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Publication Listing for the MeSH term brca1. Found 16 abstracts

Mavaddat N, Antoniou AC, Mooij TM, Hooning MJ, Heemskerk-Gerritsen BA, Nogu├Ęs C, Gauthier-Villars M, Caron O, Gesta P, Pujol P, Lortholary A, Barrowdale D, Frost D, Evans DG, Izatt L, Adlard J, Eeles R, Brewer C, Tischkowitz M, Henderson A, Cook J, Eccles D, van Engelen K, Mourits MJ, Ausems MG, Koppert LB, Hopper JL, John EM, Chung WK, Andrulis IL, Daly MB, Buys SS, Benitez J, Caldes T, Jakubowska A, Simard J, Singer CF, Tan Y, Olah E, Navratilova M, Foretova L, Gerdes AM, Roos-Blom MJ, Van Leeuwen FE, Arver B, Olsson H, Schmutzler RK, Engel C, Kast K, Phillips KA, Terry MB, Milne RL, Goldgar DE, Rookus MA, Andrieu N, Easton DF, Genepso, Embrace, Hebon, kConFab I, Ibccs, kConFab, Bcfr. Risk-reducing salpingo-oophorectomy, natural menopause, and breast cancer risk: an international prospective cohort of BRCA1 and BRCA2 mutation carriers. Breast cancer research : BCR. 2020 Jan 16;22(1):8.   PMCID: 31948486
Livaudais JC, Li C, John EM, Terry MB, Daly M, Buys SS, Habel L, Thompson B, Yanez ND, Coronado GD. Racial and Ethnic Differences in Adjuvant Hormonal Therapy Use. Journal of Womens Health. 2012 Sep;21(9):950-8.   PMCID: PMC3430474
Stevens KN, Fredericksen Z, Vachon CM, Wang XS, Margolin S, Lindblom A, Nevanlinna H, Greco D, Aittomaki K, Blomqvist C, Chang-Claude J, Vrieling A, Flesch-Janys D, Sinn HP, Wang-Gohrke S, Nickels S, Brauch H, Ko YD, Fischer HP, Schmutzler RK, Meindl A, Bartram CR, Schott S, Engel C, Godwin AK, Weaver J, Pathak HB, Sharma P, Brenner H, Muller H, Arndt V, Stegmaier C, Miron P, Yannoukakos D, Stavropoulou A, Fountzilas G, Gogas HJ, Swann R, Dwek M, Perkins A, Milne RL, Benitez J, Zamora MP, Perez JI, Bojesen SE, Nielsen SF, Nordestgaard BG, Flyger H, Guenel P, Truong T, Menegaux F, Cordina-Duverger E, Burwinkel B, Marme F, Schneeweiss A, Sohn C, Sawyer E, Tomlinson I, Kerin MJ, Peto J, Johnson N, Fletcher O, Silva ID, Fasching PA, Beckmann MW, Hartmann A, Ekici AB, Lophatananon A, Muir K, Puttawibul P, Wiangnon S, Schmidt MK, Broeks A, Braaf LM, Rosenberg EH, Hopper JL, Apicella C, Park DJ, Southey MC, Swerdlow AJ, Ashworth A, Orr N, Schoemaker MJ, Anton-Culver H, Ziogas A, Bernstein L, Dur CC, Shen CY, Yu JC, Hsu HM, Hsiung CN, Hamann U, Dunnebier T, Rudiger T, Ulmer HU, Pharoah PP, Dunning AM, Humphreys MK, Wang Q, Cox A, Cross SS, Reed MW, Hall P, Czene K, Ambrosone CB, Ademuyiwa F, Hwang H, Eccles DM, Garcia-Closas M, Figueroa JD, Sherman ME, Lissowska J, Devilee P, Seynaeve C, Tollenaar R, Hooning MJ, Andrulis IL, Knight JA, Glendon G, Mulligan AM, Winqvist R, Pylkas K, Jukkola-Vuorinen A, Grip M, John EM, Miron A, Alnaes GG, Kristensen V, Borresen-Dale AL, Giles GG, Baglietto L, McLean CA, Severi G, Kosel ML, Pankratz VS, Slager S, Olson JE, Radice P, Peterlongo P, Manoukian S, Barile M, Lambrechts D, Hatse S, Dieudonne AS, Christiaens MR, Chenevix-Trench G, Beesley J, Chen XQ, Mannermaa A, Kosma VM, Hartikainen JM, Soini Y, Easton DF, Couch FJ. 19p13.1 Is a Triple-Negative-Specific Breast Cancer Susceptibility Locus. Cancer Research. 2012 Apr;72(7):1795-803.   PMCID: PMC33199792
