Búsqueda | BVS CLAP/SMR-OPS/OMS

1.

TP53_PROF: a machine learning model to predict impact of missense mutations in TP53.

Ben-Cohen, Gil; Doffe, Flora; Devir, Michal; Leroy, Bernard; Soussi, Thierry; Rosenberg, Shai.

Brief Bioinform ; 23(2)2022 03 10.

Artículo en Inglés | MEDLINE | ID: mdl-35043155

2.

Pediatric Cancer Variant Pathogenicity Information Exchange (PeCanPIE): a cloud-based platform for curating and classifying germline variants.

Edmonson, Michael N; Patel, Aman N; Hedges, Dale J; Wang, Zhaoming; Rampersaud, Evadnie; Kesserwan, Chimene A; Zhou, Xin; Liu, Yanling; Newman, Scott; Rusch, Michael C; McLeod, Clay L; Wilkinson, Mark R; Rice, Stephen V; Soussi, Thierry; Taylor, J Paul; Benatar, Michael; Becksfort, Jared B; Nichols, Kim E; Robison, Leslie L; Downing, James R; Zhang, Jinghui.

Genome Res ; 29(9): 1555-1565, 2019 09.

Artículo en Inglés | MEDLINE | ID: mdl-31439692

3.

Letter to the editor.

Soussi, Thierry.

Hum Mol Genet ; 32(13): 2121-2123, 2023 Jun 19.

Artículo en Inglés | MEDLINE | ID: mdl-36897275

4.

High prevalence of cancer-associated TP53 variants in the gnomAD database: A word of caution concerning the use of variant filtering.

Soussi, Thierry; Leroy, Bernard; Devir, Michal; Rosenberg, Shai.

Hum Mutat ; 40(5): 516-524, 2019 05.

Artículo en Inglés | MEDLINE | ID: mdl-30720243

5.

Seshat: A Web service for accurate annotation, validation, and analysis of TP53 variants generated by conventional and next-generation sequencing.

Tikkanen, Tuomas; Leroy, Bernard; Fournier, Jean Louis; Risques, Rosa Ana; Malcikova, Jitka; Soussi, Thierry.

Hum Mutat ; 39(7): 925-933, 2018 07.

Artículo en Inglés | MEDLINE | ID: mdl-29696732

6.

Synonymous Somatic Variants in Human Cancer Are Not Infamous: A Plea for Full Disclosure in Databases and Publications.

Soussi, Thierry; Taschner, Peter E M; Samuels, Yardena.

Hum Mutat ; 38(4): 339-342, 2017 04.

Artículo en Inglés | MEDLINE | ID: mdl-28026089

7.

TP53 mutations at codon 234 are associated with chlorambucil treatment in chronic lymphocytic leukemia.

Lazarian, Grégory; Theves, Floriane; Hormi, Myriam; Letestu, Rémi; Eclache, Virginie; Bidet, Audrey; Cornillet-Lefebvre, Pascale; Davi, Frédéric; Delabesse, Eric; Estienne, Marie-Hélène; Etancelin, Pascaline; Kosmider, Olivier; Laibe, Sophy; Lode, Laurence; Muller, Marc; Nadal, Nathalie; Naguib, Dina; Pastoret, Cédric; Poulain, Stéphanie; Sujobert, Pierre; Veronese, Lauren; Imache, Samia; Lefebvre, Valérie; Cymbalista, Florence; Baran-Marszak, Fanny; Soussi, Thierry.

Am J Hematol ; 97(4): E159-E162, 2022 04.

Artículo en Inglés | MEDLINE | ID: mdl-35083778

8.

TP53 mutations are early events in chronic lymphocytic leukemia disease progression and precede evolution to complex karyotypes.

Lazarian, Gregory; Tausch, Eugen; Eclache, Virginie; Sebaa, Amel; Bianchi, Vincent; Letestu, Remi; Collon, Jean-Francois; Lefebvre, Valerie; Gardano, Laura; Varin-Blank, Nadine; Soussi, Thierry; Stilgenbauer, Stephen; Cymbalista, Florence; Baran-Marszak, Fanny.

Int J Cancer ; 139(8): 1759-63, 2016 10 15.

Artículo en Inglés | MEDLINE | ID: mdl-27270786

9.

Prevalence, distribution and predictive value of XPO1 mutation in a real-life chronic lymphocytic leukaemia cohort.

Tueur, Giulia; Lazarian, Gregory; Eclache, Virginie; Fleury, Carole; Letestu, Rémi; Lévy, Vincent; Lefebvre, Valérie; Collon, Jean-Francois; Zini, Jean-Marc; Thieblemont, Catherine; Soussi, Thierry; Cymbalista, Florence; Baran-Marszak, Fanny.

Br J Haematol ; 191(3): e90-e94, 2020 11.

Artículo en Inglés | MEDLINE | ID: mdl-32790071

10.

Shaping genetic alterations in human cancer: the p53 mutation paradigm.

Soussi, Thierry; Wiman, Klas G.

Cancer Cell ; 12(4): 303-12, 2007 Oct.

Artículo en Inglés | MEDLINE | ID: mdl-17936556

11.

Locus-specific mutation databases: pitfalls and good practice based on the p53 experience.

Soussi, Thierry; Ishioka, Chikashi; Claustres, Mireille; Béroud, Christophe.

Nat Rev Cancer ; 6(1): 83-90, 2006 01.

Artículo en Inglés | MEDLINE | ID: mdl-16397528

12.

The TP53 website: an integrative resource centre for the TP53 mutation database and TP53 mutant analysis.

