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About Conference

We are excited to share the date of our forthcoming conference “11th World Congress on Human Genetics and Genetic Diseases”, which will be held during July 10-11, 2023 Dubai, UAE .which will explore the most cutting-edge research and development in human genetics . A number of outstanding researchers, scientists, industrialists, and others will be attending to showcase their groundbreaking work, share their experiences from various perspectives, and address important questions.

The scientific community has a venue to communicate knowledge in the area of human genetics and genetic diseases. Benefits  professionals working in the fields of medicine, research, pharmacy, nursing, and other related fields who are interested in common health issues, this conference presents a thorough agenda given through plenary sessions and panel discussions.

Leading experts in the fields of genetic disease research, personalized and targeted medicine, as well as local and foreign professors, doctors, and government officials, will present sessions at this event. 

Target audience:

  • Pharmaceutical companies
  • CEO of Genetic companies
  • Directors of Genetic companies
  • Business Entrepreneurs
  • R&D department people
  • Bio-pharmacists
  • Nutritionists
  • Clinical protocol developers
  • Geneticists
  • Genetic Counselors
  • Genomics and Pharmacogenomics Faculty
  • Researchers
  • Scientists
  • Students
  • Professors
  • Training Institutes
  • Genetic engineers
  • Molecular biologists
  • Doctors
  • Data Management Companies
  • Enthusiastic people (common people, patients)
  • Software developers
  • Yoga trainers

Why to attend???

At this international conference, experts in the domains of human genetics and genetic illnesses can present their most recent findings and keep engaged on all the key developments in these areas. There will be a sizable number of scientists and top-tier professionals present at the conference. Over the course of the two-day conference, you will have the opportunity to network and hear from experts in the international academic and corporate human genetics and genetic diseases communities.

This conference seeks to bring together all such researchers, researchers, research scholars, students, and others interested in this subject and to provide them with the opportunity to discuss their innovation, share ideas, and engage with one another.

Why Dubai?

The first firm to provide complete genetic testing services in the Middle East is Eastern Biotech & Life Sciences, situated in Du Biotech, Dubai. In order to determine which genetic tests are most pertinent to this region and make them available to Middle Easterners directly, we have thoroughly investigated the biotechnological horizon.

ME Conferences chose the UAE to host its conference on "Human Genetics and Genetic Diseases" in order to enhance the participation of pioneer speakers in conference and make the attendees to explore, investigate, and exchange ideas on a worldwide scale.

Sessions and Tracks

Track 1: Classical Genetics

Classical genetics is the area of genetics that only considers the visible signs of reproduction. The experiments on Mendelian inheritance by Gregor Mendel, who made it possible to discover the fundamental mechanisms of heredity, make it the oldest field in genetics.

  • Allele
  • Phenotype
  • Genomics
  • Enzymes
  • Mutation

Track 2: Immunogenetics

The area of medical genetics and immunology known as "immunogenetics" or "immungenetics" studies how the immune system and genetics are related. Type 1 diabetes and other autoimmune illnesses are complicated genetic features brought on by immune system flaws.

  • Major Histocompatibility Complex.
  • Human Leukocyte Antigen
  • Vaccine Efficacy
  • Mono-specific Antibody

Track 3: Phylogenetics

Phylogenetics is a potent method for determining how modern species have evolved. Scientists can explain the similarities and differences between species and learn more about how species have developed by looking at phylogenetic trees. Numerous medical and biological disciplines use phylogenetics, such as forensic science, conservation biology, epidemiology, drug discovery, drug design, protein structure and function prediction, and gene function prediction.

Track 4: Comparative Genomics

In order to better understand how species arose and to discover the function of genes and noncoding areas in genomes, comparative genomics compares the entire genetic makeup of two organisms directly.

