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1. NRXN1α+/- is associated with increased excitability in ASD iPSC-derived neurons

2. Increased Ca2+ signaling in NRXN1α +/− neurons derived from ASD induced pluripotent stem cells

3. Rapid and Laboratory SARS-CoV-2 Antibody Testing in High-Risk Hospital Associated Cohorts of Unknown COVID-19 Exposure, a Validation and Epidemiological Study After the First Wave of the Pandemic

4. Rare Disease Research Partnership (RAinDRoP): a collaborative approach to identify research priorities for rare diseases in Ireland [version 2; peer review: 2 approved]

5. Author Correction: The Irish DNA Atlas: Revealing Fine-Scale Population Structure and History within Ireland

6. HGDP and HapMap analysis by Ancestry Mapper reveals local and global population relationships.

12. NRXN1α+/- is associated with increased excitability in ASD iPSC-derived neurons

13. NRXN1α

14. The role of rare compound heterozygous events in autism spectrum disorder

15. Rare Disease Research Partnership (RAinDRoP): a collaborative approach to identify the top 15 research priorities for rare diseases

16. Developing International Perspectives on Digital Competition Policy

17. Ticketing Strategies in the Sports Sector

18. Sport and Its Role and Contribution to Society and Economic Development

22. Understanding Fans and Their Consumption of Sport

25. Introduction: The Sports Sector in a Global Context

26. Sports Distribution and Media Rights

27. Formulating and Implementing Sports Marketing Strategy

28. Increased Ca2+ signaling in NRXN1α+/− neurons derived from ASD induced pluripotent stem cells

29. Genetic Associations with Aging Muscle: A Systematic Review

30. Catalogue of inherited disorders found among the Irish Traveller population

31. The Goldilocks Dilemma: When is Digital Regulation 'Just Right'?

32. A novel gain-of-function mutation in the ITPR1 suppressor domain causes spinocerebellar ataxia with altered Ca2+ signal patterns

33. P430 Identifying rare disease research priorities through (RAinDRoP) a rare disease research partnership

34. OC48 Re-interrogation of whole exome sequencing data in developmental epileptic encephalopathies

35. Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia

36. Intra-familial variability associated with recessive RYR1 mutation diagnosed prenatally by exome sequencing

37. Recessive NEK9 mutation causes a lethal skeletal dysplasia with evidence of cell cycle and ciliary defects

38. Common polygenic variation in coeliac disease and confirmation of ZNF335 and NIFA as disease susceptibility loci

39. Rare Disease Research Partnership (RAinDRoP): a collaborative approach to identify research priorities for rare diseases in Ireland

40. Sacar el mejor provecho de las recientes reformas para fortalecer la competencia

41. Fully reaping the benefits of recent competition-enhancing reforms

42. Personalized Cardio‐Metabolic Responses to an Anti‐Inflammatory Nutrition Intervention in Obese Adolescents: A Randomized Controlled Crossover Trial

43. The Irish DNA atlas: revealing fine-scale population structure and history within Ireland

44. Market Power and Wealth Distribution

45. Genomic insights into the population structure and history of the Irish Travellers

46. Inequality: A Hidden Cost of Market Power

47. Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders

48. FARS2 Causing Complex Hereditary Spastic Paraplegia With Dysphonia: Expanding the Disease Spectrum

49. <scp>NAPB</scp> – a novel <scp>SNARE</scp> ‐associated protein for early‐onset epileptic encephalopathy

50. Beaulieu-Boycott-Innes syndrome: an intellectual disability syndrome with characteristic facies

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