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1. Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity

2. Manhattan++: displaying genome-wide association summary statistics with multiple annotation layers

3. Lack of genetic support for shared aetiology of Coronary Artery Disease and Late-onset Alzheimer’s disease

4. A mouse-to-man candidate gene study identifies association of chronic otitis media with the loci TGIF1 and FBXO11

5. Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individuals

6. Genetic Determinants of the Interventricular Septum Are Linked to Ventricular Septal Defects and Hypertrophic Cardiomyopathy

7. A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape

8. Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries.

9. Vitamin D levels and susceptibility to asthma, elevated immunoglobulin E levels, and atopic dermatitis: A Mendelian randomization study.

10. Identifying systematic heterogeneity patterns in genetic association meta-analysis studies.

11. Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.

12. Abstract 11789: Genetic Determinants of Interventricular Septal Anatomy and Risk of Congenital Heart Disease

13. The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.

14. Robust estimates of heritable coronary disease risk in individuals with type 2 diabetes

15. Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants

16. Association of the PHACTR1/EDN1 Genetic Locus With Spontaneous Coronary Artery Dissection

17. Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions

18. Distribution and medical impact of loss-of-function variants in the Finnish founder population.

19. Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants

20. Heritability and family-based GWAS analyses of the N-acyl ethanolamine and ceramide plasma lipidome

21. Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits.

22. Heritability of haemodynamics in the ascending aorta

23. Genome-wide association study in a Lebanese cohort confirms PHACTR1 as a major determinant of coronary artery stenosis.

24. Large scale association analysis identifies three susceptibility loci for coronary artery disease.

25. Genome-wide association study of blood pressure extremes identifies variant near UMOD associated with hypertension.

26. Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies.

27. Targeting 160 candidate genes for blood pressure regulation with a genome-wide genotyping array.

28. Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations.

29. Genetic variation on chromosome 6 influences F cell levels in healthy individuals of African descent and HbF levels in sickle cell patients.

30. Polymorphisms in the WNK1 gene are associated with blood pressure variation and urinary potassium excretion.

31. Genetic variation in VEGF does not contribute significantly to the risk of congenital cardiovascular malformation.

32. SLC2A9 is a high-capacity urate transporter in humans.

33. Genome-wide mapping of susceptibility to coronary artery disease identifies a novel replicated locus on chromosome 17.

34. Marked variation in heritability estimates of left ventricular mass depending on modality of measurement

35. Manhattan++: displaying genome-wide association summary statistics with multiple annotation layers

36. Data-driven modelling of mutational hotspots and in-silico predictors in hypertrophic cardiomyopathy

37. Heritability and family-based GWAS analyses of the N-acyl ethanolamine and ceramide plasma lipidome

38. A multi-ancestry genome-wide study incorporating gene–smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure

39. Disruption of FOXF2 as a Likely Cause of Absent Uvula in an Egyptian Family

40. Trans-ethnic association study of blood pressure determinants in over 750,000 individuals

41. A Method to Exploit the Structure of Genetic Ancestry Space to Enhance Case-Control Studies

42. Diagnostic Yield and Clinical Utility of Sequencing Familial Hypercholesterolemia Genes in Patients With Severe Hypercholesterolemia

43. Reevaluation of the South Asian MYBPC3Δ25bp Intronic Deletion in Hypertrophic Cardiomyopathy

44. Differential Gene Expression in Macrophages From Human Atherosclerotic Plaques Shows Convergence on Pathways Implicated by Genome-Wide Association Study Risk Variants

45. Plasma cytokines and risk of coronary heart disease in the PROCARDIS study

46. A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure

47. Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

48. Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries

49. Puesta al día en estatinas. Nuevas recomendaciones

50. Genetic analysis of over one million people identifies 535 novel loci for blood pressure

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