Comparative genomics provides fresh insight into genome evolution and the way natural selection shapes DNA sequence evolution by analysing genome sequences from various species.Softwares in trend for comparitive genomics are :

  • Easyfig
  • Ensembl
  • KEGG

Track 5: Clinical Genetics

Clinical genetics is a branch of medicine that offers genetic counseling and diagnostic services to people or families who have or may develop illnesses that have a genetic foundation. Genetic disorders can affect every body system in any age group. The goal of genetic services is to assist people who have or are at risk for genetic disorders in living and reproducing as normally as possible.

Track 6: Gene Function Prediction& Genome Annotation

The approaches for predicting gene function, which automatically annotate genes with information about their functions by utilizing available resources, can be broadly categorized into experimental data-based methods and knowledge-based methods. First, a lot of techniques based on experimental data were applied.

Protein-coding genes, as well as other functional genome units like structural RNAs, tRNAs, short RNAs, pseudogenes, regulatory areas, direct and inverted repeats, insertion sequences, transposons, and other mobile elements, are predicted as part of the  multi-level process of genome annotation level process of genome annotation.

  • EuGene

Track 7: Genome Integrity

The Genome Integrity Unit focuses on cancer and early development with particular interest in how cells retain the health of their DNA. Cells respond to DNA damage by using a precise DNA repair process to preserve genomic integrity.

Track 8: Genetic Epidemiology

With conceptual and methodological input from epidemiology, genetic epidemiology initially grew out of population genetics, specifically human quantitative genetics. It is relatively recent field of study, aims to clarify how genetic and environmental variables interact to cause disease in populations.

Four main types of research study designs are used to conduct the tests of analytical epidemiology;

  • Cross-sectional studies
  • Case-control studies
  • Cohort studies
  • Controlled clinical trials

Track 9: Common Genetic Diseases

Regardless of time zone and latitude, there are some genetic faults that occur most frequently worldwide for a variety of reasons, leading to prevalent or common genetic diseases.More research is being conducted and advances are noting every day.

  • Down syndrome (Trisomy 21)
  • Fragile X syndrome
  • Klinefelter syndrome
  • Triple-X syndrome
  • Turner syndrome
  • Trisomy 18
  • Trisomy 13

Track 10: Lethal Genetic Diseases

Fatal alleles, often known as lethal genes or lethal, are alleles that result in the demise of the carrying organism. They frequently occur from mutations in genes that are crucial for development or growth. Depending on the gene or genes involved, lethal alleles might be recessive, dominant, or conditional. Lethal alleles can kill an organism before or after birth, however, they typically show up early in development.

Track 11: Nutrigenetics & Nutrigenomics

Our understanding of the processes by which nutrition impacts the metabolic pathways underlying homeostatic control has increased thanks to nutrigenomics. This can then be used to identify naturally existing chemical components in food that may delay the onset of diseases including cancer, type-2 diabetes, and obesity.  Based on genetics, nutrigenetics studies how your body reacts to foods.

Track 12: Cancer Genetics

The field of science, cancer genetics focuses on identifying the genes and metabolic processes that promote the growth of cancer. In addition, networks and pathways that contribute to tumor growth as well as the interactions between cancer genes that support tumor evolution are of concern to cancer genetics.

Track 13: Gene Therapy

Gene therapy is a medical strategy that addresses the underlying genetic issue in order to treat or prevent disease. Instead of utilizing drugs or surgery, gene therapy procedures allow doctors to treat a problem by changing a person's genetic composition.

Ex vivo, in vivo, and in situ gene therapy are the three main subtypes. Ex vivo gene therapy involves removing the patient's affected cells and modifying them genetically. In vitro gene therapy is another name for this sort of treatment, which is especially useful for blood illnesses. There is one last gene therapy plan in which the viral vector is given directly to the patient.

  • Germline therapy
  • Somatic gene therapy

Track 14: Neurogenetics

Research in neurogenetics advances knowledge of the genetic underpinnings of both normal and pathological nervous system function. efforts to comprehend the genetic basis of brain problems.

