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Nearly €19 million from NWO for development and study of “organs-on-chips”

May 2017 – Organs-on-chips: miniature organs for research purposes It may sound futuristic, but it is now possible to create miniature versions of patients’ organs to study the development and treatment of diseases. This is what researchers from Leiden University Medical Centre (LUMC), University of Twente (UT), Technical University (TU) Delft, the Hubrecht Institute, and Cisca Wijmenga of the University Medical Centre Groningen (UMCG) aim to achieve in the next ten years. Together they’ve been awarded nearly €19 million by the Netherlands Organisation for Scientific Research (NWO) to work on this innovative project. The funding comes from the Dutch Gravitation programme. See more about

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The genetics of coeliac disease

Read an interview with Cisca Wijmenga about some of her work. She “is fascinated by the study of coeliac disease; here, she discusses her close connection to the history of the field, the changes brought about by new sequencing methods and the importance of collaboration”. Read about:   Navigating the non-coding regions of the genome  –  Genome of the Netherlands   —  Non-coding RNA  –  Coeliac disease the facts  –  Genetic risk profiling The project “Coeliac disease: from lincRNAs to disease mechanism (CD-Link)”  is supported by an ERC Advanced Investigator grant. By Josh Gabbatiss. Published courtesy of International Innovation – a leading scientific dissemination service. Link to full

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Dutch genome deciphered

The family tree of the Dutch people has been deciphered by researchers at 5 Dutch universities under the leadership of Prof. Cisca Wijmenga of the UMCG in Groningen. The early history of the Dutch can be re-written and diseases can be better predicted. The research is described in a Nature Genetics article published yesterday. `Paul de Bakker, Cisca Wijmenga and colleagues report on The Genome of the Netherlands Project, including whole-genome sequencing of 769 individuals of Dutch ancestry from 250 parent-offspring families and construction of a phased haplotype map. Their intermediate-coverage population sequencing data set provides a complementary resource to

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