Mahmoud Koko - Concepedia

Author

Mahmoud Koko

Hertie Institute for Clinical Brain Research ORCID

Also Known As

Koko, M., Koko, Mahmoud, M Koko, M. KOKO, M. Koko, Mahmoud E Koko, Mahmoud E. Koko, Mahmoud Eltayeb Koko, Mahmoud Koko, Mahmoud Koko Musa

Publications

1.1K

Citations

H-Index

Concepts

All Affiliations

Hertie Institute for Clinical Brain Research University of Tübingen University of Khartoum Centre National de la Recherche Scientifique Inserm

About

Mahmoud Koko is an author at Hertie Institute for Clinical Brain Research specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	360
2	Social Sciences	2	2	194
3	Molecular Genetics	2	2	100
4	Epidemiology	1	1	73
5	Microbiology	1	1	73

Mahmoud Koko

Publications

856

Citations

H-Index

Page 1

	Year	Citations
Genotype-phenotype correlations in <i>SCN8A</i> -related disorders reveal prognostic and therapeutic implications Katrine M. Johannesen, Yuanyuan Liu, Mahmoud Koko, Brain	2021	138
Neuronal mechanisms of mutations in <i>SCN8A</i> causing epilepsy or intellectual disability Yuanyuan Liu, Julian Schubert, Lukas Sonnenberg, Brain Neurological DisorderGeneticsSynaptic TransmissionMild EpilepsyCellular Neurobiology	2018	129
Newcastle Disease Virus in Madagascar: Identification of an Original Genotype Possibly Deriving from a Died Out Ancestor of Genotype IV Olivier Fridolin Maminiaina, Patricia Gil, François‐Xavier Briand, PLoS ONE Virus EpidemiologyGeneticsNew GenotypeGenotype IvViral Evolution	2010	73
Gain-of-function variants in <i>GABRD</i> reveal a novel pathway for neurodevelopmental disorders and epilepsy Philip K. Ahring, Vivian W. Y. Liao, Elena Gardella, Brain	2021	66
<i>KCNC1</i>‐related disorders: new de novo variants expand the phenotypic spectrum Joohyun Park, Mahmoud Koko, Ulrike B. S. Hedrich, Annals of Clinical and Translational Neurology Progressive Myoclonus EpilepsyGeneticsPathologyPhenotypic SpectrumMolecular Genetics	2019	65
Examining the role of common variants in rare neurodevelopmental conditions Qin Qin Huang, Emilie M. Wigdor, Daniel Malawsky, Nature	2024	40
Hereditary spastic paraplegias: identification of a novel SPG57 variant affecting TFG oligomerization and description of HSP subtypes in Sudan Liena E. O. Elsayed, Inaam N. Mohammed, Ahlam A. Hamed, European Journal of Human Genetics Novel Spg57 VariantHereditary Spastic ParaplegiasMedicineGeneticsPathogenesis	2016	35
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 Mendelian DisorderGenetic DisorderGeneticsInherited Metabolic DiseasePathology	2019	26
Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications Katrine M. Johannesen, Yuanyuan Liu, Catherine E. Gjerulfsen, Kölner Universitäts PublikationsServer (Universität zu Köln)	2021	23
<i>KCND2</i> variants associated with global developmental delay differentially impair Kv4.2 channel gating Yongqiang Zhang, Georgios Tachtsidis, Claudia Schob, Human Molecular Genetics	2021	21

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