| Stereotyped patterns of somatic hypermutation in subsets of patients with chronic lymphocytic leukemia: implications for the role of antigen selection in leukemogenesis F Murray, N Darzentas, A Hadzidimitriou, G Tobin, M Boudjogra, ... Blood, The Journal of the American Society of Hematology 111 (3), 1524-1533, 2008 | 422 | 2008 |
| Next-generation sequencing for the diagnosis of hereditary breast and ovarian cancer using genomic capture targeting multiple candidate genes L Castéra, S Krieger, A Rousselin, A Legros, JJ Baumann, O Bruet, ... European Journal of Human Genetics 22 (11), 1305-1313, 2014 | 304 | 2014 |
| Contribution of bioinformatics predictions and functional splicing assays to the interpretation of unclassified variants of the BRCA genes JC Théry, S Krieger, P Gaildrat, F Révillion, MP Buisine, A Killian, ... European Journal of Human Genetics 19 (10), 1052-1058, 2011 | 105 | 2011 |
| Postablation 131I scintigraphy with neck and thorax SPECT–CT and stimulated serum thyroglobulin level predict the outcome of patients with differentiated thyroid … R Ciappuccini, N Heutte, G Trzepla, JP Rame, D Vaur, N Aide, S Bardet European journal of endocrinology 164 (6), 961-969, 2011 | 97 | 2011 |
| Landscape of pathogenic variations in a panel of 34 genes and cancer risk estimation from 5131 HBOC families L Castéra, V Harter, E Muller, S Krieger, N Goardon, A Ricou, A Rousselin, ... Genetics in Medicine 20 (12), 1677-1686, 2018 | 94 | 2018 |
| BRCA share: a collection of clinical BRCA gene variants C Béroud, SI Letovsky, CD Braastad, SM Caputo, O Beaudoux, YJ Bignon, ... Human Mutation 37 (12), 1318-1328, 2016 | 71 | 2016 |
| Prognosis of Binet stage A chronic lymphocytic leukemia patients: the strength of routine parameters R Letestu, V Lévy, V Eclache, F Baran-Marszak, D Vaur, D Naguib, ... Blood, The Journal of the American Society of Hematology 116 (22), 4588-4590, 2010 | 69 | 2010 |
| Guidelines for reporting secondary findings of genome sequencing in cancer genes: the SFMPP recommendations P Pujol, P Vande Perre, L Faivre, D Sanlaville, C Corsini, B Baertschi, ... European Journal of Human Genetics 26 (12), 1732-1742, 2018 | 66 | 2018 |
| Detecting splicing patterns in genes involved in hereditary breast and ovarian cancer G Davy, A Rousselin, N Goardon, L Castéra, V Harter, A Legros, E Muller, ... European Journal of Human Genetics 25 (10), 1147-1154, 2017 | 61 | 2017 |
| Stimulated thyroglobulin level at ablation in differentiated thyroid cancer: the impact of treatment preparation modalities and tumor burden R Ciappuccini, J Hardouin, N Heutte, D Vaur, E Quak, JP Rame, ... European journal of endocrinology 171 (2), 247-252, 2014 | 61 | 2014 |
| Multiple sequence variants of BRCA2 exon 7 alter splicing regulation P Gaildrat, S Krieger, D Di Giacomo, J Abdat, F Révillion, S Caputo, ... Journal of medical genetics 49 (10), 609-617, 2012 | 55 | 2012 |
| Prognostic value of microscopic lymph node involvement in patients with papillary thyroid cancer S Bardet, R Ciappuccini, E Quak, JP Rame, D Blanchard, D de Raucourt, ... The Journal of Clinical Endocrinology & Metabolism 100 (1), 132-140, 2015 | 50 | 2015 |
| XAF1 as a modifier of p53 function and cancer susceptibility EM Pinto, BC Figueiredo, W Chen, HCR Galvao, MN Formiga, ... Science advances 6 (26), eaba3231, 2020 | 49 | 2020 |
| Contribution of germline deleterious variants in the RAD51 paralogs to breast and ovarian cancers L Golmard, L Castéra, S Krieger, V Moncoutier, K Abidallah, H Tenreiro, ... European Journal of Human Genetics 25 (12), 1345-1353, 2017 | 49 | 2017 |
| Genetic profiles of cervical tumors by high‐throughput sequencing for personalized medical care E Muller, B Brault, A Holmes, A Legros, E Jeannot, M Campitelli, ... Cancer medicine 4 (10), 1484-1493, 2015 | 45 | 2015 |
| Assessment of branch point prediction tools to predict physiological branch points and their alteration by variants R Leman, H Tubeuf, S Raad, I Tournier, C Derambure, R Lanos, ... BMC genomics 21, 1-12, 2020 | 44 | 2020 |
| SPiP: Splicing Prediction Pipeline, a machine learning tool for massive detection of exonic and intronic variant effects on mRNA splicing R Leman, B Parfait, D Vidaud, E Girodon, L Pacot, G Le Gac, C Ka, ... Human Mutation 43 (12), 2308-2323, 2022 | 39 | 2022 |
| The French Genetic and Cancer Consortium guidelines for multigene panel analysis in hereditary breast and ovarian cancer predisposition J Moretta, P Berthet, V Bonadona, O Caron, O Cohen-Haguenauer, ... Bulletin du cancer 105 (10), 907-917, 2018 | 32 | 2018 |
| Germline Mutations of Inhibins in Early‐Onset Ovarian Epithelial Tumors I Tournier, R Marlin, K Walton, F Charbonnier, S Coutant, JC Théry, ... Human Mutation 35 (3), 294-297, 2014 | 32 | 2014 |
| OutLyzer: software for extracting low-allele-frequency tumor mutations from sequencing background noise in clinical practice E Muller, N Goardon, B Brault, A Rousselin, G Paimparay, A Legros, ... Oncotarget 7 (48), 79485, 2016 | 31 | 2016 |
Antoine RousselinBioinformaticien, Centre Francois Baclesse, Consortium Normand de Séquençage, Plateforme SéSAME在 baclesse.unicancer.fr 的电子邮件经过验证
