A. H. Johari

Expression analysis and genotyping of DGKZ: a GWAS-derived risk gene for schizophrenia

H. Ghaedi, H. Darvish, S. Salehi, 2019, Molecular Biology Reports.

Molecular characterization of PRKN structural variations identified through whole‐genome sequencing

C. Paisán-Ruiz, H. Darvish, A. Tafakhori, 2018, Molecular genetics & genomic medicine.

Identification of a large homozygous VPS13C deletion in a patient with early‐onset Parkinsonism

C. Paisán-Ruiz, H. Darvish, Sakineh Ranji-Burachaloo, 2018, Movement disorders : official journal of the Movement Disorder Society.

Novel Mutations in TACSTD2 Gene in Families with Gelatinous Drop-like Corneal Dystrophy (GDLD)

H. Ghaedi, N. Daftarian, H. Darvish, 2017, International journal of molecular and cellular medicine.

Phenotypic and genotypic characterization of families with complex intellectual disability identified pathogenic genetic variations in known and novel disease genes

C. Paisán-Ruiz, E. Sánchez, H. Darvish, 2020, Scientific Reports.

Phenotypic and genotypic characterization of families with complex intellectual disability identified pathogenic genetic variations in known and novel disease genes

C. Paisán-Ruiz, Y. Kajiwara, E. Sánchez, 2020, Scientific Reports.

Expression analysis and genotyping of DGKZ: a GWAS-derived risk gene for schizophrenia

H. Ghaedi, H. Darvish, S. Salehi, 2019, Molecular Biology Reports.

A novel mutation in SMOC1 and variable phenotypic expression in two patients with Waardenburg anophthalmia syndrome.

H. Ghaedi, H. Darvish, E. Alehabib, 2017, European journal of medical genetics.