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

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

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

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

5. Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study.

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

7. Risk for Chronic Kidney Disease Progression After Acute Kidney Injury: Findings From the Chronic Renal Insufficiency Cohort Study.

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

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

10. Genetic drivers of heterogeneity in type 2 diabetes pathophysiology

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

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

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

14. Rare genetic variants explain missing heritability in smoking.

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

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

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

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

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

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

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

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

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

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

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

27. APOL1 Kidney-Risk Variants Induce Mitochondrial Fission

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

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

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

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

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

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

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

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

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

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

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

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

40. Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes

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

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

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

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

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

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

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

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

50. 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.

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