Works matching IS 13899600 AND DT 2015 AND VI 14 AND IP 3

Results: 18

Analysis of PALB2 in a cohort of Italian breast cancer patients: identification of a novel PALB2 truncating mutation.

Published in:

2015

By:

Vietri, Maria;
Caliendo, Gemma;
Schiano, Concetta;
Casamassimi, Amelia;
Molinari, Anna;
Napoli, Claudio;
Cioffi, Michele

Publication type:

Letter

The analysis of a large Danish family supports the presence of a susceptibility locus for adenoma and colorectal cancer on chromosome 11q24.

Published in:

Familial Cancer, 2015, v. 14, n. 3, p. 393, doi. 10.1007/s10689-015-9791-2

By:

Rudkjøbing, Laura;
Eiberg, Hans;
Mikkelsen, Hanne;
Binderup, Marie;
Bisgaard, Marie

Publication type:

Article

Validation of an online questionnaire for identifying people at risk of familial and hereditary colorectal cancer.

Published in:

Familial Cancer, 2015, v. 14, n. 3, p. 401, doi. 10.1007/s10689-015-9792-1

By:

Kallenberg, F.;
IJspeert, J.;
Bossuyt, P.;
Aalfs, C.;
Dekker, E.

Publication type:

Article

Polymorphisms of the XRCC1 gene and breast cancer risk in the Mexican population.

Published in:

Familial Cancer, 2015, v. 14, n. 3, p. 349, doi. 10.1007/s10689-015-9787-y

By:

Macías-Gómez, Nelly;
Peralta-Leal, Valeria;
Meza-Espinoza, Juan;
Gutiérrez-Angulo, Melva;
Durán-González, Jorge;
Ramírez-González, Juan;
Gaspar-Del Toro, Alejandra;
Norberto-Rodríguez, Adolfo;
Leal-Ugarte, Evelia

Publication type:

Article

Timing of risk reducing mastectomy in breast cancer patients carrying a BRCA1/2 mutation: retrospective data from the Dutch HEBON study.

Published in:

Familial Cancer, 2015, v. 14, n. 3, p. 355, doi. 10.1007/s10689-015-9788-x

By:

Wevers, M.;
Schmidt, M.;
Engelhardt, E.;
Verhoef, S.;
Hooning, M.;
Kriege, M.;
Seynaeve, C.;
Collée, M.;
Asperen, C.;
Tollenaar, R.;
Koppert, L.;
Witkamp, A.;
Rutgers, E.;
Aaronson, N.;
Rookus, M.;
Ausems, M.

Publication type:

Article

Heterozygous germline mutations in NBS1 among Korean patients with high-risk breast cancer negative for BRCA1/2 mutation.

Published in:

Familial Cancer, 2015, v. 14, n. 3, p. 365, doi. 10.1007/s10689-015-9789-9

By:

Kim, Haeyoung;
Cho, Dae-Yeon;
Choi, Doo;
Jung, Gee;
Shin, Inkyung;
Park, Won;
Huh, Seung;
Kim, Sung-Won;
Park, Sue;
Lee, Jong;
Nam, Seok;
Lee, Jeong;
Gil, Won;
Kim, Seok

Publication type:

Article

The importance of proper bioinformatics analysis and clinical interpretation of tumor genomic profiling: a case study of undifferentiated sarcoma and a constitutional pathogenic BRCA2 mutation and an MLH1 variant of uncertain significance.

Published in:

Familial Cancer, 2015, v. 14, n. 3, p. 481, doi. 10.1007/s10689-015-9790-3

By:

Varga, Elizabeth;
Chao, Elizabeth;
Yeager, Nicholas

Publication type:

Article

Implementing a telephone based peer support intervention for women with a BRCA1/2 mutation.

Published in:

Familial Cancer, 2015, v. 14, n. 3, p. 373, doi. 10.1007/s10689-015-9797-9

By:

Farrelly, Ashley;
White, Victoria;
Young, Mary-Anne;
Jefford, Michael;
Ieropoli, Sandra;
Duffy, Jessica;
Winship, Ingrid;
Meiser, Bettina

Publication type:

Article

Pitfalls in the diagnosis of biallelic PMS2 mutations.

Published in:

Familial Cancer, 2015, v. 14, n. 3, p. 411, doi. 10.1007/s10689-015-9793-0

By:

Antelo, Marina;
Milito, Daniela;
Rhees, Jennifer;
Roca, Enrique;
Barugel, Miguel;
Cuatrecasas, Miriam;
Moreira, Leticia;
Leoz, Maria;
Carballal, Sabela;
Ocaña, Teresa;
Pellisé, Maria;
Castells, Antoni;
Boland, C.;
Goel, Ajay;
Balaguer, Francesc

Publication type:

Article

A novel POLE mutation associated with cancers of colon, pancreas, ovaries and small intestine.

