ISSN: 2161-1041

Hereditary Genetics: Current Research
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Journal Impact Factor 0.93*
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About the Journal

NLM ID: 101588596

Hereditary Genetics is disease that is inherited genetically. They are also known as genetic disorders or inherited diseases. It is a disease that is passed from one generation to another generation through defective genes by which particular characteristics are transmitted from parents to their offspring. The chromosomes are mainly responsible that these diseases are transmitted in the same family. The genes we are born with may contribute to our risk of developing certain types of hereditary diseases like cancer, Diabetes, Autosomal Dominant Diseases, Color Blindness.

Hereditary Genetics: Current Research is a peer reviewed scientific journal known for rapid dissemination of high-quality research. This Hereditary Genetics Journal with high impact factor offers an open access platform to the authors in academia and industry to publish their novel research. It serves the International Scientific Community with its standard research publications. Hereditary Genetics: Current Research is a scientific journal includes a wide range of fields in its discipline to create a platform for the authors to make their contribution towards the journal and the editorial office promises a peer review process for the submitted manuscripts for the quality of publishing. Hereditary Genetics: Current Research is one of the best Open Access journals of Scholarly publishing.

Hereditary Genetics: Current Research is scholarly Open Access journal and aims to publish the most complete and reliable source of information on the discoveries and current developments in the mode of original articles, review articles, case reports, short communications, etc. in all areas of Heredity and Genetics and making them freely available through online without any restrictions or any other subscriptions to researchers worldwide.

The journal is using the Editorial Manager System for quality in the peer review process. Editorial Manager is an online manuscript submission, review and tracking systems. The review process is performed by the Editorial board members of Hereditary Genetics: Current Research or outside experts; at least two independent reviewer’s approval followed by editor approval is required for acceptance of any citable manuscript. Authors may submit manuscripts and track their progress through the system, hopefully to publication. Reviewers can download manuscripts and submit their opinions to the editor. Editors can manage the whole submission/review/revise/publish process. 

Genetic Drift

Genetic Drift is the change in the frequency of a gene variant (allele) in a population due to random sampling of organisms. In large populations, the effects of genetic drift are negligible. Genetic drift describes random fluctuations in the numbers of gene variants in a population.

Related Journals of Genetic Drift

Molecular and Genetic MedicinePhylogenetics & Evolutionary BiologyGene TechnologyGenetic Syndromes & Gene TherapySabrao Journal of Breeding and Genetics, Topics in Current Genetics, Trends in Genetics, Molecular genetic medicine, American Journal of Medical Genetics, Cytogenetics and Cell Genetics, Japanese Journal of Genetics, Korean Journal of Genetics, Canadian Journal of Genetics and Cytology

Population Genetics

Population Genetics is the detailed study of the distributions and changes of allele frequency in a population, as it is subject to the four main evolutionary processes: genetic drift, natural selection, mutation and recombination.

Related Journals of Population Genetics

Phylogenetics & Evolutionary Biology, Genetic Disorders & Genetic ReportsGene TechnologyCellular and Molecular BiologyMathematical Population Studies, Theoretical Population Biology, Asian Population Studies, Comparative Population Studies, Journal of Population Economics, Journal of Population Research, Local Population Studies, Population and Development Review

Evolutionary Genetics

Evolutionary Genetics is the study of how genetic variations leads to evolutionary changes. It includes evolution of genome structure, genetic change in response to selection within populations, and the genetic basis of speciation and adaptation

Related Journals of Evolutionary Genetics

Genetic Syndromes & Gene TherapyPhylogenetics & Evolutionary Biology, Genetic Disorders & Genetic ReportsCell & Developmental BiologyJournal of Social, Evolutionary, and Cultural Psychology, Journal of Evolutionary Economics, Evolutionary Computation, Genetic Programming and Evolvable Machines, Genetic Counseling, Genetic Epidemiology

Genetic Disorder

A genetic disorder is a genetic problem which is caused by one or more abnormalities in the genome, especially a condition that is present from birth. Genetic disorder is caused by mutations in the chromosomal DNA of mitochondria.

Related Journals of Genetic Disorder

Genetic Disorders & Genetic ReportsGenetic Syndromes & Gene Therapy, Molecular Cloning & Genetic RecombinationCellular and Molecular BiologyGenetics Society of America, Chinese Journal of Medical Genetics, Egyptian Journal of Medical Human Genetics, Genetic Counseling, Genetic Epidemiology, Genetic Testing and Molecular Biomarkers, Genetics and Molecular Research

Genetic Syndromes

A syndrome is a collection of recognizable traits that tend to occur together and are associated with a specific disease which has more than one identifying feature or symptom. Each genetic syndrome will have many characteristic features, depending on which aspects of development are affected by the chromosomes or abnormal genes.

