Works matching IS 17312302 AND DT 2020 AND VI 18 AND IP 1

Results: 25

Retrospective review of outcomes in patients with DNA-damage repair related pancreatic cancer.

Published in:

Hereditary Cancer in Clinical Practice, 2020, v. 18, n. 1, p. 1, doi. 10.1186/s13053-020-00148-9

By:

Macklin-Mantia, Sarah K.;
Hines, Stephanie L.;
Kasi, Pashtoon M.

Publication type:

Article

Polymorphisms in MMP-1, MMP-2, MMP-7, MMP-13 and MT2A do not contribute to breast, lung and colon cancer risk in polish population.

Published in:

Hereditary Cancer in Clinical Practice, 2020, v. 18, n. 1, p. 1, doi. 10.1186/s13053-020-00147-w

By:

Białkowska, Katarzyna;
Marciniak, Wojciech;
Muszyńska, Magdalena;
Baszuk, Piotr;
Gupta, Satish;
Jaworska-Bieniek, Katarzyna;
Sukiennicki, Grzegorz;
Durda, Katarzyna;
Gromowski, Tomasz;
Lener, Marcin;
Prajzendanc, Karolina;
Łukomska, Alicja;
Cybulski, Cezary;
Huzarski, Tomasz;
Gronwald, Jacek;
Dębniak, Tadeusz;
Lubiński, Jan;
Jakubowska, Anna

Publication type:

Article

Informing patients about their mutation tests: CDKN2A c.256G>A in melanoma as an example.

Published in:

Hereditary Cancer in Clinical Practice, 2020, v. 18, n. 1, p. 1, doi. 10.1186/s13053-020-00146-x

By:

Hemminki, Kari;
Srivastava, Aayushi;
Rachakonda, Sivaramakrishna;
Bandapalli, Obul;
Nagore, Eduardo;
Hemminki, Akseli;
Kumar, Rajiv

Publication type:

Article

Prevalence of RECQL germline variants in Pakistani early-onset and familial breast cancer patients.

Published in:

Hereditary Cancer in Clinical Practice, 2020, v. 18, n. 1, p. 1, doi. 10.1186/s13053-020-00159-6

By:

Rashid, Muhammad Usman;
Muhammad, Noor;
Khan, Faiz Ali;
Shehzad, Umara;
Naeemi, Humaira;
Malkani, Naila;
Hamann, Ute

Publication type:

Article

Characteristics and genetic testing outcomes of patients with clinically suspected paraganglioma/pheochromocytoma (PGL/PCC) syndrome in Singapore.

Published in:

Hereditary Cancer in Clinical Practice, 2020, v. 18, n. 1, p. 1, doi. 10.1186/s13053-020-00156-9

By:

Ting, Kay Reen;
Ong, Pei Yi;
Wei, Samuel Ow Guan;
Parameswaran, Rajeev;
Khoo, Chin Meng;
Deepak, Doddabele Srinivasa;
Lee, Soo-Chin

Publication type:

Article

Metachronous cutaneous squamous cell carcinoma in a young patient as the only presenting symptom to uncover Lynch syndrome with MLH1 Germline mutation.

Published in:

Hereditary Cancer in Clinical Practice, 2020, v. 18, n. 1, p. N.PAG, doi. 10.1186/s13053-020-00155-w

By:

Khaddour, Karam;
Fields, Ryan C.;
Ansstas, Michael;
Rosman, Ilana S.;
Ansstas, George

Publication type:

Article

An in-depth exploration of the post-test informational needs of BRCA1 and BRCA2 pathogenic variant carriers in Asia.

Published in:

Hereditary Cancer in Clinical Practice, 2020, v. 18, n. 1, p. N.PAG, doi. 10.1186/s13053-020-00154-x

By:

Yuen, Jeanette;
Fung, Si Ming;
Sia, Chin Leong;
Venkatramani, Mallika;
Shaw, Tarryn;
Courtney, Eliza;
Li, Shao-Tzu;
Chiang, Jianbang;
Tan, Veronique Kiak-Mien;
Tan, Benita Kiat-Tee;
Ngeow, Joanne

Publication type:

Article

Biological and clinical impact of central nervous system hemangioblastomas in Chinese patients with von Hippel-Lindau disease: implications for treatment.

