Publications:

In silico analyses of Wnt1 nsSNPs reveal structurally destabilizing variants, altered interactions with Frizzled receptors and its deregulation in tumorigenesis.

Scientific Reports

Mondal, Amalesh A; Paul, Debarati D; Dastidar, Shubhra Ghosh SG; Saha, Tanima T; Goswami, Achintya Mohan AM

Publication Date: 2022-09-02

Variant appearance in text: rs148154047

PubMed Link: 36056132

Variant Present in the following documents:

• 41598_2022_19299_MOESM16_ESM.xlsx, sheet 1

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Comprehensive Genetic Analysis of 128 Candidate Genes in a Cohort With Idiopathic, Severe, or Familial Osteoporosis.

Journal Of The Endocrine Society

Rocha-Braz, Manuela G M MGM; França, Monica M MM; Fernandes, Adriana M AM; Lerario, Antonio M AM; Zanardo, Evelin A EA; de Santana, Lucas S LS; Kulikowski, Leslie D LD; Martin, Regina M RM; Mendonca, Berenice B BB; Ferraz-de-Souza, Bruno B

Publication Date: 2020-12-01

Variant appearance in text: WNT1: Thr336Met

PubMed Link: 33195954

Variant Present in the following documents:

• Main text
• bvaa148.pdf

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Genome-wide testing of putative functional exonic variants in relationship with breast and prostate cancer risk in a multiethnic population.

Plos Genetics

Haiman, Christopher A CA; Han, Ying Y; Feng, Ye Y; Xia, Lucy L; Hsu, Chris C; Sheng, Xin X; Pooler, Loreall C LC; Patel, Yesha Y; Kolonel, Laurence N LN; Carter, Erin E; Park, Karen K; Le Marchand, Loic L; Van Den Berg, David D; Henderson, Brian E BE; Stram, Daniel O DO

Publication Date: 2013-03

Variant appearance in text: rs148154047

PubMed Link: 23555315

Variant Present in the following documents:

• pgen.1003419.s009.xlsx, sheet 1

View BVdb publication page