• 2019
  Blin M, Le Tallec B, Nähse V, Schmidt M, Brossas C, Millot GA, Prioleau MN, Debatisse M, Transcription-dependent regulation of replication dynamics modulates genome stability, Nat. Struct. Mol. Biol. 2019 Jan;26(1):58-66.
• 2018
  Chaussade A, Millot G, Wells C, Brisse H, Laé M, Savignoni A, Desjardins L, Dendale R, Doz F, Aerts I, Jimenez I, Cassoux N, Stoppa Lyonnet D, Gauthier Villars M, Houdayer C, Correlation between RB1germline mutations and second primary malignancies in hereditary retinoblastoma patients treated with external beam radiotherapy, Eur J Med Genet 2018 Jul;.
• 2018
  Cossé MM, Barta ML, Fisher DJ, Oesterlin LK, Niragire B, Perrinet S, Millot GA, Hefty PS, Subtil A, The Loss of Expression of a Single Type 3 Effector (CT622) Strongly Reduces Infectivity and Growth, Front Cell Infect Microbiol 2018;8:145.
• 2018
  Millot Gael, Comprendre et réaliser les tests statistiques à l’aide de R, 4th edition, De Boeck editions, Bruxelles.
• 2017
  Benabou M, Rolland T, Leblond CS, Millot GA, Huguet G, Delorme R, Leboyer M, Pagan C, Callebert J, Maronde E, Bourgeron T, Heritability of the melatonin synthesis variability in autism spectrum disorders, Sci Rep 2017 Dec;7(1):17746.
• 2017
  Golmard L, Castéra L, Krieger S, Moncoutier V, Abidallah K, Tenreiro H, Laugé A, Tarabeux J, Millot GA, Nicolas A, Laé M, Abadie C, Berthet P, Polycarpe F, Frébourg T, Elan C, de Pauw A, Gauthier-Villars M, Buecher B, Stern MH, Stoppa-Lyonnet D, Vaur D, Houdayer C, Contribution of germline deleterious variants in the RAD51 paralogs to breast and ovarian cancers, Eur. J. Hum. Genet. 2017 Dec;25(12):1345-1353.
• 2016
  Dehainault C, Golmard L, Millot GA, Charpin A, Laugé A, Tarabeux J, Aerts I, Cassoux N, Stoppa-Lyonnet D, Gauthier-Villars M, Houdayer C, Mosaicism and prenatal diagnosis options: insights from retinoblastoma, Eur. J. Hum. Genet. 2017 02;25(3):381-383.
• 2016
  Thouvenot P, Fourrière L, Dardillac E, Ben Yamin B, Lescure A, Lejour V, Heiligenstein X, Boulé JB, Romao M, Raposo-Benedetti G, Lopez BS, Nicolas A, Millot GA, Yeast cells reveal the misfolding and the cellular mislocalization of the human BRCA1 protein, J. Cell. Sci. 2016 Dec;129(23):4366-4378.
• 2016
  Thouvenot P, Ben Yamin B, Fourrière L, Lescure A, Boudier T, Del Nery E, Chauchereau A, Goldgar DE, Houdayer C, Stoppa-Lyonnet D, Nicolas A, Millot GA, Functional Assessment of Genetic Variants with Outcomes Adapted to Clinical Decision-Making, PLoS Genet. 2016 Jun;12(6):e1006096.
• 2016
  Eloy P, Dehainault C, Sefta M, Aerts I, Doz F, Cassoux N, Lumbroso le Rouic L, Stoppa-Lyonnet D, Radvanyi F, Millot GA, Gauthier-Villars M, Houdayer C, A Parent-of-Origin Effect Impacts the Phenotype in Low Penetrance Retinoblastoma Families Segregating the c.1981C>T/p.Arg661Trp Mutation of RB1, PLoS Genet. 2016 Feb;12(2):e1005888.
