22 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
Active, last published 2026
In genomics and rare diseases
Amal
Ouskri
Scholar“Research focused on Genomics and Rare Diseases and adjacent fields.”
Claim Your Profile1
H-index
2
Citations
Amal has not officially claimed their profile. If you are Amal, claim it free.
Claim Your Profile
Pioneer
LOCKED
Pathfinder
LOCKED
Scholar
EARNED
Innovator
LOCKED
Inventor
LOCKED
Catalyst
LOCKED
Expert
UPGRADE
01 · About the work
What I study
mal Ouskri is a researcher working on Genomics and Rare Diseases. A fuller summary will appear once they update their profile.
02 · Reach
Publication output and reach
Amal's work has been cited 2 times across 2 active years. Bars show publications per year; the line shows cumulative citation totals across publications first appearing in each year.
03 · Research focus
Topics
Genomics and Rare Diseases×4BRCA gene mutations in cancer×2Prenatal Screening and Diagnostics×2Genomic variations and chromosomal abnormalities×2PARP inhibition in cancer therapy×2
04 · Where I am
Affiliations
Affiliation on published researchCentre Hospitalier Universitaire Hassan II, MoroccoDrawn from the institution listed on this researcher’s published work.
05 · Selected work
Recent publications
5 works7 May 2026Open access
Prevalence and spectrum of AZFc copy number variations in infertile Moroccan menPublisher siteDaehan saengsik uihak hoeji/Clinical and experimental reproductive medicine, Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
6 Apr 2026Open access
Novel Perspectives on ATP8A2 Regulation: Evidence for Parental Imprinting and Chimeric Transcript FormationPublisher siteEpigenomes, Genetic Syndromes and Imprinting
25 Sept 2025
A rare case of mosaic monosomy 21 in a Moroccan patient: clinical findings and insights from a systematic reviewPublisher siteClinical Dysmorphology, Genomic variations and chromosomal abnormalities
20 Sept 2025
MCLMR Syndrome: A Case Report and Systematic ReviewPublisher siteSN Comprehensive Clinical Medicine, Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
Expert Academic Profiles go further
Citation trend analytics, exportable publication records, and direct enquiry routing from industry and funders.
Are you Amal?
Claim it to verify your details, connect with industry partners, and explore Fractional Domain Expert opportunities through MARATTO™.
African researchers are full of potential that too often goes unrecognised. Your MARATTO™ profile gives your work the commercial pathway it deserves.
Claim Your Profile
Free to claim · takes a minute to verify it’s you