Francis Rousseau
Overview
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
1.
Testard Q, Vanhoye X, Yauy K, Naud M, Vieville G, Rousseau F, et al.
J Med Genet
. 2022 Sep;
59(12):1234-1240.
PMID: 36137615
Background: Despite the availability of whole exome (WES) and genome sequencing (WGS), chromosomal microarray (CMA) remains the first-line diagnostic test in most rare disorders diagnostic workup, looking for copy number...
2.
Ramon L, David C, Fontaine K, Lallet E, Marcaillou C, Martin-Lanneree S, et al.
Biomark Insights
. 2018 Mar;
13:1177271918763357.
PMID: 29568219
MiR-31-3p expression has been shown to be a predictive biomarker for response to anti-epithelial growth factor receptor therapy in patients with RAS wild-type metastatic colorectal cancer (mCRC). To aid in...
3.
Pugh S, Thiebaut R, Bridgewater J, Grisoni M, Moutasim K, Rousseau F, et al.
Oncotarget
. 2017 Dec;
8(55):93856-93866.
PMID: 29212194
Background: High miR-31-3p expression is associated with inferior outcomes in KRAS wild-type (WT) advanced colorectal cancer patients treated with anti-EGFR therapy. This study evaluated miR-31-3p expression in patients with operable...
4.
Gabriele S, Lombardi F, Sacco R, Napolioni V, Altieri L, Tirindelli M, et al.
J Psychiatr Res
. 2014 Sep;
59:108-16.
PMID: 25201284
Glyoxalase I (GLO1) is a homodimeric Zn(2+)-dependent isomerase involved in the detoxification of methylglyoxal and in limiting the formation of advanced glycation end-products (AGE). We previously found the rs4746 A332...
5.
Manceau G, Imbeaud S, Thiebaut R, Liebaert F, Fontaine K, Rousseau F, et al.
Clin Cancer Res
. 2014 Apr;
20(12):3338-47.
PMID: 24771647
Purpose: To identify microRNAs (miRNA) that predict response to anti-EGFR antibodies in patients with wild-type KRAS metastatic colorectal cancer (mCRC). Experimental Design: miRNA profiling was performed in a training set...
6.
Carayol J, Schellenberg G, Dombroski B, Amiet C, Genin B, Fontaine K, et al.
Front Genet
. 2014 Mar;
5:33.
PMID: 24600472
Autism spectrum disorders (ASD) are highly heritable complex neurodevelopmental disorders with a 4:1 male: female ratio. Common genetic variation could explain 40-60% of the variance in liability to autism. Because...
7.
Nault J, De Reynies A, Villanueva A, Calderaro J, Rebouissou S, Couchy G, et al.
Gastroenterology
. 2013 Apr;
145(1):176-187.
PMID: 23567350
Background & Aims: Due to the phenotypic and molecular diversity of hepatocellular carcinomas (HCC), it is a challenge to determine a patient's prognosis. We aimed to identify new prognostic markers...
8.
Stocks T, Angquist L, Banasik K, Harder M, Taylor M, Hager J, et al.
PLoS One
. 2012 Sep;
7(8):e43212.
PMID: 22952648
Background: Numerous gene loci are related to single measures of body weight and shape. We investigated if 55 SNPs previously associated with BMI or waist measures, modify the effects of...
9.
Hooton H, Angquist L, Holst C, Hager J, Rousseau F, Hansen R, et al.
PLoS One
. 2012 Jul;
7(7):e40394.
PMID: 22844403
Background/aims: Cathepsin S, a protein coded by the CTSS gene, is implicated in adipose tissue biology--this protein enhances adipose tissue development. Our hypothesis is that common variants in CTSS play...
10.
Hager J, Kamatani Y, Cazier J, Youhanna S, Ghassibe-Sabbagh M, Platt D, et al.
PLoS One
. 2012 Jun;
7(6):e38663.
PMID: 22745674
The manifestation of coronary artery disease (CAD) follows a well-choreographed series of events that includes damage of arterial endothelial cells and deposition of lipids in the sub-endothelial layers. Genome-wide association...