Goldgar DE, Healey S, Dowty JG, Da Silva L, Chen XQ, Spurdle AB, Terry MB, Daly MJ, Buys SM, Southey MC, Andrulis I, John EM, Khanna KK, Hopper JL, Oefner PJ, Lakhani S, Chenevix-Trench G. Rare variants in the ATM gene and risk of breast cancer. Breast Cancer Research. 2011 Jan;13(4):R73.   PMCID: PMC3236337
Rebbeck TR, Mitra N, Domchek SM, Wan F, Friebel TM, Tran TV, Singer CF, Tea MK, Blum JL, Tung N, Olopade OI, Weitzel JN, Lynch HT, Snyder CL, Garber JE, Antoniou AC, Peock S, Evans DG, Paterson J, Kennedy MJ, Donaldson A, Dorkins H, Easton DF, Rubinstein WS, Daly MB, Isaacs C, Nevanlinna H, Couch FJ, Andrulis IL, Freidman E, Laitman Y, Ganz PA, Tomlinson GE, Neuhausen SL, Narod SA, Phelan CM, Greenberg R, Nathanson KL, Epidemiological Study BB. Modification of BRCA1-Associated Breast and Ovarian Cancer Risk by BRCA1-Interacting Genes. Cancer Research. 2011 Sep;71(17):5792-805.   PMCID: PMC3170727
Schrader KA, Masciari S, Boyd N, Salamanca C, Senz J, Saunders DN, Yorida E, Maines-Bandiera S, Kaurah P, Tung N, Robson ME, Ryan PD, Olopade OI, Domchek SM, Ford J, Isaacs C, Brown P, Balmana J, Razzak AR, Miron P, Coffey K, Terry MB, John EM, Andrulis IL, Knight JA, O'Malley FP, Daly M, Bender P, Moore R, Southey MC, Hopper JL, Garber JE, Huntsman DG. Germline mutations in CDH1 are infrequent in women with early-onset or familial lobular breast cancers. Journal of Medical Genetics. 2011 Jan;48(1):64-8.   PMCID: PMC3003879
Sussner KM, Edwards TA, Thompson HS, Jandorf L, Kwate NO, Forman A, Brown K, Kapil-Pair N, Bovbjerg DH, Schwartz MD, Valdimarsdottir HB, Rter Rt HM. Ethnic, Racial and Cultural Identity and Perceived Benefits and Barriers Related to Genetic Testing for Breast Cancer among At-Risk Women of African Descent in New York City. Public Health Genomics. 2011 Jan;14(6):356-70.   PMCID: PMC3221259
Pothuri B, Leitao MM, Levine DA, Viale A, Olshen AB, Arroyo C, Bogomolniy F, Olvera N, Lin O, Soslow RA, Robson ME, Offit K, Barakat RR, Boyd J. Genetic Analysis of the Early Natural History of Epithelial Ovarian Carcinoma. Plos One. 2010 Apr;5(4).   PMCID: PMCID: PMC2859950
Apicella C, Peacock SJ, Andrews L, Tucker K, Bankier A, Daly MB, Hopper JL. Determinants of preferences for genetic counselling in Jewish women. FAMILIAL CANCER. 2006 Jan;5(2):159-67.
Longacre TA, Ennis M, Quenneville LA, Bane AL, Bleiweiss IJ, Carter BA, Catelano E, Hendrickson MR, Hibshoosh H, Layfield LJ, Memeo L, Wu H, O'Malley FP. Interobserver agreement and reproducibility in classification of invasive breast carcinoma: an NCI breast cancer family registry study. Modern Pathology. 2006 Feb;19(2):195-207.
