I. Vorechovský
Karolinska Institute
Department of Bioscience NOVUM
Huddinge
Sweden
Name/email consistency: high
- Genetic linkage of IgA deficiency to the major histocompatibility complex: evidence for allele segregation distortion, parent-of-origin penetrance differences, and the role of anti-IgA antibodies in disease predisposition. Vorechovský, I., Webster, A.D., Plebani, A., Hammarström, L. Am. J. Hum. Genet. (1999)
- A putative susceptibility locus on chromosome 18 is not a major contributor to human selective IgA deficiency: evidence from meiotic mapping of 83 multiple-case families. Vorechovský, I., Blennow, E., Nordenskjöld, M., Webster, A.D., Hammarström, L. J. Immunol. (1999)
- Clustering of missense mutations in the ataxia-telangiectasia gene in a sporadic T-cell leukaemia. Vorechovský, I., Luo, L., Dyer, M.J., Catovsky, D., Amlot, P.L., Yaxley, J.C., Foroni, L., Hammarström, L., Webster, A.D., Yuille, M.A. Nat. Genet. (1997)
- Trichoepitheliomas contain somatic mutations in the overexpressed PTCH gene: support for a gatekeeper mechanism in skin tumorigenesis. Vorechovský, I., Undén, A.B., Sandstedt, B., Toftgård, R., Ståhle-Bäckdahl, M. Cancer Res. (1997)
- ATM mutations in cancer families. Vorechovský, I., Luo, L., Lindblom, A., Negrini, M., Webster, A.D., Croce, C.M., Hammarström, L. Cancer Res. (1996)
