Works matching IS 00099163 AND DT 2014 AND VI 85 AND IP 1

Results: 20

Health care provider recommendations for reducing cancer risks among women with a BRCA1 or BRCA2 mutation.

Published in:

Clinical Genetics, 2014, v. 85, n. 1, p. 21, doi. 10.1111/cge.12233

By:

Metcalfe, KA;
Kim‐Sing, C;
Ghadirian, P;
Sun, P;
Narod, SA

Publication type:

Article

Genomic signatures of BRCA1 but not BRCA2 associated high-grade serous carcinoma resemble basal-like breast cancer.

Published in:

Clinical Genetics, 2014, v. 85, n. 1, p. 16, doi. 10.1111/cge.12302

By:

Patankar, JV

Publication type:

Article

Delineating the effects BRCA1 and BRCA2 loss of heterozygosity in pancreatic cancer progression.

Published in:

Clinical Genetics, 2014, v. 85, n. 1, p. 18, doi. 10.1111/cge.12306

By:

Fam, HK

Publication type:

Article

The spectrum of BRCA1 and BRCA2 mutations in breast cancer patients in the Bahamas.

Published in:

Clinical Genetics, 2014, v. 85, n. 1, p. 64, doi. 10.1111/cge.12132

By:

Akbari, MR;
Donenberg, T;
Lunn, J;
Curling, D;
Turnquest, T;
Krill‐Jackson, E;
Zhang, S;
Narod, SA;
Hurley, J

Publication type:

Article

RSK2 mutation co-segregates with X-linked intellectual disability and attenuated Coffin-Lowry phenotype in a three-generation family.

Published in:

Clinical Genetics, 2014, v. 85, n. 1, p. 96, doi. 10.1111/cge.12122

By:

Maystadt, I;
Destree, A;
Benoit, V;
Aeby, A;
Lederer, D;
Moortgat, S;
Jurkiewicz, D;
Krajewska‐Walasek, M;
Hanauer, A;
Thomas, GM

Publication type:

Article

The psychological impact of breast and ovarian cancer preventive options in BRCA1 and BRCA2 mutation carriers.

Published in:

Clinical Genetics, 2014, v. 85, n. 1, p. 7, doi. 10.1111/cge.12298

By:

Borreani, C;
Manoukian, S;
Bianchi, E;
Brunelli, C;
Peissel, B;
Caruso, A;
Morasso, G;
Pierotti, MA

Publication type:

Article

Clinical implications of genetic testing for BRCA1 and BRCA2 mutations in Austria.

Published in:

Clinical Genetics, 2014, v. 85, n. 1, p. 72, doi. 10.1111/cge.12216

By:

Singer, CF;
Muhr, D;
Rappaport, C;
Tea, M‐K;
Gschwantler‐Kaulich, D;
Fink‐Retter, A;
Pfeiler, G;
Berger, A;
Sun, P;
Narod, SA

Publication type:

Article

BRCA1/2 negative status predicts no extended risk of invasive ovarian cancer.

Published in:

Clinical Genetics, 2014, v. 85, n. 1, p. 17, doi. 10.1111/cge.12303

By:

Patankar, JV

Publication type:

Article

Screening for BRCA1 and BRCA2 mutations among French-Canadian breast cancer cases attending an outpatient clinic in Montreal.

Published in:

Clinical Genetics, 2014, v. 85, n. 1, p. 31, doi. 10.1111/cge.12174

By:

Ghadirian, P;
Robidoux, A;
Nassif, E;
Martin, G;
Potvin, C;
Patocskai, E;
Younan, R;
Larouche, N;
Venne, A;
Zhang, S;
Royer, R;
Narod, SA

Publication type:

Article

Geographical distribution of Slovenian BRCA1/2 families according to family origin: implications for genetic screening.

Published in:

Clinical Genetics, 2014, v. 85, n. 1, p. 59, doi. 10.1111/cge.12119

By:

Krajc, M;
Zadnik, V;
Novaković, S;
Stegel, V;
Teugels, E;
Bešič, N;
Hočevar, M;
Vakselj, A;
De Grève, J;
Žgajnar, J

Publication type:

Article

The uptake and outcome of prenatal and pre-implantation genetic diagnosis for Huntington's disease in the Netherlands (1998-2008).

