Research Topics
| Panagiotis DeloukasSummaryAffiliation: Wellcome Trust Genome Campus Country: UK Publications
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Detail Information
Publications
Replication by the Epistasis Project of the interaction between the genes for IL-6 and IL-10 in the risk of Alzheimer's diseaseOnofre Combarros
Neurology Service and Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas, Marqués de Valdecilla University Hospital University of Cantabria, 39008 Santander, Spain
J Neuroinflammation 6:22. 2009....
Association of warfarin dose with genes involved in its action and metabolismMia Wadelius
Department of Medical Sciences, Clinical Pharmacology, University Hospital, 751 85 Uppsala, Sweden
Hum Genet 121:23-34. 2007..Translation of this knowledge into clinical guidelines for warfarin prescription will be likely to have a major impact on the safety and efficacy of warfarin...
DNA sequence and structural properties as predictors of human and mouse promotersPelin Akan
Wellcome Trust Sanger Institute, Hinxton, Cambridge, UK
Gene 410:165-76. 2008..Interestingly, all mouse promoter sets showed ATG codon depletion irrespective of the presence of a TATA-box, possibly reflecting a weaker contribution to TSS specificity in mouse...
The dopamine β-hydroxylase -1021C/T polymorphism is associated with the risk of Alzheimer's disease in the Epistasis ProjectOnofre Combarros
Neurology Service and Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas, Marqués de Valdecilla University Hospital University of Cantabria, 39008 Santander, Spain
BMC Med Genet 11:162. 2010..We therefore examined the associations with AD of the DBH -1021T allele and of the above interactions in the Epistasis Project, with 1757 cases of AD and 6294 elderly controls...
Sequencing and association analysis of the type 1 diabetes-linked region on chromosome 10p12-q11Sergey Nejentsev
Juvenile Diabetes Research Foundation Wellcome Trust Diabetes and Inflammation Laboratory, Cambridge Institute for Medical Research, University of Cambridge, Cambridge, UK
BMC Genet 8:24. 2007..Here, we studied sequence polymorphisms in 23 Mb on chromosome 10p12-q11, including the putative IDDM10 region, to identify genes associated with T1D...
High-throughput analysis of candidate imprinted genes and allele-specific gene expression in the human term placentaCaroline Daelemans
Wellcome Trust Sanger Institute, Hinxton, Cambridge, CB10 1 SA, UK
BMC Genet 11:25. 2010..Using two allele-specific high-throughput technologies alongside bioinformatics predictions, normal term human placenta was screened to find new imprinted genes and to ascertain the extent of ASE in this tissue...
Data analysis issues for allele-specific expression using Illumina's GoldenGate assayMatthew E Ritchie
Bioinformatics Division, The Walter and Eliza Hall Institute of Medical Research, 1G Royal Parade, Parkville, Victoria, 3052, Australia
BMC Bioinformatics 11:280. 2010..This platform exploits coding SNPs to obtain relative expression measurements for alleles at approximately 1500 positions in the genome...
The DNA sequence and comparative analysis of human chromosome 20P Deloukas
The Wellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1SA, UK
Nature 414:865-71. 2001....
The DNA sequence and comparative analysis of human chromosome 10P Deloukas
The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton CB10 1SA, UK
Nature 429:375-81. 2004..Assessment of single base changes between the human chromosome 10 and chimpanzee sequence revealed nonsense mutations in only 21 coding genes with respect to the human sequence...
The HapMap project and its application to genetic studies of drug responseP Deloukas
Wellcome Trust Sanger Institute, Hinxton, Cambridgeshire, UK
Pharmacogenomics J 4:88-90. 2004
DNA sequence and analysis of human chromosome 9S J Humphray
The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge CB10 1SA, UK
Nature 429:369-74. 2004..We have also detected recently duplicated genes that exhibit different rates of sequence divergence, presumably reflecting natural selection...
