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1. Genome-wide analysis of mitochondrial DNA copy number reveals loci implicated in nucleotide metabolism, platelet activation, and megakaryocyte proliferation

2. Triangulating Molecular Evidence to Prioritize Candidate Causal Genes at Established Atopic Dermatitis Loci

4. Linking Physical Activity to Breast Cancer via Sex Hormones, Part 1: The Effect of Physical Activity on Sex Steroid Hormones

5. Linking Physical Activity to Breast Cancer: Text Mining Results and a Protocol for Systematically Reviewing Three Potential Mechanistic Pathways

6. Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology (vol 53, pg 1636, 2021)

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

8. Opportunities and Challenges in Functional Genomics Research in Osteoporosis: Report From a Workshop Held by the Causes Working Group of the Osteoporosis and Bone Research Academy of the Royal Osteoporosis Society on October 5th 2020

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

11. Hypertensive Disorders of Pregnancy and DNA Methylation in Newborns:Findings From the Pregnancy and Childhood Epigenetics Consortium

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

13. Appraising the causal relevance of DNA methylation for risk of lung cancer

14. Hypertensive Disorders of Pregnancy and DNA Methylation in Newborns Findings From the Pregnancy and Childhood Epigenetics Consortium

15. Cohort Profile: Pregnancy And Childhood Epigenetics (PACE) Consortium

16. MELODI: Mining Enriched Literature Objects to Derive Intermediates

17. Cohort Profile: Pregnancy And Childhood Epigenetics (PACE) Consortium

18. Identifying low density lipoprotein cholesterol associated variants in the Annexin A2 (ANXA2) gene

19. Association between telomere length and risk of cancer and non-neoplastic diseases a mendelian randomization study

20. Appraising the causal relevance of DNA methylation for risk of lung cancer

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

23. Assessing the role of insulin-like growth factors and binding proteins in prostate cancer using Mendelian randomization:Genetic variants as instruments for circulating levels

25. Replication and characterization of association between ABO SNPs and red blood cell traits by meta-analysis in Europeans

26. Plasma urate concentration and risk of coronary heart disease: a Mendelian randomisation analysis

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

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

29. Assessing the role of insulin-like growth factors and binding proteins in prostate cancer using Mendelian randomization: Genetic variants as instruments for circulating levels

30. blood pressure loci identified with a gene-centricarray

31. Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant data

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

33. The effects of height and BMI on prostate cancer incidence and mortality: a Mendelian randomization study in 20,848 cases and 20,214 controls from the PRACTICAL consortium

34. The UK10K project identifies rare variants in health and disease

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

36. Loci influencing blood pressure identified using a cardiovascular gene-centric array (vol 22, pg 1663, 2013)

37. Erratum: Meta-analysis of dense genecentric association studies reveals common and uncommon variants associated with height ((The American Journal of Human Genetics (2010) 88 (6-18))

38. Erratum: Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci (American Journal of Human Genetics (2012) 90 (410-425))

40. A multi-cohort study of polymorphisms in the GH/IGF axis and physical capability: The HALCyon programme

41. Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

43. Variants in the human insulin gene that affect pre-mRNA splicing: is -23HphI a functional single nucleotide polymorphism at IDDM2?

44. Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps

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

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

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

50. Transcriptome-wide Mendelian randomization during CD4 + T cell activation reveals immune-related drug targets for cardiometabolic diseases.

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