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S. Salehpour · SciRah

Researcher profile · Semantic Scholar

S. Salehpour

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S. Salehpour — researcher profile on SciRah

h-index: 11
Works: 69
Citations: 371

Most-cited papers

A Double-Blind, Placebo-Controlled Comparison of Letrozole to Oxandrolone Effects upon Growth and Puberty of Children with Constitutional Delay of Puberty and Idiopathic Short Stature
S. Salehpour, Parvin Alipour, M. Razzaghy-Azar, Laleh Ardeshirpour +3 more
2010Hormone Research in Paediatrics59 citations
Semantic Scholar
Cyclic Pamidronate Therapy in Children with Osteogenesis Imperfecta
S. Salehpour, S. Tavakkoli
2010Journal of Pediatric Endocrinology & Metabolism (JPEM)37 citations
Semantic Scholar
Effects of Miglustat on Stabilization of Neurological Disorder in Niemann–Pick Disease Type C
P. Karimzadeh, S. Tonekaboni, M. Ashrafi, Y. Shafeghati +11 more
2013Journal of Child Neurology29 citations
Semantic Scholar
Craniosynostosis in a patient with 2q37.3 deletion 5q34 duplication: Association of extra copy of MSX2 with craniosynostosis
A. Kariminejad, R. Kariminejad, A. Tzschach, R. Ullmann +6 more
2009American Journal of Medical Genetics. Part A29 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
Four Years of Diagnostic Challenges with Tetrahydrobiopterin Deficiencies in Iranian Patients.
S. Khatami, S. R. Dehnabeh, S. Zeinali, B. Thöny +6 more
2016JIMD Reports17 citations Open access
Semantic Scholar
ELMO Domain Containing 1 (ELMOD1) Gene Mutation Is Associated with Mental Retardation and Autism Spectrum Disorder
M. Miryounesi, Sorya Bahari, S. Salehpour, N. Alipour +1 more
2019Journal of Molecular Neuroscience13 citations
Semantic Scholar
Mutations in the VPS13B Gene in Iranian Patients with Different Phenotypes of Cohen Syndrome
N. Alipour, S. Salehpour, S. Tonekaboni, M. Rostami +4 more
2019Journal of Molecular Neuroscience12 citations
Semantic Scholar
Clinical, biochemical and molecular features of Iranian families with mucopolysaccharidosis: A case series.
V. Yassaee, Farzad Hashemi-Gorji, M. Miryounesi, Alireza Rezayi +3 more
2017Clinica chimica acta; international journal of clinical chemistry12 citations
Semantic Scholar
Co-existence of phenylketonuria either with maple syrup urine disease or Sandhoff disease in two patients from Iran: emphasizing the role of consanguinity
M. Abiri, S. Talebi, J. Uitto, L. Youssefian +4 more
2016Journal of Pediatric Endocrinology & Metabolism (JPEM)12 citations
Semantic Scholar
Effects of selenium supplementation on serum C reactive protein level: A systematic review and meta-analysis of randomized controlled clinical trials
O. Asbaghi, S. Saboori, A. Hekmatdoost, F. Abdollahpour +2 more
2020Obesity Medicine11 citations
Semantic Scholar
Association of a Novel Nonsense Mutation in KIAA1279 with Goldberg-Shprintzen Syndrome
S. Salehpour, Farzad Hashemi-Gorji, Z. Soltani, S. Ghafouri-Fard +1 more
2017Iranian journal of child neurology10 citations
Semantic Scholar
Whole-Exome Sequencing Uncovers Novel Causative Variants and Additional Findings in Three Patients Affected by Glycogen Storage Disease Type VI and Fanconi−Bickel Syndrome
M. Eghbali, K. Fatemi, S. Salehpour, M. Abiri +5 more
2021Frontiers in Genetics9 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
Three novel mutations in Iranian patients with Tay-Sachs disease.
S. Jamali, N. Eskandari, O. Aryani, S. Salehpour +3 more
2014Iranian Biomedical Journal9 citations
Semantic Scholar
Penile Agenesis: Report on 8 Cases and Review of Literature
A. Mirshemirani, A. Khaleghnejad, H. Pourang, Naser Sadeghian +2 more
20099 citations
Semantic Scholar
Identification of a novel de novo mutation in the CTNNB1 gene in an Iranian patient with intellectual disability