The DNA sequence and analysis of human chromosome 13A Dunham
The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridgeshire, CB10 1SA, UK
Nature 428:522-8. 2004..Chromosome 13 has one of the lowest gene densities (6.5 genes per Mb) among human chromosomes, and contains a central region of 38 Mb where the gene density drops to only 3.1 genes per Mb...
Relative impact of nucleotide and copy number variation on gene expression phenotypesBarbara E Stranger
Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SA, UK
Science 315:848-53. 2007..Interrogation of the genome for both types of variants may be an effective way to elucidate the causes of complex phenotypes and disease in humans...
The DNA sequence and biological annotation of human chromosome 1S G Gregory
The Wellcome Trust Sanger Institute, The Wellcome Trust Genome Campus, Hinxton, Cambridgeshire CB10 1SA, UK
Nature 441:315-21. 2006....
The DNA sequence and analysis of human chromosome 6A J Mungall
The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge CB10 1SA, UK
Nature 425:805-11. 2003..Within the essential immune loci of the major histocompatibility complex, we find HLA-B to be the most polymorphic gene on chromosome 6 and in the human genome...
RNAi--prospects for a general technique for determining gene functionP E Kuwabara
The Sanger Centre, Wellcome Trust Genome Campus, Hinxton, Cambridge, UK CB10 1SA
Parasitol Today 16:347-9. 2000....
RNA-mediated interference as a tool for identifying drug targetsN J O'Neil
Sanger Centre, Wellcome Trust Genome Campus, Hinxton, England
Am J Pharmacogenomics 1:45-53. 2001..RNAi can also help to identify the biochemical mode of action of a drug or pesticide and to identify other genes encoding products that may respond or interact with specific compounds...
Population-specific risk of type 2 diabetes conferred by HNF4A P2 promoter variants: a lesson for replication studiesInes Barroso
Wellcome Trust Sanger Institute, Hinxton, Cambridge, UK
Diabetes 57:3161-5. 2008..We aimed to investigate whether data from a large-scale mapping approach would replicate this association in novel Ashkenazi samples and in U.K. populations and whether these data would allow us to refine the association signal...
Genome-wide associations of gene expression variation in humansBarbara E Stranger
Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, United Kingdom
PLoS Genet 1:e78. 2005..In addition, we demonstrate that the HapMap cell lines themselves may serve as a useful resource for quantitative measurements at the cellular level...
High-throughput genotyping of Salmonella enterica serovar Typhi allowing geographical assignment of haplotypes and pathotypes within an urban District of Jakarta, IndonesiaStephen Baker
The Wellcome Trust Sanger Institute, Hinxton, Cambridgeshire, United Kingdom
J Clin Microbiol 46:1741-6. 2008..The study also provides insight into the evolution of serovar Typhi and demonstrates the value of a molecular epidemiological technique that is exchangeable, that is internet friendly, and that has global utility...
A histone map of human chromosome 20q13.12Pelin Akan
Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom
PLoS ONE 4:e4479. 2009..We present a systematic search for regulatory elements in a 3.5 Mb region on human chromosome 20q13.12, a region associated with a number of medical conditions such as type II diabetes and obesity...
A functional genomic analysis of cell morphology using RNA interferenceA A Kiger
Department of Genetics, Harvard Medical School, Howard Hughes Medical Institute, Boston, MA 02115, USA
J Biol 2:27. 2003..Some genes exhibited similar RNAi phenotypes in both cell types, while others appeared to have cell-type-specific functions, in part reflecting the different mechanisms used to generate a round or a flat cell morphology...
Full-genome RNAi profiling of early embryogenesis in Caenorhabditis elegansB Sönnichsen
Cenix BioScience GmbH, Tatzberg 47 51, D 01307 Dresden, Germany
Nature 434:462-9. 2005....
Caenorhabditis elegans has scores of homoeobox-containing genesT R Burglin
Department of Molecular Biology, Massachusetts General Hospital, Boston
Nature 341:239-43. 1989..We estimate that the number of homoeobox-containing genes in C. elegans is at least 60, constituting approximately 1% of the estimated total number of genes...
