Mehrnaz Narooie-Nejad

Loss of function mutations in the gene encoding latent transforming growth factor beta binding protein 2, LTBP2, cause primary congenital glaucoma

Mehrnaz Narooie-Nejad, Seyed Hassan Paylakhi, Seyedmehdi Shojaee et al. · Human Molecular Genetics · 2009 · 158 citations

Ocular Disease, Genetics, Function Mutations +16

<i>SVEP1</i> as a Genetic Modifier of <i>TEK</i>-Related Primary Congenital Glaucoma

Terri L. Young, Kristina N. Whisenhunt, Jing Jin et al. · Investigative Ophthalmology & Visual Science · 2020 · 55 citations · Full text

Association between vitamin D receptor polymorphisms and haplotypes with pulmonary tuberculosis

Saeedeh Salimi, Farzaneh Farajian‐Mashhadi, Roya Alavi-Naini et al. · Biomedical Reports · 2014 · 50 citations · Full text

Vitamin D Receptor Gene Polymorphism and the Risk of Multiple Sclerosis in South Eastern of Iran

Mehrnaz Narooie-Nejad, Maryam Moossavi, Adam Torkamanzehi et al. · Journal of Molecular Neuroscience · 2015 · 38 citations

Disease Susceptibility, Neurological Disorder, Genetic Epidemiology +8

Positive Association of Vitamin D Receptor Gene Variations with Multiple Sclerosis in South East Iranian Population

Mehrnaz Narooie-Nejad, Maryam Moossavi, Adam Torkamanzehi et al. · BioMed Research International · 2015 · 35 citations · Full text