T. Dadkhah

Individual genetic variability mainly of Proinflammatory cytokines, cytokine receptors, and toll‐like receptors dictates pathophysiology of COVID‐19 disease

Zahra Montaseri, A. Ghasemian, Y. Mansoori, 2022, Journal of medical virology.

Informative combination of CLU rs11136000, serum HDL levels, diabetes, and age as a new piece of puzzle-picture of predictive medicine for cognitive disorders

S. Hosseini, Elham Ghadami, Fatemeh Amjadi-Moheb, 2018, Molecular Biology Reports.

Informative combination of CLU rs11136000, serum HDL levels, diabetes, and age as a new piece of puzzle-picture of predictive medicine for cognitive disorders

S. Hosseini, Elham Ghadami, Fatemeh Amjadi-Moheb, 2019, Molecular Biology Reports.

PI3k/AKT signaling pathway: Erythropoiesis and beyond

Elham Ghadami, H. Akhavan-Niaki, T. Dadkhah, 2018, Journal of cellular physiology.

The analysis of association between SNCA, HUSEYO and CSMD1 gene variants and Parkinson’s disease in Iranian population

Hossein Darvish, Abbas Tafakhori, Hajar Eftekhari, 2016, Neurological Sciences.

Local application of glyceril trinitrate ointment for primary dysmenorrhea

M. Modarres, S. Ghazizadeh, T. Dadkhah, 2002, International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics.

A genetic variant in miRNA binding site of glutamate receptor 4, metabotropic (GRM4) is associated with increased risk of major depressive disorder.

H. Ghaedi, M. Ohadi, H. Darvish, 2017, Journal of affective disorders.

RIT2 Polymorphisms: Is There a Differential Association?

P. Petramfar, M. Khaniani, A. Biglarian, 2017, Molecular Neurobiology.

Mutation and Rare Polymorphisms Insight in Exons 7 and 20 of CFTR Gene in Non-Caucasian Cystic Fibrosis Patients

H. A. Niaki, Elham Ghadami, A. Shirafkan, 2016 .

IBBJ Spring 2016 , Vol 2 , No 2 Mutation and Rare Polymorphisms Insight in Exons 7 and 20 of CFTR Gene in Non-Caucasian Cystic Fibrosis Patients

Elham Ghadami, A. Shirafkan, T. Dadkhah, 2018 .