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(2024) Whole-exome sequencing revealed a novel ERCC8 variant in an Iranian large family with Cockayne syndrome. Human Gene. p. 4. ISSN 2773-0441
(2024) The role of mir-214-5p and mir-548-5p expressions in endometriosis. Molecular Biology Reports. p. 1148. ISSN 1573-4978 (Electronic) 0301-4851 (Linking)
(2023) Association of cytotoxic T-lymphocyte-associated protein 4 polymorphisms with recurrent pregnancy loss: A case-control study. International Journal of Reproductive BioMedicine. pp. 33-42. ISSN 2476-4108
(2023) Chitosan/silk fibroin/nitrogen-doped carbon quantum dot/α-tricalcium phosphate nanocomposite electrospinned as a scaffold for wound healing application: In vitro and in vivo studies. International Journal of Biological Macromolecules.
(2023) Chitosan/silk fibroin/nitrogen-doped carbon quantum dot/α-tricalcium phosphate nanocomposite electrospinned as a scaffold for wound healing application: In vitro and in vivo studies. International Journal of Biological Macromolecules. ISSN 01418130 (ISSN)
(2023) Lansoprazole as a potent HDAC2 inhibitor for treatment of colorectal cancer: An in-silico analysis and experimental validation. Computers in Biology and Medicine. p. 14. ISSN 0010-4825
(2023) Synthesis of a stimuli-sensitive PEGylated nanoniosomal doxorubicin for the treatment of acute myeloid leukemia: An <i>in vitro</i> study. Nanomedicine Journal. pp. 77-84. ISSN 2322-3049
(2023) Synthesis of a stimuli-sensitive PEGylated nanoniosomal doxorubicin for the treatment of acute myeloid leukemia: An in vitro study. Nanomedicine Journal. pp. 77-84. ISSN 23223049 (ISSN)
(2023) A new approach to the development and assessment of doxorubicin-loaded nanoliposomes for the treatment of osteosarcoma in 2D and 3D cell culture systems. Heliyon. p. 16.
(2022) Association study of ESR1 rs9340799, rs2234693, and MMP2 rs243865 variants in Iranian women with premature ovarian insufficiency: A case-control study. International Journal of Reproductive BioMedicine. pp. 841-850.
(2022) Co-segregation of variant NSUN2 Lue198Arg among Iranian family with intellectual disability: a case report. Egyptian Journal of Medical Human Genetics. p. 11. ISSN 1110-8630
(2022) Evaluation of CAG repeat length in the androgen receptor gene and polycystic ovary syndrome risk in Iranian women: A case-control study. International Journal of Reproductive BioMedicine. pp. 195-202.
(2022) GGPS1-associated muscular dystrophy with and without hearing loss. Annals of Clinical and Translational Neurology. pp. 1465-1474.
(2022) Male factor testing in recurrent pregnancy loss cases: A narrative review. International Journal of Reproductive BioMedicine. pp. 447-460.
(2022) Novel variants underlying autosomal recessive neurodevelopmental disorders with intellectual disability in Iranian consanguineous families. Journal of Clinical Laboratory Analysis.
(2022) <i>GGPS1</i>-associated muscular dystrophy with and without hearing loss. Annals of Clinical and Translational Neurology. pp. 1465-1474. ISSN 2328-9503
(2021) Apparent but unconfirmed digenism in an Iranian consanguineous family with syndromic Retinal Disease. Experimental Eye Research.
(2021) Association between <i>eNOS</i> gene promoter polymorphism (-786T>C) and idiopathic recurrent pregnancy loss in Iranian women. Asian Pacific Journal of Reproduction. pp. 269-273. ISSN 2305-0500
(2021) Association between eNOS gene promoter polymorphism (-786T>C) and idiopathic recurrent pregnancy loss in Iranian women. Asian Pacific Journal of Reproduction. pp. 269-273.
(2021) Association of M55L and Q192R polymorphisms of paraoxonase 1 gene (PON1) with recurrent pregnancy loss risk: A case–control study. International Journal of Reproductive BioMedicine. pp. 559-568.
(2021) Association of mir-146a and mir196a2 genotype with susceptibility to idiopathic recurrent pregnancy loss in iranian women: A case-control study. International Journal of Reproductive BioMedicine. pp. 725-732.
(2021) CAG repeat polymorphism in androgen receptor and infertility: A case-control study. International Journal of Reproductive BioMedicine. pp. 845-850. ISSN 2476-4108
(2021) Fertility preservation in women with ovarian cancer: Finding new pathways: A case-control study. International Journal of Reproductive BioMedicine. pp. 157-166.
