List of projects by field of study
Below you see a list of researchprojects within a certain field of study. Please use the selectbox to view researchprojects of another field of research.
It is also possible to search for keywords.
Click the title of a researchproject for more details.
A search for novel genes causing familial hypercholesterolemia on the former island of Urk |
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Cardiac care in families with an inherited heart disease: how to handle? Zinnige(r) zorg voor families met erfelijke hartziektes |
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Characteristics of breast and ovarian cancer in women with a PALB2-mutation |
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Chemical Correction of FVII Mutation |
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Chemical correction of the R175C p53 missmutation |
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Colitis ulcerosa en de ziekte van Crohn:onderzoek naar genetische en omgevings risicofactoren |
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De waarde van genetische diagnostiek (next-generation sequencing) bij jonge patiënten met nierfalen |
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De ziekte van Von Hippel-Lindau: genotype–fenotype correlatie? |
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Deciphering the role of STAP1 in cholesterol metabolism |
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Drosophila as model organism for neurodegeneration and aging |
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Duty to recontact in clinical genetics: an e-health solution? |
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Essential tremor in families |
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Evidence-based information on rare chromosomal microdeletion and –duplication syndromes for parents and doctors |
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Experiences of pregnant women and their partners with prenatal emergency diagnostics by means of genetic testing (prenatal whole exome sequencing) |
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Functional characterization of genetic susceptibility variants of Celiac disease |
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Genetic causes of hypoplastic left heart syndrome |
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Genetics in Parkinson's disease |
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Genetics of asthma: the role of Protocadherin-1 in airway epithelial integrity and function. |
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Genetische diagnostiek bij plotse hartdood en idiopathisch kamerfibrilleren |
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How do tumor cells survive genomic instability? |
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Identification of rare genetic variants contributing to the development of childhood-onset IBD-PSC using parent-offspring trios (part 2) |
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Illustrating the role of microbiome in human health |
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Inducing regeneration through manipulation of Wnt signaling |
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Interactions between CNS and immune system in neurodegenerative diseases. |
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Investigating the role of lincRNAs in autoimmune diseases |
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Investigating the role of miRNAs in autoimmune diseases |
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Liver disease and Next generation sequencing: a solution to the diagnostic problem? |
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Long non-coding RNA in liver disease |
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Microbiome analysis in gastrointestinal diseases |
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Prevalence of X-linked hypophospatemic rickets (XLH) in the Netherlands and the relation between genotype and phenotype in children. |
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Proteogenomics analysis of COPD patient derived fibroblast to reveal molecular mechanism of COPD development |
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Regulation of aging and age-related disease by transcription factors, chromatin states, and the epigenome |
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Screening future parents for serious diseases in the fertility clinic: an exploration of views of future parents and fertility doctors |
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Somatic mutations in peripheral blood of healthy individuals (clonal hematopoiesis); clinical implications and relation to ageing manifestations of the hematopoietic system |
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The airway epithelium in asthma susceptibility: towards a cure for asthma. |
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The incidence of contralateral breast cancer in women with a BRCA1/2 mutation: the role of family history |
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The outcomes of ten year follow-up of relatives at risk for sudden death due to dilatation/ dissection of the aorta: time for improvement? |
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The role of noncoding RNAs in B cell lymphoma |
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Unraveling the causative genes – and pathways - for autoimmune diseases |
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Unraveling the genetic and biological pathways of spinocerebellar ataxia |
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Unsolved cardiogenetic cases. Genetisch diagnostisch management van onopgeloste patiënten met een erfelijke hartziekte. |
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Which syndromes are associated with paediatric dilated cardiomyopathy (DCM) and how to recognize these? A systematic review of the literature. |
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