| 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 | 297 | 2014 |
| Screening BRCA1 and BRCA2 unclassified variants for splicing mutations using reverse transcription PCR on patient RNA and an ex vivo assay based on a splicing reporter minigene C Bonnet, S Krieger, M Vezain, A Rousselin, I Tournier, A Martins, ... Journal of medical genetics 45 (7), 438-446, 2008 | 137 | 2008 |
| 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 | 103 | 2011 |
| Novel diagnostic tool for prediction of variant spliceogenicity derived from a set of 395 combined in silico/in vitro studies: an international collaborative effort R Leman, P Gaildrat, G Le Gac, C Ka, Y Fichou, MP Audrezet, ... Nucleic acids research 46 (15), 7913-7923, 2018 | 97 | 2018 |
| 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 | 85 | 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 | 59 | 2017 |
| The BRCA1 c. 5434C→ G (p. Pro1812Ala) variant induces a deleterious exon 23 skipping by affecting exonic splicing regulatory elements P Gaildrat, S Krieger, JC Thery, A Killian, A Rousselin, P Berthet, ... Journal of medical genetics 47 (6), 398-403, 2010 | 54 | 2010 |
| The BRCA1 c. 5434C→ G (p. Pro1812Ala) variant induces a deleterious exon 23 skipping by affecting exonic splicing regulatory elements P Gaildrat, S Krieger, JC Thery, A Killian, A Rousselin, P Berthet, ... Journal of medical genetics 47 (6), 398-403, 2010 | 54 | 2010 |
| 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 | 44 | 2015 |
| 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 | 29 | 2016 |
| Patterns of care and the survival of elderly patients with high-risk endometrial cancer: A case-control study from the FRANCOGYN group A Rousselin, S Bendifallah, KN Timoh, L Ouldamer, G Canlorbe, ... European Journal of Surgical Oncology 43 (11), 2135-2142, 2017 | 11 | 2017 |
| Ultrasound presentation of a disseminated fetal and neonatal rhabdoid tumor Y Joueidi, A Rousselin, C Rozel, P Loget, D Ranchere Vince, S Odent, ... Case Reports in Obstetrics and Gynecology 2018, 2018 | 5 | 2018 |
| SpliceLauncher: a tool for detection, annotation and relative quantification of alternative junctions from RNAseq data R Leman, V Harter, A Atkinson, G Davy, A Rousselin, E Muller, L Castéra, ... Bioinformatics 36 (5), 1634-1636, 2020 | 4 | 2020 |
| Pap smear before 25 years old A Rousselin, L Dion, A Racin, V Lavoué, J Levêque Gynecologie, Obstetrique, Fertilite & Senologie 45 (5), 309-315, 2017 | 3 | 2017 |
| La pratique du frottis cervico-vaginal avant 25 ans A Rousselin, L Dion, A Racin, V Lavoué, J Levêque, KN Timoh Gynécologie Obstétrique Fertilité & Sénologie 45 (5), 309-315, 2017 | 3 | 2017 |
| Can new molecular profiles in epithelial ovarian cancer modify therapeutics? V Lavoue, A Rousselin, S Delplanque, M Pinsard, S Henno, F Foucher, ... Journal of Gynecology Obstetrics and Human Reproduction 46 (2), 107-112, 2017 | 2 | 2017 |
| Hicks and Richardson on industrial change: analysis and policy M Amendola, S Bruno, JL Gaffard Innovation, Economic Growth and the Firm, 2010 | 2 | 2010 |
| Erratum: Novel diagnostic tool for prediction of variant spliceogenicity derived from a set of 395 combined in silico/in vitro studies: An international collaborative effort … R Leman, P Gaildrat, G Le Gac, C Ka, Y Fichou, MP Audrezet, ... | | 2020 |
| Landscape of pathogenic variations in a panel of 34 genes in 5131 HBOC families and cancer risk estimation L Castera, V Harter, S Krieger, N Goardon, A Ricou, A Rousselin, ... EUROPEAN JOURNAL OF HUMAN GENETICS 26, 513-514, 2018 | | 2018 |
| Novel diagnostic guidelines for prediction of variant spliceogenicity derived from a set of 311 combined in silico and in vitro studies: an international collaborative effort S Krieger, R Leman, P Gaildrat, M Parsons, N Boutry-Kryza, ... Eur. J. Hum. Genet. 26, 72-74, 2018 | | 2018 |