Published in:

Hereditary Cancer in Clinical Practice, 2020, v. 18, n. 1, p. N.PAG, doi. 10.1186/s13053-020-00153-y

By:

Liu, Zhen;
Li, Liang;
Yi, Zhiqiang;
Duan, Hongzhou;
Lu, Runchun;
Li, Chunwei;
Li, Lei;
Gong, Kan

Publication type:

Article

Preferences for breast cancer prevention among women with a BRCA1 or BRCA2 mutation.

Published in:

Hereditary Cancer in Clinical Practice, 2020, v. 18, n. 1, p. N.PAG, doi. 10.1186/s13053-020-00152-z

By:

Mansfield, Carol A.;
Metcalfe, Kelly A.;
Snyder, Carrie;
Lindeman, Geoffrey J.;
Posner, Joshua;
Friedman, Sue;
Lynch, Henry T.;
Narod, Steven A.;
Evans, D. Gareth;
Liede, Alexander

Publication type:

Article

Patients with unexplained mismatch repair deficiency are interested in updated genetic testing.

Published in:

Hereditary Cancer in Clinical Practice, 2020, v. 18, n. 1, p. N.PAG, doi. 10.1186/s13053-020-00150-1

By:

Omark, Jessica;
Vilar, Eduardo;
You, Y Nancy;
Dunnington, Leslie;
Noblin, Sarah;
Stevens, Blair;
Mork, Maureen

Publication type:

Article

Public support for healthcare-mediated disclosure of hereditary cancer risk information: Results from a population-based survey in Sweden.

Published in:

Hereditary Cancer in Clinical Practice, 2020, v. 18, n. 1, p. 1, doi. 10.1186/s13053-020-00151-0

By:

Andersson, Andreas;
Hawranek, Carolina;
Öfverholm, Anna;
Ehrencrona, Hans;
Grill, Kalle;
Hajdarevic, Senada;
Melin, Beatrice;
Tham, Emma;
Hellquist, Barbro Numan;
Rosén, Anna

Publication type:

Article

An American patient with polyposis carrying a Scandinavian AXIN2 pathogenic variant.

Published in:

2020

By:

Macklin-Mantia, Sarah K.;
Riegert-Johnson, Douglas L.

Publication type:

Letter

Adherence to National Comprehensive Cancer Network Guidelines for BRCA testing among high risk breast Cancer patients: a retrospective chart review study.

Published in:

Hereditary Cancer in Clinical Practice, 2020, v. 18, n. 1, p. 1, doi. 10.1186/s13053-020-00144-z

By:

Bobbili, Priyanka;
Olufade, Temitope;
DerSarkissian, Maral;
Shenolikar, Rahul;
Yu, Hong;
Duh, Mei Sheng;
Tung, Nadine

Publication type:

Article

Increased risk for uterine cancer among first-degree relatives to Swedish gastric cancer patients.

Published in:

Hereditary Cancer in Clinical Practice, 2020, v. 18, n. 1, p. 1, doi. 10.1186/s13053-020-00145-y

By:

Samola Winnberg, Johanna;
Rudd, Eva;
Keränen, Anne;
Lagerstedt-Robinson, Kristina;
Lindblom, Annika;
Nilsson, Magnus;
Lindblad, Mats;
Sjödahl, Krister

Publication type:

Article

Correction to: Expectations and psychological issues before genetic counseling: analysis of distress determinant factors.

Published in:

2020

By:

Ballatore, Zelmira;
Bracci, Raffaella;
Maccaroni, Elena;
Svarca, Lucia;
Bianchi, Francesca;
Belvederesi, Laura;
Brugiati, Cristiana;
Pagliaretta, Silvia;
Murrone, Alberto;
Bini, Federica;
Pistelli, Mirco;
Ricci, Giulia;
Berardi, Rossana

Publication type:

Correction Notice

Expectations and psychological issues before genetic counseling: analysis of distress determinant factors.

Published in:

Hereditary Cancer in Clinical Practice, 2020, v. 18, n. 1, p. 1, doi. 10.1186/s13053-020-00142-1

By:

Ballatore, Zelmira;
Bracci, Raffaella;
Maccaroni, Elena;
Svarca, Lucia;
Bianchi, Francesca;
Belvederesi, Laura;
Bruciati, Cristiana;
Pagliaretta, Silvia;
Murrone, Alberto;
Bini, Federica;
Pistelli, Mirco;
Ricci, Giulia;
Berardi, Rossana

Publication type:

Article

Development and validation of next generation sequencing based 35-gene hereditary cancer panel.

