| The very low penetrance of cystic fibrosis for the R117H mutation: a reappraisal for genetic counselling and newborn screening C Thauvin-Robinet, A Munck, F Huet, E Génin, G Bellis, E Gautier, ... Journal of medical genetics 46 (11), 752-758, 2009 | 138 | 2009 |
| Xenobiotic metabolism and disposition in human lung cell models: comparison with in vivo expression profiles E Courcot, J Leclerc, JJ Lafitte, E Mensier, S Jaillard, P Gosset, P Shirali, ... Drug Metabolism and Disposition 40 (10), 1953-1965, 2012 | 101 | 2012 |
| Diagnosis of constitutional mismatch repair-deficiency syndrome based on microsatellite instability and lymphocyte tolerance to methylating agents S Bodo, C Colas, O Buhard, A Collura, J Tinat, N Lavoine, A Guilloux, ... Gastroenterology 149 (4), 1017-1029. e3, 2015 | 100 | 2015 |
| Profiling gene expression of whole cytochrome P450 superfamily in human bronchial and peripheral lung tissues: Differential expression in non-small cell lung cancers J Leclerc, G Tournel, ECN Ngangue, N Pottier, JJ Lafitte, S Jaillard, ... Biochimie 92 (3), 292-306, 2010 | 76 | 2010 |
| Diagnosis of Lynch syndrome and strategies to distinguish Lynch-related tumors from sporadic MSI/dMMR tumors J Leclerc, C Vermaut, MP Buisine Cancers 13 (3), 467, 2021 | 69 | 2021 |
| Genome-wide somatic copy number alterations in low-grade PanINs and IPMNs from individuals with a family history of pancreatic cancer SM Hong, A Vincent, M Kanda, J Leclerc, N Omura, M Borges, AP Klein, ... Clinical Cancer Research 18 (16), 4303-4312, 2012 | 68 | 2012 |
| Messenger RNA life-cycle in cancer cells: emerging role of conventional and non-conventional RNA-binding proteins? L Coppin, J Leclerc, A Vincent, N Porchet, P Pigny International journal of molecular sciences 19 (3), 650, 2018 | 64 | 2018 |
| Evaluation of a new panel of six mononucleotide repeat markers for the detection of DNA mismatch repair-deficient tumours A Pagin, F Zerimech, J Leclerc, A Wacrenier, S Lejeune, ... British journal of cancer 108 (10), 2079-2087, 2013 | 62 | 2013 |
| Xenobiotic metabolism and disposition in human lung: transcript profiling in non-tumoral and tumoral tissues J Leclerc, ECN Ngangue, C Cauffiez, D Allorge, N Pottier, JJ Lafitte, ... Biochimie 93 (6), 1012-1027, 2011 | 54 | 2011 |
| The serrated neoplasia pathway of colorectal tumors: Identification of MUC5AC hypomethylation as an early marker of polyps with malignant potential F Renaud, C Mariette, A Vincent, A Wacrenier, V Maunoury, J Leclerc, ... International journal of cancer 138 (6), 1472-1481, 2016 | 35 | 2016 |
| CFTR p. Arg117His associated with CBAVD and other CFTR-related disorders C Thauvin-Robinet, A Munck, F Huet, A De Becdelièvre, C Jimenez, ... Journal of medical genetics 50 (4), 220-227, 2013 | 34 | 2013 |
| Diversity of genetic events associated with MLH1 promoter methylation in Lynch syndrome families with heritable constitutional epimutation J Leclerc, C Flament, T Lovecchio, L Delattre, EA Yahya, ... Genetics in Medicine 20 (12), 1589-1599, 2018 | 32 | 2018 |
| High cyclin E staining index in blastemal, stromal or epithelial cells is correlated with tumor aggressiveness in patients with nephroblastoma D Berrebi, J Leclerc, G Schleiermacher, I Zaccaria, L Boccon-Gibod, ... PLoS One 3 (5), e2216, 2008 | 30 | 2008 |
| Colon cancer stemness as a reversible epigenetic state: Implications for anticancer therapies A Vincent, A Ouelkdite-Oumouchal, M Souidi, J Leclerc, B Neve, ... World Journal of Stem Cells 11 (11), 920, 2019 | 26 | 2019 |
| Hereditary predisposition to cancers of the digestive tract, breast, gynecological and gonadal: Focus on the Peutz-Jeghers A Turpin, S Cattan, J Leclerc, A Wacrenier, S Manouvrier-Hanu, ... Bulletin du Cancer 101 (9), 813-822, 2014 | 26 | 2014 |
| Optimization of next-generation sequencing technologies for von Hippel Lindau (VHL) mosaic mutation detection and development of confirmation methods L Coppin, P Plouvier, M Crépin, AS Jourdain, EA Yahya, S Richard, ... The Journal of Molecular Diagnostics 21 (3), 462-470, 2019 | 21 | 2019 |
| IMPDH2 Genetic Polymorphism: A Promoter Single-Nucleotide Polymorphism Disrupts a Cyclic Adenosine Monophosphate Responsive Element A Garat, C Cauffiez, R Hamdan-Khalil, F Glowacki, A Devos, J Leclerc, ... Genetic Testing and Molecular Biomarkers 13 (6), 841-847, 2009 | 18 | 2009 |
| CYP2F1 genetic polymorphism: identification of interethnic variations G Tournel, C Cauffiez, J Leclerc, I Billaut-Laden, D Allorge, D Chevalier, ... Xenobiotica 37 (12), 1433-1438, 2007 | 18 | 2007 |
| Alu element insertion in the MLH1 exon 6 coding sequence as a mutation predisposing to Lynch syndrome J Solassol, M Larrieux, J Leclerc, V Ducros, C Corsini, J Chiésa, P Pujol, ... Human Mutation 40 (6), 716-720, 2019 | 17 | 2019 |
| Characterisation of heterozygous PMS2 variants in French patients with Lynch syndrome Q Wang, J Leclerc, G Bougeard, S Olschwang, S Vasseur, K Cassinari, ... Journal of Medical Genetics 57 (7), 487-499, 2020 | 11 | 2020 |
