Heather Etchevers

Identifiants chercheurs

IdHAL :

heather-etchevers

ORCID :

0000-0003-0201-3799

IdRef :

18606179X

ResearcherID :

http://www.researcherid.com/rid/B-5813-2012

Publications

Article dans une revue (43)

A short report on melanocyte/melanoma culture, senescence, and reproducibility Lionel Larue,Duarte C Barral,Veronique Delmas,Sara Egea-Rodriguez,Daniel Aldeaet al. Pigment Cell and Melanoma Research, 2026, 39 (2), pp.e70084. ⟨10.1111/pcmr.70084⟩ Article dans une revue hal-05533385v3
The people behind the papers-Christopher De Bono, Stephane Zaffran and Heather Etchevers Christopher de Bono,Stephane Zaffran,Heather Etchevers Development, 2025, 152 (5), ⟨10.1242/dev.204734⟩ Article dans une revue hal-05264563v1
Multi-modal refinement of the human heart atlas during the first gestational trimester Christopher de Bono,Yichi Xu,Samina Kausar,Marine Herbane,Camille Humbertet al. Development (Cambridge, England), 2025, 152 (5), pp.dev.204555. ⟨10.1242/dev.204555⟩ Article dans une revue hal-04980602v1
Deconvoluted Methylation Profiles Discriminate between Closely Related Melanocytic Nevi Daniel Aldea,Nicolas Macagno,Elise Marechal,Mathias Moreno,Pauline Romanetet al. Journal of Investigative Dermatology, 2025, 145 (5), pp.1222-1226.e4. ⟨10.1016/j.jid.2024.10.595⟩ Article dans une revue hal-05458318v1
Modeling corticotroph deficiency with pituitary organoids supports the functional role of NFKB2 in human pituitary differentiation Thi Thom Mac,Teddy Fauquier,Nicolas Jullien,Pauline Romanet,Heather Etcheverset al. eLife, 2024, 12, ⟨10.7554/eLife.90875.3⟩ Article dans une revue hal-04911514v1
An epigenetic switch controls an alternative NR2F2 isoform 2 that unleashes a metastatic program in melanoma Verónica Davalos,Claudia Lovell,Richard von Itter,Igor Dolgalev,Praveen Agrawalet al. Nature Communications, In press, 14 (1), pp.1867. ⟨10.1038/s41467-023-36967-2⟩ Article dans une revue hal-04007075v1
Sustained experimental activation of FGF8/ERK in the developing chicken spinal cord models early events in ERK-mediated tumorigenesis Axelle Wilmerding,Lauranne Bouteille,Nathalie Caruso,Ghislain Bidaut,Heather C Etcheverset al. Neoplasia, 2022, 24 (2), pp.120 - 132. ⟨10.1016/j.neo.2021.12.006⟩ Article dans une revue hal-03863327v1
Somatotroph Tumors and the Epigenetic Status of the GNAS Locus Pauline Romanet,Justine Galluso,Peter Kamenicky,Mirella Hage,Marily Theodoropoulouet al. International Journal of Molecular Sciences, 2021, 22 (14), pp.7570. ⟨10.3390/ijms22147570⟩ Article dans une revue hal-03288514v1
A roadmap for the Human Developmental Cell Atlas Muzlifah Haniffa,Deanne Taylor,Sten Linnarsson,Bruce Aronow,Gary Baderet al. Nature, 2021, 597 (7875), pp.196-205. ⟨10.1038/s41586-021-03620-1⟩ Article dans une revue hal-03365045v1
Cutaneous Melanomas Arising during Childhood: An Overview of the Main Entities Arnaud de La Fouchardière,Felix Boivin,Heather Etchevers,Nicolas Macagno Dermatopathology, 2021, 8 (3), pp.301-314. ⟨10.3390/dermatopathology8030036⟩ Article dans une revue hal-03312882v1