• 2016
  Técher H, Koundrioukoff S, Carignon S, Wilhelm T, Millot GA, Lopez BS, Brison O, Debatisse M, Signaling from Mus81-Eme2-Dependent DNA Damage Elicited by Chk1 Deficiency Modulates Replication Fork Speed and Origin Usage, Cell Rep 2016 Feb;14(5):1114-27.
• 2016
  De Carli F, Gaggioli V, Millot GA, Hyrien O, Single-molecule, antibody-free fluorescent visualisation of replication tracts along barcoded DNA molecules, Int. J. Dev. Biol. 2016;60(7-8-9):297-304.
• 2015
  Jhuraney A, Velkova A, Johnson RC, Kessing B, Carvalho RS, Whiley P, Spurdle AB, Vreeswijk MP, Caputo SM, Millot GA, Vega A, Coquelle N, Galli A, Eccles D, Blok MJ, Pal T, van der Luijt RB, Santamariña Pena M, Neuhausen SL, Donenberg T, Machackova E, Thomas S, Vallée M, Couch FJ, Tavtigian SV, Glover JN, Carvalho MA, Brody LC, Sharan SK, Monteiro AN, , BRCA1 Circos: a visualisation resource for functional analysis of missense variants, J. Med. Genet. 2015 Apr;52(4):224-30.
• 2014
  Millot Gael, Comprendre et réaliser les tests statistiques à l’aide de R, 3rd edition, De Boeck editions, Bruxelles.
• 2013
  Le Tallec B, Millot GA, Blin ME, Brison O, Dutrillaux B, Debatisse M, Common fragile site profiling in epithelial and erythroid cells reveals that most recurrent cancer deletions lie in fragile sites hosting large genes, Cell Rep 2013 Aug;4(3):420-8.
• 2012
  Millot GA, Carvalho MA, Caputo SM, Vreeswijk MP, Brown MA, Webb M, Rouleau E, Neuhausen SL, Hansen Tv, Galli A, Brandão RD, Blok MJ, Velkova A, Couch FJ, Monteiro AN, , A guide for functional analysis of BRCA1 variants of uncertain significance, Hum. Mutat. 2012 Nov;33(11):1526-37.
• 2011
  Le Tallec B, Dutrillaux B, Lachages AM, Millot GA, Brison O, Debatisse M, Molecular profiling of common fragile sites in human fibroblasts, Nat. Struct. Mol. Biol. 2011 Nov;18(12):1421-3.
• 2011
  Millot GA, Berger A, Lejour V, Boulé JB, Bobo C, Cullin C, Lopes J, Stoppa-Lyonnet D, Nicolas A, Assessment of human Nter and Cter BRCA1 mutations using growth and localization assays in yeast, Hum. Mutat. 2011 Dec;32(12):1470-80.
• 2011
  Millot Gael, Comprendre et réaliser les tests statistiques à l’aide de R, 2nd edition, De Boeck editions, Bruxelles.
• 2011
  Letessier A, Millot GA, Koundrioukoff S, Lachagès AM, Vogt N, Hansen RS, Malfoy B, Brison O, Debatisse M, Cell-type-specific replication initiation programs set fragility of the FRA3B fragile site, Nature 2011 Feb;470(7332):120-3.
• 2010
  Gay S, Lachages AM, Millot GA, Courbet S, Letessier A, Debatisse M, Brison O, Nucleotide supply, not local histone acetylation, sets replication origin usage in transcribed regions, EMBO Rep. 2010 Sep;11(9):698-704.
• 2009
  Millot Gael, Comprendre et réaliser les tests statistiques à l’aide de R, De Boeck editions, Bruxelles.
