A deleterious frameshift insertion mutation in the <i>ZNF142</i> gene leads to intellectual developmental disorder with impaired speech in three affected siblings: Clinical features and literature reviewAtefeh Mir, Mohammad Amin Tabatabaiefar, Yongjun Song et al.|Molecular Genetics & Genomic Medicine|2023Cited by 8
Whole exome sequencing revealed variants in four genes underlying X-linked intellectual disability in four Iranian families: novel deleterious variants and clinical features with the review of literatureAtefeh Mir, Mohammad Amin Tabatabaiefar, Yongjun Song et al.|BMC Medical Genomics|2023Cited by 6
A novel heterozygous truncating variant in the <i>AGO1</i> gene in an Iranian family with schizophrenia as an unreported symptomAtefeh Mir, Mohammad Amin Tabatabaiefar, Erfan Khorram et al.|Annals of Human Genetics|2023Cited by 4
A novel de novo frameshift variant in the <scp><i>CHD2</i></scp> gene related to intellectual and developmental disability, seizures and speech problemsAtefeh Mir, Mohammad Amin Tabatabaiefar, Yongjun Song et al.|Molecular Genetics & Genomic Medicine|2023Cited by 1
Molecular and phenotypical findings of a novel de novo <i>SYNGAP1</i> gene variant in an 11-year-old Iranian boy with intellectual disabilityAtefeh Mir, Mohammad Amin Tabatabaiefar, Fahimeh Akbarian et al.|Laboratory Medicine|2023Cited by 1