Works matching IS 13899600 AND DT 2015 AND VI 14

Results: 80

Birt-Hogg-Dubé syndrome and intracranial vascular pathologies.

Published in:

Familial Cancer, 2015, v. 14, n. 4, p. 595, doi. 10.1007/s10689-015-9807-y

By:

Kapoor, Rahul;
Evins, Alexander;
Steitieh, Diala;
Bernardo, Antonio;
Stieg, Philip

Publication type:

Article

Prevalence and detection of psychosocial problems in cancer genetic counseling.

Published in:

Familial Cancer, 2015, v. 14, n. 4, p. 629, doi. 10.1007/s10689-015-9809-9

By:

Eijzenga, W.;
Bleiker, E.;
Hahn, D.;
Kolk, L.;
Sidharta, G.;
Aaronson, N.

Publication type:

Article

Childhood cancers in families with and without Lynch syndrome.

Published in:

Familial Cancer, 2015, v. 14, n. 4, p. 545, doi. 10.1007/s10689-015-9810-3

By:

Heath, John;
Reece, Jeanette;
Buchanan, Daniel;
Casey, Graham;
Durno, Carol;
Gallinger, Steven;
Haile, Robert;
Newcomb, Polly;
Potter, John;
Thibodeau, Stephen;
Le Marchand, Loïc;
Lindor, Noralane;
Hopper, John;
Jenkins, Mark;
Win, Aung

Publication type:

Article

Psychological distress related to BRCA testing in ovarian cancer patients.

Published in:

Familial Cancer, 2015, v. 14, n. 4, p. 495, doi. 10.1007/s10689-015-9811-2

By:

Bjørnslett, Merete;
Dahl, Alv;
Sørebø, Øystein;
Dørum, Anne

Publication type:

Article

Coexistence of paraganglioma/pheochromocytoma and papillary thyroid carcinoma: a four-case series analysis.

Published in:

Familial Cancer, 2015, v. 14, n. 4, p. 603, doi. 10.1007/s10689-015-9818-8

By:

Bugalho, Maria;
Silva, Ana;
Domingues, Rita

Publication type:

Article

BRCA1 gene variant p.P142H associated with male breast cancer: a two-generation genealogic study and literature review.

Published in:

Familial Cancer, 2015, v. 14, n. 4, p. 515, doi. 10.1007/s10689-015-9819-7

By:

Spinelli, Claudio;
Strambi, Silvia;
Piccini, Lorenzo;
Rossi, Leonardo;
Aretini, Paolo;
Caligo, Adelaide

Publication type:

Article

Survival in familial colorectal cancer: a Danish cohort study.

Published in:

Familial Cancer, 2015, v. 14, n. 4, p. 553, doi. 10.1007/s10689-015-9812-1

By:

Lautrup, Charlotte;
Mikkelsen, Ellen;
Lash, Timothy;
Katballe, Niels;
Sunde, Lone

Publication type:

Article

Supporting families with Cancer: A patient centred survivorship model of care.

Published in:

2015

By:

Craft, Emily;
Billington, Caron;
O'Sullivan, Rory;
Watson, Wendy;
Suter-Giorgini, Nicola;
Singletary, Joanne;
King, Elizabeth;
Perfirgines, Matthew;
Cashmore, Annette;
Barwell, Julian

Publication type:

Letter

Follicular variant of papillary thyroid cancer in Alström syndrome.

Published in:

Familial Cancer, 2015, v. 14, n. 4, p. 599, doi. 10.1007/s10689-015-9816-x

By:

Papadakis, M.;
Meyer, A.;
Schuster, F.;
Weyerbrock, N.;
Corinth, C.;
Dotzenrath, C.

Publication type:

Article

Challenges to clinical utilization of hereditary cancer gene panel testing: perspectives from the front lines.

Published in:

Familial Cancer, 2015, v. 14, n. 4, p. 641, doi. 10.1007/s10689-015-9817-9

By:

Marcus, Rebecca;
Geurts, Jennifer;
Grzybowski, Jessica;
Turaga, Kiran;
Clark Gamblin, T.;
Strong, Kimberly;
Johnston, Fabian

Publication type:

Article

A functional HOTAIR rs920778 polymorphism does not contributes to gastric cancer in a Turkish population: a case-control study.

Published in:

Familial Cancer, 2015, v. 14, n. 4, p. 561, doi. 10.1007/s10689-015-9813-0

By:

Bayram, Süleyman;
Ülger, Yakup;
Sümbül, Ahmet;
Kaya, Berrin;
Rencüzoğulları, Ahmet;
Genç, Ahmet;
Sevgiler, Yusuf;
Bozkurt, Onur;
Rencüzoğulları, Eyyüp

Publication type:

Article

BRCA1 and BRCA2 mutations in males with familial breast and ovarian cancer syndrome. Results of a Spanish multicenter study.

