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A. Szuto · SciRah

Researcher profile · Semantic Scholar

A. Szuto

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A. Szuto — researcher profile on SciRah

h-index: 10
Works: 17
Citations: 780

Most-cited papers

Exome sequencing identifies FUS mutations as a cause of essential tremor.
N. Merner, S. Girard, Hélène Catoire, Cynthia V. Bourassa +19 more
2012American Journal of Human Genetics188 citations Open access
Semantic Scholar
Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosis.
Hannah M Kaneb, Andrew W. Folkmann, V. Belzil, Li-En Jao +16 more
2015Human Molecular Genetics133 citations Open access
Semantic Scholar
Clinical and genetic study of hereditary spastic paraplegia in Canada
N. Chrestian, N. Dupré, Z. Gan-or, A. Szuto +17 more
2016Neurology: Genetics106 citations Open access
Semantic Scholar
Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia.
Z. Gan-or, N. Bouslam, N. Birouk, Alexandra Lissouba +23 more
2016American Journal of Human Genetics101 citations Open access
Semantic Scholar
Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosis.
C. Leblond, Z. Gan-or, D. Spiegelman, S. Laurent +12 more
2016Neurobiology of Aging69 citations
Semantic Scholar
SYNE1 mutations in autosomal recessive cerebellar ataxia.
A. Noreau, Cynthia V. Bourassa, A. Szuto, A. Levert +11 more
2013JAMA Neurology63 citations
Semantic Scholar
UBQLN2 mutations are rare in French and French-Canadian amyotrophic lateral sclerosis.
H. Daoud, Hamid Suhail, A. Szuto, W. Camu +6 more
2012Neurobiology of Aging48 citations
Semantic Scholar
Exome sequencing identifies recessive CDK5RAP2 variants in patients with isolated agenesis of corpus callosum
L. Jouan, B. O. A. Bencheikh, H. Daoud, A. Dionne-Laporte +11 more
2015European Journal of Human Genetics26 citations Open access
Semantic Scholar
C9orf72 hexanucleotide repeat expansions as the causative mutation for chromosome 9p21-linked amyotrophic lateral sclerosis and frontotemporal dementia.
H. Daoud, Hamid Suhail, Mike Sabbagh, V. Belzil +10 more
2012Archives of Neurology25 citations Open access
Semantic Scholar
A 23 years follow-up study identifies GLUT1 deficiency syndrome initially diagnosed as complicated hereditary spastic paraplegia.
M. Diomedi, Z. Gan-or, F. Placidi, P. Dion +4 more
2016European Journal of Medical Genetics12 citations Open access
Semantic Scholar
Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia.
Z. Gan-or, N. Bouslam, N. Birouk, Alexandra Lissouba +23 more
2016American Journal of Human Genetics8 citations Open access
Semantic Scholar
CYP7B1 Mutations in French-Canadian Hereditary Spastic Paraplegia Subjects
A. Noreau, P. Dion, A. Szuto, A. Levert +5 more
2012Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques3 citations Open access
Semantic Scholar
Functional Outcomes in Hereditary Spastic Paraplegia: A Prospective Cohort Study (S43.005)
N. Chrestian, N. Dupré, J. Brisson, Z. Gan-or +15 more
2016Neurology0 citations
Semantic Scholar
Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosis (P2.053)
N. Dupré, C. Leblond, D. Spiegelman, A. Szuto +3 more
2015Neurology0 citations
Semantic Scholar
Alanine Repeat in a Severe Form of Oculopharyngeal Muscular Dystrophy
L. Jouan, D. Rocheford, A. Szuto, E. Carney +1 more
20140 citations
Semantic Scholar
Exome Sequencing Identifies FUS Mutations as a Cause of Essential Tremor (P05.031)
N. Dupré, N. Merner, S. Girard, Hélène Catoire +16 more
2013Neurology0 citations
Semantic Scholar
Insensitivity to Pain: Lessons from Recent Genetics Advances
N. Merner, P. Dion, A. Szuto, G. Rouleau
20120 citations
Semantic Scholar

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