News

We have added 5 genes to our Childhood Epilepsy Panel during 2014, to keep up our synchronization with the latest research available, in line with our priority for delivering highly accurate, quality tests. You can read more about the panel in our Neurology Section and the references to research in our Publications.

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Our renewed website was launched this december with only one purpose: serving you better. Now you can easily browse through our products via the menu or our searching tool and quickly obtain the information you need about our tests, our methods, genetic testing, or simply, to get to know who we are, and the values we stand for.

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Amplexa, as a part of the Fargen project, has started sequencing a Faroese reference exome cohort for the National Biobank. The aim is to sequence whole genomes for 1% of the Faroese population, at a clinical grade quality to improve health knowledge and with it, the quality of the Faroese health system. The project will continue trough 2015 and 2016.

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Amplexa was glad to attend and sponsor the Spanish Anti Epilepsy League (LECE), which this year revolved around neurosurgery and counted with the participation of numerous field specialists, and took place in Sevilla, Spain.

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Amplexa sponsored and participated in this NGS event organized in collaboration between Odense University Hospital and Biotexcel, bringing together key opinion leaders from laboratories in the nordic countries who are using NGS technology for clinical and research purposes.

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Amplexa participated and sponsored the annual meeting of the Danish Association of Medical Genetics (Dansk Selskab for Medecinsk Genetik)in Nyborg, in line with our involvement with the relevant institutions in our field.

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Amplexa participated -and sponsored- the traditional ILAE UK Chapter Annual Scientific meeting which took place in Nottingham this year and where we had the pleasure of meeting and learning from many highly-regarded specialists in the field of epilepsy.

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Our partner, the Danish Epilepsy Center in Dianalund organized this symposium on Dravet Syndrome, titled: "How to Proceed - diagnostics, clinics, treatment, course", which Amplexa had the pleasure to support given the strong character of our mutual collaboration and our interest in Dravet Syndrome as such.

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Amplexa participated in the 11th edition of the renowned Epileptology Congress celebrated this year in Stockholm, jointly organised by the International League Against Epilepsy and the Comission of European Affairs.

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Amplexa sponsored the 16th Annual Meeting of the Infantile Seizure Society (ISS), in collaboration with the Turkish Child Neurology Association in Cappadocia (Turkey). This year, the congress focused in the Epileptic syndromes of infancy and early childhood, an area in which Amplexa is deeply involved.

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Amplexa, in collaboration with the University of the Faroe Islands, the Faroe Marine Research Institute and the Faroese Food- and Veterinary Authority Agency have formed the HerGen research group with the purpose of sequencing the genome of the North Atlantic herring, a great step towards the development of a much needed stock management tool for the industry.

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Amplexa Genetics is excited to announce Niels Christian Ganderup as the new Head of International Sales. We are sure his extensive sales experience will help us meet our objectives and drive us towards success.

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