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Author Details

David Richardson
2005
23
19
PMIDPaper TitleJournal TitlePublished Year
33863903Genetic perturbation of PU.1 binding and chromatin looping at neutrophil enhancers associates with autoimmune disease.Nat Commun2021
30407529BioSamples database: an updated sample metadata hub.Nucleic Acids Res2019
30311252FAANG, establishing metadata standards, validation and best practices for the farmed and companion animal community.Anim Genet2018
28531267Alignment of 1000 Genomes Project reads to reference assembly GRCh38.Gigascience2017
27863251Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells.Cell2016
27863955The BLUEPRINT Data Analysis Portal.Cell Syst2016
26208973Principles and application of LIMS in mouse clinics.Mamm Genome2015
25644835Whole-epigenome analysis in multiple myeloma reveals DNA hypermethylation of B cell-specific enhancers.Genome Res2015
26053498Whole-genome fingerprint of the DNA methylome during human B cell differentiation.Nat Genet2015
26214591Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics.Nat Genet2015
25258084Transcriptional diversity during lineage commitment of human blood progenitors.Science2014
19933761EuroPhenome: a repository for high-throughput mouse phenotyping data.Nucleic Acids Res2010
19377476A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation.Nat Genet2009
17236139Mutations in CUL4B, which encodes a ubiquitin E3 ligase subunit, cause an X-linked mental retardation syndrome associated with aggressive outbursts, seizures, relative macrocephaly, central obesity, hypogonadism, pes cavus, and tremor.Am J Hum Genet2007
17704778Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation.Nat Genet2007
17344846Patterns of somatic mutation in human cancer genomes.Nature2007
17485433AutoCSA, an algorithm for high throughput DNA sequence variant detection in cancer genomes.Bioinformatics2007
17668385Mutations in the BRWD3 gene cause X-linked mental retardation associated with macrocephaly.Am J Hum Genet2007
17088437Mutation analysis of 24 known cancer genes in the NCI-60 cell line set.Mol Cancer Ther2006
16618716A hypermutation phenotype and somatic MSH6 mutations in recurrent human malignant gliomas after alkylator chemotherapy.Cancer Res2006
17186471Mutations in the gene encoding the Sigma 2 subunit of the adaptor protein 1 complex, AP1S2, cause X-linked mental retardation.Am J Hum Genet2006
15681454Molecular epidemiology of simian T-cell lymphotropic virus type 1 in wild and captive sooty mangabeys.Journal of Virology2005
15681464Detection and partial characterization of simian immunodeficiency virus SIVsm strains from bush meat samples from rural Sierra Leone.Journal of Virology2005
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