Leroy, Bernard; Fournier, Jean Louis; Ishioka, Chikashi; Monti, Paola; Inga, Alberto; Fronza, Gilberto; Soussi, Thierry.

Nucleic Acids Res ; 41(Database issue): D962-9, 2013 Jan.

Artículo en Inglés | MEDLINE | ID: mdl-23161690

13.

Data-driven unbiased curation of the TP53 tumor suppressor gene mutation database and validation by ultradeep sequencing of human tumors.

Edlund, Karolina; Larsson, Ola; Ameur, Adam; Bunikis, Ignas; Gyllensten, Ulf; Leroy, Bernard; Sundström, Magnus; Micke, Patrick; Botling, Johan; Soussi, Thierry.

Proc Natl Acad Sci U S A ; 109(24): 9551-6, 2012 Jun 12.

Artículo en Inglés | MEDLINE | ID: mdl-22628563

14.

The TP53 gene network in a postgenomic era.

Soussi, Thierry.

Hum Mutat ; 35(6): 641-2, 2014 Jun.

Artículo en Inglés | MEDLINE | ID: mdl-24753184

15.

Locus-specific databases in cancer: what future in a post-genomic era? The TP53 LSDB paradigm.

Soussi, Thierry.

Hum Mutat ; 35(6): 643-53, 2014 Jun.

Artículo en Inglés | MEDLINE | ID: mdl-24478183

16.

TP53 mutations in human cancer: database reassessment and prospects for the next decade.

Leroy, Bernard; Anderson, Martha; Soussi, Thierry.

Hum Mutat ; 35(6): 672-88, 2014 Jun.

Artículo en Inglés | MEDLINE | ID: mdl-24665023

17.

Recommendations for analyzing and reporting TP53 gene variants in the high-throughput sequencing era.

Soussi, Thierry; Leroy, Bernard; Taschner, Peter E M.

Hum Mutat ; 35(6): 766-78, 2014 Jun.

Artículo en Inglés | MEDLINE | ID: mdl-24729566

18.

Analysis of TP53 mutation status in human cancer cell lines: a reassessment.

Leroy, Bernard; Girard, Luc; Hollestelle, Antoinette; Minna, John D; Gazdar, Adi F; Soussi, Thierry.

Hum Mutat ; 35(6): 756-65, 2014 Jun.

Artículo en Inglés | MEDLINE | ID: mdl-24700732

19.

ERIC recommendations for TP53 mutation analysis in chronic lymphocytic leukemia-2024 update.

Malcikova, Jitka; Pavlova, Sarka; Baliakas, Panagiotis; Chatzikonstantinou, Thomas; Tausch, Eugen; Catherwood, Mark; Rossi, Davide; Soussi, Thierry; Tichy, Boris; Kater, Arnon P; Niemann, Carsten U; Davi, Frederic; Gaidano, Gianluca; Stilgenbauer, Stephan; Rosenquist, Richard; Stamatopoulos, Kostas; Ghia, Paolo; Pospisilova, Sarka.

Leukemia ; 2024 May 16.

Artículo en Inglés | MEDLINE | ID: mdl-38755420

20.

Single-molecule DNA sequencing of acute myeloid leukemia and myelodysplastic syndromes with multiple TP53 alterations.

Lodé, Laurence; Ameur, Adam; Coste, Thibault; Ménard, Audrey; Richebourg, Steven; Gaillard, Jean-Baptiste; Le Bris, Yannick; Béné, Marie-Christine; Lavabre-Bertrand, Thierry; Soussi, Thierry.

Haematologica ; 103(1): e13-e16, 2018 01.

Artículo en Inglés | MEDLINE | ID: mdl-29079597

BVS CLAP/SMR-OPS/OMS

Centro Latinoamericano de Perinatología, Salud de la Mujer y Reproductiva

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TP53_PROF: a machine learning model to predict impact of missense mutations in TP53.

Pediatric Cancer Variant Pathogenicity Information Exchange (PeCanPIE): a cloud-based platform for curating and classifying germline variants.

Letter to the editor.

High prevalence of cancer-associated TP53 variants in the gnomAD database: A word of caution concerning the use of variant filtering.

Seshat: A Web service for accurate annotation, validation, and analysis of TP53 variants generated by conventional and next-generation sequencing.

Synonymous Somatic Variants in Human Cancer Are Not Infamous: A Plea for Full Disclosure in Databases and Publications.

TP53 mutations at codon 234 are associated with chlorambucil treatment in chronic lymphocytic leukemia.

TP53 mutations are early events in chronic lymphocytic leukemia disease progression and precede evolution to complex karyotypes.

Prevalence, distribution and predictive value of XPO1 mutation in a real-life chronic lymphocytic leukaemia cohort.

Shaping genetic alterations in human cancer: the p53 mutation paradigm.

Locus-specific mutation databases: pitfalls and good practice based on the p53 experience.

The TP53 website: an integrative resource centre for the TP53 mutation database and TP53 mutant analysis.

Data-driven unbiased curation of the TP53 tumor suppressor gene mutation database and validation by ultradeep sequencing of human tumors.

The TP53 gene network in a postgenomic era.

Locus-specific databases in cancer: what future in a post-genomic era? The TP53 LSDB paradigm.

TP53 mutations in human cancer: database reassessment and prospects for the next decade.

Recommendations for analyzing and reporting TP53 gene variants in the high-throughput sequencing era.

Analysis of TP53 mutation status in human cancer cell lines: a reassessment.

ERIC recommendations for TP53 mutation analysis in chronic lymphocytic leukemia-2024 update.

Single-molecule DNA sequencing of acute myeloid leukemia and myelodysplastic syndromes with multiple TP53 alterations.