Farideh Yousefipour

Underexpression of hsa-miR-449 family and their promoter hypermethylation in infertile men: A case-control study

S. Mousavi, R. Najafipour, S. Moghbelinejad, 2021, International journal of reproductive biomedicine.

Identification of two novel homozygous mutations in ERCC8 gene in two unrelated consanguineous families with Cockayne syndrome from Iran.

Farideh Yousefipour, Forouzandeh Mahjoobi, 2021, Clinica chimica acta; international journal of clinical chemistry.

Identification of two novel homozygous nonsense mutations in TRAPPC9 in two unrelated consanguineous families with intellectual Disability from Iran

F. Mahjoubi, H. Mozhdehipanah, Farideh Yousefipour, 2021, Molecular genetics & genomic medicine.

Identification of a novel homozygous frameshift mutation in SLC29A3 gene in a case with H syndrome from Iran.

H. Mousakhani, A. Mehrtash, A. Heidari, 2019, Current Research in Translational Medicine.