Methods used for analysis;

  • Clinical exome sequencing
  • Transgenic RNAi

Track 15: Pharmacogenomics

Pharmacogenomics, also known as pharmacogenetics, is the branch of science that looks at how a person's genes influence how they react to pharmaceuticals. Its long-term objective is to assist physicians in choosing the medications and dosages that are ideal for each patient. Each year, severe medication responses lead to more than 120,000 hospitalizations, according to estimates. By locating people who are at danger, pharmacogenomics may be able to stop these. The effectiveness and expense of healthcare may both increase. Pharmacogenomics may make it easier to find the right drugs and dosages.

Track 16: Genetics Cardiovascular Diseases

Heart failure symptoms may be caused by inherited genetic abnormalities that alter the structure of the heart muscle. The electrical system of the heart can be impacted by gene abnormalities as well, which may result in irregular cardiac rhythms.

  • Hypertrophic Cardiomyopathy (HCM) idiopathic
  • Arrhythmogenic right ventricular cardiomyopathy (ARVC)

Track 17: Population Genetics

The study of genetic diversity within and between populations, as well as the evolutionary processes that account for this variation, is known as population genetics. It is based on the Hardy-Weinberg law, which holds true as long as there is a sizable population, random mating, and minimal mutation, selection, and migration.

Tools (software) used for population genetics analysis


Track 18: Biochemical Genetics

Biochemical genetics combines genetics with biochemistry. The structure and function of cellular components, including proteins, carbohydrates, lipids, nucleic acids, and other biomolecules, as well as their roles and transformations during life processes, are a major focus of biochemistry. Clinicians must have a fundamental understanding of the benefits and drawbacks of biochemical testing in order to interpret test results, decide when to visit a specialist, or explain results to patients.

Track 19: Genetic Medicine

The area of medicine known as medical genetics deals with the diagnosis and treatment of hereditary diseases. Human genetics is a branch of science that may or may not have applications in medicine, whereas medical genetics refers to the use of genetics in the delivery of medical treatment. Research on the causes and transmission of genetic illnesses, for instance, would fall within the scope of both human genetics and medical genetics, whereas the diagnosis, treatment, and counselling of those who have genetic abnormalities would fall under the purview of medical genetics.

Track 20: Genetic counseling

You can learn more about genetic diseases and how they might impact you or your family through genetic counseling. Your personal and family health history will be gathered by the genetic counselor or other healthcare provider. They can use this data to assess the likelihood that you or a member of your family has a genetic disorder.

Track 21: Yoga practice and genetic changes

The basic genetic blueprint for all living things is found in DNA. Recent research demonstrates that yoga not only has the advantages like, but also profoundly affects how genes work. This results from non-genetic effects and is referred to as an epigenetic effect.

To Collaborate Scientific Professionals around the World

Conference Date July 10-11, 2023

For Sponsors & Exhibitors

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  • Allele
  • Allosome
  • Anemia
  • Aneuploidy
  • Autosome
  • Children
  • Chromosome
  • Chromosome Aberration
  • Cleft Palate
  • Co-dominant
  • Codon
  • Cytogenetics
  • Diallelic
  • DNA
  • Dominant
  • Dwarfism
  • Enzymes
  • Epidemics
  • Evolution
  • Ex-vivo
  • Gene
  • Genetical Characters
  • Genetics
  • Genomics
  • Gigantism
  • Haplotype
  • Histones
  • Holiday Junction
  • Human Gene
  • In-vivo
  • MRNA
  • Multiallelic
  • Muscle Cramps
  • Mutation
  • Nutrition
  • Oncology
  • Palate
  • Pediatric
  • Phenotype
  • Physical Characters
  • Polaroid
  • Polyallelic
  • Proteins
  • Psychiatry
  • Psychology
  • Recessive
  • RNA
  • Seizures
  • Spindle Fibers
  • Syndrome
  • Trait