Works matching IS 13899600 AND DT 2025 AND VI 24 AND IP 1

Results: 27

Optimizing MRI sequences and apparent diffusion coefficient parameters for small pancreatic ductal adenocarcinoma detection.

Published in:

Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-025-00447-x

By:

Mori, Naoko

Publication type:

Article

Addressing uncertainty in hereditary colorectal cancer: the role of a regional expert multidisciplinary team meeting.

Published in:

Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-025-00451-1

By:

Varde, Avani;
McVeigh, Terri;
Cuthill, Vicky;
Brady, Angela F.;
DeSouza, Bianca;
Latchford, Andrew;
Monahan, Kevin J.

Publication type:

Article

Healthcare provider-mediated cascade testing of Lynch syndrome to at-risk family members: an interview study.

Published in:

Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-025-00450-2

By:

Ong, Serene;
Chua, Zi Yang;
Yuen, Jeanette;
Chiang, Jianbang;
Zewen, Zhang;
Ngeow, Joanne;
Lysaght, Tamra

Publication type:

Article

A novel likely pathogenic germline variant in CDKN1B in a patient with MEN4 and medullary thyroid cancer.

Published in:

Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-025-00449-9

By:

Mercè, Fernández;
Asla, Queralt;
Illana, Francisco J.;
Victòria, Fusté;
Javier, Hernández-Losa;
Marta, Sesé;
Iglesias, Carmela;
Webb, Susan M.;
Aulinas, Anna

Publication type:

Article

CHEK2-related breast cancer: real-world challenges.

Published in:

Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-025-00448-w

By:

Weis, Luiza N.;
Bychkovsky, Brittany L.;
Hernandez, Adela Rodríguez;
Barroso-Sousa, Romualdo;
Sandoval, Renata L.

Publication type:

Article

New RPS20 gene variant in colorectal cancer diagnosis: insight from a large series of patients.

Published in:

Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-025-00446-y

By:

Amiot, Julie;
Gubeljak, Lara;
Fontaine, Agathe;
Smith, Denis;
Mortemousque, Isabelle;
Parodi, Nathalie;
Mauillon, Jacques;
Kasper, Edwige;
Baert-Desurmont, Stéphanie;
Tinat, Julie;
Houdayer, Claude

Publication type:

Article

Identification of a germline deep intronic PTEN-deletion leading to exonization through whole genome and targeted RNA sequencing.

Published in:

Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-025-00445-z

By:

Boedec, Morgane;
Aucouturier, Camille;
Cavaillé, Mathias;
Leman, Raphaël;
Castéra, Laurent;
Delhomelle, Hélène;
Uhrhammer, Nancy;
Bernard, Virginie;
Giraud, Sophie;
Lasseaux, Eulalie;
Jones, Natalie;
Bidart, Marie;
Boutry-Kryza, Nadia;
Noguès, Catherine;
Colas, Chrystelle;
Maugard, Christine;
Krieger, Sophie;
Bouras, Ahmed

Publication type:

Article

Myelodysplastic syndrome with dual germline RUNX1 and DDX41 variants: a rare genetic predisposition case.

Published in:

Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-025-00443-1

By:

Bove, Virginia;
Spangenberg, Maria Noel;
Ottati, Carolina;
Vázquez, Lucia;
Catalán, Ana I.;
Grille, Sofía

Publication type:

Article

Thirty-year compliance with a surveillance program for patients with familial adenomatous polyposis.

Published in:

Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-025-00441-3

By:

de Langavant, Boris Cleret;
Lefèvre, Jéremie H.;
Metras, Julie;
Dardenne, Antoine;
O'Connell, Lauren V.;
Collard, Maxime;
Parc, Yann

Publication type:

Article

Case review of perivascular epithelioid cell tumor occurring in patients with Li-Fraumeni syndrome.

Published in:

Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-025-00442-2

By:

Abe, Natsuno;
Yamazaki, Fumito;
Tsujikawa, Hanako;
Kasuga, Ryosuke;
Taniki, Nobuhito;
Shimada, Hiroyuki

Publication type:

Article

Correction: Outcomes of retesting in patients with previously uninformative cancer genetics evaluations.

Published in:

2025

By:

Sanoba, Shenin A.;
Koeppe, Erika S.;
Jacobs, Michelle F.;
Stoffel, Elena M.

Publication type:

Correction Notice

Progress report on multiple endocrine neoplasia type 1.

Published in:

Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-025-00440-4

By:

Halperin, Reut;
Tirosh, Amit

Publication type:

Article

Correction: Benign tumors and non-melanoma skin cancers in patients with fanconi anemia.

Published in:

2025

By:

Enache, Aura;
Sajjad, Bia;
Altintas, Burak;
Giri, Neelam;
J. McReynolds, Lisa;
W. Cowen, Edward

Publication type:

Correction Notice

The challenge of preventing gastric cancer in patients under surveillance for familial adenomatous polyposis.

Published in:

Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-024-00438-4

By:

Bouchiba, Hicham;
Aelvoet, Arthur S.;
van Grieken, Nicole C. T.;
Brosens, Lodewijk A. A.;
Bastiaansen, Barbara A. J.;
Dekker, Evelien

Publication type:

Article

Haplotype analysis detects MLH1 founder variant in Indian Lynch syndrome patient cohort.

Published in:

Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-024-00436-6

By:

Sheth, Harsh;
Sadhwani, Jyoti;
Jain, Abhinav;
Thenral, S. G.;
Ramprasad, Vedam;
Bishop, D. Timothy

Publication type:

Article

Bilateral familial retinoblastoma diagnosed via optical coherence tomography following a normal funduscopic exam.

