Projectenlijst per vakgebied
Hieronder ziet u een lijst van projecten behorende tot een bepaald vakgebied. Gebruik de bovenstaande keuzelijst om projecten van een ander vakgebied te tonen.
Het is ook mogelijk om te zoeken op trefwoord.
Klik op de titel van het project voor meer informatie.
A search for novel genes causing familial hypercholesterolemia on the former island of Urk |
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Characteristics of breast and ovarian cancer in women with a PALB2-mutation |
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Chromosome 6 Project: unravelling chromosome 6 aberrations with the help of Facebook |
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Clonal hematopoiesis and cardiovascular disease after autologous hematopoietic cell transplantation |
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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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Deciphering the role of STAP1 in cholesterol metabolism |
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Drosophila as model organism for neurodegeneration and aging |
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Drosophila models to understand rare genetic disorders |
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Een C. elegans model voor de ziekte van Parkinson |
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Epigenetic architecture of Dupuytren’s disease |
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Essential tremor in families |
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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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Genetic origin of Dupuytren's disease and associated fibromatosis |
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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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How do tumor cells survive genomic instability? |
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Hunting for the second gene that causes CHARGE syndrome |
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Inducing regeneration through manipulation of Wnt signaling |
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Inheritability & genetics in essential tremor |
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Investigating the role of lincRNAs in autoimmune diseases |
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Isolated echogenic bowel in prenatal diagnosis and chromosomal abnormalities. |
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Key Biological Pathways for the Complex Mixed Phenotypes in Primary Childhood Ataxia |
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Liver disease and Next generation sequencing: a solution to the diagnostic problem? |
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Onderzoek naar het ontstaan en beloop van coeliakie (glutenintolerantie). |
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Parental perspectives of the care for a rare genetic disorder: Phelan-McDermid syndrome |
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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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Rapid whole exome sequencing in prenatal genetic diagnostics for ultrasound abnormalities |
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Regulation of aging and age-related disease by transcription factors, chromatin states, and the epigenome |
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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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Survival after cancer in PMS2-associated Lynch syndrome patients |
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The airway epithelium in asthma susceptibility: towards a cure for asthma. |
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The effect of CHD7 deletions and duplications |
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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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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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Unravelling Vici-like syndrome in the Netherlands |
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Using next generation sequencing to find causative genes in patients with severe microcephaly |
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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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