Published in:

Familial Cancer, 2015, v. 14, n. 4, p. 505, doi. 10.1007/s10689-015-9814-z

By:

de Juan, Inmaculada;
Palanca, Sarai;
Domenech, Asunción;
Feliubadaló, Lidia;
Segura, Ángel;
Osorio, Ana;
Chirivella, Isabel;
de la Hoya, Miguel;
Sánchez, Ana;
Infante, Mar;
Tena, Isabel;
Díez, Orland;
Garcia-Casado, Zaida;
Vega, Ana;
Teulé, Àlex;
Barroso, Alicia;
Pérez, Pedro;
Durán, Mercedes;
Carrasco, Estela;
Juan-Fita, Mª

Publication type:

Article

High accuracy of family history of melanoma in Danish melanoma cases.

Published in:

Familial Cancer, 2015, v. 14, n. 4, p. 609, doi. 10.1007/s10689-015-9820-1

By:

Wadt, Karin;
Drzewiecki, Krzysztof;
Gerdes, Anne-Marie

Publication type:

Article

Metastatic sympathetic paraganglioma in a patient with loss of the SDHC gene.

Published in:

Familial Cancer, 2015, v. 14, n. 4, p. 615, doi. 10.1007/s10689-015-9821-0

By:

Rich, Thereasa;
Jackson, Michelle;
Roman-Gonzalez, Alejandro;
Shah, Komal;
Cote, Gilbert;
Jimenez, Camilo

Publication type:

Article

Massive gastric polyposis associated with a germline SMAD4 gene mutation.

Published in:

Familial Cancer, 2015, v. 14, n. 4, p. 569, doi. 10.1007/s10689-015-9822-z

By:

Soer, Eline;
Vos tot Nederveen Cappel, Wouter;
Ligtenberg, Marjolijn;
Moll, Freek;
Pierik, Robert;
Vecht, Juda;
Vasen, Hans;
Flierman, Antoine

Publication type:

Article

Risk reducing salpingectomy and delayed oophorectomy in high risk women: views of cancer geneticists, genetic counsellors and gynaecological oncologists in the UK.

Published in:

Familial Cancer, 2015, v. 14, n. 4, p. 521, doi. 10.1007/s10689-015-9823-y

By:

Chandrasekaran, Dhivya;
Menon, Usha;
Evans, Gareth;
Crawford, Robin;
Saridogan, Ertan;
Jacobs, Chris;
Tischkowitz, Marc;
Brockbank, Elly;
Kalsi, Jatinder;
Jurkovic, Davor;
Manchanda, Ranjit

Publication type:

Article

Risk of colorectal cancer for people with a mutation in both a MUTYH and a DNA mismatch repair gene.

Published in:

Familial Cancer, 2015, v. 14, n. 4, p. 575, doi. 10.1007/s10689-015-9824-x

By:

Win, Aung;
Reece, Jeanette;
Buchanan, Daniel;
Clendenning, Mark;
Young, Joanne;
Cleary, Sean;
Kim, Hyeja;
Cotterchio, Michelle;
Dowty, James;
MacInnis, Robert;
Tucker, Katherine;
Winship, Ingrid;
Macrae, Finlay;
Burnett, Terrilea;
Le Marchand, Loïc;
Casey, Graham;
Haile, Robert;
Newcomb, Polly;
Thibodeau, Stephen;
Lindor, Noralane

Publication type:

Article

Risk of contralateral breast cancer in BRCA1 and BRCA2 mutation carriers: a 30-year semi-prospective analysis.

Published in:

Familial Cancer, 2015, v. 14, n. 4, p. 531, doi. 10.1007/s10689-015-9825-9

By:

Basu, N.;
Ingham, S.;
Hodson, J.;
Lalloo, F.;
Bulman, M.;
Howell, A.;
Evans, D.

Publication type:

Article

POLE mutations in families predisposed to cutaneous melanoma.

Published in:

Familial Cancer, 2015, v. 14, n. 4, p. 621, doi. 10.1007/s10689-015-9826-8

By:

Aoude, Lauren;
Heitzer, Ellen;
Johansson, Peter;
Gartside, Michael;
Wadt, Karin;
Pritchard, Antonia;
Palmer, Jane;
Symmons, Judith;
Gerdes, Anne-Marie;
Montgomery, Grant;
Martin, Nicholas;
Tomlinson, Ian;
Kearsey, Stephen;
Hayward, Nicholas

Publication type:

Article

The effect of personal medical history and family history of cancer on the uptake of risk-reducing salpingo-oophorectomy.

Published in:

Familial Cancer, 2015, v. 14, n. 4, p. 539, doi. 10.1007/s10689-015-9827-7

By:

Aa, Jessica;
Hoogendam, Jacob;
Butter, Els;
Ausems, Margreet;
Verheijen, René;
Zweemer, Ronald

Publication type:

Article

Genotype-phenotype analysis of von Hippel-Lindau syndrome in fifteen Indian families.

