List of works - Mortaza Bonyadi

Association of plasminogen activator inhibitor-1 gene polymorphism with inflammatory bowel disease in Iranian Azeri Turkish patients

scientific article published on January 2014

Common MEFV mutation analysis in Iranian Azeri Turkish patients with familial Mediterranean fever.

scientific article

Common MEFV mutations in Iranian Azeri Turkish patients with Behçet's disease.

scientific article published on 30 May 2011

Common Mediterranean fever gene mutations in the Azeri Turkish population of Iran

scientific article published in February 2010

Common mutation analysis of GJB2 and GJB6 genes in affected families with autosomal recessive non-syndromic hearing loss from Iran: simultaneous detection of two common mutations (35delG/del(GJB6-D13S1830)) in the DFNB1-related deafness.

scientific article published on 21 March 2007

Effect of the C3435T polymorphism of the multidrug resistance 1 gene on the severity of inflammatory bowel disease in Iranian Azeri Turks.

scientific article published on July 2013

MEFV mutations in Iranian Azeri Turkish patients with familial Mediterranean fever.

scientific article

Mapping of a major genetic modifier of embryonic lethality in TGF beta 1 knockout mice.

scientific article published in February 1997

Mesenchymal progenitor self-renewal deficiency leads to age-dependent osteoporosis in Sca-1/Ly-6A null mice.

scientific article

Molecular analysis of the SMN and NAIP genes in Iranian spinal muscular atrophy patients

scientific article published on 01 April 2009

Mutations of the phenylalanine hydroxylase gene in Iranian Azeri Turkish patients with phenylketonuria

scientific article

Paroxonase (PON1-L55M) gene polymorphism and its association with Behçet's disease among Iranian population

scientific article published on 24 April 2020

Plasminogen activator inhibitor-1 gene polymorphism in Iranian Azeri Turkish patients with FMF disease and its association with amyloidosis.

scientific article

Polymorphisms of Promoter Region of TNF-α Gene in Iranian Azeri Turkish Patients with Behçet's Disease

scientific article published in January 2017

Regulation of Chk2 phosphorylation by interaction with protein phosphatase 2A via its B' regulatory subunit

scientific article

Role of complement factor B rs4151667 (L9H) polymorphisms and its interactional role with CFH Y402H and C3 rs2230199 (R102G) risk variants in age-related macular degeneration: a case control study

scientific article published on 06 August 2020

Spectrum of CFTR gene mutations in Iranian Azeri Turkish patients with cystic fibrosis.

scientific article

TNF-alpha gene polymorphisms in Iranian Azeri Turkish patients with Behcet's Disease.

scientific article

Thromboxane A synthase 1 gene expression and promotor haplotypes are associated with risk of large artery-atherosclerosis stroke in Iranian population

scientific article published on 26 April 2019

Tumor necrosis factor-α gene polymorphisms in FMF and their association with amyloidosis

scientific article

Whole-exome sequencing efficiently detects rare mutations in autosomal recessive nonsyndromic hearing loss

scientific article

List of works by Mortaza Bonyadi

Association of plasminogen activator inhibitor-1 gene polymorphism with inflammatory bowel disease in Iranian Azeri Turkish patients

Common MEFV mutation analysis in Iranian Azeri Turkish patients with familial Mediterranean fever.

Common MEFV mutations in Iranian Azeri Turkish patients with Behçet's disease.

Common Mediterranean fever gene mutations in the Azeri Turkish population of Iran

Common mutation analysis of GJB2 and GJB6 genes in affected families with autosomal recessive non-syndromic hearing loss from Iran: simultaneous detection of two common mutations (35delG/del(GJB6-D13S1830)) in the DFNB1-related deafness.

Effect of the C3435T polymorphism of the multidrug resistance 1 gene on the severity of inflammatory bowel disease in Iranian Azeri Turks.

MEFV mutations in Iranian Azeri Turkish patients with familial Mediterranean fever.

Mapping of a major genetic modifier of embryonic lethality in TGF beta 1 knockout mice.

Mesenchymal progenitor self-renewal deficiency leads to age-dependent osteoporosis in Sca-1/Ly-6A null mice.

Molecular analysis of the SMN and NAIP genes in Iranian spinal muscular atrophy patients

Mutations of the phenylalanine hydroxylase gene in Iranian Azeri Turkish patients with phenylketonuria

Paroxonase (PON1-L55M) gene polymorphism and its association with Behçet's disease among Iranian population

Plasminogen activator inhibitor-1 gene polymorphism in Iranian Azeri Turkish patients with FMF disease and its association with amyloidosis.

Polymorphisms of Promoter Region of TNF-α Gene in Iranian Azeri Turkish Patients with Behçet's Disease

Regulation of Chk2 phosphorylation by interaction with protein phosphatase 2A via its B' regulatory subunit

Role of complement factor B rs4151667 (L9H) polymorphisms and its interactional role with CFH Y402H and C3 rs2230199 (R102G) risk variants in age-related macular degeneration: a case control study

Spectrum of CFTR gene mutations in Iranian Azeri Turkish patients with cystic fibrosis.

TNF-alpha gene polymorphisms in Iranian Azeri Turkish patients with Behcet's Disease.

Thromboxane A synthase 1 gene expression and promotor haplotypes are associated with risk of large artery-atherosclerosis stroke in Iranian population

Tumor necrosis factor-α gene polymorphisms in FMF and their association with amyloidosis

Whole-exome sequencing efficiently detects rare mutations in autosomal recessive nonsyndromic hearing loss