Mouren MC - Search Results

1

Early-onset obsessive-compulsive disorder: a subgroup with a specific clinical and familial pattern?

Chabane N, Delorme R, Millet B, Mouren MC, Leboyer M, Pauls D. Chabane N, et al. Among authors: mouren mc. J Child Psychol Psychiatry. 2005 Aug;46(8):881-7. doi: 10.1111/j.1469-7610.2004.00382.x. J Child Psychol Psychiatry. 2005. PMID: 16033636

2

Lack of evidence for association between serotonin transporter gene (5-HTTLPR) and obsessive-compulsive disorder by case control and family association study in humans.

Chabane N, Millet B, Delorme R, Lichtermann D, Mathieu F, Laplanche JL, Roy I, Mouren MC, Hankard R, Maier W, Launay JM, Leboyer M. Chabane N, et al. Among authors: mouren mc. Neurosci Lett. 2004 Jun 10;363(2):154-6. doi: 10.1016/j.neulet.2004.03.065. Neurosci Lett. 2004. PMID: 15172105

3

[School phobia or school refusal: controversial concepts].

Mouren MC, Delorme R. Mouren MC, et al. Bull Acad Natl Med. 2006 Nov;190(8):1629-39; discussion 1639-41. Bull Acad Natl Med. 2006. PMID: 17650748 Review. French.

4

Reduced 3-O-methyl-dopa levels in OCD patients and their unaffected parents is associated with the low activity M158 COMT allele.

Delorme R, Betancur C, Chaste P, Kernéis S, Stopin A, Mouren MC, Collet C, Bourgeron T, Leboyer M, Launay JM. Delorme R, et al. Among authors: mouren mc. Am J Med Genet B Neuropsychiatr Genet. 2010 Mar 5;153B(2):542-548. doi: 10.1002/ajmg.b.31016. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 19676096 Free PMC article.

5

Search for copy number variants in chromosomes 15q11-q13 and 22q11.2 in obsessive compulsive disorder.

Delorme R, Moreno-De-Luca D, Gennetier A, Maier W, Chaste P, Mössner R, Grabe HJ, Ruhrmann S, Falkai P, Mouren MC, Leboyer M, Wagner M, Betancur C. Delorme R, et al. Among authors: mouren mc. BMC Med Genet. 2010 Jun 21;11:100. doi: 10.1186/1471-2350-11-100. BMC Med Genet. 2010. PMID: 20565924 Free PMC article.

6

Mutation screening of NOS1AP gene in a large sample of psychiatric patients and controls.

Delorme R, Betancur C, Scheid I, Anckarsäter H, Chaste P, Jamain S, Schuroff F, Nygren G, Herbrecht E, Dumaine A, Mouren MC, Råstam M, Leboyer M, Gillberg C, Bourgeron T. Delorme R, et al. Among authors: mouren mc. BMC Med Genet. 2010 Jul 5;11:108. doi: 10.1186/1471-2350-11-108. BMC Med Genet. 2010. PMID: 20602773 Free PMC article.

7

Gaze direction detection in autism spectrum disorder.

Forgeot d'Arc B, Delorme R, Zalla T, Lefebvre A, Amsellem F, Moukawane S, Letellier L, Leboyer M, Mouren MC, Ramus F. Forgeot d'Arc B, et al. Among authors: mouren mc. Autism. 2017 Jan;21(1):100-107. doi: 10.1177/1362361316630880. Epub 2016 Apr 30. Autism. 2017. PMID: 27132008

8

Atypical Social Judgment and Sensitivity to Perceptual Cues in Autism Spectrum Disorders.

Forgeot d'Arc B, Ramus F, Lefebvre A, Brottier D, Zalla T, Moukawane S, Amsellem F, Letellier L, Peyre H, Mouren MC, Leboyer M, Delorme R. Forgeot d'Arc B, et al. Among authors: mouren mc. J Autism Dev Disord. 2016 May;46(5):1574-81. doi: 10.1007/s10803-014-2208-5. J Autism Dev Disord. 2016. PMID: 25149177

9

MRI findings in 77 children with non-syndromic autistic disorder.

Boddaert N, Zilbovicius M, Philipe A, Robel L, Bourgeois M, Barthélemy C, Seidenwurm D, Meresse I, Laurier L, Desguerre I, Bahi-Buisson N, Brunelle F, Munnich A, Samson Y, Mouren MC, Chabane N. Boddaert N, et al. Among authors: mouren mc. PLoS One. 2009;4(2):e4415. doi: 10.1371/journal.pone.0004415. Epub 2009 Feb 10. PLoS One. 2009. PMID: 19204795 Free PMC article.

10

Should metabolic diseases be systematically screened in nonsyndromic autism spectrum disorders?

Schiff M, Benoist JF, Aïssaoui S, Boespflug-Tanguy O, Mouren MC, de Baulny HO, Delorme R. Schiff M, et al. Among authors: mouren mc. PLoS One. 2011;6(7):e21932. doi: 10.1371/journal.pone.0021932. Epub 2011 Jul 7. PLoS One. 2011. PMID: 21760924 Free PMC article.

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