Works matching IS 13899600 AND DT 2016 AND VI 15 AND IP 2

Results: 25

Methylation of the miR-126 gene associated with glioma progression.

Published in:

Familial Cancer, 2016, v. 15, n. 2, p. 317, doi. 10.1007/s10689-015-9846-4

By:

Cui, Hongwei;
Mu, Yongping;
Yu, Lei;
Xi, Ya-guang;
Matthiesen, Rune;
Su, Xiulan;
Sun, Wenjie

Publication type:

Article

Germline BAP1 mutations misreported as somatic based on tumor-only testing.

Published in:

Familial Cancer, 2016, v. 15, n. 2, p. 327, doi. 10.1007/s10689-016-9865-9

By:

Abdel-Rahman, Mohamed;
Rai, Karan;
Pilarski, Robert;
Davidorf, Frederick;
Cebulla, Colleen

Publication type:

Article

Migrant breast cancer patients and their participation in genetic counseling: results from a registry-based study.

Published in:

Familial Cancer, 2016, v. 15, n. 2, p. 163, doi. 10.1007/s10689-016-9871-y

By:

Baars, J.;
Dulmen, A.;
Velthuizen, M.;
Theunissen, E.;
Vrouenraets, B.;
Kimmings, A.;
Dalen, T.;
Ooijen, B.;
Witkamp, A.;
Aa, M.;
Ausems, M.

Publication type:

Article

Diagnostic values of osteopontin combined with CA125 for ovarian cancer: a meta-analysis.

Published in:

Familial Cancer, 2016, v. 15, n. 2, p. 221, doi. 10.1007/s10689-015-9847-3

By:

Lan, Zhu;
Fu, Dan;
Yu, Xiuzhang;
Xi, Mingrong

Publication type:

Article

Erratum to: Methylation of the miR-126 gene associated with glioma progression.

Published in:

2016

By:

Cui, Hongwei;
Mu, Yongping;
Yu, Lei;
Xi, Yaguang;
Matthiesen, Rune;
Su, Xiulan;
Sun, Wenjie

Publication type:

Erratum

CYP1A1 and GSTP1 gene variations in breast cancer: a systematic review and case-control study.

Published in:

Familial Cancer, 2016, v. 15, n. 2, p. 201, doi. 10.1007/s10689-015-9849-1

By:

Akhtar, Sumaira;
Mahjabeen, Ishrat;
Akram, Zertashia;
Kayani, Mahmood

Publication type:

Article

Correlation between the germline methylation status in ERβ promoter and the risk in prostate cancer: a prospective study.

Published in:

Familial Cancer, 2016, v. 15, n. 2, p. 309, doi. 10.1007/s10689-015-9850-8

By:

Wang, Lihui;
Zhang, Pan;
Meng, Xiannan;
Chen, Xiang;
Xiang, Zou;
Lin, Xiaoqian;
Liu, Ye;
Gan, Weidong;
Han, Xiaodong;
Li, Dongmei

Publication type:

Article

Development of a novel PTT assay for mutation detection in PALB2 large exons and PALB2 screening in medullary breast cancer.

Published in:

Familial Cancer, 2016, v. 15, n. 2, p. 183, doi. 10.1007/s10689-015-9851-7

By:

Poumpouridou, Nikoleta;
Goutas, Nikolaos;
Tsionou, Christina;
Dimas, Kleanthi;
Lianidou, Evi;
Kroupis, Christos

Publication type:

Article

Non-genetic health professionals' attitude towards, knowledge of and skills in discussing and ordering genetic testing for hereditary cancer.

Published in:

Familial Cancer, 2016, v. 15, n. 2, p. 341, doi. 10.1007/s10689-015-9852-6

By:

Douma, Kirsten;
Smets, Ellen;
Allain, Dawn

Publication type:

Article

Are lung cysts in renal cell cancer (RCC) patients an indication for FLCN mutation analysis?

