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Gael A Millot
Gael A Millot
Institut Pasteur
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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
4602011
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
2012013
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
1912020
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
1642012
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
1452006
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
1402011
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
862003
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
832016
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
732019
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
602019
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
582021
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
562008
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
472017
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
422020
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
392015
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
382020
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
362016
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
322017
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