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About Conference

Join us for 7th World Congress on Human Genetics and Genetic Diseases

Update your skills, enhance your knowledge base, and broaden your horizons—all in one place! 

Theme: Emerging New Innovations & Learning the Latest Trends in Genetics

Genetic Disorders, Human Genetics, Genetic Diseases, Epigenetics, Cancer Genetics, Genomics & Proteomics, Molecular Biology, Bioinformatics, Computational Biology, Genetic Counselling, Stem Cells, Neuro Genetics

Date: March  19-20, 2020

Venue: Dubai, UAE

About Human Genetics Conference

Human Genetics 2020 Conference welcomes you to attend the "7th World  Congress  on Human Genetics and Genetic Diseases" we cordially invite all the participants who are interested in sharing their knowledge and research in the arena of Genetics and Molecular Biology.

Human Genetics 2020 Conferences offers the scientific community a platform to share their knowledge in the field of Human Genetics and Genetic Diseases. This conference offers a comprehensive agenda presented through two plenary sessions and panel discussions for the benefit of professionals in the field of Medical, Dental, Pharmacy, Nursing and others, who are engaged in common health problems.

This event will feature sessions from leading experts in genetic diseases research, Personalized & Targeted Medicine including local and international professors, physicians, and government representatives. The purpose of the plenary and panel sessions is to facilitate discussions on early diagnosis, improve access and quality care, optimize the coordination of provider services, and foster high impact clinical research to expedite improved medical treatments. The conference mainly aims at the education of the medical community and dissemination of reliable information to at-risk populations, which are the most efficient ways to control genetic disorders among the people from different part of the world.

We intend to explore the challenges posed by genetic diseases and the most recent updates on pathophysiology, diagnosis, management, and prevention with emphasis on their impact on the UAE population. Certainly, this will raise awareness among medical professionals to provide effective prevention and treatment methods.

The global market for Genetic Testing is forecast to reach US$2.2 billion. Increasing knowledge about the potential benefits of genetic testing is one of the prime reasons for the growth of the genetic testing market. Advancements in the genetic testing space, aging population and a subsequent rise in the number of chronic diseases, and increasing incidence of cancer cases are the other factors propelling growth in the genetic testing market.

Who is Attending? 

  • Deans/Chairs, Vice Deans & Vice Presidents of Medical Institutions and Hospitals
  • Professors and students from academia who are in the field of research, Medical and clinical research.
  • Physicians, Business delegates, Directors / Managers & Business Intelligence Experts, Departmental Managers.

Benefits of Attending the Conference

  • The Career Guidance Workshops to the Graduates, Doctorates and Post-Doctoral Fellows, Certificate Accreditation from the Organizing Committee of presentation/ participation.
  • Accepted Abstracts will be published in the respective journals and will be labelled with a Digital Object Identification Number (DOI) provided by CrossRef (Free abstract publishing).
  • Speaker and Abstract pages created in Google on your name would get worldwide acknowledgement to your profile and Research.
  • Best Poster and Young Researcher Award.

Target Audience:

  • Genomics and Genetics Students
  • Genomics and Pharmacogenomics Researchers
  • Genomics and Pharmacogenomics Faculty
  • Genomics Scientists
  • Genomics Colleges
  • Human Genetics  Scientists
  • Pharmacology Health Professionals
  • Genetics Associations and Societies
  • Geneticists
  • Genetic Counselors
  • Bio-pharmacists
  • Business Entrepreneurs
  • Training Institutes
  • Software developing companies
  • Data Management Companies






1. Human Genetics

Human genetics is both a basic and connected science. As a key science, it is a piece of hereditary qualities the part of science that analyzes the laws of capacity, transmission, and acknowledgment of data for improvement and capacity of living beings. Inside this system, Human genetics qualities worry about the most fascinating life form the person. This worry with our very own species influences us to investigate logical outcomes in human hereditary qualities for their hypothetical noteworthiness as well as for their down to earth and incentive for human welfare. Consequently, Human genetics qualities are additionally a connected science. Its incentive for human welfare will undoubtedly have repercussions for hypothetical research too since it impacts the choice of issues by human geneticists, their preparation, and the financing of their exploration. In view of its proceeded with hypothetical and functional intrigue, human hereditary qualities offer interest and human satisfaction unparalleled by work in fields that are either fundamentally hypothetical or completely viable in the subject matter.

