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Hywel J Williams

Showing results (11-20 of 39) with videos related to

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American Journal of Human Genetics|June 13, 2003
A haplotype implicated in schizophrenia susceptibility is associated with reduced COMT expression in human brainNicholas J Bray, Paul R Buckland, Nigel M Williams, et al.
Psychiatric Genetics|November 12, 2015
Mutation screening of SCN2A in schizophrenia and identification of a novel loss-of-function mutationLiam S Carroll, Rebecca Woolf, Yousef Ibrahim, et al.
Journal of Nephrology|July 1, 2008
Further evidence for the association of MMP9 with nephropathy in type 2 diabetes and application of DNA pooling technology to candidate gene screeningSunita Nair, Aled O Phillips, Nadine Norton, et al.
The American Journal of Psychiatry|September 2, 2005
No association between schizophrenia and polymorphisms in COMT in two large samplesHywel J Williams, Beate Glaser, Nigel M Williams, et al.
Human Genetics|June 20, 2002
Universal, robust, highly quantitative SNP allele frequency measurement in DNA poolsNadine Norton, Nigel M Williams, Hywel J Williams, et al.
BMC Psychiatry|May 17, 2005
No evidence for association between polymorphisms in GRM3 and schizophreniaNadine Norton, Hywel J Williams, Sarah Dwyer, et al.
European Journal of Human Genetics : EJHG|June 11, 2015
The use of whole-exome sequencing to disentangle complex phenotypesHywel J Williams, John R Hurst, Louise Ocaka, et al.
Orphanet Journal of Rare Diseases|February 9, 2017
An example of the utility of genomic analysis for fast and accurate clinical diagnosis of complex rare phenotypesPolona Le Quesne Stabej, Chela James, Louise Ocaka, et al.
Human Molecular Genetics|November 2, 2010
Most genome-wide significant susceptibility loci for schizophrenia and bipolar disorder reported to date cross-traditional diagnostic boundariesHywel J Williams, Nicholas Craddock, Giancarlo Russo, et al.
Schizophrenia Research|March 27, 2007
Association analysis of AKT1 and schizophrenia in a UK case control sampleNadine Norton, Hywel J Williams, Sarah Dwyer, et al.
Pageof 4

Showing results (11-20 of 39) with videos related to

Sort By:
Pageof 4
American Journal of Human Genetics|June 13, 2003
A haplotype implicated in schizophrenia susceptibility is associated with reduced COMT expression in human brainNicholas J Bray, Paul R Buckland, Nigel M Williams, et al.
Psychiatric Genetics|November 12, 2015
Mutation screening of SCN2A in schizophrenia and identification of a novel loss-of-function mutationLiam S Carroll, Rebecca Woolf, Yousef Ibrahim, et al.
Journal of Nephrology|July 1, 2008
Further evidence for the association of MMP9 with nephropathy in type 2 diabetes and application of DNA pooling technology to candidate gene screeningSunita Nair, Aled O Phillips, Nadine Norton, et al.
The American Journal of Psychiatry|September 2, 2005
No association between schizophrenia and polymorphisms in COMT in two large samplesHywel J Williams, Beate Glaser, Nigel M Williams, et al.
Human Genetics|June 20, 2002
Universal, robust, highly quantitative SNP allele frequency measurement in DNA poolsNadine Norton, Nigel M Williams, Hywel J Williams, et al.
BMC Psychiatry|May 17, 2005
No evidence for association between polymorphisms in GRM3 and schizophreniaNadine Norton, Hywel J Williams, Sarah Dwyer, et al.
European Journal of Human Genetics : EJHG|June 11, 2015
The use of whole-exome sequencing to disentangle complex phenotypesHywel J Williams, John R Hurst, Louise Ocaka, et al.
Orphanet Journal of Rare Diseases|February 9, 2017
An example of the utility of genomic analysis for fast and accurate clinical diagnosis of complex rare phenotypesPolona Le Quesne Stabej, Chela James, Louise Ocaka, et al.
Human Molecular Genetics|November 2, 2010
Most genome-wide significant susceptibility loci for schizophrenia and bipolar disorder reported to date cross-traditional diagnostic boundariesHywel J Williams, Nicholas Craddock, Giancarlo Russo, et al.
Schizophrenia Research|March 27, 2007
Association analysis of AKT1 and schizophrenia in a UK case control sampleNadine Norton, Hywel J Williams, Sarah Dwyer, et al.
Pageof 4