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1. Epigenetic and proteomic signatures associate with clonal hematopoiesis expansion rate

2. Validation of human telomere length multi-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as human telomere length regulation genes

3. Epigenetic and proteomic signatures associate with clonal hematopoiesis expansion rate

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

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

6. Determinants of mosaic chromosomal alteration fitness

8. Associations of a Breast Cancer Polygenic Risk Score With Tumor Characteristics and Survival

9. Deleterious heteroplasmic mitochondrial mutations are associated with an increased risk of overall and cancer-specific mortality

10. A genome-wide gene-environment interaction study of breast cancer risk for women of European ancestry

11. Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencing

12. A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies

14. TOP-LD: A tool to explore linkage disequilibrium with TOPMed whole-genome sequence data

15. A genetic association study of circulating coagulation factor VIII and von Willebrand factor levels

16. Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project

17. Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative

18. Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program

19. Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed

20. Common variants in breast cancer risk loci predispose to distinct tumor subtypes

21. Genome-wide interaction analysis of menopausal hormone therapy use and breast cancer risk among 62,370 women

22. Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study

23. Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment

24. Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program

25. Genome-Wide Interaction Analysis of Menopausal Hormone Therapy Use and Breast Cancer Risk Among 62,370 Women

26. Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program

27. Combined Associations of a Polygenic Risk Score and Classical Risk Factors With Breast Cancer Risk.

28. Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

29. Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity

31. Transcriptome‐wide association study of breast cancer risk by estrogen‐receptor status

32. Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses.

33. Assessment of interactions between 205 breast cancer susceptibility loci and 13 established risk factors in relation to breast cancer risk, in the Breast Cancer Association Consortium

34. A network analysis to identify mediators of germline-driven differences in breast cancer prognosis.

35. Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes.

36. Allelic Heterogeneity at the CRP Locus Identified by Whole-Genome Sequencing in Multi-ancestry Cohorts

37. Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations.

38. EndoPRS: Incorporating Endophenotype Information to Improve Polygenic Risk Scores for Clinical Endpoints

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

41. Associations of obesity and circulating insulin and glucose with breast cancer risk: a Mendelian randomization analysis.

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

43. Genome-wide association study of germline variants and breast cancer-specific mortality.

44. Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes.

45. A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer

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

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

48. Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

49. Association analysis identifies 65 new breast cancer risk loci

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