Works matching IS 17312302 AND DT 2015 AND VI 13 AND IP 1

Results: 31

Ten modifiers of penetrance BRCA1 validated in a Norwegian series.

Published in:

Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0035-0

By:

Heramb, Cecilie;
Ekstrøm, Per Olaf;
Tharmaratnam, Kukatharmini;
Hovig, Eivind;
Møller, Pål;
Mæhle, Lovise

Publication type:

Article

Patient experiences living with pancreatic cancer risk.

Published in:

Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0034-1

By:

Underhill, Meghan;
Berry, Donna;
Dalton, Emily;
Schienda, Jaclyn;
Syngal, Sapna

Publication type:

Article

A case of squamous cell carcinoma of the skin due to the molecularly confirmed Lynch Syndrome.

Published in:

Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0033-2

By:

Sorscher, Steven

Publication type:

Article

Interest in genomic SNP testing for prostate cancer risk: a pilot survey.

Published in:

Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0032-3

By:

Hall, Michael J.;
Ruth, Karen J.;
Chen, David YT;
Gross, Laura M.;
Giri, Veda N.

Publication type:

Article

The missense variant increases c.470 T > C CHEK2 the risk of differentiated thyroid carcinoma in the Great Poland population.

Published in:

Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0030-5

By:

Kaczmarek-Ryś, Marta;
Ziemnicka, Katarzyna;
Hryhorowicz, Szymon T.;
Górczak, Katarzyna;
Hoppe-Gołębiewska, Justyna;
Skrzypczak-Zielińska, Marzena;
Tomys, Michalina;
Gołąb, Monika;
Szkudlarek, Malgorzata;
Budny, Bartłomiej;
Siatkowski, Idzi;
Gut, Paweł;
Ruchała, Marek;
Słomski, Ryszard;
Pławski, Andrzej

Publication type:

Article

High expression of miR-214 is associated with a worse disease-specific survival of the triple-negative breast cancer patients.

Published in:

Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0028-z

By:

Kalniete, Dagnija;
Nakazawa-Miklaševica, Miki;
Štrumfa, Ilze;
Abolinš, Arnis;
Irmejs, Arvids;
Gardovskis, Janis;
Miklaševics, Edvins

Publication type:

Article

Molecular diagnosis and comprehensive treatment of multiple endocrine neoplasia type 2 in Southeastern Chinese.

Published in:

Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0026-1

By:

Jian-Qiang Zhao;
Zhen-Guang Chen;
Xiao-Ping Qi

Publication type:

Article

Management of ovarian and endometrial cancers in women belonging to HNPCC carrier families: review of the literature and results of cancer risk assessment in Polish HNPCC families.

Published in:

Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0025-2

By:

Dębniak, Tadeusz;
Gromowski, Tomasz;
Scott, Rodney J.;
Gronwald, Jacek;
Huzarski, Tomasz;
Byrski, Tomasz;
Kurzawski, Grzegorz;
Dymerska, Dagmara;
Górski, Bohdan;
Paszkowska-Szczur, Katarzyna;
Cybulski, Cezary;
Serrano-Fernandez, Pablo;
Lubiński, Jan

Publication type:

Article

Beliefs about weight and breast cancer: an interview study with high risk women following a 12 month weight loss intervention.

Published in:

Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-014-0023-9

By:

Wright, Claire E.;
Harvie, Michelle;
Howell, Anthony;
Evans, D. Gareth;
Hulbert-Williams, Nick;
Donnelly, Louise S.

Publication type:

Article

Identification of a new large genomic BRCA2 deletion associated with high risk male breast cancer.

Published in:

Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-014-0022-x

By:

de Souza Timoteo, Ana Rafaela;
Albuquerque, Betina Menezes;
Pascoto Moura, Patricia Cristina;
de Oliveira Ramos, Carlos Cesar;
Agnez-Lima, Lucymara Fassarela;
Walsh, Tom;
King, Mary-Claire;
Lajus, Tirzah Braz Petta

Publication type:

Article

High-grade endometrial stromal sarcoma as the initial presentation of an adult patient with Peutz-Jeghers Syndrome: a case report.