2.Gene therapy and Gene editing

A number of methods are under development for treating genetic disorders, including a  inherited (eg, monogenic/Mendelian) conditions and acquired conditions such as cancer and infections. This topic reviews molecular techniques that can be used to alter the sequence or expression of a gene, including gene therapy, gene editing, and gene silencing.

  • Genetic Diseases
  • Genetic Testing
  • Genetic counselling


Genomics is an interdisciplinary field of science focusing on the structure, work, headway, mapping, and modifying of genomes. A genome is a life structure's whole plan of DNA, including most of its characteristics. As opposed to innate characteristics, which insinuates the examination of individual characteristics and their parts in inheritance, genomics goes for the total depiction and assessment of characteristics, which arrange the age of proteins with the assistance of mixes and minister particles. In this manner, proteins make up body structures, for instance, organs and tissues and also control mixture reactions and pass on movements between cells. Genomics in like manner incorporates the sequencing and examination of genomes through businesses of high throughput DNA sequencing and bioinformatics to gather and separate the limit and structure of entire genomes.

4. Human Fertilization and Embryogenesis

Fertilization :It is the process of Fusion of sperm and ovum to form ZygoteFertilization usually take place in oviduct. Ovum is in secondary oocyte stage during fertilizationSecondary oocyte is surrounded by two layer-zona pellucida and zona reticulateSperm move toward the secondary oocyte and bind to the receptor on zona pellucida. After sperm enter the oocyte, the zona pellucida become fertilization membrane preventing other sperm to enter. It is the entry of sperm that stimulate second meiotic division of Oocyte to produceOvumAcrosome of sperm release proteolytic enzyme (Hyaluronidase) that digest the egg wall and then the pro-nucleuses fuse form zygote (2n).


Zygote undergoes repeated cell division called cleavage. Cleavage starts as the zygote moves down from oviduct to uterus 3-5 days after fertilization, zygote develop into ball like structure of cell with central cavity; blastocyst (Blastula stage).Outer cell of blastocyst is known as trophoblastic cell while inner cell is known as embryonic cellTrophoblastic cell secrete HCG (human chorionic gonadotropin) hormone; similar in function as LHIt Prevent degredation  of corpus luteum, therefore corpus luteum continue to secrete progesterone and oestrogen, which help continuous growth of endometrium wall causing menstruation cycle to stop.

As blastocyst reaches to uterus, trophoblast cell invade endometrium wall and utilize nutrients for its growth and multiplication. This invasion establishes the embryo within 6-9 days in the uterus called ImplantationWith successful implantation, trophoblast form chorion membrane, which later become part of placenta.Chorion membrane develop small villi like projection on its outer layer called Chorion villi that begins to grow in the endometrium and help in exchange of nutrition between embryo and uterus.  Embryonic cell grow to become embryo. It also form other embryonic membrane covering the embryo.


Within 20 days, embryonic membrane become clearly distinguished from embryo. The amnion is a thin membrane filled with amniotic fluids that eventually surrounds the embryo and act as shock absorbent. Later allantoin membrane develop, which develop toward the chorion and get fused to form Allanto-chorion which later form Placenta. Yolk sac has no significant function in human. Embryonic disc present between yolk sac and amnion give rise to embryo. Embryonic disc differentiate into 3 germ layer(Ectoderm, mesoderm and endoderm) known as Gastulation. Embryo shows distinct from at about 4-5 weeks. Only after 6 week, embryo can be distinguished as human embryo and now embryo term as Fetus.

