Genetics Polymorphism

Genetics Polymorphism is a significant research area within Hereditary Diseases. This topic page brings together current knowledge, practical applications, and the main scientific questions that shape ongoing work in Genetics Polymorphism. It helps readers understand how the subject connects with study design, evidence quality, data interpretation, clinical or technical relevance, and the broader direction of the field. Researchers, authors, and reviewers can use this page to identify related articles, compare recent findings, and follow emerging themes that influence publication decisions and future investigation. By organizing published content around Genetics Polymorphism, the journal makes the topic easier to discover, easier to evaluate, and more useful for readers looking for focused, up-to-date scientific context.

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Related Articles

16 article(s) found
Single Nucleotide Polymorphisms associated with alimentary fatty liver disease are not genetic risk factors for treatment-associated hepatic steatosis in HIV patients on HAART
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Genetic Polymorphisms in Patients with Epilepsy: A Mini Review.
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Epigenetics and Nutrition
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A study on the association of ACE i/D gene polymorphism, Obesity, Blood pressure and susceptibility of type 2 diabetes mellitus among the Kurmis of West Bengal, India.
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Fast Screening Method for Polymorphisms in Exon 9 of the Catalase Gene.
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Single Nucleotide Polymorphism Profiles of Patients with Acute Renal Rejection to Personalize Immunosuppressive Therapy: Preliminary Results from An On-Going, Italian Study
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Scientific and Technological Interventions for Attaining Precision in Plant Genetics and Breeding
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D Allele and DD Genotype of I /D Polymorphism in The ACE Gene in Patients with Hypertension, Stroke And Cancer Prostate In Libreville: A Concern Given The High Frequencies of these Signatures in Gabonese Population
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L162v Polymorphism of Par-Α Gene, A603g Polymorphism of Tissue Factor Gene and Risk of Coronary Heart Disease in Russian Population
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Natural Selection in a Population is a Problem of Nonlinear Genetics
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Association of BsmI and ApaI Polymorphisms of the Vitamin D Receptor Gene with Dyslipidemia in Patients with Coronary Artery Disease.
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The Intersection of Cultural Characteristics and Genetics on the Prevalence of Delayed Sleep Phase Syndrome in Brazilian and Japanese Adults
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Molecular Study of Hepcidin HAMP (-582A/G) Gene Polymorphisms and Measurement of Serum Hepcidin Level among Sudanese Patients with Anemia of Chronic Kidney Disease
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Stem Cell Differentiation Stage Factors (SCDSFs) Taken from Zebrafish Embryo during Organogenesis and their Role as Epigenetics Regulators able to Reverse Neurosensory Hearing Loss
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Rbm45 Phylogenetics, Protein Domain Conservation, and Gene Architecture in Clade Metazoa
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Plasma TREM2 Levels, Alcohol Consumption, and Liver Enzymes in Patients with Alcohol use Disorder: A Sex-Dependent Relationship Involving MS4A6A Genetic Polymorphism
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