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1. Genetic variants for head size share genes and pathways with cancer

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

3. Rare variant contribution to the heritability of coronary artery disease

4. Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification

5. The genetic determinants of recurrent somatic mutations in 43,693 blood genomes

6. Genetic drivers of heterogeneity in type 2 diabetes pathophysiology

7. Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies

8. Genetic diversity fuels gene discovery for tobacco and alcohol use

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

10. Rare genetic variants explain missing heritability in smoking.

11. Whole-genome sequencing uncovers two loci for coronary artery calcification and identifies ARSE as a regulator of vascular calcification

12. Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential

13. Whole genome sequence analysis of blood lipid levels in >66,000 individuals

14. Gene Set Enrichment Analsyes Identiify Pathways Involved in Genetic Risk for Diabetic Retinopathy

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

17. Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis

18. Multiethnic Genome-Wide Association Study of Subclinical Atherosclerosis in Individuals With Type 2 Diabetes

19. Creation of a Single Institutional Review Board for Collaborative Research in Nephrology: The APOLLO Experience

20. Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices.

21. Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry

22. Fully Automatic Liver Attenuation Estimation Combing CNN Segmentation and Morphological Operations

23. Inherited causes of clonal haematopoiesis in 97,691 whole genomes

24. Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale.

25. APOL1 Kidney-Risk Variants Induce Mitochondrial Fission

26. APOL1 Long-term Kidney Transplantation Outcomes Network (APOLLO): Design and Rationale

27. Tubular Biomarkers and Chronic Kidney Disease Progression in SPRINT Participants.

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

29. Genome-wide association study identifies novel loci for type 2 diabetes-attributed end-stage kidney disease in African Americans

30. HDAC9 is implicated in atherosclerotic aortic calcification and affects vascular smooth muscle cell phenotype

31. Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria.

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

33. The African Descent and Glaucoma Evaluation Study (ADAGES) III Contribution of Genotype to Glaucoma Phenotype in African Americans: Study Design and Baseline Data

34. Genetic Architecture of Primary Open-Angle Glaucoma in Individuals of African Descent The African Descent and Glaucoma Evaluation Study III

35. Urinary Biomarkers of Tubular Damage Are Associated with Mortality but Not Cardiovascular Risk among Systolic Blood Pressure Intervention Trial Participants with Chronic Kidney Disease.

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

37. Blood-based bioenergetic profiling is related to differences in brain morphology in African Americans with Type 2 diabetes

38. Associations of coronary artery calcified plaque density with mortality in type 2 diabetes: the Diabetes Heart Study

39. Genome‐wide interaction with the insulin secretion locus MTNR1B reveals CMIP as a novel type 2 diabetes susceptibility gene in African Americans

40. Exome Chip Analysis Identifies Low-Frequency and Rare Variants in MRPL38 for White Matter Hyperintensities on Brain Magnetic Resonance Imaging

41. Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals

43. Adiponectin Isoform Patterns in Ethnic‐Specific ADIPOQ Mutation Carriers: The IRAS Family Study

44. Transancestral mapping and genetic load in systemic lupus erythematosus.

45. Type 2 Diabetes Variants Disrupt Function of SLC16A11 through Two Distinct Mechanisms

46. Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry Genetics Consortium.

47. Kidney Disease, Hypertension Treatment, and Cerebral Perfusion and Structure

48. Multiomics Analyses Identify AKR1A1 as a Biomarker for Diabetic Kidney Disease.

50. Collaboration between Dialysis Providers

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