John EM, Hopper JL, Beck JC, Knight JA, Neuhausen SL, Senie RT, Ziogas A, Andrulis IL, Anton-Culver H, Boyd N, Buys SS, Daly MB, O'Malley FP, Santella RM, Southey MC, Venne VL, Venter DJ, West DW, Whittemore AS, Seminara DG. The Breast Cancer Family Registry: an infrastructure for cooperative multinational, interdisciplinary and translational studies of the genetic epidemiology of breast cancer. Breast Cancer Research. 2004 Jan;6(4):R375-R389.
Fang CY, Miller SM, Daly MB, Hurley K. The influence of attentional style and risk perceptions on intentions to undergo prophylactic oophorectomy among first- degree relatives. Psychology & Health. 2002 Jun;17(3):365-76.
Daly M. NCCN practice guidelines: Genetics/familial high-risk cancer screening. Oncology-New York. 1999 Nov;13(11A):161-82.
Rebbeck TR, Kantoff PN, Krithivas K, Neuhausen S, Blackwood MA, Godwin AK, Daly MB, Narod SA, Garber JE, Lynch HT, Weber BL, Brown M. Modification of BRCA1-associated breast cancer risk by the polymorphic androgen-receptor CAG repeat. American journal of human genetics. 1999 May;64(5):1371-7.
Daly M, Obrams GI. Epidemiology and risk assessment for ovarian cancer. Seminars in Oncology. 1998 Jun;25(3):255-64.
Knudson AG. Hereditary cancer: Theme and variations. Journal of Clinical Oncology. 1997 Oct;15(10):3280-7.
The above publications are sorted by year, faculty last name, and first author. Click on any highlighted author listed to find all publications attributed to that individual. Click on the publication title to see the abstract. First authors who are faculty are highlighted like this. Last authors who are faculty are highlighted like this. Other authors who are faculty are highlighted like this.

MeSH cloud from publications including the MeSH term brca1

brca1 mutations susceptibility gene susceptibility gene ovarian-cancer mutation carriers expression hereditary breast carcinoma familial breast family registry history Breast cancer ataxia-telangiectasia women carriers cancer Genetic testing 2 consultations analysis disparities surface epithelium BRCA2 invasive breast cancer interobserver reproducibility-familial breast cancer-breast candidate risk single-nucleotide polymorphism hereditary breast-cancer confer united-states medullary carcinoma self-esteem information missense mutations haplotype frequencies colorectal-cancer white women communication ret protooncogene BRCA1 prophylactic pathogenesis bard1 Ashkenazi adolescents talc opportunities mutation ovarian cancer alleles decision-making Mutation Oncology breast- epidemiology prophylactic oophorectomy Risk-reducing salpingo-oophorectomy sequence dna-sequence variants li-fraumeni-syndrome attitudes kappa breast-cancer-treatment cowden-syndrome Cultural identity oophorectomy 1994 ylor rd-j res adolescence-v4-p21 prostate-cancer pathology satisfaction resource Genetics & Heredity homolog familial breast-cancer familial-ovarian-cancer tumor subtypes Racial identity palb2 complex breast cancer features decision- diffuse gastric-cancer p53 brca2-interacting protein brca2 consistency 2007 rd me-j genet couns-v16-p735 survival unknown clinical-significance increased risk genetic counselling primary peritoneal carcinoma collaborative analysis multicenter population mammography knowledge common variants states case-control variability consortium susceptibility genes 2009 shpande ad-canc control-v16-p256 follow-up perceived benefits participation client preferences protein diagnosis family-history risk-factors e-cadherin mutations human-cells american women twins ovarian cancer family registry instability stage relatives mastectomy genome-wide association Ethnic identity prediction designs black-students perceived risk 14q241 rad51l1 germline mutations rad51 monitoring retinoblastoma patient outcomes early-onset transactivation cells
Last updated on Monday, August 03, 2020