Ian Dunham

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Publications in SciGraph latest 50 shown

  • 2019-02 GARFIELD classifies disease-relevant genomic features through integration of functional annotations with association signals in NATURE GENETICS
  • 2018-12 Uncovering new disease indications for G-protein coupled receptors and their endogenous ligands in BMC BIOINFORMATICS
  • 2018-11 The COSMIC Cancer Gene Census: describing genetic dysfunction across all human cancers in NATURE REVIEWS CANCER
  • 2017-12 In silico prediction of novel therapeutic targets using gene–disease association data in JOURNAL OF TRANSLATIONAL MEDICINE
  • 2017-12 Literature evidence in open targets - a target validation platform in JOURNAL OF BIOMEDICAL SEMANTICS
  • 2016-12 Linking rare and common disease: mapping clinical disease-phenotypes to ontologies in therapeutic target validation in JOURNAL OF BIOMEDICAL SEMANTICS
  • 2015-12 Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel in NATURE COMMUNICATIONS
  • 2015-12 Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci in NATURE GENETICS
  • 2015-12 Whole-genome sequence-based analysis of thyroid function in NATURE COMMUNICATIONS
  • 2015-10 A global reference for human genetic variation in NATURE
  • 2015-10 Using human genetics to make new medicines in NATURE REVIEWS GENETICS
  • 2014-12 A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans in NATURE COMMUNICATIONS
  • 2014-03 Functional annotation of noncoding sequence variants in NATURE METHODS
  • 2013-08 Genome-wide meta-analysis identifies new susceptibility loci for migraine in NATURE GENETICS
  • 2010-12 High-throughput analysis of candidate imprinted genes and allele-specific gene expression in the human term placenta in BMC GENETICS
  • 2010-12 Systematic analysis of off-target effects in an RNAi screen reveals microRNAs affecting sensitivity to TRAIL-induced apoptosis in BMC GENOMICS
  • 2009-12 DNA methylation-histone modification relationships across the desmin locus in human primary cells in BMC MOLECULAR BIOLOGY
  • 2009-04 Mosaic 22q13 deletions: evidence for concurrent mosaic segmental isodisomy and gene conversion in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2008-08 Conservation of the H19 noncoding RNA and H19-IGF2 imprinting mechanism in therians in NATURE GENETICS
  • 2008-05 Finishing the finished human chromosome 22 sequence in GENOME BIOLOGY
  • 2008-03 A systematic library for comprehensive overexpression screens in Saccharomyces cerevisiae in NATURE METHODS
  • 2007-12 Sequencing and association analysis of the type 1 diabetes – linked region on chromosome 10p12-q11 in BMC GENETICS
  • 2007-12 The evolution of imprinting: chromosomal mapping of orthologues of mammalian imprinted domains in monotreme and marsupial mammals in BMC EVOLUTIONARY BIOLOGY
  • 2007-07 Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project in NATURE
  • 2007-02 RPS6KA2, a putative tumour suppressor gene at 6q27 in sporadic epithelial ovarian cancer in ONCOGENE
  • 2006-05 The DNA sequence and biological annotation of human chromosome 1 in NATURE
  • 2006-02 Small regions of overlapping deletions on 6q26 in human astrocytic tumours identified using chromosome 6 tile path array-CGH in ONCOGENE
  • 2005-04 Investigating chromosome organization with genomic microarrays in CHROMOSOME RESEARCH
  • 2004-09 A genome annotation-driven approach to cloning the human ORFeome in GENOME BIOLOGY
  • 2004-05 DNA sequence and analysis of human chromosome 9 in NATURE
  • 2004-05 Novel microsatellite markers and single nucleotide polymorphisms refine the tylosis with oesophageal cancer (TOC) minimal region on 17q25 to 42.5 kb: sequencing does not identify the causative gene in HUMAN GENETICS
  • 2004-04 The DNA sequence and analysis of human chromosome 13 in NATURE
  • 2003-10 The DNA sequence and analysis of human chromosome 6 in NATURE
  • 2003-08-01 DNA Rescue by the Vectorette Method in PCR PROTOCOLS
  • 2003-07 β-1,3-Glucuronyltransferase-1 gene implicated as a candidate for a schizophrenia-like psychosis through molecular analysis of a balanced translocation in MOLECULAR PSYCHIATRY
  • 2003 DNA Rescue by the Vectorette Method in PCR PROTOCOLS
  • 2002-12 The human homologue of unc-93 maps to chromosome 6q27 – characterisation and analysis in sporadic epithelial ovarian cancer in BMC GENETICS
  • 2002-08 A first-generation linkage disequilibrium map of human chromosome 22 in NATURE
  • 2002-01 Physical and transcript map of the region between D6S264 and D6S149 on chromosome 6q27, the minimal region of allele loss in sporadic epithelial ovarian cancer in ONCOGENE
  • 2001-02 The physical maps for sequencing human chromosomes 1, 6, 9, 10, 13, 20 and X in NATURE
  • 2001-02 Initial sequencing and analysis of the human genome in NATURE
  • 2000-09 An SNP map of human chromosome 22 in NATURE
  • 2000-04 A systematic, high-resolution linkage of the cytogenetic and physical maps of the human genome in NATURE GENETICS
  • 2000-04 correction: The DNA sequence of human chromosome 22 in NATURE
  • 2000-03-24 YAC Library Storage and Transport in NUCLEIC ACID PROTOCOLS HANDBOOK, THE
  • 2000-03-24 DNA Rescue by the Vectorette Method in NUCLEIC ACID PROTOCOLS HANDBOOK, THE
  • 2000-03-24 YAC Library Screening: Hybridization and PCR-Based Screening Protocols in NUCLEIC ACID PROTOCOLS HANDBOOK, THE
  • 2000-03-24 YAC Library Screening: Preparation of Hybridization Filters and Polymerase Chain Reaction Pools in NUCLEIC ACID PROTOCOLS HANDBOOK, THE
  • 2000-03 Mechanism of spreading of the highly related neurofibromatosis type 1 (NF1) pseudogenes on chromosomes 2, 14 and 22 in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 1999-12 A Molecular Cytogenetic Clone Resource for Chromosome 22 in CHROMOSOME RESEARCH
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