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

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

3. Erratum: Genomewide meta-analysis identifies loci associated with IGF-I and IGEBP-3 levels with impact on age-related traits

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

5. Serum iron levels and the risk of Parkinson Disease: a Mendelian randomization study

6. A GWAS sequence variant for platelet volume marks an alternative DNM3 promoter in megakaryocytes near a MEIS1 binding site

7. Modulation of Genetic Associations with Serum Urate Levels by Body-Mass-Index in Humans

8. Pleiotropy among common genetic loci identified for cardiometabolic disorders and C-reactive protein

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

10. Seventy-five genetic loci influencing the human red blood cell

11. Genome-Wide Association Study to Identify Common Variants Associated with Brachial Circumference: A Meta-Analysis of 14 Cohorts

12. Genome-wide association study to identify common variants associated with brachial circumference: a meta-analysis of 14 cohorts

13. New gene functions in megakaryopoiesis and platelet formation

14. Erratum: Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution (Nature Genetics (2010) 42 (949-960))

15. Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes

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

17. A global in vivo Drosophila RNAi screen identifies NOT3 as a key regulator of heart function

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

20. Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets from Blood and the Kidney

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

22. Genetic studies of body mass index yield new insights for obesity biology

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

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

25. Genome-wide association analyses identify 18 new loci associated with serum urate concentrations

26. SNP prioritization using a bayesian probability of association

27. A Genome-Wide Association Search for Type 2 Diabetes Genes in African Americans

28. Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women

29. Seventy-five genetic loci influencing the human red blood cell

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

31. Correction: Corrigendum: Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis

32. Identification of a set of endogenous reference genes for miRNA expression studies in Parkinson’s disease blood samples

33. How to communicate and what to disclose to participants in a recall-by-genotype research approach: a multistep empirical study.

34. Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits.

35. Hypoxia Sensing and Responses in Parkinson's Disease.

36. Nuclear and mitochondrial genetic variants associated with mitochondrial DNA copy number.

37. Intracellular delivery of Parkin-RING0-based fragments corrects Parkin-induced mitochondrial dysfunction through interaction with SLP-2.

38. Participant perspective on the recall-by-genotype research approach: a mixed-method embedded study with participants of the CHRIS study.

39. Fluorescent reporter of  Caenorhabditis elegans Parkin: Regulators of its abundance and role in autophagy-lysosomal dynamics.

40. Genetic insights into resting heart rate and its role in cardiovascular disease.

41. Mitochondrial DNA heteroplasmy distinguishes disease manifestation in PINK1/PRKN-linked Parkinson's disease.

42. Antithrombin, Protein C, and Protein S: Genome and Transcriptome-Wide Association Studies Identify 7 Novel Loci Regulating Plasma Levels.

43. Role of Ceramides and Sphingolipids in Parkinson's Disease.

44. Molecular phenotypes of mitochondrial dysfunction in clinically non-manifesting heterozygous PRKN variant carriers.

45. The small GTPase Rit2 modulates LRRK2 kinase activity, is required for lysosomal function and protects against alpha-synuclein neuropathology.

46. Increased Levels of the Parkinson's Disease-Associated Gene ITPKB Correlate with Higher Expression Levels of α-Synuclein, Independent of Mutation Status.

47. Pain sensitivity is modulated by affective temperament: Results from the population-based CHRIS Affective Disorder (CHRIS-AD) study.

48. Induced Pluripotent Stem Cell (iPSC) Lines from a Family with Resistant Epileptic Encephalopathy Caused by Compound Heterozygous Mutations in SZT2 Gene.

49. Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.

50. A genome on shaky ground: exploring the impact of mitochondrial DNA integrity on Parkinson's disease by highlighting the use of cybrid models.

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