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ArticlesPeer ReviewedFull Text
An epigenetic switch controls an alternative NR2F2 isoform that unleashes a metastatic program in melanoma
Author / Creator:Davalos, Veronica ; Lovell, Claudia D. ; Von Itter, Richard ; Dolgalev, Igor ; Agrawal, Praveen ; Baptiste, Gillian ; Kahler, David J. ; Sokolova, Elena ; Moran, Sebastian ; Piqué, Laia ; Vega-Saenz de Miera, Eleazar ; Fontanals-Cirera, Barbara ; Karz, Alcida ; Tsirigos, Aristotelis ; Yun, Chi ; Darvishian, Farbod ; Etchevers, Heather C. ; Osman, Iman ; Esteller, Manel ; Schober, Markus ; Hernando, Eva
Publisher:London: Nature Publishing Group UK
Journal title:Nature communications, 2023-04, Vol.14 (1), p.1867-16, Article 1867
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Outflow Tract Formation—Embryonic Origins of Conotruncal Congenital Heart Disease
Author / Creator:Stefanovic, Sonia ; Etchevers, Heather C. ; Zaffran, Stéphane
Publisher:Switzerland: MDPI AG
Journal title:Journal of cardiovascular development and disease, 2021-04, Vol.8 (4), p.42
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ISL1 Directly Regulates FGF10 Transcription during Human Cardiac Outflow Formation
Author / Creator:Golzio, Christelle ; Havis, Emmanuelle ; Daubas, Philippe ; Nuel, Gregory ; Babarit, Candice ; Munnich, Arnold ; Vekemans, Michel ; Zaffran, Stéphane ; Lyonnet, Stanislas ; Etchevers, Heather C.
Publisher:United States: Public Library of Science
Journal title:PloS one, 2012-01, Vol.7 (1), p.e30677
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Cutaneous Melanomas Arising during Childhood: An Overview of the Main Entities
Author / Creator:de la Fouchardière, Arnaud ; Boivin, Felix ; Etchevers, Heather C. ; Macagno, Nicolas
Publisher:Basel: MDPI AG
Journal title:Dermatopathology (Basel, Switzerland), 2021-09, Vol.8 (3), p.301-314
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A Subpopulation of Smooth Muscle Cells, Derived from Melanocyte-Competent Precursors, Prevents Patent Ductus Arteriosus
Author / Creator:Yajima, Ichiro ; Colombo, Sophie ; Puig, Isabel ; Champeval, Delphine ; Kumasaka, Mayuko ; Belloir, Elodie ; Bonaventure, Jacky ; Mark, Manuel ; Yamamoto, Hiroaki ; Taketo, Mark M. ; Choquet, Philippe ; Etchevers, Heather C. ; Beermann, Friedrich ; Delmas, Véronique ; Monassier, Laurent ; Larue, Lionel
Publisher:United States: Public Library of Science
Journal title:PloS one, 2013-01, Vol.8 (1), p.e53183
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The hedgehog pathway and ocular developmental anomalies
Author / Creator:Cavodeassi, Florencia ; Creuzet, Sophie ; Etchevers, Heather C.
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Human genetics, 2019-09, Vol.138 (8-9), p.917-936
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Heterogeneity of neuroblastoma cell identity defined by transcriptional circuitries
Author / Creator:Boeva, Valentina ; Louis-Brennetot, Caroline ; Peltier, Agathe ; Durand, Simon ; Pierre-Eugène, Cécile ; Raynal, Virginie ; Etchevers, Heather C ; Thomas, Sophie ; Lermine, Alban ; Daudigeos-Dubus, Estelle ; Geoerger, Birgit ; Orth, Martin F ; Grünewald, Thomas G P ; Diaz, Elise ; Ducos, Bertrand ; Surdez, Didier ; Carcaboso, Angel M ; Medvedeva, Irina ; Deller, Thomas ; Combaret, Valérie ; Lapouble, Eve ; Pierron, Gaelle ; Grossetête-Lalami, Sandrine ; Baulande, Sylvain ; Schleiermacher, Gudrun ; Barillot, Emmanuel ; Rohrer, Hermann ; Delattre, Olivier ; Janoueix-Lerosey, Isabelle
Publisher:New York: Nature Publishing Group US
Journal title:Nature genetics, 2017-09, Vol.49 (9), p.1408-1413
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Hiding in Plain Sight: Molecular Genetics Applied to Giant Congenital Melanocytic Nevi
Author / Creator:Etchevers, Heather C.
Publisher:United States: Elsevier Inc
Journal title:Journal of investigative dermatology, 2014-04, Vol.134 (4), p.879-882
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Analysis of mouse models carrying the I26T and R160C substitutions in the transcriptional repressor HESX1 as models for septo-optic dysplasia and hypopituitarism
Author / Creator:Sajedi, Ezat ; Gaston-Massuet, Carles ; Signore, Massimo ; Andoniadou, Cynthia L. ; Kelberman, Daniel ; Castro, Sandra ; Etchevers, Heather C. ; Gerrelli, Dianne ; Dattani, Mehul T. ; Martinez-Barbera, Juan Pedro
Publisher:England: The Company of Biologists Ltd
Journal title:Disease models & mechanisms, 2008-11, Vol.1 (4-5), p.241-254
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Epigenetic deregulation of GATA3 in neuroblastoma is associated with increased GATA3 protein expression and with poor outcomes
Author / Creator:Almutairi, Bader ; Charlet, Jessica ; Dallosso, Anthony R. ; Szemes, Marianna ; Etchevers, Heather C. ; Malik, Karim T. A. ; Brown, Keith W.
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2019-12, Vol.9 (1), p.18934-12, Article 18934
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Somatotroph Tumors and the Epigenetic Status of the GNAS Locus
Author / Creator:Romanet, Pauline ; Galluso, Justine ; Kamenicky, Peter ; Hage, Mirella ; Theodoropoulou, Marily ; Roche, Catherine ; Graillon, Thomas ; Etchevers, Heather C. ; De Murat, Daniel ; Mougel, Grégory ; Figarella-Branger, Dominique ; Dufour, Henry ; Cuny, Thomas ; Assié, Guillaume ; Barlier, Anne