5. Thalassemia

Thalassemia is an inherited blood disorder that reduces the production of functional hemoglbin (the protein in red blood cells that carries oxygen ).This causes a shortage of red blood cells and low levels of oxygen ).This causes a shortage of red blood cells and low levels of oxygen in the blood stream,leadig to a variety of health problems .There are two main types of thalassemia, alpha thalassemia and beta thalassemia. Signs and symptoms vary but may include mild to serve anaemia ,paleness, fatigue ,yellow discoloration of skin (jaundice ),and bone problems .Beta thalassemia is caused by changes (mutations ) in the HBB gene while alpha thalassemia is caused by mutations in the HBA1 and HBA2 genes .Both are Inherited in an autosomal recessive manner.Treatment depends on the type and severity of the condition but may include blood transfusions and /or folic acid supplements

6. Evolutionary and Population Genetics

Mutation is the source of genetic variation, contributing to adaptive evolution and population stratification. The fields of evolutionary and population genetics apply quantitative and statistical analytical methods to models of populations, endeavoring to understand the dynamics of genetic variation and change in natural populations. The focus of these fields includes molecular population genetics such as allele frequency, quantitative genetics, and the phenomena of recombination and its impact on genetic linkage.

The research projects of our Evolutionary and Population Genetics faculty employ genome-wide statistical analytic approaches to understand the genetic structure and sequence variation among populations and species  as well as complex phenotypes and evolutionary history (Li). In addition, we are interested in the evolutionary history and functional mechanisms of specific elements in the human genome, such as the retrotransposon (Moran) and X-amplicons and their impact on male fertility (Mueller).

7. Developmental Genetics & Quantitative Genetics 

Developmental genetics is the investigation of the manner by which qualities control the development and advancement of a living being for a mind-blowing duration cycle. A recently prepared egg cell or zygote contains a remarkable gathering of qualities that will control its improvement from a solitary cell into a fetus through examples of differential quality articulation during the time spent embryogenesis.

8. Genome Editing and Gene Regulation

Genome Editing and gene regulation was introduce CRISPR” (pronounced “crisper”) stands for Clustered Regularly Interspaced Short Palindromic Repeats, which are the hallmark of a bacterial defense system that forms the basis for CRISPR-Cas9 genome editing technology. In the field of genome engineering, the term “CRISPR” or “CRISPR-Cas9” is often used loosely to refer to the various CRISPR-Cas9 and -CPF1, (and other) systems that can be programmed to target specific stretches of genetic code and to edit DNA at precise locations, as well as for other purposes, such as for new diagnostic tools. With these systems, researchers can permanently modify genes in living cells and organisms and, in the future, may make it possible to correct mutations at precise locations in the human genome in order to treat genetic causes of disease. Other systems are now available, such as CRISPR-Cas13’s, that target RNA provide alternate avenues for use, and with unique characteristics that have been leveraged for sensitive diagnostic tools, such as SHERLOCK.

9. Paediatrics and Genetics

Fortunately, most children are born healthy with no medical problems or birth  defects. However, some children are born with differences in body structure, brain development, or body chemistry that can lead to problems with health, development, school performance, and/or social interaction. Pediatric geneticists are trained to identify the causes and natural history of these disorders. They may suggest tests and treatments that can help in understanding and caring for your child’s condition. Pediatric geneticists also can help families understand whether some conditions are hereditary (coming from the genes) and offer testing to family members who may be at risk for having children with similar problems.

10. Cytogenetics

Cytogenetics is the investigation of chromosomal structure, area, and capacity in cells. It incorporates the investigation of chromosome number and appearance (karyotyping), the physical area of qualities on chromosomes, and chromosomal conduct in procedures, for example, cell division. The ordinary human cell is comprised of 46 chromosomes: 22 sets of autosomes, numbered 1-22 by request of diminishing length, 1 set of gonosomes, or sex chromosomes.

