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Heather C. Etchevers, Ph.D. - Publications

Affiliations: 
2001-2007 Handicaps génétiques de l'enfant INSERM U393, Paris, France 
 2006-2009 Centre de Physiopathologie de Toulouse Purpan INSERM U563, Toulouse, France 
 2007-2010 Génétique et épigénétique des maladies métaboliques, neurosensorielles et du développement INSERM U781, Paris, France 
 2010-2017 Génétique Médicale et Génomique Fonctionnelle Faculté de Médecine de La Timone, INSERM U910, Marseille, France 
 2018- Marseille Medical Genetics INSERM - France 
Area:
neural crest, congenital malformations, human embryo
Website:
https://www.marseille-medical-genetics.org/h-etchevers/
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Year Citation  Score
2021 Wilmerding A, Bouteille L, Caruso N, Bidaut G, Etchevers HC, Graba Y, Delfini MC. Sustained experimental activation of FGF8/ERK in the developing chicken spinal cord models early events in ERK-mediated tumorigenesis. Neoplasia (New York, N.Y.). 24: 120-132. PMID 34959031 DOI: 10.1016/j.neo.2021.12.006  0.322
2021 Haniffa M, Taylor D, Linnarsson S, Aronow BJ, Bader GD, Barker RA, Camara PG, Camp JG, Chédotal A, Copp A, Etchevers HC, Giacobini P, Göttgens B, Guo G, Hupalowska A, et al. A roadmap for the Human Developmental Cell Atlas. Nature. 597: 196-205. PMID 34497388 DOI: 10.1038/s41586-021-03620-1  0.365
2021 de la Fouchardière A, Boivin F, Etchevers HC, Macagno N. Cutaneous Melanomas Arising during Childhood: An Overview of the Main Entities. Dermatopathology (Basel, Switzerland). 8: 301-314. PMID 34449585 DOI: 10.3390/dermatopathology8030036  0.629
2021 Romanet P, Galluso J, Kamenicky P, Hage M, Theodoropoulou M, Roche C, Graillon T, Etchevers HC, De Murat D, Mougel G, Figarella-Branger D, Dufour H, Cuny T, Assié G, Barlier A. Somatotroph Tumors and the Epigenetic Status of the Locus. International Journal of Molecular Sciences. 22. PMID 34299200 DOI: 10.3390/ijms22147570  0.258
2021 Fledderus AC, Pasmans SGMA, Wolkerstorfer A, Oei W, Etchevers HC, van Kessel MS, van der Horst CMAM, Spuls PI. Domains and outcomes of the core outcome set of congenital melanocytic naevi for clinical practice and research, part 2 (the OCOMEN project). The British Journal of Dermatology. PMID 33959942 DOI: 10.1111/bjd.20437  0.207
2021 Stefanovic S, Etchevers HC, Zaffran S. Outflow Tract Formation-Embryonic Origins of Conotruncal Congenital Heart Disease. Journal of Cardiovascular Development and Disease. 8. PMID 33918884 DOI: 10.3390/jcdd8040042  0.609
2021 Etchevers HC. Pericyte Ontogeny: The Use of Chimeras to Track a Cell Lineage of Diverse Germ Line Origins. Methods in Molecular Biology (Clifton, N.J.). 2235: 61-87. PMID 33576971 DOI: 10.1007/978-1-0716-1056-5_6  0.319
2020 Oei W, Fledderus AC, Spuls PI, Eggen CAM, Kottner J, van der Horst CMAM, Wolkerstorfer A, van Kessel MS, Krengel S, Etchevers HC, Korfage IJ, Pasmans SGM. Development of an international core domain set for medium, large and giant congenital melanocytic naevi as a first step towards a core outcome set for clinical practice and research. The British Journal of Dermatology. PMID 33237568 DOI: 10.1111/bjd.19694  0.26
