Works matching IS 17312302 AND DT 2025 AND VI 23 AND IP 1

Results: 18

BRCA1 promoter hypermethylation is not associated with germline variants in Polish breast cancer patients.

Published in:

Hereditary Cancer in Clinical Practice, 2025, v. 23, n. 1, p. 1, doi. 10.1186/s13053-025-00317-8

By:

Prajzendanc, Karolina;
Domagała, Paweł;
Hybiak, Jolanta;
Kluźniak, Wojciech;
Cybulski, Cezary;
Białkowska, Katarzyna;
Ogrodniczak, Alicja;
Ryś, Janusz;
Sejda, Aleksandra;
Szwiec, Marek;
Tomiczek-Szwiec, Joanna;
Kluz, Tomasz;
Dwornik, Roksana;
Cylwik, Dagmara;
Gronwald, Jacek;
Lubiński, Jan;
Jakubowska, Anna

Publication type:

Article

High familial risks in some rare cancers may pinpoint to hidden germline genetics: focus on esophageal, stomach, small intestinal, testis, thyroid and bone cancers.

Published in:

2025

By:

Hemminki, Kari;
Hemminki, Otto;
Koskinen, Anni;
Hemminki, Akseli;
Försti, Asta

Publication type:

Literature Review

Translation, cultural adaptation, and pilot testing of the German cancer worry scale among BRCA1/2 pathogenic variant carriers in Austria.

Published in:

Hereditary Cancer in Clinical Practice, 2025, v. 23, n. 1, p. 1, doi. 10.1186/s13053-025-00316-9

By:

Parger, Anna-Maria;
Muhr, Daniela;
Singer, Christian F.;
Tan, Yen Y.

Publication type:

Article

Prostate Cancer: genetics in practice now and in the future.

Published in:

Hereditary Cancer in Clinical Practice, 2025, v. 23, n. 1, p. 1, doi. 10.1186/s13053-025-00310-1

By:

McHugh, Jana;
Bancroft, Elizabeth;
Kote-Jarai, Zsofia;
Eeles, Rosalind

Publication type:

Article

Tumour mutational burden using a targeted panel approach for comprehensive tumour profiling focusing on colorectal cancer.

Published in:

2025

By:

Scott, Rodney J.;
Ziolkowski, Andrew;
Mossman, David;
Hipwell, Michael

Publication type:

Literature Review

Endoscopic surveillance for colorectal cancer and its precursor lesions in Lynch syndrome; time for some policy shifts?

Published in:

Hereditary Cancer in Clinical Practice, 2025, v. 23, n. 1, p. 1, doi. 10.1186/s13053-025-00312-z

By:

Kuipers, Romy N;
Burggraaff, Marissa F;
Maas, Michiel HJ;
van der Biessen – van Beek, Dorien TJ;
van Kouwen, Mariëtte CA;
Bisseling, Tanya M

Publication type:

Article

Association between single nucleotide polymorphisms of DNA repair genes (BRCA1, BRCA2, and PALB2) and breast cancer incidence in a subset of Iranian population.

Published in:

Hereditary Cancer in Clinical Practice, 2025, v. 23, n. 1, p. 1, doi. 10.1186/s13053-025-00311-0

By:

Jahangiri, Sepideh;
Abdan, Zahra;
Houshmand, Massoud;
Souroush, Ali;
Aznab, Mozaffar

Publication type:

Article

Knowledge and perceptions of genetic testing for patients with breast cancer in Nigeria: a survey of healthcare providers.

Published in:

Hereditary Cancer in Clinical Practice, 2025, v. 23, n. 1, p. 1, doi. 10.1186/s13053-025-00315-w

By:

Wuraola, Funmilola Olanike;
Dare, Anna;
Ramruthan, Jenine;
Reel, Emma;
Santiago, Anna T.;
Sharif, Folorunso;
Olayide, Agodirin;
Sunday-Nweke, Nneka;
Alatise, Olusegun;
Cil, Tulin D.

Publication type:

Article

Insights into genetic modifiers of breast cancer risk in carriers of BRCA1 and BRCA2 pathogenic variants.

Published in:

Hereditary Cancer in Clinical Practice, 2025, v. 23, n. 1, p. 1, doi. 10.1186/s13053-025-00313-y

By:

Dwornik, Roksana;
Białkowska, Katarzyna

Publication type:

Article

Chemotherapy receipt in affected BRCA1/2 and PALB2 carriers with operable breast cancer: the impact of early detection and pre-diagnostic awareness on clinical outcomes and treatment.

