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1. Multi‐phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations

2. Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

3. Diversity in genetic risk of recurrent stroke: a genome-wide association study meta-analysis

4. Hepatocyte growth factor demonstrates racial heterogeneity as a biomarker for coronary heart disease

5. Genetic associations with lipoprotein subfraction measures differ by ethnicity in the multi-ethnic study of atherosclerosis (MESA)

6. 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.

7. Elevated Levels of Adhesion Proteins Are Associated With Low Ankle-Brachial Index.

8. Impact of adiposity on cellular adhesion: The Multi‐Ethnic Study of atherosclerosis (MESA)

9. Genome-wide association of body fat distribution in African ancestry populations suggests new loci.

10. A genome-wide association search for type 2 diabetes genes in African Americans.

11. Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting

13. Serum magnesium and calcium levels in relation to ischemic stroke: Mendelian randomization study

15. Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

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

17. Stroke genetics informs drug discovery and risk prediction across ancestries

18. GRECOS Project (Genotyping Recurrence Risk of Stroke): The Use of Genetics to Predict the Vascular Recurrence After Stroke

19. Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): a meta-analysis of genome-wide association studies

25. Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors

27. Mutations at the BLK locus linked to maturity onset diabetes of the young and [beta]-cell dysfunction

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

29. Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis

30. Genome-Wide Analysis of Blood Pressure Variability and Ischemic Stroke

32. Mutations in a novel gene, NHS, cause the pleiotropic effects of Nance-Horan Syndrome, including severe congenital cataract, dental anomalies, and mental retardation

33. Genetic dissection of the human leukocyte antigen region by use of haplotypes of Tasmanians with multiple sclerosis

34. Are Myocardial Infarction–Associated Single-Nucleotide Polymorphisms Associated With Ischemic Stroke?

35. Otitis media susceptibility and shifts in the head and neck microbiome due to SPINK5 variants

38. Genome-wide linkage scan in Gullah-Speaking African American families with type 2 diabetes: the Sea Islands Genetic African American Registry (Project SuGAR)

39. Relative effects of LDL-C on ischemic stroke and coronary disease A Mendelian randomization study

40. Association of the distal region of the ectonucleotide pyrophosphatase/phosphodiesterase 1 gene with type 2 diabetes in an African-American population enriched for nephropathy

42. Variants of the transcription factor 7-like 2 (TCF7L2) gene are associated with type 2 diabetes in an African-American population enriched for nephropathy

43. Association of the estrogen receptor-α gene with the metabolic syndrome and its component traits in African-American families: the Insulin Resistance Atherosclerosis Family Study

48. Investigation of the estrogen receptor-α gene with type 2 diabetes and/or nephropathy in African-American and European-American populations

50. A genome-wide scan for type 2 diabetes in African-American families reveals evidence for a locus on chromosome 6q

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