2020 Macagno N, Pissaloux D, Etchevers H, Haddad V, Vergier B, Sierra-Fortuny S, Tirode F, de la Fouchardière A. Cutaneous Melanocytic Tumors With Concomitant NRASQ61R and IDH1R132C Mutations: A Report of 6 Cases. The American Journal of Surgical Pathology. PMID 32732488 DOI: 10.1097/Pas.0000000000001500  0.701
2020 Calbet-Llopart N, Pascini-Garrigos M, Tell-Martí G, Potrony M, da Silva VM, Barreiro A, Puig S, Captier G, James I, Degardin N, Carrera C, Malvehy J, Etchevers HC, Puig-Butillé JA. Melanocortin-1 receptor (MC1R) genotypes do not correlate with size in two cohorts of medium-to-giant congenital melanocytic nevi. Pigment Cell & Melanoma Research. PMID 32323445 DOI: 10.1111/Pcmr.12883  0.432
2019 Almutairi B, Charlet J, Dallosso AR, Szemes M, Etchevers HC, Malik KTA, Brown KW. Epigenetic deregulation of GATA3 in neuroblastoma is associated with increased GATA3 protein expression and with poor outcomes. Scientific Reports. 9: 18934. PMID 31831790 DOI: 10.1038/S41598-019-55382-6  0.431
2019 Jaouadi H, Chehida AB, Kraoua L, Etchevers HC, Argiro L, Kasdallah N, Blibech S, Delague V, Lévy N, Tebib N, Mrad R, Abdelhak S, Benkhalifa R, Zaffran S. A severe clinical phenotype of Noonan syndrome with neonatal hypertrophic cardiomyopathy in the second case worldwide with RAF1 S259Y neomutation. Genetics Research. 101: e6. PMID 31030682 DOI: 10.1017/S0016672319000041  0.752
2019 Etchevers HC, Dupin E, Le Douarin NM. The diverse neural crest: from embryology to human pathology. Development (Cambridge, England). 146. PMID 30858200 DOI: 10.1242/Dev.169821  0.681
2018 Fultang L, Gamble LD, Gneo L, Berry AM, Egan SA, De Bie F, Yogev O, Eden GL, Booth S, Brownhill S, Vardon A, McConville CM, Cheng PN, Norris MD, Etchevers HC, et al. Macrophage-derived IL-1β and TNF-α regulate arginine metabolism in neuroblastoma. Cancer Research. PMID 30545920 DOI: 10.1158/0008-5472.Can-18-2139  0.246
2018 Zaffran S, Odelin G, Stefanovic S, Lescroart F, Etchevers HC. Ectopic expression of Hoxb1 induces cardiac and craniofacial malformations. Genesis (New York, N.Y. : 2000). 56: e23221. PMID 30134070 DOI: 10.1002/Dvg.23221  0.697
2018 Cavodeassi F, Creuzet S, Etchevers HC. The hedgehog pathway and ocular developmental anomalies. Human Genetics. PMID 30073412 DOI: 10.1007/S00439-018-1918-8  0.38
2018 Macagno N, Etchevers HC, Malissen N, Rome A, Hesse S, Mallet S, Degardin N, Gaudy C. Reduced H3K27me3 Expression is Common in Nodular Melanomas of Childhood Associated With Congenital Melanocytic Nevi But Not in Proliferative Nodules. The American Journal of Surgical Pathology. 42: 701-704. PMID 29369061 DOI: 10.1097/Pas.0000000000001026  0.668
2018 Thomas AC, Heux P, Santos C, Arulvasan W, Solanky N, Carey ME, Gerrelli D, Kinsler VA, Etchevers HC. Widespread dynamic and pleiotropic expression of the melanocortin-1-receptor (MC1R) system is conserved across chick, mouse and human embryonic development. Birth Defects Research. PMID 29316344 DOI: 10.1002/Bdr2.1183  0.783
2018 Etchevers HC, Rose C, Kahle B, Vorbringer H, Fina F, Heux P, Berger I, Schwarz B, Zaffran S, Macagno N, Krengel S. Giant congenital melanocytic nevus with vascular malformation and epidermal cysts associated with a somatic activating mutation in BRAF. Pigment Cell & Melanoma Research. PMID 29316280 DOI: 10.1111/Pcmr.12685  0.786
