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2. Understanding the genetic complexity of puberty timing across the allele frequency spectrum

3. Genome-wide characterization of circulating metabolic biomarkers

4. Publisher Correction: Understanding the genetic complexity of puberty timing across the allele frequency spectrum

5. Author Correction: Trans-ancestral genome-wide association study of longitudinal pubertal height growth and shared heritability with adult health outcomes

7. Trans-ancestral genome-wide association study of longitudinal pubertal height growth and shared heritability with adult health outcomes

8. Genetic drivers of heterogeneity in type 2 diabetes pathophysiology

9. Considering Collective Motivation to Read: A Narrative, Inquiry

11. Accounting Standards Codification 326: Three Years of Expected Credit Loss Reporting

12. Plasma proteomic associations with genetics and health in the UK Biobank

13. Multilingual Implications for Reading Prosody Assessment

14. Genome-wide meta-analysis and omics integration identifies novel genes associated with diabetic kidney disease

16. GWAS of random glucose in 476,326 individuals provide insights into diabetes pathophysiology, complications and treatment stratification

17. Evaluating human genetic support for hypothesized metabolic disease genes

18. Thrombosis risk in single- and double-heterozygous carriers of factor V Leiden and prothrombin G20210A in FinnGen and the UK Biobank

19. High-Resolution Genotyping of Formalin-Fixed Tissue Accurately Estimates Polygenic Risk Scores in Human Diseases

20. Genetic analysis of blood molecular phenotypes reveals common properties in the regulatory networks affecting complex traits

22. Nutrient Cycling

23. Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus

25. Genetic effects on the timing of parturition and links to fetal birth weight

27. Discovery of drug–omics associations in type 2 diabetes with generative deep-learning models

28. FinnGen provides genetic insights from a well-phenotyped isolated population

29. Improving reporting standards for polygenic scores in risk prediction studies

30. Genome-wide association study identifies 48 common genetic variants associated with handedness

31. The public health impact of poor sleep on severe COVID-19, influenza and upper respiratory infections

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

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

34. Complement genes contribute sex-biased vulnerability in diverse disorders

35. Identification of type 2 diabetes loci in 433,540 East Asian individuals

36. An effector index to predict target genes at GWAS loci

37. Risk of Midlife Stroke After Adverse Pregnancy Outcomes: The FinnGen Study

39. Comprehensive Inherited Risk Estimation for Risk-Based Breast Cancer Screening in Women

41. Author Correction: Discovery of drug–omics associations in type 2 diabetes with generative deep-learning models

42. Author Correction: Genetic effects on the timing of parturition and links to fetal birth weight

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

45. Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 associate with gestational duration.

46. Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology

47. Multiethnic Genome-wide Association Study of Diabetic Retinopathy using Liability Threshold Modeling of Duration of Diabetes and Glycemic Control

48. A genome‐wide association study suggests new evidence for an association of the NADPH Oxidase 4 (NOX4) gene with severe diabetic retinopathy in type 2 diabetes

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

50. Author Correction: Identification of genetic effects underlying type 2 diabetes in South Asian and European populations

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