Cell-type-specific replication initiation programs set fragility of the FRA3B fragile site A Letessier, GA Millot, S Koundrioukoff, AM Lachagès, N Vogt, ... Nature 470 (7332), 120-123, 2011 | 460 | 2011 |
Severe ADAMTS13 deficiency in adult idiopathic thrombotic microangiopathies defines a subset of patients characterized by various autoimmune manifestations, lower platelet … P Coppo, D Bengoufa, A Veyradier, M Wolf, A Bussel, GA Millot, S Malot, ... Medicine 83 (4), 233-244, 2004 | 203* | 2004 |
Common fragile site profiling in epithelial and erythroid cells reveals that most recurrent cancer deletions lie in fragile sites hosting large genes B Le Tallec, GA Millot, ME Blin, O Brison, B Dutrillaux, M Debatisse Cell reports 4 (3), 420-428, 2013 | 201 | 2013 |
High-throughput single-cell activity-based screening and sequencing of antibodies using droplet microfluidics A Gérard, A Woolfe, G Mottet, M Reichen, C Castrillon, V Menrath, ... Nature biotechnology 38 (6), 715-721, 2020 | 191 | 2020 |
A guide for functional analysis of BRCA1 variants of uncertain significance GA Millot, MA Carvalho, SM Caputo, MPG Vreeswijk, MA Brown, M Webb, ... Human mutation 33 (11), 1526-1537, 2012 | 164 | 2012 |
Prognostic value of inhibitory anti‐ADAMTS13 antibodies in adult‐acquired thrombotic thrombocytopenic purpura P Coppo, M Wolf, A Veyradier, A Bussel, S Malot, GA Millot, C Daubin, ... British journal of haematology 132 (1), 66-74, 2006 | 145 | 2006 |
Molecular profiling of common fragile sites in human fibroblasts B Le Tallec, B Dutrillaux, AM Lachages, GA Millot, O Brison, M Debatisse Nature structural & molecular biology 18 (12), 1421-1423, 2011 | 140 | 2011 |
Constitutive and specific activation of STAT3 by BCR-ABL in embryonic stem cells P Coppo, I Dusanter-Fourt, G Millot, MM Nogueira, A Dugray, ML Bonnet, ... Oncogene 22 (26), 4102-4110, 2003 | 86 | 2003 |
Signaling from Mus81-Eme2-dependent DNA damage elicited by Chk1 deficiency modulates replication fork speed and origin usage H Techer, S Koundrioukoff, S Carignon, T Wilhelm, GA Millot, BS Lopez, ... Cell reports 14 (5), 1114-1127, 2016 | 83 | 2016 |
Comprendre et réaliser les tests statistiques à l'aide de R: manuel de biostatistique G Millot De Boeck Supérieur, 2018 | 80* | 2018 |
Transcription-dependent regulation of replication dynamics modulates genome stability M Blin, B Le Tallec, V Nähse, M Schmidt, C Brossas, GA Millot, ... Nature structural & molecular biology 26 (1), 58-66, 2019 | 73 | 2019 |
LGP2 binds to PACT to regulate RIG-I–and MDA5-mediated antiviral responses RY Sanchez David, C Combredet, V Najburg, GA Millot, G Beauclair, ... Science signaling 12 (601), eaar3993, 2019 | 60 | 2019 |
MetaHiC phage-bacteria infection network reveals active cycling phages of the healthy human gut M Marbouty, A Thierry, GA Millot, R Koszul Elife 10, e60608, 2021 | 58 | 2021 |
Human immunodeficiency virus‐associated thrombotic microangiopathies: clinical characteristics and outcome according to ADAMTS13 activity S Malak, M Wolf, GA Millot, E Mariotte, A Veyradier, JL Meynard, ... Scandinavian journal of immunology 68 (3), 337-344, 2008 | 56 | 2008 |
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 | 47 | 2017 |
Variants of uncertain clinical significance in hereditary breast and ovarian cancer genes: best practices in functional analysis for clinical annotation AN Monteiro, P Bouwman, AN Kousholt, DM Eccles, GA Millot, JY Masson, ... Journal of medical genetics 57 (8), 509-518, 2020 | 42 | 2020 |
BRCA1 Circos: a visualisation resource for functional analysis of missense variants A Jhuraney, A Velkova, RC Johnson, B Kessing, RS Carvalho, P Whiley, ... Journal of medical genetics 52 (4), 224-230, 2015 | 39 | 2015 |
The anti-IgE mAb omalizumab induces adverse reactions by engaging Fcγ receptors B Balbino, P Herviou, O Godon, J Stackowicz, O Richard-Le Goff, ... The Journal of clinical investigation 130 (3), 1330-1335, 2020 | 38 | 2020 |
A Parent-of-Origin Effect Impacts the Phenotype in Low Penetrance Retinoblastoma Families Segregating the c.1981C>T/p.Arg661Trp Mutation of RB1 P Eloy, C Dehainault, M Sefta, I Aerts, F Doz, N Cassoux, ... PLoS Genetics 12 (2), e1005888, 2016 | 36 | 2016 |
Heritability of the melatonin synthesis variability in autism spectrum disorders M Benabou, T Rolland, CS Leblond, GA Millot, G Huguet, R Delorme, ... Scientific reports 7 (1), 17746, 2017 | 32 | 2017 |