Domains and outcomes of the core outcome set of congenital melanocytic naevi for clinical practice and research (the OCOMEN project): part 2* A.C. Fledderus,S.G.M.A. Pasmans,A. Wolkerstorfer,W. Oei,H.C. Etcheverset al. British Journal of Dermatology, 2021, 185 (5), pp.970-977. ⟨10.1111/bjd.20437⟩ Article dans une revue hal-03662367v1
Outflow Tract Formation—Embryonic Origins of Conotruncal Congenital Heart Disease Sonia Stefanovic,Heather Etchevers,Stéphane Zaffran Journal of Cardiovascular Development and Disease, 2021, 8 (4), pp.42. ⟨10.3390/jcdd8040042⟩ Article dans une revue hal-03663016v1
Melanocortin‐1 receptor ( MC1R ) genotypes do not correlate with size in two cohorts of medium‐to‐giant congenital melanocytic nevi Neus Calbet-Llopart,Mirella Pascini-Garrigos,Gemma Tell-Martí,Miriam Potrony,Vanessa Martins da Silvaet al. Pigment Cell & melanoma research, 2020, 33 (5), pp.685-694. ⟨10.1111/pcmr.12883⟩ Article dans une revue hal-03609329v1
Cutaneous melanocytic tumors with concomitant NRAS Q61R and IDH1 R132C mutations: a report of six cases Nicolas Macagno,Daniel Pissaloux,Heather Etchevers,Véronique Haddad,Béatrice Vergieret al. American Journal of Surgical Pathology, 2020 Article dans une revue hal-02540120v1
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 W Oei,a C Fledderus,P I Spuls,C a M Eggen,J Kottneret al. British Journal of Dermatology, 2020, ⟨10.1111/bjd.19694⟩ Article dans une revue hal-03156673v1
Cutaneous Melanocytic Tumors With Concomitant NRAS Q61R and IDH1 R132C Mutations Nicolas Macagno,Daniel Pissaloux,Heather Etchevers,Heather Etchevers,Véronique Haddadet al. American Journal of Surgical Pathology, 2020, 44 (10), pp.1398-1405. ⟨10.1097/PAS.0000000000001500⟩ Article dans une revue hal-03882539v1
The hedgehog pathway and ocular developmental anomalies Florencia Cavodeassi,Sophie Creuzet,Heather Etchevers Human Genetics, 2019, 138 (8-9), pp.917-936. ⟨10.1007/s00439-018-1918-8⟩ Article dans une revue hal-01853948v1
The diverse neural crest: from embryology to human pathology Heather Etchevers,Elisabeth Dupin,Nicole M. Le Douarin Development, 2019, 146 (5), ⟨10.1242/dev.169821⟩ Article dans une revue hal-02478901v1
Macrophage-Derived IL1 beta and TNF alpha Regulate Arginine Metabolism in Neuroblastoma Livingstone Fultang,Laura D. Gamble,Luciana Gneo,Andrea M. Berry,Sharon A. Eganet al. Cancer Research, 2019, 79 (3), pp.611-624. ⟨10.1158/0008-5472.CAN-18-2139⟩ Article dans une revue hal-02462178v1
A severe clinical phenotype of Noonan syndrome with neonatal hypertrophic cardiomyopathy in the second case worldwide with RAF1 S259Y neomutation Hager Jaouadi,Amel Ben Chehida,Lilia Kraoua,Heather Etchevers,Laurent Argiroet al. Genetics Research, 2019, 101, pp.e6. ⟨10.1017/S0016672319000041⟩ Article dans une revue hal-02461305v1
Epigenetic deregulation of GATA3 in neuroblastoma is associated with increased GATA3 protein expression and with poor outcomes Bader Almutairi,Jessica Charlet,Anthony R Dallosso,Marianna Szemes,Heather Etcheverset al. Scientific Reports, 2019, 9, pp.18934. ⟨10.1038/s41598-019-55382-6⟩ Article dans une revue hal-02407665v1
Widespread dynamic and pleiotropic expression of the melanocortin-1-receptor (MC1R) system is conserved across chick, mouse and human embryonic development Anna C. Thomas,Pauline Heux,Chloe Santos,Wisenave Arulvasan,Nita Solankyet al. Birth Defects Research, 2018, 110 (5), pp.443-455. ⟨10.1002/bdr2.1183⟩ Article dans une revue hal-01847993v1