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Genetic Syndromes & Gene Therapy, Genetic Disorders & Genetic Reports, Molecular Cloning & Genetic RecombinationCellular and Molecular BiologyProteins: Structure, Function and Genetics, Developmental Genetics, Ophthalmic Paediatrics and Genetics, Journal of Craniofacial Genetics and Developmental Biology, UCLA Immunogenetics Center, Genetics Society of America, Cancer genetics, Chinese Journal of Medical Genetics

Gene Flow

In population genetics, gene flow which is also known as gene migration. Gene flow is the transfer of alleles or genes from one population to another. Migration into or out of a population may be responsible for a marked change in allele frequencies.

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Fungal Genomics & BiologyClinical & Medical Genomics, Molecular Cloning & Genetic RecombinationGene TechnologyMolecular Phylogenetics and Evolution, Mutagenesis, Mutation Research- Fundamental and Molecular Mechanisms of Mutagenesis, Mutation Research- Genetic Toxicology and Environmental Mutagenesis, Nature Genetics, Nature Reviews Genetics, Neurogenetics, Russian Journal of Genetics, Russian Journal of Genetics: Applied Research

Genetic Skin Disorders

Genetic diseases are mainly affecting the skin and its appendages. These are caused by single-gene mutations. Genetic skin disorders are also called as genodermatoses. Nearly forty four skin diseases are there some of them are skin cancer, lupus, acne, psoriasis, hives, warts, carbuncle, and hyperhidrosis.

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Genetic Diversity

Genetic diversity means the total number of genetic characteristics in the genetic makeup of a species. It is distinguished from genetic variations, which describes about the tendency of genetic characteristics to vary.

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Molecular and Genetic MedicinePhylogenetics & Evolutionary BiologyGene TechnologyGenetic Syndromes & Gene TherapyGenetic Testing and Molecular Biomarkers, Genetics and Molecular Research, Journal of Community Genetics, Journal of Genetic Counseling, Twin Research and Human Genetics, Developmental Genetics, Genetics Society of America

Genetic Testing for Diseases

This is the analysis of chromosomes, proteins, and metabolites. Genetic testing for diseases can provide important information for diagnosing, treating and preventing illness. Genetic testing identifies the changes in chromosomes, genes, or proteins. These are performed on a sample of blood, hair, skin, amniotic fluid, or other tissue.

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Advancements in Genetic EngineeringClinical & Medical GenomicsMolecular Biomarkers & DiagnosisMolecular and Genetic MedicineSoviet genetics, Genetics Society of Japan/Nihon Iden Gakkai, The Korean Society of Genetics, Genetics Society of America, Annual Review of Genetics

Genetic Diseases Screening

It is used to determine whether a couple is at increased risk of having baby with a hereditary genetic disorder. This is called as new-born screening. These are used just after birth to identify genetic disorders. Genetic diseases creening is particularly recommended when family members having genetic abnormality, one or both partners know they have a genetic abnormality.

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Genetic Syndromes & Gene Therapy, Genetic Disorders & Genetic ReportsCellular and Molecular BiologyPhylogenetics & Evolutionary BiologySoviet genetics, Genetics Society of Japan/Nihon Iden Gakkai, The Korean Society of Genetics, Genetics Society of America, Annual Review of Genetics, Mutation Research, Mutation Research Letters, Human Mutation, Application of Clinical Genetics

Hereditary Mutation

A change of gene that occurs in germ cell and is then incorporated into every cell in the developing body of the new organism. For hereditary mutations to affect on organism descendants, they must occur in the cells that produce the next generation and affect the hereditary materials.

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Carcinogenesis & MutagenesisPhylogenetics & Evolutionary BiologyGenetic Syndromes & Gene TherapyPhylogenetics & Evolutionary Biology, Mutation Research, Mutation Research Letters, Human Mutation, Mutation Research- Reviews in Mutation Research, Mutation Research- Fundamental and Molecular Mechanisms of Mutagenesis, Mutation Research- Genetic Toxicology and Environmental Mutagenesis, Mutagenesis

Hereditary Disorders

Hereditary Disorders is applied to diseases such as hemophilia and characteristics such as the tendency toward baldness that pass from parents to children. These are caused by disturbances in storage, transmission, and production of genetic information. These are caused primarily by chromosomal and gene mutations.

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Genetic Syndromes & Gene Therapy, Genetic Disorders & Genetic Reports, Molecular Cloning & Genetic RecombinationCellular and Molecular BiologySoviet genetics, Genetics Society of Japan/Nihon Iden Gakkai, The Korean Society of Genetics, Genetics Society of America, Annual Review of Genetics, Mutation Research- Mutation Research Letters, Human Mutation, Mutation Research- Reviews in Mutation Research

Hereditary Blood Disorders

Hereditary Blood Disorders occur in red blood cells, white blood cells, and platelets. These can also affect the liquid portion of blood, called plasma. Symptoms of blood disorders include unexplained nosebleeds, excessive bruising, bleeding into joints, muscles and soft tissues.

