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1. Autochthonous Human Babesia divergens Infection, England

2. SCGB1D2 inhibits growth of Borrelia burgdorferi and affects susceptibility to Lyme disease

3. TWINGEN: protocol for an observational clinical biobank recall and biomarker cohort study to identify Finnish individuals with high risk of Alzheimer’s disease

4. The Exponential Shapeshifting Response of N-Vinylcaprolactam Hydrogel Bilayers Due to Temperature Change for Potential Minimally Invasive Surgery

5. A chromosome scale assembly of the tarnished plant bug, Lygus lineolaris (Palisot de Beauvois), genome

6. Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality

7. O11: An atlas of 1.2M structural variants across global populations in the Genome Aggregation Database (gnomAD)

8. O43: Analysis of >800,000 diverse sequenced humans in gnomAD improves clinical interpretation and provides insight into gene function

9. Risk and protection of different rare protein-coding variants of complement component C4A in age-related macular degeneration

10. Inflammatory and infectious upper respiratory diseases associate with 41 genomic loci and type 2 inflammation

11. Genetic analyses implicate complex links between adult testosterone levels and health and disease

12. Efficient and accurate frailty model approach for genome-wide survival association analysis in large-scale biobanks

13. The 22q11.2 region regulates presynaptic gene-products linked to schizophrenia

14. Comprehensive genome-wide association study of different forms of hernia identifies more than 80 associated loci

15. Cohort profile: SUPER-Finland – the Finnish study for hereditary mechanisms of psychotic disorders

16. Identifying Novel Genes and Variants in Immune and Coagulation Pathways Associated with Macular Degeneration

17. Recontacting biobank participants to collect lifestyle, behavioural and cognitive information via online questionnaires: lessons from a pilot study within FinnGen

18. Publisher Correction: Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality

19. Integrated analyses of growth differentiation factor-15 concentration and cardiometabolic diseases in humans

20. The role of polygenic risk and susceptibility genes in breast cancer over the course of life

21. GWAS of thyroid stimulating hormone highlights pleiotropic effects and inverse association with thyroid cancer

22. Sleep apnoea is a risk factor for severe COVID-19

23. Author Correction: GWAS of thyroid stimulating hormone highlights the pleiotropic effects and inverse association with thyroid cancer

24. Correction: A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease.

25. A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease.

26. Quantifying unobserved protein-coding variants in human populations provides a roadmap for large-scale sequencing projects

27. High-Quality Exome Sequencing of Whole-Genome Amplified Neonatal Dried Blood Spot DNA.

28. Allele-specific methylation occurs at genetic variants associated with complex disease.

32. Risk of Midlife Stroke After Adverse Pregnancy Outcomes: The FinnGen Study

34. New insights into the genetic etiology of Alzheimer's disease and related dementias

35. LAVAA: A lightweight association viewer across ailments

36. Simulating Solar Radio Bursts Using Generative Adversarial Networks

37. Improving fine-mapping by modeling infinitesimal effects

38. Integrated analyses of growth differentiation factor-15 concentration and cardiometabolic diseases in humans

39. A Chromosome-Length Reference Genome for the Endangered Pacific Pocket Mouse Reveals Recent Inbreeding in a Historically Large Population

41. Cohort profile: SUPER-Finland – the Finnish study for hereditary mechanisms of psychotic disorders

43. REPLACING GWAS ARRAYS: CAPTURING GENOMIC DIVERSITY WITH A NOVEL WHOLE-EXOME PLUS LOW-PASS WHOLE GENOME PRODUCT

44. ANALYSIS OF RARE CODING AND COMMON VARIANTS IN AUTISM AND COMORBID SUBGROUPS

45. Secretoglobin family 1D member 2 (SCGB1D2) protein inhibits growth of Borrelia burgdorferi and affects susceptibility to Lyme disease

46. Identifying Novel Genes and Variants in Immune and Coagulation Pathways Associated with Macular Degeneration

47. Implementation of CYP2D6 copy-number imputation panel and frequency of key pharmacogenetic variants in Finnish individuals with a psychotic disorder

50. GENOME-WIDE ANALYSIS IDENTIFIES SORCS3 AS A NOVEL SUSCEPTIBILITY LOCUS FOR PANIC DISORDER IN THE FINNGEN STUDY

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