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Author Details

Christine P Bird
The Wellcome Trust Sanger Institute
1999
25
22
PMIDPaper TitleJournal TitlePublished Year
20364136Mutation spectrum revealed by breakpoint sequencing of human germline CNVs.Nat Genet2010
20364136Mutation spectrum revealed by breakpoint sequencing of human germline CNVs.Nat Genet2010
17289997Relative impact of nucleotide and copy number variation on gene expression phenotypes.Science2007
17943131Genome-wide detection and characterization of positive selection in human populations.Nature2007
17943122A second generation human haplotype map of over 3.1 million SNPs.Nature2007
17895424Islands of euchromatin-like sequence and expressed polymorphic sequences within the short arm of human chromosome 21.Genome Res2007
17578567Fast-evolving noncoding sequences in the human genome.Genome Biol2007
17571346Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project.Nature2007
17873874Population genomics of human gene expression.Nat Genet2007
17289997Relative impact of nucleotide and copy number variation on gene expression phenotypes.Science2007
17333537Genes flanking Xist in mouse and human are separated on the X chromosome in American marsupials.Chromosome Res2007
17895424Islands of euchromatin-like sequence and expressed polymorphic sequences within the short arm of human chromosome 21.Genome Res2007
17943131Genome-wide detection and characterization of positive selection in human populations.Nature2007
17943122A second generation human haplotype map of over 3.1 million SNPs.Nature2007
17571346Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project.Nature2007
17578567Fast-evolving noncoding sequences in the human genome.Genome Biol2007
17873874Population genomics of human gene expression.Nat Genet2007
17333537Genes flanking Xist in mouse and human are separated on the X chromosome in American marsupials.Chromosome Res2007
16380714Conserved noncoding sequences are selectively constrained and not mutation cold spots.Nat Genet2006
17055246Functional variation and evolution of non-coding DNA.Curr Opin Genet Dev2006
16710414The DNA sequence and biological annotation of human chromosome 1.Nature2006
16380714Conserved noncoding sequences are selectively constrained and not mutation cold spots.Nat Genet2006
17055246Functional variation and evolution of non-coding DNA.Curr Opin Genet Dev2006
16710414The DNA sequence and biological annotation of human chromosome 1.Nature2006
15772651The DNA sequence of the human X chromosome.Nature2005
15772651The DNA sequence of the human X chromosome.Nature2005
16030148Progressive proximal expansion of the primate X chromosome centromere.Proc Natl Acad Sci U S A2005
16030148Progressive proximal expansion of the primate X chromosome centromere.Proc Natl Acad Sci U S A2005
15164053DNA sequence and analysis of human chromosome 9.Nature2004
15574953Complete nucleotide sequence of the conjugative tetracycline resistance plasmid pFBAOT6, a member of a group of IncU plasmids with global ubiquity.Appl Environ Microbiol2004
15057823The DNA sequence and analysis of human chromosome 13.Nature2004
15020831BAC finishing strategies.Methods Mol Biol2004
15164054The DNA sequence and comparative analysis of human chromosome 10.Nature2004
15164053DNA sequence and analysis of human chromosome 9.Nature2004
15574953Complete nucleotide sequence of the conjugative tetracycline resistance plasmid pFBAOT6, a member of a group of IncU plasmids with global ubiquity.Appl Environ Microbiol2004
15020831BAC finishing strategies.Methods Mol Biol2004
15057823The DNA sequence and analysis of human chromosome 13.Nature2004
15164054The DNA sequence and comparative analysis of human chromosome 10.Nature2004
12659809Comparative and functional analyses of LYL1 loci establish marsupial sequences as a model for phylogenetic footprinting.Genomics2003
12659809Comparative and functional analyses of LYL1 loci establish marsupial sequences as a model for phylogenetic footprinting.Genomics2003
14574404The DNA sequence and analysis of human chromosome 6.Nature2003
12704239Dispersal of NK homeobox gene clusters in amphioxus and humans.Proc Natl Acad Sci U S A2003
14574404The DNA sequence and analysis of human chromosome 6.Nature2003
12704239Dispersal of NK homeobox gene clusters in amphioxus and humans.Proc Natl Acad Sci U S A2003
11668635Matroshka and ectopic polymorphisms: Two new classes of DNA sequence variation identified at the Van der Woude syndrome locus on 1q32-q41.Hum Mutat2001
11780052The DNA sequence and comparative analysis of human chromosome 20.Nature2001
11668635Matroshka and ectopic polymorphisms: Two new classes of DNA sequence variation identified at the Van der Woude syndrome locus on 1q32-q41.Hum Mutat2001
11780052The DNA sequence and comparative analysis of human chromosome 20.Nature2001
10591208The DNA sequence of human chromosome 22.Nature1999
10591208The DNA sequence of human chromosome 22.Nature1999
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Collaborators

The Wellcome Trust Sanger Institute
Co-authored papers 12
4Wellcome Trust Sanger Institute
Co-authored papers 11
Illumina Cambridge Ltd.
Co-authored papers 10
University of Cambridge
Co-authored papers 10
Co-authored papers 9
Co-authored papers 9
European Bioinformatics Institute
Co-authored papers 9
Illumina Cambridge Ltd.
Co-authored papers 9
Inivata Ltd.
Co-authored papers 9
Institute of Biotechnology, University of Cambridge
Co-authored papers 9
University of Geneva
Co-authored papers 8
Co-authored papers 8
Co-authored papers 8
University of Cambridge
Co-authored papers 7
Co-authored papers 7
Center for Genetic Medicine, Northwestern University Feinberg School of Medicine
Co-authored papers 7
UCL Cancer Institute, University College London
Co-authored papers 7
Co-authored papers 7
Wellcome Sanger Institute
Co-authored papers 7
Co-authored papers 7
University of Oxford
Co-authored papers 7
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 7
Co-authored papers 6
Co-authored papers 6
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 6
European Bioinformatics Institute (EMBL-EBI)
Co-authored papers 6
Wellcome Trust Sanger Institute
Co-authored papers 6
Wellcome Trust Sanger Institute
Co-authored papers 6
Harvard University
Co-authored papers 5
University of California at Santa Cruz
Co-authored papers 5