11. Genome Integrity:

Our genomes are composed of the sum total of genetic material necessary to encode the blueprint for human life. The effective maintenance of genome integrity and stability is essential for normal cell division, normal function of our tissues and organs, healthy aging, and the prevention of diseases such as cancer. The processes that regulate genome integrity maintenance include sensing, signaling, and repair of DNA damage, processing of DNA damage in the context of chromatin and chromosomes, cell cycle checkpoint control, and control of cell death. Many of the basic aspects of genome integrity—such as how cells sense and process DNA damage—are still not well understood.

12. Cancer Genetics   

Cancer is a genetic issue in which the typical control of cell improvement is lost. Cancer genetics is presently one of the quickest stretching out restorative distinguishing strengths. At the nuclear dimension, the tumor is brought about by a mutation(s) in DNA, which result in twisted cell development. An expansive part of these changes is secured and occur in physical cells. In any case, a couple of individuals secure mutation(s) in the germ line. The mutation(s) occur in two classes of cell characteristics: oncogenes and tumor silencer characteristics. Under standard conditions, tumor silencer characteristics oversee cell division and camouflage of extension. Changes in these characteristics result in unchecked cell duplication realizing tumors with strange cell cycles and tumor development. The tumor silencer characteristics add to malady by the inactivating of loss of limit change.

13. Neurogenetics

Neurogenetics studies the role of genetics in the development and function of the nervous system. It considers neural characteristics as phenotypes (i.e. manifestations, measurable or not, of the genetic make-up of an individual), and is mainly based on the observation that the nervous systems of individuals, even of those belonging to the same species, may not be identical. As the name implies, it draws aspects from both the studies of neuroscience and genetics, focusing in particular how the genetic code an organism carries affects its expressed traits. Mutations in this genetic sequence can have a wide range of effects on the quality of life of the individual. Neurological diseases, behavior and personality are all studied in the context of neurogenetics. The field of neurogenetics emerged in the mid to late 1900s with advances closely following advancements made in available technology. Currently, neurogenetics is the center of much research utilizing cutting edge techniques.

14. Nutrigenetics

Nutrigenetics refers to the application of genomic principles in nutritional research, enables us to formulate associations between specific nutrients and genetic factors, e.g. the way in which food or food ingredients influence gene expression. It aims to identify the genes that influence the risk of diet-related diseases and also helpful to solve the mechanisms that underlie these genetic predispositions. In contrast, nutrigenetics reveals the coordination of genetic makeup of individuals with their responses to various dietary nutrients. It clarifies different responses to same nutrient by different individuals. Interaction of genetic background and diet with regard to development of chronic conditions as obesity, cardiovascular disease, hypertension and cancer are discussed in present review. These two branches of nutrition resemble with two sides of a coin, facing towards opposite sides but simultaneously, they are intimately attached with each other. Collective efforts by the scientific community are needed to strictly follow guidelines put forth regarding experimental designs, analysis, and data storage for nutritional research. This strategy will be helpful to generate a sound database useful for clinicians and dietetic practitioners.

15. pharmacogenetics 

Pharmacogenetics is the study of how people respond differently to drug therapy based upon their genetic makeup or genes. Diet, overall health, and environment also have significant influence on medication response, but none are stronger indicators of how you will process medication than your genetics.

16. Regenerative-Medicine Approach

Regenerative medicine may be defined as the process of replacing or "regenerating" human cells, tissues or organs to restore or establish normal function. Regenerative Medicine refers to a group of biomedical approaches to clinical therapies that may involve the use of stem cells.

17. Cardiovascular Disorders

The cardiovascular, or circulatory, system supplies the body with blood. It consists of the heartarteriesveins, and capillaries.CVD is now the most common cause of death worldwide. However, there are many ways to reduce the risk of developing these conditions. There are also many treatment options available if do they occur.The treatment, symptoms, and prevention of the conditions that are part of CVD often overlap.In this article, we look at the different types of CVD, their symptoms and causes, and how to prevent and treat them.

