Zakia Abdelhamed - Concepedia

Author

Zakia Abdelhamed

Al-Azhar University

Also Known As

Z Abdelhamed, Z. Abdelhamed, Zakia Abdel-Hamed, Zakia Abdelhamed, Zakia I.A. Abdelhamed, Zakia I.A. Abdelhamed

Publications

661

Citations

H-Index

Concepts

All Affiliations

Al-Azhar University University of Leeds Cincinnati Children's Hospital Medical Center St James's University Hospital Seattle Children's Hospital

About

Zakia Abdelhamed is an author at Al-Azhar University specializing in medicine, developmental biology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	453
2	Cell Biology	3	3	170
3	Molecular Genetics	3	3	173
4	Cellular Physiology	2	2	169
5	Pathology	1	1	17

Zakia Abdelhamed

Publications

568

Citations

H-Index

Page 1

	Year	Citations
A meckelin–filamin A interaction mediates ciliogenesis Matthew Adams, Roslyn Simms, Zakia Abdelhamed, Human Molecular Genetics Developmental BiologyMendelian DisorderGenetic DisorderDevelopmental GeneticsCell Interaction	2011	107
Next generation sequencing identifies mutations in Atonal homolog 7 (ATOH7) in families with global eye developmental defects Kamron N. Khan, Clare V. Logan, Martin McKibbin, Human Molecular Genetics Ocular DiseaseGeneticsMolecular GeneticsDisease Gene IdentificationGenomics	2011	94
Homozygous Mutations in PXDN Cause Congenital Cataract, Corneal Opacity, and Developmental Glaucoma Kamron N. Khan, Adam K Rudkin, David Parry, The American Journal of Human Genetics Homozygous MutationsCongenital Cataract-microcorneaOcular DiseaseDevelopmental BiologyOphthalmology	2011	79
A mutation in <i>Ccdc39</i> causes neonatal hydrocephalus with abnormal motile cilia development in mice Zakia Abdelhamed, Shawn M. Vuong, Lauren M. Hill, Development	2018	78
Differential requirements of tubulin genes in mammalian forebrain development Elizabeth Bittermann, Zakia Abdelhamed, Ryan P. Liegel, PLoS Genetics GeneticsCytoskeletonMolecular GeneticsCellular PhysiologyEmbryology	2019	62
Biallelic Mutations in the Autophagy Regulator DRAM2 Cause Retinal Dystrophy with Early Macular Involvement Mohammed E. El‐Asrag, Panagiotis I. Sergouniotis, Martin McKibbin, The American Journal of Human Genetics Cell AutophagyBiallelic MutationsEarly Macular InvolvementDevelopmental BiologyRetina	2015	48
Aberrant Wnt signalling and cellular over-proliferation in a novel mouse model of Meckel–Gruber syndrome Gabrielle Wheway, Zakia Abdelhamed, Subaashini Natarajan, Developmental Biology Developmental BiologySignal TransductionTissue DevelopmentGenetic DisorderGenetics	2013	46
Novel C8orf37 mutations cause retinitis pigmentosa in consanguineous families of Pakistani origin. Zeinab Ravesh, Mohammed E El Asrag, Nicole Weisschuh, PubMed	2015	17
A novel hypomorphic allele of <i>Spag17</i> causes primary ciliary dyskinesia phenotypes in mice Zakia Abdelhamed, Marshall Lukacs, Sandra Cindrić, Disease Models & Mechanisms SpermatogenesisGeneticsPathologyMolecular GeneticsDisease Gene Identification	2020	17
Gpr63 is a modifier of microcephaly in Ttc21b mouse mutants John Snedeker, William E. Gibbons, David Paulding, PLoS Genetics	2019	10

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