Publications by authors named "Sepideh Mehvari"

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Contribution of genetic variants in the development of familial premature coronary artery disease in a cohort of cardiac patients.
Sepideh Mehvari, Nahid Karimian Fathi, Sara Saki, Maryam Asadnezhad, Sanaz Arzhangi

Clin Genet· June 2024

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Comprehensive genotype-phenotype correlation in AP-4 deficiency syndrome; Adding data from a large cohort of Iranian patients.
Maryam Beheshtian, Tara Akhtarkhavari, Sepideh Mehvari, Marzieh Mohseni, Zohreh Fattahi

Clin Genet· January 2021

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Whole genome sequencing identifies a duplicated region encompassing Xq13.2q13.3 in a large Iranian family with intellectual disability.
Sepideh Mehvari, Farzaneh Larti, Hao Hu, Zohreh Fattahi, Maryam Beheshtian

Mol Genet Genomic Med· October 2020

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Genetics of intellectual disability in consanguineous families.
Hao Hu, Kimia Kahrizi, Luciana Musante, Zohreh Fattahi, Ralf Herwig, Sepideh Mehvari

Mol Psychiatry· July 2019

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Effect of inbreeding on intellectual disability revisited by trio sequencing.
Kimia Kahrizi, Hao Hu, Masoumeh Hosseini, Vera M Kalscheuer, Zohreh Fattahi, Sepideh Mehvari

Clin Genet· January 2019

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