Works matching IS 13899600 AND DT 2013 AND VI 12 AND IP 4

Results: 23

Whole exome sequencing identifies mutation of EDNRA involved in ACTH-independent macronodular adrenal hyperplasia.

Published in:

Familial Cancer, 2013, v. 12, n. 4, p. 657, doi. 10.1007/s10689-013-9642-y

By:

Zhu, Jie;
Cui, Liang;
Wang, Wei;
Hang, Xing-Yi;
Xu, A-Xiang;
Yang, Su-Xia;
Dou, Jing-Tao;
Mu, Yi-Ming;
Zhang, Xu;
Gao, Jiang-Ping

Publication type:

Article

Can we test for hereditary cancer at 18 years when we start surveillance at 25? Patient reported outcomes.

Published in:

Familial Cancer, 2013, v. 12, n. 4, p. 675, doi. 10.1007/s10689-013-9644-9

By:

Sie, Aisha S.;
Prins, Judith B.;
Spruijt, Liesbeth;
Kets, C. Marleen;
Hoogerbrugge, Nicoline

Publication type:

Article

Rectal cancers in patients with familial adenomatous polyposis.

Published in:

Familial Cancer, 2013, v. 12, n. 4, p. 749, doi. 10.1007/s10689-013-9656-5

By:

Liang, Jennifer;
Church, James M.

Publication type:

Article

Polymorphisms in arachidonic acid metabolism-related genes and the risk and prognosis of colorectal cancer.

Published in:

Familial Cancer, 2013, v. 12, n. 4, p. 755, doi. 10.1007/s10689-013-9659-2

By:

Li, Shuying;
Zhao, Xiaojuan;
Wu, Zhiwei;
Li, Ye;
Zhu, Lin;
Cui, Binbin;
Dong, Xinshu;
Tian, Suli;
Hu, Fulan;
Zhao, Yashuang

Publication type:

Article

Case report: metachronous central nervous system desmoid tumours and thyroid carcinoma in a young familial adenomatous polyposis patient.

Published in:

Familial Cancer, 2013, v. 12, n. 4, p. 647, doi. 10.1007/s10689-013-9640-0

By:

Butel-Simoes, G. I.;
Spigelman, A. D.

Publication type:

Article

The incidence of PALB2 c.3113G>A in women with a strong family history of breast and ovarian cancer attending familial cancer centres in Australia.

Published in:

2013

By:

Teo, Zhi L.;
Sawyer, Sarah D.;
James, Paul A.;
Mitchell, Gillian;
Trainer, Alison H.;
Lindeman, Geoffrey J.;
Shackleton, Kylie;
Cicciarelli, Linda;
Southey, Melissa C.

Publication type:

Letter

Psychosocial consequences of predictive genetic testing for lynch syndrome and associations to surveillance behaviour in a 7-year follow-up study.

Published in:

Familial Cancer, 2013, v. 12, n. 4, p. 639, doi. 10.1007/s10689-013-9628-9

By:

Aktan-Collan, Katja;
Kääriäinen, Helena;
Järvinen, Heikki;
Peltomäki, Päivi;
Pylvänäinen, Kirsi;
Mecklin, Jukka-Pekka;
Haukkala, Ari

Publication type:

Article

Phenotypic heterogeneity of hereditary gynecologic cancers: a report from the Creighton hereditary cancer registry.

Published in:

Familial Cancer, 2013, v. 12, n. 4, p. 719, doi. 10.1007/s10689-013-9651-x

By:

Casey, Murray Joseph;
Bewtra, Chhanda;
Lynch, Henry T.;
Snyder, Carrie;
Stacy, Mark;
Watson, Patrice

Publication type:

Article

Is the psychological impact of genetic testing moderated by support and sharing of test results to family and friends?

Published in:

Familial Cancer, 2013, v. 12, n. 4, p. 601, doi. 10.1007/s10689-013-9621-3

By:

Lapointe, Julie;
Dorval, Michel;
Noguès, Catherine;
Fabre, Roxane;
Julian-Reynier, Claire

Publication type:

Article

Prevalence of HOXB13 mutation in a population of Ashkenazi Jewish men treated for prostate cancer.

Published in:

Familial Cancer, 2013, v. 12, n. 4, p. 597, doi. 10.1007/s10689-013-9618-y

By:

Alanee, Shaheen;
Shah, Sohela;
Vijai, Joseph;
Schrader, Kasmintan;
Hamilton, Robert;
Rau-Murthy, Rohini;
Sarrel, Kara;
Manschreck, Christopher;
Eastham, James;
Offit, Kenneth

Publication type:

Article

Novel and recurrent BRCA1/BRCA2 mutations in early onset and familial breast and ovarian cancer detected in the Program of Genetic Counseling in Cancer of Valencian Community (eastern Spain). Relationship of family phenotypes with mutation prevalence.

