دانشگاه شاهد

زهرا ظفری

استاد یار - دکتری تخصصی ژنتیک پزشکی


نام دانشکده : دانشکده علوم پایه
گروه آموزشی : زیست شناسی
شماره اتاق : 324
پست الکترونیک :
تلفن محل کار :00982151212231
پیوندها :
 

سوابق تحصیلی

دکتری تخصصی ژنتیک پزشکی، دانشگاه تربیت مدرس، تهران، ایران

مقالات ژورنالی (7)   Download XML   Download TXT

●  Identification of a Novel KCNQ1 Frameshift Mutation and Review of the Literature among Iranian Long QT Families
   ◂ Azam Amirian, Zahra Zafari, Morteza Karimipoor, Alireza Kordafshari, Mohammad Dalili, Siamak Saber, Amir Farjam Fazelifar, Sirous Zeinali
   ✔ 1398/03/02  2019/05/23
    Iranian Biomedical Journal


●  Characterization and haplotype study of 6 novel STR markers related to the KCNQ1 gene in heterogeneous cardiovascular disorders in the Iranian population
   ◂ Azam Amirian, Zahra Zafari, Zohre Sharifi, Alireza Kordafshari, Morteza Karimipoor, Sirous Zeinali
   ✔ 1398/01/29  2019/04/18
    Turkish Journal of Medical Sciences


●  Molecular Analysis of KCNQ1, KCNH2 and SCN5A Genes in Iranian Patients with Long QT Syndrome
   ◂ Amirian A, Karimipoor M, Zafari Z, Kallhor M, Dalili M, Saber S, Fazelifar Af, Zeinali S
   ✔ 1397/06/02  2018/08/24
    Journal of Molecular and Genetic Medicine


●  Detection of a new KCNQ1 frameshift mutation associated with Jervell and Lange-Nielsen syndrome in 2 Iranian families
   ◂ Azam Amirian, Zahra Zafari, Mohammad Dalili, Siamak Saber, Morteza Karimipoor, Samira Dabbagh Bagheri, Amir Farjam Fazelifar, Sirous Zeinali
   ✔ 1397/01/27  2018/04/16
    Journal of Arrhythmia


●  Development and diversity of a novel panel of short tandem repeat markers encompassing the SCN5A gene in Iranian population
   ◂ Zahra Zafari, Azam Amirian, Faezeh Rahimi Nejad, Vahid Akbari, Mohammad Taghi Akbari, Sirus Zeinali
   ✔ 1397/01/22  2018/04/11
    Journal of Genetics


●   Novel frameshift mutation in the KCNQ1 gene responsible for Jervell and Lange-Nielsen syndrome
   ◂ Sirous Zeinali, Amirfarjam Fazelifar, Vahid Akbari, Morteza Karimipour, Siamak Saber, Zahra Zafari, Seyed Mohammad Dalili, Azam Amirian
   ✔ 1396/10/11  2018/01/01
    Iranian Journal of Basic Medical Sciences


●  Identification and characterization of a novel recessive KCNQ1 mutation associated with Romano-Ward Long-QT syndrome in two Iranian families
   ◂ Zahra Zafari, Mohammad Dalili, Sirus Zeinali, Siamak Saber, Amir Farjam Fazeli Far, Mohammad Taghi Akbari
   ✔ 1396/04/21  2017/07/12
    Journal of Electrocardiology


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