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Hussein Daoud

De Novo Mutations in Moderate or Severe Intellectual Disability
2014 · Fadi F. Hamdan, Myriam Srour, et al. · PLoS Genetics · 417
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Excess of De Novo Deleterious Mutations in Genes Associated with Glutamatergic Systems in Nonsyndromic Intellectual Disability
2011 · Fadi F. Hamdan, Julie Gauthier, et al. · The American Journal of Human Genetics · 348
Genetics of motor neuron disorders: new insights into pathogenic mechanisms
2009 · Patrick A. Dion, Hussein Daoud, et al. · Nature Reviews Genetics · 313
Direct Measure of the De Novo Mutation Rate in Autism and Schizophrenia Cohorts
2010 · Philip Awadalla, Julie Gauthier, et al. · The American Journal of Human Genetics · 239
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De Novo Mutations in FOXP1 in Cases with Intellectual Disability, Autism, and Language Impairment
2010 · Fadi F. Hamdan, Hussein Daoud, et al. · The American Journal of Human Genetics · 235
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CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia
2016 · Kelly L. Williams, Simon Topp, et al. · Nature Communications · 207
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Contribution of TARDBP mutations to sporadic amyotrophic lateral sclerosis
2008 · H Daoud, P N Valdmanis, et al. · Journal of Medical Genetics · 194
De Novo SYNGAP1 Mutations in Nonsyndromic Intellectual Disability and Autism
2011 · Fadi F. Hamdan, Hussein Daoud, et al. · Biological Psychiatry · 187
Mutations in FUS cause FALS and SALS in French and French Canadian populations
2009 · V. V. Belzil, P. N. Valdmanis, et al. · Neurology · 133
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ATXN2 trinucleotide repeat length correlates with risk of ALS
2016 · William Sproviero, Aleksey Shatunov, et al. · Neurobiology of Aging · 132
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Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosis
2014 · Hannah M. Kaneb, Andrew W. Folkmann, et al. · Human Molecular Genetics · 131
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A blinded international study on the reliability of genetic testing for GGGGCC-repeat expansions in C9orf72 reveals marked differences in results among 14 laboratories
2014 · Chizuru Akimoto, Alexander E Volk, et al. · Journal of Medical Genetics · 131
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Recent advances in the genetics of amyotrophic lateral sclerosis
2009 · Paul N. Valdmanis, Hussein Daoud, et al. · Current Neurology and Neuroscience Reports · 122
Mutations in POLR3A and POLR3B are a major cause of hypomyelinating leukodystrophies with or without dental abnormalities and/or hypogonadotropic hypogonadism
2013 · Hussein Daoud, Martine Tétreault, et al. · Journal of Medical Genetics · 106
Exome sequencing reveals SPG11 mutations causing juvenile ALS
2011 · Hussein Daoud, Sirui Zhou, et al. · Neurobiology of Aging · 105
Association of Long ATXN2 CAG Repeat Sizes With Increased Risk of Amyotrophic Lateral Sclerosis
2011 · Hussein Daoud, Véronique Belzil, et al. · Archives of Neurology · 103
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Next-generation sequencing for diagnosis of rare diseases in the neonatal intensive care unit
2016 · Hussein Daoud, Stephanie M. Luco, et al. · Canadian Medical Association Journal · 99
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Phenotype and genotype analysis in amyotrophic lateral sclerosis with TARDBP gene mutations
2012 · P. Corcia, P. Valdmanis, et al. · Neurology · 85
Identification of rare protein disulfide isomerase gene variants in amyotrophic lateral sclerosis patients
2015 · Paloma Gonzalez-Perez, Ute Woehlbier, et al. · Gene · 79
Autism and Nonsyndromic Mental Retardation Associated with a De Novo Mutation in the NLGN4X Gene Promoter Causing an Increased Expression Level
2009 · Hussein Daoud, Frédérique Bonnet-Brilhault, et al. · Biological Psychiatry · 63
Identification of a pathogenic FTO mutation by next-generation sequencing in a newborn with growth retardation and developmental delay
2015 · Hussein Daoud, Dong Zhang, et al. · Journal of Medical Genetics · 59
Resequencing of 29 Candidate Genes in Patients With Familial and Sporadic Amyotrophic Lateral Sclerosis
2011 · Hussein Daoud, Paul N. Valdmanis, et al. · Archives of Neurology · 52
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Analysis of OPTN as a causative gene for amyotrophic lateral sclerosis
2010 · Véronique V. Belzil, Hussein Daoud, et al. · Neurobiology of Aging · 51
Case report of novel DYRK1A mutations in 2 individuals with syndromic intellectual disability and a review of the literature
2016 · Stephanie M. Luco, Daniela Pohl, et al. · BMC Medical Genetics · 49
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UBQLN2 mutations are rare in French and French–Canadian amyotrophic lateral sclerosis
2012 · Hussein Daoud, Hamid Suhail, et al. · Neurobiology of Aging · 42
Works count: 72
Citation count: 4,281
H-index: 31
I10-index: 49
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