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Nigel Williams | doi.page

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Nigel Williams

NHS EnglandCardiff University(GB)

Publications by Year

Research Areas

Genetic Associations and Epidemiology, Parkinson's Disease Mechanisms and Treatments, Genetics and Neurodevelopmental Disorders, Genomic variations and chromosomal abnormalities, Congenital heart defects research

Most-Cited Works

→ Biological insights from 108 schizophrenia-associated genetic loci(2014)8,017 cited
→ Common polygenic variation contributes to risk of schizophrenia and bipolar disorder(2009)5,009 cited
→ A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD(2011)4,423 cited
→ Rare chromosomal deletions and duplications increase risk of schizophrenia(2008)1,501 cited
→ Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study(2012)1,213 cited
→ Genome Scan Meta-Analysis of Schizophrenia and Bipolar Disorder, Part II: Schizophrenia(2003)1,146 cited

→ Identification of loci associated with schizophrenia by genome-wide association and follow-up(2008)

1,080 cited

→ Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis(2010)575 cited

→ Meta-Analysis of Genome-Wide Association Studies of Attention-Deficit/Hyperactivity Disorder(2010)467 cited

→ Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: Implications for 22q11 deletion syndrome(2006)388 cited