Gholamreza Shariati
Ahvaz Jundishapur University of Medical Sciences(IR)HealthPartners(US)
Publications by Year
Research Areas
Hemoglobinopathies and Related Disorders, Genomics and Rare Diseases, Iron Metabolism and Disorders, RNA regulation and disease, Mitochondrial Function and Pathology
Most-Cited Works
- → Loss of the sphingolipid desaturase DEGS1 causes hypomyelinating leukodystrophy(2019)103 cited
- → Mutations in INPP5K Cause a Form of Congenital Muscular Dystrophy Overlapping Marinesco-Sjögren Syndrome and Dystroglycanopathy(2017)70 cited
- → Wound Healing Activity of Extracts and Formulations of Aloe vera, Henna, Adiantum capillus-veneris, and Myrrh on Mouse Dermal Fibroblast Cells(2017)62 cited
- → Homozygous Missense Variants in NTNG2, Encoding a Presynaptic Netrin-G2 Adhesion Protein, Lead to a Distinct Neurodevelopmental Disorder(2019)57 cited
- → Effect of the herbal mixture composed of Aloe Vera, Henna, Adiantum capillus-veneris, and Myrrha on wound healing in streptozotocin-induced diabetic rats(2016)53 cited
- → Biallelic SQSTM1 mutations in early-onset, variably progressive neurodegeneration(2018)52 cited
- → Autosomal recessive cardiomyopathy and sudden cardiac death associated with variants in MYL3(2020)36 cited
- → Neurologic Phenotypes Associated With Mutations in RTN4IP1 (OPA10) in Children and Young Adults(2017)35 cited
- → TMEM63C mutations cause mitochondrial morphology defects and underlie hereditary spastic paraplegia(2022)35 cited
- → Analysis of enriched rare variants in JPH2-encoded junctophilin-2 among Greater Middle Eastern individuals reveals a novel homozygous variant associated with neonatal dilated cardiomyopathy(2019)34 cited