elahe elahi
University of Tehran
H-index: 34
Asia-Iran
Top articles of elahe elahi
A comparison between the effects of two liposome-encapsulated bevacizumab formulations on ocular neovascularization inhibition
Colloids and Surfaces B: Biointerfaces
2024/2/1
Identification of a mutation in TNRC18 in a patient with clinical features of Fazio‐Londe disease
Clinical Case Reports
2024/1
Najmeh Salehi
H-Index: 3
Elahe Elahi
H-Index: 20
Identification of RNF13 as cause of recessively inherited ALS in a multi-case pedigree
Journal of Medical Genetics
2023/3/1
Elahe Elahi
H-Index: 20
An overview of amyotrophic lateral sclerosis (ALS) and its genetic status
2023/1/1
Elahe Elahi
H-Index: 20
Adding the Molecular Diversity Information of the Common Fouling Barnacle Amphibalanus amphitrite (Darwin, 1854)(Crustacea: Cirripedia) from the Persian Gulf and Gulf of Oman …
Zoological Studies
2023
Alireza Sari
H-Index: 13
Elahe Elahi
H-Index: 20
Prenatal diagnosis of primary congenital glaucoma and histopathological features in a fetal globe with cytochrome p4501B1 mutations
European Journal of Ophthalmology
2022/3
Evolution of the SARS-CoV-2 genome and emergence of variants of concern
2022/2
Iman Safari
H-Index: 5
Elahe Elahi
H-Index: 20
Ophthalmogenetic Epidemiology in Iran
Archives of Persian Ophthalmology
2022/1/10
Multi-stage analysis of FOXM1, PYROXD1, hTERT, PPARA, PIM3, BMI1 and MCTP1 expression patterns in colorectal cancer
Gastroenterology and Hepatology From Bed to Bench
2022
Elahe Elahi
H-Index: 20
Alireza Sadeghpour
H-Index: 9
Mutation Screening of Six Exons of ABCA4 in Iranian Stargardt Disease Patients
Journal of Ophthalmic & Vision Research
2022/1
Fatemeh Suri
H-Index: 9
Elahe Elahi
H-Index: 20
Identification of UBA1 as the causative gene of an X‐linked non‐Kennedy spinal–bulbar muscular atrophy
European Journal of Neurology
2022/12
Najmeh Salehi
H-Index: 3
Elahe Elahi
H-Index: 20
Genetic screening of TGFBI in Iranian patients with TGFBI-associated corneal dystrophies and a meta-analysis of global variation frequencies
Ophthalmic Genetics
2022/7/4
Erratum: Carrier Status for p. Gly61Glu and p. Arg368His CYP1B1 Mutations Causing Primary Congenital Glaucoma in Iran
Journal of Ophthalmic & Vision Research
2022/4
Carrier Status for p. Gly61Glu and p. Arg368His CYP1B1 Mutations Causing Primary Congenital Glaucoma in Iran
Journal of Ophthalmic & Vision Research
2021/10
Study on SARS-CoV-2 strains in Iran reveals potential contribution of co-infection with and recombination between different strains to the emergence of new strains
Virology
2021/10/1
A case of adult onset Sandhoff disease that mimics Brown-Vialetto-Van Laere syndrome
Neuromuscular Disorders
2021/6/1
Niloofar Farboodi
H-Index: 2
Elahe Elahi
H-Index: 20
World‐wide tracking of major SARS‐CoV‐2 genome haplotypes in sequences of June 1 to November 15, 2020 and discovery of rapid expansion of a new haplotype
Journal of Medical Virology
2021/5
Iman Safari
H-Index: 5
Elahe Elahi
H-Index: 20
Evolution of SARS‐CoV‐2 genome from December 2019 to late March 2020: Emerged haplotypes and informative Tag nucleotide variations
Journal of Medical Virology
2021/4
Iman Safari
H-Index: 5
Elahe Elahi
H-Index: 20
BVVL/FL: features caused by SLC52A3 mutations; WDFY4 and TNFSF13B may be novel causative genes
Neurobiology of aging
2021/3/1
Deep geno-and phenotyping in two consanguineous families with CMT2 reveals HADHA as an unusual disease-causing gene and an intronic variant in GDAP1 as an unusual mutation
Journal of Neurology
2021/2
John Hardy
H-Index: 9
Elahe Elahi
H-Index: 20
