Rapid diagnosis of Long QT syndrome protects family from major health risk
Congenica supports the rapid diagnosis of Long QT syndrome and enables consideration of potentially life-saving interventions for baby and mother.
Clinical OMICs interview with David Atkins CEO Congenica
Clinical OMICs features an interview with Congenica CEO David Atkins who talks about the genomic medicine landscape and Congenica's plans for the future.
Raising awareness of Dravet Syndrome
Galia Wilson and Claire Eldred have provided us with today's article in recognition of International Dravet Syndrome Awareness day, Wednesday 23rd June.
Genomics in the Clinic & the Promise of Precision Medicine
At PMLS Precision Medicine and Rare Disease event, Congenica took part in a panel entitled 'Genomics in the Clinic and the Promise of Precision Medicine'.
Our story of Norrie Disease
We welcome guest blogger Carla Golledge, who shares her story about son Cameron who was born with Norrie disease.
Congenica funded to reduce fatal drug interactions by mapping genes
New software to reduce the number of adverse drug reactions is being developed thanks to a joint investment of £2 million provided by UKRI and L& G.
The challenges and opportunities for growth during a global pandemic
Congenica's Chairman Andy Richards and CEO David Atkins join leaders from biotech / pharma sector to discuss the impact of pandemic in the last 18 months.
Enhanced whole exome analysis enables Veritas Intercontinental to solve more cases
Veritas Genetics partnered with Congenica to improve diagnostic yield & increase the efficiency, throughput and speed of analysis in diagnostic laboratory
Genomic sequencing in a prenatal setting - posters presented at ISPD
Two members of Congenica’s Clinical Interpretation Services team presented posters at the International Conference on Prenatal Diagnosis and Therapy (ISPD)
Mutual Collaboration focus for CRDN Companies Forum
Alastair Kent and Dr Charles Steward attended the virtual Cambridge Rare Disease Network (CRDN) Companies Forum Patient Group and Industry Partnering event
Helping to Further the Patient Impact of Genomics
Dr Charles Steward was interviewed for podcast, Once Upon a Gene, where Effie speaks to others about their journey through life with rare disease.
How Schinzel-Giedion Syndrome (SGS) has changed our lives
Nuala Summerfield tells the story of her daughter's diagnosis of rare disease Schinzel-Giedion Syndrome (SGS) and setting up The SGS Foundation