Published in:

Familial Cancer, 2015, v. 14, n. 3, p. 437, doi. 10.1007/s10689-015-9803-2

By:

Hansen, Maren;
Johansen, Jostein;
Bjørnevoll, Inga;
Sylvander, Anna;
Steinsbekk, Kristin;
Sætrom, Pål;
Sandvik, Arne;
Drabløs, Finn;
Sjursen, Wenche

Publication type:

Article

Genetic screening in patients with Retinoblastoma in Israel.

Published in:

Familial Cancer, 2015, v. 14, n. 3, p. 471, doi. 10.1007/s10689-015-9794-z

By:

Sagi, Michal;
Frenkel, Avishag;
Eilat, Avital;
Weinberg, Naomi;
Frenkel, Shahar;
Pe'er, Jacob;
Abeliovich, Dvorah;
Lerer, Israela

Publication type:

Article

Clinical characterization and mutation spectrum in Caribbean Hispanic families with Lynch syndrome.

Published in:

Familial Cancer, 2015, v. 14, n. 3, p. 415, doi. 10.1007/s10689-015-9795-y

By:

Cruz-Correa, Marcia;
Diaz-Algorri, Yaritza;
Pérez-Mayoral, Julyann;
Suleiman-Suleiman, Wasilah;
Mar Gonzalez-Pons, Maria;
Bertrán, Carlos;
Casellas, Nicolás;
Rodríguez, Natalia;
Pardo, Sherly;
Rivera, Keyla;
Mosquera, Rafael;
Rodriguez-Quilichini, Segundo

Publication type:

Article

Germline mutations predisposing to non-small cell lung cancer.

Published in:

Familial Cancer, 2015, v. 14, n. 3, p. 463, doi. 10.1007/s10689-015-9796-x

By:

Clamon, Gerald;
Bossler, Aaron;
Hejleh, Taher;
Furqan, Muhammad

Publication type:

Article

Risk factors for endometrial cancer among women with a BRCA1 or BRCA2 mutation: a case control study.

Published in:

Familial Cancer, 2015, v. 14, n. 3, p. 383, doi. 10.1007/s10689-015-9798-8

By:

Segev, Yakir;
Rosen, Barry;
Lubinski, Jan;
Gronwald, Jacek;
Lynch, Henry;
Moller, Pal;
Kim-Sing, Charmaine;
Ghadirian, Parviz;
Karlan, Beth;
Eng, Charis;
Gilchrist, Dawna;
Neuhausen, Susan;
Eisen, Andrea;
Friedman, Eitan;
Euhus, David;
Ping, Sun;
Narod, Steven

Publication type:

Article

Increased risk for colorectal adenomas and cancer in mono-allelic MUTYH mutation carriers: results from a cohort of North-African Jews.

Published in:

Familial Cancer, 2015, v. 14, n. 3, p. 427, doi. 10.1007/s10689-015-9799-7

By:

Rosner, Guy;
Bercovich, Dani;
Daniel, Yael;
Strul, Hana;
Fliss-Isakov, Naomi;
Ben-Yehoiada, Meirav;
Santo, Erwin;
Halpern, Zamir;
Kariv, Revital

Publication type:

Article

Specific Alu elements involved in a significant percentage of copy number variations of the STK11 gene in patients with Peutz-Jeghers syndrome.

Published in:

Familial Cancer, 2015, v. 14, n. 3, p. 455, doi. 10.1007/s10689-015-9800-5

By:

Borun, Pawel;
Rosa, Marina;
Nedoszytko, Boguslaw;
Walkowiak, Jaroslaw;
Plawski, Andrzej

Publication type:

Article

Zebrafish xenotransplantation as a tool for in vivo cancer study.

Published in:

Familial Cancer, 2015, v. 14, n. 3, p. 487, doi. 10.1007/s10689-015-9802-3

By:

Zhang, Beibei;
Xuan, Chao;
Ji, Yunxi;
Zhang, Weiming;
Wang, Daogang

Publication type:

Article

3′-UTR poly(T/U) repeat of EWSR1 is altered in microsatellite unstable colorectal cancer with nearly perfect sensitivity.

Published in:

Familial Cancer, 2015, v. 14, n. 3, p. 449, doi. 10.1007/s10689-015-9804-1

By:

Kondelin, Johanna;
Tuupanen, Sari;
Gylfe, Alexandra;
Aavikko, Mervi;
Renkonen-Sinisalo, Laura;
Järvinen, Heikki;
Böhm, Jan;
Mecklin, Jukka-Pekka;
Andersen, Claus;
Vahteristo, Pia;
Pitkänen, Esa;
Aaltonen, Lauri

Publication type:

Article