Works matching IS 13899600 AND DT 2010 AND VI 9

Results: 103

Breast cancer susceptibility variants alter risk in familial ovarian cancer.

Published in:

Familial Cancer, 2010, v. 9, n. 4, p. 503, doi. 10.1007/s10689-010-9349-2

By:

Latif, A.;
McBurney, H.;
Roberts, S.;
Lalloo, F.;
Howell, A.;
Evans, D.;
Newman, W.

Publication type:

Article

Predicting BRCA1 and BRCA2 gene mutation carriers: comparison of PENN II model to previous study.

Published in:

Familial Cancer, 2010, v. 9, n. 4, p. 495, doi. 10.1007/s10689-010-9348-3

By:

Lindor, Noralane;
Johnson, Kiley;
Harvey, Hayden;
Shane Pankratz, V.;
Domchek, Susan;
Hunt, Katherine;
Wilson, Marcia;
Cathie Smith, M.;
Couch, Fergus

Publication type:

Article

MYH biallelic mutation can inactivate the two genetic pathways of colorectal cancer by APC or MLH1 transversions.

Published in:

Familial Cancer, 2010, v. 9, n. 4, p. 589, doi. 10.1007/s10689-010-9367-0

By:

Lefevre, Jérémie;
Colas, Chrystelle;
Coulet, Florence;
Bonilla, Carolina;
Mourra, Najat;
Flejou, Jean-Francois;
Tiret, Emmanuel;
Bodmer, Walter;
Soubrier, Florent;
Parc, Yann

Publication type:

Article

Associations of 9p21 variants with cutaneous malignant melanoma, nevi, and pigmentation phenotypes in melanoma-prone families with and without CDKN2A mutations.

Published in:

Familial Cancer, 2010, v. 9, n. 4, p. 625, doi. 10.1007/s10689-010-9356-3

By:

Yang, Xiaohong;
Liang, Xueying;
Pfeiffer, Ruth;
Wheeler, William;
Maeder, Dennis;
Burdette, Laurie;
Yeager, Meredith;
Chanock, Stephen;
Tucker, Margaret;
Goldstein, Alisa

Publication type:

Article

Complete BRCA mutation screening in breast and ovarian cancer predisposition families from a North-Eastern Romanian population.

Published in:

Familial Cancer, 2010, v. 9, n. 4, p. 519, doi. 10.1007/s10689-010-9361-6

By:

Negura, Lucian;
Uhrhammer, Nancy;
Negura, Anca;
Artenie, Vlad;
Carasevici, Eugen;
Bignon, Yves-Jean

Publication type:

Article

Clinical and molecular characterization of Brazilian families with von Hippel-Lindau disease: a need for delineating genotype-phenotype correlation.

Published in:

Familial Cancer, 2010, v. 9, n. 4, p. 635, doi. 10.1007/s10689-010-9357-2

By:

Gomy, Israel;
Molfetta, Greice;
Andrade Barreto, Ester;
Ferreira, Cristiane;
Zanette, Dalila;
Casali-da-Rocha, José;
Silva, Wilson

Publication type:

Article

Can a phenotype for recessive inheritance in breast cancer be defined?

Published in:

Familial Cancer, 2010, v. 9, n. 4, p. 525, doi. 10.1007/s10689-010-9355-4

By:

Ellberg, Carolina;
Jönsson, Göran;
Olsson, Håkan

Publication type:

Article

Magnetic resonance colonography for colorectal cancer screening in patients with Lynch syndrome gene mutation.

Published in:

Familial Cancer, 2010, v. 9, n. 4, p. 555, doi. 10.1007/s10689-010-9350-9

By:

Lim, Eu;
Leung, Christopher;
Pitman, Alex;
Stella, Damien;
Brown, Gregor;
Slattery, Masha;
Marion, Kaye;
Macrae, Finlay

Publication type:

Article

Selective COX-2 inhibition affects fatty acids, but not COX mRNA expression in patients with FAP.

Published in:

Familial Cancer, 2010, v. 9, n. 4, p. 571, doi. 10.1007/s10689-010-9365-2

By:

Almendingen, Kari;
Larsen, Laila;
Fausa, Olav;
Bratlie, Jorunn;
Høstmark, Arne;
Aabakken, Lars

Publication type:

Article

Pancreatic cancer risk counselling and screening: impact on perceived risk and psychological functioning.

