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Hardy-Weinberg Equilibrium in Meta-Analysis Studies and Large-Scale Genomic Sequencing Era.
- Published in:
- Asian Pacific Journal of Cancer Prevention, 2024, v. 25, n. 7, p. 2229, doi. 10.31557/APJCP.2024.25.7.2229
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- Article
Correlation of TNF-α polymorphisms with susceptibility to lung cancer: evidence from a meta-analysis based on 29 studies.
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- BMC Cancer, 2024, v. 24, n. 1, p. 1, doi. 10.1186/s12885-024-12854-x
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- Article
A meta-analysis for association of eNOS VNTR 4b/a, – 786 T > C and + 894G > T polymorphisms with risk of recurrent pregnancy loss.
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- Archives of Gynecology & Obstetrics, 2021, v. 304, n. 5, p. 1135, doi. 10.1007/s00404-021-06172-x
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- Article
Clinical Features of Okur-Chung Neurodevelopmental Syndrome: Case Report and Literature Review.
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- Molecular Syndromology, 2022, v. 13, n. 5, p. 381, doi. 10.1159/000522353
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- Article
A meta-analysis for association of TNF-α -308G>A polymorphism with susceptibility to Ankylosing Spondylitis.
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- Journal of Orthopaedics, 2021, v. 26, p. 79, doi. 10.1016/j.jor.2021.07.015
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- Article
Association of catechol-O-methyltranferase 472G>A (Val158Met) polymorphism with susceptibility to fibromyalgia syndrome.
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- Journal of Orthopaedics, 2020, v. 20, p. 257, doi. 10.1016/j.jor.2020.01.013
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- Publication type:
- Article
A meta-analysis for the risk and prevalence of preeclampsia among pregnant women with COVID-19.
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- Turkish Journal of Obstetrics & Gynecology, 2021, v. 18, n. 3, p. 224, doi. 10.4274/tjod.galenos.2021.66750
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- Article
Meta-analysis of the frequency of intrauterine growth restriction and preterm premature rupture of the membranes in pregnant women with COVID-19.
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- Turkish Journal of Obstetrics & Gynecology, 2021, v. 18, n. 3, p. 236, doi. 10.4274/tjod.galenos.2021.74829
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- Article
A meta-analysis of the association of the ACE I/D and PAI-1 4G/5G polymorphisms with recurrent pregnancy loss in Iranian women: Are the investigations adequate?
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- Turkish Journal of Obstetrics & Gynecology, 2021, v. 18, n. 2, p. 139, doi. 10.4274/tjod.galenos.2021.58997
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- Article
A thorough analysis of data on the correlation between COL9A1 polymorphisms and the susceptibility to congenital talipes equinovarus: a meta-analysis.
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- Journal of Orthopaedic Surgery & Research, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13018-024-04834-5
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- Article
Clinical and molecular characterization of three patients with Hepatocerebral form of mitochondrial DNA depletion syndrome: a case series.
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- BMC Medical Genetics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12881-019-0893-9
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- Article
A novel mutation in SEPN1 causing rigid spine muscular dystrophy 1: a Case report.
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- BMC Medical Genetics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12881-018-0743-1
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- Article
EPS8 variant causes deafness, autosomal recessive 102 (DFNB102) and literature review.
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- Human Genome Variation, 2023, v. 10, n. 1, p. 1, doi. 10.1038/s41439-023-00229-w
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- Article
Association of NAD (P) H Quinine Oxidoreductase 1 rs1800566 Polymorphism with Bladder and Prostate Cancers - a Systematic Review and Meta-Analysis.
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- Journal of the Czech & Slovak Societies for Oncology / Klinická Onkologie, 2020, v. 33, n. 2, p. 92, doi. 10.14735/amko202092
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- Article
Association of MTHFR 677C>T, 1298A>C and MTR 2756A>G Polymorphisms with Risk of Retinoblastoma.
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- Journal of the Czech & Slovak Societies for Oncology / Klinická Onkologie, 2019, v. 32, n. 5, p. 375, doi. 10.14735/amko2019375
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- Article
Expression Levels of LINC01296 and LINC00152 in Breast Cancer Tissue: Association with the Use of Oral Contraceptives.
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- Eurasian Journal of Medicine & Oncology, 2022, v. 6, n. 1, p. 83, doi. 10.14744/ejmo.2022.33174
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- Article
Association of MATN-3 and ADIPOQ Polymorphisms with Susceptibility to Knee Osteoarthritis.
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- Eurasian Journal of Medicine & Oncology, 2021, v. 5, n. 4, p. 291, doi. 10.14744/ejmo.2021.23898
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- Article
A pathogenic variant of TULP3 causes renal and hepatic fibrocystic disease.
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- Frontiers in Genetics, 2022, v. 13, p. 01, doi. 10.3389/fgene.2022.1021037
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- Article
Altered Expression of hsa_circ_0001445 and hsa_circ_0020397 in Breast Cancer Representing Associations with BMI and Reproductive Factors.
