| Transcription factors: specific DNA binding and specific gene regulation AL Todeschini, A Georges, RA Veitia Trends in genetics 30 (6), 211-219, 2014 | 204 | 2014 |
| Association of the PHACTR1/EDN1 Genetic Locus With Spontaneous Coronary Artery Dissection D Adlam, TM Olson, N Combaret, JC Kovacic, SE Iismaa, A Al-Hussaini, ... Journal of the American College of Cardiology 73 (1), 58-66, 2019 | 186 | 2019 |
| FOXL2: a central transcription factor of the ovary A Georges, A Auguste, L Bessiere, A Vanet, AL Todeschini, RA Veitia Journal of molecular endocrinology 52 (1), R17-R33, 2014 | 183 | 2014 |
| Kinesin's cover-neck bundle folds forward to generate force AS Khalil, DC Appleyard, AK Labno, A Georges, M Karplus, AM Belcher, ... Proceedings of the National Academy of Sciences 105 (49), 19247-19252, 2008 | 166 | 2008 |
| Transcription factor FOXL2 protects granulosa cells from stress and delays cell cycle: role of its regulation by the SIRT1 deacetylase BA Benayoun, AB Georges, D L'Hôte, N Andersson, A Dipietromaria, ... Human molecular genetics 20 (9), 1673-1686, 2011 | 107 | 2011 |
| Generic binding sites, generic DNA‐binding domains: where does specific promoter recognition come from? AB Georges, BA Benayoun, S Caburet, RA Veitia The FASEB Journal 24 (2), 346-356, 2010 | 107 | 2010 |
| The transcription factor FOXL2 mobilizes estrogen signaling to maintain the identity of ovarian granulosa cells A Georges, D L'Hôte, AL Todeschini, A Auguste, B Legois, A Zider, ... Elife 3, e04207, 2014 | 93 | 2014 |
| The transcription factor FOXL2: at the crossroads of ovarian physiology and pathology S Caburet, A Georges, D L’Hôte, AL Todeschini, BA Benayoun, RA Veitia Molecular and cellular endocrinology 356 (1-2), 55-64, 2012 | 88 | 2012 |
| Functional Exploration of the Adult Ovarian Granulosa Cell Tumor-Associated Somatic FOXL2 Mutation p.Cys134Trp (c.402C>G) BA Benayoun, S Caburet, A Dipietromaria, A Georges, B d'Haene, ... PloS one 5 (1), e8789, 2010 | 83 | 2010 |
| FOXL2, GATA4, and SMAD3 co-operatively modulate gene expression, cell viability and apoptosis in ovarian granulosa cell tumor cells M Anttonen, M Pihlajoki, N Andersson, A Georges, D L'hôte, S Vattulainen, ... PLoS One 9 (1), e85545, 2014 | 70 | 2014 |
| Discovery of novel protein partners of the transcription factor FOXL2 provides insights into its physiopathological roles D L'Hôte, A Georges, AL Todeschini, JH Kim, BA Benayoun, J Bae, ... Human molecular genetics 21 (14), 3264-3274, 2012 | 51 | 2012 |
| Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases A Georges, ML Yang, TE Berrandou, MK Bakker, O Dikilitas, SR Kiando, ... Nature communications 12 (1), 6031, 2021 | 45 | 2021 |
| Genomics of fibromuscular dysplasia S Di Monaco, A Georges, JP Lengelé, M Vikkula, A Persu International journal of molecular sciences 19 (5), 1526, 2018 | 45 | 2018 |
| Genome-wide association study reveals novel genetic loci: a new polygenic risk score for mitral valve prolapse C Roselli, M Yu, V Nauffal, A Georges, Q Yang, K Love, LC Weng, ... European heart journal 43 (17), 1668-1680, 2022 | 37 | 2022 |
| Genome-Wide Association Study–Driven Gene-Set Analyses, Genetic, and Functional Follow-Up Suggest GLIS1 as a Susceptibility Gene for Mitral Valve Prolapse M Yu, A Georges, NR Tucker, S Kyryachenko, K Toomer, JJ Schott, ... Circulation: Genomic and Precision Medicine 12 (5), e002497, 2019 | 34 | 2019 |
| A plasma proteogenomic signature for fibromuscular dysplasia JW Olin, AF Di Narzo, V d’Escamard, D Kadian-Dodov, H Cheng, ... Cardiovascular research 116 (1), 63-77, 2020 | 32 | 2020 |
| Design and analysis for assessment of water quality RH Norris, A Georges Limnology in Australia, 555-572, 1986 | 31 | 1986 |
| SUMOylation of the Forkhead transcription factor FOXL2 promotes its stabilization/activation through transient recruitment to PML bodies A Georges, BA Benayoun, M Marongiu, A Dipietromaria, D L'Hôte, ... PLoS One 6 (10), e25463, 2011 | 30 | 2011 |
| Mutational probing of the forkhead domain of the transcription factor FOXL2 provides insights into the pathogenicity of naturally occurring mutations AL Todeschini, A Dipietromaria, D L'hôte, FZ Boucham, AB Georges, ... Human molecular genetics 20 (17), 3376-3385, 2011 | 25 | 2011 |
| Rare loss-of-function mutations of PTGIR are enriched in fibromuscular dysplasia A Georges, J Albuisson, T Berrandou, D Dupré, A Lorthioir, V D’escamard, ... Cardiovascular Research 117 (4), 1154-1165, 2021 | 23 | 2021 |
