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1. GWAS for executive function and processing speed suggests involvement of the CADM2 gene

2. Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53949).

3. Drug–gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval

4. Genome-wide association study of Tourette's syndrome.

7. Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits (vol 50, pg 1412, 2018)

9. Quality control and conduct of genome-wide association meta-analyses

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

11. Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure

12. Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

13. Biological interpretation of genome-wide association studies using predicted gene functions

14. Trans-ethnic meta-analysis of white blood cell phenotypes

15. Segregation of FRAXE in a large family: clinical, psychometric, cytogenetic, and molecular data

18. Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity

19. Genome of the Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels

20. Meta-analysis of Genome-Wide Association Studies Identifies Novel Loci Associated With Optic Disc Morphology

21. Multiethnic Genome-Wide Association Study of Cerebral White Matter Hyperintensities on MRI

22. Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations

23. Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function

24. The Lin28/let-7 axis regulates glucose metabolism

25. Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process

26. ROBO2 gene variants are associated with familial vesicouretral reflux

27. Genetic contributions to variation in general cognitive function: A meta-analysis of genome-wide association studies in the CHARGE consortium (N=53 949)

28. New genetic loci link adipose and insulin biology to body fat distribution.

29. Biological interpretation of genome-wide association studies using predicted gene functions

30. Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium

31. New genetic loci link adipose and insulin biology to body fat distribution

32. A genome-wide association study of depressive symptoms

33. Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders

34. Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits

36. PARK6-linked parkinsonism occurs in several European families

37. Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure

38. Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (Nature Genetics (2010) 42 (105-116))

39. New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (vol 42, pg 105, 2010)

40. Genome-Wide Meta-Analysis of Myopia and Hyperopia Provides Evidence for Replication of 11 Loci

41. Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma

42. Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization

43. Erratum

44. GIGYF2 mutations are not a frequent cause of familial Parkinson's disease

45. ATP13A2 missense mutations in juvenile parkinsonism and young onset Parkinson disease

46. Comprehensive analysis of the LRRK2 gene in sixty families with Parkinson's disease

48. Novel parkin mutations detected in patients with early-onset Parkinson's disease

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