List of works - Ian Dunham

Initial sequencing and analysis of the human genome

scientific article published on 15 February 2001

Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project

scientific article published in June 2007

Ensembl 2012

scientific article

Ensembl 2013

scientific article

Ensembl 2011

scientific article

The DNA sequence of human chromosome 22

scientific article (publication date: 2 December 1999)

An anthropoid-specific locus of orphan C to U RNA-editing enzymes on chromosome 22

scientific article

A Gene Map of the Human Genome

scientific article

The Human Cell Atlas

scientific article

Defining functional DNA elements in the human genome

scientific article

Integrative annotation of chromatin elements from ENCODE data

scientific article

Functional annotation of noncoding sequence variants.

scientific article published on 2 February 2014

The landscape of histone modifications across 1% of the human genome in five human cell lines

scientific article

Ensembl's 10th year

scientific article

A first-generation linkage disequilibrium map of human chromosome 22

scientific article published in Nature

Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsy

scientific article

Genome-wide meta-analysis identifies new susceptibility loci for migraine

scientific article

hORFeome v3.1: a resource of human open reading frames representing over 10,000 human genes

scientific article

ATR-X syndrome protein targets tandem repeats and influences allele-specific expression in a size-dependent manner.

scientific article published in October 2010

Rapid assessment of S. cerevisiae mating type by PCR.

scientific article published in August 1990

Replication timing of the human genome

scientific article

Human major histocompatibility complex contains genes for the major heat shock protein HSP70

scientific article

The DNA sequence and analysis of human chromosome 6

scientific article

Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci

scientific article

Complete MHC haplotype sequencing for common disease gene mapping

scientific article published on 12 May 2004

Molecular mapping of the human major histocompatibility complex by pulsed-field gel electrophoresis

scientific article

The extent of linkage disequilibrium in four populations with distinct demographic histories

scientific article

Systematic evaluation of variability in ChIP-chip experiments using predefined DNA targets

scientific article published on 7 February 2008

Open Targets: a platform for therapeutic target identification and validation

scientific article

Conservation of the H19 noncoding RNA and H19-IGF2 imprinting mechanism in therians

scientific article

The evolution of the DLK1-DIO3 imprinted domain in mammals

scientific article (publication date: 3 June 2008)

Identification of multiple HTF-island associated genes in the human major histocompatibility complex class III region

scientific article

The DNA sequence and biological annotation of human chromosome

scientific article

The COSMIC Cancer Gene Census: describing genetic dysfunction across all human cancers

article

A systematic library for comprehensive overexpression screens in Saccharomyces cerevisiae

scientific article

Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congenital heart disease

scientific article

A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applications

scientific article published in December 2002

Molecular definition of the 22q11 deletions in velo-cardio-facial syndrome

scientific article published on June 1995

An SNP map of human chromosome 22.

scientific article

Organization of the human immunoglobulin lambda light-chain locus on chromosome 22q11.2.

scientific article

Cell-type-specific long-range looping interactions identify distant regulatory elements of the CFTR gene

scientific article

The human LARGE gene from 22q12.3-q13.1 is a new, distinct member of the glycosyltransferase gene family

scientific article

The portability of tagSNPs across populations: a worldwide survey

scientific article published on 8 February 2006

RPS6KA2, a putative tumour suppressor gene at 6q27 in sporadic epithelial ovarian cancer

scientific article

Functional diversity for REST (NRSF) is defined by in vivo binding affinity hierarchies at the DNA sequence level

scientific article published on 28 April 2009

Butyrate mediates decrease of histone acetylation centered on transcription start sites and down-regulation of associated genes

scientific article published in June 2007

Binding sites for metabolic disease related transcription factors inferred at base pair resolution by chromatin immunoprecipitation and genomic microarrays

scientific article

Applications of machine learning in drug discovery and development

scientific article

Characterization of a new member of the human beta-adaptin gene family from chromosome 22q12, a candidate meningioma gene

scientific article

Replication timing of human chromosome 6.

scientific article

List of works by Ian Dunham

Initial sequencing and analysis of the human genome

Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project

Ensembl 2012

Ensembl 2013

Ensembl 2011

The DNA sequence of human chromosome 22

An anthropoid-specific locus of orphan C to U RNA-editing enzymes on chromosome 22

A Gene Map of the Human Genome

The Human Cell Atlas

Defining functional DNA elements in the human genome

Integrative annotation of chromatin elements from ENCODE data

Functional annotation of noncoding sequence variants.

The landscape of histone modifications across 1% of the human genome in five human cell lines

Ensembl's 10th year

A first-generation linkage disequilibrium map of human chromosome 22

Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsy

Genome-wide meta-analysis identifies new susceptibility loci for migraine

hORFeome v3.1: a resource of human open reading frames representing over 10,000 human genes

ATR-X syndrome protein targets tandem repeats and influences allele-specific expression in a size-dependent manner.

Rapid assessment of S. cerevisiae mating type by PCR.

Replication timing of the human genome

Human major histocompatibility complex contains genes for the major heat shock protein HSP70

The DNA sequence and analysis of human chromosome 6

Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci

Complete MHC haplotype sequencing for common disease gene mapping

Molecular mapping of the human major histocompatibility complex by pulsed-field gel electrophoresis

The extent of linkage disequilibrium in four populations with distinct demographic histories

Systematic evaluation of variability in ChIP-chip experiments using predefined DNA targets

Open Targets: a platform for therapeutic target identification and validation

Conservation of the H19 noncoding RNA and H19-IGF2 imprinting mechanism in therians

The evolution of the DLK1-DIO3 imprinted domain in mammals

Identification of multiple HTF-island associated genes in the human major histocompatibility complex class III region

The DNA sequence and biological annotation of human chromosome

The COSMIC Cancer Gene Census: describing genetic dysfunction across all human cancers

A systematic library for comprehensive overexpression screens in Saccharomyces cerevisiae

Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congenital heart disease

A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applications

Molecular definition of the 22q11 deletions in velo-cardio-facial syndrome

An SNP map of human chromosome 22.

Organization of the human immunoglobulin lambda light-chain locus on chromosome 22q11.2.

Cell-type-specific long-range looping interactions identify distant regulatory elements of the CFTR gene

The human LARGE gene from 22q12.3-q13.1 is a new, distinct member of the glycosyltransferase gene family

The portability of tagSNPs across populations: a worldwide survey

RPS6KA2, a putative tumour suppressor gene at 6q27 in sporadic epithelial ovarian cancer

Functional diversity for REST (NRSF) is defined by in vivo binding affinity hierarchies at the DNA sequence level

Butyrate mediates decrease of histone acetylation centered on transcription start sites and down-regulation of associated genes

Binding sites for metabolic disease related transcription factors inferred at base pair resolution by chromatin immunoprecipitation and genomic microarrays

Applications of machine learning in drug discovery and development

Characterization of a new member of the human beta-adaptin gene family from chromosome 22q12, a candidate meningioma gene

Replication timing of human chromosome 6.