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Zahra Anvar

TitlePostdoc Fellows and Associates
InstitutionBaylor College of Medicine
DepartmentPostDoc
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    1. Demond H, Anvar Z, Jahromi BN, Sparago A, Verma A, Davari M, Calzari L, Russo S, Jahromi MA, Monk D, Andrews S, Riccio A, Kelsey G. A KHDC3L mutation resulting in recurrent hydatidiform mole causes genome-wide DNA methylation loss in oocytes and persistent imprinting defects post-fertilisation. Genome Med. 2019 12 17; 11(1):84. PMID: 31847873.
      View in: PubMed
    2. Akbari A, Pipitone GB, Anvar Z, Jaafarinia M, Ferrari M, Carrera P, Totonchi M. ADCY10 frameshift variant leading to severe recessive asthenozoospermia and segregating with absorptive hypercalciuria. Hum Reprod. 2019 Jun 04; 34(6):1155-1164. PMID: 31119281.
      View in: PubMed
    3. Anvar Z, Acurzio B, Roma J, Cerrato F, Verde G. Origins of DNA methylation defects in Wilms tumors. Cancer Lett. 2019 Aug 10; 457:119-128. PMID: 31103718.
      View in: PubMed
    4. Fallahi J, Razban V, Momtahan M, Akbarzadeh-Jahromi M, Namavar-Jahromi B, Anvar Z, Fardaei M. A Novel Mutation in NLRP7 Related to Recurrent Hydatidiform Mole and Reproductive Failure. Int J Fertil Steril. 2019 Jul; 13(2):135-138. PMID: 31037924.
      View in: PubMed
    5. Namavar Jahromi B, Zolghadri J, Rahmani E, Alipour S, Anvar Z, Zarei A, Keramati P. 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. Taiwan J Obstet Gynecol. 2019 Mar; 58(2):255-260. PMID: 30910149.
      View in: PubMed
    6. Jahromi BN, Dabbaghmanesh MH, Bakhshaie P, Parsanezhad ME, Anvar Z, Alborzi M, Zarei A, Bakhshaei M. Assessment of oxytocin level, glucose metabolism components and cutoff values for oxytocin and anti-mullerian hormone in infertile PCOS women. Taiwan J Obstet Gynecol. 2018 Aug; 57(4):555-559. PMID: 30122578.
      View in: PubMed
    7. Poorang S, Abdollahi S, Anvar Z, Tabei SMB, Jahromi BN, Moein-Vaziri N, Gharesi-Fard B, Banaei M, Dastgheib SA. The Impact of Methylenetetrahydrofolate Reductase (MTHFR) Sperm Methylation and Variants on Semen Parameters and the Chance of Recurrent Pregnancy Loss in the Couple. Clin Lab. 2018 Jul 01; 64(7):1121-1128. PMID: 30146842.
      View in: PubMed
    8. Namavar Jahromi B, Parsanezhad ME, Shomali Z, Bakhshai P, Alborzi M, Moin Vaziri N, Anvar Z. Ovarian Hyperstimulation Syndrome: A Narrative Review of Its Pathophysiology, Risk Factors, Prevention, Classification, and Management. Iran J Med Sci. 2018 May; 43(3):248-260. PMID: 29892142.
      View in: PubMed
    9. Bahmanimehr A, Zeighami S, Namavar Jahromi B, Anvar Z, Parsanezhad ME, Davari M, Montazeri S. Detection of Y Chromosome Microdeletions and Hormonal Profile Analysis of Infertile Men undergoing Assisted Reproductive Technologies. Int J Fertil Steril. 2018 Jul; 12(2):173-177. PMID: 29707937.
      View in: PubMed
    10. Moein-Vaziri N, Fallahi J, Namavar-Jahromi B, Fardaei M, Momtahan M, Anvar Z. Clinical and genetic-epignetic aspects of recurrent hydatidiform mole: A review of literature. Taiwan J Obstet Gynecol. 2018 Feb; 57(1):1-6. PMID: 29458875.
      View in: PubMed
    11. Nasri F, Gharesi-Fard B, Namavar Jahromi B, Farazi-Fard MA, Banaei M, Davari M, Ebrahimi S, Anvar Z. Sperm DNA methylation of H19 imprinted gene and male infertility. Andrologia. 2017 Dec; 49(10). PMID: 28295500.
      View in: PubMed
    12. Riso V, Cammisa M, Kukreja H, Anvar Z, Verde G, Sparago A, Acurzio B, Lad S, Lonardo E, Sankar A, Helin K, Feil R, Fico A, Angelini C, Grimaldi G, Riccio A. ZFP57 maintains the parent-of-origin-specific expression of the imprinted genes and differentially affects non-imprinted targets in mouse embryonic stem cells. Nucleic Acids Res. 2016 09 30; 44(17):8165-78. PMID: 27257070.
      View in: PubMed
    13. Anvar Z, Cammisa M, Riso V, Baglivo I, Kukreja H, Sparago A, Girardot M, Lad S, De Feis I, Cerrato F, Angelini C, Feil R, Pedone PV, Grimaldi G, Riccio A. ZFP57 recognizes multiple and closely spaced sequence motif variants to maintain repressive epigenetic marks in mouse embryonic stem cells. Nucleic Acids Res. 2016 Feb 18; 44(3):1118-32. PMID: 26481358.
      View in: PubMed
    14. Baglivo I, Esposito S, De Cesare L, Sparago A, Anvar Z, Riso V, Cammisa M, Fattorusso R, Grimaldi G, Riccio A, Pedone PV. Genetic and epigenetic mutations affect the DNA binding capability of human ZFP57 in transient neonatal diabetes type 1. FEBS Lett. 2013 May 21; 587(10):1474-81. PMID: 23499433.
      View in: PubMed
    15. Saadat M, Anvar Z, Namavar-Jahromi B, Saadat I. Genetic polymorphisms of glutathione S-transferase Z1 (GSTZ1) and susceptibility to preeclampsia. Mol Biol Rep. 2012 Sep; 39(9):8995-8. PMID: 22729907.
      View in: PubMed
    16. Anvar Z, Saadat I, Namavar-Jahromi B, Saadat M. Genetic polymorphisms of glutathione S-transferase M1 (GSTM1) and T1 (GSTT1) and susceptibility to pre-eclampsia: a case-control study and a meta-analysis. EXCLI J. 2011; 10:44-51. PMID: 27857664.
      View in: PubMed
    17. Anvar Z, Namavar-Jahromi B, Saadat M. Association between consanguineous marriages and risk of pre-eclampsia. Arch Gynecol Obstet. 2011 Mar; 283 Suppl 1:5-7. PMID: 20517614.
      View in: PubMed
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