• 2008
  Malak S, Wolf M, Millot GA, Mariotte E, Veyradier A, Meynard JL, Korach JM, Malot S, Bussel A, Azoulay E, Boulanger E, Galicier L, Devaux E, Eschwège V, Gallien S, Adrie C, Schlemmer B, Rondeau E, Coppo P, , Human immunodeficiency virus-associated thrombotic microangiopathies: clinical characteristics and outcome according to ADAMTS13 activity, Scand. J. Immunol. 2008 Sep;68(3):337-44.
• 2008
  Gonnet F, Bouazza B, Millot GA, Ziaei S, Garcia L, Butler-Browne GS, Mouly V, Tortajada J, Danos O, Svinartchouk F, Proteome analysis of differentiating human myoblasts by dialysis-assisted two-dimensional gel electrophoresis (DAGE), Proteomics 2008 Jan;8(2):264-78.
• 2006
  Coppo P, Wolf M, Veyradier A, Bussel A, Malot S, Millot GA, Daubin C, Bordessoule D, Pène F, Mira JP, Heshmati F, Maury E, Guidet B, Boulanger E, Galicier L, Parquet N, Vernant JP, Rondeau E, Azoulay E, Schlemmer B, , Prognostic value of inhibitory anti-ADAMTS13 antibodies in adult-acquired thrombotic thrombocytopenic purpura, Br. J. Haematol. 2006 Jan;132(1):66-74.
• 2004
  Coppo P, Bengoufa D, Veyradier A, Wolf M, Bussel A, Millot GA, Malot S, Heshmati F, Mira JP, Boulanger E, Galicier L, Durey-Dragon MA, Frémeaux-Bacchi V, Ramakers M, Pruna A, Bordessoule D, Gouilleux V, Scrobohaci ML, Vernant JP, Moreau D, Azoulay E, Schlemmer B, Guillevin L, Lassoued K, , Severe ADAMTS13 deficiency in adult idiopathic thrombotic microangiopathies defines a subset of patients characterized by various autoimmune manifestations, lower platelet count, and mild renal involvement, Medicine (Baltimore) 2004 Jul;83(4):233-44.
• 2004
  Millot GA, Vainchenker W, Duménil D, Svinarchuk F, Differential signalling of NH2-terminal flag-labelled thrombopoietin receptor activated by TPO or anti-FLAG antibodies, Cell. Signal. 2004 Mar;16(3):355-63.
• 2003
  Coppo P, Dusanter-Fourt I, Millot G, Nogueira MM, Dugray A, Bonnet ML, Mitjavila-Garcia MT, Le Pesteur D, Guilhot F, Vainchenker W, Sainteny F, Turhan AG, Constitutive and specific activation of STAT3 by BCR-ABL in embryonic stem cells, Oncogene 2003 Jun;22(26):4102-10.
• 2002
  Millot GA, Vainchenker W, Duménil D, Svinarchuk F, Distinct effects of thrombopoietin depending on a threshold level of activated Mpl in BaF-3 cells, J. Cell. Sci. 2002 Jun;115(Pt 11):2329-37.
• 2002
  Filippi MD, Porteu F, Le Pesteur F, Schiavon V, Millot GA, Vainchenker W, de Sauvage FJ, Dubart Kupperschmitt A, Sainteny F, Requirement for mitogen-activated protein kinase activation in the response of embryonic stem cell-derived hematopoietic cells to thrombopoietin in vitro, Blood 2002 Feb;99(4):1174-82.
• 2002
  Millot GA, Feger F, Garçon L, Vainchenker W, Dumenil D, Svinarchuk F, MplK, a natural variant of the thrombopoietin receptor with a truncated cytoplasmic domain, binds thrombopoietin but does not interfere with thrombopoietin-mediated cell growth, Exp. Hematol. 2002 Feb;30(2):166-75.
• 2001
  Millot GA, Svinarchuk F, Lacout C, Vainchenker W, Dumenil D, The granulocyte colony-stimulating factor receptor supports erythroid differentiation in the absence of the erythropoietin receptor or Stat5, Br. J. Haematol. 2001 Feb;112(2):449-58.