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| Human neural tube defects: developmental biology, epidemiology, and genetics ER Detrait, TM George, HC Etchevers, JR Gilbert, M Vekemans, ... Neurotoxicology and teratology 27 (3), 515-524, 2005 | 477 | 2005 |
| Highly conserved non-coding elements on either side of SOX9 associated with Pierre Robin sequence S Benko, JA Fantes, J Amiel, DJ Kleinjan, S Thomas, J Ramsay, ... Nature genetics 41 (3), 359-364, 2009 | 471 | 2009 |
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| PAX8, TITF1, and FOXE1 Gene Expression Patterns during Human Development: New Insights into Human Thyroid Development and Thyroid Dysgenesis … SS Trueba, J Augé, G Mattei, H Etchevers, J Martinovic, P Czernichow, ... The Journal of Clinical Endocrinology & Metabolism 90 (1), 455-462, 2005 | 270 | 2005 |
| Phenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human development D Sanlaville, HC Etchevers, M Gonzales, J Martinovic, M Clément-Ziza, ... Journal of medical genetics 43 (3), 211-317, 2006 | 256 | 2006 |
| Homozygous silencing of T-box transcription factor EOMES leads to microcephaly with polymicrogyria and corpus callosum agenesis L Baala, S Briault, HC Etchevers, F Laumonnier, A Natiq, J Amiel, ... Nature genetics 39 (4), 454-456, 2007 | 252 | 2007 |
| Matthew-Wood syndrome is caused by truncating mutations in the retinol-binding protein receptor gene STRA6 C Golzio, J Martinovic-Bouriel, S Thomas, S Mougou-Zrelli, ... The American Journal of Human Genetics 80 (6), 1179-1187, 2007 | 203 | 2007 |
| Mutational, functional, and expression studies of the TCF4 gene in Pitt‐Hopkins syndrome L de Pontual, Y Mathieu, C Golzio, M Rio, V Malan, N Boddaert, C Soufflet, ... Human mutation 30 (4), 669-676, 2009 | 164 | 2009 |
| Antenatal presentation of Bardet-Biedl syndrome may mimic Meckel syndrome H Karmous-Benailly, J Martinovic, MC Gubler, Y Sirot, L Clech, C Ozilou, ... The American Journal of Human Genetics 76 (3), 493-504, 2005 | 142 | 2005 |
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| Molecular bases of human neurocristopathies HC Etchevers, J Amiel, S Lyonnet Neural crest induction and differentiation, 213-234, 2006 | 127 | 2006 |
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| The diverse neural crest: from embryology to human pathology HC Etchevers, E Dupin, NM Le Douarin Development 146 (5), dev169821, 2019 | 96 | 2019 |
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| Epistasis between RET and BBS mutations modulates enteric innervation and causes syndromic Hirschsprung disease L De Pontual, NA Zaghloul, S Thomas, EE Davis, DM Mcgaughey, ... Proceedings of the National Academy of Sciences 106 (33), 13921-13926, 2009 | 71 | 2009 |
Stanislas LyonnetInstitut imagineVerified email at inserm.fr
