Afagh Alavi

A Pathogenic Homozygous Mutation in The Pleckstrin Homology Domain of RASA1 Is Responsible for Familial Tricuspid Atresia in An Iranian Consanguineous Family

F. Behjati, Ahoura Nozari, Ehsan Aghaei-Moghadam, 2018, Cell journal.

Study on SARS-CoV-2 strains in Iran reveals potential contribution of co-infection with and recombination between different strains to the emergence of new strains

A. Heidarzadeh, A. Heshmati, H. Galehdari, 2021, Virology.

Clinical and genetic spectrum of a large cohort of patients with δ-sarcoglycan muscular dystrophy

T. Crawford, C. Bruno, E. Zanoteli, 2021, Brain : a journal of neurology.

Identification of PROS1 as a Novel Candidate Gene for Juvenile Retinitis Pigmentosa

H. K. Khorram Khorshid, Afagh Alavi, A. Dehghani, 2019, International journal of molecular and cellular medicine.

MFSD8 gene mutations; evidence for phenotypic heterogeneity

H. K. Khorram Khorshid, P. Jamali, Afagh Alavi, 2019, Ophthalmic genetics.

Intellectual disability associated with craniofacial dysmorphism due to POLR3B mutation and defect in spliceosomal machinery

K. Kahrizi, H. Najmabadi, Afagh Alavi, 2022, BMC Medical Genomics.

Spinocerebellar Ataxia 40: Another Etiology Underlying Essential Tremor Syndrome

A. Lang, R. Munhoz, M. Rohani, 2021, Movement disorders clinical practice.

Identification of let-7f and miR-338 as plasma-based biomarkers for sporadic amyotrophic lateral sclerosis using meta-analysis and empirical validation

B. Panahi, S. Teimourian, M. Joghataei, 2022, Scientific Reports.

Pantothenate kinase 2 mutation with eye-of-the-tiger sign on magnetic resonance imaging in three siblings

E. Elahi, M. Rezvani, M. Rohani, 2012, Iranian journal of neurology.