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University of Groningen Genetic susceptibility for inflammatory bowel disease across ethnicities and diseases van Sommeren, Suzanne

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University of Groningen

Genetic susceptibility for inflammatory bowel disease across ethnicities and diseases

van Sommeren, Suzanne

DOI:

10.33612/diss.100597247

IMPORTANT NOTE: You are advised to consult the publisher's version (publisher's PDF) if you wish to cite from

it. Please check the document version below.

Document Version

Publisher's PDF, also known as Version of record

Publication date:

2019

Link to publication in University of Groningen/UMCG research database

Citation for published version (APA):

van Sommeren, S. (2019). Genetic susceptibility for inflammatory bowel disease across ethnicities and

diseases. Rijksuniversiteit Groningen. https://doi.org/10.33612/diss.100597247

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(2)

Stellingen behorende bij het proefschrift

Genetic Susceptibility for Inflammatory Bowel Disease across ethnicities and diseases

1. Identifying an increasing number of genetic risk loci for inflam-matory bowel disease hardly increases the explained disease va-riance, but contributes to biological insights (this thesis). 2. The majority of genetic risk loci for inflammatory bowel disease

are shared across populations, with a few exceptions, for example

NOD2 and ATG16L1 (this thesis).

3. To take into account the influence of ethnicity and certain sub-phenotypes of inflammatory bowel disease in genetic association studies, individuals under study should be deeply phenotyped (this thesis).

4. The shared pathogenesis of inflammatory bowel disease and its extra-intestinal manifestations is underscored by overlapping genetic associations and biological pathways (this thesis). 5. Gene co-expression networks and protein-protein interactions

of candidate genes residing in associated disease loci pinpoint shared biological pathways between inflammatory bowel disease and its extra-intestinal manifestations (this thesis).

6. The shared genetic risk loci between inflammatory bowel disease and gastro-intestinal graft-versus-host disease suggests possibi-lities for drug repositioning (this thesis).

7. Gene expression studies should take cell-type specificity into account (this thesis).

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