A genetic explanation for the rising incidence of type 1 diabetes, a polygenic disease von Awdeh, Z.L., Yunis, Edmond J., Audeh, Mark J., Fici, Dolores, Pugliese, Alberto, Larsen, Charles E., Alper, Chester A.

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Conserved extended haplotypes discriminate HLA-DR3-homozygous Basque patients with type 1 diabetes mellitus and celiac disease von Bilbao, J R, Calvo, B, Aransay, A M, Martin-Pagola, A, Perez de Nanclares, G, Aly, T A, Rica, I, Vitoria, J C, Gaztambide, S, Noble, J, Fain, P R, Awdeh, Z L, Alper, C A, Castaño, L

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Mendelian inheritance of polygenic diseases: a hypothetical basis for increasing incidence von Awdeh, Z.L., Alper, Chester A.

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Major Histocompatibility Complex Haplotype Studies in Ashkenazi Jewish Patients with Pemphigus Vulgaris von Ahmed, A. Razzaque, Yunis, Edmond J., Khatri, Khalil, Wagner, Rene, Notani, Gur, Awdeh, Zuheir, Alper, Chester A.

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Major Histocompatibility Complex Haplotypes and Class II Genes in Non- Jewish Patients with Pemphigus Vulgaris von Ahmed, A. Razzaque, Wagner, Rene, Khatri, Khalil, Notani, Gur, Awdeh, Zuheir, Alper, Chester A., Yunis, Edmond J.

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Strategies and technical challenges in allele level Class II typing in 2578 bone marrow transplantation donor–recipient pairs von Williams, T.M, Winden, T, Setterholm, M, Vierra-Green, C.A, Spellman, S, Flesch, S, Awdeh, Z, Baxter-Lowe, L.A, Begovich, A.B, Fernandez-Vina, M, Hegland, J, Hurley, C.K, Johnson, D, Noreen, H, Salazar, M, Schmeckpeper, B, Yunis, E.J

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The extent of HLA class II allele level disparity in unrelated bone marrow transplantation : analysis of 1259 National Marrow Donor Program donor-recipient pairs von HURLEY, C. K, BAXTER-LOWE, L. A, YUNIS, E. J, KITAJIMA, D, SHIPP, K, SPLETT, J, WINDEN, T, KOLLMAN, C, JOHNSON, D, NG, J, HARTZMAN, R. J, HEGLAND, J, BEGOVICH, A. B, FERNANDEZ-VINA, M, NOREEN, H, SCHMECKPEPER, B, AWDEH, Z, CHOPCK, M, SALAZAR, M, WILLIAMS, T. M

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The cellular basis for lack of antibody response to hepatitis B vaccine in humans von EGEA, E, IGLESIAS, A, SALAZAR, M, MORIMOTO, C, KRUSKALL, M. S, AWDEH, Z, SCHLOSSMAN, S. F, ALPER, C. A, YUNIS, E. J

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Extended HLA/Complement Allele Haplotypes: Evidence for T/t-Like Complex in Man von Awdeh, Z. L., Raum, D., Yunis, E. J., Alper, C. A.

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Hepatitis B surface antigen- and tetanus toxoid-specific clonal expansion of CD4+ cells in vitro determined by TCRBV CDR3 length and nucleotide sequence von UKO, G. P, FRASER, P. A, AWDEH, Z. L, FICI, D. A, CRAWFORD, K. D, LARSEN, C. E, ALPER, C. A

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Inherited Structural Polymorphism of the Fourth Component of Human Complement von Awdeh, Zuheir L., Alper, Chester A.

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Association of DQw7 (DQB10301) with Ocular Cicatricial Pemphigoid von Ahmed, A R, Foster, S, Zaltas, M, Notani, G, Awdeh, Z, Alper, C A, Yunis, E J

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The Paternally Inherited Insulin Gene B Allele (1,428 FokI site) Confers Protection from Insulin-dependent Diabetes in Families von Pugliese, Alberto, Awdeh, Zuheir L., Alper, Chester A., Jackson, Richard A., Eisenbarth, George S.

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Characterization of type I complement C2 deficiency MHC haplotypes. Strong conservation of the complotype/HLA-B-region and absence of disease association due to linked class II gen... von Truedsson, L, Alper, CA, Awdeh, ZL, Johansen, P, Sjoholm, AG, Sturfelt, G

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Inheritable variable sizes of DNA stretches in the human MHC: conserved extended haplotypes and their fragments or blocks von Yunis, E.J., Larsen, C.E., Fernandez-Viña, M., Awdeh, Z.L., Romero, T., Hansen, J.A., Alper, C.A.

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Linkage disequilibrium between HLA-DPB1 alleles and retinoid X receptor β haplotypes von Rajsbaum, Ricardo, Fici, Dolores, Boggs, Deborah A, Fraser, Patricia A, Flores-Villanueva, Pedro O, Awdeh, Zuheir L

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The MHC type 1 diabetes susceptibility gene is centromeric to HLA-DQB1 von Husain, Zaheed, Kelly, M. Ann, Eisenbarth, George S, Pugliese, Alberto, Awdeh, Zuheir L, Larsen, Charles E, Alper, Chester A

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HLA‐DRB1 leprogenic motifs in Nigerian population groups von UKO, G. P, LU, L.-Y, FRASER, P. A, ASUQUO, M. A, FICI, D, MAHAN, S, AWDEH, Z, UDIM, E. R, DING, W, UMANA, U, ADEWOLE, T

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A DNA oligonucleotide microarray for detecting human astrovirus serotypes von Brown, David W., Gunning, Kerry B., Henry, Dorothy M., Awdeh, Zuheir L., Brinker, James P., Tzipori, Saul, Herrmann, John E.

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CD4 TCRBV CDR3 Analysis in prevalent SLE Cases from two ethnic Groups von Fraser, P A, Lu, L-Y, DeCeulaer, K, Schur, P H, Fici, D, Awdeh, Z, Ding, W-Z, Levitan, E, Lew, R, Uko, G, Gonzalez, C

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