Francis Rousseau
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Explore the profile of Francis Rousseau including associated specialties, affiliations and a list of published articles.
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20
Citations
590
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Recent Articles
11.
Carayol J, Schellenberg G, Dombroski B, Genin E, Rousseau F, Dawson G
Mol Autism
. 2011 Oct;
2(1):17.
PMID: 22017886
Background: The inheritance pattern in most cases of autism is complex. The risk of autism is increased in siblings of children with autism and previous studies have indicated that the...
12.
Carayol J, Sacco R, Tores F, Rousseau F, Lewin P, Hager J, et al.
Biol Psychiatry
. 2011 Jul;
70(9):880-7.
PMID: 21757185
Background: Autism is a severe developmental disorder, with strong genetic underpinnings. Previous genome-wide scans unveiled a linkage region spanning 3.5 Mb, located on human chromosome 3p25. This region encompasses the...
13.
Hooton H, Dubern B, Henegar C, Paternoster L, Nohr E, Alili R, et al.
Obes Facts
. 2011 May;
4(2):131-44.
PMID: 21577020
Objective: Cystatin C, a protein coded by CST3 gene, is implicated in adipose tissue biology. Our hypothesis is that common variants in CST3 gene could play a role in the...
14.
Edery P, Marcaillou C, Sahbatou M, Labalme A, Chastang J, Touraine R, et al.
Science
. 2011 Apr;
332(6026):240-3.
PMID: 21474761
The spliceosome, a ribonucleoprotein complex that includes proteins and small nuclear RNAs (snRNAs), catalyzes RNA splicing through intron excision and exon ligation to produce mature messenger RNAs, which, in turn...
15.
Napolioni V, Lombardi F, Sacco R, Curatolo P, Manzi B, Alessandrelli R, et al.
Eur J Hum Genet
. 2010 Nov;
19(3):353-9.
PMID: 21102624
The integrin-β 3 gene (ITGB3), located on human chromosome 17q21.3, was previously identified as a quantitative trait locus (QTL) for 5-HT blood levels and has been implicated as a candidate...
16.
Brooks P, Marcaillou C, Vanpeene M, Saraiva J, Stockholm D, Francke S, et al.
BMC Genet
. 2009 Apr;
10:16.
PMID: 19331686
Background: The monogenic disease osteogenesis imperfecta (OI) is due to single mutations in either of the collagen genes ColA1 or ColA2, but within the same family a given mutation is...
17.
Maussion G, Carayol J, Lepagnol-Bestel A, Tores F, Loe-Mie Y, Milbreta U, et al.
Hum Mol Genet
. 2008 May;
17(16):2541-51.
PMID: 18492799
Autism spectrum disorders (ASDs) are common, heritable, but genetically heterogeneous neurodevelopmental conditions. We recently defined a susceptibility locus for ASDs on chromosome 1q41-q42. High-resolution single-nucleotide polymorphisms (126 SNPs) genotyping across...
18.
Philippi A, Tores F, Carayol J, Rousseau F, Letexier M, Roschmann E, et al.
BMC Med Genet
. 2007 Dec;
8:74.
PMID: 18053270
Background: Autism is a complex, heterogeneous, behaviorally-defined disorder characterized by disruptions of the nervous system and of other systems such as the pituitary-hypothalamic axis. In a previous genome wide screen,...
19.
Sacco R, Papaleo V, Hager J, Rousseau F, Moessner R, Militerni R, et al.
BMC Med Genet
. 2007 Mar;
8:11.
PMID: 17346350
Background: The TPH2 gene encodes the enzyme responsible for serotonin (5-HT) synthesis in the Central Nervous System (CNS). Stereotypic and repetitive behaviors are influenced by 5-HT, and initial studies report...
20.
Cancel-Tassin G, Latil A, Rousseau F, Mangin P, Bottius E, Escary J, et al.
Eur Urol
. 2003 Sep;
44(4):487-90.
PMID: 14499686
Objectives: Prostate cancer is a very common hormone-related malignancy in Western countries. It is initially dependent on androgen stimulation but in vitro growth of prostate cancer cells are also dependent...