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Publications by Hossein Najmabadi
Mutations in NSUN2 Cause Autosomal- Recessive Intellectual Disability
American Journal of Human Genetics
Genetics
ST3GAL3 Mutations Impair the Development of Higher Cognitive Functions
American Journal of Human Genetics
Genetics
BOD1 Is Required for Cognitive Function in Humans and Drosophila
PLoS Genetics
Evolution
Ecology
Genetics
Molecular Biology
Cancer Research
Systematics
Behavior
Integrated Sequence Analysis Pipeline Provides One-Stop Solution for Identifying Disease-Causing Mutations
Human Mutation
Genetics
Iranome: A Catalogue of Genomic Variations in the Iranian Population
Human Mutation
Genetics
GPR126 : A Novel Candidate Gene Implicated in Autosomal Recessive Intellectual Disability
American Journal of Medical Genetics, Part A
Genetics
Identification of a Nonsense Mutation in the Very Low-Density Lipoprotein Receptor Gene (VLDLR) in an Iranian Family With Dysequilibrium Syndrome
European Journal of Human Genetics
Genetics
An Autosomal Recessive Syndrome of Severe Mental Retardation, Cataract, Coloboma and Kyphosis Maps to the Pericentromeric Region of Chromosome 4
European Journal of Human Genetics
Genetics
Mutations in the First MyTH4 Domain ofMYO15Aare a Common Cause of DFNB3 Hearing Loss
Laryngoscope
Otorhinolaryngology
A Novel Splice Site Mutation in theRDXgene Causes DFNB24 Hearing Loss in an Iranian Family
American Journal of Medical Genetics, Part A
Genetics
