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1. Mendelian randomization implies no direct causal association between leukocyte telomere length and amyotrophic lateral sclerosis

2. Smoking-by-genotype interaction in type 2 diabetes risk and fasting glucose

3. Associations of autozygosity with a broad range of human phenotypes

4. Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration

5. Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions

6. Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia

7. Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity

8. Erratum to: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

9. GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes

10. Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K i

11. Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index

12. Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis

13. Rare and low-frequency coding variants alter human adult height

14. Lack of evidence for a role of genetic variation in TMEM230 in the risk for Parkinson's disease in the Caucasian population

15. Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing

16. Genetic variation at 16q24.2 is associated with small vessel stroke

17. Novel genetic loci associated with hippocampal volume

18. Meta-analysis of rare and common exome chip variants identifies S1PR4 and other loci influencing blood cell traits

19. ABCA7 p.G215S as potential protective factor for Alzheimer's disease

20. Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits

21. DNA methylation-based measures of biological age: Meta-analysis predicting time to death

22. Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals

23. GWAS for executive function and processing speed suggests involvement of the CADM2 gene

24. GWAS for executive function and processing speed suggests involvement of the CADM2 gene

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

26. Consumption of meat is associated with higher fasting glucose and insulin concentrations regardless of glucose and insulin genetic risk scores: A meta-analysis of 50,345 Caucasians

27. New genetic loci link adipose and insulin biology to body fat distribution

28. The transcriptional landscape of age in human peripheral blood

29. Genetic overlap between diagnostic subtypes of ischemic stroke

30. Common genetic variants influence human subcortical brain structures

31. Genome-wide studies of verbal declarative memory in nondemented older people: The Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium

32. Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption

33. Frontotemporal dementia and its subtypes: A genome-wide association study

34. Prospective associations of coronary heart disease loci in African Americans using the MetaboChip

35. Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease

36. Pleiotropic genes for metabolic syndrome and inflammation

37. Multilocus genetic risk score associates with ischemic stroke in case-control and prospective cohort studies

38. Genetic diversity is a predictor of mortality in humans

39. Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization

40. Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease

41. Systematic identification of trans eQTLs as putative drivers of known disease associations

42. A genome-wide association study of depressive symptoms

43. Genome-Wide Association Study of Retinopathy in Individuals without Diabetes

44. The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism

45. Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: A cross-sectional study

46. Common variants at 6q22 and 17q21 are associated with intracranial volume

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

48. Genome-wide association studies of cerebral white matter lesion burden

49. Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

50. Identification of nine novel loci associated with white blood cell subtypes in a Japanese population

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