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Esraa Eltaraifee
Institution:
University of Khartoum
Observed institution:
University of Khartoum
ORCID:
0009-0004-0339-6749
Observed ORCID:
0009-0004-0339-6749
OpenAlex ID:
A5042234952
Clinical phenotyping and genetic diagnosis of a large cohort of Sudanese families with hereditary spinocerebellar degenerations
2023
·
Ashraf Yahia
, Ahlam A. A. Hamed
, et al.
·
European Journal of Human Genetics
·
13
PDF
Advancing Parkinson's Disease Research in Africa: A Strategic Training Framework of the Global Parkinson's Genetics Program
2024
·
Kathryn Step
, Esraa Eltaraifee
, et al.
·
Movement Disorders
·
9
PDF
A novel homozygous mutation in TRAPPC9 gene causing autosomal recessive non-syndromic intellectual disability
2022
·
Mutaz Amin
, Cedric Vignal
, et al.
·
BMC Medical Genomics
·
9
PDF
Novel variants causing megalencephalic leukodystrophy in Sudanese families
2021
·
Mutaz Amin
, Cedric Vignal
, et al.
·
Journal of Human Genetics
·
8
Case Report: A New Family With Pontocerebellar Hypoplasia 10 From Sudan
2022
·
Mutaz Amin
, Cedric Vignal
, et al.
·
Frontiers in Genetics
·
4
PDF
Genome‐Wide Assessment Reveals Ancestral Differences in Homozygosity Patterns Potentially Linked to Parkinson's Disease Etiology
2026
·
Kathryn Step
, Carlos F. Hernández
, et al.
·
Movement Disorders
·
3
Bi-allelic PRRT2 variants may predispose to Self-limited Familial Infantile Epilepsy
2024
·
Mahmoud Koko
, Maha A. Elseed
, et al.
·
European Journal of Human Genetics
·
3
PDF
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Works count:
7
Citation count:
49
H-index:
4
I10-index:
1
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