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1. Algorithmic Ghost in the Research Shell: Large Language Models and Academic Knowledge Creation in Management Research

10. ARC OF A DIVER

12. Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophrenia

13. Development of an Innovation Corridor Testbed for Shared Electric Connected and Automated Transportation

16. Genome-wide determinants of mortality and motor progression in Parkinson’s disease

17. Genotype–phenotype correlation in PRKN-associated Parkinson’s disease

18. Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association study

20. Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome

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

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

25. The genetic and clinico-pathological profile of early-onset progressive supranuclear palsy.

28. Conclusion

29. Introduction

34. Haunting

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

40. Exome sequencing of individuals with Huntington’s disease implicates FAN1 nuclease activity in slowing CAG expansion and disease onset

42. The endocytic membrane trafficking pathway plays a major role in the risk of Parkinson's disease

46. Rates of Bile Acid Diarrhoea After Cholecystectomy: A Multicentre Audit

50. Investigation of the genetic aetiology of Lewy body diseases with and without dementia

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