Egyptian Journal of Medical Human Genetics

The association between angiotensin II type 1 receptor A1166C gene polymorphism and the risk of essential hypertension: a meta-analysis

Telomere reprogramming during fetal life in low socioeconomic mothers

Association study of TAAAA polymorphism in the first intron of p53 gene with risk of colorectal cancer in Iranian population

Study of the impact of consanguinity on abortion and mortality in the population of Beni Abbes (southwestern Algeria)

Non-randomness distribution of micro-RNAs on human chromosomes

Plasminogen activator inhibitor-1 gene polymorphism as a risk factor for vascular complications in type 2 diabetes mellitus

Serum level and single-nucleotide polymorphisms of toll-like receptor-7 among urinary bladder cancer Iraqi patients

Therapeutic potential of Hsp27 in neurological diseases

Adiponectin and human eating behaviour: a Mendelian randomization study

Aberrant p16 methylation as an early diagnostic marker in blood of hepatocellular carcinoma patients

MPL W515\u2009L/K mutations in myeloproliferative neoplasms

Aberrant methylation of yes-associated protein (YAP1) as a potential biomarker in breast cancer

The demographic data and the high frequency of chromosome/chromatid breaks as biomarkers for genome integrity have a role in predicting the susceptibility to have Down syndrome in a cohort of Egyptian young-aged mothers

Association of insulin gene VNTR INS -23/Hph1 A>T (rs689) polymorphism with type 1 diabetes mellitus in Egyptian children

Association between calcium-sensing receptor (CaSR) R990G, CaSR A986S, and CaSR Q1011E gene polymorphisms and the risk of urolithiasis: a meta-analysis

Omphalocele: a review of common genetic etiologies

The role of protein inhibitor of activated STAT3 and miRNA-18a expressions in breast cancer

Determinants of p14/ARF methylation in healthy females: association with reproductive and non-reproductive risk factors of breast cancer

D76V, L161R, and C117S are the most pathogenic amino acid substitutions with several dangerous consequences on leptin structure, function, and stability

MTHFR gene polymorphism and associated nutritional deficiency in the etiology and pathogenesis of Down syndrome

Screening for B cell, T cell and natural killer cell defects among children with methylmalonic and propionic acidemias

Influence of dopaminergic system gene polymorphisms on mixed amphetamine-type stimulants and opioid dependence in Malaysian Malays

Induction of inflammatory response in human cell lines by arsenic-contaminated soil-isolated bacterium Micrococcus sp. KUMAs15

Clinicopathological features of Egyptian colorectal cancer patients regarding somatic genetic mutations especially in KRAS gene and microsatellite instability status: a pilot study

Toxoplasmosis and abortion: pro- and anti-inflammatory cytokines gene expression of the host immune cells

Detection of high level aminoglycoside resistance genes among clinical isolates of Enterococcus species

Protective association of VDR gene polymorphisms and haplotypes with multiple sclerosis patients in Egyptian population

Association study of APOE gene polymorphisms with diabetes and the main cardiometabolic risk factors, in the Algerian population

Telomerase reverse transcriptase gene amplification in hematological malignancies

Association between fibrinogen receptor (Glycoprotein IIb) polymorphism and the risk of venous thromboembolism: a systematic review

Characterization of plasmid-mediated qnrA and qnrB genes among Enterobacteriaceae strains: quinolone resistance and ESBL production in Ismailia, Egypt

Prognostic implications of IDH1rs11554137 and IDH2R140Q SNPs mutations in cytogenetically normal acute myeloid leukemia

Flavanones from Sorghum bicolor selectively inhibit COX-2: in-silico and in-vivo validation

Gene-environment and gene-gene interactions between CHRNA3 rs1051730, XRCC1 rs25487, and ERCC1 rs735482 variants highly elevate the risk of lung cancer

Detection of some metabolic disorders in suspected neonates admitted at Assiut University Children Hospital