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1. An LGR6 frameshift variant abrogates receptor expression on select leukocyte subsets and is associated with viral infections

2. Defining the clinical validity of genes reported to cause pulmonary arterial hypertension

3. PIK3R3 is a candidate regulator of platelet count in people of Bangladeshi ancestry

4. Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations

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

6. Global Biobank analyses provide lessons for developing polygenic risk scores across diverse cohorts

7. Meta-analysis fine-mapping is often miscalibrated at single-variant resolution

8. Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease

9. Population‐based identity‐by‐descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia

10. Genetic correlations among psychiatric and immune‐related phenotypes based on genome‐wide association data

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

12. Transferability of genetic loci and polygenic scores for cardiometabolic traits in British Pakistani and Bangladeshi individuals

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

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

15. Identification of rare sequence variation underlying heritable pulmonary arterial hypertension.

16. Allele-specific control of rodent and human lncRNA KMT2E-AS1 promotes hypoxic endothelial pathology in pulmonary hypertension

17. Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci

18. Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysis

19. Integrating polygenic risk scores in the prediction of type 2 diabetes risk and subtypes in British Pakistanis and Bangladeshis: A population-based cohort study

20. Genome-wide association analysis identifies 13 new risk loci for schizophrenia

21. Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity

22. Initiation codon mutation in betaB1-crystallin (CRYBB1) associated with autosomal recessive nuclear pulverulent cataract.

23. PIK3R3 is a candidate regulator of platelet count in people of Bangladeshi ancestry

24. Integrative Multiomics to Dissect the Lung Transcriptional Landscape of Pulmonary Arterial Hypertension

25. Global Biobank analyses provide lessons for developing polygenic risk scores across diverse cohorts

26. Health and population effects of rare gene knockouts in adult humans with related parents

27. Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease

28. Integrative Multiomics to Dissect the Lung Transcriptional Landscape of Pulmonary Arterial Hypertension

29. Additional file 26 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

30. Additional file 34 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

31. Additional file 16 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

32. Author Correction : The power of genetic diversity in genome-wide association studies of lipids

33. Additional file 6 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

34. Additional file 9 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

36. Genome-wide meta-analysis implicates mediators of hair follicle development and morphogenesis in risk for severe acne

37. Genetic counselling and testing in pulmonary arterial hypertension: a consensus statement on behalf of the International Consortium for Genetic Studies in PAH

38. Abstract 14753: Loss of Function ABCC8 Mutations Are Associated With Pulmonary Arterial Hypertension

39. Exome-wide association study reveals novel psoriasis susceptibility locus at TNFSF15 and rare protective alleles in genes contributing to type I IFN signalling

41. A polygenic resilience score moderates the genetic risk for schizophrenia

42. Mendelian randomisation and experimental medicine approaches to IL-6 as a drug target in PAH

43. Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders

45. Mutations in the Pericentrin (PCNT) Gene Cause Primordial Dwarfism

46. HUMAN GENOMICS: Health and population effects of rare gene knockouts in adult humans with related parents

47. Pulmonary Arterial Hypertension: A Current Perspective on Established and Emerging Molecular Genetic Defects

48. Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAH

49. Mendelian randomisation and experimental medicine approaches to interleukin-6 as a drug target in pulmonary arterial hypertension

50. Additional file 1 of Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAH

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