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Blood Disorders & Transfusion, Blood, Blood & Lymph, Insights in Blood PressureBMC Blood Disorders, Clinical Medicine Insights: Blood Disorders, Pediatric Blood and Cancer, Biology of Blood and Marrow Transplantation, Indian Journal of Hematology and Blood Transfusion, Journal of Cerebral Blood Flow and Metabolism

Hereditary Diseases

It is a disease or disorder that is inherited genetically. Hereditary Diseases are passed on from one generation to another through defective genes. These diseases are transmitted in the same family. The chromosomes in the humans are responsible for passing the traits from the parent to the offspring.

Related Journals of Hereditary Diseases

Genetic Syndromes & Gene Therapy, Genetic Disorders & Genetic Reports, Molecular Cloning & Genetic RecombinationCellular and Molecular BiologySoviet genetics, Genetics Society of Japan/Nihon Iden Gakkai, The Korean Society of Genetics, Genetics Society of America, Annual Review of Genetics, Mutation Research, Mutation Research Letters, Human Mutation

Cancer Genetics

Cancer is a genetic disease. It is caused by certain changes to genes that control the way of cells function. Cancer Genetic changes include mutations in the DNA. Genetic changes that occur after conception are called somatic changes. They arise at any time during a person’s life.

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Cancer SurgeryCancer Science & TherapyCancer Medicine & Anti Cancer DrugsCancer Clinical TrialsCancer genetics, Cancer Discovery, Cancer and Chemotherapy Reviews, Cancer Epidemiology Biomarkers and Prevention, Cancer Imaging, Cancer Letters, Cancer Immunity, Cancer Prevention Research, Balkan Journal of Medical Genetics

Inherited Diseases

It is a genetic problem caused by one or more abnormalities in the genome. There are some conditions in which the genetic changes are responsible for causing the condition. These are called inherited diseases or genetic disorder. Sometimes this change can cause mistakes in the protein instructions.

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Chromosomal Abnormalities

The condition of having an abnormal number of chromosomes, or having chromosomes with missing or extra pieces. These can be organized into two basic groups: numerical abnormalities and structural abnormalities. Chromosome abnormalities are occurring as an accident in the egg or sperm.

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Genetic Codon

The means by which DNA and RNA molecules carry genetic information in living cells. The code defines how sequences of these nucleotide triplets, called codons, specify which amino acid will be added next during protein synthesis. The genetic codon determines the protein sequence for a given coding region.

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Gene Sequencing

It is the laboratory process that determines the complete DNA sequence of an organism’s genome at a single time. The genome sequencing of a single cell selected from a mixed population of cells can be determined using techniques of single cell genome sequencing.

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Genetic Syndromes & Gene TherapyCell & Developmental BiologyMolecular Cloning & Genetic RecombinationGene TechnologyGenes Chromosomes and Cancer, Genes, Brain and Behavior, Chromosoma, Genes and Immunity, Genetica, Genetical Research, Genetics and Molecular Biology, Genome Biology and Evolution, Genetics Society of Japan/Nihon Iden Gakkai, The Korean Society of Genetics

Human Mutation

A human mutation occurs when a DNA gene is damaged or changed in such a way that as to alter the genetic message carried by that gene. A Mutagen is an agent of substance that can bring about a permanent alteration to the physical composition of a DNA gene such that the genetic message is changed.

Related Journals of Human Mutation

Carcinogenesis & MutagenesisPhylogenetics & Evolutionary BiologyGenetic Syndromes & Gene TherapyPhylogenetics & Evolutionary Biology, Mutation Research, Mutation Research Letters, Human Mutation, Mutation Research- Reviews in Mutation Research, Mutation Research- Fundamental and Molecular Mechanisms of Mutagenesis, Mutation Research- Genetic Toxicology and Environmental Mutagenesis, Mutagenesis

 

Journal of Hereditary Genetics: Current Research is associated with our international conference "World Congress on Human Genetics", October 31- November 2, 2016 Valencia, Spain. We are particularly interested in Hereditary Genetics in the areas of Types of Biomarkers, Functional Genomics and Cytogenetic Biomarkers, Biomarkers of Exposure Response and Susceptibility, Biomarkers for Disorders, Biomarkers in Nanoscience, Biomarkers Industry & Market Analysis, We encourage articles involving Hereditary angioedema, Hereditary-spastic, Hereditary-cancer, Hereditary neuropathy, Hereditary colorectal, Epigenetics, Haemo chromatosis, Schizophrenia, Hereditary breast cancer

Journal Highlights

 

Major Disease Statistics

*Unofficial 2015 Journal Impact Factor was established by dividing the number of articles published in 2013 and 2014 with the number of times they are cited in 2015 based on Google search and the Scholar Citation Index database. If 'X' is the total number of articles published in 2013 and 2014, and 'Y' is the number of times these articles were cited in indexed journals during 2015 then, impact factor = Y/X
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