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William P Gilks

Showing results (1-10 of 10) with videos related to

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Trends in Genetics : TIG|September 21, 2014
Sex differences in disease genetics: evidence, evolution, and detectionWilliam P Gilks, Jessica K Abbott, Edward H Morrow
F1000Research|January 20, 2017
Whole genome resequencing of a laboratory-adapted <i>Drosophila melanogaster </i>population sampleWilliam P Gilks, Tanya M Pennell, Ilona Flis, et al.
The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry|March 6, 2012
Functional investigation of a schizophrenia GWAS signal at the CDC42 geneWilliam P Gilks, Matthew Hill, Michael Gill, et al.
Neuroscience Letters|November 17, 2009
Replicated genetic evidence supports a role for HOMER2 in schizophreniaWilliam P Gilks, Emma H Allott, Gary Donohoe, et al.
DNA Research : an International Journal for Rapid Publication of Reports on Genes and Genomes|December 18, 2010
Multiplex target enrichment using DNA indexing for ultra-high throughput SNP detectionElaine M Kenny, Paul Cormican, William P Gilks, et al.
Lancet (London, England)|February 1, 2005
A common LRRK2 mutation in idiopathic Parkinson's diseaseWilliam P Gilks, Patrick M Abou-Sleiman, Sonia Gandhi, et al.
Journal of Neurochemistry|June 30, 2006
Altered cleavage and localization of PINK1 to aggresomes in the presence of proteasomal stressMiratul M K Muqit, Patrick M Abou-Sleiman, Adrian T Saurin, et al.
Neuron|November 16, 2004
Cloning of the gene containing mutations that cause PARK8-linked Parkinson's diseaseCoro Paisán-Ruíz, Shushant Jain, E Whitney Evans, et al.
Science (New York, N.Y.)|April 17, 2004
Hereditary early-onset Parkinson's disease caused by mutations in PINK1Enza Maria Valente, Patrick M Abou-Sleiman, Viviana Caputo, et al.
Brain : a Journal of Neurology|November 8, 2005
Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic dataNaheed L Khan, Shushant Jain, John M Lynch, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Trends in Genetics : TIG|September 21, 2014
Sex differences in disease genetics: evidence, evolution, and detectionWilliam P Gilks, Jessica K Abbott, Edward H Morrow
F1000Research|January 20, 2017
Whole genome resequencing of a laboratory-adapted <i>Drosophila melanogaster </i>population sampleWilliam P Gilks, Tanya M Pennell, Ilona Flis, et al.
The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry|March 6, 2012
Functional investigation of a schizophrenia GWAS signal at the CDC42 geneWilliam P Gilks, Matthew Hill, Michael Gill, et al.
Neuroscience Letters|November 17, 2009
Replicated genetic evidence supports a role for HOMER2 in schizophreniaWilliam P Gilks, Emma H Allott, Gary Donohoe, et al.
DNA Research : an International Journal for Rapid Publication of Reports on Genes and Genomes|December 18, 2010
Multiplex target enrichment using DNA indexing for ultra-high throughput SNP detectionElaine M Kenny, Paul Cormican, William P Gilks, et al.
Lancet (London, England)|February 1, 2005
A common LRRK2 mutation in idiopathic Parkinson's diseaseWilliam P Gilks, Patrick M Abou-Sleiman, Sonia Gandhi, et al.
Journal of Neurochemistry|June 30, 2006
Altered cleavage and localization of PINK1 to aggresomes in the presence of proteasomal stressMiratul M K Muqit, Patrick M Abou-Sleiman, Adrian T Saurin, et al.
Neuron|November 16, 2004
Cloning of the gene containing mutations that cause PARK8-linked Parkinson's diseaseCoro Paisán-Ruíz, Shushant Jain, E Whitney Evans, et al.
Science (New York, N.Y.)|April 17, 2004
Hereditary early-onset Parkinson's disease caused by mutations in PINK1Enza Maria Valente, Patrick M Abou-Sleiman, Viviana Caputo, et al.
Brain : a Journal of Neurology|November 8, 2005
Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic dataNaheed L Khan, Shushant Jain, John M Lynch, et al.
Pageof 1