Published in:

Familial Cancer, 2016, v. 15, n. 2, p. 297, doi. 10.1007/s10689-015-9853-5

By:

Johannesma, Paul;
Houweling, Arjan;
Menko, Fred;
Beek, I.;
Reinhard, Rinze;
Gille, Johan;
Waesberghe, JanHein;
Thunnissen, Erik;
Starink, Theo;
Postmus, Pieter;
Moorselaar, R.

Publication type:

Article

The impact of an interventional counselling procedure in families with a BRCA1/2 gene mutation: efficacy and safety.

Published in:

Familial Cancer, 2016, v. 15, n. 2, p. 155, doi. 10.1007/s10689-015-9854-4

By:

Sermijn, Erica;
Delesie, Liesbeth;
Deschepper, Ellen;
Pauwels, Ingrid;
Bonduelle, Maryse;
Teugels, Erik;
Grève, Jacques

Publication type:

Article

Associations between allergic conditions and pediatric brain tumors in Neurofibromatosis type 1.

Published in:

Familial Cancer, 2016, v. 15, n. 2, p. 301, doi. 10.1007/s10689-015-9855-3

By:

Porcelli, Bree;
Zoellner, Nancy;
Abadin, Salmafatima;
Gutmann, David;
Johnson, Kimberly

Publication type:

Article

Mismatch repair deficiency concordance between primary colorectal cancer and corresponding metastasis.

Published in:

Familial Cancer, 2016, v. 15, n. 2, p. 253, doi. 10.1007/s10689-015-9856-2

By:

Haraldsdottir, Sigurdis;
Roth, Rachel;
Pearlman, Rachel;
Hampel, Heather;
Arnold, Christina;
Frankel, Wendy

Publication type:

Article

Mutation analysis of MUTYH in Japanese colorectal adenomatous polyposis patients.

Published in:

Familial Cancer, 2016, v. 15, n. 2, p. 261, doi. 10.1007/s10689-015-9857-1

By:

Taki, Keiko;
Sato, Yuri;
Nomura, Sachio;
Ashihara, Yuumi;
Kita, Mizuho;
Tajima, Ikufumi;
Sugano, Kokichi;
Arai, Masami

Publication type:

Article

Screening of the BRCA1 gene in Brazilian patients with breast and/or ovarian cancer via high-resolution melting reaction analysis.

Published in:

Familial Cancer, 2016, v. 15, n. 2, p. 173, doi. 10.1007/s10689-015-9858-0

By:

Oliveira, Eneida;
Soares, Bárbara;
Lemos, Sara;
Rosa, Reginaldo;
Rodrigues, Angélica;
Barbosa, Leandro;
Oliveira Lopes, Débora;
Santos, Luciana

Publication type:

Article

Recurrent candidiasis and early-onset gastric cancer in a patient with a genetically defined partial MYD88 defect.

Published in:

Familial Cancer, 2016, v. 15, n. 2, p. 289, doi. 10.1007/s10689-015-9859-z

By:

Vogelaar, Ingrid;
Ligtenberg, Marjolijn;
Post, Rachel;
Voer, Richarda;
Kets, C.;
Jansen, Trees;
Jacobs, Liesbeth;
Schreibelt, Gerty;
Vries, I.;
Netea, Mihai;
Hoogerbrugge, Nicoline

Publication type:

Article

Determining the familial risk distribution of colorectal cancer: a data mining approach.

Published in:

Familial Cancer, 2016, v. 15, n. 2, p. 241, doi. 10.1007/s10689-015-9860-6

By:

Chau, Rowena;
Jenkins, Mark;
Buchanan, Daniel;
Ait Ouakrim, Driss;
Giles, Graham;
Casey, Graham;
Gallinger, Steven;
Haile, Robert;
Le Marchand, Loic;
Newcomb, Polly;
Lindor, Noralane;
Hopper, John;
Win, Aung

Publication type:

Article

Gatekeeper role of gastroenterologists and surgeons in recognising and discussing familial colorectal cancer.

