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Sahar Sadat Sedighzadeh

Observed names: S. Sedighzadeh, Sahar Sedighzadeh, Sedighzadeh, Sahar
ORCID: 0000-0002-6973-4809
Observed ORCID: 0000-0002-6973-4809
OpenAlex ID: A5016586135
A narrative review of tumor-associated macrophages in lung cancer: regulation of macrophage polarization and therapeutic implications
2021 · Sahar Sadat Sedighzadeh, Amin Pastaki Khoshbin, et al. · Translational Lung Cancer Research · 204
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The clinical and genetic spectrum of autosomal-recessive TOR1A-related disorders
2023 · Afshin Saffari, Tracy Lau, et al. · Brain · 16
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Biallelic loss of LDB3 leads to a lethal pediatric dilated cardiomyopathy
2022 · Tamara T. Koopmann, Yalda Jamshidi, et al. · European Journal of Human Genetics · 16
A common form of dominant human IFNAR1 deficiency impairs IFN-α and -ω but not IFN-β-dependent immunity
2024 · Fahd Al Qureshah, Jérémie Le Pen, et al. · The Journal of Experimental Medicine · 14
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Clinicogenetic characterisation of SLC29A3-related syndromes: a case series, tracing ancestral variants and molecular dynamics simulation
2025 · Sajjad Biglari, Mohammad Shahrooei, et al. · Journal of Medical Genetics · 9
Whole exome sequencing reveals several novel variants in congenital disorders of glycosylation and glycogen storage diseases in seven patients from Iran
2022 · Atefe Papi, Mina Zamani, et al. · Molecular Genetics & Genomic Medicine · 9
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Childhood‐Onset Choreo‐Dystonia Due to a Recurrent Novel Homozygous Nonsense HPCA Variant: Case Series and Literature Review
2022 · Francesca Magrinelli, Kailash P. Bhatia, et al. · Movement Disorders Clinical Practice · 8
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Identification of Three Novel Mutations in the FANCA, FANCC, and ITGA2B Genes by Whole Exome Sequencing
2020 · Samira Negahdari, Mina Zamani, et al. · International Journal of Preventive Medicine · 6
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Whole exome sequencing identified a novel frameshift variant in the BHLHA9 in an Iranian family with mesoaxial synostotic syndactyly
2021 · Sahar Sadat Sedighzadeh, Alireza Sedaghat, et al. · Congenital Anomalies · 4
Human LFA-1 governs T cell immune surveillance of the skin
2026 · Ahmad Yatim, Leila Youssefian, et al. · Science Immunology · 3
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Whole-exome sequencing deciphers the genetic profile of visual impairments in patients from Southwest Iran
2022 · Mina Zamani, Sahar Sedighzadeh, et al. · Molecular Genetics and Genomics · 3
Whole-Exome Sequencing Application for Genetic Diagnosis of Kidney Diseases: A Study from Southwest of Iran
2021 · Mina Zamani, Tahereh Seifi, et al. · Kidney360 · 3
Fusion Protein Strategy to Increase Expression and Solubility of Hypervariable Region of VP2 Protein of Infectious Bursal Disease Virus in Escherichia coli
2012 · Sahar Sadat Sedighzadeh, Mehdi Shamsara, et al. · The Protein Journal · 3
Monoallelic and biallelic KDM5A variants identified in patients with autism spectrum disorder
2026 · Lauretta El Hayek, Ashlesha Gogate, et al. · Human Genetics and Genomics Advances · 2
Neonatal Refractory Seizures and Hyperammonemia in a Neonate With ALDH7A1 Deficiency
2025 · Maryam Saeedi, Kayvan Mirnia, et al. · Clinical Case Reports · 1
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Biallelic NDUFA9 variants cause a progressive neurodevelopmental disorder with prominent dystonia and mitochondrial complex I deficiency
2025 · Francesca Magrinelli, Lucie S Taylor, et al. · Brain Communications · 1
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Biallelic loss-of-function PTPN6 variants lead to inflammatory lung disease and hemolytic anemia
2026 · S. Farshid Moussavi-Harami, Matt S. Zinter, et al. · The Journal of Experimental Medicine
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Expanded clinical and genetic characterization of autosomal recessive HMGCR-related muscular dystrophy
2026 · Stephany El-Hayek, Aboulfazl Rad, et al. · Journal of Neuromuscular Diseases
XPOT Deficiency causes a human disorder through impaired tRNA nuclear export
2026 · S. von Hardenberg, I. Niehaus, et al. · medRxiv
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Atypical presentation of Acrodermatitis enteropathica in a child: later onset with life-threatening severe extensive dermatitis and septic shock
2025 · Elaheh Foroughi, Bahareh Abtahi-Naeini, et al. · BMC Pediatrics
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Expanded Clinical and Genetic Characterization of Autosomal Recessive HMGCR-RelatedLimb-Girdle Muscular Dystrophy
2025 · Aboulfazl Rad, El-Hayek, Stephany, et al.
The LPS-Treated Human Gastric Cancer Cells (AGS) Show a Significant Higher Tendency to Proliferation, Inflammation and Cannabinoid Receptor 1 Expression
2020 · Sahar Sadat Sedighzadeh, Hamid Galehdari, et al. · Jentashapir Journal of Cellular and Molecular Biology
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Cloning and Codon-optimized Expression of Structural Protein Hypervariable Region of VP2 from Infectious Bursal Disease Virus
2012 · Sahar Sedighzadeh, Mehdi Shamsara, et al. · International journal of molecular and clinical microbiology
Works count: 23
Citation count: 302
H-index: 7
I10-index: 4
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