Andres CR - Search Results

1

Effect of familial clustering in the genetic screening of 235 French ALS families.

Corcia P, Camu W, Brulard C, Marouillat S, Couratier P, Camdessanché JP, Cintas P, Verschueren A, Soriani MH, Desnuelle C, Fleury MC, Guy N, Cassereau J, Viader F, Pittion-Vouyovitch S, Danel V, Kolev I, Le Masson G, Beltran S, Salachas F, Bernard E, Pradat PF, Blasco H, Lanznaster D, Hergesheimer R, Laumonnier F, Andres CR, Meininger V, Vourc'h P. Corcia P, et al. Among authors: andres cr. J Neurol Neurosurg Psychiatry. 2021 May;92(5):479-484. doi: 10.1136/jnnp-2020-325064. Epub 2021 Jan 6. J Neurol Neurosurg Psychiatry. 2021. PMID: 33408239

2

Abnormal SMN1 gene copy number is a susceptibility factor for amyotrophic lateral sclerosis.

Corcia P, Mayeux-Portas V, Khoris J, de Toffol B, Autret A, Müh JP, Camu W, Andres C; French ALS Research Group. Amyotrophic Lateral Sclerosis. Corcia P, et al. Ann Neurol. 2002 Feb;51(2):243-6. doi: 10.1002/ana.10104. Ann Neurol. 2002. PMID: 11835381

3

Molecular analysis of the oligodendrocyte myelin glycoprotein gene in autistic disorder.

Vourc'h P, Martin I, Marouillat S, Adrien JL, Barthélémy C, Moraine C, Müh JP, Andres C. Vourc'h P, et al. Neurosci Lett. 2003 Feb 27;338(2):115-8. doi: 10.1016/s0304-3940(02)01338-1. Neurosci Lett. 2003. PMID: 12566166

4

Mutation screening and association study of the UBE2H gene on chromosome 7q32 in autistic disorder.

Vourc'h P, Martin I, Bonnet-Brilhault F, Marouillat S, Barthélémy C, Pierre Müh J, Andres C. Vourc'h P, et al. Psychiatr Genet. 2003 Dec;13(4):221-5. doi: 10.1097/00041444-200312000-00005. Psychiatr Genet. 2003. PMID: 14639049

5

Oligodendrocyte myelin glycoprotein (OMgp): evolution, structure and function.

Vourc'h P, Andres C. Vourc'h P, et al. Brain Res Brain Res Rev. 2004 May;45(2):115-24. doi: 10.1016/j.brainresrev.2004.01.003. Brain Res Brain Res Rev. 2004. PMID: 15145622 Review.

6

Transmission disequilibrium study of an oligodendrocyte and myelin glycoprotein gene allele in 431 families with an autistic proband.

Martin I, Gauthier J, D'Amelio M, Védrine S, Vourc'h P, Rouleau GA, Persico AM, Andres CR. Martin I, et al. Among authors: andres cr. Neurosci Res. 2007 Dec;59(4):426-30. doi: 10.1016/j.neures.2007.08.009. Epub 2007 Aug 19. Neurosci Res. 2007. PMID: 17897745

7

Mutations of the ANG gene in French patients with sporadic amyotrophic lateral sclerosis.

Paubel A, Violette J, Amy M, Praline J, Meininger V, Camu W, Corcia P, Andres CR, Vourc'h P; French Amyotrophic Lateral Sclerosis (ALS) Study Group. Paubel A, et al. Among authors: andres cr. Arch Neurol. 2008 Oct;65(10):1333-6. doi: 10.1001/archneur.65.10.1333. Arch Neurol. 2008. PMID: 18852347

8

Haploinsufficiency of the GPD2 gene in a patient with nonsyndromic mental retardation.

Daoud H, Gruchy N, Constans JM, Moussaoui E, Saumureau S, Bayou N, Amy M, Védrine S, Vu PY, Rötig A, Laumonnier F, Vourc'h P, Andres CR, Leporrier N, Briault S. Daoud H, et al. Among authors: andres cr. Hum Genet. 2009 Jan;124(6):649-58. doi: 10.1007/s00439-008-0588-3. Epub 2008 Nov 16. Hum Genet. 2009. PMID: 19011903

9

What was the set of ubiquitin and ubiquitin-like conjugating enzymes in the eukaryote common ancestor?

Michelle C, Vourc'h P, Mignon L, Andres CR. Michelle C, et al. Among authors: andres cr. J Mol Evol. 2009 Jun;68(6):616-28. doi: 10.1007/s00239-009-9225-6. Epub 2009 May 19. J Mol Evol. 2009. PMID: 19452197 Free PMC article.

10

Deficit in BDNF does not increase vulnerability to stress but dampens antidepressant-like effects in the unpredictable chronic mild stress.

Ibarguen-Vargas Y, Surget A, Vourc'h P, Leman S, Andres CR, Gardier AM, Belzung C. Ibarguen-Vargas Y, et al. Among authors: andres cr. Behav Brain Res. 2009 Sep 14;202(2):245-51. doi: 10.1016/j.bbr.2009.03.040. Epub 2009 Apr 5. Behav Brain Res. 2009. PMID: 19463708

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