| An RNA gene expressed during cortical development evolved rapidly in humans KS Pollard, SR Salama, N Lambert, MA Lambot, S Coppens, JS Pedersen, ... Nature 443 (7108), 167-172, 2006 | 1148 | 2006 |
| Pyramidal neurons derived from human pluripotent stem cells integrate efficiently into mouse brain circuits in vivo I Espuny-Camacho, KA Michelsen, D Gall, D Linaro, A Hasche, ... Neuron 77 (3), 440-456, 2013 | 575 | 2013 |
| Inhibition of SRGAP2 function by its human-specific paralogs induces neoteny during spine maturation C Charrier, K Joshi, J Coutinho-Budd, JE Kim, N Lambert, J De Marchena, ... Cell 149 (4), 923-935, 2012 | 458 | 2012 |
| Human-specific NOTCH2NL genes expand cortical neurogenesis through delta/notch regulation IK Suzuki, D Gacquer, R Van Heurck, D Kumar, M Wojno, A Bilheu, ... Cell 173 (6), 1370-1384. e16, 2018 | 381 | 2018 |
| Kinetochore KMN network gene CASC5 mutated in primary microcephaly A Genin, J Desir, N Lambert, M Biervliet, N Van Der Aa, G Pierquin, ... Human molecular genetics 21 (24), 5306-5317, 2012 | 138 | 2012 |
| tRNA Methyltransferase Homolog Gene TRMT10A Mutation in Young Onset Diabetes and Primary Microcephaly in Humans M Igoillo-Esteve, A Genin, N Lambert, J Desir, I Pirson, B Abdulkarim, ... PLoS genetics 9 (10), e1003888, 2013 | 128 | 2013 |
| FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly N Simonis, I Migeotte, N Lambert, C Perazzolo, DC de Silva, B Dimitrov, ... Journal of medical genetics 50 (9), 585-592, 2013 | 95 | 2013 |
| Birth and rapid subcellular adaptation of a hominoid-specific CDC14 protein L Rosso, AC Marques, M Weier, N Lambert, MA Lambot, ... PLoS biology 6 (6), e140, 2008 | 87 | 2008 |
| Genes expressed in specific areas of the human fetal cerebral cortex display distinct patterns of evolution N Lambert, MA Lambot, A Bilheu, V Albert, Y Englert, F Libert, JC Noel, ... PloS one 6 (3), e17753, 2011 | 86 | 2011 |
| Novel NEXMIF pathogenic variant in a boy with severe autistic features, intellectual disability, and epilepsy, and his mildly affected mother N Lambert, C Dauve, E Ranza, P Makrythanasis, F Santoni, F Sloan-Béna, ... Journal of human genetics 63 (7), 847-850, 2018 | 21 | 2018 |
| A familial heterozygous null mutation of MET in autism spectrum disorder N Lambert, V Wermenbol, B Pichon, S Acosta, J Van Den Ameele, ... Autism research 7 (5), 617-622, 2014 | 20 | 2014 |
| L’attachement. De Konrad Lorenz à Larry Young: de l’éthologie à la neurobiologie N Lambert 1, F Lotstra 2 Cahiers critiques de thérapie familiale et de pratiques de réseaux, 83-97, 2005 | 13 | 2005 |
| Génétique et transmission transgénérationnelle N Lambert Cahiers de psychologie clinique 43 (2), 11-28, 2014 | 9 | 2014 |
| The end, themes and variations in psychodramatic improvisation C Diricq, L Jönck, N Lambert Revue de psychotherapie psychanalytique de groupe 74 (1), 55-67, 2020 | | 2020 |
| La fin, thèmes et variations en improvisation psychodramatique C Diricq, L Jönck, N Lambert Revue de psychothérapie psychanalytique de groupe, 55-67, 2019 | | 2019 |
| Care for unaccompanied minor migrant adolescents at the Youth Health Consultation: Support, psychotherapy and resilience C Devillé, N Lambert Revue Medicale Suisse 14 (603), 822-824, 2018 | | 2018 |
| Genetics and transgenerational transmission N Lambert Cahiers de psychologie clinique 43 (2), 11-28, 2014 | | 2014 |
| Loss-of-function of TRMT10A causes young onset diabetes and microcephaly M Igoillo Esteve, A Genin, N Lambert, J Désir, I Pirson, B Abdulkarim, ... | | 2013 |
| ISDN2012_0241: Developmental and evolutionary functions of a human‐specific gene duplication of srGAP2 during brain development C Charrier, K Joshi, T Sassa, J Coutinho‐Budd, N Lambert, ... International Journal of Developmental Neuroscience 30 (8), 628-628, 2012 | | 2012 |
| Developmental and evolutionary functions of a human-specific gene duplication of SRGAP2 during brain development K Joshi, C Charrier, T Sassa, J Coutinho-Budd, N Lambert, ... INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE 30 (8), 668-668, 2012 | | 2012 |
