Search

Your search keyword '"Daly, MJ"' showing total 947 results

Search Constraints

Start Over You searched for: Author "Daly, MJ" Remove constraint Author: "Daly, MJ"
947 results on '"Daly, MJ"'

Search Results

1. The female protective effect against autism spectrum disorder

2. Largest GWAS of PTSD (N=20 070) yields genetic overlap with schizophrenia and sex differences in heritability

3. Integrated Model of De Novo and Inherited Genetic Variants Yields Greater Power to Identify Risk Genes

4. A first update on mapping the human genetic architecture of COVID-19

5. GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture

6. Enhancing Discovery of Genetic Variants for Posttraumatic Stress Disorder Through Integration of Quantitative Phenotypes and Trauma Exposure Information

7. Mapping the human genetic architecture of COVID-19

8. Evaluating drug targets through human loss-of-function genetic variation (vol 581, pg 459, 2020)

9. The mutational constraint spectrum quantified from variation in 141,456 humans

10. The mutational constraint spectrum quantified from variation in 141,456 humans (vol 581, pg 434, 2020)

11. Evaluating potential drug targets through human loss-of-function genetic variation

12. Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17458 subjects

14. IBD risk loci are enriched in multigenic regulatory modules encompassing putative causative genes

16. Association of Genetic Variants in NUDT15 With Thiopurine-Induced Myelosuppression in Patients With Inflammatory Bowel Disease

17. Genetic and Transcriptomic Variation Linked to Neutrophil Granulocyte-Macrophage Colony-Stimulating Factor Signaling in Pediatric Crohn's Disease

18. Genome wide meta-analysis identifies genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders

19. International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci

20. Genetic architecture of human plasma lipidome and its link to cardiovascular disease

21. Polygenic burden in focal and generalized epilepsies

22. Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia

23. Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness

24. Rare Variant, Gene-Based Association Study of Hereditary Melanoma Using Whole-Exome Sequencing

25. Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.

26. Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population.

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

28. Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases

29. Variability in Working Memory Performance Explained by Epistasis vs Polygenic Scores in the ZNF804A Pathway

30. Data Descriptor: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

31. A second generation human haplotype map of over 3.1 million SNPs

33. Inherited determinants of Crohn's disease and ulcerative colitis phenotypes:a genetic association study

34. Genome-wide meta-analysis identifies new susceptibility loci for migraine

35. High-density mapping of the MHC identifies a shared role for HLA-DRB1∗01:03 in inflammatory bowel diseases and heterozygous advantage in ulcerative colitis

36. Genetic influences on schizophrenia and subcortical brain volumes: Large-scale proof of concept

37. Schizophrenia risk from complex variation of complement component 4

38. Three-Dimensional Virtual Navigation Versus Conventional Image Guidance: A Randomized Controlled Trial

39. Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies

40. The Lin28/let-7 axis regulates glucose metabolism

41. Localization of an acromesomelic dysplasia on chromosome 9 by homozygosity mapping

42. Genetic schizophrenia risk variants jointly modulate total brain and white matter volume

43. An integrated map of genetic variation from 1,092 human genomes

44. Bayesian inference analyses of the polygenic architecture of rheumatoid arthritis

45. Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease

46. Genome-wide association study of serious blistering skin rash caused by drugs

47. Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

48. Susceptibility to amoxicillin-clavulanate-induced liver injury is influenced by multiple HLA class I and class II alleles

49. Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes

50. Genome-wide association identifies multiple ulcerative colitis susceptibility loci (vol 42, pg 332, 2010)

Catalog

Books, media, physical & digital resources