·         Angina

·         Arrhythmia

·         Congential heart disease

·         Coronary artery disease

·         Heart attack

·         Heart failure

18. Personalized Medicine and Pharmacogenomics

Personalized medicine holds the promise that treatments will one day be tailored to your genetic makeup.Modern medications save millions of lives a year. Yet any one medication might not work for you, even if it works for other people. Or it might cause severe side effects for you but not for someone else.Your age, lifestyle and health all influence your response to medications. But so do your genes. Pharmacogenomics is the study of how a person's unique genetic makeup (genome) influences his or her response to medications.

19.Genetic Counselling :

Genetic counseling is the process of advising individuals and families affected by or at risk of genetic disorders to help them understand and adapt to the medical, psychological and familial implications of genetic contributions to disease.[1] The process integrates:

Interpretation of family and medical histories to assess the chance of disease occurrence or recurrence

Education about inheritance, testing, management, prevention, resources

Counseling to promote informed choices and adaptation to the risk or condition.

20. Reproductive Genetics/Prenatal Genetics:

Part of the Division of Maternal-Fetal Medicine, the Reproductive Genetics Service was created to help women with medical conditions encountered or made worse by a pregnancy or whose prenatal testing reveals a birth defect or genetic condition in the fetus.Genetics in obstetrics can be complicated because the genetic make-up of three people – the mother, the father of the baby, and the unborn child – must be considered. Many women have a genetic condition that is unrecognized until they become pregnant.Reproductive Genetics Service geneticists and seven board-certified counselors help couples understand how genetics can affect their pregnancy, offering counseling for those planning to have a baby or women who are already pregnant.

21. Immunogenetics 

Immunogenetics or immungenetics is the branch of medical genetics that explores the relationship between the immune system and genetics.Autoimmune diseases, such as type , diabetes, are complex genetic traits which result from defects in the immune system. Identification of genes defining the immune defects may identify new target genes for therapeutic approaches. Alternatively, genetic variations can also help to 


Market Analysis Report

Market Analysis

Market Scenario

Genetics is nothing but the study of genes, their capacities and impacts. Atomic genetics, formative genetics, populace genetics and quantitative genetics, and human genetics are different sorts of hereditary investigations. Human genetics is the investigation of legacy in people, i.e., it is the investigation of legacy of attributes in kids from guardians. It incorporates the investigation of quality articulation, quality structure, transformation examination, cytogenetic and genomic imaging, genome structure and association, hereditary and physical mapping, malady affiliation contemplates, atomic diagnostics, genetics of complex illnesses, epistatic collaborations, and different ideas. It additionally decides different hereditary components in charge of ailments. It offers different points of interest, for example, distinguishing proof and determination and treatment of different illnesses, for example, malignant growth, cardiovascular sicknesses, and other hereditary maladies.

The worldwide human genetics advertise is driven by the expanding number of patients with hereditary ailments and expanding social insurance use by significant economies over the globe. Besides, the developing mindfulness about hereditary maladies, expanding interests in innovative work, and rising government bolster fuel the market development. Be that as it may, different variables control the development of the market, for example, greater expense of instruments and absence of gifted experts.

Worldwide Human Genetics Market is anticipating a solid development at a CAGR of 11.5% amid the estimate time frame.

