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1. Genome-wide copy number variation association study in anorexia nervosa

6. Publisher Correction: Genetic correlates of vitamin D-binding protein and 25-hydroxyvitamin D in neonatal dried blood spots

7. Lithium response in bipolar disorder is associated with focal adhesion and PI3K-Akt networks: a multi-omics replication study

9. Leveraging base-pair mammalian constraint to understand genetic variation and human disease

10. Functional characterisation of the amyotrophic lateral sclerosis risk locus GPX3/TNIP1

11. Phenotypic and genetic factors associated with donation of DNA and consent to record linkage for prescription history in the Australian Genetics of Depression Study

15. Genetic correlates of vitamin D-binding protein and 25-hydroxyvitamin D in neonatal dried blood spots

17. Common Alleles: Next Steps in the Study of Common Variants

20. Interactions between the lipidome and genetic and environmental factors in autism

21. The correlates of neonatal complement component 3 and 4 protein concentrations with a focus on psychiatric and autoimmune disorders

23. Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions

26. Using brain cell-type-specific protein interactomes to interpret neurodevelopmental genetic signals in schizophrenia

28. GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores

29. Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection

30. A genome-wide association study of shared risk across psychiatric disorders implicates gene regulation during fetal neurodevelopment

31. Attention deficit hyperactivity disorder symptoms as antecedents of later psychotic outcomes in 22q11.2 deletion syndrome

32. Polygenic risk score analysis for amyotrophic lateral sclerosis leveraging cognitive performance, educational attainment and schizophrenia

33. Mapping genomic loci implicates genes and synaptic biology in schizophrenia

35. Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease

37. Lithium carbonate in amyotrophic lateral sclerosis patients homozygous for the C-allele at SNP rs12608932 in UNC13A: protocol for a confirmatory, randomized, group-sequential, event-driven, double-blind, placebo-controlled trial

38. Identifying the Common Genetic Basis of Antidepressant Response

39. Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

40. Age at first birth in women is genetically associated with increased risk of schizophrenia.

41. Estimation of Genetic Correlation via Linkage Disequilibrium Score Regression and Genomic Restricted Maximum Likelihood.

42. Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection

43. GWAS of epigenetic aging rates in blood reveals a critical role for TERT.

45. Autism-related dietary preferences mediate autism-gut microbiome associations

46. Large-scale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitness.

47. Association of Body Mass Index with DNA Methylation and Gene Expression in Blood Cells and Relations to Cardiometabolic Disease: A Mendelian Randomization Approach.

48. Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology

49. The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls

50. Classical Human Leukocyte Antigen Alleles and C4 Haplotypes Are Not Significantly Associated With Depression

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