Afsaneh Taghipour‐Sheshdeh

Expanding the molecular and clinical phenotypes of FUT8‐CDG

Bobby G. Ng, Hassan Dastsooz, Mohammad Silawi et al. · Journal of Inherited Metabolic Disease · 2020 · 31 citations · Full text

Genomic prediction for growth using a low-density SNP panel in dromedary camels

Morteza Bitaraf Sani, Javad Zare Harofte, Mohammad Hossein Banabazi et al. · Scientific Reports · 2021 · 22 citations · Full text

Genetic Testing in Various Neurodevelopmental Disorders Which Manifest as Cerebral Palsy: A Case Study From Iran

Marzieh Nejabat, Soroor Inaloo, Afsaneh Taghipour‐Sheshdeh et al. · Frontiers in Pediatrics · 2021 · 18 citations · Full text

Identification and Clinical Implications of a Novel MYO15A Variant in a Consanguineous Iranian Family by Targeted Exome Sequencing

Narges Zarepour, Mahbobeh Koohiyan, Afsaneh Taghipour‐Sheshdeh et al. · Audiology and Neurotology · 2019 · 16 citations

A novel pathogenic variant in the MARVELD2 gene causes autosomal recessive non-syndromic hearing loss in an Iranian family

Afsaneh Taghipour‐Sheshdeh, Fatemeh Nemati-Zargaran, Narges Zarepour et al. · Genomics · 2018 · 11 citations

Mendelian Disorder, Genetic Disorder, Genetics +9