Published in:

Familial Cancer, 2013, v. 12, n. 4, p. 767, doi. 10.1007/s10689-013-9622-2

By:

de Juan Jiménez, Inmaculada;
García Casado, Zaida;
Palanca Suela, Sarai;
Esteban Cardeñosa, Eva;
López Guerrero, José Antonio;
Segura Huerta, Ángel;
Chirivella González, Isabel;
Sánchez Heras, Ana Beatriz;
Juan Fita, Mª José;
Tena García, Isabel;
Guillen Ponce, Carmen;
Martínez de Dueñas, Eduardo;
Romero Noguera, Ignacio;
Salas Trejo, Dolores;
Goicoechea Sáez, Mercedes;
Bolufer Gilabert, Pascual

Publication type:

Article

Multivariate analysis of MLH1 c.1664T>C (p.Leu555Pro) mismatch repair gene variant demonstrates its pathogenicity.

Published in:

Familial Cancer, 2013, v. 12, n. 4, p. 741, doi. 10.1007/s10689-013-9652-9

By:

Farrell, M. P.;
Hughes, D. J.;
Drost, M.;
Wallace, A. J.;
Cummins, R. J.;
Fletcher, T. A.;
Meany, M. A.;
Kay, E. W.;
de Wind, N.;
Power, D. G.;
Andrews, E. J.;
Green, A. J.;
Gallagher, D. J.

Publication type:

Article

The Proceedings of the Collaborative Group of the Americas on Inherited Colorectal Cancer Sheraton Boston Hotel, Boston, Massachusetts, October 27–29, 2012.

Published in:: Familial Cancer, 2013, v. 12, n. 4, p. 779, doi. 10.1007/s10689-012-9592-9
Publication type:: Article

Interest of individuals from BRCA families to participate in research studies focused on male BRCA carriers.

Published in:

Familial Cancer, 2013, v. 12, n. 4, p. 615, doi. 10.1007/s10689-013-9624-0

By:

Pal, Tuya;
Vadaparampil, Susan;
Kim, Jongphil;
Xu, Yan;
Friedman, Sue;
Narod, Steven A.;
Metcalfe, Kelly

Publication type:

Article

Do individuals with a family history of colorectal cancer adhere to medical recommendations for the prevention of colorectal cancer?

Published in:

Familial Cancer, 2013, v. 12, n. 4, p. 629, doi. 10.1007/s10689-013-9627-x

By:

Bronner, Karen;
Mesters, Ilse;
Weiss-Meilnik, Ahuva;
Geva, Ravit;
Rozner, Guy;
Strul, Hana;
Inbar, Moshe;
Halpern, Zamir;
Kariv, Revital

Publication type:

Article

Extracolonic cancer risk in patients with serrated polyposis syndrome and their first-degree relatives.

Published in:

Familial Cancer, 2013, v. 12, n. 4, p. 669, doi. 10.1007/s10689-013-9643-x

By:

Hazewinkel, Yark;
Reitsma, Johannes B.;
Nagengast, Fokko M.;
Vasen, Hans F.;
van Os, Theo A. M.;
van Leerdam, Monique E.;
Koornstra, Jan-Jacob;
Dekker, Evelien

Publication type:

Article

Chemoprevention in Lynch syndrome.

Published in:

Familial Cancer, 2013, v. 12, n. 4, p. 707, doi. 10.1007/s10689-013-9650-y

By:

Burn, John;
Mathers, John C.;
Bishop, D. Tim

Publication type:

Article

Self administered screening for hereditary cancers in conjunction with mammography and ultrasound.

Published in:

Familial Cancer, 2013, v. 12, n. 4, p. 651, doi. 10.1007/s10689-013-9641-z

By:

McDonnell, Charles H.;
Seidenwurm, David J.;
McDonnell, Diana E.;
Bobolis, Kristie A.

Publication type:

Article

Factors affecting the decision to undergo risk-reducing salpingo-oophorectomy among women with BRCA gene mutation.

Published in:

Familial Cancer, 2013, v. 12, n. 4, p. 621, doi. 10.1007/s10689-013-9625-z

By:

Kim, Dongwon;
Kang, Eunyoung;
Hwang, Euijun;
Sun, Young;
Hwang, Yoonsun;
Yom, Cha Kyong;
Kim, Kidong;
No, Jae Hong;
Kim, Yong-Beom;
Kim, Sung-Won

Publication type:

Article

Underestimated survival predictions of the prognostic tools Adjuvant! Online and PREDICT in BRCA1-associated breast cancer patients.