Published in:

Familial Cancer, 2016, v. 15, n. 2, p. 231, doi. 10.1007/s10689-015-9861-5

By:

Douma, Kirsten;
Dekker, Evelien;
Smets, Ellen;
Aalfs, Cora

Publication type:

Article

Risk of thyroid cancer among Caribbean Hispanic patients with familial adenomatous polyposis.

Published in:

Familial Cancer, 2016, v. 15, n. 2, p. 267, doi. 10.1007/s10689-015-9862-4

By:

Casellas-Cabrera, Nicolás;
Díaz-Algorri, Yaritza;
Carlo-Chévere, Víctor;
González-Pons, María;
Rodríguez-Mañón, Natalia;
Pérez-Mayoral, Julyann;
Bertrán-Rodríguez, Carlos;
Soto-Salgado, Marievelisse;
Giardiello, Francis;
Rodríguez-Quilichini, Segundo;
Cruz-Correa, Marcia

Publication type:

Article

Initial clinical validation of Health Heritage, a patient-facing tool for personal and family history collection and cancer risk assessment.

Published in:

Familial Cancer, 2016, v. 15, n. 2, p. 331, doi. 10.1007/s10689-015-9863-3

By:

Baumgart, Leigh;
Postula, Kristen;
Knaus, William

Publication type:

Article

Relationship of immunohistochemistry, copy number aberrations and epigenetic disorders with BRCAness pattern in hereditary and sporadic breast cancer.

Published in:

Familial Cancer, 2016, v. 15, n. 2, p. 193, doi. 10.1007/s10689-015-9864-2

By:

Murria Estal, Rosa;
Palanca Suela, Sarai;
de Juan Jiménez, Inmaculada;
Alenda Gonzalez, Cristina;
Egoavil Rojas, Cecilia;
García-Casado, Zaida;
López Guerrero, Jose;
Juan Fita, María;
Sánchez Heras, Ana;
Segura Huerta, Ángel;
Santaballa Bertrán, Ana;
Chirivella González, Isabel;
Llop García, Marta;
Pérez Simó, Gema;
Barragán González, Eva;
Bolufer Gilabert, Pascual

Publication type:

Article

Developing and assessing the utility of a You-Tube based clinical genetics video channel for families affected by inherited tumours.

Published in:

2016

By:

Jones, G.;
Singletary, J.;
Cashmore, A.;
Jain, V.;
Abhulimhen, J.;
Chauhan, J.;
Musson, H.;
Barwell, J.

Publication type:

Letter

Constitutional MLH1 methylation presenting with colonic polyposis syndrome and not Lynch syndrome.

Published in:

Familial Cancer, 2016, v. 15, n. 2, p. 275, doi. 10.1007/s10689-016-9868-6

By:

Kidambi, Trilokesh;
Blanco, Amie;
Ziffle, Jessica;
Terdiman, Jonathan

Publication type:

Article

CDH1 germline mutations and hereditary lobular breast cancer.

Published in:

Familial Cancer, 2016, v. 15, n. 2, p. 215, doi. 10.1007/s10689-016-9869-5

By:

Corso, Giovanni;
Intra, Mattia;
Trentin, Chiara;
Veronesi, Paolo;
Galimberti, Viviana

Publication type:

Article

Exome sequencing identifies potential novel candidate genes in patients with unexplained colorectal adenomatous polyposis.

Published in:

Familial Cancer, 2016, v. 15, n. 2, p. 281, doi. 10.1007/s10689-016-9870-z

By:

Spier, Isabel;
Kerick, Martin;
Drichel, Dmitriy;
Horpaopan, Sukanya;
Altmüller, Janine;
Laner, Andreas;
Holzapfel, Stefanie;
Peters, Sophia;
Adam, Ronja;
Zhao, Bixiao;
Becker, Tim;
Lifton, Richard;
Holinski-Feder, Elke;
Perner, Sven;
Thiele, Holger;
Nöthen, Markus;
Hoffmann, Per;
Timmermann, Bernd;
Schweiger, Michal;
Aretz, Stefan

Publication type:

Article