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1. Yield of genetic association signals from genomes, exomes and imputation in the UK Biobank

2. Genetic risk factors for COVID-19 and influenza are largely distinct

3. Association Between Whole Blood–Derived Mitochondrial DNA Copy Number, Low‐Density Lipoprotein Cholesterol, and Cardiovascular Disease Risk

4. The genetic determinants of recurrent somatic mutations in 43,693 blood genomes

5. Genetics of Latin American Diversity Project: Insights into population genetics and association studies in admixed groups in the Americas

6. Association analysis of mitochondrial DNA heteroplasmic variants: Methods and application

8. Prioritization of Kidney Cell Types Highlights Myofibroblast Cells in Regulating Human Blood Pressure

9. Converging evidence from exome sequencing and common variants implicates target genes for osteoporosis

10. A genetic association study of circulating coagulation factor VIII and von Willebrand factor levels

11. Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative

12. Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program

13. The Type 2 Diabetes Knowledge Portal: An open access genetic resource dedicated to type 2 diabetes and related traits

14. Association of mitochondrial DNA copy number with cardiometabolic diseases

15. Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program

16. Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis

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

18. Clonal hematopoiesis associated with epigenetic aging and clinical outcomes

19. Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program

20. Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices.

21. Epigenome-wide DNA methylation association study of circulating IgE levels identifies novel targets for asthma

22. Whole genome sequence analysis of pulmonary function and COPD in 19,996 multi-ethnic participants.

23. De novo mutations across 1,465 diverse genomes reveal mutational insights and reductions in the Amish founder population

24. Identification of CFTR variants in Latino patients with cystic fibrosis from the Dominican Republic and Puerto Rico

25. Whole Genome Sequencing Identifies CRISPLD2 as a Lung Function Gene in Children With Asthma

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

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

29. Whole-genome sequencing reveals host factors underlying critical COVID-19

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

31. The HUNT study: A population-based cohort for genetic research

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

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

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

37. Population-scale analysis of common and rare genetic variation associated with hearing loss in adults

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

39. Genetic Susceptibility to Mood Disorders and Risk of Stroke: A Polygenic Risk Score and Mendelian Randomization Study

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

41. Deep-coverage whole genome sequences and blood lipids among 16,324 individuals.

42. Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence

43. Publisher Correction: Whole genome sequencing in psychiatric disorders: the WGSPD consortium.

44. Correction: A 32 kb Critical Region Excluding Y402H in CFH Mediates Risk for Age-Related Macular Degeneration

45. Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes

46. Whole genome sequencing in psychiatric disorders: the WGSPD consortium.

47. Presence and transmission of mitochondrial heteroplasmic mutations in human populations of European and African ancestry

48. De novo mutations across 1,465 diverse genomes reveal mutational insights and reductions in the Amish founder population

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

50. Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline

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