Published in:

Familial Cancer, 2015, v. 14, n. 4, p. 585, doi. 10.1007/s10689-015-9806-z

By:

Vikkath, Narendranath;
Valiyaveedan, Sindhu;
Nampoothiri, Sheela;
Radhakrishnan, Natasha;
Pillai, Gopal;
Nair, Vasantha;
Pooleri, Ginil;
Mathew, Georgie;
Menon, Krishnakumar;
Ariyannur, Prasanth;
Pillai, Ashok

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

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

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

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

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

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

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

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

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

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

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

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

International society for gastrointestinal hereditary tumours-InSiGHT.

Published in:: 2015
Publication type:: Abstract

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

Health professionals' evaluation of delivering treatment-focused genetic testing to women newly diagnosed with breast cancer.

Published in:

Familial Cancer, 2015, v. 14, n. 2, p. 265, doi. 10.1007/s10689-014-9770-z

By:

Douma, Kirsten;
Meiser, Bettina;
Kirk, Judy;
Mitchell, Gillian;
Saunders, Christobel;
Rahman, Belinda;
Sousa, Mariana;
Barlow-Stewart, Kristine;
Gleeson, Margaret;
Tucker, Kathy

Publication type:

Article

A risk of digestive tract neoplasms susceptibility in miR-146a and miR-196a2.

Published in:

Familial Cancer, 2015, v. 14, n. 2, p. 229, doi. 10.1007/s10689-014-9776-6

By:

Xie, Mingkun;
Li, Yating;
Wu, Jing;
Wu, Jin

Publication type:

Article

Desmoid tumors: clinical features and outcome of an unpredictable and challenging manifestation of familial adenomatous polyposis.

Published in:

Familial Cancer, 2015, v. 14, n. 2, p. 211, doi. 10.1007/s10689-014-9772-x

By:

Campos, Fábio;
Martinez, Carlos;
Novaes, Marleny;
Nahas, Sérgio;
Cecconello, Ivan

Publication type:

Article

Comparison of proctocolectomy and ileal pouch-anal anastomosis to colectomy and ileorectal anastomosis in familial adenomatous polyposis.

Published in:

Familial Cancer, 2015, v. 14, n. 2, p. 221, doi. 10.1007/s10689-014-9773-9

By:

Koskenvuo, L.;
Mustonen, H.;
Renkonen-Sinisalo, L.;
Järvinen, H.;
Lepistö, A.

Publication type:

Article

Parental age and Neurofibromatosis Type 1: a report from the NF1 Patient Registry Initiative.

Published in:

Familial Cancer, 2015, v. 14, n. 2, p. 317, doi. 10.1007/s10689-014-9774-8

By:

Liu, Qian;
Zoellner, Nancy;
Gutmann, David;
Johnson, Kimberly

Publication type:

Article

The roles of AXIN2 in tumorigenesis and epigenetic regulation.

Published in:

Familial Cancer, 2015, v. 14, n. 2, p. 325, doi. 10.1007/s10689-014-9775-7

By:

Li, Shuang;
Wang, Chunpeng;
Liu, Xiaodong;
Hua, Shucheng;
Liu, Xin

Publication type:

Article

First-Line sunitinib in patients with renal cell carcinoma (RCC) in von Hippel-Lindau (VHL) disease: clinical outcome and patterns of radiological response.

Published in:

Familial Cancer, 2015, v. 14, n. 2, p. 309, doi. 10.1007/s10689-014-9771-y

By:

Roma, Anna;
Maruzzo, Marco;
Basso, Umberto;
Brunello, Antonella;
Zamarchi, Rita;
Bezzon, Elisabetta;
Pomerri, Fabio;
Zovato, Stefania;
Opocher, Giuseppe;
Zagonel, Vittorina

Publication type:

Article

The effect of oral 3,3′-diindolylmethane supplementation on the 2:16α-OHE ratio in BRCA1 mutation carriers.

Published in:

Familial Cancer, 2015, v. 14, n. 2, p. 281, doi. 10.1007/s10689-015-9783-2

By:

Nikitina, Dina;
Llacuachaqui, Marcia;
Sepkovic, Daniel;
Bradlow, H.;
Narod, Steven;
Kotsopoulos, Joanne

Publication type:

Article

Impact of BRCA1/ 2 mutation on young women's 5-year parenthood rates: a prospective comparative study (GENEPSO-PS cohort).

Published in:

Familial Cancer, 2015, v. 14, n. 2, p. 273, doi. 10.1007/s10689-014-9777-5

By:

Mancini, Julien;
Mouret-Fourme, Emmanuelle;
Noguès, Catherine;
Julian-Reynier, Claire

Publication type:

Article

The breast cancer immunophenotype of TP53-p.R337H carriers is different from that observed among other pathogenic TP53 mutation carriers.

Published in:

Familial Cancer, 2015, v. 14, n. 2, p. 333, doi. 10.1007/s10689-015-9779-y

By:

Fitarelli-Kiehl, Mariana;
Giacomazzi, Juliana;
Santos-Silva, Patricia;
Graudenz, Marcia;
Palmero, Edenir;
Michelli, Rodrigo;
Achatz, Maria;
Toledo Osório, Cynthia;
Faria Ferraz, Victor;
Picanço, Clarissa;
Ashton-Prolla, Patricia

Publication type:

Article