‪Niloofar Bazazzadegan, Assistant professor, PhD in Medical Genetics‬

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Kimia KahriziProfessor of Medicine, Thessaly UniversityVerified email at uth.gr
Richard J SmithUniversity of IowaVerified email at uiowa.edu
zohreh FattahiGenetics Research Center,University of social welfare and rehabilitation sciencesVerified email at uswr.ac.ir
Mojgan BabanejadGenetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.Verified email at uswr.ac.ir
Ahmad DaneshiProfessor of Otolaryngology, IUMSVerified email at ent-hns.org
Mohammad FarhadiENT and Head&Neck Research Center, Iran University of Medical SciencesVerified email at iums.ac.ir
Nicole C MeyerResearch Associate, University of IowaVerified email at uiowa.edu
Matthew AvenariusAssistant professor, The Ohio State UniversityVerified email at osumc.edu
Koorosh KamaliAssisstant professor of Epidemiology, Zanjan University of Medical SciencesVerified email at zums.ac.ir
A. Eliot Shearer, MD, PhDDept of Otolaryngology, Boston Children's Hospital, Harvard Medical SchoolVerified email at childrens.harvard.edu
Fatemehsadat (Sahar) EsteghamatHarvard Medical schoolVerified email at enders.tch.harvard.edu
Maryam BeheshtianGenetics Research Center, University of Social Welfare and Rehabilitation SciencesVerified email at uswr.ac.ir
Kioomars Saliminejad, PhDAvicenna Research Institute, Tehran, IranVerified email at avicenna.ac.ir
marzieh dehghan Shasaltanehuniversity of zanjanVerified email at znu.ac.ir
Farzaneh LartiDepartment of Molecular Biology and Genetics, Bogaziçi UniversityVerified email at boun.edu.tr
Fereidoun AziziProfessor of Endocrinology & Metabolism, Shahid Beheshti University of Medical SciencesVerified email at sbmu.ac.ir
Seyedeh Sedigheh AbediniUniversity of New South WalesVerified email at unsw.edu.au
Hela AzaiezUniversity of IowaVerified email at uiowa.edu
behzad davarniaDepartment of Genetics, Ardabil University Of Medical ScienceVerified email at arums.ac.ir
Masoud Motasaddi ZarandyTehran University of Medical SciencesVerified email at sina.tums.ac.ir

Niloofar Bazazzadegan, Assistant professor, PhD in Medical Genetics

Genetics Research Center, University of Social Welfare and Rehabilitation Sciences