Published in:

Hereditary Cancer in Clinical Practice, 2025, v. 23, n. 1, p. 1, doi. 10.1186/s13053-025-00314-x

By:

Wong, Stephanie M.;
Apostolova, Carla;
Ferroum, Amina;
Alhassan, Basmah;
Prakash, Ipshita;
Basik, Mark;
Martel, Karyne;
Meterissian, Sarkis;
Fleiszer, David;
Wong, Nora;
Sadinsky, Michaela Bercovitch;
Malagon, Talia;
Boileau, Jean Francois;
Foulkes, William D.

Publication type:

Article

Analysis of informed consent forms of patients undergoing cancer genetic testing in the era of next-generation sequencing.

Published in:

Hereditary Cancer in Clinical Practice, 2025, v. 23, n. 1, p. 1, doi. 10.1186/s13053-025-00309-8

By:

Kerševan, Tina;
Kogovšek, Tina;
Blatnik, Ana;
Krajc, Mateja

Publication type:

Article

De novo familial adenomatous polyposis with germline double heterozygosity of APC/BRCA2: a case report and literature review.

Published in:

Hereditary Cancer in Clinical Practice, 2025, v. 23, n. 1, p. 1, doi. 10.1186/s13053-025-00306-x

By:

Zhang, Tian-Qi;
Cai, Ji-Dong;
Li, Cong;
Xu, Yun;
Xu, Ye

Publication type:

Article

Assessing germline TP53 mutations in cancer patients: insights into Li-Fraumeni syndrome and genetic testing guidelines.

Published in:

Hereditary Cancer in Clinical Practice, 2025, v. 23, n. 1, p. 1, doi. 10.1186/s13053-025-00307-w

By:

Danishevich, Anastasiia;
Fedorova, Daria;
Bodunova, Natalia;
Makarova, Maria;
Byakhova, Maria;
Semenova, Anna;
Galkin, Vsevolod;
Litvinova, Maria;
Nikolaev, Sergey;
Efimova, Irina;
Osinin, Pavel;
Lisitsa, Tatyana;
Khakhina, Anastasiya;
Shipulin, German;
Nasedkina, Tatiana;
Shumilova, Syuykum;
Gusev, Oleg;
Bilyalov, Airat;
Shagimardanova, Elena;
Shigapova, Leyla

Publication type:

Article

Age-specific familial risks in cancer as clues to germline genetic and environmental causes: focus on colorectal, endometrial, prostate, kidney, breast and lung cancers.

Published in:

2025

By:

Hemminki, Kari;
Försti, Asta;
Hemminki, Otto;
Scott, Rodney J.;
Hemminki, Akseli

Publication type:

Literature Review

Colorectal carcinogenesis in the Lynch syndromes and familial adenomatous polyposis: trigger events and downstream consequences.

Published in:

Hereditary Cancer in Clinical Practice, 2025, v. 23, n. 1, p. 1, doi. 10.1186/s13053-025-00305-y

By:

Møller, Pål;
Ahadova, Aysel;
Kloor, Matthias;
Seppälä, Toni T.;
Burn, John;
Haupt, Saskia;
Macrae, Finlay;
Dominguez-Valentin, Mev;
Möslein, Gabriela;
Lindblom, Annika;
sunde, Lone;
Winship, Ingrid;
Capella, Gabriel;
Monahan, Kevin;
Buchanan, Daniel D.;
Evans, D. Gareth;
Hovig, Eivind;
Sampson, Julian R.

Publication type:

Article

Time to rethink colorectal cancer prevention strategies for lynch syndrome.

Published in:

Hereditary Cancer in Clinical Practice, 2025, v. 23, n. 1, p. 1, doi. 10.1186/s13053-024-00295-3

By:

Lubinski, Jan;
Scott, Rodney J.

Publication type:

Article

Clinician perspectives on designing and implementing a hereditary cancer transition clinic.

Published in:

Hereditary Cancer in Clinical Practice, 2025, v. 23, n. 1, p. 1, doi. 10.1186/s13053-024-00304-5

By:

Gabriel, Jazmine L.;
Schlieder, Victoria;
Goehringer, Jessica M.;
Leitzel, Tracey;
Sugrue, Emily Ann;
Zultevicz, Sarah;
Davis, Thomas W.;
Campbell-Salome, Gemme;
Romagnoli, Katrina

Publication type:

Article

Two independent families with de novo whole APC gene deletion and intellectual disability: a case report.

Published in:

2025

By:

Iwaizumi, Moriya;
Taniguchi, Terumi;
Kojima, Risa;
Osawa, Harumo;
Tatsuta, Kyota;
Sakata, Mayu;
Osawa, Satoshi;
Kurachi, Kiyotaka;
Sugimoto, Ken

Publication type:

Case Study