Published in:

Familial Cancer, 2010, v. 9, n. 4, p. 617, doi. 10.1007/s10689-010-9354-5

By:

Maheu, Christine;
Vodermaier, Andrea;
Rothenmund, Heidi;
Gallinger, Steve;
Ardiles, Paola;
Semotiuk, Kara;
Holter, Spring;
Thayalan, Saumea;
Esplen, Mary

Publication type:

Article

Regular surveillance for Li-fraumeni syndrome: advice, adherence and perceived benefits.

Published in:

Familial Cancer, 2010, v. 9, n. 4, p. 647, doi. 10.1007/s10689-010-9368-z

By:

Lammens, C.;
Bleiker, E.;
Aaronson, N.;
Wagner, A.;
Sijmons, R.;
Ausems, M.;
Vriends, A.;
Ruijs, M.;
Os, T.;
Spruijt, L.;
Gómez García, E.;
Cats, A.;
Nagtegaal, T.;
Verhoef, S.

Publication type:

Article

FAP, gastric cancer, and genetic counseling featuring children and young adults: a family study and review.

Published in:

Familial Cancer, 2010, v. 9, n. 4, p. 581, doi. 10.1007/s10689-010-9352-7

By:

Lynch, Henry;
Snyder, Carrie;
Davies, Janine;
Lanspa, Stephen;
Lynch, Jane;
Gatalica, Zoran;
Graeve, Victoria;
Foster, Jason

Publication type:

Article

Report of the Combined Meeting of the International Society for Gastrointestinal Hereditary Tumours, the Human Variome Project and the National Cancer Institute Colon Cancer Family Registry, Duesseldorf, Germany, 24 June 2009.

Published in:

2010

By:

Kohonen-Corish, Maija;
Weber, Thomas;
Lindblom, Annika;
Macrae, Finlay

Publication type:

Report

Carney triad versus Carney Stratakis syndrome: two cases which illustrate the difficulty in distinguishing between these conditions in individual patients.

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 443, doi. 10.1007/s10689-010-9323-z

By:

Alrashdi, Ismail;
Bano, Gul;
Maher, Eamonn;
Hodgson, Shirley

Publication type:

Article

Differences in clinical and pathological characteristics of colorectal cancer in Arab as compared to Jewish patients in Northern Israel.

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 327, doi. 10.1007/s10689-010-9337-6

By:

Glushko, Yelena;
Basher, Walid;
Barchana, Micha;
Zidan, Jamal

Publication type:

Article

Abstracts 3rd Biennial Meeting of InSiGHT (International Society for Gastrointestinal Hereditary Tumours).

Published in:: Familial Cancer, 2010, v. 9, n. 4, p. 713, doi. 10.1007/s10689-010-9351-8
Publication type:: Article

A novel mutation of the Succinate Dehydrogenase B Gene in a Korean Family with Pheochromocytoma.

Published in:

Familial Cancer, 2010, v. 9, n. 4, p. 643, doi. 10.1007/s10689-010-9359-0

By:

Lee, Sang;
Kim, Eun;
Lee, Yu;
Lee, Woochang;
Min, Won;
Lee, Young-Joo;
Huh, Joo;
Lee, Woo

Publication type:

Article

Screening for large genomic rearrangements of the BRIP1 and CHK1 genes in Finnish breast cancer families.

Published in:

Familial Cancer, 2010, v. 9, n. 4, p. 537, doi. 10.1007/s10689-010-9360-7

By:

Solyom, Szilvia;
Pylkäs, Katri;
Winqvist, Robert

Publication type:

Article

Peutz-Jeghers syndrome: a study of long-term surgical morbidity and causes of mortality.

Published in:

Familial Cancer, 2010, v. 9, n. 4, p. 609, doi. 10.1007/s10689-010-9358-1

By:

You, Y.;
Wolff, Bruce;
Boardman, Lisa;
Riegert-Johnson, Douglas;
Qin, Rui

Publication type:

Article

The contribution of breast cancer pathology to statistical models to predict mutation risk in BRCA carriers.

