Mathias Schwartz

6PUBLICATIONS
14CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)MechanobiologyCancer geneticsGene expression (incl. microarray and other genome-wide approaches)
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Publications (6)

|Aug 12, 2026
Simultaneous single-cell profiling of chromatin, transcriptome and surface markers with OneCell CUT&Tag captures epigenomic reprogramming.

|Sep 25, 2023
Mosaic BRCA1 promoter methylation contribution in hereditary breast/ovarian cancer pedigrees.

Mathias Schwartz, Sabrina Ibadioune, Albain Chansavang

|Aug 29, 2022
Can abnormal chromatin folding cause high-penetrance cancer predisposition?

Mathias Schwartz

|Aug 22, 2019
Familial pancreatic adenocarcinoma: A retrospective analysis of germline genetic testing in a French multicentre cohort.

Mathias Schwartz, Clement Korenbaum, Meriem Benfoda

|Jul 04, 2018
Optimization of the diagnosis of inherited colorectal cancer using NGS and capture of exonic and intronic sequences of panel genes.

Stéphanie Baert-Desurmont, Sophie Coutant, Françoise Charbonnier

|Nov 14, 2017
How chromosomal deletions can unmask recessive mutations? Deletions in 10q11.2 associated with CHAT or SLC18A3 mutations lead to congenital myasthenic syndrome.

Mathias Schwartz, Damien Sternberg, Sandra Whalen

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Frequent Collaborators

1 joint publications

Sandrine M Caputo

1 joint publications

Chrystelle Colas

1 joint publications

Dominique Stoppa-Lyonnet

1 joint publications

Lisa Golmard