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261.
Common genetic variation at BARD1 is not associated with breast cancer risk in BRCA1 or BRCA2 mutation carriers. [electronic resource] by
Producer: 20110915 In: Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology vol. 20
Availability: No items available.

262.
Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant. [electronic resource] by
Producer: 20170515 In: American journal of human genetics vol. 98
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263.
Common breast cancer-predisposition alleles are associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers. [electronic resource] by
Producer: 20080513 In: American journal of human genetics vol. 82
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264.
7q21-rs6964587 and breast cancer risk: an extended case-control study by the Breast Cancer Association Consortium. [electronic resource] by
Producer: 20120315 In: Journal of medical genetics vol. 48
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265.
Genome-wide association study identifies novel breast cancer susceptibility loci. [electronic resource] by
Producer: 20070808 In: Nature vol. 447
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266.
Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers. [electronic resource] by
Producer: 20120222 In: Human molecular genetics vol. 20
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267.
A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24. [electronic resource] by
Producer: 20101028 In: Nature genetics vol. 42
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268.
Corrigendum: Common variants at 19p13 are associated with susceptibility to ovarian cancer. [electronic resource] by
Producer: 20160425 In: Nature genetics vol. 48
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269.
Heterogeneity of breast cancer associations with five susceptibility loci by clinical and pathological characteristics. [electronic resource] by
Producer: 20080612 In: PLoS genetics vol. 4
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270.
Common variants at 19p13 are associated with susceptibility to ovarian cancer. [electronic resource] by
Producer: 20101028 In: Nature genetics vol. 42
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271.
Common genetic variants and modification of penetrance of BRCA2-associated breast cancer. [electronic resource] by
Producer: 20110307 In: PLoS genetics vol. 6
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272.
Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers. [electronic resource] by
Producer: 20100203 In: Human molecular genetics vol. 18
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273.
Interplay between BRCA1 and RHAMM regulates epithelial apicobasal polarization and may influence risk of breast cancer. [electronic resource] by
Producer: 20120319 In: PLoS biology vol. 9
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274.
9q31.2-rs865686 as a susceptibility locus for estrogen receptor-positive breast cancer: evidence from the Breast Cancer Association Consortium. [electronic resource] by
Producer: 20121227 In: Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology vol. 21
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275.
Breast cancer risk and 6q22.33: combined results from Breast Cancer Association Consortium and Consortium of Investigators on Modifiers of BRCA1/2. [electronic resource] by
Producer: 20121127 In: PloS one vol. 7
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276.
Exploring the link between MORF4L1 and risk of breast cancer. [electronic resource] by
Producer: 20120525 In: Breast cancer research : BCR vol. 13
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277.
Confirmation of 5p12 as a susceptibility locus for progesterone-receptor-positive, lower grade breast cancer. [electronic resource] by
Producer: 20120202 In: Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology vol. 20
Availability: No items available.

278.
Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers. [electronic resource] by
Producer: 20110214 In: Journal of the National Cancer Institute vol. 103
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279.
11q13 is a susceptibility locus for hormone receptor positive breast cancer. [electronic resource] by
Producer: 20120927 In: Human mutation vol. 33
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280.
Associations of common variants at 1p11.2 and 14q24.1 (RAD51L1) with breast cancer risk and heterogeneity by tumor subtype: findings from the Breast Cancer Association Consortium. [electronic resource] by
Producer: 20120222 In: Human molecular genetics vol. 20
Availability: No items available.