The Journal emphasizes on structural and functional analysis of the genome which allows us to understand the function and contribution of genetic factors in terms of health and disease. It aims to the development of technologies for providing insights into the molecular, genetic and cellular basis of diseases, with growing opportunities for improving individualized patient care. It also focuses on genome technologies, including high-throughput genotyping, sequencing and the study of gene expression.
Journal of Clinical & Medical Genomics is an Open Access, peer-reviewed journal which aims to provide the most rapid and reliable source of information on current developments in the field of Clinical Trials. The emphasis will be on publishing quality papers quickly and freely available to researchers worldwide.
Journal of Clinical & Medical Genomics is an Open Access journal and aims to publish 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 the field and making them freely available through online without any restrictions or any other subscriptions to researchers worldwide.
The journal is using Editorial Manager System for quality in review process. Editorial Manager is an online manuscript submission, review and tracking systems. Review processing is performed by the editorial board members of Journal of Clinical & Medical Genomics or outside experts; at least two independent reviewers 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.
Genome sequencing is the process through which we can determine the whole DNA sequence of an organism at a single time. This genomic sequencing describes the both chromosomal and mitochondrial DNA Sequencing. Whole genome sequence data will be a significant device to guide therapeutic interpolation. As genome sequencing becomes more reachable, the ability to study the whole human genome quickens occasions for discovery of human disease.
Related Journals of Genomic Sequencing
Pharmacogenetics and Genomics, Genomics, BMC Genomics, Recent Patents on DNA and Gene Sequences, Journal of Gene Medicine, Mouse Genome, Genome Dynamics, Genome Integrity.
It is the branch of genomics science that deal with sequencing, analysis of genome sequence of the individual person. Genome sequence of individuals are discovered by using some different techniques like partial or full genome sequencing by using Next Generation Sequencing techniques and after that it is compared with the already published literature to discover the likelihood of disease risks and trait expressions. Personalized genomics builds on principles established by the integration of genetics into medical practice.
Related Journals of Personised Genomics
Comparative and Functional Genomics, Briefings in Functional Genomics, General Hospital Psychiatry, Genetics in Medicine, Molecular Genetics and Metabolism, Mutation Research - Genetic Toxicology and Environmental MutaGenesis.
Cancer start when normal cells start under go to some mutational changes and grow uncontrollably, result into a mass of cells called a tumor. Genes are made up of deoxyribonucleic acid (DNA), which comprises all of the chemical information that expresses cells what to do and when to do it. The biggest project started to understand the cancer genome is “the cancer genome atlas”. Project started in 2006 by the National Cancer Institute and the National Human Genome Research Institute. They create a “map” of various cancer genomes to better understand a normal cell compared to cancer cell and what makes one cancer different from another.
Related Journals of Cancer Genomics
Cancer Genomics and Proteomics, British Journal of Cancer, Genomics Proteomics Bioinformatics, European Journal of Cancer, Cancer Epidemiology Biomarkers and Prevention, Cancer and Metastasis Reviews, Molecular Cancer Research, Genes Chromosomes and Cancer.
Pharmacogenomics is the science to find out the gene of the individual organism response to drugs substances. Pharmacogenomics works by uniting traditional pharmaceutical sciences like biochemistry with the understanding of common DNA dissimilarities in the human genome. The applications of pharmacogenomics are the study of human variability in drug response. In the upcoming future pharmacogenomics help in the development of designer drugs to indulgence a wide range of health complications, including cardiovascular disease, Alzheimer disease, cancer, HIV/AIDS, and asthma.
Related Journals of Pharmacogenomics
Pharmacogenomics, Pharmacogenomics Journal, American Journal of PharmacoGenomics, Epigenomics, General and Comparative Endocrinology, Genome Research, Genome Biology, Cytogenetic and Genome Research.
Personalized medicine research utilizes all the genetic related information of a patient's genotype to: begin a curative measure against the start of a disease or condition, or select the most suitable treatment for a disease or condition that is good to that individual. The whole genome sequence of human help in the understanding of genetic disease and its cure, In future diagnosed the individual disease with specific medicine related to its genome map.
Related Journals of Personalized Medical Research
AIDS Care - Psychological and Socio-Medical Aspects of AIDS/HIV, Medical Science Monitor, Canadian Medical Association Journal, Annual Review of Biomedical Engineering, Current Medical Research and Opinion, Annals of Biomedical Engineering.
The medical science branch that involves the utilization of individual genomic information for his complete health care management. Now a day Genomic medicine is going to be an integral part of primary care for an individual person. By the help of genetic information doctor can easily diagnosis for genetic disease when it should going to happen in future before it will occur. Application of genomic medicine is: today’s oncology practice utilizing tumor genotyping of cancers such as melanoma, breast, colon and lung for targeting of therapy. Genetic screening of patients with a family history of breast or colon cancer can easily treat before it will become severe.
Related Journals of Genetics and Genomic Medicine
Pharmacogenetics and Genomics, Genome Medicine, Genome Biology and Evolution, Advances in Genome Biology, Genome Mapping and Genomics in Animals, Mammalian Genome, Nature Genetics American Journal of Human Genetics, Human Molecular Genetics.
Biomarker are the measurable indicator that indicates the presence or amount or severity of the disease state in the individual person. Existing genomics and biotechnology tools provide the assurance of the development of biomarkers to guess individual disease risk, empower initial recognition of disease, and enhance diagnostic classification to better inform individualized management. One of the extreme problems in the improvement and authentication of biomarkers is the uncertainty of the term and the catastrophe to distinguish that biomarker validity means fitness for proposed use. One greatest application of the Human Genome Project was the identification and development of biomarkers for ‘personalized, preventive and predictive medicine’.
