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Results: 1 to 20 of 78

1.

Breast cancer risk assessment using genetic variants and risk factors in a Singapore Chinese population.

Lee CP, Irwanto A, Salim A, Yuan JM, Liu J, Koh WP, Hartman M.

Breast Cancer Res. 2014 Jun 18;16(3):R64. doi: 10.1186/bcr3678.

PMID:
24941967
[PubMed - in process]
Free PMC Article
2.

Frequent germline deleterious mutations in DNA repair genes in familial prostate cancer cases are associated with advanced disease.

Leongamornlert D, Saunders E, Dadaev T, Tymrakiewicz M, Goh C, Jugurnauth-Little S, Kozarewa I, Fenwick K, Assiotis I, Barrowdale D, Govindasami K, Guy M, Sawyer E, Wilkinson R; UKGPCS Collaborators, Antoniou AC, Eeles R, Kote-Jarai Z.

Br J Cancer. 2014 Mar 18;110(6):1663-72. doi: 10.1038/bjc.2014.30. Epub 2014 Feb 20.

PMID:
24556621
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Quantitative assessment of common genetic variants on chromosome 5p12 and hormone receptor status with breast cancer risk.

Yu Y, Chen Z, Wang H, Zhang Y.

PLoS One. 2013 Aug 19;8(8):e72154. doi: 10.1371/journal.pone.0072154. eCollection 2013.

PMID:
23977236
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Breast cancer in the young: role of the geneticist.

Woodson AH, Profato JL, Muse KI, Litton JK.

J Thorac Dis. 2013 Jun;5 Suppl 1:S19-26. doi: 10.3978/j.issn.2072-1439.2013.04.13.

PMID:
23819023
[PubMed]
Free PMC Article
5.

Analysis and prediction of pathways in HeLa cells by integrating biological levels of organization with systems-biology approaches.

Higareda-Almaraz JC, Valtierra-Gutiérrez IA, Hernandez-Ortiz M, Contreras S, Hernandez E, Encarnación-Guevara S.

PLoS One. 2013 Jun 10;8(6):e65433. doi: 10.1371/journal.pone.0065433. Print 2013. Erratum in: PLoS One. 2013;8(7). doi:10.1371/annotation/b212d5e5-7c4b-48c1-80ff-ba0d4ce87cfc. Encarnacion, Sergio [corrected to Encarnación-Guevara, Sergio].

PMID:
23785426
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

Estimating single nucleotide polymorphism associations using pedigree data: applications to breast cancer.

Barnes DR, Barrowdale D, Beesley J, Chen X; kConFab Investigators; Australian Ovarian Cancer Study Group, James PA, Hopper JL, Goldgar D, Chenevix-Trench G, Antoniou AC, Mitchell G.

Br J Cancer. 2013 Jun 25;108(12):2610-22. doi: 10.1038/bjc.2013.277. Epub 2013 Jun 11.

PMID:
23756864
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Risk factors for second screen-detected or interval breast cancers in women with a personal history of breast cancer participating in mammography screening.

Houssami N, Abraham LA, Kerlikowske K, Buist DS, Irwig L, Lee J, Miglioretti DL.

Cancer Epidemiol Biomarkers Prev. 2013 May;22(5):946-61. doi: 10.1158/1055-9965.EPI-12-1208-T. Epub 2013 Mar 19.

PMID:
23513042
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Exome sequencing of germline DNA from non-BRCA1/2 familial breast cancer cases selected on the basis of aCGH tumor profiling.

Hilbers FS, Meijers CM, Laros JF, van Galen M, Hoogerbrugge N, Vasen HF, Nederlof PM, Wijnen JT, van Asperen CJ, Devilee P.

PLoS One. 2013;8(1):e55734. doi: 10.1371/journal.pone.0055734. Epub 2013 Jan 31.

PMID:
23383274
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Recognizing BRCA gene mutation risk subsequent to breast cancer diagnosis in southwestern Ontario.

Vanstone M, Chow W, Lester L, Ainsworth P, Nisker J, Brackstone M.

Can Fam Physician. 2012 May;58(5):e258-66.

PMID:
22734169
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

The application of nonsense-mediated mRNA decay inhibition to the identification of breast cancer susceptibility genes.

Johnson JK, Waddell N; kConFab Investigators, Chenevix-Trench G.

BMC Cancer. 2012 Jun 15;12:246. doi: 10.1186/1471-2407-12-246.

PMID:
22703186
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

BRCA1/2 mutations, fertility and the grandmother effect.

da Silva J.

Proc Biol Sci. 2012 Aug 7;279(1740):2926-9. doi: 10.1098/rspb.2012.0542. Epub 2012 May 9. No abstract available.

PMID:
22572204
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

The role of BRCA1 and BRCA2 in prostate cancer.

Castro E, Eeles R.

Asian J Androl. 2012 May;14(3):409-14. doi: 10.1038/aja.2011.150. Epub 2012 Apr 23. Review.