2017 Boeva V, Louis-Brennetot C, Peltier A, Durand S, Pierre-Eugène C, Raynal V, Etchevers HC, Thomas S, Lermine A, Daudigeos-Dubus E, Geoerger B, Orth MF, Grünewald TGP, Diaz E, Ducos B, et al. Heterogeneity of neuroblastoma cell identity defined by transcriptional circuitries. Nature Genetics. PMID 28740262 DOI: 10.1038/Ng.3921  0.626
2016 Charlet J, Tomari A, Dallosso AR, Szemes M, Kaselova M, Curry TJ, Almutairi B, Etchevers HC, McConville C, Malik KT, Brown KW. Genome-wide DNA methylation analysis identifies MEGF10 as a novel epigenetically repressed candidate tumour suppressor gene in neuroblastoma. Molecular Carcinogenesis. PMID 27862318 DOI: 10.1002/Mc.22591  0.452
2016 Chassaing N, Davis EE, McKnight KL, Niederriter AR, Causse A, David V, Desmaison A, Lamarre S, Vincent-Delorme C, Pasquier L, Coubes C, Lacombe D, Rossi M, Dufier JL, Dollfus H, ... ... Etchevers HC, et al. Targeted resequencing identifies PTCH1 as a major contributor to ocular developmental anomalies and extends the SOX2 regulatory network. Genome Research. PMID 26893459 DOI: 10.1101/Gr.196048.115  0.694
2016 Xu P, Thomas S, Dellinger A, Etchevers H, Vekemans M, Gilbert JR, Speer MC. Transcriptome analysis of genes involved in neural tube closure during human embryonic development using Long-SAGE F1000research. 5. DOI: 10.7490/F1000Research.1111340.1  0.778
2016 Thomas S, Thomas M, Wincker P, Babarit C, Xu P, Speer MC, Munnich A, Lyonnet S, Vekemans M, Etchevers H. Isolation and transcriptional profiling of embryonic human neural crest cells F1000research. 5. DOI: 10.7490/F1000Research.1111339.1  0.785
2016 Goudefroye G, Guirchon J, Ozilou C, Morichon-Delvallez N, Munnich A, Vekemans M, Attie-Bitach T, Etchevers H. Chromosomal, molecular and morphological analysis of a human embryo with homogeneous trisomy of chromosome 8 F1000research. 5. DOI: 10.7490/F1000Research.1111338.1  0.724
2016 Sanlaville D, Etchevers H, Clément-Ziza M, Goudefroye G, Audollent S, Detrait E, Attié-Bitach T, Vekemans M. Comparative expression patterns of CHD7 , TBX1, FOXG1b ( BF1 ) , DLX5 and FGF10 during human craniofacial development F1000research. 5. DOI: 10.7490/F1000Research.1111318.1  0.778
2016 Carey M, Lechat S, Etchevers H. The melanocortin 1 receptor ( Mc1r ) and prepro-opiomelanocortin ( Pomc ) are transcribed in numerous extracutaneous sites of the developing avian embryo F1000research. 5. DOI: 10.7490/F1000Research.1111317.1  0.363
2016 Heux P, Matonti J, Schwarz B, Bentatou Z, Viola A, Etchevers H. Early constitutive activation of Nras in the dorsal neural tube leads to cutaneous and extra-cutaneous melanocytosis F1000research. 5. DOI: 10.7490/F1000Research.1111316.1  0.759
2015 El Robrini N, Etchevers HC, Ryckebüsch L, Faure E, Eudes N, Niederreither K, Zaffran S, Bertrand N. Cardiac outflow morphogenesis depends on effects of retinoic acid signaling on multiple cell lineages. Developmental Dynamics : An Official Publication of the American Association of Anatomists. PMID 26442704 DOI: 10.1002/Dvdy.24357  0.736
2015 Price HN, O'Haver J, Marghoob A, Badger K, Etchevers H, Krengel S. Practical application of the new classification scheme for congenital melanocytic nevi. Pediatric Dermatology. 32: 23-7. PMID 25346440 DOI: 10.1111/Pde.12428  0.359
