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Year Number of Results
1995 1
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1999 3
2000 4
2001 4
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2003 1
2004 3
2005 4
2006 3
2007 3
2008 4
2009 5
2010 7
2011 3
2012 2
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2020 3
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62 results

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Page 1
De novo TBR1 variants cause a neurocognitive phenotype with ID and autistic traits: report of 25 new individuals and review of the literature.
Nambot S, Faivre L, Mirzaa G, Thevenon J, Bruel AL, Mosca-Boidron AL, Masurel-Paulet A, Goldenberg A, Le Meur N, Charollais A, Mignot C, Petit F, Rossi M, Metreau J, Layet V, Amram D, Boute-Bénéjean O, Bhoj E, Cousin MA, Kruisselbrink TM, Lanpher BC, Klee EW, Fiala E, Grange DK, Meschino WS, Hiatt SM, Cooper GM, Olivié H, Smith WE, Dumas M, Lehman A; CAUSES Study; Inglese C, Nizon M, Guerrini R, Vetro A, Kaplan ES, Miramar D, Van Gils J, Fergelot P, Bodamer O, Herkert JC, Pajusalu S, Õunap K, Filiano JJ, Smol T, Piton A, Gérard B, Chantot-Bastaraud S, Bienvenu T, Li D, Juusola J, Devriendt K, Bilan F, Poé C, Chevarin M, Jouan T, Tisserant E, Rivière JB, Tran Mau-Them F, Philippe C, Duffourd Y, Dobyns WB, Hevner R, Thauvin-Robinet C. Nambot S, et al. Among authors: charollais a. Eur J Hum Genet. 2020 Jun;28(6):770-782. doi: 10.1038/s41431-020-0571-6. Epub 2020 Jan 31. Eur J Hum Genet. 2020. PMID: 32005960 Free PMC article. Review.
Connexins and secretion.
Serre-Beinier V, Mas C, Calabrese A, Caton D, Bauquis J, Caille D, Charollais A, Cirulli V, Meda P. Serre-Beinier V, et al. Among authors: charollais a. Biol Cell. 2002 Nov;94(7-8):477-92. doi: 10.1016/s0248-4900(02)00024-2. Biol Cell. 2002. PMID: 12566221 Review.
Lipoprotein (a), birth weight and neonatal stroke.
Renaud C, Bonneau C, Presles E, Laporte S, Depeyre A, Varlet MN, Chabrier S; AVCnn Group. Renaud C, et al. Neonatology. 2010;98(3):225-8. doi: 10.1159/000281015. Epub 2010 Apr 13. Neonatology. 2010. PMID: 20428016
[Indications of electroencephalogram in the newborn].
Lamblin MD, André M, Auzoux M, Bednarek N, Bour F, Charollais A, Cheliout-Heraut F, D'Allest AM, De Bellecize J, Delanoe C, Furby A, Frenkel AL, Keo-Kosal P, Mony L, Moutard ML, Navelet Y, Nedelcoux H, Nguyen TT, Nogues B, Plouin P, Salefranque F, Soufflet C, Touzery de Villepin A, Vecchierini MF, Wallois F, Esquivel-Walls E. Lamblin MD, et al. Among authors: charollais a. Arch Pediatr. 2004 Jul;11(7):829-33. doi: 10.1016/j.arcped.2004.01.031. Arch Pediatr. 2004. PMID: 15234381 Review. French.
De novo variants in TCF7L2 are associated with a syndromic neurodevelopmental disorder.
Dias C, Pfundt R, Kleefstra T, Shuurs-Hoeijmakers J, Boon EMJ, van Hagen JM, Zwijnenburg P, Weiss MM, Keren B, Mignot C, Isapof A, Weiss K, Hershkovitz T, Iascone M, Maitz S, Feichtinger RG, Kotzot D, Mayr JA, Ben-Omran T, Mahmoud L, Pais LS, Walsh CA, Shashi V, Sullivan JA, Stong N, Lecoquierre F, Guerrot AM, Charollais A, Rodan LH. Dias C, et al. Among authors: charollais a. Am J Med Genet A. 2021 Aug;185(8):2384-2390. doi: 10.1002/ajmg.a.62254. Epub 2021 May 18. Am J Med Genet A. 2021. PMID: 34003604 Free PMC article.
Promises and pitfalls of a Pannexin1 transgenic mouse line.
Hanstein R, Negoro H, Patel NK, Charollais A, Meda P, Spray DC, Suadicani SO, Scemes E. Hanstein R, et al. Among authors: charollais a. Front Pharmacol. 2013 May 9;4:61. doi: 10.3389/fphar.2013.00061. eCollection 2013. Front Pharmacol. 2013. PMID: 23675350 Free PMC article.
Involvement of gap junctional communication in secretion.
Michon L, Nlend Nlend R, Bavamian S, Bischoff L, Boucard N, Caille D, Cancela J, Charollais A, Charpantier E, Klee P, Peyrou M, Populaire C, Zulianello L, Meda P. Michon L, et al. Among authors: charollais a. Biochim Biophys Acta. 2005 Dec 20;1719(1-2):82-101. doi: 10.1016/j.bbamem.2005.11.003. Epub 2005 Nov 18. Biochim Biophys Acta. 2005. PMID: 16359942 Free article. Review.
62 results