Published in:

Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0027-0

By:

Noriega-Iriondo, Maria Fernanda;
Colon-Otero, Gerardo;
Kipp, Benjamin R.;
Copland, John A.;
Ferber, Matthew J.;
Marlow, Laura A.;
Roberts, Maegan E.;
Robertson, Matthew W.;
Dinh, Tri A.;
Attia, Steven;
Geiger, Xochiquetzal J.;
Riegert-Johnson, Douglas L.

Publication type:

Article

Next-generation sequencing for genetic testing of familial colorectal cancer syndromes.

Published in:

Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0039-9

By:

Simbolo, Michele;
Mafficini, Andrea;
Agostini, Marco;
Pedrazzani, Corrado;
Bedin, Chiara;
Urso, Emanuele D.;
Nitti, Donato;
Turri, Giona;
Scardoni, Maria;
Fassan, Matteo;
Scarpa, Aldo

Publication type:

Article

The role of BRCA1 and BRCA2 mutations in prostate, pancreatic and stomach cancers.

Published in:

Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0038-x

By:

Cavanagh, Helen;
Rogers, Katherine M. A.

Publication type:

Article

Cumulative BRCA mutation analysis in the Greek population confirms that homogenous ethnic background facilitates genetic testing.

Published in:

Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0037-y

By:

Tsigginou, Alexandra;
Vlachopoulos, Fotios;
Arzimanoglou, Iordanis;
Zagouri, Flora;
Dimitrakakis, Constantine

Publication type:

Article

Tumour spectrum in non-BRCA hereditary breast cancer families in Sweden.

Published in:

Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0036-z

By:

Wendt, Camilla;
Lindblom, Annika;
Arver, Brita;
von Wachenfeldt, Anna;
Margolin, Sara

Publication type:

Article

Ten modifiers of BRCA1 penetrance validated in a Norwegian series.

Published in:

Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0035-0

By:

Heramb, Cecilie;
Ekstrøm, Per Olaf;
Tharmaratnam, Kukatharmini;
Hovig, Eivind;
Møller, Pål;
Mæhle, Lovise

Publication type:

Article

Patient experiences living with pancreatic cancer risk.

Published in:

Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0034-1

By:

Underhill, Meghan;
Berry, Donna;
Dalton, Emily;
Schienda, Jaclyn;
Syngal, Sapna

Publication type:

Article

A case of squamous cell carcinoma of the skin due to the molecularly confirmed Lynch Syndrome.

Published in:

Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0033-2

By:

Sorscher, Steven

Publication type:

Article

Interest in genomic SNP testing for prostate cancer risk: a pilot survey.

Published in:

Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0032-3

By:

Hall, Michael J.;
Ruth, Karen J.;
Chen, David Y. T.;
Gross, Laura M.;
Giri, Veda N.

Publication type:

Article

Decisions about prophylactic gynecologic surgery: a qualitative study of the experience of female Lynch syndrome mutation carriers.

Published in:

Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0031-4

By:

Etchegary, Holly;
Dicks, Elizabeth;
Watkins, Kathy;
Alani, Sabrina;
Dawson, Lesa

Publication type:

Article

The c.470 T > C CHEK2 missense variant increases the risk of differentiated thyroid carcinoma in the Great Poland population.

Published in:

Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0030-5

By:

Kaczmarek-Ryś, Marta;
Ziemnicka, Katarzyna;
Hryhorowicz, Szymon T.;
Górczak, Katarzyna;
Hoppe-Gołębiewska, Justyna;
Skrzypczak-Zielińska, Marzena;
Tomys, Michalina;
Gołąb, Monika;
Szkudlarek, Malgorzata;
Budny, Bartłomiej;
Siatkowski, Idzi;
Gut, Paweł;
Ruchała, Marek;
Słomski, Ryszard;
Pławski, Andrzej

Publication type:

Article

Thank you to all our manuscript reviewers in 2014.

Published in:

Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0029-y

By:

Lubinski, Jan;
Scott, Rodney J.;
Sijmons, Rolf;
Bayliss, Katie

Publication type:

Article

PARP inhibitors.

