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Genetic Epidemiology
|
December 24, 2003
Bayesian trio models for association in the presence of genotyping errors
L Bernardinelli, C Berzuini, S Seaman, et al.
Annals of Human Genetics
|
September 6, 2005
Design of case-controls studies with unscreened controls
V Moskvina, P Holmans, K M Schmidt, et al.
Molecular Psychiatry
|
March 1, 1996
Increasing the efficiency of genomic searches for linkage in complex disorders by DNA pooling of affected sib-pairs
N Craddock, J Daniels, P Holmans, et al.
Lancet (London, England)
|
October 31, 1997
Association of slow acetylator genotype for N-acetyltransferase 2 with familial Parkinson's disease
O Bandmann, J Vaughan, P Holmans, et al.
Kidney International
|
July 20, 1999
Familial phenotype differences in PKD11
N Hateboer, L P Lazarou, A J Williams, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
October 1, 1994
No linkage or association between multiple sclerosis and the myelin basic protein gene in affected sibling pairs
N W Wood, P Holmans, D Clayton, et al.
Genetic Epidemiology
|
October 31, 2000
Clustering methods applied to allele sharing data
R J Neuman, N L Saccone, P Holmans, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
January 14, 2000
Detailed genotyping demonstrates association between the slow acetylator genotype for N-acetyltransferase 2 (NAT2) and familial Parkinson's disease
O Bandmann, J R Vaughan, P Holmans, et al.
Genes, Brain, and Behavior
|
August 19, 2007
Brain gene expression correlates with changes in behavior in the R6/1 mouse model of Huntington's disease
A Hodges, G Hughes, S Brooks, et al.
Cellular Signalling
|
December 19, 2016
SMAD transcription factors are altered in cell models of HD and regulate HTT expression
K R Bowles, T Stone, P Holmans, et al.
Page
of 9
Search research articles
Search
Showing results (11-20 of 82) with videos related to
Sort By:
Page
of 9
Genetic Epidemiology
|
December 24, 2003
Bayesian trio models for association in the presence of genotyping errors
L Bernardinelli, C Berzuini, S Seaman, et al.
Annals of Human Genetics
|
September 6, 2005
Design of case-controls studies with unscreened controls
V Moskvina, P Holmans, K M Schmidt, et al.
Molecular Psychiatry
|
March 1, 1996
Increasing the efficiency of genomic searches for linkage in complex disorders by DNA pooling of affected sib-pairs
N Craddock, J Daniels, P Holmans, et al.
Lancet (London, England)
|
October 31, 1997
Association of slow acetylator genotype for N-acetyltransferase 2 with familial Parkinson's disease
O Bandmann, J Vaughan, P Holmans, et al.
Kidney International
|
July 20, 1999
Familial phenotype differences in PKD11
N Hateboer, L P Lazarou, A J Williams, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
October 1, 1994
No linkage or association between multiple sclerosis and the myelin basic protein gene in affected sibling pairs
N W Wood, P Holmans, D Clayton, et al.
Genetic Epidemiology
|
October 31, 2000
Clustering methods applied to allele sharing data
R J Neuman, N L Saccone, P Holmans, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
January 14, 2000
Detailed genotyping demonstrates association between the slow acetylator genotype for N-acetyltransferase 2 (NAT2) and familial Parkinson's disease
O Bandmann, J R Vaughan, P Holmans, et al.
Genes, Brain, and Behavior
|
August 19, 2007
Brain gene expression correlates with changes in behavior in the R6/1 mouse model of Huntington's disease
A Hodges, G Hughes, S Brooks, et al.
Cellular Signalling
|
December 19, 2016
SMAD transcription factors are altered in cell models of HD and regulate HTT expression
K R Bowles, T Stone, P Holmans, et al.
Page
of 9