Macrophage IL-1B and TNF-a create an immune-metabolic loop regulating Arginase2 in neuroblastoma Livingstone Fultang,Laura D Gamble,Luciana Gneo,Andrea M Berry,Sharon A Eganet al. Cancer Research, In press Article dans une revue hal-01920354v1
Ectopic expression of Hoxb1 induces cardiac and craniofacial malformations Stéphane Zaffran,Gaelle Odelin,Sonia Stefanovic,Fabienne Lescroart,Heather Etchevers Genesis - The Journal of Genetics and Development, 2018, 6-7, pp.e23221. ⟨10.1101/300368⟩ Article dans une revue hal-01851980v1
The diverse neural crest: from embryology to human pathology Heather Etchevers,Elisabeth Dupin,Nicole Le Douarin Development (Cambridge, England), In press Article dans une revue hal-01851974v2
Giant congenital melanocytic nevus with vascular malformation and epidermal cysts associated with a somatic activating mutation in BRAF Heather C. Etchevers,Christian Rose,Birgit Kahle,Helmuth Vorbringer,Frederic Finaet al. Pigment Cell and Melanoma Research, In press, ⟨10.1111/pcmr.12685⟩ Article dans une revue hal-01613153v2
Reduced H3K27me3 Expression is Common in Nodular Melanomas of Childhood Associated With Congenital Melanocytic Nevi But Not in Proliferative Nodules Reply Nicolas Macagno,Heather C. Etchevers,Nausicaa Malissen,Angelique Rome,Sylvie Hesseet al. American Journal of Surgical Pathology, 2018, 42 (5), pp.701-704 Article dans une revue hal-02000327v1
Heterogeneity of neuroblastoma cell identity defined by transcriptional circuitries Valentina Boeva,Caroline Louis-Brennetot,Agathe Peltier,Simon Durand,Cecile Pierre-Eugeneet al. Nature Genetics, 2017, 49 (9), pp.1408-1413. ⟨10.1038/ng.3921⟩ Article dans une revue hal-01741718v1
Cardiac outflow morphogenesis depends on effects of retinoic acid signaling on multiple cell lineages Nicolas El Robrini,Heather C. Etchevers,Lucile Ryckebüsch,Emilie Faure,Nathalie Eudeset al. Developmental Dynamics, 2016, 245 (3), pp.388-401. ⟨10.1002/dvdy.24357⟩ Article dans une revue hal-01469053v1
Targeted resequencing identifies PTCH1 as a major contributor to ocular developmental anomalies and extends the SOX2 regulatory network Nicolas Chassaing,Erica E. Davis,Kelly L. Mcknight,Adrienne R. Niederriter,Alexandre Causseet al. Genome Research, 2016, 26 (4), pp.474-485. ⟨10.1101/gr.196048.115⟩ Article dans une revue hal-01282340v1
A Subpopulation of Smooth Muscle Cells, Derived from Melanocyte-Competent Precursors, Prevents Patent Ductus Arteriosus Ichiro Yajima,Sophie Colombo,Isabel Puig,Delphine Champeval,Mayuko Kumasakaet al. PLoS ONE, 2013, 8 (1), pp.e53183. ⟨10.1371/journal.pone.0053183⟩ Article dans une revue hal-04985637v1
ISL1 directly regulates FGF10 transcription during human cardiac outflow formation. Christelle Golzio,Emmanuelle Havis,Philippe Daubas,Gregory Nuel,Candice Babaritet al. PLoS ONE, 2012, 7 (1), pp.e30677. ⟨10.1371/journal.pone.0030677⟩ Article dans une revue hal-00686361v1
