Hamid Galehdari - Concepedia

Author

Hamid Galehdari

Shahid Chamran University of Ahvaz ORCID

Also Known As

G Abdel Hamid, Galehdari Hamid, Galehdari, Hamid, H Galehdari, H. Galehdari, Hamid GALEHDARI, Hamid Galehdari, Mina Zamani, Samira Negahdari, Seyed Reza Kazemi Nezhad

269

Publications

2.8K

Citations

H-Index

Concepts

All Affiliations

Shahid Chamran University of Ahvaz Ahvaz Jundishapur University of Medical Sciences University College London National Hospital for Neurology and Neurosurgery St George's, University of London

About

Hamid Galehdari is an author at Shahid Chamran University of Ahvaz specializing in medicine, genetics, and neuroscience.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	13	17	974
2	Natural Sciences	5	5	64
3	Social Sciences	3	3	107
4	Biochemistry	2	2	22
5	Biology	2	2	29

Hamid Galehdari

Publications

2.2K

Citations

H-Index

Page 1

	Year	Citations
Deficiency of terminal ADP‐ribose protein glycohydrolase TARG1/C6orf130 in neurodegenerative disease Reza Seyed Sharifi, Rosa Morra, C. Denise Appel, The EMBO Journal	2013	298
Allelic Loss Is Often the First Hit in the Biallelic Inactivation of the p53 and DPC4 Genes During Pancreatic Carcinogenesis Jutta Lüttges, Hamid Galehdari, Verena Bröcker, American Journal Of Pathology Biallelic InactivationPancreatic CarcinogenesisPancreatic CancerPathologyDpc4 Genes	2001	236
Mutations of the DPC4/Smad4 gene in biliary tract carcinoma. Stephan A. Hahn, Detlef K. Bartsch, Anja Schroers, PubMed Tumor BiologyPancreatic CancerBiliary TractDpc4/smad4 GeneGenetics	1998	147
Mutations of the DPC4/Smad4 gene in neuroendocrine pancreatic tumors Detlef K. Bartsch, Stephan A. Hahn, Kirill D Danichevski, Oncogene Pancreatic CancerDpc4/smad4 GeneMedicinePathologyMolecular Diagnostics	1999	130
Loss of the sphingolipid desaturase DEGS1 causes hypomyelinating leukodystrophy Devesh C. Pant, Imen Dorboz, Agatha Schlüter, Journal of Clinical Investigation Myelin DevelopmentMyelin SheathNeurodegenerative DiseasesAmyotrophic Lateral SclerosisNeurological Disease	2019	101
NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular disease Paige Martin, Yu Kigoshi-Tansho, Roger B. Sher, Nature Communications	2020	91
Mutations in INPP5K Cause a Form of Congenital Muscular Dystrophy Overlapping Marinesco-Sjögren Syndrome and Dystroglycanopathy Daniel P. S. Osborn, Heather L. Pond, Neda Mazaheri, The American Journal of Human Genetics Inpp5k CauseRare DiseasesMendelian DisorderGenetic DisorderGenetics	2017	66
Homozygous Missense Variants in NTNG2, Encoding a Presynaptic Netrin-G2 Adhesion Protein, Lead to a Distinct Neurodevelopmental Disorder Caroline Dias, Jaya Punetha, Céline Zheng, The American Journal of Human Genetics Brain DevelopmentExome SequencingSynaptic TransmissionGeneticsDisease Gene Identification	2019	57
Effect of the herbal mixture composed of Aloe Vera, Henna, Adiantum capillus-veneris, and Myrrha on wound healing in streptozotocin-induced diabetic rats Hamid Galehdari, Samira Negahdari, Mahnaz Kesmati, BMC Complementary and Alternative Medicine	2016	53
Biallelic <i>SQSTM1</i> mutations in early-onset, variably progressive neurodegeneration Valentina Muto, Elisabetta Flex, Zachary A Kupchinsky, Neurology	2018	52

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