Sepideh Dashti, S. Salehpour, M. Ghasemi, H. Sadeghi +6 more
2022Neurological Sciences7 citations
Semantic Scholar
Exome sequencing reveals neurodevelopmental genes in simplex consanguineous Iranian families with syndromic autism
M. Ghasemi, Hossein Sadeghi, Farzad Hashemi-Gorji, R. Mirfakhraie +12 more
2024BMC Medical Genomics6 citations Open access
Semantic Scholar
The effect of omega-3 fatty acids and vitamin E co-supplementation on glycemic profile: A systematic review and meta-analysis of randomized controlled trials
O. Asbaghi, S. Saboori, E. Falahi, S. Salehpour +3 more
20206 citations
Semantic Scholar
Relationship of generalized joint hypermobility with vesicoureteral reflux and urinary tract infection.
Zahra Pournasiri, A. Madani, H. Zandi, S. Salehpour +2 more
2014Iranian Journal of Kidney Diseases6 citations
Semantic Scholar
Extending and outlining the genotypic and phenotypic spectrum of novel mutations of NALCN gene in IHPRF1 syndrome: identifying recurrent urinary tract infection
Sahand Tehrani Fateh, Saman Bagheri, H. Sadeghi, S. Salehpour +7 more
2023Neurological Sciences5 citations
Semantic Scholar
Molecular characterization of a large cohort of mucopolysaccharidosis patients: Iran Mucopolysaccharidosis RE‐diagnosis study (IMPRESsion)
S. Ghaffari, M. Rafati, Mahdi Shadnoush, Shokooh Pourbabaee +35 more
2021Human Mutation5 citations Open access
Semantic Scholar
A novel splice site mutation in the GNPTAB gene in an Iranian patient with mucolipidosis II α/β
Farzad Hashemi-Gorji, S. Ghafouri-Fard, S. Salehpour, V. Yassaee +1 more
2016Journal of Pediatric Endocrinology & Metabolism (JPEM)4 citations
Semantic Scholar
Frequency of Pediatric Acute Respiratory Tract Infections in Iran; A Systematic Review
A. Shamshiri, A. Fahimzad, S. Tabatabaie, F. Shiva +4 more
20134 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
The treatment and clinical follow-up outcome in Iranian patients with tetrahydrobiopterin deficiency
S. Khani, Mina Barzegari, Zahra Esmaeilizadeh, Pantea Farsian +9 more
2021Journal of Pediatric Endocrinology & Metabolism (JPEM)3 citations
Semantic Scholar
Long-Term Effect of Nephrocalcinosis on Renal Function and Body Growth Index in Children: A Retrospective Single Center Study
Zahra Pournasiri, A. Madani, A. Ghaemi, Zahra Adl +1 more
2018Iranian Journal of Pediatrics3 citations Open access
Semantic Scholar
MOLECULAR INVESTIGATION OF GLUTARIC ACIDURIA TYPE1 IN IRAN
M. Houshmand, O. Aryani, Z. Pirzadeh, Fereshteh Ghasemi +2 more
20123 citations
Semantic Scholar
Safety and effectiveness of a biosimilar somatropin (Cinnatropin®) in children and adolescents receiving growth hormone therapy over 1 year: a registry-based phase IV study
A. Rabbani, M. Razzaghy-Azar, Z. Karamizadeh, M. Hashemipour +12 more
2025European Journal of Pediatrics2 citations
Semantic Scholar
A Double-Blind, Placebo-Controlled Comparison of Cinnamon Extract to Metformin Effects upon Insulin Resistance, Apolipoprotein B:Apolipoprotein A1 Ratio, and BMI of Obese Adolescent Girls with Polycystic Ovary Syndrome
S. Salehpour, Somayeh Setavand, S. Onsori
20152 citations
Semantic Scholar
Effects of Growth Hormone on Muscle Strength, Tone and Mobility of Children with Prader-Willi Syndrome
S. Salehpour, O. Aryani
2011Pediatric Research2 citations
Semantic Scholar
Clinical and Genetic Characterization of Woodhouse-Sakati Syndrome in Iranian Patients: A Case Series
Sepehr Khosravi, Toktam Moosavian, S. Salehpour, S. Habibi +2 more
2025Journal of Movement Disorders1 citations Open access
Semantic Scholar
Whole exome sequencing in pediatric hyperammonemia: significant diagnostic yield and identification of three novel variants
Reza Hajati, F. Hashemian, S. Salehpour, A. Sayad
2025BMC Medical Genomics1 citations Open access
Semantic Scholar
Gaucher syndrome: report of six cases and review of genetic mutations among Iranian patients