Published in:

Familial Cancer, 2010, v. 9, n. 4, p. 545, doi. 10.1007/s10689-010-9362-5

By:

Vargas, Ana;
Silva, Leonard;
Lakhani, Sunil

Publication type:

Article

Disclosing cancer genetic information within families: perspectives of counselees and their at-risk relatives.

Published in:

Familial Cancer, 2010, v. 9, n. 4, p. 669, doi. 10.1007/s10689-010-9364-3

By:

Hayat Roshanai, Afsaneh;
Lampic, Claudia;
Rosenquist, Richard;
Nordin, Karin

Publication type:

Article

Papillary thyroid cancer in a patient with MUTYH-associated polyposis (MAP).

Published in:

Familial Cancer, 2010, v. 9, n. 4, p. 595, doi. 10.1007/s10689-010-9366-1

By:

Pervaiz, Muhammad;
Eppolito, Amanda;
Schmidt, Karen

Publication type:

Article

CDH1 gene mutations do not contribute in hereditary diffuse gastric cancer in Poland.

Published in:

Familial Cancer, 2010, v. 9, n. 4, p. 605, doi. 10.1007/s10689-010-9381-2

By:

Jakubowska, Anna;
Ławniczak, Małgorzata;
Wojnarska, Beata;
Cybulski, Cezary;
Huzarski, Tomasz;
Byrski, Tomasz;
Tołoczko-Grabarek, Aleksandra;
Jaworska, Katarzyna;
Durda, Katarzyna;
Starzyńska, Teresa;
Lubiński, Jan

Publication type:

Article

Frequency of extracolonic tumors in Brazilian families with Lynch syndrome: analysis of a hereditary colorectal cancer institutional registry.

Published in:

Familial Cancer, 2010, v. 9, n. 4, p. 563, doi. 10.1007/s10689-010-9373-2

By:

Silva, Felipe;
Oliveira, Ligia;
Santos, Érika;
Nakagawa, Wilson;
Aguiar Junior, Samuel;
Valentin, Mev;
Rossi, Benedito;
Oliveira Ferreira, Fábio

Publication type:

Article

Comprehensive BRCA1 and BRCA2 mutation analyses and review of French Canadian families with at least three cases of breast cancer.

Published in:

Familial Cancer, 2010, v. 9, n. 4, p. 507, doi. 10.1007/s10689-010-9372-3

By:

Cavallone, Luca;
Arcand, Suzanna;
Maugard, Christine;
Nolet, Serge;
Gaboury, Louis;
Mes-Masson, Anne-Marie;
Ghadirian, Parviz;
Provencher, Diane;
Tonin, Patricia

Publication type:

Article

A functional varient in microRNA-146a is associated with risk of esophageal squamous cell carcinoma in Chinese Han.

Published in:

Familial Cancer, 2010, v. 9, n. 4, p. 599, doi. 10.1007/s10689-010-9370-5

By:

Guo, Hong;
Wang, Kai;
Xiong, Gang;
Hu, Huamei;
Wang, Dongmei;
Xu, Xueqing;
Guan, Xingying;
Yang, Kang;
Bai, Yun

Publication type:

Article

Similarities in solar ultraviolet irradiance and other environmental factors may explain much of the family link between uveal melanoma and other cancers.

Published in:

2010

By:

Grant, William;
Moan, Johan;
Micu, Emanuela;
Porojnicu, Alina;
Juzeniene, Asta

Publication type:

Letter

Hereditary predisposition rather than environmental factor are likely to explain the familial link between uveal melanoma and other cancers.

Published in:

2010

By:

Abdel-Rahman, M.;
Pilarski, R.

Publication type:

Letter

BRCA1 and BRCA2 families and the risk of skin cancer.

Published in:

Familial Cancer, 2010, v. 9, n. 4, p. 489, doi. 10.1007/s10689-010-9377-y

By:

Ginsburg, Ophira;
Kim-Sing, Charmaine;
Foulkes, William;
Ghadirian, Parviz;
Lynch, Henry;
Sun, Ping;
Narod, Steven

Publication type:

Article

Thymoma associated with malignancies may herald a hereditary cancer syndrome.