2014 Etchevers HC. Hiding in plain sight: molecular genetics applied to giant congenital melanocytic nevi. The Journal of Investigative Dermatology. 134: 879-882. PMID 24646799 DOI: 10.1038/Jid.2013.531  0.422
2013 Yajima I, Colombo S, Puig I, Champeval D, Kumasaka M, Belloir E, Bonaventure J, Mark M, Yamamoto H, Taketo MM, Choquet P, Etchevers HC, Beermann F, Delmas V, Monassier L, et al. A subpopulation of smooth muscle cells, derived from melanocyte-competent precursors, prevents patent ductus arteriosus. Plos One. 8: e53183. PMID 23382837 DOI: 10.1371/Journal.Pone.0053183  0.426
2012 Krupp DR, Xu PT, Thomas S, Dellinger A, Etchevers HC, Vekemans M, Gilbert JR, Speer MC, Ashley-Koch AE, Gregory SG. Transcriptome profiling of genes involved in neural tube closure during human embryonic development using long serial analysis of gene expression (long-SAGE). Birth Defects Research. Part a, Clinical and Molecular Teratology. 94: 683-92. PMID 22806986 DOI: 10.1002/Bdra.23040  0.782
2012 Chassaing N, Sorrentino S, Davis EE, Martin-Coignard D, Iacovelli A, Paznekas W, Webb BD, Faye-Petersen O, Encha-Razavi F, Lequeux L, Vigouroux A, Yesilyurt A, Boyadjiev SA, Kayserili H, Loget P, ... ... Etchevers HC, et al. OTX2 mutations contribute to the otocephaly-dysgnathia complex. Journal of Medical Genetics. 49: 373-9. PMID 22577225 DOI: 10.1136/Jmedgenet-2012-100892  0.665
2012 Golzio C, Havis E, Daubas P, Nuel G, Babarit C, Munnich A, Vekemans M, Zaffran S, Lyonnet S, Etchevers HC. ISL1 directly regulates FGF10 transcription during human cardiac outflow formation. Plos One. 7: e30677. PMID 22303449 DOI: 10.1371/Journal.Pone.0030677  0.787
2012 Van Der Werf CS, Wabbersen TD, Hsiao NH, Paredes J, Etchevers HC, Kroisel PM, Tibboel D, Babarit C, Schreiber RA, Hoffenberg EJ, Vekemans M, Zeder SL, Ceccherini I, Lyonnet S, Ribeiro AS, et al. CLMP is required for intestinal development, and loss-of-function mutations cause congenital short-bowel syndrome. Gastroenterology. 142: 453-462.e3. PMID 22155368 DOI: 10.1053/J.Gastro.2011.11.038  0.797
2012 Wilms S, Etchevers H, Beckwith M. The "Global Naevus Initiative" case study F1000research. 3. DOI: 10.7490/F1000Research.1090105.1  0.416
2011 De Pontual L, Kettaneh D, Gordon CT, Oufadem M, Boddaert N, Lees M, Balu L, Lachassinne E, Petros A, Mollet J, Wilson LC, Munnich A, Brugière L, Delattre O, Vekemans M, ... Etchevers H, et al. Germline gain-of-function mutations of ALK disrupt central nervous system development Human Mutation. 32: 272-276. PMID 21972109 DOI: 10.1002/Humu.21442  0.794
2011 Etchevers H. Primary culture of chick, mouse or human neural crest cells. Nature Protocols. 6: 1568-77. PMID 21959239 DOI: 10.1038/Nprot.2011.398  0.449
2011 Macé M, Galiacy SD, Erraud A, Mejía JE, Etchevers H, Allouche M, Desjardins L, Calvas P, Malecaze F. Comparative transcriptome and network biology analyses demonstrate antiproliferative and hyperapoptotic phenotypes in human keratoconus corneas. Investigative Ophthalmology & Visual Science. 52: 6181-91. PMID 21676910 DOI: 10.1167/Iovs.10-70981  0.453
2011 Krengel S, Breuninger H, Beckwith M, Etchevers HC. Meeting report from the 2011 International Expert Meeting on Large Congenital Melanocytic Nevi and Neurocutaneous Melanocytosis, Tübingen. Pigment Cell & Melanoma Research. 24: E1-6. PMID 21672181 DOI: 10.1111/J.1755-148X.2011.00875.X  0.406
