Francois Rousseau
Francois Rousseau
Professeur, Faculté de médecine, Université Laval
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Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome
I Oberle, F Rousseau, D Heitz, C Kretz, D Devys, A Hanauer, J Boue, ...
Science, 1097-1102, 1991
Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture
K Estrada, U Styrkarsdottir, E Evangelou, YH Hsu, EL Duncan, EE Ntzani, ...
Nature genetics 44 (5), 491-501, 2012
Direct diagnosis by DNA analysis of the fragile X syndrome of mental retardation
F Rousseau, D Heitz, V Biancalana, S Blumenfeld, C Kretz, J Boué, ...
New England Journal of Medicine 325 (24), 1673-1681, 1991
Prevalence of carriers of premutation-size alleles of the FMRI gene--and implications for the population genetics of the fragile X syndrome.
F Rousseau, P Rouillard, ML Morel, EW Khandjian, K Morgan
American journal of human genetics 57 (5), 1006, 1995
Prevalence and detection of delirium in elderly emergency department patients
M Élie, F Rousseau, M Cole, F Primeau, J McCusker, F Bellavance
Cmaj 163 (8), 977-981, 2000
Expansion of the fragile X CGG repeat in females with premutation or intermediate alleles
SL Nolin, WT Brown, A Glicksman, GE Houck Jr, AD Gargano, A Sullivan, ...
The American Journal of Human Genetics 72 (2), 454-464, 2003
A multicenter study on genotype-phenotype correlations in the fragile X syndrome, using direct diagnosis with probe StB12. 3: the first 2,253 cases
F Rousseau, D Heitz, J Tarleton, J MacPherson, H Malmgren, N Dahl, ...
American journal of human genetics 55 (2), 225, 1994
Whole‐genome sequencing identifies EN1 as a determinant of bone density and fracture
HF Zheng, V Forgetta, YH Hsu, K Estrada, A Rosello‐Diez, PJ Leo, ...
Nature 526 (7571), 112-117, 2015
Premutation and intermediate-size FMR1 alleles in 10 572 males from the general population: loss of an AGG interruption is a late event in the generation of fragile X syndrome …
C Dombrowski, S Levesque, ML Morel, P Rouillard, K Morgan, ...
Human Molecular Genetics 11 (4), 371-378, 2002
The fragile X mental retardation protein is associated with ribosomes
EW Khandjian, F Corbin, S Woerly, F Rousseau
Nature genetics 12 (1), 91-93, 1996
The fragile X mental retardation protein is associated with poly (A)+ mRNA in actively translating polyribosomes
F Corbin, M Bouillon, A Fortin, S Morin, F Rousseau, EW Khandjian
Human molecular genetics 6 (9), 1465-1472, 1997
Large-scale analysis of association between LRP5 and LRP6 variants and osteoporosis
JBJ van Meurs, TA Trikalinos, SH Ralston, S Balcells, ML Brandi, K Brixen, ...
Jama 299 (11), 1277-1290, 2008
FORGE Canada Consortium: outcomes of a 2-year national rare-disease gene-discovery project
CL Beaulieu, J Majewski, J Schwartzentruber, ME Samuels, ...
The American Journal of Human Genetics 94 (6), 809-817, 2014
Combining biochemical and ultrasonographic markers in predicting preeclampsia: a systematic review
Y Giguere, M Charland, E Bujold, N Bernard, S Grenier, F Rousseau, ...
Clinical chemistry 56 (3), 361-375, 2010
Isolation of sequences that span the fragile X and identification of a fragile X-related CpG island
D Heitz, F Rousseau, D Devys, S Saccone, H Abderrahim, D Le Paslier, ...
Science 251 (4998), 1236-1239, 1991
Missense FGFR3 Mutations Create Cysteine Residues in Thanatophoric Dwarfism Type I (TD1)
F Rousseau, V El Ghouzzi, AL Delezoide, L Legeai-Mallet, M Le Merrer, ...
Human molecular genetics 5 (4), 509-512, 1996
Reduced Seminal Parameters Associated With Environmental DDT Exposure and p,p′‐DDE Concentrations in Men in Chiapas, Mexico: A Cross‐Sectional Study
C De Jager, P Farias, A Barraza‐Villarreal, MH Avila, P Ayotte, E Dewailly, ...
Journal of andrology 27 (1), 16-27, 2006
Analysis of full fragile X mutations in fetal tissues and monozygotic twins indicate that abnormal methylation and somatic heterogeneity are established early in development
D Devys, V Biancalana, F Rousseau, J Boue, JL Mandel, I Oberle
American journal of medical genetics 43 (1‐2), 208-216, 1992
A polymorphic autoregulatory hormone response element in the human estrogen-related receptor α (ERRα) promoter dictates peroxisome proliferator-activated receptor γ coactivator …
J Laganière, GB Tremblay, CR Dufour, S Giroux, F Rousseau, V Giguère
Journal of Biological Chemistry 279 (18), 18504-18510, 2004
Identification of a novel truncating PALB2 mutation and analysis of its contribution to early-onset breast cancer in French-Canadian women
WD Foulkes, P Ghadirian, MR Akbari, N Hamel, S Giroux, N Sabbaghian, ...
Breast Cancer Research 9 (6), 1-9, 2007
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