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H. Bagherian · SciRah

Researcher profile · Semantic Scholar

H. Bagherian

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H. Bagherian — researcher profile on SciRah

h-index: 10
Works: 45
Citations: 348

Most-cited papers

Multigene Next-Generation Sequencing Panel Identifies Pathogenic Variants in Patients with Unknown Subtype of Epidermolysis Bullosa: Subclassification with Prognostic Implications.
H. Vahidnezhad, L. Youssefian, A. Saeidian, A. Touati +12 more
2017Journal of Investigative Dermatology42 citations Open access
Semantic Scholar
Impact of Consanguineous Marriages in GJB2-Related Hearing Loss in the Iranian Population: A Report of a Novel Variant
N. Mahdieh, B. Rabbani, Atefeh Shirkavand, H. Bagherian +6 more
2011Genetic Testing and Molecular Biomarkers34 citations
Semantic Scholar
High level of intrafamilial phenotypic variability of non-syndromic hearing loss in a Lur family due to delE120 mutation in GJB2 gene.
N. Mahdieh, H. Bagherian, Atefeh Shirkavand, M. Sharafi +1 more
2010International Journal of Pediatric Otorhinolaryngology28 citations
Semantic Scholar
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.
Elham Davoudi-Dehaghani, S. Zeinali, N. Mahdieh, Atefeh Shirkavand +2 more
2013International Journal of Pediatric Otorhinolaryngology26 citations
Semantic Scholar
Molecular genetics of a cohort of 635 cases of phenylketonuria in a consanguineous population
T. Shirzadeh, A. Saeidian, H. Bagherian, S. Salehpour +17 more
2018Journal of Inherited Metabolic Disease23 citations
Semantic Scholar
Th‐1 cytokines gene polymorphism in human brucellosis
S. Davoudi, A. Amirzargar, Mahboubeh Hajiabdolbaghi, M. Rasoolinejad +7 more
2006International Journal of Immunogenetics21 citations
Semantic Scholar
Comprehensive Mutation Analysis and Report of 12 Novel Mutations in a Cohort of Patients with Spinal Muscular Atrophy in Iran
Z. Sharifi, M. Taheri, M. Fallah, M. Abiri +11 more
2021Journal of Molecular Neuroscience17 citations
Semantic Scholar
Identification of six novel mutations in Iranian patients with maple syrup urine disease and their in silico analysis.
M. Abiri, Razieh Karamzadeh, M. Karimipoor, S. Ghadami +6 more
2016Mutation research15 citations
Semantic Scholar
Molecular genetic diagnosis of Glanzmann syndrome in Iranian population; reporting novel and recurrent mutations
F. Z. Motlagh, M. Fallah, H. Bagherian, T. Shirzadeh +6 more
2019Orphanet Journal of Rare Diseases14 citations Open access
Semantic Scholar
GJB2 c.−23+1G>A mutation is second most common mutation among Iranian individuals with autosomal recessive hearing loss
S. Zeinali, Elham Davoudi-Dehaghani, Sarah Azadmehr, Samira DabbaghBagheri +7 more
2015European Archives of Oto-Rhino-Laryngology14 citations
Semantic Scholar
Mutational screening through comprehensive bioinformatics analysis to detect novel germline mutations in the APC gene in patients with familial adenomatous polyposis (FAP)
F. Ghadamyari, M. Heidari, S. Zeinali, Mehri Khatami +4 more
2021Journal of clinical laboratory analysis (Print)10 citations Open access
Semantic Scholar
Autozygosity mapping of methylmalonic acidemia associated genes by short tandem repeat markers facilitates the identification of five novel mutations in an Iranian patient cohort
Mehdi Shafaat, Mohammad Alaee, Ali Rahmanifar, A. Setoodeh +7 more
2018Metabolic brain disease10 citations
Semantic Scholar
Investigation of GJB6 large deletions in Iranian patients using quantitative real-time PCR.
N. Mahdieh, M. Raeisi, Atefeh Shirkavand, H. Bagherian +2 more
2010Clinical Laboratory10 citations
Semantic Scholar
Biallelic variants in MESD, which encodes a WNT-signaling-related protein, in four new families with recessively inherited osteogenesis imperfecta
T. Tran, R. Keller, Brecht Guillemyn, M. Pepin +14 more
2021HGG advances9 citations Open access
Semantic Scholar
Molecular Characterization of QDPR Gene in Iranian Families with BH4 Deficiency: Reporting Novel and Recurrent Mutations.
Hannaneh Foroozani, M. Abiri, S. Salehpour, H. Bagherian +8 more