2011 Cognet M, Nougayrede A, Malan V, Callier P, Cretolle C, Faivre L, Genevieve D, Goldenberg A, Heron D, Mercier S, Philip N, Sigaudy S, Verloes A, Sarnacki S, Munnich A, ... ... Etchevers H, et al. Dissection of the MYCN locus in Feingold syndrome and isolated oesophageal atresia. European Journal of Human Genetics : Ejhg. 19: 602-6. PMID 21224895 DOI: 10.1038/Ejhg.2010.225  0.804
2011 van der Werf CS, Wabbersen TD, Hsiao N, Paredes J, Etchevers HC, Kroisel PM, Tibboel D, Schreiber RA, Hoffenberg EJ, Zeder SL, Ceccherini I, Lyonnet S, Ribeiro AS, Seruca R, te Meerman GJ, et al. Identification of the Gene Underlying Congenital Short Bowel Syndrome, Pointing to Its Major Role in Intestinal Development Gastroenterology. 140: S-89. DOI: 10.1016/S0016-5085(11)60364-8  0.668
2010 Thomas S, Encha-Razavi F, Devisme L, Etchevers H, Bessieres-Grattagliano B, Goudefroye G, Elkhartoufi N, Pateau E, Ichkou A, Bonnière M, Marcorelle P, Parent P, Manouvrier S, Holder M, Laquerrière A, et al. High-throughput sequencing of a 4.1 Mb linkage interval reveals FLVCR2 deletions and mutations in lethal cerebral vasculopathy. Human Mutation. 31: 1134-41. PMID 20690116 DOI: 10.1002/Humu.21329  0.797
2010 Chaabouni M, Etchevers H, De Blois MC, Calvas P, Waill-Perrier MC, Vekemans M, Romana SP. Identification of the IRXB gene cluster as candidate genes in severe dysgenesis of the ocular anterior segment. Investigative Ophthalmology & Visual Science. 51: 4380-6. PMID 20164457 DOI: 10.1167/Iovs.09-4111  0.663
2010 Arnaud A, Crétolle C, Babarit C, Galmiche L, Munnich A, Lyonnet S, Vekemans M, Etchevers H, Sarnacki S. CL004 - Expression de marqueurs de pluripotence dans des cellules de tératome sacro-coccygien Archives De Pediatrie. 17: 2. DOI: 10.1016/S0929-693X(10)70220-7  0.705
2009 de Pontual L, Zaghloul NA, Thomas S, Davis EE, McGaughey DM, Dollfus H, Baumann C, Bessling SL, Babarit C, Pelet A, Gascue C, Beales P, Munnich A, Lyonnet S, Etchevers H, et al. Epistasis between RET and BBS mutations modulates enteric innervation and causes syndromic Hirschsprung disease. Proceedings of the National Academy of Sciences of the United States of America. 106: 13921-6. PMID 19666486 DOI: 10.1073/Pnas.0901219106  0.814
2009 Bessières-Grattagliano B, Foliguet B, Devisme L, Loeuillet L, Marcorelles P, Bonnière M, Laquerrière A, Fallet-Bianco C, Martinovic J, Zrelli S, Leticee N, Cayol V, Etchevers HC, Vekemans M, Attie-Bitach T, et al. Refining the clinicopathological pattern of cerebral proliferative glomeruloid vasculopathy (Fowler syndrome): report of 16 fetal cases. European Journal of Medical Genetics. 52: 386-92. PMID 19635601 DOI: 10.1016/J.Ejmg.2009.07.006  0.762
2009 Boissel S, Reish O, Proulx K, Kawagoe-Takaki H, Sedgwick B, Yeo GS, Meyre D, Golzio C, Molinari F, Kadhom N, Etchevers HC, Saudek V, Farooqi IS, Froguel P, Lindahl T, et al. Loss-of-function mutation in the dioxygenase-encoding FTO gene causes severe growth retardation and multiple malformations. American Journal of Human Genetics. 85: 106-11. PMID 19559399 DOI: 10.1016/J.Ajhg.2009.06.002  0.752