(2021) Homozygous females for a X-linked RPGR-ORF15 mutation in an Iranian family with retinitis pigmentosa. Experimental Eye Research.
(2020) Frequency of the rs 14035 polymorphism of <i>RAN</i> gen in recurrent pregnancy loss: A case-control study. International Journal of Reproductive BioMedicine. pp. 359-366. ISSN 2476-4108
(2020) Key Regulatory miRNAs and their Interplay with Mechanosensing and Mechanotransduction Signaling Pathways in Breast Cancer Progression. Molecular Cancer Research. pp. 1113-1128. ISSN 1541-7786
(2020) Posterior column ataxia with retinitis pigmentosa (PCARP) in an Iranian patient associated with the <i>FLVCR1</i> gene. Ophthalmic Genetics. pp. 90-92. ISSN 1381-6810
(2020) Posterior column ataxia with retinitis pigmentosa (PCARP) in an Iranian patient associated with the FLVCR1 gene. Ophthalmic Genetics. pp. 90-92.
(2020) Testicular expression of <i>TDRD1</i>, <i>TDRD5</i>, <i>TDRD9</i> and <i>TDRD12</i> in azoospermia. BMC medical genetics. p. 7.
(2020) Upregulation of the <i>RNF8</i> gene can predict the presence of sperm in azoospermic individuals. Clinical and Experimental Reproductive Medicine-Cerm. pp. 61-67. ISSN 2233-8233
(2019) Expression patterns of cofilin and scinderin in breast cancer and their association with clinicopathological features in Iranian patients. Clinical Cancer Investigation Journal. pp. 215-221. ISSN 2278-0513
(2019) Protective Effects of Antioxidant Supplements on Sperm Parameters, Sperm DNA Damage and Level of Seminal ROS in RPL Patients: A Clinical Trial Study. Iranian Red Crescent Medical Journal. p. 8. ISSN 2074-1804
(2019) Utilization of Whole Exome Sequencing in Lethal Form of Multiple Pterygium Syndrome: Identification of Mutations in Embryonal Subunit of Acetylcholine Receptor. International Journal of Molecular and Cellular Medicine. pp. 258-270. ISSN 2251-9637
(2018) Anatomic Features of C-shaped Mandibular Second Molars in a Selected Iranian Population Using CBCT. Iranian Endodontic Journal. pp. 120-125. ISSN 1735-7497 (Print) 2008-2746 (Electronic) 1735-7497 (Linking)
(2018) Detection of 4977-bp deletion of mitochondrial DNA in in vitro fertilization failure women: A case-control study. International Journal of Reproductive BioMedicine. pp. 571-576. ISSN 2476-4108 (Print) 2476-3772 (Electronic) 2476-3772 (Linking)
(2018) Variable localization of Toll-like receptors in human fallopian tube epithelial cells. Clinical and Experimental Reproductive Medicine. pp. 1-9. ISSN 2233-8233 (Print) 2233-8241 (Electronic) 2093-8896 (Linking)
(2017) Frequency of TNFR1 36 A/G gene polymorphism in azoospermic infertile men: A case-control study. International Journal of Reproductive BioMedicine. pp. 521-526. ISSN 2476-4108 (Print) 2476-3772 (Electronic) 2476-3772 (Linking)
(2016) An Association Study of the <i>SLC19A1</i> Gene Polymorphisms/Haplotypes with Idiopathic Recurrent Pregnancy Loss in an Iranian Population. Genetic Testing and Molecular Biomarkers. pp. 235-240. ISSN 1945-0265
(2015) The accuracy of Breastlight in detection of breast lesions. Indian Journal of Cancer. pp. 513-516.
(2014) Effectiveness of aspirin compare with heparin plus aspirin in recurrent pregnancy loss treatment: A quasi experimental study. Iranian Journal of Reproductive Medicine. pp. 73-76. ISSN 16806433 (ISSN)
(2013) Analysis of <i>MLH3</i> C2531T polymorphism in Iranian women with unexplained infertility. Iranian Journal of Reproductive Medicine. pp. 19-24. ISSN 1680-6433
(2010) Frequency of poly cystic ovary syndrome in patients with premenopausal breast cancer. Iranian Journal of Reproductive Medicine. pp. 86-89. ISSN 1680-6433
(2007) Genetics of polycystic ovary syndrome. Iranian Journal of Reproductive Medicine. pp. 1-5. ISSN 1680-6433
(2007) Pathological findings of osteoarthritis in sternoclavicular joint. Iranian Journal of Medical Sciences. pp. 156-162. ISSN 02530716 (ISSN)