2015JIMD Reports9 citations Open access
Semantic Scholar
Genetic attributes of Iranian cystic fibrosis patients: the diagnostic efficiency of CFTR mutations in over a decade
Amin Hosseini Nami, M. Kabiri, Fatemeh Zafarghandi Motlagh, T. Shirzadeh +8 more
2023Frontiers in Genetics8 citations Open access
Semantic Scholar
Allelic heterogeneity among Iranian DFNB7/11 families: report of a new Iranian deaf family with TMC1 mutation identified by next-generation sequencing
Elham Davoudi-Dehaghani, M. Fallah, J. Tavakkoly-Bazzaz, H. Bagherian +1 more
2015Acta Oto-Laryngologica8 citations
Semantic Scholar
Molecular study of alpha-thalassemia mutations in Iranian potential carriers
B. Zarbakhsh, E. Farshadi, A. Kashani, Karimipour Morteza +8 more
20107 citations
Semantic Scholar
Molecular genetic study of Calpainopathy in Iran.
Marzieh Mojbafan, A. Khajeh, Haleh Habibi, H. Bagherian +1 more
2018Gene5 citations
Semantic Scholar
A rare form of limb girdle muscular dystrophy (type 2E) seen in an Iranian family detected by autozygosity mapping
Marzieh Mojbafan, Y. Nilipour, S. Tonekaboni, S. Bagheri +5 more
2016Journal of neurogenetics5 citations
Semantic Scholar
Reporting the presence of three different diseases causing GJB2 mutations in a consanguineous deaf family
Elham Davoudi-Dehaghani, M. Fallah, Tina Shirzad, J. Tavakkoly-Bazzaz +2 more
2014International Journal of Audiology5 citations
Semantic Scholar
The Spectrum of Pathogenic Variants in Iranian Families with Hemophilia A.
Sarah Azadmehr, F. Rahiminejad, Fatemeh Zafarghandi Motlagh, M. Jamali +6 more
2021Archives of Iranian medicine4 citations Open access
Semantic Scholar
Mutational Analysis and Genotype Investigation of Less Known Gaucher Mutations through Haplotype Analysis in Iranian Gaucher Patients
Negar Sardarpour, H. Bagherian, Fatemeh Zafarghandi Motlagh, T. Shirzadeh +6 more
2023International journal of molecular and cellular medicine3 citations
Semantic Scholar
Amplicon Secondary Structure Formation and Elongation during the Process of Sequencing
Elham Davoudi-Dehaghani, S. Zeinali, N. Mahdieh, Atefeh Shirkav +1 more
20123 citations
Semantic Scholar
Lymphocyte subsets, immunoglobulin levels, complement activity CH50, and phagocytic peroxide production in 19 Iranian patients with first episode of bacterial meningitis.
Z. Ahmadinejad, H. Bagherian, Lida Atarord, A. Soodbakhsh +1 more
2011Journal of microbiology, immunology, and infection = Wei mian yu gan ran za zhi3 citations Open access
Semantic Scholar
Identification of Novel Mutations in the MMAA and MUT Genes among Methylmalonic Aciduria Families
Mahboobeh Jafari, Fatemeh Karami, A. Setoodeh, Ali Rahmanifar +4 more
2023Iranian Biomedical Journal2 citations Open access
Semantic Scholar
Autozygosity Mapping by Genome-wide Single Nucleotide Polymorphism Array Identifies a Novel Homozygous HR Mutation in a Consanguineous Family with Universal Hereditary Hair Loss
S. Zeinali, L. Youssefian, H. Vahidnezhad, A. Saeidian +3 more
2021International Journal of Dermatology and Venereology2 citations Open access
Semantic Scholar
A decade of molecular preimplantation genetic diagnosis of 350 blastomeres for beta-thalassemia combined with HLA typing, aneuploidy screening and sex selection in Iran
Yeganeh Keshvar, Solmaz Sabeghi, Z. Sharifi, K. Fatemi +10 more
2021BMC Pregnancy and Childbirth2 citations Open access
Semantic Scholar
Hemorrhagic Pleural Effusion as a First Presentation of Chronic Lymphocytic Leukemia (A Case Report)
H. Bagherian, Z. Ahmadinejad, F. A. Ardalan
20072 citations Open access
Semantic Scholar
Demographic and clinical findings of pediatric trauma patients of Bam earthquake in 2003
Z. Ahmadinezhad, V. Zieaei, H. Bagherian, N. Zarinfar +1 more
20042 citations
Semantic Scholar
Identification and in silico structural analysis for the first de novo mutation in the cystic fibrosis transmembrane conductance regulator protein in Iran: case report and developmental insight using microsatellite markers
Amin Hosseini Nami, M. Kabiri, Fatemeh Zafarghandi Motlagh, T. Shirzadeh +4 more