Published in:

2010

By:

Tehrani, Omid;
Chen, Emily;
Schaebler, David;
Mughal, Abdul

Publication type:

Letter

Real world experience with cancer genetic counseling via telephone.

Published in:

Familial Cancer, 2010, v. 9, n. 4, p. 681, doi. 10.1007/s10689-010-9369-y

By:

Sutphen, Rebecca;
Davila, Barbara;
Shappell, Heather;
Holtje, Tricia;
Vadaparampil, Susan;
Friedman, Sue;
Toscano, Michele;
Armstrong, Joanne

Publication type:

Article

A PALB2 germline mutation associated with hereditary breast cancer in Italy.

Published in:

Familial Cancer, 2010, v. 9, n. 2, p. 181, doi. 10.1007/s10689-009-9295-z

By:

Papi, Laura;
Putignano, Anna;
Congregati, Caterina;
Piaceri, Irene;
Zanna, Ines;
Sera, Francesco;
Morrone, Doralba;
Genuardi, Maurizio;
Palli, Domenico

Publication type:

Article

RASSF1A polymorphism in familial breast cancer.

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 263, doi. 10.1007/s10689-010-9335-8

By:

Bergqvist, J.;
Latif, A.;
Roberts, S.;
Hadfield, K.;
Lalloo, F.;
Howell, A.;
Evans, D.;
Newman, W.

Publication type:

Article

Contribution of CDKN2A/P16, P14, CDK4 and BRCA1/2 germline mutations in individuals with suspected genetic predisposition to uveal melanoma.

Published in:

Familial Cancer, 2010, v. 9, n. 4, p. 663, doi. 10.1007/s10689-010-9379-9

By:

Buecher, B.;
Gauthier-Villars, M.;
Desjardins, L.;
Lumbroso-Le Rouic, L.;
Levy, C.;
Pauw, A.;
Bombled, J.;
Tirapo, C.;
Houdayer, C.;
Bressac-de Paillerets, B.;
Stoppa-Lyonnet, D.

Publication type:

Article

PALB2: a novel inactivating mutation in a Italian breast cancer family.

Published in:

Familial Cancer, 2010, v. 9, n. 4, p. 531, doi. 10.1007/s10689-010-9382-1

By:

Balia, Cristina;
Sensi, Elisa;
Lombardi, Grazia;
Roncella, Manuela;
Bevilacqua, Generoso;
Caligo, Maria

Publication type:

Article

Communicating genetic risk information within families: a review.

Published in:

Familial Cancer, 2010, v. 9, n. 4, p. 691, doi. 10.1007/s10689-010-9380-3

By:

Wiseman, Mel;
Dancyger, Caroline;
Michie, Susan

Publication type:

Article

Identification of the first case of germline duplication of BRCA1 exon 13 in an Italian family.

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 275, doi. 10.1007/s10689-009-9315-z

By:

Cerutti, Roberta;
Sahnane, Nora;
Carnevali, Ileana;
Furlan, Daniela;
Tibiletti, Maria;
Chiaravalli, Anna;
Capella, Carlo

Publication type:

Article

BRCA1 mutations and colorectal cancer in Poland.

Published in:

Familial Cancer, 2010, v. 9, n. 4, p. 541, doi. 10.1007/s10689-010-9378-x

By:

Suchy, Janina;
Cybulski, Cezary;
Górski, Bohdan;
Huzarski, Tomasz;
Byrski, Tomasz;
Dębniak, Tadeusz;
Gronwald, Jacek;
Jakubowska, Anna;
Wokołorczyk, Dominika;
Kurzawski, Grzegorz;
Kładny, Józef;
Jawień, Arkadiusz;
Banaszkiewicz, Zbigniew;
Wiśniowski, Rafał;
Wandzel, Piotr;
Starzewski, Jacek;
Lorenc, Zbigniew;
Korobowicz, Elżbieta;
Krokowicz, Piotr;
Horbacka, Karolina

Publication type:

Article

Identification of a Danish breast/ovarian cancer family double heterozygote for BRCA1 and BRCA2 mutations.

