Heather C. Etchevers, Ph.D.
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 embryoWebsite:
https://www.marseille-medical-genetics.org/h-etchevers/Google:
"Heather Etchevers"Mean distance: (not calculated yet)
Parents
Sign in to add mentor| Barbara S. Beltz | research assistant | 1991-1992 | Wellesley |
| Nicole Marthe Le Douarin | grad student | 1994-2000 | Collège de France CNRS |
| Stanislas Lyonnet | post-doc | 2001-2002 | Université René Descartes (Paris). Faculté de médecine Necker enfants malades |
| Michel Vekemans | research scientist | 2001-2002 | Université René Descartes (Paris). Faculté de médecine Necker enfants malades |
Children
Sign in to add trainee| Elise Maréchal | grad student | 2020- | Université Aix-Marseille, INSERM U1251 |
| Christelle Golzio | grad student | 2005-2009 | Université René Descartes Paris V |
| Nicolas Chassaing | grad student | 2009-2013 | Université Toulouse III - Paul Sabatier |
| Nicolas El Robrini | grad student | 2010-2014 | Université Aix-Marseille |
| Pauline Heux | grad student | 2014-2017 | Université Aix-Marseille |
| Eric Detrait | post-doc | 2003-2005 | INSERM U393, Paris, France |
| Lekbir Baala | post-doc | 2005-2007 | INSERM U393, Paris, France |
| Sophie Thomas | post-doc | 2005-2010 | INSERM U781, Paris, France |
| Nicolas Macagno | research scientist | 2018- | Aix-Marseille Université & INSERM |
Collaborators
Sign in to add collaborator| Stéphane Zaffran | collaborator | 2010- | Université Aix-Marseille, INSERM U1251 |
| Tania Attié-Bitach | collaborator | 2000-2010 | Université René Descartes (Paris). Faculté de médecine Necker enfants malades |
| Stanislas Lyonnet | collaborator | 2002-2012 | INSERM U781, Paris, France |
| Michel Vekemans | collaborator | 2002-2012 | Université René Descartes (Paris). Faculté de médecine Necker enfants malades |
| Nicolas Lévy | collaborator | 2010-2021 | Université Aix-Marseille |
BETA: Related publications
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Publications
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| Wilmerding A, Bouteille L, Caruso N, et al. (2021) 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 |
| Haniffa M, Taylor D, Linnarsson S, et al. (2021) A roadmap for the Human Developmental Cell Atlas. Nature. 597: 196-205 |
| de la Fouchardière A, Boivin F, Etchevers HC, et al. (2021) Cutaneous Melanomas Arising during Childhood: An Overview of the Main Entities. Dermatopathology (Basel, Switzerland). 8: 301-314 |
| Romanet P, Galluso J, Kamenicky P, et al. (2021) Somatotroph Tumors and the Epigenetic Status of the Locus. International Journal of Molecular Sciences. 22 |
| Fledderus AC, Pasmans SGMA, Wolkerstorfer A, et al. (2021) 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 |
| Stefanovic S, Etchevers HC, Zaffran S. (2021) Outflow Tract Formation-Embryonic Origins of Conotruncal Congenital Heart Disease. Journal of Cardiovascular Development and Disease. 8 |
| Etchevers HC. (2021) 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 |
| Oei W, Fledderus AC, Spuls PI, et al. (2020) 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 |
| Macagno N, Pissaloux D, Etchevers H, et al. (2020) Cutaneous Melanocytic Tumors With Concomitant NRASQ61R and IDH1R132C Mutations: A Report of 6 Cases. The American Journal of Surgical Pathology |
| Calbet-Llopart N, Pascini-Garrigos M, Tell-Martí G, et al. (2020) Melanocortin-1 receptor (MC1R) genotypes do not correlate with size in two cohorts of medium-to-giant congenital melanocytic nevi. Pigment Cell & Melanoma Research |