2 Sept 2026
High frequency of LRRK2 p.Gly2019Ser in Moroccan Parkinson’s disease: RFLP as a reliable genotyping approachPublisher siteNeurogenetics, Parkinson's Disease Mechanisms and Treatments
Active, last published 2026
In genetic neurodegenerative diseases
Karim
Ouldim
Scholar“Research focused on Genetic Neurodegenerative Diseases and adjacent fields.”
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01 · About the work
What I study
arim Ouldim is a researcher working on Genetic Neurodegenerative Diseases. A fuller summary will appear once they update their profile.
02 · Reach
Publication output and reach
Karim's work has been cited 16 times across 3 active years. Bars show publications per year; the line shows cumulative citation totals across publications first appearing in each year.
03 · Research focus
Topics
Genetic Neurodegenerative Diseases×3Genomics and Rare Diseases×2Genetics and Neurodevelopmental Disorders×2Genetic Syndromes and Imprinting×2Glycogen Storage Diseases and Myoclonus×2
04 · Where I am
Affiliations
Affiliation on published researchAgence pour le Développement et la Réhabilitation de la Ville de Fès, MoroccoDrawn from the institution listed on this researcher’s published work.
05 · Selected work
Recent publications
6 works22 Aug 2026
Progressive ataxia and orolingual chorea revealing a novel VPS13A variant: a case report of chorea-acanthocytosis without peripheral acanthocytosis with a literature reviewPublisher siteNeurogenetics, Blood groups and transfusion
22 Feb 2026Open access
First combined analysis of SMN1, SMN2, and NAIP copy numbers in Moroccan SMA patients and their correlation with disease severityPublisher siteMolecular Genetics and Metabolism Reports, Neurogenetic and Muscular Disorders Research
1 Jan 2026Open access2cites
Idiopathic Pulmonary Fibrosis: A Comprehensive Review of Risk Factors, Genetics, Diagnosis, and Therapeutic ApproachesPublisher siteBiomedicines, Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
19 Nov 2025Open access
Novel Variant in the <i>NLRP12</i> Gene: Insights From a Case Report and Systematic ReviewPublisher siteInternational Journal of Immunogenetics
23 Mar 2024Open access1cites
Conventional and molecular cytogenetic characterization of a Moroccan patient with WAGR syndromePublisher siteEgyptian Journal of Medical Human Genetics, Renal and related cancers
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