| Human Splicing Finder: an online bioinformatics tool to predict splicing signals FO Desmet, D Hamroun, M Lalande, G Collod-Béroud, M Claustres, ... Nucleic acids research 37 (9), e67-e67, 2009 | 2900 | 2009 |
| Assessing TP53 status in human tumours to evaluate clinical outcome T Soussi, C Béroud Nature Reviews Cancer 1 (3), 233-239, 2001 | 932 | 2001 |
| The TREAT‐NMD DMD Global Database: analysis of more than 7,000 Duchenne muscular dystrophy mutations CL Bladen, D Salgado, S Monges, ME Foncuberta, K Kekou, K Kosma, ... Human mutation 36 (4), 395-402, 2015 | 803 | 2015 |
| Effect of mutation type and location on clinical outcome in 1,013 probands with Marfan syndrome or related phenotypes and FBN1 mutations: an international study L Faivre, G Collod-Beroud, BL Loeys, A Child, C Binquet, E Gautier, ... The American Journal of Human Genetics 81 (3), 454-466, 2007 | 635 | 2007 |
| Low mitochondrial respiratory chain content correlates with tumor aggressiveness in renal cell carcinoma H Simonnet, N Alazard, K Pfeiffer, C Gallou, C Béroud, J Demont, ... Carcinogenesis 23 (5), 759-768, 2002 | 454 | 2002 |
| Update of the UMD‐FBN1 mutation database and creation of an FBN1 polymorphism database G Collod‐Béroud, S Le Bourdelles, L Ades, L Ala‐Kokko, P Booms, ... Human mutation 22 (3), 199-208, 2003 | 426 | 2003 |
| Genotype–phenotype analysis in 2,405 patients with a dystrophinopathy using the UMD–DMD database: a model of nationwide knowledgebase S Tuffery‐Giraud, C Béroud, F Leturcq, RB Yaou, D Hamroun, ... Human mutation 30 (6), 934-945, 2009 | 424 | 2009 |
| APC gene: database of germline and somatic mutations in human tumors and cell lines C Béroud, T Soussi Nucleic acids research 24 (1), 121-124, 1996 | 412 | 1996 |
| p53 website and analysis of p53 gene mutations in human cancer: forging a link between epidemiology and carcinogenesis T Soussi, K Dehouche, C Béroud Human mutation 15 (1), 105-113, 2000 | 384 | 2000 |
| Diagnostic approach to the congenital muscular dystrophies CG Bönnemann, CH Wang, S Quijano-Roy, N Deconinck, E Bertini, ... Neuromuscular disorders 24 (4), 289-311, 2014 | 367 | 2014 |
| Impact of cytomorphological detection of circulating tumor cells in patients with liver cancer G Vona, L Estepa, C Béroud, D Damotte, F Capron, B Nalpas, A Mineur, ... Hepatology 39 (3), 792-797, 2004 | 290 | 2004 |
| Comparison of Clinical Presentations and Outcomes Between Patients With TGFBR2 and FBN1 Mutations in Marfan Syndrome and Related Disorders D Attias, C Stheneur, C Roy, G Collod-Béroud, D Detaint, L Faivre, ... Circulation 120 (25), 2541-2549, 2009 | 285 | 2009 |
| Consensus statement on standard of care for congenital muscular dystrophies CH Wang, CG Bonnemann, A Rutkowski, T Sejersen, J Bellini, V Battista, ... Journal of child neurology 25 (12), 1559-1581, 2010 | 258 | 2010 |
| UMD (Universal mutation database): a generic software to build and analyze locus‐specific databases C Béroud, G Collod‐Béroud, C Boileau, T Soussi, C Junien Human mutation 15 (1), 86-94, 2000 | 248 | 2000 |
| p53 gene mutation: software and database C Béroud, T Soussi Nucleic acids research 26 (1), 200-204, 1998 | 247 | 1998 |
| Multiexon skipping leading to an artificial DMD protein lacking amino acids from exons 45 through 55 could rescue up to 63% of patients with Duchenne muscular dystrophy C Béroud, S Tuffery‐Giraud, M Matsuo, D Hamroun, V Humbertclaude, ... Human mutation 28 (2), 196-202, 2007 | 245 | 2007 |
| Aortic event rate in the Marfan population: a cohort study G Jondeau, D Detaint, F Tubach, F Arnoult, O Milleron, F Raoux, ... Circulation 125 (2), 226-232, 2012 | 240 | 2012 |
| APC gene: database of germline and somatic mutations in human tumors and cell lines P Laurent-Puig, C Béroud, T Soussi Nucleic acids research 26 (1), 269-270, 1998 | 229 | 1998 |
| Cardiovascular manifestations in men and women carrying a FBN1 mutation D Détaint, L Faivre, G Collod-Beroud, AH Child, BL Loeys, C Binquet, ... European heart journal 31 (18), 2223-2229, 2010 | 222 | 2010 |
| The UMD‐p53 database: new mutations and analysis tools C Béroud, T Soussi Human mutation 21 (3), 176-181, 2003 | 217 | 2003 |
