ÌÇÐÄÊÓƵ

Email

zanvar@bcm.edu

Positions

Instructor

ÌÇÐÄÊÓƵ of Medicine
houston, Texas, United States

Education

PhD from Università degli Studi della Campania "Luigi Vanvitelli"

12/2013 - Naples, campania, Italy

MSc from Khatam University

07/2010 - Tehran

BA from Shiraz University

07/2007 - Shiraz

Selected Publications

• ADCY10 frameshift variant leading to severe recessive asthenozoospermia and segregating with absorptive hypercalciuria. " ;
• A KHDC3L mutation resulting in recurrent hydatidiform mole causes genome-wide DNA methylation loss in oocytes and persistent imprinting defects post-fertilisation. " ;
• A Novel Mutation in NLRP7 Related to Recurrent Hydatidiform Mole and Reproductive Failure. " ;
• Assessment of oxytocin level, glucose metabolism components and cutoff values for oxytocin and anti-mullerian hormone in infertile PCOS women. " ;
• Clinical and genetic-epignetic aspects of recurrent hydatidiform mole: A review of literature. " ;
• Detection of Y Chromosome Microdeletions and Hormonal Profile Analysis of Infertile Men undergoing Assisted Reproductive Technologies. " ;
• Effect of low-dose aspirin on the development of ovarian hyperstimulation syndrome and outcomes of assisted reproductive techniques in the women with PCOS, a randomized double-blinded clinical trial. " ;
• Genetic and epigenetic mutations affect the DNA binding capability of human ZFP57 in transient neonatal diabetes type 1.. " ;
• Origins of DNA methylation defects in Wilms tumors. " ;
• Ovarian Hyperstimulation Syndrome: A Narrative Review of Its Pathophysiology, Risk Factors, Prevention, Classification, and Management. " ;
• Sperm DNA methylation of H19 imprinted gene and male infertility. " ;
• The Impact of Methylenetetrahydrofolate Reductase (MTHFR) Sperm Methylation and Variants on Semen Parameters and the Chance of Recurrent Pregnancy Loss in the Couple. " ;
• ZFP57 maintains the parent-of-origin-specific expression of the imprinted genes and differentially affects non-imprinted targets in mouse embryonic stem cells.. " ;
• ZFP57 recognizes multiple and closely spaced sequence motif variants to maintain repressive epigenetic marks in mouse embryonic stem cells.. " ;
• Pre-implantation genetic diagnosis in an Iranian family with a novel mutation in MUT gene. " BMC Med Genet. ; 21
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Show 18 more publications

Projects

Methylome and transcriptome profiling in Nlrp2 KO mouse model

Languages

Farsi, Italian