Concepedia

Author

Ashraf Yahia

University of KhartoumORCID

Also Known As

Ashraf Mohamed, Ashraf Y O Mohamed, Ashraf Y. O. Mohamed, Ashraf Yahia, Ashraf Yahia Osman Mohamed

35

Publications

368

Citations

10

H-Index

6

Concepts

All Affiliations

University of KhartoumKing Saud UniversityNational UniversityCentre National de la Recherche ScientifiqueInserm
AY

About

Ashraf Yahia is an author at University of Khartoum specializing in inherited metabolic disease, pathology, and neurogenetics.

Top Concepts

#ConceptH-IndexPublicationsCitations

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Medicine

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2

Pathology

1

1

26

3

Clinical Genetics

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26

4

Genetics

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26

5

Inherited Metabolic Disease

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26

Ashraf Yahia

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9

Publications

157

Citations

9

H-Index

YearCitations

Machine Learning Prediction of Autism Spectrum Disorder From a Minimal Set of Medical and Background Information

Shyam Sundar Rajagopalan, Yali Zhang, Ashraf Yahia,

JAMA Network Open

2024

44

Overlap of polymicrogyria, hydrocephalus, and Joubert syndrome in a family with novel truncating mutations in ADGRG1/GPR56 and KIAA0556

Edmund Cauley, Ahlam A. Hamed, Inaam N. Mohamed,

Neurogenetics

2019

26

Intra-familial phenotypic heterogeneity in a Sudanese family with DARS2-related leukoencephalopathy, brainstem and spinal cord involvement and lactate elevation: a case report

Ashraf Yahia, Liena E. O. Elsayed, Arwa Babai,

BMC Neurology

2018

19

Case report of a novel homozygous splice site mutation in PLA2G6 gene causing infantile neuroaxonal dystrophy in a Sudanese family

Liena E. O. Elsayed, Inaam N. Mohammed, Ahlam A. Hamed,

BMC Medical Genetics

2018

13

A heterozygous mutation in the CCDC88C gene likely causes early-onset pure hereditary spastic paraplegia: a case report

Ashraf Yahia, Zhefan Stephen Chen, Ammar Ahmed,

BMC Neurology

2021

12

Clinical phenotyping and genetic diagnosis of a large cohort of Sudanese families with hereditary spinocerebellar degenerations

Ashraf Yahia, Ahlam A. Hamed, Inaam N. Mohamed,

European Journal of Human Genetics

2023

12

Genetic diagnosis in Sudanese and Tunisian families with syndromic intellectual disability through exome sequencing

Ashraf Yahia, Ikhlas Ben Ayed, Ahlam A. Hamed,

Annals of Human Genetics

2022

11

Pathogenic Variants in ABHD16A Cause a Novel Psychomotor Developmental Disorder With Spastic Paraplegia

Ashraf Yahia, Liena E. O. Elsayed, Rémi Valter,

Frontiers in Neurology

2021

10

Consanguinity and willingness to perform premarital genetic screening in Sudan

Yasir Ahmed Mohammed Elhadi, Salma S. Alrawa, Esraa S. A. Alfadul,

European Journal of Human Genetics

2023

10

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