Lista de obras - Hamid Ghaedi - Dominio Público Uruguay

A Bioinformatics Approach to the Identification of Variants Associated with Type 1 and Type 2 Diabetes Mellitus that Reside in Functionally Validated miRNAs Binding Sites.

artículo científico publicado en 2016

A genetic variant in CAMKK2 gene is possibly associated with increased risk of bipolar disorder.

artículo científico publicado en 2015

A genetic variant in miRNA binding site of glutamate receptor 4, metabotropic (GRM4) is associated with increased risk of major depressive disorder.

artículo científico publicado en 2016

A novel mutation and variable phenotypic expression in a large consanguineous pedigree with Jalili syndrome.

artículo científico publicado en 2016

An Association Study between Longitudinal Changes of Leukocyte Telomere and the Risk of Azoospermia in a Population of Iranian Infertile Men

artículo científico publicado en 2018

Analysis of beta-hemolysis in human blood agars by Streptococcus pyogenes

artículo científico publicado en 2011

Association of miR-146a rs2910164 and miR-149 rs2292832 Variants with Susceptibility to Type 2 Diabetes.

artículo científico publicado en 2016

Bioinformatics prioritization of SNPs perturbing microRNA regulation of hematological malignancy-implicated genes.

artículo científico publicado en 2015

Copy Number Variants in Patients with Autism and Additional Clinical Features: Report of VIPR2 Duplication and a Novel Microduplication Syndrome.

artículo científico publicado en 2016

Genetic Variants of Cytochrome b-245, Alpha Polypeptide Gene and Premature Acute Myocardial Infarction Risk in an Iranian Population.

artículo científico publicado en 2015

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

scientific article published on 19 November 2019

Impact of ATM and SLC22A1 Polymorphisms on Therapeutic Response to Metformin in Iranian Diabetic Patients

scientific article published on January 2016

In silico dissection of miRNA targetome polymorphisms and their role in regulating miRNA-mediated gene expression in esophageal cancer.

artículo científico publicado en 2016

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

artículo científico publicado en 2020

Single-Nucleotide Polymorphisms Within MicroRNAs Sequences and Their 3' UTR Target Sites May Regulate Gene Expression in Gastrointestinal Tract Cancers.

artículo científico publicado en 2014

The clinical significance of miR-335, miR-124, miR-218 and miR-484 downregulation in gastric cancer

scientific article published on 31 August 2018

The effects of somatic mutations on EGFR interaction with anti-EGFR monoclonal antibodies: Implication for acquired resistance

artículo científico publicado en 2019

The pre-mir-27a variant rs895819 may contribute to type 2 diabetes mellitus susceptibility in an Iranian cohort.

artículo científico publicado en 2016

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

artículo científico publicado en 2016

Variation in the miRNA-433 binding site of FGF20 is a risk factor for Parkinson's disease in Iranian population

artículo científico publicado en 2015

c.376G>A mutation in WFS1 gene causes Wolfram syndrome without deafness.

artículo científico publicado en 2016

Lista de obras de Hamid Ghaedi

A Bioinformatics Approach to the Identification of Variants Associated with Type 1 and Type 2 Diabetes Mellitus that Reside in Functionally Validated miRNAs Binding Sites.

A genetic variant in CAMKK2 gene is possibly associated with increased risk of bipolar disorder.

A genetic variant in miRNA binding site of glutamate receptor 4, metabotropic (GRM4) is associated with increased risk of major depressive disorder.

A novel mutation and variable phenotypic expression in a large consanguineous pedigree with Jalili syndrome.

An Association Study between Longitudinal Changes of Leukocyte Telomere and the Risk of Azoospermia in a Population of Iranian Infertile Men

Analysis of beta-hemolysis in human blood agars by Streptococcus pyogenes

Association of miR-146a rs2910164 and miR-149 rs2292832 Variants with Susceptibility to Type 2 Diabetes.

Bioinformatics prioritization of SNPs perturbing microRNA regulation of hematological malignancy-implicated genes.

Copy Number Variants in Patients with Autism and Additional Clinical Features: Report of VIPR2 Duplication and a Novel Microduplication Syndrome.

Genetic Variants of Cytochrome b-245, Alpha Polypeptide Gene and Premature Acute Myocardial Infarction Risk in an Iranian Population.

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

Impact of ATM and SLC22A1 Polymorphisms on Therapeutic Response to Metformin in Iranian Diabetic Patients

In silico dissection of miRNA targetome polymorphisms and their role in regulating miRNA-mediated gene expression in esophageal cancer.

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

Single-Nucleotide Polymorphisms Within MicroRNAs Sequences and Their 3' UTR Target Sites May Regulate Gene Expression in Gastrointestinal Tract Cancers.

The clinical significance of miR-335, miR-124, miR-218 and miR-484 downregulation in gastric cancer

The effects of somatic mutations on EGFR interaction with anti-EGFR monoclonal antibodies: Implication for acquired resistance

The pre-mir-27a variant rs895819 may contribute to type 2 diabetes mellitus susceptibility in an Iranian cohort.

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

Variation in the miRNA-433 binding site of FGF20 is a risk factor for Parkinson's disease in Iranian population

c.376G>A mutation in WFS1 gene causes Wolfram syndrome without deafness.