Qing Wang

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 7

Top Topics

Dna Methylation

Top Venues

Genes, chromosomes & cancer

Molecular genetics & genomic medicine

JCO precision oncology

European journal of human genetics : EJHG

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

Publications

Ahmed Bouras, Aurélie Fabre, Hélène Zattara, Sandrine Handallou, Françoise Desseigne, Caroline Kientz, Fabienne Prieur, Magalie Peysselon, Clémentine Legrand, Laura Calavas, Jean-Christophe Saurin, Qing Wang
Hereditary Colorectal Cancer and Polyposis Syndromes Caused by Variants in Uncommon Genes. Genes, chromosomes & cancer 63 (8) (2024)
Ahmed Bouras, Clementine Legrand, Jihen Kourda, Eric Ruano, Chloé Grand-Masson, Cedrick Lefol, Qing Wang
From variant of unknown significance to likely pathogenic: Characterization and pathogenicity determination of a large genomic deletion in the MLH1 gene. Molecular genetics & genomic medicine (2023)
Ahmed Bouras, Cedrick Lefol, Eric Ruano, Chloé Grand-Masson, Qing Wang
PMS2 or PMS2CL? Characterization of variants detected in the 3' of the PMS2 gene. Genes, chromosomes & cancer (2023)
Ahmed Bouras, Pierre Naibo, Clémentine Legrand, François Le Marc'hadour, Eric Ruano, Chloé Grand-Masson, Cedrick Lefol, Qing Wang
A PMS2 non-canonical splicing site variant leads to aberrant splicing in a patient suspected for lynch syndrome. Familial cancer (2022)
Xiaolan Feng, Haocheng Li, Joanna Fourquet, Mehdi Brahmi, Armelle Dufresne, Alexandra Meurgey, Isabelle L Ray-Coquard, Qing Wang, Julien Bollard, Francoise Ducimetiere, Frederic Chibon, Jean Yves Blay
Refining Prognosis in Localized Gastrointestinal Stromal Tumor: Clinical Significance of Phosphatase and Tensin Homolog Low Expression and Gene Loss. JCO precision oncology 6 (2022)
Qing Wang, Julie Leclerc, Gaëlle Bougeard, Sylviane Olschwang, Stéphanie Vasseur, Kévin Cassinari, Denis Boidin, Cédrick Lefol, Pierre Naïbo, Thierry Frébourg, Marie Pierre Buisine, Stéphanie Baert-Desurmont, null null
Characterisation of heterozygous PMS2 variants in French patients with Lynch syndrome. Journal of medical genetics 57 (7) (2020)
Cedrick Lefol, Emilie Sohier, Christian Baudet, Pierre Naïbo, Eric Ruano, Chloé Grand-Masson, Alain Viari, Qing Wang
Acquired somatic MMR deficiency is a major cause of MSI tumor in patients suspected for "Lynch-like syndrome" including young patients. European journal of human genetics : EJHG 29 (3) (2020)