Nejat Mahdieh

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Bahareh RabbaniIran University of Medical SciencesVerified email at modares.ac.ir
Majid MalekiProfessor of Cardiology, Rajaie Cardiovascular Medical & Research CenterVerified email at rhc.ac.ir
Mohammad Taghi AkbariAssociate Professor of Medical GeneticsVerified email at modares.ac.ir
Mortaza Bonyadi, Mortaza Jabbarpour...University of TabrizVerified email at tabrizu.ac.ir
Ibis MenendezUniversity of Miami. Hussman Institute of Human GenomicsVerified email at med.miami.edu
Oscar Diaz-HortaJohn P. Hussman Institute for Human Genomics University of Miami | Miller School of MedicineVerified email at med.miami.edu
Ahmad DaneshiProfessor of Otolaryngology, IUMSVerified email at ent-hns.org
Nikou FotouhiUniversity of Miami, Miller School of MedicineVerified email at med.miami.edu
Michael GonzalezChildren's Hospital of PhiladelphiaVerified email at email.chop.edu
Dr. Salar BakhtiyariDepartment of Clinical Biochemistry, Ilam University of Medical Sciences, Ilam, Iran.Verified email at medilam.ac.ir
Shahin AkhondzadehPsychiatric Research Center, Roozbeh Hospital, Tehran University of Medical Sciences, IranVerified email at neda.net
Mohammad FarhadiENT and Head&Neck Research Center, Iran University of Medical SciencesVerified email at iums.ac.ir
Matthew AvenariusAssistant professor, The Ohio State UniversityVerified email at osumc.edu
Mehdi TotonchiGenetics & Stem cell Departments, Royan InstituteVerified email at royaninstitute.org
Nosratollah Zarghami SoltanahmadiDept. of Clin. Biochem; Dept of Med. Biotechnology, Istanbul Aydin UniversityVerified email at aydin.edu.tr
Professor S. FarajniaTabriz University of Medical sciencesVerified email at tbzmed.ac.ir
Bagher Larijani, MDProfessor of Medicine/Endocrinology Division Chief, Head of EMRI, Tehran University (TUMS)Verified email at tums.ac.ir
M.Amin TabatabaiefarProfessor of Medical Genetics, Isfahan University of Medical SciencesVerified email at med.mui.ac.ir
Mohammadreza HavasianAlborz University of Medical Sciences, Karaj, IranVerified email at medilam.ac.ir
Jafar Panahiilam university of medical sciencesVerified email at medilam.ac.ir

Nejat Mahdieh

Rajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences, Tehran, Iran

Verified email at rhc.ac.ir

Medical Genetics


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The promise of whole-exome sequencing in medical genetics B Rabbani, M Tekin, N Mahdieh Journal of human genetics 59 (1), 5-15, 2014	677	2014
Next-generation sequencing: impact of exome sequencing in characterizing Mendelian disorders B Rabbani, N Mahdieh, K Hosomichi, H Nakaoka, I Inoue Journal of human genetics 57 (10), 621-632, 2012	279	2012
Whole-exome sequencing efficiently detects rare mutations in autosomal recessive nonsyndromic hearing loss O Diaz-Horta, D Duman, J Foster, A Sırmacı, M Gonzalez, N Mahdieh, ... PloS one 7 (11), e50628, 2012	170	2012
An overview of mutation detection methods in genetic disorders N Mahdieh, B Rabbani Iranian journal of pediatrics 23 (4), 375, 2013	166	2013
Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort G Bademci, J Foster, N Mahdieh, M Bonyadi, D Duman, FB Cengiz, ... Genetics in Medicine 18 (4), 364-371, 2016	151	2016
Next generation sequencing: implications in personalized medicine and pharmacogenomics B Rabbani, H Nakaoka, S Akhondzadeh, M Tekin, N Mahdieh Molecular biosystems 12 (6), 1818-1830, 2016	121	2016
Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populations N Mahdieh, B Rabbani, S Wiley, MT Akbari, S Zeinali Journal of human genetics 55 (10), 639-648, 2010	120	2010
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
Statistical study of 35delG mutation of GJB2 gene: a meta-analysis of carrier frequency N Mahdieh, B Rabbani International journal of audiology 48 (6), 363-370, 2009	111	2009
Beta thalassemia in 31,734 cases with HBB gene mutations: pathogenic and structural analysis of the common mutations; Iran as the crossroads of the Middle East N Mahdieh, B Rabbani Blood reviews 30 (6), 493-508, 2016	48	2016
The frequency of GJB2 mutations and the Δ (GJB6‐D13S1830) deletion as a cause of autosomal recessive non‐syndromic deafness in the Kurdish population N Mahdieh, C Nishimura, K Ali‐Madadi, Y Riazalhosseini, H Yazdan, ... Clinical genetics 65 (6), 506-508, 2004	46	2004
Next generation sequencing applications for cardiovascular disease S Kalayinia, H Goodarzynejad, M Maleki, N Mahdieh Annals of Medicine 50 (2), 91-109, 2018	45	2018
Variations in multiple syndromic deafness genes mimic non-syndromic hearing loss G Bademci, FB Cengiz, J Foster Ii, D Duman, L Sennaroglu, O Diaz-Horta, ... Scientific reports 6 (1), 31622, 2016	45	2016
The frequency of eight common point mutations in CYP21 gene in Iranian patients with congenital adrenal hyperplasia ALI RAMEZANI, K Kahrizi, AM RAZAGHI, N Mahdieh, P Koppens Iranian Biomedical Journal 12 (1), 49-53, 2008	45	2008
Screening of OTOF mutations in Iran: a novel mutation and review N Mahdieh, A Shirkavand, B Rabbani, M Tekin, B Akbari, MT Akbari, ... International journal of pediatric otorhinolaryngology 76 (11), 1610-1615, 2012	42	2012
Mutation Analysis of the CYP21A2 Gene in the Iranian Population B Rabbani, N Mahdieh, MTH Ashtiani, B Larijani, MT Akbari, M New, ... Genetic Testing and Molecular Biomarkers 16 (2), 82-90, 2012	36	2012
Impact of consanguineous marriages in GJB2-related hearing loss in the Iranian population: a report of a novel variant N Mahdieh, B Rabbani, A Shirkavand, H Bagherian, ZS Movahed, ... Genetic testing and molecular biomarkers 15 (7-8), 489-493, 2011	35	2011
In silico structural, functional and pathogenicity evaluation of a novel mutation: an overview of HSD3B2 gene mutations B Rabbani, N Mahdieh, MTH Ashtiani, A Setoodeh, A Rabbani Gene 503 (2), 215-221, 2012	31	2012
Molecular diagnosis of congenital adrenal hyperplasia in Iran: focusing on CYP21A2 gene B Rabbani, N Mahdieh, MTH Ashtiani, MT Akbari, A Rabbani Iranian journal of pediatrics 21 (2), 139, 2011	31	2011
A transversion mutation in non-coding exon 3 of the TMC1 gene in two ethnically related Iranian deaf families from different geographical regions; evidence for founder effect E Davoudi-Dehaghani, S Zeinali, N Mahdieh, A Shirkavand, H Bagherian, ... International Journal of Pediatric Otorhinolaryngology 77 (5), 821-826, 2013	28	2013

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