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Publications by Mohammad Ali Faghihi

Inhibition of Natural Antisense Transcripts in Vivo Results in Gene-Specific Transcriptional Upregulation

Nature Biotechnology

Applied Microbiology

Biomedical Engineering

Molecular Medicine

English

Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia

American Journal of Human Genetics

English

Transcriptomic Profiling of Extracellular RNAs Present in Cerebrospinal Fluid Identifies Differentially Expressed Transcripts in Parkinson’s Disease

Journal of Parkinson's Disease

Molecular Neuroscience

English

A Novel Mutation in ERCC8 Gene Causing Cockayne Syndrome

Frontiers in Pediatrics

English

A Novel Splice Site Mutation in WAS Gene in Patient With Wiskott-Aldrich Syndrome and Chronic Colitis: A Case Report

BMC Medical Genetics

English

Pre-Implantation Genetic Diagnosis in an Iranian Family With a Novel Mutation in MUT Gene

BMC Medical Genetics

English