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Clinical Genetics|April 6, 2019
Identification of disease-causing variants in the EXOSC gene family underlying autosomal recessive intellectual disability in Iranian familiesMaryam Beheshtian, Zohreh Fattahi, Mahsa Fadaee, et al.
European Journal of Human Genetics : EJHG|July 16, 2015
Missense variants in AIMP1 gene are implicated in autosomal recessive intellectual disability without neurodegenerationZafar Iqbal, Lucia Püttmann, Luciana Musante, et al.
Human Molecular Genetics|June 13, 2018
Biallelic missense variants in ZBTB11 can cause intellectual disability in humansZohreh Fattahi, Taimoor I Sheikh, Luciana Musante, et al.
Translational Psychiatry|January 8, 2021
Biallelic mutations in the death domain of PIDD1 impair caspase-2 activation and are associated with intellectual disabilityTaimoor I Sheikh, Nasim Vasli, Stephen Pastore, et al.
Brain : a Journal of Neurology|February 1, 2022
ZBTB11 dysfunction: spectrum of brain abnormalities, biochemical signature and cellular consequencesDulika Sumathipala, Petter Strømme, Zohreh Fattahi, et al.
Human Mutation|July 26, 2019
Iranome: A catalog of genomic variations in the Iranian populationZohreh Fattahi, Maryam Beheshtian, Marzieh Mohseni, et al.
Plos Genetics|September 25, 2019
Distinct genetic variation and heterogeneity of the Iranian populationZohreh Mehrjoo, Zohreh Fattahi, Maryam Beheshtian, et al.
NPJ Genomic Medicine|February 19, 2024
Clinical application of next generation sequencing for Mendelian disease diagnosis in the Iranian populationAyda Abolhassani, Zohreh Fattahi, Maryam Beheshtian, et al.
Clinical Genetics|October 14, 2018
Effect of inbreeding on intellectual disability revisited by trio sequencingKimia Kahrizi, Hao Hu, Masoumeh Hosseini, et al.
Transboundary and Emerging Diseases|April 9, 2021
SARS-CoV-2 outbreak in Iran: The dynamics of the epidemic and evidence on two independent introductionsZohreh Fattahi, Marzieh Mohseni, Khadijeh Jalalvand, et al.
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