Difference between revisions of "Etchevers:Publications list"

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'''2007'''<cite>Pontual-Cancer-2007 pmid=17765533</cite>
Pontual-Cancer-2007 pmid=17765533
Loic-2007 pmid=17765533
// This is a test for future updates as we do hope to keep publishing. I'd like to figure out how to not have to cite as above to get automatic formatting.
// This is a test for future updates as we do hope to keep publishing. I'd like to figure out how to not have to cite as above to get automatic formatting.

Revision as of 08:32, 17 October 2007


Reprints available upon request; erase the final "a" in my address when you send the message .

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  1. de Pontual L, Trochet D, Bourdeaut F, Thomas S, Etchevers H, Chompret A, Minard V, Valteau D, Brugieres L, Munnich A, Delattre O, Lyonnet S, Janoueix-Lerosey I, and Amiel J. Methylation-associated PHOX2B gene silencing is a rare event in human neuroblastoma. Eur J Cancer. 2007 Nov;43(16):2366-72. DOI:10.1016/j.ejca.2007.07.016 | PubMed ID:17765533 | HubMed [Loic-2007]
    This is a test for future updates as we do hope to keep publishing. I'd like to figure out how to not have to cite as above to get automatic formatting.

• Golzio C, Martinovic-Bouriel J, Thomas S, Mougou-Zrelli S, Grattagliano-Bessieres B, Bonniere M, Delahaye S, Munnich A, Encha-Razavi F, Lyonnet S, Vekemans M, Attie-Bitach T, Etchevers HC. Matthew-Wood syndrome is caused by truncating mutations in the retinol-binding protein receptor gene STRA6. Am J Hum Genet. 2007 Jun;80(6):1179-87. Epub 2007 Apr 11. PMID: 17503335

• Etchevers HC, Amiel J, Lyonnet S. [Genetic and molecular bases of neurocristopathies.] Arch Pediatr. 2007 Jun;14(6):668-672. Epub 2007 Apr 16. French. PMID: 17434298

• Baala L, Briault S, Etchevers HC, Laumonnier F, Natiq A, Amiel J, Boddaert N, Picard C, Sbiti A, Asermouh A, Attie-Bitach T, Encha-Razavi F, Munnich A, Sefiani A, Lyonnet S. Homozygous silencing of T-box transcription factor EOMES leads to microcephaly with polymicrogyria and corpus callosum agenesis. Nat Genet. 2007 Apr;39(4):454-6. Epub 2007 Mar 11. PMID: 17353897

• Martinovic-Bouriel J, Bernabe-Dupont C, Golzio C, Grattagliano-Bessieres B, Malan V, Bonniere M, Esculpavit C, Fallet-Bianco C, Mirlesse V, Le Bidois J, Aubry MC, Vekemans M, Morichon N, Etchevers H, Attie-Bitach T, Encha-Razavi F, Benachi A. Matthew-Wood syndrome: report of two new cases supporting autosomal recessive inheritance and exclusion of FGF10 and FGFR2. Am J Med Genet A. 2007 Feb 1;143(3):219-28. PMID: 17236193


• Etchevers HC, Amiel J, Lyonnet S. Molecular bases of human neurocristopathies. Adv Exp Med Biol. 2006;589:213-34. A comprehensive review.
Actually, this is what is listed in PubMed but I thought it was here: Neural Crest Induction and Differentiation, ed. J.-P. Saint-Jeannet. Landes Biosciences, Georgetown, TX. ISBN: 1-58706-070-1.

• Golzio C, Guirchoun J, Ozilou C, Thomas S, Goudefroye G, Morichon-Delvallez N, Vekemans M, Attie-Bitach T, Etchevers HC. Cytogenetic and histological features of a human embryo with homogeneous chromosome 8 trisomy. Prenat Diagn. 2006 Dec;26(13):1201-1205

• Sanlaville D, Etchevers HC, Gonzales M, Martinovic J, Clement-Ziza M, Delezoide AL, Aubry MC, Pelet A, Chemouny S, Cruaud C, Audollent S, Esculpavit C, Goudefroye G, Ozilou C, Fredouille C, Joye N, Morichon-Delvallez N, Dumez Y, Weissenbach J, Munnich A, Amiel J, Encha-Razavi F, Lyonnet S, Vekemans M, Attie-Bitach T. Phenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human development. J Med Genet. 2006 Mar;43(3):211-217. Epub 2005 Sep 16.


• Detrait E, Etchevers HC. Vascularization of the head and neck during development. J Neuroradiol. 2005 Jun;32(3):147-56. Review, in French.

