• 2022
  Freyer L, Lallemand Y, Dardenne P, Sommer A, Biton A, Gomez Perdiguero E, , Erythro-myeloid progenitor origin of Hofbauer cells in the early mouse placenta., Development 2022 Apr; 149(8): .
• 2021
  Iturri L, Freyer L, Biton A, Dardenne P, Lallemand Y, Gomez Perdiguero E, , Megakaryocyte production is sustained by direct differentiation from erythromyeloid progenitors in the yolk sac until midgestation., Immunity 2021 May; (): .
• 2017
  Iturri L, Saenz Coronilla J, Lallemand Y, Gomez Perdiguero E, Identification Of Erythromyeloid Progenitors And Their Progeny In The Mouse Embryo By Flow Cytometry, J Vis Exp 2017 Jul;(125).
• 2013
  Vieux-Rochas M, Bouhali K, Mantero S, Garaffo G, Provero P, Astigiano S, Barbieri O, Caratozzolo MF, Tullo A, Guerrini L, Lallemand Y, Robert B, Levi G, Merlo GR, BMP-mediated functional cooperation between Dlx5;Dlx6 and Msx1;Msx2 during mammalian limb development, PLoS ONE 2013;8(1):e51700.
• 2012
  Lallemand Y, Moreau J, Cloment CS, Vives FL, Robert B, Generation and characterization of a tamoxifen inducible Msx1(CreERT2) knock-in allele, Genesis 2013 Feb;51(2):110-9.
• 2011
  Lopes M, Goupille O, Saint Cloment C, Lallemand Y, Cumano A, Robert B, Msx genes define a population of mural cell precursors required for head blood vessel maturation, Development 2011 Jul;138(14):3055-66.
• 2011
  Bensoussan-Trigano V, Lallemand Y, Saint Cloment C, Robert B, Msx1 and Msx2 in limb mesenchyme modulate digit number and identity, Dev. Dyn. 2011 May;240(5):1190-202.
• 2009
  Lallemand Y, Bensoussan V, Cloment CS, Robert B, Msx genes are important apoptosis effectors downstream of the Shh/Gli3 pathway in the limb, Dev. Biol. 2009 Jul;331(2):189-98.
• 2007
  Coolen M, Sauka-Spengler T, Nicolle D, Le-Mentec C, Lallemand Y, Da Silva C, Plouhinec JL, Robert B, Wincker P, Shi DL, Mazan S, Evolution of axis specification mechanisms in jawed vertebrates: insights from a chondrichthyan, PLoS ONE 2007;2(4):e374.
• 2006
  Robert B, Lallemand Y, Anteroposterior patterning in the limb and digit specification: contribution of mouse genetics, Dev. Dyn. 2006 Sep;235(9):2337-52.
• 2005
  Lallemand Y, Nicola MA, Ramos C, Bach A, Cloment CS, Robert B, Analysis of Msx1; Msx2 double mutants reveals multiple roles for Msx genes in limb development, Development 2005 Jul;132(13):3003-14.
• 2004
  Fernández-Llebrez P, Grondona JM, Pérez J, López-Aranda MF, Estivill-Torrús G, Llebrez-Zayas PF, Soriano E, Ramos C, Lallemand Y, Bach A, Robert B, Msx1-deficient mice fail to form prosomere 1 derivatives, subcommissural organ, and posterior commissure and develop hydrocephalus, J. Neuropathol. Exp. Neurol. 2004 Jun;63(6):574-86.
• 2003
  Blanc I, Bach A, Lallemand Y, Perrin-Schmitt F, Guénet JL, Robert B, A new mouse limb mutation identifies a Twist allele that requires interacting loci on chromosome 4 for its phenotypic expression, Mamm. Genome 2003 Dec;14(12):797-804.
• 2003
  Bach A, Lallemand Y, Nicola MA, Ramos C, Mathis L, Maufras M, Robert B, Msx1 is required for dorsal diencephalon patterning, Development 2003 Sep;130(17):4025-36.
• 1998
  Lallemand Y, Luria V, Haffner-Krausz R, Lonai P, Maternally expressed PGK-Cre transgene as a tool for early and uniform activation of the Cre site-specific recombinase, Transgenic Res. 1998 Mar;7(2):105-12.
• 1997
  Rallu M, Loones M, Lallemand Y, Morimoto R, Morange M, Mezger V, Function and regulation of heat shock factor 2 during mouse embryogenesis, Proc. Natl. Acad. Sci. U.S.A. 1997 Mar;94(6):2392-7.
• 1996
  Acampora D, Mazan S, Avantaggiato V, Barone P, Tuorto F, Lallemand Y, Brûlet P, Simeone A, Epilepsy and brain abnormalities in mice lacking the Otx1 gene, Nat. Genet. 1996 Oct;14(2):218-22.
• 1995
  Acampora D, Mazan S, Lallemand Y, Avantaggiato V, Maury M, Simeone A, Brûlet P, Forebrain and midbrain regions are deleted in Otx2-/- mutants due to a defective anterior neuroectoderm specification during gastrulation, Development 1995 Oct;121(10):3279-90.
• 1995
  Picciotto MR, Zoli M, Léna C, Bessis A, Lallemand Y, Le Novère N, Vincent P, Pich EM, Brûlet P, Changeux JP, Abnormal avoidance learning in mice lacking functional high-affinity nicotine receptor in the brain, Nature 1995 Mar;374(6517):65-7.
• 1992
  Le Mouellic H, Lallemand Y, Brûlet P, Homeosis in the mouse induced by a null mutation in the Hox-3.1 gene, Cell 1992 Apr;69(2):251-64.
• 1990
  Lallemand Y, Brûlet P, An in situ assessment of the routes and extents of colonisation of the mouse embryo by embryonic stem cells and their descendants, Development 1990 Dec;110(4):1241-8.
• 1990
  Le Mouellic H, Lallemand Y, Brûlet P, Targeted replacement of the homeobox gene Hox-3.1 by the Escherichia coli lacZ in mouse chimeric embryos, Proc. Natl. Acad. Sci. U.S.A. 1990 Jun;87(12):4712-6.