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Verified ScholarVerified at Centre Hospitalo-Universitaire Bab El OuedASIDASID-4375-3034-0256 orcid.org/0000-0003-1735-7471
Mériem Tazir
Centre Hospitalo-Universitaire Bab El Oued
Faculty researcher at Centre Hospitalo-Universitaire Bab El Oued (DZ), specializing in Physical Sciences & Engineering. [Discipline: Physical Sciences & Engineering] [Scholar Type: Journal Research Scientist] [Career Tier: Distinguished Scholar] [Region: North Africa]
#Hereditary Neurological Disorders#Genetic Neurodegenerative Diseases#Peripheral Neuropathies and Disorders#Genomics and Rare Diseases
Scholarly Profiles: Google Scholar
Citation Indices
Standard Scientometrics| All | Since 2021 | |
|---|---|---|
| Citations | 7,379 | 3,542 |
| h-index | 41 | 31 |
| i10-index | 71 | 50 |
Annual Citation Growth
Verified Citations / Year0
2020354
2021+40%496
2022+29%638
2023+33%850
2024-8%779
2025-45%425
2026Scholarship Distribution & Proportions159 Articles • 0 Books & Monographs • 0 Applied Assignments
Continental Provenance:25% African Regional Citations (1,845) • 75% Global Research Impact (5,534)
159 Indexed WorksAuthentic Data
Co-Authors & Academic Collaborators
No verified co-authors registered on AfriJournal Index yet.
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Articles & Books (159)
Homozygous Defects in LMNA, Encoding Lamin A/C Nuclear-Envelope Proteins, Cause Autosomal Recessive Axonal Neuropathy in Human (Charcot-Marie-Tooth Disorder Type 2) and Mouse
Published in The American Journal of Human Genetics•2002
DOI: 10.1086/339274 Verified Peer-Reviewed
LRRK2G2019S as a Cause of Parkinson's Disease in North African Arabs
Published in New England Journal of Medicine•2006
DOI: 10.1056/nejmc055540 Verified Peer-Reviewed
Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2
Published in Nature Genetics•2004
DOI: 10.1038/ng1303 Verified Peer-Reviewed
Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy
Published in The American Journal of Human Genetics•2016
DOI: 10.1016/j.ajhg.2016.01.014 Verified Peer-Reviewed
The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy
Published in Nature Genetics•2000
DOI: 10.1038/81701 Verified Peer-Reviewed
Showing 1 – 5 of 159 publications
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