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Genotype–phenotype associations in hereditary spastic paraplegia: a systematic review and meta-analysis on 13,570 patients

Journal of neurology, 2021-06, Vol.268 (6), p.2065-2082

2021

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An updated review of the H19 lncRNA in human cancer: molecular mechanism and diagnostic and therapeutic importance

Molecular biology reports, 2020-08, Vol.47 (8), p.6357-6374

2020

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P628: Genomic hot spots in coding regions: Identifying regions enriched for heterozygote excess variants

Genetics in Medicine Open, 2024, Vol.2, p.101534, Article 101534

2024

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Mutually exclusive mutation profiles define functionally related genes in muscle invasive bladder cancer

PloS one, 2022-01, Vol.17 (1), p.e0259992-e0259992

2022

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SUCLG1 mutations and mitochondrial encephalomyopathy: a case study and review of the literature

Molecular biology reports, 2020-12, Vol.47 (12), p.9699-9714

2020

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The genetic basis for the inverse relationship between rheumatoid arthritis and schizophrenia

Molecular genetics & genomic medicine, 2020-11, Vol.8 (11), p.e1483-n/a

2020

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Association of MiR-146a Expression and Type 2 Diabetes Mellitus: A Meta-Analysis

International journal of molecular and cellular medicine, 2017, Vol.6 (3), p.156-163

2017

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Up-regulation of FOXN3-AS1 in invasive ductal carcinoma of breast cancer patients

Heliyon, 2021-10, Vol.7 (10), p.e08179-e08179, Article e08179

2021

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Whole-exome sequencing identified a novel mutation of MLH1 in an extended family with lynch syndrome

Genes & diseases, 2020-12, Vol.7 (4), p.614-619

2020

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Association of Lin-28A rs3811464 Variant with Susceptibility to Type 2 Diabetes

Journal of clinical and diagnostic research, 2017-11, Vol.11 (11), p.GC01-GC04

2017

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Association Between Two Common Polymorphisms of Vitamin D Binding Protein and the Risk of Coronary Artery Disease: a Case-Control Study

Journal of medical biochemistry, 2017-08, Vol.36 (4), p.349-357

2017

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Valproic acid may exerts its cytotoxic effect through rassf1a expression induction in acute myeloid leukemia

Tumor biology, 2016-08, Vol.37 (8), p.11001-11006

2016

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Variant Classification Discordance

The Journal of molecular diagnostics : JMD, 2024-02, Vol.26 (2), p.115-126

2024

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Variant Classification Discordance: Contributing Factors and Predictive Models

The Journal of molecular diagnostics : JMD, 2024-02, Vol.26 (2), p.115-126

2024

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MAP3K1 May be a Promising Susceptibility Gene for Type 2 Diabetes Mellitus in an Iranian Population

International journal of molecular and cellular medicine, 2016, Vol.5 (3), p.134-140

2016

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Genetic variants in long noncoding RNA H19 and MEG3 confer risk of type 2 diabetes in an Iranian population

Gene, 2018-10, Vol.675, p.265-271

2018

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Sphingosine 1-phosphate interacts with Survivin pathway to enhance tumorigenesis in cancer cells

Iranian journal of basic medical sciences, 2015-08, Vol.18 (8), p.813-821

2015

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Co-expression profiling of plasma miRNAs and long noncoding RNAs in gastric cancer patients

Gene, 2019-03, Vol.687, p.135-142

2019

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Circular RNAs in β-cell function and type 2 diabetes-related complications: a potential diagnostic and therapeutic approach

Molecular biology reports, 2019-10, Vol.46 (5), p.5631-5643

2019

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Genetic Variants Of Cytochrome b-245, Alpha Polypeptide Gene And Premature Acute Myocardial Infarction Risk In An Iranian Population

Journal of medical biochemistry, 2015-10, Vol.34 (4), p.402-408

2015

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Variation in the expression level of MALAT1, MIAT and XIST lncRNAs in coronary artery disease patients with and without type 2 diabetes mellitus

Archives of physiology and biochemistry, 2022-09, Vol.128 (5), p.1308-1315

2022

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Clinical significance of long noncoding RNA VIM‐AS1 and CTBP1‐AS2 expression in type 2 diabetes

Journal of cellular biochemistry, 2019-06, Vol.120 (6), p.9315-9323

2019

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MicroRNA-copy number variations in coronary artery disease patients with or without type 2 diabetes mellitus

Archives of physiology and biochemistry, 2021-11, Vol.127 (6), p.497-503

2021

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Long non-coding RNA LY86-AS1 and HCG27_201 expression in type 2 diabetes mellitus

Molecular biology reports, 2018-12, Vol.45 (6), p.2601-2608

2018

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Association between chronic obstructive pulmonary disease and interleukins gene variants: A systematic review and meta-analysis

Cytokine (Philadelphia, Pa.), 2019-05, Vol.117, p.65-71

2019

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Genotype–phenotype associations in hereditary spastic paraplegia: a systematic review and meta-analysis on 13,570 patients

An updated review of the H19 lncRNA in human cancer: molecular mechanism and diagnostic and therapeutic importance

P628: Genomic hot spots in coding regions: Identifying regions enriched for heterozygote excess variants

Mutually exclusive mutation profiles define functionally related genes in muscle invasive bladder cancer

SUCLG1 mutations and mitochondrial encephalomyopathy: a case study and review of the literature

The genetic basis for the inverse relationship between rheumatoid arthritis and schizophrenia

Association of MiR-146a Expression and Type 2 Diabetes Mellitus: A Meta-Analysis

Up-regulation of FOXN3-AS1 in invasive ductal carcinoma of breast cancer patients

Whole-exome sequencing identified a novel mutation of MLH1 in an extended family with lynch syndrome

Association of Lin-28A rs3811464 Variant with Susceptibility to Type 2 Diabetes

Association Between Two Common Polymorphisms of Vitamin D Binding Protein and the Risk of Coronary Artery Disease: a Case-Control Study

Valproic acid may exerts its cytotoxic effect through rassf1a expression induction in acute myeloid leukemia

Variant Classification Discordance

Variant Classification Discordance: Contributing Factors and Predictive Models

MAP3K1 May be a Promising Susceptibility Gene for Type 2 Diabetes Mellitus in an Iranian Population

Genetic variants in long noncoding RNA H19 and MEG3 confer risk of type 2 diabetes in an Iranian population

Sphingosine 1-phosphate interacts with Survivin pathway to enhance tumorigenesis in cancer cells

Co-expression profiling of plasma miRNAs and long noncoding RNAs in gastric cancer patients

Circular RNAs in β-cell function and type 2 diabetes-related complications: a potential diagnostic and therapeutic approach

Genetic Variants Of Cytochrome b-245, Alpha Polypeptide Gene And Premature Acute Myocardial Infarction Risk In An Iranian Population

Variation in the expression level of MALAT1, MIAT and XIST lncRNAs in coronary artery disease patients with and without type 2 diabetes mellitus

Clinical significance of long noncoding RNA VIM‐AS1 and CTBP1‐AS2 expression in type 2 diabetes

MicroRNA-copy number variations in coronary artery disease patients with or without type 2 diabetes mellitus

Long non-coding RNA LY86-AS1 and HCG27_201 expression in type 2 diabetes mellitus

Association between chronic obstructive pulmonary disease and interleukins gene variants: A systematic review and meta-analysis

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