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 embryo
Website:
https://www.marseille-medical-genetics.org/h-etchevers/
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Publications

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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
Almutairi B, Charlet J, Dallosso AR, et al. (2019) Epigenetic deregulation of GATA3 in neuroblastoma is associated with increased GATA3 protein expression and with poor outcomes. Scientific Reports. 9: 18934
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