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1. Agonist antibody to guanylate cyclase receptor NPR1 regulates vascular tone

2. A deep catalogue of protein-coding variation in 983,578 individuals

3. Genetic drivers of heterogeneity in type 2 diabetes pathophysiology

4. Integrating transcriptomics, metabolomics, and GWAS helps reveal molecular mechanisms for metabolite levels and disease risk

5. Genome-wide association meta-analysis identifies risk loci for abdominal aortic aneurysm and highlights PCSK9 as a therapeutic target

6. A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids

7. A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation

8. Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia

9. Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci

10. The power of genetic diversity in genome-wide association studies of lipids

11. Mitochondrial genome copy number measured by DNA sequencing in human blood is strongly associated with metabolic traits via cell-type composition differences

12. Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder.

13. Sequencing of 640,000 exomes identifies GPR75 variants associated with protection from obesity

14. Association of structural variation with cardiometabolic traits in Finns

15. Common and rare variant associations with clonal haematopoiesis phenotypes

16. Colocalization of GWAS and eQTL signals at loci with multiple signals identifies additional candidate genes for body fat distribution.

17. A saturated map of common genetic variants associated with human height

18. “PMS2CL interference leading to erroneous identification of a pathogenic PMS2 variant in Black Patients”

19. Adipose Tissue Gene Expression Associations Reveal Hundreds of Candidate Genes for Cardiometabolic Traits.

20. Exome sequencing of Finnish isolates enhances rare-variant association power

21. Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution

22. Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation

23. Genome-wide analysis provides genetic evidence that ACE2 influences COVID-19 risk and yields risk scores associated with severe disease

24. Multiancestry exome sequencing reveals INHBE mutations associated with favorable fat distribution and protection from diabetes

25. Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

27. Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.

28. Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.

29. Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees

30. Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

31. Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.

32. Variants in autophagy genes MTMR12 and FAM134A are putative modifiers of the hepatic phenotype in α1-antitrypsin deficiency

34. Exome sequencing and analysis of 454,787 UK Biobank participants

35. Biallelic BRCA Loss and Homologous Recombination Deficiency in Nonbreast/Ovarian Tumors in Germline BRCA1/2 Carriers

36. Author Correction: Common and rare variant associations with clonal haematopoiesis phenotypes

37. A Low-Frequency Inactivating Akt2 Variant Enriched in the Finnish Population is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk.

38. Rare and low-frequency coding variants alter human adult height

40. Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci

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

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

43. Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locus.

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

45. Rare variants in PPARG with decreased activity in adipocyte differentiation are associated with increased risk of type 2 diabetes

46. Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol

48. PMS2CL interference leading to erroneous identification of a pathogenic PMS2 variant in Black patients

49. Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder

50. Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

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