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

by Zeynab Shaghaghi, Mortaza Bonyadi, Mohammad H Somi, Manouchehr Khoshbaten
Published 2014-01-01

Association study of the BDNF gene polymorphism (G196A) with overweight/obesity among women from Northwest of Iran

by Haneieh Honarmand, Mortaza Bonyadi, Abbas Rafat, Reza Mahdavi, Fereshteh Aliasghari
Published 2021-02-01

Association of CFI p.Gly119Arg gene polymorphism with age-related macular degeneration (AMD) disease in the population living in Tehran

by Neda Norouzi, Mortaza Bonyadi, Esmaeil Babaei, Mohammad Hossein Jabbarpour Bonyadi
Published 2017-08-01

TNF-alpha gene polymorphisms in Iranian Azari Turkish patients with inflammatory bowel diseases

by Mortaza Bonyadi, Reza Abdolmohammadi, Zohreh Jahanafrooz, Mohammad-Hosein Somy, Manoochehr Khoshbaten
Published 2014-01-01

Association between Common Single- nucleotide Polymorphism of Reelin Gene, rs736707 (C/T) with Autism Spectrum Disorder in Iranian-Azeri Patients

by Leila Mehdizadeh Fanid, Hassan Shahrokhi, Mina Adampourezare, Mohamad Ali Hosseinpour Feizi, Mortaza Bonyadi, A Eslami
Published 2015-11-01

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 ca...

by Nasrin Roshanipour, Maryam Ghaffari Laleh, Mortaza Bonyadi, Mohammad Hossein Jabbarpoor Bonyadi, Masoud Soheilian, Alireza Javadzadeh, Mehdi Yaseri
Published 2020-08-01

Correction: Whole-Exome Sequencing Efficiently Detects Rare Mutations in Autosomal Recessive Nonsyndromic Hearing Loss

by Oscar Diaz-Horta, Duygu Duman, Joseph Foster, Aslı Sırmacı, Michael Gonzalez, Nejat Mahdieh, Nikou Fotouhi, Mortaza Bonyadi, Filiz Başak Cengiz, Ibis Menendez, Rick H. Ulloa, Yvonne J. K. Edwards, Stephan Züchner, Susan Blanton, Mustafa Tekin
Published 2013-01-01

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

by Oscar Diaz-Horta, Duygu Duman, Joseph Foster, Aslı Sırmacı, Michael Gonzalez, Nejat Mahdieh, Nikou Fotouhi, Mortaza Bonyadi, Filiz Başak Cengiz, Ibis Menendez, Rick H Ulloa, Yvonne J K Edwards, Stephan Züchner, Susan Blanton, Mustafa Tekin
Published 2012-01-01

Correction: Whole-Exome Sequencing Efficiently Detects Rare Mutations in Autosomal Recessive Nonsyndromic Hearing Loss.

by Oscar Diaz-Horta, Duygu Duman, Joseph Foster, Aslı Sırmacı, Michael Gonzalez, Nejat Mahdieh, Nikou Fotouhi, Mortaza Bonyadi, Filiz Başak Cengiz, Ibis Menendez, Rick H. Ulloa, Yvonne J. K. Edwards, Stephan Züchner, Susan Blanton, Mustafa Tekin
Published 2013-01-01