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1. Increased frequency of repeat expansion mutations across different populations

3. Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits.

4. Global sequence properties for superfamily prediction: a machine learning approach

5. Large-Scale Pharmacogenomics Analysis of Patients With Cancer Within the 100,000 Genomes Project Combining Whole-Genome Sequencing and Medical Records to Inform Clinical Practice

6. GWAS of CRP response to statins further supports the role of APOE in statin response: A GIST consortium study

7. Insights for precision oncology from the integration of genomic and clinical data of 13,880 tumors from the 100,000 Genomes Cancer Programme

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

13. Prioritization of Kidney Cell Types Highlights Myofibroblast Cells in Regulating Human Blood Pressure

14. The Pharmacogenetics of Statin Therapy on Clinical Events: No Evidence that Genetic Variation Affects Statin Response on Myocardial Infarction

15. Sex, Genotype, and Liver Volume Progression as Risk of Hospitalization Determinants in Autosomal Dominant Polycystic Liver Disease

18. Predicting deleterious nsSNPs: an analysis of sequence and structural attributes

20. Certain heterozygous variants in the kinase domain of the serine/threonine kinase NEK8 can cause an autosomal dominant form of polycystic kidney disease

21. Rare variants in the sodium-dependent phosphate transporter gene SLC34A3 explain missing heritability of urinary stone disease

24. The Deep Genome Project

25. Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction.

26. A national initiative in data science for health: an evaluation of the UK Farr Institute

27. Stretch-activated ion channel TMEM63B associates with developmental and epileptic encephalopathies and progressive neurodegeneration

28. Late-Onset Autosomal Dominant Macular Degeneration Caused by Deletion of the CRX Gene

30. Whole-genome sequencing of chronic lymphocytic leukemia identifies subgroups with distinct biological and clinical features

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

32. Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution

33. Allopurinol versus usual care in UK patients with ischaemic heart disease (ALL-HEART): a multicentre, prospective, randomised, open-label, blinded-endpoint trial

34. Whole-genome sequencing reveals host factors underlying critical COVID-19

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

37. SOX11 variants cause a neurodevelopmental disorder with infrequent ocular malformations and hypogonadotropic hypogonadism and with distinct DNA methylation profile

38. Whole genome sequencing for the diagnosis of neurological repeat expansion disorders in the UK: a retrospective diagnostic accuracy and prospective clinical validation study

39. Prediction of Susceptibility to First-Line Tuberculosis Drugs by DNA Sequencing

40. Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.

41. Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

42. Evaluating the performance of a clinical genome sequencing program for diagnosis of rare genetic disease, seen through the lens of craniosynostosis

44. The power of genetic diversity in genome-wide association studies of lipids

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

46. SARS-CoV-2 susceptibility and COVID-19 disease severity are associated with genetic variants affecting gene expression in a variety of tissues

47. Scaling national and international improvement in virtual gene panel curation via a collaborative approach to discordance resolution

48. Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

49. A genome-wide interaction analysis of tricyclic/tetracyclic antidepressants and RR and QT intervals: a pharmacogenomics study from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium

50. Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

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