Related Journals of Biomarkers in Genomic Medicine
Cancer Epidemiology Biomarkers and Prevention, Biomarkers, Genetic Testing and Molecular Biomarkers, Biomarkers in Medicine, Cancer Biomarkers, Genomic Medicine, Biomarkers, and Health Sciences, Open Biomarkers Journal.
Genetic engineering is the scientific method by which researchers transform the genome of an organism. Genetic engineering technique mainly requires recombinant DNA. Recombinant DNA is a combination of DNA from one source with the other DNA from the different organism’s sources or different locations in a specified genome that would not normally be found in nature. New DNA inserted in the host genome DNA using molecular is a combination of DNA from one source with the other DNA from the different organism’s sources or different locations in a specified genome that would not normally be found in nature. New DNA inserted in the host genome DNA using molecular cloning methods to generate a new DNA sequence. The transfer of genes within and across species boundaries to produce improved or novel organisms.
Related Journals of Genetic Engineering
Biotechnology and Genetic Engineering Reviews, Genetic engineering, Genetic Engineering and Biotechnology News, Genetic Engineering and Biotechnology Journal.
Genes are the building blocks of inheritance and genes are passed from one generation to next generation. Genes simply contain the DNA that holds the Information for the protein synthesis. Protein works main building block for the cells. If any regularity occurs in this process result in genetic disease. Sometimes, a mutation change in the DNA content of the cell i.e. a change in a genae or genes. The mutation changes in the gene's causes irregularities in the instructions for making a protein, as result the protein does not work properly. This can result in a medical situation called a genetic disorder.
Related Journals of Genetic Diseases
Inflammatory Bowel Diseases, Digestive Diseases and Sciences, Cerebrovascular Diseases, Progress in Cardiovascular Diseases, International Journal of Infectious Diseases, Journal of Gastrointestinal and Liver Diseases, Chronic Diseases in Canada.
Due to the fresh development in high-throughput sequencing technique for cancer genomes has supported a growing molecular classification of cancer. Due to advancement of various New technology like next-generation sequencing 1, 2 (NGS) has enabled a systematic cataloguing of cancer genomes through national and international genomics projects, for example, the Cancer Genome Atlas and the International Cancer Genomics Consortium. The quick improvement in the Next Generation Sequencing (NGS) has opened a wealth of opportunities for research in many fields: personalized medicine, cancer biology, neuro-degeneration, epigenetics, tumor evolution, microbiome and infectious disease ambulation etc.
Related Journals of Clinical Research in Genome
Journal of AIDS and Clinical Research, Journal of Anesthesia and Clinical Research, Multivariate Experimental Clinical Research, Scrip Clinical Research, Breast Cancer: Basic and Clinical Research, Diabetes and Metabolic Syndrome: Clinical Research and Reviews, Clinical Research in Cardiology.
There are so many types of heart disease but genetic diseases related to heart disease are very few in number. Coronary artery blockage, Congenital heart defect (CHD) or congenital heart anomaly is a type of genetic disease that occurs in inborn baby in which is a defect in the structure of the heart and great vessels at the time of birth. This will cause blood to flow through the heart in an abnormal pattern. The most of the known reason of congenital heart disease are focal mutations, either sporadic genetic changes or deletion or addition in the segments of DNA.
Related Journals of Genetic Heart Disease
European Heart Journal, American Journal of Physiology - Heart and Circulatory Physiology, American Heart Journal, Journal of Heart and Lung Transplantation, Heart Rhythm, Journal of Heart Valve Disease, European Heart Journal Cardiovascular Imaging, World journal for pediatric & congenital heart surgery.
The clinical trial is an experimental study that investigates that the drug is usable to human being or not, in the term of treatment, safety and effectiveness. Clinical trials are controlled by the respective government of that country in which clinical trial is going. Clinical studies provide us an improved idea or understanding of how genes can cause or influence diseases. Participants in clinical studies help current and future generations. From these studies, researchers will develop new diagnostic tests; provide more effective treatments, and better ways of managing diseases with genetic components.
Related Journals of Clinical Trial for Genetic Disease
Controlled Clinical Trials, HIV Clinical Trials, Contemporary Clinical Trials, Reviews on Recent Clinical Trials, PLoS Clinical Trials, Open Access Journal of Clinical Trials, Online journal of current clinical trials, Open Clinical Trials Journal.
Diabetes is also known as diabetes mellitus, categories as a group of metabolic diseases which is characterized by high blood glucose (blood sugar) level in the body, either because of low insulin production from liver, or because the body's cells do not respond to insulin (insensitiveness), or both. Diabetic disorder divided into two types: Type 1 diabetes- body does not produce insulin (Autoimmune pancreatic β-cell destruction perhaps triggered by an environmental exposure in genetically susceptible person), Type 2 diabetes- body does not produce enough insulin, or the cells in the body do not react to insulin.
Related Journals of Genetic Diabetic Disorder
Diabetic Medicine, Review of Diabetic Studies, Diabetic Medicine Supplement, Diabetic Foot and Ankle, Diabetic Hypoglycemia, Journal of the Diabetic Association of India.
Genomics is the study of genes and their function. Genomics objective is the understanding of the structure of the genome, comprising the mapping genes and sequencing the DNA. Genomics investigate the molecular mechanisms and the transaction of genetic and environmental factors in disease. Medical Genomics is a discipline in genetics that applies the application of recombinant DNA techniques, DNA sequencing methods, and bioinformatics to sequence, assemble, and investigate the function and structure of genomes (the complete set of DNA within a single cell of an organism).
Related Journals of Medical Genomics
Journal of Medical Genetics, JAMA - Journal of the American Medical Association, British Medical Journal, American Journal of Medical Genetics, Journal of the American Medical Informatics Association : JAMIA, Journal of Biomedical Materials Research, Current Medical Research and Opinion.
*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