S. Taghavi

发表

A novel c.240_241insGG mutation in NDP gene in a family with Norrie disease

H. Ghaedi, N. Daftarian, H. Darvish, 2018, Clinical & experimental optometry.

Identification of a Large DNAJB2 Deletion in a Family with Spinal Muscular Atrophy and Parkinsonism

Hossein Darvish, Abbas Tafakhori, Ruth H Walker, 2016, Human mutation.

Support for "Disease-Only" Genotypes and Excess of Homozygosity at the CYTH4 Primate-Specific GTTT-Repeat in Schizophrenia.

C. Paisán-Ruiz, M. Ohadi, H. Darvish, 2017, Genetic testing and molecular biomarkers.

A genetic variant in miRNA binding site of glutamate receptor 4, metabotropic (GRM4) is associated with increased risk of major depressive disorder.

H. Ghaedi, M. Ohadi, H. Darvish, 2017, Journal of affective disorders.