Verified email at uswr.ac.ir

Medical genetics human genetics Molecular genetics


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Utilizing ethnic-specific differences in minor allele frequency to recategorize reported pathogenic deafness variants AE Shearer, RW Eppsteiner, KT Booth, SS Ephraim, J Gurrola, A Simpson, ... The American Journal of Human Genetics 95 (4), 445-453, 2014	167	2014
Characterising the spectrum of autosomal recessive hereditary hearing loss in Iran CM Sloan-Heggen, M Babanejad, M Beheshtian, AC Simpson, KT Booth, ... Journal of medical genetics 52 (12), 823-829, 2015	116	2015
GJB2 mutations: Passage through Iran H Najmabadi, C Nishimura, K Kahrizi, Y Riazalhosseini, M Malekpour, ... American Journal of Medical Genetics Part A 133 (2), 132-137, 2005	112	2005
A comprehensive study to determine heterogeneity of autosomal recessive nonsyndromic hearing loss in Iran M Babanejad, Z Fattahi, N Bazazzadegan, C Nishimura, N Meyer, ... American journal of medical genetics Part A 158 (10), 2485-2492, 2012	71	2012
Screening for MYO15A gene mutations in autosomal recessive nonsyndromic, GJB2 negative Iranian deaf population Z Fattahi, AE Shearer, M Babanejad, N Bazazzadegan, SN Almadani, ... American Journal of Medical Genetics Part A 158 (8), 1857-1864, 2012	65	2012
The spectrum of GJB2 mutations in the Iranian population with non-syndromic hearing loss—a twelve year study N Bazazzadegan, N Nikzat, Z Fattahi, C Nishimura, N Meyer, S Sahraian, ... International journal of pediatric otorhinolaryngology 76 (8), 1164-1174, 2012	63	2012
A large deletion in GPR98 causes type IIC Usher syndrome in male and female members of an Iranian family N Hilgert, K Kahrizi, N Dieltjens, N Bazazzadegan, H Najmabadi, ... Journal of medical genetics 46 (4), 272-276, 2009	50	2009
Identification of SLC26A4 gene mutations in Iranian families with hereditary hearing impairment K Kahrizi, M Mohseni, C Nishimura, N Bazazzadegan, SM Fischer, ... European journal of pediatrics 168, 651-653, 2009	46	2009
Heterogeneity of hereditary hearing loss in Iran: a comprehensive review M Beheshtian, M Babanejad, H Azaiez, N Bazazzadegan, D Kolbe, ... Archives of Iranian medicine 19 (10), 720, 2016	36	2016
Mutations in TMC1 are a Common Cause of DFNB7/11 Hearing Loss in the Iranian Population MS Hildebrand, K Kahrizi, CJ Bromhead, AE Shearer, JA Webster, ... Annals of otology, rhinology & laryngology 119 (12), 830-835, 2010	36	2010
Spectrum of GJB2 (Cx26) gene mutations in Iranian Azeri patients with nonsyndromic autosomal recessive hearing loss B Davarnia, M Babanejad, Z Fattahi, N Nikzat, N Bazazzadegan, ... International journal of pediatric otorhinolaryngology 76 (2), 268-271, 2012	28	2012
GJB2 mutations in Baluchi population A Naghavi, C Nishimura, K Kahrizi, Y Riazalhosseini, N Bazazzadegan, ... Journal of genetics 87, 195-197, 2008	28	2008
A defect in the CLIP1 gene (CLIP-170) can cause autosomal recessive intellectual disability F Larti, K Kahrizi, L Musante, H Hu, E Papari, Z Fattahi, N Bazazzadegan, ... European Journal of Human Genetics 23 (3), 331-336, 2015	27	2015
Did the GJB2 35delG mutation originate in Iran? V Norouzi, H Azizi, Z Fattahi, F Esteghamat, N Bazazzadegan, ... American journal of medical genetics Part A 155 (10), 2453-2458, 2011	19	2011
A novel mutation of the USH2C (GPR98) gene in an Iranian family with Usher syndrome type II K Kahrizi, N Bazazzadegan, L Jamali, N Nikzat, A Kashef, H Najmabadi Journal of genetics 93, 837-841, 2014	16	2014
Two Iranian families with a novel mutation in GJB2 causing autosomal dominant nonsyndromic hearing loss N Bazazzadegan, AM Sheffield, M Sobhani, K Kahrizi, NC Meyer, ... American Journal of Medical Genetics Part A 155 (5), 1202-1211, 2011	15	2011
Effects of ectoine on behavior and candidate genes expression in ICV-STZ rat model of sporadic Alzheimer’s disease N Bazazzadegan, MD Shasaltaneh, K Saliminejad, K Kamali, M Banan, ... Advanced pharmaceutical bulletin 7 (4), 629, 2017	14	2017
The effects of Melilotus officinalis extract on expression of Daxx, Nfkb and Vegf genes in the streptozotocin-induced rat model of sporadic alzheimer’s disease N Bazazzadegan, MD Shasaltaneh, K Saliminejad, K Kamali, M Banan, ... Avicenna Journal of Medical Biotechnology 9 (3), 133, 2017	14	2017
CNKSR1 gene defect can cause syndromic autosomal recessive intellectual disability S Kazeminasab, II Taskiran, Z Fattahi, N Bazazzadegan, M Hosseini, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 177 …, 2018	13	2018
An association study on IL16 gene polymorphisms with the risk of sporadic Alzheimer's disease T Khoshbakht, M Soosanabadi, M Neishaboury, K Kamali, M Karimlou, ... Avicenna journal of medical biotechnology 7 (3), 128, 2015	13	2015

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