Williams, Nigel

The relative contribution of common and rare genetic variants to ADHD

Martin, J., O'Donovan, M. C., Thapar, A., Langley, K., & Williams, N. (2015) · Translational Psychiatry

Attention Deficit Hyperactivity DisorderGenetic Associations and Epidemiology

Cited by 85

Familial frontotemporal dementia with amyotrophic lateral sclerosis and a shared haplotype on chromosome 9p

Pearson, J. P., Williams, N. M., Majounie, E., Waite, A., Stott, J., Newsway, V., Murray, A., Hernandez, D., Guerreiro, R., Singleton, A. B., et al. (2011) · Journal of Neurology

Amyotrophic Lateral Sclerosis ResearchAlzheimer's disease research and treatments

Cited by 84

Additional rare variant analysis in Parkinson’s disease cases with and without known pathogenic mutations: Evidence for oligogenic inheritance

Lubbe, S. J., Escott-Price, V., Gibbs, J. R., Nalls, M. A., Bras, J., Price, T. R., Nicolas, A., Jansen, I. E., Mok, K. Y., Pittman, A. M., et al. (2016) · Human Molecular Genetics

Parkinson's Disease Mechanisms and TreatmentsLysosomal Storage Disorders Research

Cited by 61

Ehlers-Danlos Syndrome with Severe Early-Onset Periodontal Disease (EDS-VIII) Is a Distinct, Heterogeneous Disorder with One Predisposition Gene at Chromosome 12p13

Rahman, N., Dunstan, M., Teare, M. D., Hanks, S., Douglas, J., Coleman, K., Bottomly, W. E., Campbell, M. E., Berglund, B., Nordenskjöld, M., et al. (2003) · The American Journal of Human Genetics

Connective tissue disorders researchOral microbiology and periodontitis research

Cited by 55

C9ORF72 expansion in amyotrophic lateral sclerosis/frontotemporal dementia also causes parkinsonism

O'Dowd, S., Curtin, D., Waite, A. J., Roberts, K., Pender, N., Reid, V., O'Connell, M., Williams, N. M., Morris, H. R., Traynor, B. J., et al. (2012) · Movement Disorders

Amyotrophic Lateral Sclerosis ResearchParkinson's Disease Mechanisms and Treatments

Cited by 52

Genetic risk for schizophrenia and developmental delay is associated with shape and microstructure of midline white-matter structures

Drakesmith, M., Parker, G. D., Smith, J., Linden, S. C., Rees, E., Williams, N., Owen, M. J., van den Bree, M., Hall, J., Jones, D. K., et al. (2019) · Translational Psychiatry

Genomic variations and chromosomal abnormalitiesSchizophrenia research and treatment

Cited by 31

Excessive appetitive arousal in Prader–Willi syndrome

Hinton, E. C., Isles, A. R., Williams, N. M., & Parkinson, J. A. (2010) · Appetite

Regulation of Appetite and ObesityGenetic Syndromes and Imprinting

Cited by 19

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

Tan, M. M. X., Lawton, M. A., Pollard, M. I., Brown, E., Real, R., Carrasco, A. M., Bekadar, S., Jabbari, E., Reynolds, R. H., Iwaki, H., et al. (2024) · npj Parkinson's Disease

Parkinson's Disease Mechanisms and TreatmentsGenetic Associations and Epidemiology

Cited by 17

Electrophysiological network alterations in adults with copy number variants associated with high neurodevelopmental risk

Dima, D. C., Adams, R., Linden, S. C., Baird, A., Smith, J., Foley, S., Perry, G., Routley, B. C., Magazzini, L., Drakesmith, M., et al. (2020) · Translational Psychiatry

Genomic variations and chromosomal abnormalitiesFunctional Brain Connectivity Studies

Cited by 14