De novo mutations in schizophrenia implicate synaptic networks
2014 · Nature · 1,690 citations
https://doi.org/10.1038/nature12929
H
Hywel Williams
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Hywel Williams is an academic researcher from Cardiff University. The author has contributed to research in topics: Genetic Associations and Epidemiology & Genetics and Neurodevelopmental Disorders & Genomics and Rare Diseases. The author has an h-index of 60, co-authored 193 publications.
ORCID: 0000-0001-7758-0312Papers by this author
worksConvergent evidence that <i>oligodendrocyte lineage transcription factor 2</i> ( <i>OLIG2</i> ) and interacting genes influence susceptibility to schizophrenia
2006 · Proceedings of the National Academy of Sciences · 117 citations
https://doi.org/10.1073/pnas.0603029103
Mutations in SNX14 Cause a Distinctive Autosomal-Recessive Cerebellar Ataxia and Intellectual Disability Syndrome
2014 · The American Journal of Human Genetics · 100 citations
https://doi.org/10.1016/j.ajhg.2014.10.007
STAG3 truncating variant as the cause of primary ovarian insufficiency
2015 · European Journal of Human Genetics · 81 citations
https://doi.org/10.1038/ejhg.2015.107
A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans
2014 · Nature Communications · 74 citations
https://doi.org/10.1038/ncomms5871
Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity
2017 · Scientific Reports · 71 citations
https://doi.org/10.1038/s41598-017-03054-8
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