Researcher profile · Semantic Scholar

N. Nouri

h-index: 10
Works: 34
Citations: 242

Most-cited papers

Consanguineous marriages in the genetic counseling centers of Isfahan and the ethical issues of clinical consultations
N. Nouri, N. Nouri, Samaneh Tirgar, E. Soleimani +3 more
2017Journal of Medical Ethics and History of Medicine17 citations
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Evaluation of multiplex ligation-dependent probe amplification analysis versus multiplex polymerase chain reaction assays in the detection of dystrophin gene rearrangements in an Iranian population subset
N. Nouri, Esmat Fazel-Najafabadi, Mansoor Salehi, M. Hosseinzadeh +3 more
2014Advanced Biomedical Research17 citations Open access
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Non-syndromic cleft lip with or without cleft palate in Asian populations: Association analysis on three gene polymorphisms of the folate pathway.
M. Martinelli, A. Girardi, F. Cura, N. Nouri +5 more
2016Archives of Oral Biology15 citations Open access
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Biallelic loss of LDB3 leads to a lethal pediatric dilated cardiomyopathy
T. Koopmann, Y. Jamshidi, Mohammad Naghibi-Sistani, H. M. van der Klift +19 more
2022European Journal of Human Genetics14 citations Open access
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Family-based association analysis between nonsyndromic cleft lip with or without cleft palate and IRF6 polymorphism in an Iranian population
N. Nouri, M. Memarzadeh, F. Carinci, F. Cura +6 more
2014Clinical Oral Investigations14 citations
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Autozygosity-driven genetic diagnosis in consanguineous families from Italy and the Greater Middle East
Flavia Palombo, C. Graziano, N. Al Wardy, N. Nouri +17 more
2020Human Genetics13 citations Open access
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Decline in peripheral blood NKG2D+CD3+CD56+ NKT cells in metastatic colorectal cancer patients
M. Gharagozloo, A. Rezaei, H. Kalantari, A. Bahador +6 more
2018Bratislava Medical Journal13 citations Open access
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Association between mismatch repair gene MSH3 codons 1036 and 222 polymorphisms and sporadic prostate cancer in the Iranian population.
F. Jafary, Mansoor Salehi, M. Sedghi, N. Nouri +4 more
2012Asian Pacific Journal of Cancer Prevention13 citations Open access
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Genotype-phenotype correlation of survival motor neuron and neuronal apoptosis inhibitory protein genes in spinal muscular atrophy patients from Iran
M. Sedghi, M. Behnam, Esmat Fazel, Mansoor Salehi +4 more
2014Advanced Biomedical Research12 citations Open access
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Detection of Intragenic SMN1 Mutations in Spinal Muscular Atrophy Patients With a Single Copy of SMN1
H. Ganji, N. Nouri, Mansoor Salehi, O. Aryani +4 more
2015Journal of Child Neurology11 citations
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Use of in silico tools for classification of novel missense mutations identified in dystrophin gene in developing countries.
N. Nouri, Esmat Fazel-Najafabadi, Mahdieh Behnam, N. Nouri +4 more
2014Gene10 citations
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A case report of 22q11 deletion syndrome confirmed by array-CGH method
M. Sedghi, N. Nouri, H. Abdali, M. Memarzadeh +1 more
2012Journal of Research in Medical Sciences10 citations
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Possible effect of SNAIL family transcriptional repressor 1 polymorphisms in non-syndromic cleft lip with or without cleft palate
F. Cura, A. Palmieri, A. Girardi, F. Carinci +5 more
2018Clinical Oral Investigations9 citations
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Mutations in the Key Autophagy Tethering Factor EPG5 Link Neurodevelopmental and Neurodegenerative Disorders Including Early‐Onset Parkinsonism
H. Dafsari, Celine Deneubourg, Kritarth Singh, R. Maroofian +137 more
2025Annals of Neurology8 citations Open access
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Clinical and genetic profile of children with unexplained intellectual disability/developmental delay and epilepsy.
N. Nouri, Amir Bahreini, J. Nasiri, Mansoor Salehi
2021Epilepsy Research8 citations
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Cutis Laxa Type II with Mutation in the Pyrroline‐5‐Carboxylate Reductase 1 Gene
N. Nouri, O. Aryani, N. Nouri, Behnam Kamalidehghan +1 more
2013Pediatric dermatology7 citations
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ROCK1 is associated with non-syndromic cleft palate.
A. Palmieri, L. Scapoli, M. Carrozzo, F. Cura +6 more