2009 Chassaing N, Golzio C, Odent S, Lequeux L, Vigouroux A, Martinovic-Bouriel J, Tiziano FD, Masini L, Piro F, Maragliano G, Delezoide AL, Attié-Bitach T, Manouvrier-Hanu S, Etchevers HC, Calvas P. Phenotypic spectrum of STRA6 mutations: from Matthew-Wood syndrome to non-lethal anophthalmia. Human Mutation. 30: E673-81. PMID 19309693 DOI: 10.1002/Humu.21023  0.806
2009 De Pontual L, Mathieu Y, Golzio C, Rio M, Malan V, Boddaert N, Soufflet C, Picard C, Durandy A, Dobbie A, Heron D, Isidor B, Motte J, Newburry-Ecob R, Pasquier L, ... ... Etchevers H, et al. Mutational, functional, and expression studies of the TCF4 gene in pitt-hopkins syndrome Human Mutation. 30: 669-676. PMID 19235238 DOI: 10.1002/Humu.20935  0.818
2009 Benko S, Fantes JA, Amiel J, Kleinjan DJ, Thomas S, Ramsay J, Jamshidi N, Essafi A, Heaney S, Gordon CT, McBride D, Golzio C, Fisher M, Perry P, Abadie V, ... ... Etchevers HC, et al. Highly conserved non-coding elements on either side of SOX9 associated with Pierre Robin sequence. Nature Genetics. 41: 359-64. PMID 19234473 DOI: 10.1038/Ng.329  0.789
2009 Golzio C, Havis E, Nuel G, Babarit C, Munnich A, Vekemans M, Lyonnet S, Etchevers H. Program/Abstract # 500 Developmental Biology. 331: 528. DOI: 10.1016/J.Ydbio.2009.05.528  0.734
2009 Cluzeau C, Mou C, Fraitag S, Bodemer C, Munnich A, Courtois G, Etchevers H, Headon DJ, Smahi A. Crosstalk between NF-kappaB and Wnt/beta-catenin pathways involved in skin appendages development Developmental Biology. 331: 391. DOI: 10.1016/J.Ydbio.2009.05.029  0.44
2008 Sajedi E, Gaston-Massuet C, Signore M, Andoniadou CL, Kelberman D, Castro S, Etchevers HC, Gerrelli D, Dattani MT, Martinez-Barbera JP. Analysis of mouse models carrying the I26T and R160C substitutions in the transcriptional repressor HESX1 as models for septo-optic dysplasia and hypopituitarism. Disease Models & Mechanisms. 1: 241-54. PMID 19093031 DOI: 10.1242/Dmm.000711  0.49
2008 Lequeux L, Rio M, Vigouroux A, Titeux M, Etchevers H, Malecaze F, Chassaing N, Calvas P. Confirmation of RAX gene involvement in human anophthalmia. Clinical Genetics. 74: 392-5. PMID 18783408 DOI: 10.1111/J.1399-0004.2008.01078.X  0.698
2008 Thomas S, Thomas M, Wincker P, Babarit C, Xu P, Speer MC, Munnich A, Lyonnet S, Vekemans M, Etchevers HC. Human neural crest cells display molecular and phenotypic hallmarks of stem cells. Human Molecular Genetics. 17: 3411-25. PMID 18689800 DOI: 10.1093/Hmg/Ddn235  0.781
2007 de Pontual L, Trochet D, Bourdeaut F, Thomas S, Etchevers H, Chompret A, Minard V, Valteau D, Brugieres L, Munnich A, Delattre O, Lyonnet S, Janoueix-Lerosey I, Amiel J. Methylation-associated PHOX2B gene silencing is a rare event in human neuroblastoma. European Journal of Cancer (Oxford, England : 1990). 43: 2366-72. PMID 17765533 DOI: 10.1016/J.Ejca.2007.07.016  0.795
2007 Golzio C, Martinovic-Bouriel J, Thomas S, Mougou-Zrelli S, Grattagliano-Bessieres B, Bonniere M, Delahaye S, Munnich A, Encha-Razavi F, Lyonnet S, Vekemans M, Attie-Bitach T, Etchevers HC. Matthew-Wood syndrome is caused by truncating mutations in the retinol-binding protein receptor gene STRA6. American Journal of Human Genetics. 80: 1179-87. PMID 17503335 DOI: 10.1086/518177  0.794