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 283, doi. 10.1007/s10689-010-9345-6

By:

Steffensen, Ane;
Jønson, Lars;
Ejlertsen, Bent;
Gerdes, Anne-Marie;
Nielsen, Finn;
Hansen, Thomas

Publication type:

Article

Detection of allelic imbalance in MLH1 expression by pyrosequencing serves as a tool for the identification of germline defects in Lynch syndrome.

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 345, doi. 10.1007/s10689-009-9314-0

By:

Kwok, Chau-To;
Ward, Robyn;
Hawkins, Nicholas;
Hitchins, Megan

Publication type:

Article

Pregnancy after prophylactic total gastrectomy.

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 331, doi. 10.1007/s10689-009-9316-y

By:

Kaurah, Pardeep;
Fitzgerald, Rebecca;
Dwerryhouse, Sarah;
Huntsman, David

Publication type:

Article

Update multiple endocrine neoplasia type 2.

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 449, doi. 10.1007/s10689-010-9320-2

By:

Raue, Friedhelm;
Frank-Raue, Karin

Publication type:

Article

High risk for neoplastic transformation of endometriosis in a carrier of lynch syndrome.

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 383, doi. 10.1007/s10689-010-9321-1

By:

Nyiraneza, Christine;
Marbaix, Etienne;
Smets, Mireille;
Galant, Christine;
Sempoux, Christine;
Dahan, Karin

Publication type:

Article

“ I have always believed I was at high risk...” The role of expectation in emotional responses to the receipt of an average, moderate or high cancer genetic risk assessment result: a thematic analysis of free-text questionnaire comments.

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 469, doi. 10.1007/s10689-010-9324-y

By:

Hilgart, J.;
Phelps, C.;
Bennett, P.;
Hood, K.;
Brain, K.;
Murray, A.

Publication type:

Article

A distinct mutation on the alternative splice site of APC exon 9 results in attenuated familial adenomatous polyposis phenotype.

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 395, doi. 10.1007/s10689-009-9317-x

By:

Fostira, Florentia;
Yannoukakos, Drakoulis

Publication type:

Article

Can self-esteem, mastery and perceived stigma predict long-term adjustment in women carrying a BRCA1/2-mutation? Evidence from a multi-center study.

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 305, doi. 10.1007/s10689-010-9325-x

By:

Vodermaier, Andrea;
Esplen, Mary;
Maheu, Christine

Publication type:

Article

Assessment of clinical practices among cancer genetic counselors.

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 459, doi. 10.1007/s10689-010-9326-9

By:

Wham, Deborah;
Vu, Thuy;
Chan-Smutko, Gayun;
Kobelka, Christine;
Urbauer, Diana;
Heald, Brandie

Publication type:

Article

Relationship of BRCA1 and BRCA2 mutations with cancer burden in the family and tumor incidence.

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 291, doi. 10.1007/s10689-010-9327-8

By:

Esteban Cardeñosa, Eva;
Bolufer Gilabert, Pascual;
Juan Jiménez, Inmaculada;
Palanca Suela, Sarai;
Barragán González, Eva;
González Anguix, Virginia;
Lerma Alejos, Enrique;
Chirivella González, Isabel;
Segura Huerta, Ángel;
Guillén Ponce, Carmen;
Martínez de Dueñas, Eduardo;
Cuevas Cuerda, Dolores;
Salas Trejo, Dolores

Publication type:

Article

Knowledge, attitudes, and clinical experience of physicians regarding preimplantation genetic diagnosis for hereditary cancer predisposition syndromes.

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 479, doi. 10.1007/s10689-010-9343-8

By:

Brandt, Amanda;
Tschirgi, Matthew;
Ready, Kaylene;
Sun, Charlotte;
Darilek, Sandra;
Hecht, Jacqueline;
Arun, Banu;
Lu, Karen

Publication type:

Article

Analysis of mismatch repair gene mutations in Turkish HNPCC patients.

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 365, doi. 10.1007/s10689-010-9336-7

By:

Tunca, Berrin;
Pedroni, Monica;
Cecener, Gulsah;
Egeli, Unal;
Borsi, Enrica;
Zorluoglu, Abdullah;
Gregorio, Carmela;
Yilmazlar, Tuncay;
Yerci, Omer;
Leon, Maurizio

Publication type:

Article