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Paria Alipour
Paria Alipour
PhD in Human Genetics, McGill University
Verified email at mail.mcgill.ca
Title
Cited by
Cited by
Year
Spinal cord extracts of amyotrophic lateral sclerosis spread TDP-43 pathology in cerebral organoids
Y Tamaki, JP Ross, P Alipour, CÉ Castonguay, B Li, H Catoire, ...
PLoS Genetics 19 (2), e1010606, 2023
232023
A novel pathogenic variant in an Iranian Ataxia telangiectasia family revealed by next-generation sequencing followed by in silico analysis
MA Tabatabaiefar, P Alipour, A Pourahmadiyan, N Fattahi, L Shariati, ...
Journal of the Neurological Sciences 379, 212-216, 2017
132017
Investigation of the causal relationship between ALS and autoimmune disorders: a Mendelian randomization study
P Alipour, K Senkevich, JP Ross, D Spiegelman, D Manousaki, PA Dion, ...
BMC Medicine 20 (1), 1-7, 2022
92022
Potential Protective Link Between Type I Diabetes and Parkinson's Disease Risk and Progression
K Senkevich, P Alipour, E Chernyavskaya, E Yu, AJ Noyce, Z Gan‐Or
Movement Disorders 38 (7), 1350-1355, 2023
52023
A pathogenic variant in SLC26A4 is associated with Pendred syndrome in a consanguineous Iranian family
A Pourahmadiyan, P Alipour, N Fattahi, M Kasiri, F Rezaeian, ...
International Journal of Audiology 58 (10), 628-634, 2019
32019
Next-generation sequencing reveals a novel pathogenic variant in the ATM gene
A Pourahmadiyan, P Alipour, N Golchin, MA Tabatabaiefar
International Journal of Neuroscience 132 (6), 558-562, 2022
22022
Exploring ALS differential vulnerability using single-cell transcriptomic analysis
P Alipour, P Dion, G Rouleau, J Ross
Journal of the Neurological Sciences 455, 2023
2023
Copy-number variants and polygenic risk for intelligence confer risk for autism spectrum disorder irrespective of their effects on cognitive ability
Z Schmilovich, VR Bourque, E Douard, G Huguet, C Poulain, J Ross, ...
Frontiers in Psychiatry 15, 1369767, 2023
2023
Evidence of a causal relationship between Parkinson's disease and autoimmune disorders driven by HLA
K Senkevich, P Alipour, E Chernyavskaya, E Yu, A Noyce, Z Gan-Or
EUROPEAN JOURNAL OF NEUROLOGY 29, 307-308, 2022
2022
Profiling of the oculomotor nucleus and spinal cord in amyotrophic lateral sclerosis using single-nuclei RNA sequencing (snRNA-seq)
P Alipour, JP Ross, D Spiegelman, D Rochefort, PA Dion, GA Rouleau
EUROPEAN JOURNAL OF HUMAN GENETICS 28 (SUPPL 1), 446-447, 2020
2020
Genetic linkage analysis of DFNB40 and DFNB48 loci in families with autosomal recessive non-syndromic hearing loss (ARNSHL) from western provinces of Iran
A Pourahmadiyan, MA Tabatabaiefar, S Reiisi, P Alipour, N Fattahi, ...
Journal of Isfahan Medical School 34 (374), 214-220, 2016
2016
Genetic linkage analysis of DFNB7/11 locus in patients with autosomal recessive non syndromic hearing loss from Hamedan province
A POURAHMADIYAN, MA TABATABAIEFAR, S Reiisi, P Alipour, ...
Journal of Shahrekord University of Medical Sciences 18 (3), 8-18, 2016
2016
Genetic linkage analysis of the DFNB63 locus in families with autosomal recessive nonsyndromic hearing loss from Hamadan and Kohgiluyeh and Boyer-Ahmad Provinces, Iran
P Alipour, MA Tabatabaiefar, S Reiisi, N Fattahi, A Pourahmadian, ...
Journal of Isfahan Medical School 33 (346), 1308-1317, 2015
2015
GENETIC LINKAGE ANALYSIS OF DFNB59 LOCI INVOLVED IN AUTOSOMAL RECESSIVE NON-SYNDROMIC HEARING LOSS (ARNSHL) IN 3 WESTERN PROVINCES OF IRAN
N Fattahi, FARMA TABATABAIE, S REIISI, P Alipour, A Pourahmadian, ...
Journal of Shahrekord University of Medical Sciences 17 (4), 39-46, 2015
2015
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Articles 1–14