Search

Your search keyword '"WH Ouwehand"' showing total 23 results

Search Constraints

Start Over You searched for: Author "WH Ouwehand" Remove constraint Author: "WH Ouwehand" Journal nature genetics Remove constraint Journal: nature genetics
23 results on '"WH Ouwehand"'

Search Results

1. Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction.

2. Polygenic basis and biomedical consequences of telomere length variation.

3. Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression.

4. A catalog of genetic loci associated with kidney function from analyses of a million individuals.

5. Genome-wide association study of primary sclerosing cholangitis identifies new risk loci and quantifies the genetic relationship with inflammatory bowel disease.

6. Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing.

7. Defining the role of common variation in the genomic and biological architecture of adult human height.

8. Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.

9. SMIM1 underlies the Vel blood group and influences red blood cell traits.

10. Large-scale association analysis identifies new risk loci for coronary artery disease.

11. Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome.

12. Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndrome.

13. Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.

14. Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.

15. Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region.

16. A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium.

17. Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.

18. Cell-specific protein phenotypes for the autoimmune locus IL2RA using a genotype-selectable human bioresource.

19. New susceptibility locus for coronary artery disease on chromosome 3q22.3.

20. Six new loci associated with body mass index highlight a neuronal influence on body weight regulation.

21. Common variants near MC4R are associated with fat mass, weight and risk of obesity.

22. Genome-wide association analysis identifies 20 loci that influence adult height.

23. Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants.

Catalog

Books, media, physical & digital resources