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Nassima Addour-Boudrahem

Observed names: Boudrahem-Addour, Nassima, N Addour, N. Addour, N. Boudrahem-Addour, Nassima Addour, Nassima Boudrahem-Addour, Nassima Boudrahem‐Addour
Observed institutions: University of Sciences and Technology Houari Boumediene, Montreal Children's Hospital, McGill University Health Centre, Hôpital Cochin, Research Institute of the McGill University Health Centre, McGill University
ORCID: 0000-0002-9231-9806
Observed ORCID: 0000-0002-9231-9806
OpenAlex ID: A5046529550
Neurogenesis, neuronal migration, and axon guidance
2020 · Andrea Accogli, Nassima Addour-Boudrahem, et al. · Handbook of clinical neurology · 68
De Novo Pathogenic Variants in N-cadherin Cause a Syndromic Neurodevelopmental Disorder with Corpus Callosum, Axon, Cardiac, Ocular, and Genital Defects
2019 · Andrea Accogli, Sara Calabretta, et al. · The American Journal of Human Genetics · 53
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Diagnostic Approach to Cerebellar Hypoplasia
2021 · Andrea Accogli, Nassima Addour-Boudrahem, et al. · The Cerebellum · 46
Diagnostic Yield of Intellectual Disability Gene Panels
2018 · Heather Pekeles, Andrea Accogli, et al. · Pediatric Neurology · 36
Oxidative Status and Plasma Lipid Profile in β-Thalassemia Patients
2014 · Nassima Boudrahem-Addour, Malika Izem-Meziane, et al. · Hemoglobin · 34
Human Oligodendrocyte Myelination Potential; Relation to Age and Differentiation
2021 · Julia Xiao Xuan Luo, Qiao‐Ling Cui, et al. · Annals of Neurology · 24
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Molecular Heterogeneity of β-Thalassemia in Algeria: How to Face Up to a Major Health Problem
2009 · Nassima Boudrahem-Addour, Nadia Zidani, et al. · Hemoglobin · 21
Pathogenic variants in AIMP1 cause pontocerebellar hypoplasia
2019 · Andrea Accogli, Laura Russell, et al. · Neurogenetics · 19
Defining the Genetic Landscape of Congenital Mirror Movements in 80 Affected Individuals
2024 · Meagan L. Collins Hutchinson, Judith St‐Onge, et al. · Movement Disorders · 18
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Heterozygous Missense Pathogenic Variants Within the Second Spectrin Repeat of SPTBN2 Lead to Infantile-Onset Cerebellar Ataxia
2019 · Andrea Accogli, Judith St-Onge, et al. · Journal of Child Neurology · 13
mTOR Pathway Somatic Pathogenic Variants in Focal Malformations of Cortical Development
2023 · Eric Krochmalnek, Andrea Accogli, et al. · Neurology Genetics · 12
PCDH12 variants are associated with basal ganglia anomalies and exudative vitreoretinopathy
2021 · Andrea Accogli, Charbel El Kosseifi, et al. · European Journal of Medical Genetics · 8
Classic “PCH” Genes are a Rare Cause of Radiologic Pontocerebellar Hypoplasia
2023 · Rohaya Binti Mohamad Zakaria, Maisa Malta, et al. · The Cerebellum · 7
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Twins with psychiatric features and a nonsense HRAS variant affecting transcript processing
2023 · Andrea Accogli, Meagan L. Collins Hutchinson, et al. · Psychiatry Research Case Reports · 1
Posterior Fossa Malformations in a Cohort of 116 Fetuses: A Retrospective Analysis of Imaging Characteristics, Postnatal Imaging Concordance, Pregnancy Outcomes and Yield of Genetic Testing
2026 · Maisa Malta, Olivier Fortin, et al. · The Cerebellum
C.4 Clinical, radiological, and etiological features in a cohort of 94 patients with schizencephaly
2025 · E Rodriguez, M Severino, et al. · Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques
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A recurrent MCF2 variant which disrupts DCC binding leads to congenital mirror movements and corpus callosum agenesis
2024 · Andrea Accogli, Victoria Veas Roy, et al. · Research Square
P.07 Characterization of MRI brain abnormalities in X-linked myotubular myopathy
2022 · L. Vogt, A. Marefi, et al. · Neuromuscular Disorders
P.048 Characterization of somatic mutations in mTOR pathway genes in focal cortical dysplasias
2019 · E Krochmalnek, A Accogli, et al. · Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques
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Screening of PI3K-AKT-mTOR pathway genes in focal cortical dysplasias in a clinical setting (P2.283)
2018 · Andrea Accogli, Judith St-Onge, et al. · Neurology
Exploration moléculaire des lissencéphalies : à propos de quatre cas
2014 · N. Boudrahem-Addour, N. Carion, et al. · Revue Neurologique
BIOCHEMISTRY: P-6: MUTATION OF CODON 6 OF THE β GLOBIN GENE AND OXIDATIVE STRESS
2011 · Nassima Addour, A Taleb Bahmed, et al.
Works count: 23
Citation count: 365
H-index: 11
I10-index: 11
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