J. I et al.American journal of medical genetics. 2000, Vol 93, Num 5, pp 403-409, issn 0148-7299Article

Linkage of Crohn's disease to the major histocompatibility complex region is detected by multiple non-parametric analysesYANG, H; PLEVY, S. E; TAYLOR, K et al.Gut. 1999, Vol 44, Num 4, pp 519-526, issn 0017-5749Article

The GENNID study : A resource for mapping the genes that cause NIDDMRAFFEL, L. J; ROBBINS, D. C; CHIU, K. C et al.Diabetes care. 1996, Vol 19, Num 8, pp 864-872, issn 0149-5992Article

Intercellular adhesion molecule 1 gene associations with immunologic subsets of inflammatory bowel diseaseHUIYING YANG; VORA, D. K; TARGAN, S. R et al.Gastroenterology (New York, NY. 1943). 1995, Vol 109, Num 2, pp 440-448, issn 0016-5085Article

Regional mapping of the gene for familial Mediterranean fever on human chromosome 16p13FISCHEL-GHODSIAN, N; XIANGDONG BU; PREZANT, T. R et al.American journal of medical genetics. 1993, Vol 46, Num 6, pp 689-693, issn 0148-7299Article

The aggregation of the 5' insulin gene polymorphism in insulin dependent (type I) diabetes mellitus familiesRAFFEL, L. J; HITMAN, G. A; TOYODA, H et al.Journal of medical genetics. 1992, Vol 29, Num 7, pp 447-450, issn 0022-2593Article

Two-locus mitochondrial and nuclear gene models for mitochondrial disordersBU, X; YANG, H.-Y; SHOHAT, M et al.Genetic epidemiology. 1992, Vol 9, Num 1, pp 27-44, issn 0741-0395Article

HLA-DR and the 5' insulin gene polymorphism in insulin-dependent diabetesRAFFEL, L. J; VADHEIM, C. M; KLEIN, R et al.Metabolism, clinical and experimental. 1991, Vol 40, Num 12, pp 1244-1248, issn 0026-0495Article

The 5' insulin gene polymorphism and the genetics of vascular complications in type 1 (insulin-dependent) diabetes mellitusRAFFEL, L. J; VADHEIM, C. M; ROTH, M.-P et al.Diabetologia (Berlin). 1991, Vol 34, Num 9, pp 680-683, issn 0012-186XArticle

Familial visceral neuropathy with autosomal dominant transmissionMAYER, E. A; SCHUFFLER, M. D; ROTTER, J. I et al.Gastroenterology (New York, NY. 1943). 1986, Vol 91, Num 6, pp 1528-1535, issn 0016-5085Article

Disease risk estimates from marker association data. Application to individuals at risk for hemochromatosisLIN, H. J; CONTE, W. J; ROTTER, J. I et al.Clinical genetics. 1985, Vol 27, Num 2, pp 127-133, issn 0009-9163Article

Consanguinity and common adult diseases in Israeli Arab communitiesJABER, L; SHOHAT, T; ROTTER, J. I et al.American journal of medical genetics. 1997, Vol 70, Num 4, pp 346-348, issn 0148-7299Article

A form of sensorineural deafness is determined by a mitochondrial and an autosomal locus : evidence from pedigree segregation analysisXIANGDONG BU; SHOHAT, M; JABER, L et al.Genetic epidemiology. 1993, Vol 10, Num 1, pp 3-15, issn 0741-0395Article

Sample-size considerations and strategies for linkage analysis in autosomal recessive disordersWONG, F. L; CANTOR, R. M; ROTTER, J. I et al.American journal of human genetics. 1986, Vol 39, Num 1, pp 25-37, issn 0002-9297Article

Use of HLA marker associations and HLA haplotype linkage to estimate disease risks in families with gluten-sensitive enteropathyLIN, H. J; ROTTER, J. I; CONTE, W. J et al.Clinical genetics. 1985, Vol 28, Num 3, pp 185-198, issn 0009-9163Article

Characterization of Statin Dose Response in Electronic Medical RecordsWEI, W.-Q; FENG, Q; NICKERSON, D. A et al.Clinical pharmacology and therapeutics. 2014, Vol 95, Num 3, pp 331-338, issn 0009-9236, 8 p.Article

Common genetic variants differentially influence the transition from clinically defined states of fasting glucose metabolismWALFORD, G. A; GREEN, T; SISCOVICK, D. S et al.Diabetologia (Berlin). 2012, Vol 55, Num 2, pp 331-339, issn 0012-186X, 9 p.Article

A high-resolution genetic map of the familial Mediterranean fever candidate region allows identification of haplotype-sharing among ethnic groupsBALOW, J. E; SHELTON, D. A; LEVY, E. N et al.Genomics (San Diego, Calif.). 1997, Vol 44, Num 3, pp 280-291, issn 0888-7543Article

Association between Serum amyloid A proteins and coronary artery disease: Evidence from two distinct arteriosclerotic processesFYFE, A. I; ROTHENBERG, L. S; DEBEER, F. C et al.Circulation (New York, N.Y.). 1997, Vol 96, Num 9, pp 2914-2919, issn 0009-7322Article