Ahmed Bouras

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 13

Top Topics

Pseudomonas Aeruginosa

Genome Wide Identification

Prostate Cancer

Top Venues

Human molecular genetics

Genes, chromosomes & cancer

Pediatric blood & cancer

Molecular genetics & genomic medicine

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

Publications

Ahmed Bouras, Cedrick Lefol, Eric Ruano, Chloé Grand-Masson, Jessie Auclair-Perrossier, Qing Wang
Splicing analysis of 24 potential spliceogenic variants in MMR genes and clinical interpretation based on refined ACMG/AMP criteria. Human molecular genetics 33 (10) (2024)
Ahmed Bouras, Cedrick Lefol, Eric Ruano, Chloé Grand-Masson, Jessie Auclair-Perrossier, Qing Wang
Splicing analysis of 24 potential spliceogenic variants in MMR genes and clinical interpretation based on refined ACMG/AMP criteria. Human molecular genetics (2024)
Clémentine Legrand, Magalie Peysselon, Marie Bidart, Ahmed Bouras
Germline POT1 mutation and neuroblastoma: A mere coincidence or true association. Pediatric blood & cancer (2024)
Ahmed Bouras, Cedrick Lefol, Eric Ruano, Chloé Grand-Masson, Jessie Auclair-Perrossier, Qing Wang
Splicing analysis of 24 potential spliceogenic variants in MMR genes and clinical interpretation based on refined ACMG/AMP criteria. Human molecular genetics 33 (10) (2024)
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, Cedrick Lefol, Eric Ruano, Chloé Grand-Masson, Jessie Auclair-Perrossier, Qing Wang
Splicing analysis of 24 potential spliceogenic variants in MMR genes and clinical interpretation based on refined ACMG/AMP criteria. Human molecular genetics 33 (10) (2024)
Clémentine Legrand, Magalie Peysselon, Marie Bidart, Ahmed Bouras
Germline POT1 mutation and neuroblastoma: A mere coincidence or true association. Pediatric blood & cancer 71 (7) (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, Souhir Guidara, Mélanie Leone, Adrien Buisson, Tanguy Martin-Denavit, Sophie Dussart, Christine Lasset, Sophie Giraud, Marie-Noëlle Bonnet-Dupeyron, Zine-Eddine Kherraf, Damien Sanlaville, Sandra Fert-Ferrer, Marine Lebrun, Valerie Bonadona, Alain Calender, Nadia Boutry-Kryza
Overview of the Genetic Causes of Hereditary Breast and Ovarian Cancer Syndrome in a Large French Patient Cohort. Cancers 15 (13) (2023)
Ahmed Bouras, Cyril Lafaye, Melanie Leone, Zine-Eddine Kherraf, Tanguy Martin-Denavit, Sandra Fert-Ferrer, Alain Calender, Nadia Boutry-Kryza
Identification and Characterization of an Exonic Duplication in PALB2 in a Man with Synchronous Breast and Prostate Cancer. International journal of molecular sciences 23 (2) (2022)
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)
Ahmed Bouras, Melanie Leone, Valerie Bonadona, Marine Lebrun, Alain Calender, Nadia Boutry-Kryza
Identification and Characterization of New Alu Element Insertion in the BRCA1 Exon 14 Associated with Hereditary Breast and Ovarian Cancer. Genes 12 (11) (2021)