Your Scientific Adventure in Becoming a Gene Discoverer Starts Here…
Collaborate with us in rare disease research studies
Publish Scientific Papers
Save & Improve More Lives
Leave a Lasting Legacy
Embedding a research culture in a clinical setting is challenging. We get it!
Many clinicians identify rare genomic disorders in distinct phenotype or VUS cases, but majority are missing the opportunity of presenting their findings to wider community through paper publication because…
- They are tied up by other responsibilities
- No research budget whatsoever
- No community to inspire them
Your collaboration with our scholars vanish all obstacles on your way in becoming a gene discoverer.
As a Gene Discoverer You Get Access to…
Genome Medicine Research Lab ( GMRL) is located at St.George’s Hospital, University of London. GMRL investigates the role of mutations in DNA on development and disease susceptibility. Researchers explore the function of disease associated genes using cutting edge technologies and biological models. The focus of the lab is on Rare Disease, Complex Trait, and Development & disease.... Read More Rare Disease: Children account for 50% of rare disease patients. At least 40% of these children don’t have a diagnosis. With advances in analysing and interpreting genomic data, the center uncovers new genes for rare previously undiagnosed conditions. Each one of these provides an opportunity to improve understanding of disease mechanisms which help inform better clinical management. Complex trait: GMRL analyses available genomic data in phenotyped human populations to identify genes associated with these traits and diseases. These studies have provided a greater understanding of the biology linking genotype and phenotype. Whether it’s a new gene in which mutations cause a rare disease, or a novel gene pathway involved in a complex trait, GMRL is interested in identifying the potential mechanisms that link the genotype to the phenotype using zebrafish as an in vivo model to functionally characterise novel findings. Apply Now to Become a Gene Discoverer…Ongoing Projects
Development disease:
In collaboration with Genome Medicine Research Lab, we investigate a variety of Mendelian diseases (i.e. predominantly due to a DNA change in a single gene) in the Middle East region.... Read More As a result of cultural, historical, regional, and socio-economic factors in the Middle East, a higher proportion of families are consanguineous. With the increased levels of consanguinity (and hence higher incidence of Mendelian recessive disorders), and the lack of representation of middle eastern genomes in the public domain at present, this project will provide a unique opportunity for healthcare community across the globe to uncover previously undiagnosed cases.
Collaborate with us as we investigate the underlying genetic cause in families with rare inherited conditions.
The Panel represents a global network of recognized experts in medical genetics community. You’ll be given an opportunity to collaborate with other experts while uncovering genes for undiagnosed cases. Your findings will be then an opportunity for scientific paper publication.
Becoming a Gene Discoverer Is as Easy as 1,2,3
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Become a Gene Discoverer
Don't be Held Back!
Collaborate with us as we discover genes and publish scientific papers.