PMID:
22522501
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Germline BRCA1 mutations increase prostate cancer risk.

Leongamornlert D, Mahmud N, Tymrakiewicz M, Saunders E, Dadaev T, Castro E, Goh C, Govindasami K, Guy M, O'Brien L, Sawyer E, Hall A, Wilkinson R, Easton D; UKGPCS Collaborators, Goldgar D, Eeles R, Kote-Jarai Z.

Br J Cancer. 2012 May 8;106(10):1697-701. doi: 10.1038/bjc.2012.146.

PMID:
22516946
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

A genomewide screen for suppressors of Alu-mediated rearrangements reveals a role for PIF1.

Chisholm KM, Aubert SD, Freese KP, Zakian VA, King MC, Welcsh PL.

PLoS One. 2012;7(2):e30748. doi: 10.1371/journal.pone.0030748. Epub 2012 Feb 9.

PMID:
22347400
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Accuracy of BRCA1/2 mutation prediction models for different ethnicities and genders: experience in a southern Chinese cohort.

Kwong A, Wong CH, Suen DT, Co M, Kurian AW, West DW, Ford JM.

World J Surg. 2012 Apr;36(4):702-13. doi: 10.1007/s00268-011-1406-y.

PMID:
22290208
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Elevated breast cancer risk among mothers of a population-based series of 2668 children with cancer.

Pang D, Evans G, Birch J.

Ecancermedicalscience. 2008;2:57. doi: 10.3332/ecancer.2008.57. Epub 2008 Jan 17.

PMID:
22275959
[PubMed]
Free PMC Article
17.

Breast cancer risk assessment with five independent genetic variants and two risk factors in Chinese women.

Dai J, Hu Z, Jiang Y, Shen H, Dong J, Ma H, Shen H.

Breast Cancer Res. 2012 Jan 23;14(1):R17.

PMID:
22269215
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

CHEK2 contribution to hereditary breast cancer in non-BRCA families.

Desrichard A, Bidet Y, Uhrhammer N, Bignon YJ.

Breast Cancer Res. 2011;13(6):R119. doi: 10.1186/bcr3062. Epub 2011 Nov 24.

PMID:
22114986
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers.

Cox DG, Simard J, Sinnett D, Hamdi Y, Soucy P, Ouimet M, Barjhoux L, Verny-Pierre C, McGuffog L, Healey S, Szabo C, Greene MH, Mai PL, Andrulis IL; Ontario Cancer Genetics Network, Thomassen M, Gerdes AM, Caligo MA, Friedman E, Laitman Y, Kaufman B, Paluch SS, Borg Å, Karlsson P, Askmalm MS, Bustinza GB; SWE-BRCA Collaborators, Nathanson KL, Domchek SM, Rebbeck TR, Benítez J, Hamann U, Rookus MA, van den Ouweland AM, Ausems MG, Aalfs CM, van Asperen CJ, Devilee P, Gille HJ; HEBON; EMBRACE, Peock S, Frost D, Evans DG, Eeles R, Izatt L, Adlard J, Paterson J, Eason J, Godwin AK, Remon MA, Moncoutier V, Gauthier-Villars M, Lasset C, Giraud S, Hardouin A, Berthet P, Sobol H, Eisinger F, Bressac de Paillerets B, Caron O, Delnatte C; GEMO Study Collaborators, Goldgar D, Miron A, Ozcelik H, Buys S, Southey MC, Terry MB; Breast Cancer Family Registry, Singer CF, Dressler AC, Tea MK, Hansen TV, Johannsson O, Piedmonte M, Rodriguez GC, Basil JB, Blank S, Toland AE, Montagna M, Isaacs C, Blanco I, Gayther SA, Moysich KB, Schmutzler RK, Wappenschmidt B, Engel C, Meindl A, Ditsch N, Arnold N, Niederacher D, Sutter C, Gadzicki D, Fiebig B, Caldes T, Laframboise R, Nevanlinna H, Chen X, Beesley J, Spurdle AB, Neuhausen SL, Ding YC, Couch FJ, Wang X, Peterlongo P, Manoukian S, Bernard L, Radice P, Easton DF, Chenevix-Trench G, Antoniou AC, Stoppa-Lyonnet D, Mazoyer S, Sinilnikova OM; Consortium of Investigators of Modifiers of BRCA1/2.

Hum Mol Genet. 2011 Dec 1;20(23):4732-47. doi: 10.1093/hmg/ddr388. Epub 2011 Sep 2.

PMID:
21890493
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Identification of germline alterations of the mad homology 2 domain of SMAD3 and SMAD4 from the Ontario site of the breast cancer family registry (CFR).

Tram E, Ibrahim-Zada I, Briollais L, Knight JA, Andrulis IL, Ozcelik H.

Breast Cancer Res. 2011 Aug 11;13(4):R77. doi: 10.1186/bcr2926.

PMID:
21835029
[PubMed - indexed for MEDLINE]
Free PMC Article

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