Dr Hussein Daoud
Dr Hussein Daoud
Scientist - Genomics Specialist, Genetics Diagnostic Laboratory - Children's Hospital of Eastern
Verified email at cheo.on.ca
Cited by
Cited by
Excess of de novo deleterious mutations in genes associated with glutamatergic systems in nonsyndromic intellectual disability
FF Hamdan, J Gauthier, Y Araki, DT Lin, Y Yoshizawa, K Higashi, A Park, ...
The American Journal of Human Genetics 88 (3), 306-316, 2011
Genetics of motor neuron disorders: new insights into pathogenic mechanisms
PA Dion, H Daoud, GA Rouleau
Nature Reviews Genetics 10 (11), 769-782, 2009
De novo mutations in moderate or severe intellectual disability
FF Hamdan, M Srour, JM Capo-Chichi, H Daoud, C Nassif, L Patry, ...
PLoS genetics 10 (10), 2014
Direct measure of the de novo mutation rate in autism and schizophrenia cohorts
P Awadalla, J Gauthier, RA Myers, F Casals, FF Hamdan, AR Griffing, ...
The American Journal of Human Genetics 87 (3), 316-324, 2010
Contribution of TARDBP mutations to sporadic amyotrophic lateral sclerosis
H Daoud, PN Valdmanis, E Kabashi, P Dion, N Dupre, W Camu, ...
Journal of medical genetics 46 (2), 112-114, 2009
De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment
FF Hamdan, H Daoud, D Rochefort, A Piton, J Gauthier, M Langlois, ...
The American Journal of Human Genetics 87 (5), 671-678, 2010
De novo SYNGAP1 mutations in nonsyndromic intellectual disability and autism
FF Hamdan, H Daoud, A Piton, J Gauthier, S Dobrzeniecka, MO Krebs, ...
Biological psychiatry 69 (9), 898-901, 2011
Mutations in FUS cause FALS and SALS in French and French Canadian populations
VV Belzil, PN Valdmanis, PA Dion, H Daoud, E Kabashi, A Noreau, ...
Neurology 73 (15), 1176-1179, 2009
Recent advances in the genetics of amyotrophic lateral sclerosis
PN Valdmanis, H Daoud, PA Dion, GA Rouleau
Current neurology and neuroscience reports 9 (3), 198-205, 2009
Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosis
HM Kaneb, AW Folkmann, VV Belzil, LE Jao, CS Leblond, SL Girard, ...
Human molecular genetics 24 (5), 1363-1373, 2015
CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia
KL Williams, S Topp, S Yang, B Smith, JA Fifita, ST Warraich, KY Zhang, ...
Nature communications 7 (1), 1-8, 2016
A blinded international study on the reliability of genetic testing for GGGGCC-repeat expansions in C9orf72 reveals marked differences in results among 14 laboratories
C Akimoto, AE Volk, M Van Blitterswijk, M Van den Broeck, CS Leblond, ...
Journal of medical genetics 51 (6), 419-424, 2014
Association of long ATXN2 CAG repeat sizes with increased risk of amyotrophic lateral sclerosis
H Daoud, V Belzil, S Martins, M Sabbagh, P Provencher, L Lacomblez, ...
Archives of neurology 68 (6), 739-742, 2011
Exome sequencing reveals< i> SPG11</i> mutations causing juvenile ALS
H Daoud, S Zhou, A Noreau, M Sabbagh, V Belzil, A Dionne-Laporte, ...
Neurobiology of aging, 2011
Mutations in POLR3A and POLR3B are a major cause of hypomyelinating leukodystrophies with or without dental abnormalities and/or hypogonadotropic hypogonadism
H Daoud, M Tétreault, W Gibson, K Guerrero, A Cohen, ...
Journal of medical genetics 50 (3), 194-197, 2013
Autism and nonsyndromic mental retardation associated with a de novo mutation in the NLGN4X gene promoter causing an increased expression level
H Daoud, F Bonnet-Brilhault, S Védrine, MV Demattéi, P Vourc'h, N Bayou, ...
Biological psychiatry 66 (10), 906-910, 2009
Next-generation sequencing for diagnosis of rare diseases in the neonatal intensive care unit
H Daoud, SM Luco, R Li, E Bareke, C Beaulieu, O Jarinova, N Carson, ...
Cmaj 188 (11), E254-E260, 2016
Phenotype and genotype analysis in amyotrophic lateral sclerosis with TARDBP gene mutations
P Corcia, P Valdmanis, S Millecamps, C Lionnet, H Blasco, K Mouzat, ...
Neurology 78 (19), 1519-1526, 2012
Analysis of OPTN as a causative gene for amyotrophic lateral sclerosis
VV Belzil, H Daoud, A Desjarlais, JP Bouchard, N Dupré, W Camu, ...
Neurobiology of aging 32 (3), 555. e13-555. e14, 2011
Identification of rare protein disulfide isomerase gene variants in amyotrophic lateral sclerosis patients
P Gonzalez-Perez, U Woehlbier, RJ Chian, P Sapp, GA Rouleau, ...
Gene 566 (2), 158-165, 2015
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