Published in:

Familial Cancer, 2013, v. 12, n. 4, p. 683, doi. 10.1007/s10689-013-9646-7

By:

Plakhins, Grigorijs;
Irmejs, Arvids;
Gardovskis, Andris;
Subatniece, Signe;
Liepniece-Karele, Inta;
Purkalne, Gunta;
Teibe, Uldis;
Trofimovics, Genadijs;
Miklasevics, Edvins;
Gardovskis, Janis

Publication type:

Article

Association of the BRCA1 promoter polymorphism rs11655505 with the risk of familial breast and/or ovarian cancer.

Published in:

Familial Cancer, 2013, v. 12, n. 4, p. 691, doi. 10.1007/s10689-013-9647-6

By:

Bielinska, Beata;
Gaj, Pawel;
Kluska, Anna;
Nowakowska, Dorota;
Balabas, Aneta;
Dabrowska, Michalina;
Niwinska, Anna;
Gruchota, Jakub;
Zub, Renata;
Skasko, Elzbieta;
Steffen, Jan;
Ostrowski, Jerzy;
Siedlecki, Janusz A.

Publication type:

Article

“High rate of recurrent adenomatosis during endoscopic surveillance after duodenectomy in patients with familial adenomatous polyposis”.

Published in:

Familial Cancer, 2013, v. 12, n. 4, p. 699, doi. 10.1007/s10689-013-9648-5

By:

Alderlieste, Yasser A.;
Bastiaansen, Barbara A.;
Mathus-Vliegen, Elisabeth M. H.;
Gouma, Dirk J.;
Dekker, Evelien

Publication type:

Article

Frameshift mutation in the PTCH2 gene can cause nevoid basal cell carcinoma syndrome.

Published in:

Familial Cancer, 2013, v. 12, n. 4, p. 611, doi. 10.1007/s10689-013-9623-1

By:

Fujii, Katsunori;
Ohashi, Hirofumi;
Suzuki, Maiko;
Hatsuse, Hiromi;
Shiohama, Tadashi;
Uchikawa, Hideki;
Miyashita, Toshiyuki

Publication type:

Article

Works matching IS 13899600 AND DT 2013 AND VI 12 AND IP 4

Whole exome sequencing identifies mutation of EDNRA involved in ACTH-independent macronodular adrenal hyperplasia.

Can we test for hereditary cancer at 18 years when we start surveillance at 25? Patient reported outcomes.

Rectal cancers in patients with familial adenomatous polyposis.

Polymorphisms in arachidonic acid metabolism-related genes and the risk and prognosis of colorectal cancer.

Case report: metachronous central nervous system desmoid tumours and thyroid carcinoma in a young familial adenomatous polyposis patient.

The incidence of <i>PALB2</i> c.3113G>A in women with a strong family history of breast and ovarian cancer attending familial cancer centres in Australia.

Psychosocial consequences of predictive genetic testing for lynch syndrome and associations to surveillance behaviour in a 7-year follow-up study.

Phenotypic heterogeneity of hereditary gynecologic cancers: a report from the Creighton hereditary cancer registry.

Is the psychological impact of genetic testing moderated by support and sharing of test results to family and friends?

Prevalence of <i>HOXB13</i> mutation in a population of Ashkenazi Jewish men treated for prostate cancer.

Novel and recurrent <i>BRCA1/BRCA2</i> mutations in early onset and familial breast and ovarian cancer detected in the Program of Genetic Counseling in Cancer of Valencian Community (eastern Spain). Relationship of family phenotypes with mutation prevalence.

Multivariate analysis of <i>MLH1</i> c.1664T>C (p.Leu555Pro) mismatch repair gene variant demonstrates its pathogenicity.

The Proceedings of the Collaborative Group of the Americas on Inherited Colorectal Cancer Sheraton Boston Hotel, Boston, Massachusetts, October 27–29, 2012.

Interest of individuals from <i>BRCA</i> families to participate in research studies focused on male <i>BRCA</i> carriers.

Do individuals with a family history of colorectal cancer adhere to medical recommendations for the prevention of colorectal cancer?

Extracolonic cancer risk in patients with serrated polyposis syndrome and their first-degree relatives.

Chemoprevention in Lynch syndrome.

Self administered screening for hereditary cancers in conjunction with mammography and ultrasound.

Factors affecting the decision to undergo risk-reducing salpingo-oophorectomy among women with <i>BRCA</i> gene mutation.

Underestimated survival predictions of the prognostic tools Adjuvant! Online and PREDICT in BRCA1-associated breast cancer patients.

Association of the BRCA1 promoter polymorphism rs11655505 with the risk of familial breast and/or ovarian cancer.

“High rate of recurrent adenomatosis during endoscopic surveillance after duodenectomy in patients with familial adenomatous polyposis”.

Frameshift mutation in the <i>PTCH2</i> gene can cause nevoid basal cell carcinoma syndrome.