Hamid Galehdari

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Alihossein SaberiAhvaz Jundishapur Univesity of Medical SciencesVerified email at ajums.ac.ir
Mohammad HamidAssociate Professor of Molecular Genetics (Medical) Pasteur Institute of IranVerified email at pasteur.ac.ir
Reza MaroofianThe UCL Queen Square Institute of NeurologyVerified email at ucl.ac.uk
Amir JalaliSchool of Paramedical Sciences, Guilan University of Medical SciencesVerified email at gums.ac.ir
Mahnaz KesmatiProfessor of Neurophysiology, Shahid Chamran UniversityVerified email at scu.ac.ir
mohammad pedramAhvaz jundishapur University of Medical SciencesVerified email at ajums.ac.ir
bijan keikhaeiThalassemia & Hemoglobinopathy Research Center, Health Research Institute, Ahvaz JundishapurVerified email at ajums.ac.ir
Stephan HahnProfessor of Molecular Medicine, Ruhr University BochumVerified email at rub.de
Mohammad ShafieiDepartment of Genetics, Faculty of science, ShahidChamran University of Ahvaz, Ahvaz, Iran.Verified email at scu.ac.ir
masoumeh baradaranToxicology Research Center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, IranVerified email at ajums.ac.ir
Fakher RahimDepartment of Medical Laboratory Technologies, Alnoor University, Mousl, Nineveh, IraqVerified email at alnoor.edu.iq
Annahita RezaieProfessor in veterinary pathology, Shahid Chamran University of AhvazVerified email at scu.ac.ir
Yalda JamshidiSt George's University of LondonVerified email at sgul.ac.uk
kaveh jasebThalassemia & Hemoglobinopathy Research Center, Health Research Institute, Ahvaz JundishapurVerified email at ajums.ac.ir
Nastaran MajdinasabProfessor of Neurology, Ahvaz Jundishapur University of Medical SciencesVerified email at ajums.ac.ir
Abolfazl GholipourAssistant Professor of Medical Bacteriology, Shahrekord University of Medical SciencesVerified email at skums.ac.ir
Manoochehr MakvandiAhvaz Jundishapur University of Medical Sciences, Ahvaz-IranVerified email at ajums.ac.ir
Andreas LadurnerChair of Physiological Chemistry, LMU Munich; Founder, Managing Director and CSO, Eisbach Bio GmbHVerified email at med.lmu.de
Roy WilliamsCalifornia Institute of TechnologyVerified email at caltech.edu

Hamid Galehdari

Department of Genetics, Faculty of Sciences, Shahid Chamran University of Ahvaz, Ahvaz, Iran

