Annique Claringbould

Zoekresultaten

• 2019

  Allele specific expression identifies rare variants as cause for extreme allelic imbalance

  BIOS Consortium, jul.-2019, In: European Journal of Human Genetics. 27, blz. 601 1 blz.

  Onderzoeksoutput › Academic
• 2017

  MR-Link: Mendelian Randomization Under Linkage Disequilibrium and Unobserved Pleiotropy

  BIOS Consortium, 2017, In: Human heredity. 83, 5, blz. 233 1 blz.

  Onderzoeksoutput › Academic

• Multi-Phenotype Genome-Wide Meta-Analysis of Lipid Levels and BMI in 64,736 Europeans Suggests Shared Genetic Architecture

  Kaakinen, M., Magi, R., Lagou, V., Claringbould, A., Gaulton, K., Fischer, K., Morris, A., Prokopenko, I., BIOS Consortium & ENGAGE Consortium, nov.-2017, In: Genetic epidemiology. 41, 7, blz. 652-653 2 blz.

  Onderzoeksoutput: Meeting Abstract › Academic

• New Quality Measure for CNV: A Multi-Omics Approach

  Lepamets, M., Lepik, K., Kals, M., Carmeli, C., Claringbould, A., Bochud, M., Stringhini, S., Wijmenga, C., Franke, L., Magi, R. & Kutalik, Z., 2017, In: Human heredity. 83, 1, blz. 16-16 1 blz.

  Onderzoeksoutput › Academic
• 2016

  Genome-Wide Multiphenotype and eQTL Analyses Provide Novel Insights into Omega Fatty Acid Metabolism and Type 2 Diabetes

  Kaakinen, M., Claringbould, A., Hagenbeek, F., Magi, R., Ala-Korpela, M., Jarvelin, M.-R., Prokopenko, I. & BIOS Consortium, jun.-2016, In: Diabetes. 65, blz. A52-A52 1 blz.

  Onderzoeksoutput: Meeting Abstract › Academic