Publications:

Sequence variations of ACVRL1 play a critical role in hepatic vascular malformations in hereditary hemorrhagic telangiectasia.

Orphanet Journal Of Rare Diseases

Giraud, Sophie S; Bardel, Claire C; Dupuis-Girod, Sophie S; Carette, Marie-France MF; Gilbert-Dussardier, Brigitte B; Riviere, Sophie S; Saurin, Jean-Christophe JC; Eyries, Mélanie M; Patri, Sylvie S; Decullier, Evelyne E; Calender, Alain A; Lesca, Gaëtan G

Publication Date: 2020-09-22

Variant appearance in text: rs11466338

PubMed Link: 32962750

Variant Present in the following documents:

• Main text
• 13023_2020_Article_1533.pdf

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A population-based case-control study of genetic variation in cytokine genes associated with risk of cervical and vulvar cancers.

Gynecologic Oncology

Hardikar, Sheetal S; Johnson, Lisa G LG; Malkki, Mari M; Petersdorf, Effie W EW; Galloway, Denise A DA; Schwartz, Stephen M SM; Madeleine, Margaret M MM

Publication Date: 2015-10

Variant appearance in text: rs11466338

PubMed Link: 26241630

Variant Present in the following documents:

• Main text

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A replicated association between polymorphisms near TNFα and risk for adverse reactions to radiotherapy.

British Journal Of Cancer

Talbot, C J CJ; Tanteles, G A GA; Barnett, G C GC; Burnet, N G NG; Chang-Claude, J J; Coles, C E CE; Davidson, S S; Dunning, A M AM; Mills, J J; Murray, R J S RJ; Popanda, O O; Seibold, P P; West, C M L CM; Yarnold, J R JR; Symonds, R P RP

Publication Date: 2012-08-07

Variant appearance in text: rs11466338

PubMed Link: 22767148

Variant Present in the following documents:

• Main text
• bjc2012290a.pdf

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