Publications:

CCND2, CTNNB1, DDX3X, GLI2, SMARCA4, MYC, MYCN, PTCH1, TP53, and MLL2 gene variants and risk of childhood medulloblastoma.

Journal Of Neuro-Oncology

Dahlin, Anna M AM; Hollegaard, Mads V MV; Wibom, Carl C; Andersson, Ulrika U; Hougaard, David M DM; Deltour, Isabelle I; Hjalmars, Ulf U; Melin, Beatrice B

Publication Date: 2015-10

Variant appearance in text: rs11564447

PubMed Link: 26290144

Variant Present in the following documents:

• 11060_2015_1891_MOESM1_ESM.pdf

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Wnt signaling pathway pharmacogenetics in non-small cell lung cancer.

The Pharmacogenomics Journal

Stewart, D J DJ; Chang, D W DW; Ye, Y Y; Spitz, M M; Lu, C C; Shu, X X; Wampfler, J A JA; Marks, R S RS; Garces, Y I YI; Yang, P P; Wu, X X

Publication Date: 2014-12

Variant appearance in text: rs11564447

PubMed Link: 24980784

Variant Present in the following documents:

• Main text

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Haplotype association analysis of genes within the WNT signalling pathways in diabetic nephropathy.

Bmc Nephrology

Kavanagh, David H DH; Savage, David A DA; Patterson, Christopher C CC; McKnight, Amy Jayne AJ; Crean, John K JK; Maxwell, Alexander P AP; McKay, Gareth J GJ; ,

Publication Date: 2013-06-18

Variant appearance in text: rs11564447

PubMed Link: 23777469

Variant Present in the following documents:

• Main text
• 1471-2369-14-126.pdf

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Stabilizing mutation of CTNNB1/beta-catenin and protein accumulation analyzed in a large series of parathyroid tumors of Swedish patients.

Molecular Cancer

Björklund, Peyman P; Lindberg, Daniel D; Akerström, Göran G; Westin, Gunnar G

Publication Date: 2008-06-09

Variant appearance in text: rs11564447

PubMed Link: 18541010

Variant Present in the following documents:

• Main text
• 1476-4598-7-53.pdf

View BVdb publication page