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Expert Opinion on Biological Therapy|August 22, 2017
Prospects and progress of Listeria-based cancer vaccinesAzam Bolhassani, Niloofar Naderi, Sepehr Soleymani
Journal of Medical Case Reports|May 29, 2008
Clear lens phacoemulsification in the anterior lenticonus due to Alport Syndrome: two case reportsGhassem Amir Aslanzadeh, Davoud Gharabaghi, Niloofar Naderi
Hematology (Amsterdam, Netherlands)|February 14, 2019
Analysis of long non-coding RNA expression in hemophilia A patientsNiloofar Naderi, Ali Namvar, Nooshin Amani, et al.
European Journal of Medical Research|September 10, 2022
Identification of a novel de novo pathogenic variant in GFAP in an Iranian family with Alexander disease by whole-exome sequencingKatayoun Heshmatzad, Niloofar Naderi, Tannaz Masoumi, et al.
BMC Medical Genomics|May 7, 2024
Detection of a novel pathogenic variant in KCNH2 associated with long QT syndrome 2 using whole exome sequencingErfan Kohansal, Niloofar Naderi, Amir Farjam Fazelifar, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|August 3, 2025
Pharmacogenomics in cardiac therapy: Personalizing treatment for heart healthNiloofar Naderi, Amir Ghaffari Jolfayi, Amir Azimi, et al.
Hematology (Amsterdam, Netherlands)|July 12, 2018
Polymorphisms in the TGF-β1 (rs1982037) and IL-2 (rs2069762, rs4833248) genes are not associated with inhibitor development in Iranian patients with hemophilia ANiloofar Naderi, Fariba Ebrahimzadeh, Mohammad Jazebi, et al.
Cardiology Research and Practice|November 19, 2025
Unlocking the Secrets of Andersen-Tawil Syndrome: The Role of Next-Generation Sequencing in a Family With Long QT SyndromeMansoor Namazi, Niloofar Naderi, Amir Askarinejad, et al.
Laboratory Medicine|June 10, 2022
Whole-Exome Sequencing Revealed a Pathogenic Nonsense Variant in the SLC19A2 Gene in an Iranian Family with Thiamine-Responsive Megaloblastic AnemiaNeda Mohsen-Pour, Niloofar Naderi, Serwa Ghasemi, et al.
BMC Cardiovascular Disorders|October 4, 2023
A novel heterozygous missense MYH7 mutation potentially causes an autosomal dominant form of myosin storage myopathy with dilated cardiomyopathyNiloofar Naderi, Neda Mohsen-Pour, Yalda Nilipour, et al.
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