A genome-wide association study identifies susceptibility loci for Wilms tumor-Reference-Cited by-同舟云学术

A genome-wide association study identifies susceptibility loci for Wilms tumor

Published:2012-04-29 Issue:6 Volume:44 Page:681-684
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Turnbull Clare,Perdeaux Elizabeth R,Pernet David,Naranjo Arlene,Renwick Anthony,Seal Sheila,Munoz-Xicola Rosa Maria,Hanks Sandra,Slade Ingrid,Zachariou Anna,Warren-Perry Margaret,Ruark Elise,Gerrard Mary,Hale Juliet,Hewitt Martin,Kohler Janice,Lane Sheila,Levitt Gill,Madi Mabrook,Morland Bruce,Neefjes Veronica,Nicholson James,Picton Susan,Pizer Barry,Ronghe Milind,Stevens Michael,Traunecker Heidi,Stiller Charles A,Pritchard-Jones Kathy,Dome Jeffrey,Grundy Paul,Rahman Nazneen

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.2251.pdf

Reference15 articles.

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2. Breslow, N.E., Beckwith, J.B., Perlman, E.J. & Reeve, A.E. Age distributions, birth weights, nephrogenic rests, and heterogeneity in the pathogenesis of Wilms tumor. Pediatr. Blood Cancer 47, 260–267 (2006).

3. Scott, R.H., Stiller, C.A., Walker, L. & Rahman, N. Syndromes and constitutional chromosomal abnormalities associated with Wilms tumour. J. Med. Genet. 43, 705–715 (2006).

4. Scott, R.H. et al. Constitutional 11p15 abnormalities, including heritable imprinting center mutations, cause nonsyndromic Wilms tumor. Nat. Genet. 40, 1329–1334 (2008).

5. Little, S.E. et al. Frequency and heritability of WT1 mutations in nonsyndromic Wilms' tumor patients: a UK Children's Cancer Study Group Study. J. Clin. Oncol. 22, 4140–4146 (2004).

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