Published in:

Clinical Genetics, 2014, v. 85, n. 1, p. 87, doi. 10.1111/cge.12089

By:

van Rij, MC;
de Koning Gans, PAM;
van Belzen, MJ;
Roos, RAC;
Geraedts, JPM;
De Rademaeker, M;
Bijlsma, EK;
de Die‐Smulders, CEM

Publication type:

Article

Breast cancer genetics: 20 years later.

Published in:

Clinical Genetics, 2014, v. 85, n. 1, p. 5, doi. 10.1111/cge.12293

By:

Lubinski, J

Publication type:

Article

BRCA1 and BRCA2 - update and implications on the genetics of breast cancer: a clinical perspective.

Published in:

Clinical Genetics, 2014, v. 85, n. 1, p. 1, doi. 10.1111/cge.12291

By:

Foulkes, WD

Publication type:

Article

Risk of having BRCA1 mutation in high-risk women with triple-negative breast cancer: a meta-analysis.

Published in:

Clinical Genetics, 2014, v. 85, n. 1, p. 43, doi. 10.1111/cge.12270

By:

Tun, NM;
Villani, G;
Ong, K;
Yoe, L;
Bo, ZM

Publication type:

Article

High prevalence of BRCA1 founder mutations in Greek breast/ovarian families.

Published in:

Clinical Genetics, 2014, v. 85, n. 1, p. 36, doi. 10.1111/cge.12274

By:

Konstantopoulou, I;
Tsitlaidou, M;
Fostira, F;
Pertesi, M;
Stavropoulou, A‐V;
Triantafyllidou, O;
Tsotra, E;
Tsiftsoglou, AP;
Tsionou, C;
Droufakou, S;
Dimitrakakis, C;
Fountzilas, G;
Yannoukakos, D

Publication type:

Article

Modes of delivery of genetic testing services and the uptake of cancer risk management strategies in BRCA1 and BRCA2 carriers.

Published in:

Clinical Genetics, 2014, v. 85, n. 1, p. 49, doi. 10.1111/cge.12130

By:

Pal, T;
Lee, J‐H;
Besharat, A;
Thompson, Z;
Monteiro, ANA;
Phelan, C;
Lancaster, JM;
Metcalfe, K;
Sellers, TA;
Vadaparampil, S;
Narod, SA

Publication type:

Article

Prenatal testing for Huntington's disease in the Netherlands from 1998 to 2008.

Published in:

Clinical Genetics, 2014, v. 85, n. 1, p. 78, doi. 10.1111/cge.12090

By:

van Rij, MC;
de Koning Gans, PAM;
Aalfs, CM;
Elting, M;
Ippel, PF;
Maat‐Kievit, JA;
Vermeer, S;
Verschuuren‐Bemelmans, CC;
van Belzen, MJ;
Belfroid, RDM;
Losekoot, M;
Geraedts, JPM;
Roos, RAC;
Tibben, A;
de Die‐Smulders, CEM;
Bijlsma, EK

Publication type:

Article

Huntington disease in 2013 - genetic choices across the life cycle.

Published in:

Clinical Genetics, 2014, v. 85, n. 1, p. 76, doi. 10.1111/cge.12093

By:

Morrison, PJ

Publication type:

Article

Linking distant relatives with BRCA gene mutations: potential for cost savings.

Published in:

Clinical Genetics, 2014, v. 85, n. 1, p. 54, doi. 10.1111/cge.12211

By:

Senter, L;
O'Connor, M;
Oriyo, F;
Sweet, K;
Toland, AE

Publication type:

Article

Rates of risk-reducing surgery in Israeli BRCA1 and BRCA2 mutation carriers.

Published in:

Clinical Genetics, 2014, v. 85, n. 1, p. 68, doi. 10.1111/cge.12149

By:

Laitman, Y;
Vaisman, Y;
Feldman, D;
Helpman, L;
Gitly, M;
Paluch Shimon, S;
Berger, R;
Cohen, L;
Narod, SA;
Friedman, E

Publication type:

Article