Target Group

  • Medical Research Laboratories
  • Academic Medical Institutes and Universities
  • Research and Development Companies
  • Genetics & Genomic Industries

Regional Analysis

  • America is the biggest market for human genetics inferable from the advancement in the diagnostics and medicinal innovation and broad utilization of new advances in genetics. Furthermore, the nearness of key players in the market likewise fills the market development. The U.S. is the biggest market for human genetics with an expansion in the number of concentrates in genetics and its significance in social insurance.
  • The European market for human genetics is driven by the rising pervasiveness of various unending hereditary infections and expanding government support for innovative work exercises. In Germany, being the biggest market, the development is represented by the rising spotlight on research exercises by real market players in the field of genetics and innovative headway.
  • In the Asia Pacific, the market is energized by the expanding mindfulness about research in hereditary infections and consistent ascent in the predominance of hereditary illnesses. Significant nations adding to the market development are China, Japan, and India because of expanding accessibility of research offices and nearness of talented workforce, for example, explore researchers and others.
  • The Middle East and Africa holds minimal offer in the worldwide human genetics market and demonstrates a consistent development because of the rising interest for social insurance administrations and research exercises, poor financial condition, and less improvement in medicinal offices, particularly, in Africa.

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New Updates: Human Genetics Meet 2020

Past Conference Report

Human Genetics Meet 2019

6th World Congress on Human Genetics and Genetic Diseases was hosted by ME Conferences during April 08-09, 2019 in Abu Dhabi, UAE on the theme of Know the current generation to save the future generation.

Active responses and great reviews are given by the Organizing Committee Member, the scientists and the young community students who came to attend the Conference from different parts of the world. The Conference marked the presence of renowned speakers, young researchers, business delegate, Students who made the Conference a most successful and productive event of 2019.

The conference marked its start by an opening ceremony which included introduction by the Honourable Guest: Dr. Mariam Fida, Al Jawhara Center, Bahrain.

We are very overwhelmed by her presence and her generous response.

Human Genetics Meet 2019 Organizing Committee extends its gratitude and congratulates the honourable moderators of the conference, Dr. Nigora Mavlyanova, Ministry of Health of the Republic of Uzbekistan, Uzbekistan and Dr. Salma Alyssa Ferouz, Guyana Cancer Foundation, Guyana for their preeminent contribution towards the smooth functioning of this esteemed event.

We have taken a privilege of felicitating our keynote Speakers:

  • Dr. Manohar Furtado | Apton Biosystems Inc. | USA

  • Dr. Vojin Rakić | Center for the Study of Bioethics- University of Belgrade | Serbia

  • Dr. Pravin Potdar  | Dr. A P J Abdul Kalam Education & Research Centre | India

  • Dr. Meena Upadhyaya  | Cardiff University | UK

Who shared their innovative researches and vast experience through their fabulous presentations during the event.

The eminent personalities at the conference were

•           Dr. Manohar Furtado  | Apton Biosystems Inc. | USA

•           Dr. Meena Upadhyaya | Cardiff University | UK

•           Dr. Pravin Potdar | Dr. A P J Abdul Kalam Education & Research Centre | India

•           Dr. Mariam Fida | Al Jawhara Center | Bahrain

 •          And many more

Exhibitor: EDgene, India

Last but not the least; we are obliged to various delegate experts, Company representatives, eminent personalities who supported the Conference by facilitating active discussion forums. We would like to convey our sincere gratitude to all the supporters from Editorial Board Members of our Open Access Journals, Keynote Speakers, Honourable guests, Valuable Speakers, Students, delegates and special thank s to Media Partners  for their promotions to make this event a successful one.

With the unique feedbacks from the Conference Human Genetics Meet 2019, we would like to announce the commencement of the 7th World Congress on Human Genetics and Genetic Diseases to be held during March 19-20, 2020 in Dubai, UAE.