2007 Etchevers HC, Amiel J, Lyonnet S. [Genetic and molecular bases of neurocristopathies]. Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie. 14: 668-72. PMID 17434298 DOI: 10.1016/J.Arcped.2007.02.072  0.554
2007 Baala L, Briault S, Etchevers HC, Laumonnier F, Natiq A, Amiel J, Boddaert N, Picard C, Sbiti A, Asermouh A, Attié-Bitach T, Encha-Razavi F, Munnich A, Sefiani A, Lyonnet S. Homozygous silencing of T-box transcription factor EOMES leads to microcephaly with polymicrogyria and corpus callosum agenesis. Nature Genetics. 39: 454-6. PMID 17353897 DOI: 10.1038/Ng1993  0.801
2007 Martinovic-Bouriel J, Bernabé-Dupont C, Golzio C, Grattagliano-Bessières B, Malan V, Bonnière M, Esculpavit C, Fallet-Bianco C, Mirlesse V, Le Bidois J, Aubry MC, Vekemans M, Morichon N, Etchevers H, Attié-Bitach T, et al. Matthew-Wood syndrome: report of two new cases supporting autosomal recessive inheritance and exclusion of FGF10 and FGFR2. American Journal of Medical Genetics. Part A. 143: 219-28. PMID 17236193 DOI: 10.1002/Ajmg.A.31599  0.805
2007 Etchevers H. DNA sequencing and quick clean-up Nature Protocols. DOI: 10.1038/Nprot.2007.167  0.304
2006 Etchevers HC, Amiel J, Lyonnet S. Molecular bases of human neurocristopathies. Advances in Experimental Medicine and Biology. 589: 213-34. PMID 17076285 DOI: 10.1007/978-0-387-46954-6_14  0.65
2006 Golzio C, Guirchoun J, Ozilou C, Thomas S, Goudefroye G, Morichon-Delvallez N, Vekemans M, Attié-Bitach T, Etchevers HC. Cytogenetic and histological features of a human embryo with homogeneous chromosome 8 trisomy. Prenatal Diagnosis. 26: 1201-5. PMID 17075794 DOI: 10.1002/Pd.1588  0.78
2006 Sanlaville D, Etchevers HC, Gonzales M, Martinovic J, Clément-Ziza M, Delezoide AL, Aubry MC, Pelet A, Chemouny S, Cruaud C, Audollent S, Esculpavit C, Goudefroye G, Ozilou C, Fredouille C, et al. Phenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human development. Journal of Medical Genetics. 43: 211-217. PMID 16169932 DOI: 10.1136/Jmg.2005.036160  0.788
2005 Detrait E, Etchevers HC. [Vascularization of the head and neck during development]. Journal of Neuroradiology = Journal De Neuroradiologie. 32: 147-56. PMID 16134296 DOI: 10.1016/s0150-9861(05)83132-3  0.274
2005 Detrait ER, George TM, Etchevers HC, Gilbert JR, Vekemans M, Speer MC. Human neural tube defects: developmental biology, epidemiology, and genetics. Neurotoxicology and Teratology. 27: 515-24. PMID 15939212 DOI: 10.1016/J.Ntt.2004.12.007  0.784
2005 Etchevers HC. The cap 'n' collar family member NF-E2-related factor 3 (Nrf3) is expressed in mesodermal derivatives of the avian embryo. The International Journal of Developmental Biology. 49: 363-7. PMID 15906252 DOI: 10.1387/Ijdb.041942He  0.476
2005 Deak KL, Boyles AL, Etchevers HC, Melvin EC, Siegel DG, Graham FL, Slifer SH, Enterline DS, George TM, Vekemans M, McClay D, Bassuk AG, Kessler JA, Linney E, Gilbert JR, et al. SNPs in the neural cell adhesion molecule 1 gene (NCAM1) may be associated with human neural tube defects. Human Genetics. 117: 133-42. PMID 15883837 DOI: 10.1007/S00439-005-1299-7  0.674
2005 Cai J, Ash D, Kotch LE, Jabs EW, Attie-Bitach T, Auge J, Mattei G, Etchevers H, Vekemans M, Korshunova Y, Tidwell R, Messina DN, Winston JB, Lovett M. Gene expression in pharyngeal arch 1 during human embryonic development. Human Molecular Genetics. 14: 903-12. PMID 15703188 DOI: 10.1093/Hmg/Ddi083  0.762