Published in:

Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 31, doi. 10.1186/s13053-014-0024-8

By:

Anwar, Maheen;
Muhammad Aslam, Hafiz;
Anwar, Shahzad

Publication type:

Article

High expression of miR-214 is associated with a worse disease-specific survival of the triple-negative breast cancer patients.

Published in:

Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0028-z

By:

Kalniete, Dagnija;
Nakazawa-Miklaševiča, Miki;
Štrumfa, Ilze;
Āboliņš, Arnis;
Irmejs, Arvīds;
Gardovskis, Jānis;
Miklaševičs, Edvīns

Publication type:

Article

Beliefs about weight and breast cancer: an interview study with high risk women following a 12 month weight loss intervention.

Published in:

Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 14, doi. 10.1186/s13053-014-0023-9

By:

Wright, Claire E.;
Harvie, Michelle;
Howell, Anthony;
Evans, D. Gareth;
Hulbert-Williams, Nick;
Donnelly, Louise S.

Publication type:

Article

High-grade endometrial stromal sarcoma as the initial presentation of an adult patient with Peutz-Jeghers Syndrome: a case report.

Published in:

2015

By:

Noriega-Iriondo, Maria Fernanda;
Colon-Otero, Gerardo;
Kipp, Benjamin R.;
Copland, John A.;
Ferber, Matthew J.;
Marlow, Laura A.;
Roberts, Maegan E.;
Robertson, Matthew W.;
Dinh, Tri A.;
Attia, Steven;
Geiger, Xochiquetzal J.;
Riegert-Johnson, Douglas L.

Publication type:

Case Study

Molecular diagnosis and comprehensive treatment of multiple endocrine neoplasia type 2 in Southeastern Chinese.

Published in:

Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 57, doi. 10.1186/s13053-015-0026-1

By:

Jian-Qiang Zhao;
Zhen-Guang Chen;
Xiao-Ping Qi

Publication type:

Article

Management of ovarian and endometrial cancers in women belonging to HNPCC carrier families: review of the literature and results of cancer risk assessment in Polish HNPCC families.

Published in:

Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 39, doi. 10.1186/s13053-015-0025-2

By:

Debniak, Tadeusz;
Gromowski, Tomasz;
Scott, Rodney J.;
Gronwald, Jacek;
Huzarski, Tomasz;
Byrski, Tomasz;
Kurzawski, Grzegorz;
Dymerska, Dagmara;
Górski, Bohdan;
Paszkowska-Szczur, Katarzyna;
Cybulski, Cezary;
Serrano-Fernandez, Pablo;
Lubinski, Jan

Publication type:

Article

High-grade endometrial stromal sarcoma as the initial presentation of an adult patient with Peutz-Jeghers Syndrome: a case report.

Published in:

Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0027-0

By:

Noriega-Iriondo, Maria Fernanda;
Colon-Otero, Gerardo;
Kipp, Benjamin R.;
Copland, John A.;
Ferber, Matthew J.;
Marlow, Laura A.;
Roberts, Maegan E.;
Robertson, Matthew W.;
Dinh, Tri A.;
Attia, Steven;
Geiger, Xochiquetzal J.;
Riegert-Johnson, Douglas L.

Publication type:

Article

Beliefs about weight and breast cancer: an interview study with high risk women following a 12 month weight loss intervention.

Published in:

Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-014-0023-9

By:

Wright, Claire E.;
Harvie, Michelle;
Howell, Anthony;
Gareth Evans, D.;
Hulbert-Williams, Nick;
Donnelly, Louise S.

Publication type:

Article

Identification of a new BRCA2 large genomic deletion associated with high risk male breast cancer.

Published in:

Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-014-0022-x

By:

de Souza Timoteo, Ana Rafaela;
Menezes Albuquerque, Betina;
Pascoto Moura, Patricia Cristina;
de Oliveira Ramos, Carlos Cesar;
Fassarela Agnez-Lima, Lucymara;
Walsh, Tom;
King, Mary-Claire;
Petta Lajus, Tirzah Braz

Publication type:

Article