2024Therapeutic Advances in Respiratory Disease1 citations Open access
Semantic Scholar
Mutations in COL6A Gene Family Responsible for Muscular Dystrophies in Three Unrelated Families
Nasibeh Soltani, Z. Shahbazi, M. Karimipoor, M. Fallah +6 more
2023Iranian Biomedical Journal1 citations
Semantic Scholar
First report of a patient with homozygous hemoglobin Ernz: Evidence to support a non-pathogenic variant.
Z. Shojaei, M. Abiri, Fatemeh Zafarghandi Motlagh, Masoumeh Amini +5 more
2023Blood Cells, Molecules & Diseases1 citations
Semantic Scholar
Homozygosity mapping and CDH23 mutation analysis in Iranian deaf families
Elham Davoudi-Dehaghani, H. Bagherian, Samira DabbaghBagheri, N. Mahdieh +2 more
20161 citations
Semantic Scholar
Comparing clinical and laboratory findings of infective endocarditis among intravenous drug users and non-drug users
A. Soudbakhsh, Mahboobe Hagiabdolbaghi, H. Bagherian, Omid Yussefnejad
20071 citations
Semantic Scholar
Whole‐Exome Sequencing in Undiagnosed Muscular Dystrophies: A High Diagnostic Yield and Novel Insights From Iranian Families
Nasibeh Soltani, Z. Shahbazi, M. Fallah, M. Karimipoor +10 more
2026Human Mutation0 citations Open access
Semantic Scholar
Genetic variability in maple syrup urine disease: novel mutations and their pathogenicity in the Iranian population
Mansooreh Jafari, Fatemeh Karami, I. Salahshourifar, A. Setoodeh +5 more
2025Molecular Biology Reports0 citations
Semantic Scholar
Sjögren-Larsson syndrome. Pathogenic variant analysis of ALDH3A2 gene in six Iranian families.
S. Ahmadi, Elham Davoudi-Dehaghani, H. Bagherian, P. Jamali +5 more
20190 citations
Semantic Scholar
SLC26A4 pathogenic variants as a third cause of hearing loss: Role of three exons in DFNB4 deafness in Iran
Elham Davoudi-Dehaghani, N. Mahdieh, Atefeh Shirkavand, H. Bagherian +2 more
2019Indian Journal of Otology0 citations
Semantic Scholar
Cryptic de novo deletion at 2q23.3-q24.1 in a patient with intellectual disability
J. Malbin, M. Fallah, Z. Sharifi, MAHSA SHAFAEI +4 more
2016Journal Genetika0 citations
Semantic Scholar
Cryptic de novo deletion at 2q23.3-q24.1 in a patient with intellectual disability
J. Malbin, M. Fallah, Z. Sharifi, Mahsa Shafaei +4 more
2016Journal Genetika0 citations
Semantic Scholar
P-67 Early aneuploidy detection by means of QF-PCR using uterine fetal cell free DNA: A non-invasive approach
S. Zeinali, F. Savadkoohi, A. Farzad, H. Bagherian +5 more
20130 citations Open access
Semantic Scholar
SURVEYING NECROTIZING FASCIITIS IN A TEACHING HOSPITAL IN TEHRAN, 1999-2003
H. Mahboubeh, H. Faezipour, H. Bagherian, R. Mohammadi
20060 citations
Semantic Scholar
Surveying necrotizing fasciitis in a teaching
Mahboobe Hagiabdolbaghi, H. Faezipour, H. Bagherian, Reza Aghamohammadi
20060 citations
Semantic Scholar
PROGNOSTIC FACTORS IN ACUTE BACTERIA MENINGITIS
V. Ziyaee, Z. Ahmadinezhad, A. Yalda, H. Bagherian +1 more
20030 citations
Semantic Scholar

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S. Zeinali×35
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S. Zeinali — researcher profile on SciRah
M. Fallah×10
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M. Fallah — researcher profile on SciRah
Elham Davoudi-Dehaghani×9
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Elham Davoudi-Dehaghani — researcher profile on SciRah
Fatemeh Zafarghandi Motlagh×9
M. Abiri×8
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M. Abiri — researcher profile on SciRah

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N. Mahdieh — researcher profile on SciRah

T. Shirzadeh×7

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T. Shirzadeh — researcher profile on SciRah

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A. Setoodeh — researcher profile on SciRah

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M. Jamali — researcher profile on SciRah

Atefeh Shirkavand×6

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M. Alaei — researcher profile on SciRah

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Z. Sharifi — researcher profile on SciRah