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1. Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes (vol 50, pg 524, 2018)

2. Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (vol 50, pg 26, 2018)

3. Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (vol 50, pg 765, 2017)

4. 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

5. Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity

6. Genome of the Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels

7. Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility

8. Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant data

9. A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry

10. Exome sequencing and directed clinical phenotyping diagnose cholesterol ester storage disease presenting as autosomal recessive hypercholesterolemia

11. Erratum: Meta-analysis of dense genecentric association studies reveals common and uncommon variants associated with height ((The American Journal of Human Genetics (2010) 88 (6-18))

12. Sweet liking and high novelty seeking: independent phenotypes associated with alcohol-related problems.

14. AKT1 and neurocognition in schizophrenia [corrected] [published erratum appears in AUST NZ J PSYCHIATRY 2009 Oct;43(10):983].

16. Correlation of membranous glomerular ultrastructural changes with disease severity and outcome in lupus patients initiating cyclophosphamide therapy.

17. Association of adipose tissue deposition and beta-2 adrenergic receptor variants: the IRAS family study.

19. Longitudinal influence of age, menopause, hormone replacement therapy, and other medications on parotid flow rates in healthy women.

20. A catalog of genetic loci associated with kidney function from analyses of a million individuals

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

22. Proteomic networks and related genetic variants associated with smoking and chronic obstructive pulmonary disease.

23. A methylation risk score for chronic kidney disease: a HyperGEN study.

24. Single-Ancestry versus Multi-Ancestry Polygenic Risk Scores for CKD in Black American Populations.

25. Variant level heritability estimates of type 2 diabetes in African Americans.

26. Time-to-Event Genome-Wide Association Study for Incident Cardiovascular Disease in People With Type 2 Diabetes.

27. Polygenic Risk for Type 2 Diabetes in African Americans.

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

29. Lac-Phe mediates the effects of metformin on food intake and body weight.

30. Genetic drivers of heterogeneity in type 2 diabetes pathophysiology.

31. X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements.

32. Genome-wide study investigating effector genes and polygenic prediction for kidney function in persons with ancestry from Africa and the Americas.

33. Whole genome sequence analysis of apparent treatment resistant hypertension status in participants from the Trans-Omics for Precision Medicine program.

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

35. Type 2 Diabetes Modifies the Association of CAD Genomic Risk Variants With Subclinical Atherosclerosis.

36. Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease.

37. Lac-Phe mediates the anti-obesity effect of metformin.

38. Clonal Hematopoiesis of Indeterminate Potential (CHIP) and Incident Type 2 Diabetes Risk.

39. Large-scale exome array summary statistics resources for glycemic traits to aid effector gene prioritization.

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

41. Mendelian randomization study of diabetes and dementia in the Million Veteran Program.

42. The predominant PAR4 variant in individuals of African ancestry worsens murine and human stroke outcomes.

43. Plasma neurofilament light chain concentrations are elevated in youth-onset type 2 diabetes and associated with neuropathy.

44. WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE.

45. The Microbiome, Epigenome, and Diet in Adults with Obesity during Behavioral Weight Loss.

46. Time-to-Event Genome-Wide Association Study for Incident Cardiovascular Disease in People with Type 2 Diabetes Mellitus.

47. Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles.

48. Large scale proteomic studies create novel privacy considerations.

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

50. Canonical correlation analysis for multi-omics: Application to cross-cohort analysis.

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