Hisham Megahed - Concepedia

Author

Hisham Megahed

Université Paris Cité ORCID

Also Known As

Hisham Megahed

Publications

1.4K

Citations

H-Index

Concepts

All Affiliations

Université Paris Cité Singleton Hospital National Water Research Center Newcastle University St. Jude Children's Research Hospital

About

Hisham Megahed is an author at Université Paris Cité specializing in medicine, neuroscience, and neurodegenerative diseases.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	889
2	Neurology	2	2	612
3	Neuroscience	2	2	612
4	Biostatistics	1	1	169
5	Pathology	1	1	108

Hisham Megahed

Publications

1.4K

Citations

H-Index

Page 1

	Year	Citations
Exome Sequencing Links Corticospinal Motor Neuron Disease to Common Neurodegenerative Disorders Gaia Novarino, Ali G. Fenstermaker, Maha S. Zaki, Science Neurological DisorderGeneticsNetwork AnalysisGene DiscoveryDisease Gene Identification	2014	526
Definition of Disease-Risk Stratification Groups in Childhood Medulloblastoma Using Combined Clinical, Pathologic, and Molecular Variables David W. Ellison, Mehmet Koçak, James Dalton, Journal of Clinical Oncology	2010	299
DNA methylation profiling of medulloblastoma allows robust subclassification and improved outcome prediction using formalin-fixed biopsies Ed C. Schwalbe, Daniel Williamson, Janet C. Lindsey, Acta Neuropathologica Robust SubclassificationFormalin-fixed BiopsiesMedicineGeneticsDna Methylation	2013	169
MYC family amplification and clinical risk-factors interact to predict an extremely poor prognosis in childhood medulloblastoma Sarra Ryan, Ed C. Schwalbe, Michael Cole, Acta Neuropathologica Hematological MalignancyNeuro-oncologyMyc Family AmplificationMedicinePediatrics	2011	108
Biallelic loss of human CTNNA2, encoding αN-catenin, leads to ARP2/3 complex overactivity and disordered cortical neuronal migration Ashleigh E. Schaffer, Martin W. Breuss, Ahmet Okay Çağlayan, Nature Genetics Neurodegenerative DiseasesHuman Ctnna2Arp2/3 Complex OveractivityNeurologyNeuroscience	2018	86
Rapid Diagnosis of Medulloblastoma Molecular Subgroups Ed C. Schwalbe, Janet C. Lindsey, Debbie Straughton, Clinical Cancer Research	2011	80
Utility of whole exome sequencing for the early diagnosis of pediatric-onset cerebellar atrophy associated with developmental delay in an inbred population Hisham Megahed, Michaël Nicouleau, Giulia Barcia, Orphanet Journal of Rare Diseases	2016	42
Inherited glycosylphosphatidylinositol defects cause the rare Emm-negative blood phenotype and developmental disorders Romain Duval, Gaël Nicolas, Alexandra Willemetz, Blood	2021	29
Biallelic loss of <scp><i>EMC10</i></scp> leads to mild to severe intellectual disability Rauan Kaiyrzhanov, Clarissa Rocca, Mohnish Suri, Annals of Clinical and Translational Neurology	2022	14
Association of GSTP1 p.Ile105Val (rs1695, c.313A > G) Variant with the Risk of Breast Carcinoma among Egyptian Women Magdy M. Youssef, Afaf Elsaid, Rasha A. El‐Saeed, Biochemical Genetics	2021	12

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