Reach Us +44-7480-724769
Journal of Genetics and DNA Research- Open Access Journals

Journal of Genetics and DNA Research
Open Access

OMICS International organises 3000+ Global Conferenceseries Events every year across USA, Europe & Asia with support from 1000 more scientific Societies and Publishes 700+ Open Access Journals which contains over 50000 eminent personalities, reputed scientists as editorial board members.

Open Access Journals gaining more Readers and Citations
700 Journals and 15,000,000 Readers Each Journal is getting 25,000+ Readers

This Readership is 10 times more when compared to other Subscription Journals (Source: Google Analytics)
All submissions of the EM system will be redirected to Online Manuscript Submission System. Authors are requested to submit articles directly to Online Manuscript Submission System of respective journal.
Editorial Board
Editor Image

Dr. E. Shyam P. Reddy
Department of Obstetrics and Gynecology
Morehouse School of Medicine

Editor Image

Dr. Esteban Galeano Gomez
Director of research and development projects
ACSAS Company

Editor Image

Dr. Xinmin An
Department of Horticulture
Zhejiang University

Recommended Conferences
Submit Manuscript

Submit manuscript at or send as an e-mail attachment to the Editorial Office at [email protected]

Table of Contents
About the Journal

Indexed in - Open Jgate, CNKI, Journal Guide

Index Copernicus Value (ICV 2016): 110.89

Journal of Genetics and DNA Research is a reputed peer reviewed, open access journal that aims to publish research articles that explore the role of genetics to various human disorders and the way to address them effectively.

The journal thus aim at geneticists, DNA experts, counsellors, medical professionals, clinical and diagnostic practitioners, researchers and students that work on various evolutionary and developmental genetics.

It encompasses a broad spectrum of themes in the field of genetics , including Genetic Code; Genetic Disorder; Genetic linkages; Genome Biology; Genome Sequencing; Human Genetics; Mendelian Genetics; DNA Replication; Functional Genomics; Gene cloning; Genetic Probes; Genetically engineering foods; Recombinant DNA; Trans-Genesis; RNA Splicing; DNA fingerprinting; Chromosomal Abnormalities; Gene Flow; Genetic Diversity; Genetic Syndromes; Hereditary Diseases; Mutation; Inherited Diseases; Population Genetics, etc.

Indexing: The journal is registered with the following abstracting partners: Google Scholar, Index Copernicus, Open JGate, Baidu Scholar, CNKI (China National Knowledge Infrastructure), EBSCO Publishing's Electronic Databases, Exlibris-Primo Central, Hinari, Infotrieve, Journal Guide, National Science Library, ProQuest, TdNet.

The journal encourages original manuscripts for publication in the form of research articles, reviews, commentaries, short communication, letters to the editors, editorials, etc.

The authors can submit the manuscript online at or send it as an e-mail attachment at [email protected] 


A gene is a sequence of DNA or RNA that is needed to contribute to a function. They are the working subunits of DNA that contains a particular set of instructions, usually coding for a particular protein or for a particular function. They are the basic physical and functional units of heredity.

DNA Mutations

DNA mutations are permanent changes in the DNA sequence of a gene, such that the sequence differs from what is found in most people. Mutations range in size; they can affect anywhere from a single DNA base pair to a large segment of a chromosome that includes multiple genes. They change the way a cell or whole organism functions. Some mutations even cause lethality, while others have no effect.

Single Nucleotide Polymorphisms

Single nucleotide polymorphisms, abbreviated as SNPs, are the most common type of genetic variations among people. Each SNP represents a difference in a single DNA building block, called a nucleotide. It is a variation in a single nucleotide that occurs at a specific position in the genome, where each variation is present to some appreciable degree within a population. It occurrs when a single nucleotide adenine (A), thymine (T), cytosine (C), or guanine (G) in the genome (or other shared sequence) differs between members of a species or paired chromosomes in an individual. SNPs in humans can affect how humans develop diseases and respond to pathogens, chemicals, medication, vaccines, and other agents.

Chromosomal Aberrations

Chromosomal abberations are the alterations in the structure of individual chromosome which may occur spontaneously or by induction through mutagenic agents. Such changes may result in quantitative alteration of genes or rearrangement of genes through loss, gain or reallocation of chromosomal segments.

Inherited Disorders

An inherited disease is caused by a change or mutation in an individual’s DNA. Since genes are passed from parent to child, any changes in the DNA within a gene are also passed. Families at risk for such inherited diseases should consult a certified genetic counsellor. It may be necessary to check each parent's DNA to learn about some genetic inheritance patterns. A careful family pedigree (chart of members of the family) and history may help determine risks for certain problems.

Recombinant DNA Technology

Recombinant DNA technology is the deliberate, controlled manipulation of the genes in an organism with the intent of making that organism better in some way. It includes a bunch of techniques that produce unlimited amounts of otherwise unavailable or scarce biological product by introducing DNA isolated from animals or plants into bacteria and then harvesting the product from a bacterial colony.

Recently Published Articles

Leave Your Message 24x7