Published in:

Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-024-00424-w

By:

Allphin, Mitchell T.;
Ramasubramanian, Aparna

Publication type:

Article

Recurrent paraneoplastic nephrotic syndrome; insights from a Lynch syndrome patient with multiple malignancies.

Published in:

Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-024-00435-7

By:

de Jong, Myrthe A.;
Slingerland, Marije;
Hawinkels, Lukas J. A. C.;
Nielsen, Maartje;
Crobach, Augustinus S. L. P.;
de Jonge-Muller, Eveline S. M.;
Rabelink, Antonius J.;
Langers, Alexandra M. J.

Publication type:

Article

Sarcomas arising in MEN1 patients: demonstrating LOH of the MEN1 locus and loss of menin expression.

Published in:

Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-024-00433-9

By:

van Leeuwaarde, Rachel S.;
Halfdanarson, Thorvardur R.;
Sudhakar, Shwetha M.;
Meijers, Ruud W. J.;
Folpe, Andrew L.;
Brosens, Lodewijk A. A.

Publication type:

Article

A family-based approach to cascade genetic testing in a pediatric cancer genetics clinic.

Published in:

Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-024-00434-8

By:

Haider, Rida;
Desrosiers-Battu, Lauren;
Scollon, Sarah;
Stankiewicz, Pawel;
Lupo, Philip J.;
Plon, Sharon E.

Publication type:

Article

Cascade genetic testing in hereditary cancer: exploring the boundaries of the Italian legal framework.

Published in:

Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-024-00430-y

By:

Varesco, Liliana;
Di Tano, Francesco;
Monducci, Juri;
Sciallero, Stefania;
Turchetti, Daniela;
Bighin, Claudia;
Buzzatti, Giulia;
Giannubilo, Irene;
Trevisan, Lucia;
Battistuzzi, Linda

Publication type:

Article

Hereditary breast and ovarian cancer genetic testing in unselected patients: example of private supplementation of public healthcare service.

Published in:

Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-024-00426-8

By:

Fiorentino, Francesca;
Innella, Giovanni;
Balducci, Federica;
Marullo, Laura;
Lanzoni, Giulia;
Miccoli, Sara;
Cardarelli, Laura;
Turchetti, Daniela;
Tempesta, Sergio

Publication type:

Article

The genetic landscape of Lynch syndrome in the Israeli population.

Published in:

Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-024-00432-w

By:

Shtaya, Aasem Abu;
Nathan, Sofia Naftaly;
Kedar, Inbal;
Friedman, Eitan;
Half, Elizabeth;
Lidzbarsky, Gabi;
Levi, Gili Reznick;
Laish, Ido;
Katz, Lior;
Bazak, Lily;
Peretz, Lilach Peled;
Salmon, Lina Basel;
Douiev, Liza;
Kalis, Marina Lifshitc;
Schechter, Menachem;
Barzily-Rokni, Michal;
Samra, Nadra Nasser;
Abu-Freha, Naim;
Hagari-Bechar, Ofir;
Segol, Ori

Publication type:

Article

Prevalence of cardiometabolic outcomes in women who underwent salpingo-oophorectomy to prevent hereditary breast and ovarian cancer: a meta-analysis.

Published in:

2025

By:

Moraes, Francisco Cezar Aquino de;
Moro, Lucca Dal;
Souza, Maria Eduarda Cavalcanti;
Rodrigues, Anna Luíza Soares de Oliveira;
Sano, Vitor Kendi Tsuchiya;
Barbosa, Bárbara Ferraz;
Pacheco, Lucas Gama;
Cunha, Daniel Ferreira;
Queiroz, Otávio Luiz de;
Souza, Dilma do Socorro Moraes de;
Feio, Danielle;
Stecca, Carlos;
Burbano, Rommel Mario Rodríguez

Publication type:

Literature Review

BRCAIndica: a resource for ACMG/AMP classified BRCA1 and BRCA2 variants.

Published in:

Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-024-00429-5

By:

Vatsyayan, Aastha;
Anu, R. I.;
Mathur, Prerika;
Uchil, Divya;
Joshi, Ashish;
Dwivedi, Aradhana;
Sirohi, Bhawna;
Mathew, Aju;
Damodaran, Dileep;
Panda, Soumya Surath;
Kolluri, Spoorthy;
Ayillath, Shaji K.;
Amalnath, Deepak;
Shankar, Gomathi;
Pandhare, Kavita;
Scaria, Vinod

Publication type:

Article

Germline pathogenic variants in RNF43 in patients with and without serrated polyposis syndrome.

Published in:

Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-024-00428-6

By:

Brinch, Heidi Hesselø;
Byrjalsen, Anna;
Lohse, Zuzana;
Rasmussen, Andreas Ørslev;
Karstensen, John Gásdal;
Kristiansen, Britta Schlott;
Jelsig, Anne Marie

Publication type:

Article

Mainstreaming cancer genetics: feasibility of an advanced nurse practitioner-led service diagnosing Lynch syndrome from colorectal cancer in Ireland.

Published in:

Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-024-00427-7

By:

Loughrey, Mechelle;
O'Connell, Lauren V.;
McSorley, Lynda;
Martin, Sean;
Hanly, Ann;
Winter, Des C.;
Frayling, Ian M.;
Sheahan, Kieran;
Kennelly, Rory

Publication type:

Article

Overlap syndrome of hereditary hemorrhagic telangiectasia and juvenile polyposis syndrome: ten years follow-up-case series and review of literature.

Published in:

2025

By:

Gonzalez, Maria Laura;
Vazquez, Carolina;
Argüero, Maria J.;
Santino, Juan P.;
Braslavsky, Ana;
Serra, Marcelo M.

Publication type:

Literature Review