2019Journal of Oral Pathology & Medicine6 citations Open access
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A novel mutation in the aprataxin (APTX) gene in an Iranian individual suffering early-onset ataxia with oculomotor apraxia type 1(AOA1) disease.
N. Nouri, N. Nouri, O. Aryani, Behnam Kamalidehghan +2 more
2012Iranian Biomedical Journal6 citations
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Mutations in EPG5 are associated with a wide spectrum of neurodevelopmental and neurodegenerative disorders
H. Dafsari, Celine Deneubourg, Kritarth Singh, R. Maroofian +123 more
2024medRxiv5 citations Open access
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Prevalence of 22q11.2 microdeletion syndrome in Iranian patients with cleft palate
N. Nouri, M. Memarzadeh, Mansoor Salehi, N. Nouri +5 more
2016Advanced Biomedical Research5 citations Open access
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Non-syndromic cleft palate: Association analysis on three gene polymorphisms of the folate pathway in Asian and Italian populations
F. Carinci, A. Palmieri, L. Scapoli, F. Cura +8 more
2019International Journal of Immunopathology and Pharmacology4 citations Open access
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Identification of Proximal and Distal 22q11.2 Microduplications among Patients with Cleft Lip and/or Palate: A Novel Inherited Atypical 0.6 Mb Duplication
M. Sedghi, H. Abdali, M. Memarzadeh, Mansoor Salehi +3 more
2015Genetics Research International4 citations Open access
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Investigation of TBX1 gene deletion in Iranian children with 22q11.2 deletion syndrome: correlation with conotruncal heart defects
H. Ganji, Mansoor Salehi, M. Sedghi, H. Abdali +5 more
2013Heart Asia4 citations Open access
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Mutation analysis of CACNA1A gene in Iranian migrainous and review literatures
Rokhsareh Meamar, Maryam Ostadsharif, M. Saadatnia, A. Ghorbani +3 more
2013Journal of Research in Medical Sciences4 citations
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Bi-allelic variants in BRF2 are associated with perinatal death and craniofacial anomalies
Francesca Mattioli, Rún Friðriksdóttir, Anne Hébert, S. Bassani +19 more
2025Genome Medicine3 citations Open access
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Significant association between nonsyndromic cleft lip with or without cleft palate and IRF6rs2235371 polymorphism in Iranian familiar population
F. Jafary, Z. Nadeali, Mansoor Salehi, M. Hosseinzadeh +3 more
2015Molecular Biology3 citations
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An insight into genetics of non-syndromic cleft palate
N. Nouri, Padideh Karimi, Mansoor Salehi, M. Memarzadeh +2 more
2013Advanced Biomedical Research3 citations Open access
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Ultra-Rare Variants Identify Biological Pathways and Candidate Genes in the Pathobiology of Non-Syndromic Cleft Palate Only
Emanuela Iovino, L. Scapoli, A. Palmieri, R. Sgarzani +6 more
2023Biomolecules2 citations Open access
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Significant association between nonsyndromic cleft lip with or without cleft palate and IRF6rs2235371 polymorphism in Iranian familiar population
F. Jafary, Z. Nadeali, Mansoor Salehi, M. Hosseinzadeh +3 more
2015Molecular Biology2 citations
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Reciprocal 22q11.2 Deletion and Duplication in Siblings with Karyotypically Normal Parents
Wolfram Demaerel, M. Hosseinzadeh, N. Nouri, M. Sedghi +6 more
2016Cytogenetic and Genome Research1 citations
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Genetic Counseling in Central Iran: Lack of Public Awareness about Genetic Diseases?
N. Nouri, E. Soleimani, Esmat Fazel-Najafabadi, F. Zahedi +2 more
20161 citations
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Chromodomain helicase DNA-binding proteins and orofacial cleft
Mehran Dehghanian, Majid Hosseinzadeh, H. Abdali, N. Nouri +1 more
2026Journal of Research in Medical Sciences0 citations Open access
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Comparison of three Diagnostic Methods of Real time PCR, Reverse Dot Blot and DNA Sequencing for Analysis of KRAS Mutations in Patients with Colorectal Cancer
N. Nouri
2021Cancer Therapy & Oncology International Journal0 citations Open access
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confirmed by array-CGH method
M. Sedghi, N. Nouri, H. Abdali, M. Memarzadeh +1 more
20120 citations
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M. Hosseinzadeh

×7

M. Memarzadeh×7

F. Carinci×6

L. Scapoli×6

M. Martinelli×5

F. Cura×5

F. Jafary×5

Esmat Fazel-Najafabadi×4