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- Archives of Iranian Medicine (AIM), 2022, v. 25, n. 12, p. 817, doi. 10.34172/aim.2022.127
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- Article
Gender difference in determinant factors of being overweight among the 40-70-year-old population of Kharameh cohort study, Iran.
- Published in:
- 2021
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- Publication type:
- journal article
Association of IL-10 -1082A>G, -819C>T, and -592C>A polymorphisms with susceptibility to chronic and aggressive periodontitis: a systematic review and meta-analysis.
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- Inflammation Research, 2021, v. 70, n. 5, p. 509, doi. 10.1007/s00011-021-01448-z
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- Article
Correction: A novel frameshift pathogenic variant in ST3GAL5 causing salt and pepper developmental regression syndrome (SPDRS): a case report.
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- 2021
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- Correction Notice
Two novel Warburg micro syndrome 1 cases caused by pathogenic variants in RAB3GAP1.
- Published in:
- Human Genome Variation, 2021, v. 8, n. 1, p. 1, doi. 10.1038/s41439-021-00171-9
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- Publication type:
- Article
A novel frameshift pathogenic variant in ST3GAL5 causing salt and pepper developmental regression syndrome (SPDRS): A case report.
- Published in:
- Human Genome Variation, 2021, v. 8, n. 1, p. 1, doi. 10.1038/s41439-021-00164-8
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- Publication type:
- Article
A single-amino-acid in-frame deletion in CYP17A1 results in combined 17-hydroxylase and 17,20-lyase deficiency in an Iranian family despite the protein mutation site.
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- Human Genome Variation, 2021, v. 8, n. 1, p. 1, doi. 10.1038/s41439-021-00160-y
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- Publication type:
- Article
A novel PTRH2 missense mutation causing IMNEPD: a case report.
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- Human Genome Variation, 2021, v. 8, n. 1, p. 1, doi. 10.1038/s41439-021-00147-9
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- Article
A Candidate Gene Association Study of Bone Mineral Density in an Iranian Population.
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- Frontiers in Endocrinology, 2016, v. 7, p. 1, doi. 10.3389/fendo.2016.00141
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- Article
Association of PAI-1 rs1799889 Polymorphism with Susceptibility to Ischemic Stroke: a Huge Meta-Analysis based on 44 Studies.
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- Acta Medica, 2020, v. 63, n. 1, p. 31, doi. 10.14712/18059694.2020.13
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- Publication type:
- Article
Association of IL-6 -174 G>C Polymorphism with Susceptibility to Colorectal Cancer and Gastric Cancer: a Systematic Review and Meta-Analysis.
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- Acta Medica, 2019, v. 62, n. 4, p. 137, doi. 10.14712/18059694.2020.2
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- Publication type:
- Article
Association of Transforming Growth Factor-β1 rs1982073 Polymorphism with Susceptibility to Acute Renal Rejection: a Systematic Review and Meta-Analysis.
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- 2021
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- Publication type:
- journal article
Association of Endothelial Nitric Oxide Synthase Gene Polymorphisms with Susceptibility to Prostate Cancer: a Comprehensive Systematic Review and Meta-Analysis.
- Published in:
- 2020
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- Publication type:
- journal article
Correlation between rs1800871, rs1800872 and rs1800896 Polymorphisms at IL-10 Gene and Lung Cancer Risk.
- Published in:
- Asian Pacific Journal of Cancer Prevention, 2024, v. 25, n. 1, p. 287, doi. 10.31557/APJCP.2024.25.1.287
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- Publication type:
- Article
Novel insight into the ectodermal dysplasia 11A: Splicing variant of the EDARADD gene in a family with clinical variability and literature review.
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- Journal of Dermatology, 2023, v. 50, n. 10, p. 1357, doi. 10.1111/1346-8138.16849
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- Article
Intronic OTOF mutation causes an atypical splicing defect resulting in auditory neuropathy spectrum disorder.
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- Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-023-01420-2
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- Publication type:
- Article
MCM2 mutation causes autosomal dominant nonsyndromic hearing loss (DFNA70): novel variant in the second family.
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- Journal of Genetics, 2022, v. 101, n. 1, p. 1, doi. 10.1007/s12041-022-01364-z
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- Publication type:
- Article
Exome sequencing identified a de novo frameshift pathogenic variant of CTBP1 in an extremely rare case of HADDTS.
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- Journal of Genetics, 2021, v. 100, n. 2, p. 1, doi. 10.1007/s12041-021-01315-0
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- Article
A novel nonsense variant in the ATL3 gene is associated with disturbed pain sensitivity, numbness of distal limbs and muscle weakness.
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- Annals of Human Genetics, 2023, v. 87, n. 4, p. 147, doi. 10.1111/ahg.12501
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- Article
Clinical features of patients with Yin Yang 1 deficiency causing Gabriele‐de Vries syndrome: A new case and review of the literature.
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- Annals of Human Genetics, 2022, v. 86, n. 1, p. 52, doi. 10.1111/ahg.12448
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- Publication type:
- Article