Dissection of the MYCN locus in Feingold Syndrome and isolated esophageal atresia Loic de Pontual,Marie Cognet,Agnès Nougayrede,Valérie Malan,Patrick Callieret al. European Journal of Human Genetics, 2011, ⟨10.1038/ejhg.2010.225⟩ Article dans une revue hal-00608020v1
GERMLINE GAIN-OF-FUNCTION MUTATIONS of ALK DISRUPT CENTRAL NERVOUS SYSTEM DEVELOPMENT Loic de Pontual,Dania Kettaneh,Chris Gordon,Myriam Oufadem,Nathalie Boddaertet al. Human Mutation, 2011, 32 (3), pp.272. ⟨10.1002/humu.21442⟩ Article dans une revue hal-00616287v1
High-throughput Sequencing of a 4.1 Mb Linkage Interval Reveals &lt;i&gt;FLVCR2&lt;/i&gt; Deletions and Mutations in Lethal Cerebral Vasculopathy Sophie Thomas,Ferechte Encha-Razavi,Louise Devisme,Heather C Etchevers,Bettina Bessieres-Grattaglianoet al. Human Mutation, 2010, 31 (10), pp.1134. ⟨10.1002/humu.21329⟩ Article dans une revue hal-00574003v1
Phenotypic spectrum of STRA6 mutations: from Matthew-Wood syndrome to non-lethal anophthalmia. Nicolas Chassaing,Christelle Golzio,Sylvie Odent,Léopoldine Lequeux,Adeline Vigourouxet al. Human Mutation, 2009, 30 (5), pp.E673-81. ⟨10.1002/humu.21023⟩ Article dans une revue inserm-00372285v1
Loss-of-Function Mutation in the Dioxygenase-Encoding FTO Gene Causes Severe Growth Retardation and Multiple Malformations Sarah Boissel,Orit Reish,Karine Proulx,Hiroko Kawagoe-Takaki,Barbara Sedgwicket al. American Journal of Human Genetics, 2009, 85 (1), pp.106-111. ⟨10.1016/j.ajhg.2009.06.002⟩ Article dans une revue hal-02044723v1
Highly conserved non-coding elements on either side of SOX9 associated with Pierre Robin sequence. S. Benko,Fantes Ja,J. Amiel,Kleinjan Dj,S. Thomaset al. Nature Genetics, 2009, 41(3), pp.359-364 Article dans une revue hal-00406268v1
Mutational, functional, and expression studies of the TCF4 gene in Pitt-Hopkins syndrome Loic de Pontual,Yves Mathieu,Christelle Golzio,Marlène Rio,Valérie Malanet al. Human Mutation, 2009, 30 (4), pp.669-676. ⟨10.1002/humu.20935⟩ Article dans une revue istex hal-02134020v1
Epistasis between RET and BBS mutations modulates enteric innervation and causes syndromic Hirschsprung disease. Loïc de Pontual,Norann A Zaghloul,Sophie Thomas,Erica E Davis,David M Mcgaugheyet al. Proceedings of the National Academy of Sciences of the United States of America, 2009, 106 (33), pp.13921-6. ⟨10.1073/pnas.0901219106⟩ Article dans une revue pasteur-00604838v1
Confirmation of RAX gene involvement in human anophthalmia. L. Lequeux,Marlène Rio,Armelle Vigouroux,Matthias Titeux,Heather C. Etcheverset al. Clinical Genetics, 2008, 74 (4), pp.392-395. ⟨10.1111/j.1399-0004.2008.01078.x⟩ Article dans une revue inserm-00322979v1
Matthew-Wood syndrome is caused by truncating mutations in the retinol-binding protein receptor gene STRA6. Christelle Golzio,Jelena Martinovic-Bouriel,Sophie Thomas,Soumaya Mougou-Zrelli,Bettina Grattagliano-Bessiereset al. American Journal of Human Genetics, 2007, 80 (6), pp.1179-87. ⟨10.1086/518177⟩ Article dans une revue hal-00172593v1
Methylation-associated PHOX2B gene silencing is a rare event in human neuroblastoma. Loïc de Pontual,Delphine Trochet,Franck Bourdeaut,Sophie Thomas,Heather C. Etcheverset al. European Journal of Cancer, 2007, 43 (16), pp.2366-72. ⟨10.1016/j.ejca.2007.07.016⟩ Article dans une revue inserm-00323027v1

