Hywel Williams - Concepedia

Author

Hywel Williams

Also Known As

Camps, C, D Wakelin, David Skuse, David St Clair, F Ward, Fend Zhang, Freimer, Nelson B, GOSgene, H J Williams, H Williams

229

Publications

21K

Citations

H-Index

103

Concepts

All Affiliations

Cardiff University University of Wales University College London Great Ormond Street Hospital Guy's Hospital

About

Hywel Williams is an author at Cardiff University specializing in medicine, genetics, and schizophrenia.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	30	41	4.7K
2	Public Health	8	8	389
3	Social Sciences	7	7	1.9K
4	Natural Sciences	1	1	20
5	Biology	1	1	20

Hywel Williams

Publications

9.5K

Citations

H-Index

Page 1

	Year	Citations
De novo mutations in schizophrenia implicate synaptic networks Menachem Fromer, Andrew Pocklington, David H. Kavanagh, Nature Synaptic PlasticityPsychotic DisorderPsychiatric GeneticsSchizophreniaConnectomics	2014	1.7K
Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel Jie Huang, Bryan Howie, Shane McCarthy, Nature Communications	2015	374
A Haplotype Implicated in Schizophrenia Susceptibility Is Associated with Reduced COMT Expression in Human Brain Nicholas J. Bray, Paul R. Buckland, Nigel Williams, The American Journal of Human Genetics PsychiatryRisk PredictionPsychiatric GeneticsSchizophreniaNeuropsychiatry	2003	339
The UK10K project identifies rare variants in health and disease Klaudia Walter, Josine L. Min, Jie Huang, Kölner Universitäts PublikationsServer (Universität zu Köln)	2015	299
Fine mapping of ZNF804A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder Hywel Williams, N Norton, Sarah Dwyer, Molecular Psychiatry PsychiatryGenome-wide Significant EvidenceGeneticsPsychiatric GeneticsSchizophrenia	2010	281
Support for genetic variation in neuregulin 1 and susceptibility to schizophrenia Nigel Williams, Anna Preece, Gillian Spurlock, Molecular Psychiatry PsychiatryGeneticsPsychiatric GeneticsGenetic EpidemiologyNeuregulin 1	2003	235
Exome sequencing for prenatal diagnosis of fetuses with sonographic abnormalities Suzanne Drury, Hywel Williams, Natalie Trump, Prenatal Diagnosis	2015	225
Full genome screen for Alzheimer disease: Stage II analysis* Amanda Myers, Fabienne Wavrant DeVriéze, Peter Holmans, American Journal of Medical Genetics	2002	208
Tumour compartment transcriptomics demonstrates the activation of inflammatory and odontogenic programmes in human adamantinomatous craniopharyngioma and identifies the MAPK/ERK pathway as a novel therapeutic target John Apps, Gabriela Carreno, José Mario González-Meljem, Acta Neuropathologica	2018	206
Identification in 2 Independent Samples of a Novel Schizophrenia RiskHaplotype of the Dystrobrevin Binding Protein Gene (DTNBP1) Nigel Williams, Anna Preece, Derek W. Morris, Archives of General Psychiatry	2004	194

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