2005 Karmous-Benailly H, Martinovic J, Gubler MC, Sirot Y, Clech L, Ozilou C, Auge J, Brahimi N, Etchevers H, Detrait E, Esculpavit C, Audollent S, Goudefroye G, Gonzales M, Tantau J, et al. Antenatal presentation of Bardet-Biedl syndrome may mimic Meckel syndrome. American Journal of Human Genetics. 76: 493-504. PMID 15666242 DOI: 10.1086/428679  0.809
2005 Trueba SS, Augé J, Mattei G, Etchevers H, Martinovic J, Czernichow P, Vekemans M, Polak M, Attié-Bitach T. PAX8, TITF1, and FOXE1 gene expression patterns during human development: new insights into human thyroid development and thyroid dysgenesis-associated malformations. The Journal of Clinical Endocrinology and Metabolism. 90: 455-62. PMID 15494458 DOI: 10.1210/Jc.2004-1358  0.712
2004 Pinson L, Augé J, Audollent S, Mattéi G, Etchevers H, Gigarel N, Razavi F, Lacombe D, Odent S, Le Merrer M, Amiel J, Munnich A, Meroni G, Lyonnet S, Vekemans M, et al. Embryonic expression of the human MID1 gene and its mutations in Opitz syndrome. Journal of Medical Genetics. 41: 381-6. PMID 15121778 DOI: 10.1136/Jmg.2003.014829  0.815
2003 Amiel J, Laudier B, Attié-Bitach T, Trang H, de Pontual L, Gener B, Trochet D, Etchevers H, Ray P, Simonneau M, Vekemans M, Munnich A, Gaultier C, Lyonnet S. Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome. Nature Genetics. 33: 459-61. PMID 12640453 DOI: 10.1038/Ng1130  0.831
2003 Etchevers HC. Early expression of hypoxia-inducible factor 1alpha in the chicken embryo. Gene Expression Patterns : Gep. 3: 49-52. PMID 12609602 DOI: 10.1016/S1567-133X(02)00076-5  0.414
2003 Etchevers H. Vasculo- and Angio-Genesis in the Head and Neck Rivista Di Neuroradiologia. 16: 735-738. DOI: 10.1177/197140090301600508  0.284
2002 Etchevers HC, Couly G, Le Douarin NM. Morphogenesis of the branchial vascular sector. Trends in Cardiovascular Medicine. 12: 299-304. PMID 12458092 DOI: 10.1016/S1050-1738(02)00178-0  0.657
2001 Etchevers HC, Vincent C, Le Douarin NM, Couly GF. The cephalic neural crest provides pericytes and smooth muscle cells to all blood vessels of the face and forebrain Development. 1059-68. PMID 11245571  0.318
2001 Etchevers HC, Vincent C, Le Douarin NM, Couly GF. The cephalic neural crest provides pericytes and smooth muscle cells to all blood vessels of the face and forebrain. Development (Cambridge, England). 128: 1059-68. PMID 11245571  0.643
1999 Duprez D, Leyns L, Bonnin MA, Lapointe F, Etchevers H, De Robertis EM, Le Douarin N. Expression of Frzb-1 during chick development. Mechanisms of Development. 89: 179-83. PMID 10559495 DOI: 10.1016/S0925-4773(99)00206-3  0.69
1999 Duprez D, Leyns L, Bonnin MA, Lapointe F, Etchevers H, De Robertis EM, Le Douarin N. Expression of Frzb-1 during chick development Mechanisms of Development. 179-83. PMID 10559495  0.363
1999 Etchevers HC, Couly G, Vincent C, Le Douarin NM. Anterior cephalic neural crest is required for forebrain viability. Development (Cambridge, England). 126: 3533-43. PMID 10409500  0.647
1999 Etchevers HC, Couly G, Vincent C, Le Douarin NM. Anterior cephalic neural crest is required for forebrain viability Development. 3533-43. PMID 10409500  0.325
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