No verified email

Human Genetics


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Allelic loss is often the first hit in the biallelic inactivation of the p53 and DPC4 genes during pancreatic carcinogenesis J Lüttges, H Galehdari, V Bröcker, I Schwarte-Waldhoff, D Henne-Bruns, ... The American journal of pathology 158 (5), 1677-1683, 2001	315	2001
Deficiency of terminal ADP‐ribose protein glycohydrolase TARG1/C6orf130 in neurodegenerative disease R Sharifi, R Morra, C Denise Appel, M Tallis, B Chioza, G Jankevicius, ... The EMBO journal 32 (9), 1225-1237, 2013	311	2013
Mutations of the DPC4/Smad4 Gene in Biliary Tract Carcinoma SA Hahn, D Bartsch, A Schroers, H Galehdari, M Becker, A Ramaswamy, ... Cancer research 58 (6), 1124-1126, 1998	224	1998
Mutations of the DPC4/Smad4 gene in neuroendocrine pancreatic tumors D Bartsch, SA Hahn, KD Danichevski, A Ramaswamy, D Bastian, ... Oncogene 18 (14), 2367-2371, 1999	167	1999
Loss of the sphingolipid desaturase DEGS1 causes hypomyelinating leukodystrophy DC Pant, I Dorboz, A Schluter, S Fourcade, N Launay, J Joya, ... The Journal of clinical investigation 129 (3), 1240-1256, 2019	69	2019
Wound healing activity of extracts and formulations of aloe vera, henna, adiantum capillus-veneris, and myrrh on mouse dermal fibroblast cells S Negahdari, H Galehdari, M Kesmati, A Rezaie, G Shariati International journal of preventive medicine 8 (1), 18, 2017	64	2017
NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular disease PB Martin, Y Kigoshi-Tansho, RB Sher, G Ravenscroft, JE Stauffer, ... Nature communications 11 (1), 4625, 2020	62	2020
Mutations in INPP5K cause a form of congenital muscular dystrophy overlapping Marinesco-Sjögren syndrome and dystroglycanopathy DPS Osborn, HL Pond, N Mazaheri, J Dejardin, CJ Munn, K Mushref, ... The American Journal of Human Genetics 100 (3), 537-545, 2017	62	2017
Effect of the herbal mixture composed of Aloe Vera, Henna, Adiantum capillus-veneris, and Myrrha on wound healing in streptozotocin-induced diabetic rats H Galehdari, S Negahdari, M Kesmati, A Rezaie, G Shariati BMC complementary and alternative medicine 16, 1-9, 2016	51	2016
Association between the G1001C polymorphism in the GRIN1 gene promoter and schizophrenia in the Iranian population H Galehdari Journal of molecular neuroscience 38, 178-181, 2009	48	2009
Homozygous missense variants in NTNG2, encoding a presynaptic netrin-G2 adhesion protein, lead to a distinct neurodevelopmental disorder CM Dias, J Punetha, C Zheng, N Mazaheri, A Rad, S Efthymiou, ... The American Journal of Human Genetics 105 (5), 1048-1056, 2019	42	2019
Biallelic SQSTM1 mutations in early-onset, variably progressive neurodegeneration V Muto, E Flex, Z Kupchinsky, G Primiano, H Galehdari, M Dehghani, ... Neurology 91 (4), e319-e330, 2018	42	2018
VMD DisRg: New User-Friendly Implement for calculation distance and radius of gyration in VMD program S Falsafi-Zadeh, Z Karimi, H Galehdari Bioinformation 8 (7), 341, 2012	37	2012
Comprehensive spectrum of the β-thalassemia mutations in Khuzestan, Southwest Iran H Galehdari, B Salehi, S Azmoun, B Keikhaei, KM Zandian, M Pedram Hemoglobin 34 (5), 461-468, 2010	36	2010
VMD-SS: A graphical user interface plug-in to calculate the protein secondary structure in VMD program M Yahyavi, S Falsafi-Zadeh, Z Karimi, G Kalatarian, H Galehdari Bioinformation 10 (8), 548, 2014	32	2014
The first molecular genetics analysis of individuals suffering from nephropatic cystinosis in the Southwestern Iran S Shahkarami, H Galehdari, A Ahmadzadeh, M Babaahmadi, M Pedram Nefrologia 33 (3), 308-315, 2013	32	2013
CYP2E1^5B, CYP2E1^6, CYP2E1^7B, CYP2E1^2, and CYP2E1^*3 Allele Frequencies in Iranian Populations GM Shahriary, H Galehdari, A Jalali, F Zanganeh, SMR Alavi, ... Asian Pacific Journal of Cancer Prevention 13 (12), 6505-6510, 2012	30	2012
Expression of VEGF and TGF-β genes in skin wound healing process induced using phenytoin in male rats R Savari, M Shafiei, H Galehdari, M Kesmati Jundishapur Journal of Health Sciences 11 (1), 2019	28	2019
Molecular analysis of exons 6 and 7 of phenylalanine hydroxylase gene mutations in Phenylketonuria patients in Western Iran K Moradi, R Alibakhshi, K Ghadiri, SR Khatami, H Galehdari Indian journal of human genetics 18 (3), 290, 2012	28	2012
Analysis of enriched rare variants in JPH2-encoded junctophilin-2 among Greater Middle Eastern individuals reveals a novel homozygous variant associated with … EG Jones, N Mazaheri, R Maroofian, M Zamani, T Seifi, A Sedaghat, ... Scientific reports 9 (1), 9038, 2019	27	2019

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