Communication dans un congrès (2)

Refinement of the four-dimensional human heart atlas during the first trimester of gestation with rare and diverse cell states Kausar Samina,Herbane Marine,Marechal Elise,Fabienne Lescroart,Lenfant Nicolaset al. Cardiovascular Development and Regeneration, May 2022, Marseille, France Communication dans un congrès hal-04237843v1
Refinement of the four-dimensional human heart atlas during the first trimester of gestation with rare and diverse cell states Kausar Samina,Herbane Marine,Marechal Elise,Fabienne Lescroart,Lenfant Nicolaset al. HCA Developmental and Pediatric Cell Atlas Meeting, Human Cell Atlas, Nov 2022, PARIS, France Communication dans un congrès hal-04237856v1

Chapitre d'ouvrage (1)

Embryologie de l'oeil Sophie Creuzet,Heather Etchevers Denis, Danièle; Qui Buoc, Emmanuel; Aziz Alessi, Aurore. Ophtalmologie pédiatrique : Rapport SFO 2017, Elsevier-Masson, pp.739-756, 2017, 978-2-294-75022-9. ⟨10.6084/m9.figshare.4983362.v1⟩ Chapitre d'ouvrage hal-01586398v2

Pré-publication, Document de travail (6)

Oncogenic MAPK pathway activation induces a congenital and progressively lethal rare neuropathy in mice Elise Marechal,Daniel Aldea,Patrice Quintana,Grégoire Mondielli,Nathalie Bernard- Marissalet al. 2026 Pré-publication, Document de travail hal-05461289v1
RIPOR2 promotes multinucleation of melanoma cells downstream of the RAS/ERK oncogenic pathway Axelle Wilmerding,Aurélie Richard,Nicolas Macagno,Estelle Hirsinger,Tarek Gharsalliet al. 2025 Pré-publication, Document de travail hal-05393365v1
Multi-modal refinement of the human heart atlas during the first gestational trimester Christopher de Bono,Yichi Xu,Samina Kausar,Marine Herbane,Camille Humbertet al. 2025 Pré-publication, Document de travail hal-04800957v1
Multiple congenital malformations arise from somatic mosaicism for constitutively active Pik3ca signalling Elise Marechal,Anne Poliard,Kilian Henry,Mathias Moreno,Mathilde Legrixet al. 2023 Pré-publication, Document de travail hal-03809038v1
Melanocortin-1 receptor (MC1R) genotypes do not correlate with size in two cohorts of medium-to-giant congenital melanocytic nevi Institutional affiliations Neus Calbet-Llopart,Mirella Pascini-Garrigos,Gemma Tell-Martí,Miriam Potrony,Vanessa Martins da Silvaet al. 2020 Pré-publication, Document de travail hal-02540105v1
Pericyte ontogeny: the use of chimeras to track a cell lineage of diverse germ line origins Heather C. Etchevers 2017 Pré-publication, Document de travail hal-01586419v1

HDR (2)

University habilitation to direct research Heather Etchevers Embryology and Organogenesis. Université de la Méditerranée - Aix-Marseille II, 2012 HDR tel-00709758v1
Qualification thesis to directing research at the University of the Mediterranean Aix-Marseille II Heather C. Etchevers Development Biology. Aix-Marseille Université (AMU), 2012 HDR tel-01469161v1