SwePub - search: WFRF:(Evans D. Gareth)

Enumeration	Reference	Cover
1.	Jiang, Xia (author) Shared heritability and functional enrichment across six solid cancers 2019 In: Nature Communications. - 2041-1723. ; 10 swepub:Mat__t	Read full
2.	Dareng, Eileen O. (author) Polygenic risk modeling for prediction of epithelial ovarian cancer risk 2022 In: European Journal of Human Genetics. - 1018-4813. ; 30:3, 349-362 swepub:Mat__t	Read full
3.	Kapoor, Pooja Middha (author) Combined associations of a polygenic risk score and classical risk factors with breast cancer risk 2021 In: Journal of the National Cancer Institute. - 0027-8874. ; 113:3, 329-337 swepub:Mat__t	Read full
4.	Vigorito, Elena (author) Fine-Scale Mapping at 9p22.2 Identifies Candidate Causal Variants That Modify Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers 2016 In: PLoS ONE. - 1932-6203. ; 11 7 swepub:Mat__t	Read full
5.	Escala-Garcia, Maria (author) A network analysis to identify mediators of germline-driven differences in breast cancer prognosis 2020 In: Nature Communications. - 2041-1723. ; 11:1 swepub:Mat__t	Read full
6.	Coignard, Juliette (author) A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers 2021 In: Nature Communications. - 2041-1723. ; 12:1 swepub:Mat__t	Read full
7.	Tye, Andrew M. (author) Dissolved inorganic carbon export from rivers of Great Britain 2022 In: Journal of Hydrology. - 0022-1694. ; 615 swepub:Mat__t	Read full
8.	Kirchhoff, Tomas (author) Breast cancer risk and 6q22.33 2012 In: PLoS ONE. - 1932-6203. ; 7:6 swepub:Mat__t	Read full
9.	Morra, Anna (author) Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment 2021 In: Breast Cancer Research. - 1465-5411. ; 23:1 swepub:Mat__t	Read full
10.	Vertis in usum 2002 swepub:Mat__t
11.	Antoniou, Antonis C. (author) Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers 2012 In: Breast Cancer Research. - 1465-5411. ; 14:1, R33 swepub:Mat__t	Read full
12.	Mulligan, Anna Marie (author) Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2 2011 In: Breast Cancer Research. - 1465-5411. ; 13:6 swepub:Mat__t	Read full
13.	Dörk, Thilo (author) Two truncating variants in FANCC and breast cancer risk 2019 In: Scientific Reports. - 2045-2322. ; 9 swepub:Mat__t	Read full
14.	Johnson, Nichola (author) CYP3A71C allele 2021 In:* British Journal of Cancer. - 0007-0920. ; 124:4, 842-854 swepub:Mat__t	Read full
15.	Ahearn, Thomas U. (author) Common variants in breast cancer risk loci predispose to distinct tumor subtypes 2022 In: Breast Cancer Research. - 1465-5411. ; 24:1 swepub:Mat__t	Read full
16.	Dennis, Joe (author) Rare germline copy number variants (CNVs) and breast cancer risk 2022 In: Communications Biology. ; 5:1 swepub:Mat__t	Read full
17.	Park, Hanla A (author) Mendelian randomisation study of smoking exposure in relation to breast cancer risk 2021 In: British Journal of Cancer. - 0007-0920. ; 125:8, 1135-1145 swepub:Mat__t	Read full
18.	Mueller, Stefanie H. (author) Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry 2023 In: Genome Medicine. - 1756-994X. ; 15 swepub:Mat__t	Read full
19.	Garcia-Martin, E. Elena (author) Sources, Composition, and Export of Particulate Organic Matter Across British Estuaries 2023 In: Journal of Geophysical Research - Biogeosciences. - 2169-8953. ; 128:4 swepub:Mat__t	Read full
20.	Middha, Pooja K. (author) A genome-wide gene-environment interaction study of breast cancer risk for women of European ancestry 2023 In: Breast Cancer Research. - 1465-5411. ; 25:1 swepub:Mat__t	Read full
21.	A history of Wales. 1815-1906 / D. Gareth Evans 1989 swepub:Mat__t
22.	A history of Wales. 1906-2000 / D. Gareth Evans 2000 swepub:Mat__t
23.	Zanti, Maria (author) A Likelihood Ratio Approach for Utilizing Case-Control Data in the Clinical Classification of Rare Sequence Variants 2023 In: Human Mutation. - 1059-7794. ; 2023 swepub:Mat__t	Read full
24.	Ferner, Rosalie E. (author) Neurofibromatoses in Clinical Practice 2011 swepub:Mat__t
25.	Evans, D. Gareth R. (author) CIM - Mechanical Aspects State of the Art Report swepub:Mat__t

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