Human genome sequences: enigmatic variationsDUNHAM, Ian.Mutagenesis. 2002, Vol 17, Num 6, pp 457-461, issn 0267-8357, 5 p.Article

Genomics : the new rock and roll?DUNHAM, Ian.Trends in genetics (Regular ed.). 2000, Vol 16, Num 10, pp 456-461, issn 0168-9525Article

GenomicsDUNHAM, Ian; KWOK, Pui-Yan.Human molecular genetics (Print). 2006, Vol 15, issn 0964-6906, 102 p., NSSerial Issue

The characteristics of human genes: analysis of human chromosome 22 : Functional Genomics and Disease 2003DUNHAM, Ian; BEARE, David M; COLLINS, John E et al.Comparative and functional genomics. 2003, Vol 4, Num 6, pp 635-646, issn 1531-6912, 12 p.Conference Paper

From genome to proteome : developing expression clone resources for the human genomeTEMPLE, Gary; LAMESCH, Philippe; MILSTEIN, Stuart et al.Human molecular genetics (Print). 2006, Vol 15, issn 0964-6906, R31-R43, NSArticle

The extent of linkage disequilibrium in four populations with distinct demographic historiesDUNNING, Alison M; DUROCHER, Francine; LAI, Eric et al.American journal of human genetics. 2000, Vol 67, Num 6, pp 1544-1554, issn 0002-9297Article

Pharmacogenomics : from bedside to clinical practiceMARSH, Sharon; MCLEOD, Howard L.Human molecular genetics (Print). 2006, Vol 15, issn 0964-6906, R89-R93, NSArticle

Genome-wide location analysis : insights on transcriptional regulationHAWKINS, R. David; BING REN.Human molecular genetics (Print). 2006, Vol 15, issn 0964-6906, R1-R7, NSArticle

Evolution at the nucleotide level : the problem of multiple whole-genome alignmentDEWEY, Colin N; PACHTER, Lior.Human molecular genetics (Print). 2006, Vol 15, issn 0964-6906, R51-R56, NSArticle

Conservation of the H19 noncoding RNA and H19-IGF2 imprinting mechanism in theriansSMITS, Guillaume; MUNGALL, Andrew J; MCCARREY, John R et al.Nature genetics. 2008, Vol 40, Num 8, pp 971-976, issn 1061-4036, 6 p.Article

Physical and transcript map of the region between D6S264 and D6S149 on chromosome 6q27, the minimal region of allele loss in sporadic epithelial ovarian cancerYING LIU; EMILION, Gracy; MUNGALL, Andrew J et al.Oncogene (Basingstoke). 2002, Vol 21, Num 3, pp 387-399, issn 0950-9232Article

A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applicationsBUCKLEY, Patrick G; MANTRIPRAGADA, Kiran K; SINDER WILEN, Birgitta et al.Human molecular genetics (Print). 2002, Vol 11, Num 25, pp 3221-3229, issn 0964-6906, 9 p.Article

Ethical issues in medical-sequencing research : implications of genotype-phenotype studies for individuals and populationsFOSTER, Morris W; SHARP, Richard R.Human molecular genetics (Print). 2006, Vol 15, issn 0964-6906, R45-R49, NSArticle

Integrating biological data through the genomeREEVES, Gabrielle A; THORNTON, Janet M.Human molecular genetics (Print). 2006, Vol 15, issn 0964-6906, R81-R87, NSArticle

Non-coding RNAMATTICK, John S; MAKUNIN, Igor V.Human molecular genetics (Print). 2006, Vol 15, issn 0964-6906, R17-R29, NSArticle

Structural variants : changing the landscape of chromosomes and design of disease studiesFEUK, Lars; MARSHALL, Christian R; WINTLE, Richard F et al.Human molecular genetics (Print). 2006, Vol 15, issn 0964-6906, R57-R66, NSArticle

Sleeping beauty : a novel cancer gene discovery toolDUPUY, Adam J; JENKINS, Nancy A; COPELAND, Neal G et al.Human molecular genetics (Print). 2006, Vol 15, issn 0964-6906, R75-R79, NSArticle

Binding sites for metabolic disease related transcription factors inferred at base pair resolution by chromatin immunoprecipitation and genomic microarraysRADA-IGLESIAS, Alvaro; WALLERMAN, Ola; WRAIGHT, Vicki L et al.Human molecular genetics (Print). 2005, Vol 14, Num 22, pp 3435-3447, issn 0964-6906, 13 p.Article

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 geneLANGAN, Joanne E; COLE, Charlotte G; DUNHAM, Ian et al.Human genetics. 2004, Vol 114, Num 6, pp 534-540, issn 0340-6717, 7 p.Article

hORFeome v3.1 : A resource of human open reading frames representing over 10,000 human genesLAMESCH, Philippe; NING LI; ROGERS, Jane et al.Genomics (San Diego, Calif.). 2007, Vol 89, Num 3, pp 307-315, issn 0888-7543, 9 p.Article

Tissue-specific histone modification and transcription factor binding in a globin gene expressionDE GOBBI, Marco; ANGUITA, Eduardo; HUGHES, Jim et al.Blood. 2007, Vol 110, Num 13, pp 4503-4510, issn 0006-4971, 8 p.Article

Evidence for widespread reticulate evolution within human dupliconsJACKSON, Michael S; OLIVER, Karen; LOVELAND, Jane et al.American journal of human genetics. 2005, Vol 77, Num 5, pp 824-840, issn 0002-9297, 17 p.Article

Replication timing of the human genomeWOODFINE, Kathryn; FIEGLER, Heike; BEARE, David M et al.Human molecular genetics (Print). 2004, Vol 13, Num 2, pp 191-202, issn 0964-6906, 12 p.Article

Mosaic 22q13 deletions : evidence for concurrent mosaic segmental isodisomy and gene conversionBONAGLIA, Maria Clara; GIORDA, Roberto; DUNHAM, Ian et al.European journal of human genetics. 2009, Vol 17, Num 4, pp 426-433, issn 1018-4813, 8 p.Article

The role of the polycomb complex in silencing α-globin gene expression in nonerythroid cellsGARRICK, David; DE GOBBI, Marco; DUNHAM, Ian et al.Blood. 2008, Vol 112, Num 9, pp 3889-3899, issn 0006-4971, 11 p.Article