Published in:

Hereditary Cancer in Clinical Practice, 2020, v. 18, n. 1, p. 1, doi. 10.1186/s13053-020-00141-2

By:

Chan, Wing;
Lee, Mianne;
Yeo, Zhen Xuan;
Ying, Dingge;
Grimaldi, Keith A.;
Pickering, Craig;
Yang, Michael M. S.;
Sundaram, Senthil K.;
Tzang, Lawrence C. H.

Publication type:

Article

A rare missense variant in APC interrupts splicing and causes AFAP in two Danish families.

Published in:

Hereditary Cancer in Clinical Practice, 2020, v. 18, n. 1, p. 1, doi. 10.1186/s13053-020-00140-3

By:

Djursby, Malene;
Wadt, Karin;
Frederiksen, Jane Hübertz;
Madsen, Majbritt Busk;
Berchtold, Lukas Adrian;
Hasselby, Jane Preuss;
Willemoe, Gro Linno;
Hansen, Thomas v. O.;
Gerdes, Anne-Marie

Publication type:

Article

An interesting case of likely BRCA2 related bilateral breast cancer with metastasis in the fimbrial part of fallopian tube.

Published in:

Hereditary Cancer in Clinical Practice, 2020, v. 18, n. 1, p. 1, doi. 10.1186/s13053-020-00139-w

By:

Boltežar, Lučka;
Gašljević, Gorana;
Novaković, Srdjan;
Stegel, Vida;
Škof, Erik

Publication type:

Article

The Prospective Lynch Syndrome Database reports enable evidence-based personal precision health care.

Published in:

Hereditary Cancer in Clinical Practice, 2020, v. 18, n. 1, p. 1, doi. 10.1186/s13053-020-0138-0

By:

Møller, Pål

Publication type:

Article

Diet, weight management, physical activity and Ovarian & Breast Cancer Risk in women with BRCA1/2 pathogenic Germline gene variants: systematic review.

Published in:

Hereditary Cancer in Clinical Practice, 2020, v. 18, n. 1, p. 1, doi. 10.1186/s13053-020-0137-1

By:

Coletta, Adriana M.;
Peterson, Susan K.;
Gatus, Leticia A.;
Krause, Kate J.;
Schembre, Susan M.;
Gilchrist, Susan C.;
Arun, Banu;
You, Y. Nancy;
Rodriguez-Bigas, Miguel A.;
Strong, Larkin L.;
Lu, Karen H.;
Basen-Engquist, Karen

Publication type:

Article

Ubiquitous neurocognitive dysfunction in familial adenomatous polyposis: proof-of-concept of the role of APC protein in neurocognitive function.

Published in:

Hereditary Cancer in Clinical Practice, 2020, v. 18, n. 1, p. 1, doi. 10.1186/s13053-020-0135-3

By:

Cruz-Correa, Marcia Roxana;
Sala, Ana Cecilia;
Cintrón, Beatriz;
Hernández, Jessica;
Olivera, Myrta;
Cora, Adrian;
Moore, Constance M.;
Luciano, Carlos A.;
Soto-Salgado, Marievelisse;
Giardiello, Francis M.;
Hooper, Stephen R.

Publication type:

Article

Group plus "mini" individual pre-test genetic counselling sessions for hereditary cancer shorten provider time and improve patient satisfaction.

Published in:

Hereditary Cancer in Clinical Practice, 2020, v. 18, n. 1, p. 1, doi. 10.1186/s13053-020-0136-2

By:

Hynes, Jaclyn;
MacMillan, Andrée;
Fernandez, Sara;
Jacob, Karen;
Carter, Shannon;
Predham, Sarah;
Etchegary, Holly;
Dawson, Lesa

Publication type:

Article

On the road with Henry Lynch.

Published in:

2020

By:

Narod, Steven A.

Publication type:

Editorial

Whole-body MRI within a surveillance program for carriers with clinically actionable germline TP53 variants - the Swedish constitutional TP53 study SWEP53.

Published in:

Hereditary Cancer in Clinical Practice, 2020, v. 18, n. 1, p. 1, doi. 10.1186/s13053-020-0133-5

By:

Omran, Meis;
Blomqvist, Lennart;
Brandberg, Yvonne;
Pal, Niklas;
Kogner, Per;
Ståhlbom, Anne Kinhult;
Tham, Emma;
Bajalica-Lagercrantz, Svetlana

Publication type:

Article