Publisher:Basel: MDPI AG
Journal title:International journal of molecular sciences, 2021-07, Vol.22 (14), p.7570
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Homozygous silencing of T-box transcription factor EOMES leads to microcephaly with polymicrogyria and corpus callosum agenesis
Author / Creator:Baala, Lekbir ; Briault, Sylvain ; Etchevers, Heather C ; Laumonnier, Frédéric ; Natiq, Abdelhafid ; Amiel, Jeanne ; Boddaert, Nathalie ; Picard, Capucine ; Sbiti, Aziza ; Asermouh, Abdellah ; Attié-Bitach, Tania ; Encha-Razavi, Féréchté ; Munnich, Arnold ; Sefiani, Abdelaziz ; Lyonnet, Stanislas
Publisher:New York: Nature Publishing Group US
Journal title:Nature genetics, 2007-04, Vol.39 (4), p.454-456
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OTX2 mutations contribute to the otocephaly-dysgnathia complex
Author / Creator:Chassaing, Nicolas ; Sorrentino, Susanna ; Davis, Erica E ; Martin-Coignard, Dominique ; Iacovelli, Anthony ; Paznekas, William ; Webb, Bryn D ; Faye-Petersen, Ona ; Encha-Razavi, Férechté ; Lequeux, Leopoldine ; Vigouroux, Adeline ; Yesilyurt, Ahmet ; Boyadjiev, Simeon A ; Kayserili, Hülya ; Loget, Philippe ; Carles, Dominique ; Sergi, Consolato ; Puvabanditsin, Surasak ; Chen, Chih-Ping ; Etchevers, Heather C ; Katsanis, Nicholas ; Mercer, Catherine L ; Calvas, Patrick ; Jabs, Ethylin Wang
Publisher:London: BMJ Publishing Group Ltd
Journal title:Journal of medical genetics, 2012-06, Vol.49 (6), p.373-379
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ArticlesPeer ReviewedFull Text
Ectopic expression of Hoxb1 induces cardiac and craniofacial malformations
Author / Creator:St phane Zaffran ; Ga lle Odelin ; Stefanovic, Sonia ; Lescroart, Fabienne ; Etchevers, Heather C
Publisher:Cold Spring Harbor: Cold Spring Harbor Laboratory Press
Journal title:bioRxiv, 2018-07
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SNPs in the neural cell adhesion molecule 1 gene (NCAM1) may be associated with human neural tube defects
Author / Creator:Deak, Kristen L. ; Boyles, Abee L. ; Etchevers, Heather C. ; Melvin, Elizabeth C. ; Siegel, Deborah G. ; Graham, Felicia L. ; Slifer, Susan H. ; Enterline, David S. ; George, Timothy M. ; Vekemans, Michel ; McClay, David ; Bassuk, Alexander G. ; Kessler, John A. ; Linney, Elwood ; Gilbert, John R. ; Speer, Marcy C.
Publisher:Heidelberg: Springer
Journal title:Human genetics, 2005-07, Vol.117 (2-3), p.133-142
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A severe clinical phenotype of Noonan syndrome with neonatal hypertrophic cardiomyopathy in the second case worldwide with RAF1 S259Y neomutation
Author / Creator:Jaouadi, Hager ; Chehida, Amel Ben ; Kraoua, Lilia ; Etchevers, Heather C. ; Argiro, Laurent ; Kasdallah, Nadia ; Blibech, Sonia ; Delague, Valérie ; Lévy, Nicolas ; Tebib, Néji ; Mrad, Ridha ; Abdelhak, Sonia ; Benkhalifa, Rym ; Zaffran, Stéphane
Publisher:England: Cambridge University Press
Journal title:Genetical research, 2019, Vol.101, p.e6, Article e6
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A roadmap for the Human Developmental Cell Atlas
Author / Creator:Haniffa, Muzlifah ; Taylor, Deanne ; Linnarsson, Sten ; Aronow, Bruce J. ; Bader, Gary D. ; Barker, Roger A. ; Camara, Pablo G. ; Camp, J. Gray ; Chédotal, Alain ; Copp, Andrew ; Etchevers, Heather C. ; Giacobini, Paolo ; Göttgens, Berthold ; Guo, Guoji ; Hupalowska, Ania ; James, Kylie R. ; Kirby, Emily ; Kriegstein, Arnold ; Lundeberg, Joakim ; Marioni, John C. ; Meyer, Kerstin B. ; Niakan, Kathy K. ; Nilsson, Mats ; Olabi, Bayanne ; Pe’er, Dana ; Regev, Aviv ; Rood, Jennifer ; Rozenblatt-Rosen, Orit ; Satija, Rahul ; Teichmann, Sarah A. ; Treutlein, Barbara ; Vento-Tormo, Roser ; Webb, Simone
Publisher:London: Nature Publishing Group UK
Journal title:Nature (London), 2021-09, Vol.597 (7875), p.196-205
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Acknowledgment to Reviewers of Journal of Cardiovascular Development and Disease in 2021
Publisher:Basel: MDPI AG
Journal title:Journal of cardiovascular development and disease, 2022-01, Vol.9 (2), p.45
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Multi-modal refinement of the human heart atlas during the first gestational trimester
Author / Creator:De Bono, Christopher ; Xu, Yichi ; Kausar, Samina ; Herbane, Marine ; Humbert, Camille ; Rafatov, Sevda ; Missirian, Chantal ; Moreno, Mathias ; Shi, Weiyang ; Gitton, Yorick I ; Lombardini, Alberto ; Vanzetta, Ivo ; Mazaud-Guittot, Severine ; Chedotal, Alain ; Baudot, Anais ; Zaffran, Stephane ; Etchevers, Heather C
Publisher:Cold Spring Harbor: Cold Spring Harbor Laboratory Press
Journal title:bioRxiv, 2025-01
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Multiple congenital malformations arise from somatic mosaicism for constitutively active Pik3ca signalling
Author / Creator:Marechal, Elise ; Poliard, Anne ; Moreno, Mathias ; Legrix, Mathilde ; Macagno, Nicolas ; Gregoire Mondielli ; Fauquier, Teddy ; Barlier, Anne ; Etchevers, Heather C
Publisher:Cold Spring Harbor: Cold Spring Harbor Laboratory Press
Journal title:bioRxiv, 2022-04
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An epigenetic switch controls an alternative NR2F2 isoform that unleashes a metastatic program in melanoma

