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Heather Etchevers, Ph. D.'s Publications

Staff scientist (CR1) , INSERM
Marseille, France

Research field: Biological Sciences - Embryology
congenital malformations, genetics, epigenetics, stem cells
Web Page (1) | Book Section (3) | Journal Article (48)

Journal Article

Heather C Etchevers (2014) Hiding in plain sight: molecular genetics applied to giant congenital melanocytic nevi., 879-82. In The Journal of Investigative Dermatology 134 (4).
Ichiro Yajima, Sophie Colombo, Isabel Puig, Delphine Champeval, Mayuko Kumasaka, Elodie Belloir, Jacky Bonaventure, Manuel Mark, Hiroaki Yamamoto, Mark M Taketo, Philippe Choquet, Heather C Etchevers, Friedrich Beermann, Véronique Delmas, Laurent Monassier, Lionel Larue (2013) A subpopulation of smooth muscle cells, derived from melanocyte-competent precursors, prevents patent ductus arteriosus., e53183. In PloS one 8 (1).
H Etchevers, T Bret (2013) Au coeur des actions sociales, 40-41. In Kiwanis Magazine 132 (mars-avril).
Christine S Van Der Werf, Tara D Wabbersen, Nai-Hua Hsiao, Joana Paredes, Heather C Etchevers, Peter M Kroisel, Dick Tibboel, Candice Babarit, Richard a Schreiber, Edward J Hoffenberg, Michel Vekemans, Sirkka L Zeder, Isabella Ceccherini, Stanislas Lyonnet, Ana S Ribeiro, Raquel Seruca, Gerard J Te Meerman, Sven C D van Ijzendoorn, Iain T Shepherd, Joke B G M Verheij, Robert M W Hofstra (2012) CLMP is required for intestinal development, and loss-of-function mutations cause congenital short-bowel syndrome., 453-462.e3. In Gastroenterology 142 (3).
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Christelle Golzio, Emmanuelle Havis, Philippe Daubas, Gregory Nuel, Candice Babarit, Arnold Munnich, Michel Vekemans, Stéphane Zaffran, Stanislas Lyonnet, Heather C Etchevers (2012) ISL1 Directly Regulates FGF10 Transcription during Human Cardiac Outflow Formation., e30677. In PLoS ONE 7 (1).
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Nicolas Chassaing, Susanna Sorrentino, Erica E Davis, Dominique Martin-Coignard, Anthony Iacovelli, William Paznekas, Bryn D Webb, Ona Faye-Petersen, Férechté Encha-Razavi, Leopoldine Lequeux, Adeline Vigouroux, Ahmet Yesilyurt, Simeon A Boyadjiev, Hülya Kayserili, Philippe Loget, Dominique Carles, Consolato Sergi, Surasak Puvabanditsin, Chih-Ping Chen, Heather C Etchevers, Nicholas Katsanis, Catherine L Mercer, Patrick Calvas, Ethylin Wang Jabs (2012) OTX2 mutations contribute to the otocephaly-dysgnathia complex., 373-9. In Journal of Medical Genetics 49 (6).
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Deidre R Krupp, Pu-Ting Xu, Sophie Thomas, Andrew Dellinger, Heather C Etchevers, Michel Vekemans, John R Gilbert, Marcy C Speer, Allison E Ashley-Koch, Simon G Gregory (2012) Transcriptome profiling of genes involved in neural tube closure during human embryonic development using long serial analysis of gene expression (long-SAGE).. In Birth Defects Research. Part A.
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Matthias Macé, Stéphane D Galiacy, Angélique Erraud, José Enrique Mejía, Heather Etchevers, Michèle Allouche, Laurence Desjardins, Patrick Calvas, François Malecaze (2011) Comparative transcriptome and network biology analyses demonstrate antiproliferative and hyperapoptotic phenotypes in human keratoconus corneas., 6181-91. In Investigative Ophthalmology & Visual Science 52 (9).
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Marie Cognet, Agnés Nougayrede, Valérie Malan, Patrick Callier, Celia Cretolle, Laurence Faivre, David Genevieve, Alice Goldenberg, Delphine Heron, Sandra Mercier, Nicole Philip, Sabine Sigaudy, Alain Verloes, Sabine Sarnacki, Arnold Munnich, Michel Vekemans, Stanislas Lyonnet, Heather Etchevers, Jeanne Amiel, Loïc de Pontual (2011) Dissection of the MYCN locus in Feingold syndrome and isolated oesophageal atresia., 602-6. In European Journal of Human Genetics 19 (5).
Loïc de Pontual, Dania Kettaneh, Christopher T. Gordon, Myriam Oufadem, Nathalie Boddaert, Melissa Lees, Laurent Balu, Eric Lachassinne, Andy Petros, Julie Mollet, Louise C. Wilson, Arnold Munnich, Laurence Brugière, Olivier Delattre, Michel Vekemans, Heather Etchevers, Stanislas Lyonnet, Isabelle Janoueix-Lerosey, Jeanne Amiel (2011) Germline gain-of-function mutations of ALK disrupt central nervous system development., 272-6. In Human Mutation 32 (3).
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Sven Krengel, Helmut Breuninger, Mark Beckwith, Heather C Etchevers (2011) Meeting report from the 2011 international expert meeting ... authors version, E1-6. In Pigment Cell & Melanoma Research 24 (4).
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Heather Etchevers (2011) Primary culture of chick, mouse or human neural crest cells, 1568-1577. In Nature Protocols 6 (10).
