Javad Mohammadiasl

8PUBLICATIONS
17CO-AUTHORS
Developmental genetics (incl. sex determination)Epigenetics (incl. genome methylation and epigenomics)Gene mappingGenetic immunologyCancer genetics
Featured researcher

Get your video featured.

JoVEPublish with JoVE
Journal

Publications (8)

|Oct 24, 2024
Identification and characterization of NMNAT1 gene mutations in an Iranian patient with Leber congenital amaurosis 9.

Mostafa Neissi, Motahareh Sheikh-Hosseini, Misagh Mohammadi-Asl

|Aug 18, 2024
Usher Syndrome Type 2 in An Iranian Family: A Novel Founder Variation in The USH2A Gene.

Mostafa Neissi, Javad Mohammadi-Asl, Misagh Mohammadi-Asl

|Mar 15, 2024
Retinitis pigmentosa-1 due to an RP1 mutation in a consanguineous Iranian family: Report of a novel mutation.

Mostafa Neissi, Motahareh Sheikh-Hosseini, Javad Mohammadi-Asl

|Nov 01, 2021
AHI1 gene mutation in a consanguineous Iranian family affected by Joubert syndrome: A case report.

Mostafa Neissi, Hadideh Mabudi, Javad Mohammadi-Asl

|Jul 27, 2020
Influence of Two DNA Repair Pathway Polymorphisms in Colorectal Cancer Risk in Southwest Iran.

Seyed Mohammad Hosseini, Javad Mohammadiasl, Abdulhasan Talaiezadeh

Pageof 2