Mathias Schwartz

ORCID

Publication Activity (10 Years)

Years Active: 2017-2023
Publications (10 Years): 5

Top Venues

American journal of medical genetics. Part A

European journal of human genetics : EJHG

Journal of medical genetics

Physiological genomics

This page only lists publications with an associated author ORCID identifier.

Publications

Mathias Schwartz, Sabrina Ibadioune, Albain Chansavang, Sophie Vacher, Sandrine M Caputo, Hélène Delhomelle, Jennifer Wong, Khadija Abidallah, Virginie Moncoutier, Véronique Becette, Tatiana Popova, Voreak Suybeng, Antoine De Pauw, Marc-Henri Stern, Chrystelle Colas, Emmanuelle Mouret-Fourme, Dominique Stoppat-Lyonnet, Lisa Golmard, Ivan Bieche, Julien Masliah-Planchon
Mosaic BRCA1 promoter methylation contribution in hereditary breast/ovarian cancer pedigrees. Journal of medical genetics (2023)
Mathias Schwartz
Can abnormal chromatin folding cause high-penetrance cancer predisposition? Physiological genomics 54 (10) (2022)
Mathias Schwartz, Clement Korenbaum, Meriem Benfoda, Mickael Mary, Chrystelle Colas, Florence Coulet, Melissa Parrin, Philippe Jonveaux, Olivier Ingster, Sandra Granier, Louis De Mestier, Jerome Cros, Angelique Riffault, Marie Muller, Philippe Levy, Vinciane Rebours, William Greenhalf, Nadem Soufir, Pascal Hammel
Familial pancreatic adenocarcinoma: A retrospective analysis of germline genetic testing in a French multicentre cohort. Clinical genetics 96 (6) (2019)
Stéphanie Baert-Desurmont, Sophie Coutant, Françoise Charbonnier, Pierre Macquere, François Lecoquierre, Mathias Schwartz, Maud Blanluet, Myriam Vezain, Raphaël Lanos, Olivier Quenez, Jacqueline Bou, Emilie Bouvignies, Steeve Fourneaux, Sandrine Manase, Stéphanie Vasseur, Jacques Mauillon, Marion Gerard, Régine Marlin, Gaëlle Bougeard, Julie Tinat, Thierry Frebourg, Isabelle Tournier
Optimization of the diagnosis of inherited colorectal cancer using NGS and capture of exonic and intronic sequences of panel genes. European journal of human genetics : EJHG 26 (11) (2018)
Mathias Schwartz, Damien Sternberg, Sandra Whalen, Alexandra Afenjar, Arnaud Isapof, Brigitte Chabrol, Marie-France Portnoï, Solveig Heide, Boris Keren, Sandra Chantot-Bastaraud, Jean-Pierre Siffroi
How chromosomal deletions can unmask recessive mutations? Deletions in 10q11.2 associated with CHAT or SLC18A3 mutations lead to congenital myasthenic syndrome. American journal of medical genetics. Part A 176 (1) (2017)

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Publication Activity (10 Years)

Top Topics

Top Venues

Mathias Schwartz