Alibakhshi R

References (2)

Title : MDGA2 homozygous loss-of-function variants cause developmental and epileptic encephalopathy - Morsy_2026_Am.J.Hum.Genet__
Author(s) : Morsy H , Kim H , Jang G , Zaki MS , Severino M , Abdelrazek IM , Hussien H , Self E , Albaradie RS , Bakur K , Firoozfar Z , Efthymiou S , Noureldeen MM , Nabil A , Alvi JR , Molavi F , Alavi S , Alibakhshi R , Topcu V , Mancilar H , Uctepe E , Yesilyurt A , Aldhalaan H , Showki Tous ES , Alhaddad B , Elbendary HM , Scardamaglia A , Murphy D , Yepez VA , Gagneur J , Omar TI , Abd Elmaksoud M , Vandrovocova J , Abdalla E , Reilly MM , Sultan T , Alkuraya FS , Gleeson JG , Um JW , Houlden H , Ko J , Maroofian R
Ref : American Journal of Human Genetics , : , 2026
Abstract :
PubMedSearch : Morsy_2026_Am.J.Hum.Genet__
PubMedID: 41570816

Title : Association between activity and genotypes of paraoxonase1 L55M (rs854560) increases the disease activity of rheumatoid arthritis through oxidative stress - Tanhapour_2019_Mol.Biol.Rep_46_741
Author(s) : Tanhapour M , Shahmohamadnejad S , Vaisi-Raygani A , Kiani A , Shakiba Y , Rahimi Z , Bahrehmand F , Shakiba E , Vaisi-Raygani AA , Alibakhshi R , Eivazi A , Pourmotabbed T
Ref : Mol Biol Rep , 46 :741 , 2019
Abstract :
PubMedSearch : Tanhapour_2019_Mol.Biol.Rep_46_741
PubMedID: 30506510