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Outflow Tract Formation—Embryonic Origins of Conotruncal Congenital Heart Disease

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ISL1 Directly Regulates FGF10 Transcription during Human Cardiac Outflow Formation

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Cutaneous Melanomas Arising during Childhood: An Overview of the Main Entities

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A Subpopulation of Smooth Muscle Cells, Derived from Melanocyte-Competent Precursors, Prevents Patent Ductus Arteriosus

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The hedgehog pathway and ocular developmental anomalies

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Heterogeneity of neuroblastoma cell identity defined by transcriptional circuitries

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Hiding in Plain Sight: Molecular Genetics Applied to Giant Congenital Melanocytic Nevi

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Analysis of mouse models carrying the I26T and R160C substitutions in the transcriptional repressor HESX1 as models for septo-optic dysplasia and hypopituitarism

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Epigenetic deregulation of GATA3 in neuroblastoma is associated with increased GATA3 protein expression and with poor outcomes

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Somatotroph Tumors and the Epigenetic Status of the GNAS Locus

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Homozygous silencing of T-box transcription factor EOMES leads to microcephaly with polymicrogyria and corpus callosum agenesis

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OTX2 mutations contribute to the otocephaly-dysgnathia complex

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Ectopic expression of Hoxb1 induces cardiac and craniofacial malformations

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SNPs in the neural cell adhesion molecule 1 gene (NCAM1) may be associated with human neural tube defects

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A severe clinical phenotype of Noonan syndrome with neonatal hypertrophic cardiomyopathy in the second case worldwide with RAF1 S259Y neomutation

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A roadmap for the Human Developmental Cell Atlas

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Acknowledgment to Reviewers of Journal of Cardiovascular Development and Disease in 2021

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Multi-modal refinement of the human heart atlas during the first gestational trimester

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Multiple congenital malformations arise from somatic mosaicism for constitutively active Pik3ca signalling

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