Javad Mohammadi‐Asl

Ahvaz Jundishapur University of Medical Sciences — IR

Neuroscience · Life Sciences

19h-index1.3kcitations166works1.42yr avg
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Research Topics

Hearing, Cochlea, Tinnitus, Genetics(15), Epigenetics and DNA Methylation(12), Vestibular and auditory disorders(10), RNA modifications and cancer(10), Reproductive Biology and Fertility(9)

Publications166 total

PIGC-related encephalopathy: Lessons learned from 18 new probands
European Journal of Human Genetics·2025Open Access
Expression of concern ‘Randomized, triple-blind, placebo-controlled clinical trial examining the effects of alpha-lipoic acid supplement on the spermatogram and seminal oxidative stress in infertile men’ [Fertil Steril 2015; 104:318-24]
Fertility and Sterility·2025Open Access
Genetic investigation of an Iraqi family with Emery-Dreifuss muscular dystrophy
Journal of Rare Diseases·2025Open Access
Clinical and genetic findings in an Iraqi family with TMEM67-associated Joubert syndrome
Neurology Asia·2025Open Access
ARV1 p.Gln62Ter, a novel mutation linked to developmental and epileptic encephalopathy-38
Journal of Rare Diseases·2025· 1 citedOpen Access
Effect of Weight-Loss Diet Combined with Taurine Supplementation on Fasting Levels of Fibroblast Growth Factors19, 21, and β -klothoCo-Receptor in Obese Women: A Randomized Clinical Trial
Journal of Nutrition and Food Security·2025Open Access
Crosstalk between non-coding RNAs and programmed cell death in colorectal cancer: implications for targeted therapy
Epigenetics & Chromatin·2025· 15 citedOpen Access
Identification and characterization of <scp><i>NMNAT1</i></scp> gene mutations in an Iranian patient with Leber congenital amaurosis 9
Clinical Case Reports·2024· 2 citedOpen Access
Usher Syndrome Type 2 in An Iranian Family: A Novel Founder Variation in The <i>USH2A</i> Gene.
PubMed·2024Open Access
Clinical and genetic analysis of Niemann-Pick disease type C with a novel NPC1 variant
Journal of Rare Diseases·2024· 1 citedOpen Access
Designing a multi-epitope candidate vaccine against SARS-CoV-2 through in silico approach for producing in plant systems
Studia Universitatis Babeş-Bolyai Biologia·2024Open Access
Unveiling a Novel THOC2 Mutation's Role in X-linked Intellectual Disability
International Journal of Biomedicine·2024Open Access
Joubert syndrome caused by a TMEM67 mutation: Genotype-phenotype analysis
Neurology Asia·2024Open Access
Folate gene polymorphisms CBS 844ins68 and RFC1 A80G and risk of Down syndrome offspring in young Iranian women: A cross-sectional study
International Journal of Reproductive BioMedicine (IJRM)·2024Open Access
Retinitis pigmentosa‐1 due to an <scp><i>RP1</i></scp> mutation in a consanguineous Iranian family: Report of a novel mutation
Clinical Case Reports·2024· 4 citedOpen Access
Mutation Detection in MYO15A Gene in an Iranian Family with Non-Syndromic Hearing Loss
International Journal of Biomedicine·2024· 1 citedOpen Access
The fertility of dairy heifers and cows is not influenced by the follicular wave of the ovulatory follicle
Journal of Reproduction and Development·2024Open Access
A Novel Deleterious MYO15A Gene Mutation Causes Nonsyndromic Hearing Loss.
PubMed·2024· 1 citedOpen Access
Evaluate the Effect of Dendrosomal Curcumin on Expression Level of HOTAIR Long Noncoding RNA in MCF-7 Breast Cancer Cell Line
Journal of Shahid Sadoughi University of Medical Sciences·2023· 1 citedOpen Access
Exome Sequencing Identifies a Novel SGCA Gene Mutation in an Iranian Family with Limb Girdle Muscular Dystrophy: A Case Report
Gene Cell and Tissue·2023Open Access
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Frequent Co-authors

Parvin Mehdipour(6), Najmaldin Saki(6), Neda Golchin(6), Mohammadreza Hajjari(6), Maryam Tahmasebi Birgani(6), Fatemeh Haidari(5), Ghasem Saki(5), Masoud Hemadi(5), Ali Khodadadi(5), Mohammad Shahjahani(4), Hossein Ansari(4), Mohammad Amin Tabatabaiefar(4), Vahid Haghpanah(3), Mohammad Seghatoleslami(3), Mohammadreza Gholami(3), Kambiz Ahmadi Angali(3), Hamid Galehdari(3), Fakher Rahim(3), Morteza Hashemzadeh Chaleshtori(3), Arman Shahrisa(3)