Mohammed Zain Seidahmed

Author

Also Known As

Heba Morsy, M Seidahmed, M. Seidahmed, M.Z. Seidahmed, Mohammed Z Seidahmed, Mohammed Z. Seidahmed, Mohammed Zain Seidahmed, Mohammed Z. Seidahmed, Mohammed Zain Seidahmed, Seidahmed, Mohammed

Publications

2.6K

Citations

H-Index

Concepts

All Affiliations

Security Forces Hospital King Faisal Specialist Hospital & Research Centre King Saud University Alfaisal University King Abdulaziz City for Science and Technology

About

Mohammed Zain Seidahmed is an author at Security Forces Hospital specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	16	16	1.2K
2	Public Health	2	2	72
3	Engineering	1	1	17
4	Health Sciences	1	1	196
5	Anatomy	1	1	69

Mohammed Zain Seidahmed

Publications

2.4K

Citations

H-Index

Page 1

	Year	Citations
Accelerating Novel Candidate Gene Discovery in Neurogenetic Disorders via Whole-Exome Sequencing of Prescreened Multiplex Consanguineous Families Anas M. Alazami, Nisha Patel, Hanan E. Shamseldin, Cell Reports	2014	465
The landscape of genetic diseases in Saudi Arabia based on the first 1000 diagnostic panels and exomes Dorota Monies, Mohamed Abouelhoda, Moeenaldeen AlSayed, Human Genetics	2017	296
Alteration of Fatty-Acid-Metabolizing Enzymes Affects Mitochondrial Form and Function in Hereditary Spastic Paraplegia Christelle Tesson, Magdalena Nawara, Mustafa A. Salih, The American Journal of Human Genetics Metabolic SyndromeEnergy MetabolismMetabolic DisorderMitochondrial FunctionBiochemistry	2012	196
The genetic landscape of familial congenital hydrocephalus Ranad Shaheen, Mohammed Adeeb Sebai, Nisha Patel, Annals of Neurology	2017	144
Genomic and phenotypic delineation of congenital microcephaly Ranad Shaheen, Sateesh Maddirevula, Nour Ewida, Genetics in Medicine Developmental AnomalyDevelopmental BiologyBrain DevelopmentDevelopmental GeneticsGenetics	2018	120
Autozygome and high throughput confirmation of disease genes candidacy Sateesh Maddirevula, Fatema Alzahrani, Mohammed Al‐Owain, Genetics in Medicine	2018	112
Mutations in DONSON disrupt replication fork stability and cause microcephalic dwarfism John J. Reynolds, Louise S. Bicknell, Paula Carroll, Nature Genetics Genome InstabilityDevelopmental BiologyGenetic DisorderGeneticsGenomic Mechanism	2017	109
The morbid genome of ciliopathies: an update Hanan E. Shamseldin, Ranad Shaheen, Nour Ewida, Genetics in Medicine Genetic DisorderMedicineGeneticsPathologyGenome Analysis	2020	103
Mutations in CSPP1, Encoding a Core Centrosomal Protein, Cause a Range of Ciliopathy Phenotypes in Humans Ranad Shaheen, Hanan E. Shamseldin, Catrina M. Loucks, The American Journal of Human Genetics Ciliopathy PhenotypesPathologyCore Centrosomal ProteinCell BiologyMedicine	2013	86
A TCTN2 mutation defines a novel Meckel Gruber syndrome locus Ranad Shaheen, Eissa Faqeih, Mohammed Zain Seidahmed, Human Mutation Developmental BiologyMendelian DisorderGenetic DisorderMedicineGenetics	2011	79

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