Search

Your search keyword '"Overton, John"' showing total 1,346 results

Search Constraints

Start Over You searched for: Author "Overton, John" Remove constraint Author: "Overton, John"
1,346 results on '"Overton, John"'

Search Results

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

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

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

5. NOTCH3 p.Arg1231Cys is markedly enriched in South Asians and associated with stroke

8. Genotyping, sequencing and analysis of 140,000 adults from Mexico City

9. Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects

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

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

24. Reviews

25. Author Correction: Genotyping, sequencing and analysis of 140,000 adults from Mexico City

27. Common and rare variant associations with clonal haematopoiesis phenotypes

33. Self-describing Digital Assets and Their Applications in an Integrated Science and Engineering Ecosystem

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

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

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

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

42. Student Perceptions of Effective Lecturers: The Need to Recognise the Role of Ethnicity and Choice of Discipline

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

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

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

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

Catalog

Books, media, physical & digital resources