Let us meet again @ Human Genetics Meet 2020

Email us at:


Past Reports  Gallery  

To Collaborate Scientific Professionals around the World

Conference Date March 19-20, 2020

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  • Animal Epigenetics
  • Asthma
  • Bacterial Genome Size
  • Behavioral Epigenetics
  • Bioinformatics In Genomics
  • Biomarkers
  • Blood Group
  • Breeding
  • Cancer Biomarkers
  • Cancer Epigenetics
  • Cancer Genetics
  • Cancer Genomics
  • Cancers
  • Cardiovascular Disorders
  • Cell Biology
  • Cell Biotechnology
  • Chromosomal Sisorder
  • Ciliopathies
  • Cleft Palate
  • Clinical Epigenetics
  • Clinical Genomics
  • Cloning
  • Comparative Genomics
  • Complete & Incomplete Dominance
  • Congenital Disorders
  • Creation Of Transgenic Organisms
  • Cryoconservation Of Animal Genetic Resources
  • Cytogenetics
  • Cytogenetics & Karyotyping
  • Developmental Epigenetics
  • Developmental Genetics & Quantitative Genetics
  • Diabetes
  • Diagnosis
  • DNA Fingerprinting
  • DNA Methylation
  • DNA Technology
  • Drug Treatments
  • Embryology
  • Epigenetics
  • Epigenetics Alteration
  • Epigenome
  • Etymoloagy
  • Eugenics
  • Evolution
  • Evolutionary And Population Genetics
  • Forensic Genetics
  • Functional Genomics
  • Future Trends In Genomics
  • Gene Allele
  • Gene Cloning
  • Gene Editing
  • Gene Expression
  • Gene Expression
  • Gene Isolation
  • Gene Mutations
  • Gene Splicing
  • Gene Therapy
  • Gene Therapy And Gene Editing
  • Genes And Sex
  • Genes For Noncoding RNA
  • Genes?Mutation
  • Genetic Analysis Of DNA Structure
  • Genetic Counselling
  • Genetic Disorder
  • Genetic Diversity
  • Genetic Engineering
  • Genetic Enhancement
  • Genetic Genealogy
  • Genetic Transformation
  • Genetic Variation
  • Genetics And Cancer
  • Genetics And Parkinson?s Disease
  • Genetics Disorders
  • Genome Editing And Gene Regulation
  • Genome Engineering
  • Genome Integrity
  • Genome Medicine
  • Genomics
  • Genotype
  • Germ Immunization
  • Germ Line Mutations
  • Heart Disease
  • Human Chromosomes
  • Human Fertilization And Embryogenesis
  • Human Genetic Clustering
  • Human Genetics
  • Human Genome Mapping
  • Human Genome Project
  • Human Genomics
  • Hypertension
  • Immunogenetics
  • In Vitro Fertilisation
  • Infertility
  • Inflammatory Bowel Disease
  • Intellectual Disability
  • Medical Genetics
  • Micro RNA
  • Microbial Genomics
  • Mitochondrial DNA
  • Mitochondrial Genetics
  • Molecular Basis For Inheritance
  • Molecular Biology
  • Molecular Genetics
  • Molecular Tools For Gene Study
  • Mood Disorder
  • Mutagenesis
  • Mutation
  • Neurodevelopmental Genetics
  • Neuroepigenetics
  • Neurogenetics
  • Neuronal Epigenetics
  • Next Generation Sequencing
  • Nucleic Acids
  • Nucleotide
  • Nutrigenetics
  • Nutritional Epigenetics
  • Nutritional Genomics
  • Obesity
  • Oncogenes
  • Organ Transplantation
  • Organ Transplants
  • Paediatrics And Genetics
  • Personalized Medicine And Pharmacogenomics
  • Pharmacogenetics
  • Pharmacogenomics
  • Phenotype
  • Phylogenetics
  • Plant Genetic Resources
  • Plant Genomics And Molecular Plant Sciences
  • Polymerization
  • Poplation Genetics
  • Prion
  • Proteomics
  • Pseudogenes
  • Recombinant DNA Construction
  • Recombinant DNA Technology
  • Refractive Rrror
  • Regenerative-medicine Approach
  • Reproductive Cloning
  • Reproductive Genetics/Prenatal Genetics
  • Stem Cell
  • Stem Cell Research
  • Thalassemia
  • Therapeutic Cloning
  • Tissue Biomarkers
  • Transgenic Engineering
  • Xenograft