Mahmoud F. Elsaid - Concepedia

Author

Mahmoud F. Elsaid

Also Known As

Dr. Mahmoud Mohamed Elsaid, M F El-Said, M F Elsaid, M. F. Elsaid, M.F. Elsaid, Mahmoud El-Said, Mahmoud Elsaid, Mahmoud F El-Said, Mahmoud F Elsaid, Mahmoud F. El-Said

Publications

649

Citations

H-Index

Concepts

All Affiliations

Hamad Medical Corporation Weill Cornell Medical College in Qatar Cornell University MIND Research Institute Radboud University Nijmegen

About

Mahmoud F. Elsaid is an author at Hamad Medical Corporation specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	209
2	Pathology	4	4	159
3	Molecular Genetics	2	2	117
4	Neurology	2	2	42
5	Biology	1	1	48

Mahmoud F. Elsaid

Publications

561

Citations

H-Index

Page 1

	Year	Citations
Mutation in noncoding <scp>RNA RNU12</scp> causes early onset cerebellar ataxia Mahmoud F. Elsaid, Nader Chalhoub, Tawfeg Ben‐Omran, Annals of Neurology	2016	89
Autosomal Recessive Inheritance of GLUT1 Deficiency Syndrome Jörg Klepper, Hans Scheffer, Mahmoud F. Elsaid, Neuropediatrics Down SyndromeSporadic TransmissionDevelopmental BiologyAutoimmune DiseaseSlc2a1 Gene	2009	69
Gene therapy for spinal muscular atrophy: the Qatari experience Hossamaldein Gaber Ali, Khalid Ibrahim, Mahmoud F. Elsaid, Gene Therapy	2021	49
A common mutation in the<i>CBS</i>gene explains a high incidence of homocystinuria in the Qatari population Mahmoud F. Elsaid, Ramin Badii, Mohammed Bessisso, Human Mutation GeneticsQatari PopulationGenetic EpidemiologyNuclear FamiliesPathology	2006	48
Altered<i>PLP1</i>splicing causes hypomyelination of early myelinating structures Sietske H. Kevelam, Jennifer R. Taube, Rosalina M.L. van Spaendonk, Annals of Clinical and Translational Neurology	2015	41
Clinical and genomic characteristics of LAMA2 related congenital muscular dystrophy in a patients’ cohort from Qatar. A population specific founder variant Alice Abdel Aleem, Mahmoud F. Elsaid, Nader Chalhoub, Neuromuscular Disorders Rare DiseasesPatients ’ CohortGenetic DisorderGeneticsGenetic Epidemiology	2020	38
W44X mutation in the WWOX gene causes intractable seizures and developmental delay: a case report Loai Elsaadany, Mahmoud F. Elsaid, Rehab Ali, BMC Medical Genetics	2016	27
Identification of a novel CNTNAP1 mutation causing arthrogryposis multiplex congenita with cerebral and cerebellar atrophy Shenela Lakhani, Ryan N. Doan, Mariam Al‐Mureikhi, European Journal of Medical Genetics Neurodegenerative DiseasesCerebellar AtrophyMendelian DisorderGenetic DisorderGenetics	2017	27
Recurrence risk after a first febrile convulsion. Mohamed S. Bessisso, Mahmoud F. Elsaid, Naama A. Almula, PubMed	2001	24
Acute bacterial meningitis in Qatar. Mahmoud F. Elsaid, Amina A. Flamerzi, Mohammed Bessisso, PubMed	2006	23

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