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1. A first update on mapping the human genetic architecture of COVID-19

2. Cohort Profile: The United Kingdom Research study into Ethnicity and COVID-19 outcomes in Healthcare workers (UK-REACH)

3. S109 Genome-wide analysis of longitudinal lung function and gas transfer in individuals with idiopathic pulmonary fibrosis

5. Longitudinal lung function and gas transfer in individuals with idiopathic pulmonary fibrosis: a genome-wide association study

6. Persistent hesitancy for SARS-CoV-2 vaccines among healthcare workers in the United Kingdom: analysis of longitudinal data from the UK-REACH cohort study

7. Healthcare workers' views on mandatory SARS-CoV-2 vaccination in the UK: A cross-sectional, mixed- methods analysis from the UK-REACH study

8. Access to personal protective equipment in healthcare workers during the COVID-19 pandemic in the United Kingdom: results from a nationwide cohort study (UK-REACH)

10. Genome-wide association study of chronic sputum production implicates loci involved in mucus production and infection

11. S65 Genome-wide association study of survival times after diagnosis of idiopathic pulmonary fibrosis

12. Publisher Correction:Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals

13. Variants associated with HHIP expression have sexdifferential effects on lung function

14. Ethnic differences in SARS-CoV-2 vaccine hesitancy in United Kingdom healthcare workers: Results from the UK-REACH prospective nationwide cohort study

15. The United Kingdom Research study into Ethnicity And COVID-19 outcomes in Healthcare workers (UK-REACH): protocol for a prospective longitudinal cohort study of healthcare and ancillary workers in UK healthcare settings.

16. Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci

17. Variants associated with HHIP expression have sex-differential effects on lung function [version 1; peer review: 2 approved]

18. Fibroadenoma of the breast

19. Variants associated withHHIP expression have sex-differential effects on lung function

20. Chronic obstructive pulmonary disease and related phenotypes: polygenic risk scores in population-based and case-control cohorts

21. Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals

23. Corrigendum to: Cohort profile: Extended Cohort for E-health, Environment and DNA (EXCEED)

24. Cohort Profile: Extended Cohort for E-health, Environment and DNA (EXCEED)

25. Low-frequency variation in TP53 has large effects on head circumference and intracranial volume

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

27. T1 Meta-analysis of idiopathic pulmonary fibrosis genome-wide analyses identifies three novel genetic signals associated with disease susceptibility

28. SNPs associated withHHIPexpression have differential effects on lung function in males and females

29. Meta-analysis of exome array data identifies six novel genetic loci for lung function.

30. ExomeChip-Wide Analysis of 95 626 Individuals Identifies 10 Novel Loci Associated With QT and JT Intervals

31. Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis

32. Evidence for large-scale gene-by-smoking interaction effects on pulmonary function

33. Large-scale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitness

34. Phenotypic and pharmacogenetic evaluation of patients with thiazide-induced hyponatremia

35. Discovery of novel heart rate-associated loci using the Exome Chip

36. Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits

37. Genome-wide association study of copy number variation with lung function identifies a novel signal of association near BANP for forced vital capacity

38. Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants

39. Common Variants in the ATP2B1 Gene Are Associated With Susceptibility to Hypertension

40. Shared polygenic effects of FEV1 in the first genetic study in UK Biobank

41. A Meta-analysis of Gene Expression Signatures of Blood Pressure and Hypertension

42. Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel

43. Hypothesis-based analysis of gene-gene interactions and risk of myocardial infarction

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

45. Exome-wide analysis of rare coding variation identifies novel associations with COPD and airflow limitation in MOCS3, IFIT3 and SERPINA12

46. Genome-wide association study identifies 74 loci associated with educational attainment

47. Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies

48. blood pressure loci identified with a gene-centricarray

49. Four novel loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation In vivo

50. Common variants in the ATP2B1 gene are associated with susceptibility to hypertension: the Japanese Millennium GenomeProject

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