• Detrait ER, George TM, Etchevers HC, Gilbert JR, Vekemans M, Speer MC. Human neural tube defects: developmental biology, epidemiology, and genetics. Neurotoxicol Teratol. 2005 May-Jun;27(3):515-24. Epub 2005 Mar 5. Review.

• Etchevers HC. The cap 'n' collar family member NF-E2-related factor 3 (Nrf3) is expressed in mesodermal derivatives of the avian embryo. Int J Dev Biol. 2005;49(2-3):363-7.

• Deak KL, Boyles AL, Etchevers HC, Melvin EC, Siegel DG, Graham FL, Slifer SH, Enterline DS, George TM, Vekemans M, McClay D, Bassuk AG, Kessler JA, Linney E, Gilbert JR, Speer MC. SNPs in the neural cell adhesion molecule 1 gene (NCAM1) may be associated with human neural tube defects. Hum Genet. 2005 Jul;117(2-3):133-42. Epub 2005 May 10.

• Cai J, Ash D, Kotch LE, Jabs EW, Attie-Bitach T, Auge J, Mattei G, Etchevers H, Vekemans M, Korshunova Y, Tidwell R, Messina DN, Winston JB, Lovett M. Gene expression in pharyngeal arch 1 during human embryonic development. Hum Mol Genet. 2005 Apr 1;14(7):903-12. Epub 2005 Feb 9.

• Karmous-Benailly H, Martinovic J, Gubler MC, Sirot Y, Clech L, Ozilou C, Auge J, Brahimi N, Etchevers H, Detrait E, Esculpavit C, Audollent S, Goudefroye G, Gonzales M, Tantau J, Loget P, Joubert M, Gaillard D, Jeanne-Pasquier C, Delezoide AL, Peter MO, Plessis G, Simon-Bouy B, Dollfus H, Le Merrer M, Munnich A, Encha-Razavi F, Vekemans M, Attie-Bitach T. Antenatal presentation of Bardet-Biedl syndrome may mimic Meckel syndrome. Am J Hum Genet. 2005 Mar;76(3):493-504. Epub 2005 Jan 21.

• Trueba SS, Auge J, Mattei G, Etchevers H, Martinovic J, Czernichow P, Vekemans M, Polak M, Attie-Bitach T. PAX8, TITF1, and FOXE1 gene expression patterns during human development: new insights into human thyroid development and thyroid dysgenesis-associated malformations. J Clin Endocrinol Metab. 2005 Jan;90(1):455-62. Epub 2004 Oct 19.


• Pinson L, Auge J, Audollent S, Mattei G, Etchevers H, Gigarel N, Razavi F, Lacombe D, Odent S, Le Merrer M, Amiel J, Munnich A, Meroni G, Lyonnet S, Vekemans M, Attie-Bitach T. Embryonic expression of the human MID1 gene and its mutations in Opitz syndrome. J Med Genet. 2004 May;41(5):381-6.


• Amiel J, Laudier B, Attie-Bitach T, Trang H, de Pontual L, Gener B, Trochet D, Etchevers H, Ray P, Simonneau M, Vekemans M, Munnich A, Gaultier C, Lyonnet S. Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome. Nat Genet. 2003 Apr;33(4):459-61. Epub 2003 Mar 17.

• Etchevers HC. Early expression of hypoxia-inducible factor 1 alpha in the chicken embryo. Gene Expr Patterns. 2003 Mar;3(1):49-52.

Before 2003:

• Etchevers HC, Couly G, Le Douarin NM. Morphogenesis of the branchial vascular sector. Trends Cardiovasc Med. 2002 Oct;12(7):299-304. Review.

• Etchevers HC, Vincent C, Le Douarin NM, Couly GF. The cephalic neural crest provides pericytes and smooth muscle cells to all blood vessels of the face and forebrain. Development. 2001 Apr;128(7):1059-68.

• Etchevers HC, Vincent C, Couly GF. "Neural crest and pituitary development". In: Hypothalamic-Pituitary Development: Genetic and Clinical Aspects. R. Rappaport, ed. S. Karger AG, Basel, Suisse, 2001;13-29.

• Duprez D, Leyns L, Bonnin MA, Lapointe F, Etchevers H, De Robertis EM, Le Douarin N. Expression of Frzb-1 during chick development. Mech Dev. 1999 Dec;89(1-2):179-83.

• Etchevers HC, Couly G, Vincent C, Le Douarin NM. Anterior cephalic neural crest is required for forebrain viability. Development. 1999 Aug;126(16):3533-43.

Sophie Thomas, Lekbir Baala, Jean-Claude Quintyn, Nicolas Chassaing and Eric Detrait have published other work outside of our laboratory. See under their names at PubMed.

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