ZAHRA ANVAR

TitleInstructor
InstitutionBaylor College of Medicine
DepartmentDepartment of Obstetrics & Gynecology
Address1250 MOURSUND STREET
Houston, TX 77030
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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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    PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Anvar Z, Jochum MD, Chakchouk I, Sharif M, Demond H, To AK, Kraushaar DC, Wan YW, Andrews S, Kelsey G, Veyver IB. Maternal loss-of-function of Nlrp2 results in failure of epigenetic reprogramming in mouse oocytes. Res Sq. 2024 Jun 04. PMID: 38883732; PMCID: PMC11177987.
      Citations:    
    2. Anvar Z, Chakchouk I, Sharif M, Mahadevan S, Su L, Anikar S, Naini FA, Utama AB, Van den Veyver IB. Comparison of Four Protocols for In Vitro Differentiation of Human Embryonic Stem Cells into Trophoblast Lineages by BMP4 and Dual Inhibition of Activin/Nodal and FGF2 Signaling. Reprod Sci. 2024 Jan; 31(1):173-189. PMID: 37658178; PMCID: PMC10784360.
      Citations:    Fields:    Translation:HumansCells
    3. Anvar Z, Chakchouk I, Sharif M, Mahadevan S, Nasiotis ET, Su L, Liu Z, Wan YW, Van den Veyver IB. Loss of the Maternal Effect Gene Nlrp2 Alters the Transcriptome of Ovulated Mouse Oocytes and Impacts Expression of Histone Demethylase KDM1B. Reprod Sci. 2023 09; 30(9):2780-2793. PMID: 36976514; PMCID: PMC10524210.
      Citations:    Fields:    Translation:AnimalsCells
    4. Jahromi BN, Borzou N, Parsanezhad ME, Anvar Z, Ghaemmaghami P, Sabetian S. Associations of insulin resistance, sex hormone-binding globulin, triglyceride, and hormonal profiles in polycystic ovary syndrome: A cross-sectional study. Int J Reprod Biomed. 2021 Jul; 19(7):653-662. PMID: 34458674; PMCID: PMC8387712.
      Citations: 1     
    5. Anvar Z, Chakchouk I, Demond H, Sharif M, Kelsey G, Van den Veyver IB. DNA Methylation Dynamics in the Female Germline and Maternal-Effect Mutations That Disrupt Genomic Imprinting. Genes (Basel). 2021 08 06; 12(8). PMID: 34440388; PMCID: PMC8394515.
      Citations: 5     Fields:    Translation:HumansCells
    6. Zal F, Ahmadi P, Davari M, Khademi F, Jahromi MA, Anvar Z, Jahromi BN. Glutathione-dependent enzymes in the follicular fluid of the first-retrieved oocyte and their impact on oocyte and embryos in polycystic ovary syndrome: A cross-sectional study. Int J Reprod Biomed. 2020 Jun; 18(6):415-424. PMID: 32754677; PMCID: PMC7340988.
      Citations:    
    7. Jahromi BN, Yaghobi R, Matlub N, Fazelzadeh A, Ramzi A, Anvar Z, Zare N, Salarian L, Fallahi J. Prevalence of Cytomegalovirus in Semen of Male Partners of Infertile Couples and the Virus Impact on Sperm Parameters. J Reprod Infertil. 2020 Apr-Jun; 21(2):124-129. PMID: 32500015; PMCID: PMC7253934.
      Citations: 1     
    8. Fallahi J, Anvar Z, Razban V, Momtahan M, Namavar-Jahromi B, Fardaei M. Founder Effect of KHDC3L, p.M1V Mutation, on Iranian Patients with Recurrent Hydatidiform Moles. Iran J Med Sci. 2020 Mar; 45(2):118-124. PMID: 32210488; PMCID: PMC7071548.
      Citations: 2     Fields:    
    9. Habibzadeh P, Tabatabaei Z, Farazi Fard MA, Jamali L, Hafizi A, Nikuei P, Salarian L, Nasr Esfahani MH, Anvar Z, Faghihi MA. Pre-implantation genetic diagnosis in an Iranian family with a novel mutation in MUT gene. BMC Med Genet. 2020 02 03; 21(1):22. PMID: 32013889; PMCID: PMC6998079.
      Citations: 1     Fields:    Translation:Humans
    10. Demond H, Anvar Z, Jahromi BN, Verma A, Davari M, Calzari L, Russo S, Jahromi MA, Monk D, Andrews S, Riccio A, Kelsey G, Sparago A. 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; PMCID: PMC6918611.
      Citations: 19     Fields:    Translation:HumansCells
    11. 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 06 04; 34(6):1155-1164. PMID: 31119281.
      Citations: 13     Fields:    Translation:Humans
    12. Anvar Z, Acurzio B, Cerrato F, Roma J, Verde G. Origins of DNA methylation defects in Wilms tumors. Cancer Lett. 2019 08 10; 457:119-128. PMID: 31103718.
      Citations: 13     Fields:    Translation:HumansCells
    13. 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; PMCID: PMC6500085.
      Citations: 7     
    14. 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.
      Citations: 3     Fields:    Translation:HumansCells
    15. 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.
      Citations: 7     Fields:    Translation:Humans
    16. 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.
      Citations: 2     Fields:    Translation:HumansCells
    17. 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; PMCID: PMC5993897.
      Citations: 16     Fields:    
    18. 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; PMCID: PMC5936618.
      Citations: 5     
    19. 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.
      Citations: 4     Fields:    Translation:Humans
    20. 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.
      Citations: 6     Fields:    Translation:HumansCells
    21. 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; PMCID: PMC5041456.
      Citations: 27     Fields:    Translation:AnimalsCells
    22. 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; PMCID: PMC4756812.
      Citations: 27     Fields:    Translation:AnimalsCells
    23. Esposito S, De Cesare L, Sparago A, Anvar Z, Riso V, Cammisa M, Fattorusso R, Grimaldi G, Riccio A, Pedone PV, Baglivo I. 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; PMCID: PMC3655262.
      Citations: 18     Fields:    Translation:HumansAnimalsCells
    24. 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.
      Citations: 1     Fields:    Translation:Humans
    25. 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; PMCID: PMC5109005.
      Citations: 4     
    26. 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.
      Citations: 4     Fields:    Translation:Humans
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