M. Miryounesi, Mohadeseh Fathi, Sheyda Khalilian, Faezeh Sherafat +2 more
2025Neurogenetics1 citations
Semantic Scholar
Comprehensive review and expanding the genetic landscape of Cornelia-de-Lange spectrum: insights from novel mutations and skin biopsy in exome-negative cases
Sahand Tehrani Fateh, Nadia Mohammad Zadeh, S. Salehpour, Farzad Hashemi-Gorji +8 more
2024BMC Medical Genomics1 citations Open access
Semantic Scholar
Broadening the Phenotype and Genotype Spectrum of Glycogen Storage Disease by Unraveling Novel Variants in an Iranian Patient Cohort
Parinaz Moghimi, Farzad Hashemi-Gorji, Sanaz Jamshidi, Sahand Tehrani Fateh +6 more
2024Biochemical Genetics1 citations
Semantic Scholar
Analysis of the HEXA, HEXB, ARSA, and SMPD1 Genes in 68 Iranian Patients
Rezvan Abtahi, P. Karimzadeh, Alireza Rezayi, S. Salehpour +4 more
2021Journal of Molecular Neuroscience1 citations
Semantic Scholar
A novel SRD5A2 mutation in an Iranian family with sex development disorder
Farzad Hashemi-Gorji, S. Salehpour, M. Miryounesi, R. Mirfakhraie +1 more
2020Andrologia1 citations Open access
Semantic Scholar
A New Nonsense Mutation in CDKL5 Gene in a Male Patient with Early Onset Refractory Epilepsy: a Case Report
S. Ghafouri-Fard, S. Salehpour, V. Yassaee, M. Miryounesi
20161 citations
Semantic Scholar
Clinical and Molecular Study of NPC in Iran: Report of 5 Novel Mutations
S. Tonekaboni, O. Aryani, P. Karimzadeh, T. Zaman +5 more
20151 citations
Semantic Scholar
[Freeman-Sheldon syndrome. A case report].
S. Salehpour, S. Saket
20091 citations
Semantic Scholar
Mismanagement of Phenylketonuria: An Underlying Cause of Kwashiorkor
S. Salehpour, D. Babaie
20081 citations
Semantic Scholar
CYSTINOSIS: REPORT OF A CASE
F. Imanzadeh, S. Salehpour, S. Nariman, A. Sayyari
20031 citations
Semantic Scholar
Analysis of whole-exome sequencing data from nearly 10,000 Iranian individuals: identification of recessive mitochondrial disease variants and proposal of a population-specific carrier screening panel
Mohadeseh Fathi, P. Karimzadeh, F. Ahmadabadi, Damoun Nashta Ali +6 more
2026Human Genomics0 citations Open access
Semantic Scholar
The effect of reduced carbohydrate diet on cardiometabolic risk factors and gut microbiota in children and adolescents with obesity: a randomized controlled trial
Yasaman Khorshidi, F. Hadaegh, Nazgoli Rafiei, P. Hadaegh +4 more
2026BMC Pediatrics0 citations Open access
Semantic Scholar
Whole-exome sequencing reveals the molecular diagnoses of pediatric patients presenting with hyperammonemia
Reza Hajati, Sharareh Kamfar, Azadeh Reshadmanesh, Mohammad Saberi +5 more
2026Discover Genetics and Evolution0 citations Open access
Semantic Scholar
Exploring the Genetic Landscape of Knobloch Syndrome: Novel Variant Identification and Literature Review
M. Ghasemi, Maryam Mirahmadi, Hadi Bayat, Morteza Sheikhi Nooshabadi +6 more
2025OBM Genetics0 citations Open access
Semantic Scholar
Unraveling and Expanding the Genotypic Spectrum of Kabuki Syndrome with Identification of de Novo Protein-Truncating Mutations in the KMT2D Gene: Insights into the Role of Premature Stop Codons in the Etiology of the Disorder
M. Ghasemi, Maryam Mirahmadi, Hadi Bayat, M. Miryounesi +6 more
2025OBM Genetics0 citations Open access
Semantic Scholar
Spectrum of Genetic Mutations Among Iranian Patients with Gangliosidosis
Sheyda Khalilian, Mohadeseh Fathi, Mona Alizadeh, Fatemeh Larki Darabi +4 more
2025Biochemical Genetics0 citations
Semantic Scholar
Exome Sequencing in 9 Iranian Patients Expands the Mutational and Clinical Spectrum of Bardet-Biedl Syndrome.
Mohammad Reza Seyedtaghia, Mohsen Habibi, Farzad Hashemi-Gorji, Sahand Tehrani-Fateh +8 more
2025Biochemical Genetics0 citations Open access
Semantic Scholar

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