Sophie Thomas, Ferechté Encha-Razavi, Louise Devisme, Heather Etchevers, Bettina Bessieres-Grattagliano, Géraldine Goudefroye, Nadia Elkhartoufi, Emilie Pateau, Amale Ichkou, Maryse Bonnière, Pascale Marcorelle, Philippe Parent, Sylvie Manouvrier, Muriel Holder, Annie Laquerrière, Laurence Loeuillet, Joelle Roume, Jelena Martinovic, Soumaya Mougou-Zerelli, Marie Gonzales, Vincent Meyer, Marc Wessner, Christine Bole Feysot, Patrick Nitschke, Nadia Leticee, Arnold Munnich, Stanislas Lyonnet, Peter Wookey, Gabor Gyapay, Bernard Foliguet, Michel Vekemans, Tania Attié-Bitach (2010) High-throughput sequencing of a 4.1 Mb linkage interval reveals FLVCR2 deletions and mutations in lethal cerebral vasculopathy, 1134-41. In Human Mutation 31 (10).
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Myriam Chaabouni, Heather Etchevers, Marie Christine De Blois, Patrick Calvas, Marie Christine Waill-Perrier, Michel Vekemans, Serge Pierrick Romana (2010) Identification of the IRXB gene cluster as candidate genes in severe dysgenesis of the ocular anterior segment., 4380-6. In Investigative Ophthalmology & Visual Science 51 (9).
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Loïc de Pontual, Norann A Zaghloul, Sophie Thomas, Erica E Davis, David M McGaughey, Hélène Dollfus, Clarisse Baumann, Seneca L Bessling, Candice Babarit, Anna Pelet, Cecilia Gascue, Philip Beales, Arnold Munnich, Stanislas Lyonnet, Heather Etchevers, Tania Attie-Bitach, Jose L Badano, Andrew S McCallion, Nicholas Katsanis, Jeanne Amiel (2009) Epistasis between RET and BBS mutations modulates enteric innervation and causes syndromic Hirschsprung disease, 13921-6. In Proceedings of the National Academy of Sciences of the United States of America 106 (33).
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Sabina Benko, Judy A Fantes, Jeanne Amiel, Dirk-Jan Kleinjan, Sophie Thomas, Jacqueline Ramsay, Negar Jamshidi, Abdelkader Essafi, Simon Heaney, Christopher T Gordon, David McBride, Christelle Golzio, Malcolm Fisher, Paul Perry, Véronique Abadie, Carmen Ayuso, Muriel Holder-Espinasse, Nicky Kilpatrick, Melissa M Lees, Arnaud Picard, I Karen Temple, Paul Thomas, Marie-Paule Vazquez, Michel Vekemans, Hugues Roest Crollius, Nicholas D Hastie, Arnold Munnich, Heather C Etchevers, Anna Pelet, Peter G Farlie, David R Fitzpatrick, Stanislas Lyonnet (2009) Highly conserved non-coding elements on either side of SOX9 associated with Pierre Robin sequence., 359-64. In Nature Genetics 41 (3).
Sarah Boissel, Orit Reish, Karine Proulx, Hiroko Kawagoe-Takaki, Barbara Sedgwick, Giles S H Yeo, David Meyre, Christelle Golzio, Florence Molinari, Noman Kadhom, Heather C Etchevers, I Sadaf Farooqi, Philippe Froguel, Tomas Lindahl, Stephen O Rahilly, Arnold Munnich, Vladimir Saudek, Stephen O'Rahilly, Laurence Colleaux (2009) Loss-of-function mutation in the dioxygenase-encoding FTO gene causes severe growth retardation and multiple malformations, 106-11. In American Journal of Human Genetics 85 (1).
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Loïc de Pontual, Yves Mathieu, Christelle Golzio, Marlene Rio, Valérie Malan, Nathalie Boddaert, Christine Soufflet, Capucine Picard, Anne Durandy, Angus Dobbie, Delphine Heron, Bertrand Isidor, Jacques Motte, Ruth Newburry-Ecob, Laurent Pasquier, Marc Tardieu, Géraldine Viot, Francis Jaubert, Arnold Munnich, Laurence Colleaux, Michel Vekemans, Heather Etchevers, Stanislas Lyonnet, Jeanne Amiel (2009) Mutational, functional, and expression studies of the TCF4 gene in Pitt-Hopkins syndrome., 669-76. In Human Mutation 30 (4).
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B Bessières-Grattagliano, B Foliguet, L Devisme, L Loeuillet, P Marcorelles, M Bonnière, A Laquerrière, C Fallet-Bianco, J Martinovic, S Zrelli, N Leticee, V Cayol, H C Etchevers, M Vekemans, T Attie-Bitach, F Encha-Razavi (2009) Refining the clinicopathological pattern of cerebral proliferative glomeruloid vasculopathy (Fowler syndrome): report of 16 fetal cases., 386-92. In European Journal of Medical Genetics 52 (6).
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Sabina Benko, Judy A Fantes, Jeanne Amiel, Dirk-Jan Kleinjan, Sophie Thomas, Jacqueline Ramsay, Negar Jamshidi, Abdelkader Essafi, Simon Heaney, Christopher T Gordon, David McBride, Christelle Golzio, Malcolm Fisher, Paul Perry, Véronique Abadie, Carmen Ayuso, Muriel Holder-Espinasse, Nicky Kilpatrick, Melissa M Lees, Arnaud Picard, I Karen Temple, Paul Thomas, Marie-Paule Vazquez, Michel Vekemans, Hugues Roest Crollius, Nicholas D Hastie, Arnold Munnich, Heather C Etchevers, Anna Pelet, Peter G Farlie, David R Fitzpatrick, Stanislas Lyonnet (2009) SI: Highly conserved non-coding elements on either side of SOX9 associated with Pierre Robin sequence., 359-64. In Nature Genetics 41 (3).