Research Areas
I am interested in understanding how genetic variation affects health and disease with a focus on pregnancy-related outcomes (birthweight and gestational duration) and selected childhood diseases. I often use the genome-wide association study (GWAS) approach, but my projects also include other types of data, such as metabolomics profiles. In terms of childhood diseases, I am particularly interested in 1) the gastrointestinal disorder pyloric stenosis, and 2) febrile seizures.
Educations |
|
2006 |
PhD in Statistical Genetics. The Royal Veterinary and Agricultural University of Denmark |
2002 |
MSc in Biology and Statistics. University of Copenhagen.
|
1997 |
BSc in Biology. University of Copenhagen |
Employments |
|
2011- |
Senior Researcher, Dept. of Epidemiology Research, SSI |
2007-2011 |
Research Scientist, Dept. of Epidemiology Research, SSI |
2006-2007 |
Research Scientist, Dept. of Statistics, deCODE genetics, Iceland |
2004-2005 |
Visiting Scientist, Dept. of Biostatistics, Johns Hopkins University, Baltimore (4 months) |
2003-2005 |
Statistics Instructor. The Royal Veterinary and Agricultural University of Denmark. |
2002 |
Visiting Research Assistant, Dept. of Biostatistics, Columbia University, New York (6 months) |
1999-2001 |
Assistant Editor of Biology, Danish National Encyclopedia |
Professional Activities and Leadership Positions |
2016- |
Research Group Leader, Dept. of Epidemiology Research, SSI. |
2007- |
Project leadership on numerous GWAS projects. |
Prizes and Honours |
2012 |
The Thorvald Madsen Prize |
International Collaborations |
A number of collaborative projects with the Early Growth Genetics (EGG) consortium and the iPSYCH consortium. Many international collaborations, e.g., for replication of genetic association findings or functional follow-up experiments.
|
Selected, recent publications |
Liu X, Helenius D, Skotte L, …, Buil A, Feenstra B. Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 are associated with gestational duration. bioRxiv 2018; 423897, https://doi.org/10.1101/423897
|
Fadista J, Skotte L, …, Feenstra B. Genome-wide meta-analysis identifies BARX1 and EML4-MTA3 as new loci associated with infantile hypertrophic pyloric stenosis. Human Molecular Genetics 2018; ddy347, https://doi.org/10.1093/hmg/ddy347 |
Beaumont RN, Warrington NM, …, Evans DM*, Lawlor DA*, Feenstra B*, Freathy RM*. Genome-wide association study of offspring birth weight in 86,577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics. Human Molecular Genetics 2018; 27, 742-756, https://doi.org/10.1093/hmg/ddx429 *Shared last author |
Zhang G, Feenstra B, …, Muglia LJ. Genetic Associations with Gestational Duration and Spontaneous Preterm Birth. New England Journal of Medicine 2017; 377, 1156-
1167, https://doi.org/10.1056/NEJMoa1612665 |
Feenstra B, …, Hviid A. Common variants associated with general and MMR vaccine-related febrile seizures. Nature Genetics 2014; 46: 1274-1282, https://doi.org/10.1038/ng.3129 |