Exploring the Genomes of Cancer Cells: Progress and Promise : Cancer Crusade at 40STRATTON, Michael R.Science (Washington, D.C.). 2011, Vol 331, Num 6024, pp 1553-1558, issn 0036-8075, 6 p.Article

The emerging landscape of breast cancer susceptibilitySTRATTON, Michael R; RAHMAN, Nazneen.Nature genetics. 2008, Vol 40, Num 1, pp 17-22, issn 1061-4036, 6 p.Article

Genomics and the Continuum of Cancer CareMCDERMOTT, Ultan; DOWNING, James R; STRATTON, Michael R et al.The New England journal of medicine. 2011, Vol 364, Num 4, pp 340-350, issn 0028-4793, 11 p.Article

Lessons learnt from large-scale exon re-sequencing of the X chromosomeRAYMOND, F. Lucy; WHIBLEY, Annabel; STRATTON, Michael R et al.Human molecular genetics (Print). 2009, Vol 18, issn 0964-6906, R60-R64, NS1Article

The cancer genomeSTRATTON, Michael R; CAMPBELL, Peter J; FUTREAL, P. Andrew et al.Nature (London). 2009, Vol 458, Num 7239, pp 719-724, issn 0028-0836, 6 p.Article

Submicroscopic Duplications of the Hydroxysteroid Dehydrogenase HSD17B10 and the E3 Ubiquitin Ligase HUWE1 Are Associated with Mental RetardationFROYEN, Guy; CORBETT, Mark; CHELLY, Jamel et al.American journal of human genetics. 2008, Vol 82, Num 2, pp 432-443, issn 0002-9297, 12 p.Article

A common coding variant in CASP8 is associated with breast cancer riskCOX, Angela; DUNNING, Alison M; LISSOWSKA, Jolanta et al.Nature genetics. 2007, Vol 39, Num 3, pp 352-358, issn 1061-4036, 7 p.Article

Genome-wide association study identifies novel breast cancer susceptibility lociEASTON, Douglas F; POOLEY, Karen A; WAREHAM, Nicholas et al.Nature (London). 2007, Vol 447, Num 7148, pp 1087-1093, issn 0028-0836, 7 p.Article

Mutations in the gene encoding the sigma 2 subunit of the adaptor protein 1 complex, AP1S2, cause X-linked mental retardationTARPEY, Patrick S; STEVENS, Claire; DICKS, Ed et al.American journal of human genetics. 2006, Vol 79, Num 6, pp 1119-1124, issn 0002-9297, 6 p.Article

Mutations in the DLG3 gene cause nonsyndromic X-linked mental retardationTARPEY, Patrick; PARNAU, Josep; KORNY, Angelique et al.American journal of human genetics. 2004, Vol 75, Num 2, pp 318-324, issn 0002-9297, 7 p.Article

Cancer and genomics : The human genomeFUTREAL, P. Andrew; KASPRZYK, Arek; BIRNEY, Ewan et al.Nature (London). 2001, Vol 409, Num 6822, pp 850-852, issn 0028-0836Article

DICER1 syndrome: clarifying the diagnosis, clinical features and management implications of a pleiotropic tumour predisposition syndromeSLADE, Ingrid; BACCHELLI, Chiara; JENKINSON, Helen et al.Journal of medical genetics. 2011, Vol 48, Num 4, pp 273-278, issn 0022-2593, 6 p.Article

A comprehensive catalogue of somatic mutations from a human cancer genomePLEASANCE, Erin D; CHEETHAM, R. Keira; KAI YE et al.Nature (London). 2010, Vol 463, Num 7278, pp 191-196, issn 0028-0836, 6 p.Article

Systematic sequencing of renal carcinoma reveals inactivation of histone modifying genesDALGLIESH, Gillian L; FURGE, Kyle; TEAGUE, Jon et al.Nature (London). 2010, Vol 463, Num 7279, pp 360-363, issn 0028-0836, 4 p.Article

Natural History of Christianson SyndromeSCHROER, Richard J; HOLDEN, Kenton R; STRATTON, Michael R et al.American journal of medical genetics. Part A. 2010, Vol 152, Num 11, pp 2775-2783, issn 1552-4825, 9 p.Article

ATM mutations that cause ataxia- telangiectasia are breast cancer susceptibility allelesRENWICK, Anthony; THOMPSON, Deborah; MCGUFFOG, Lesley et al.Nature genetics. 2006, Vol 38, Num 8, pp 873-875, issn 1061-4036, 3 p.Article

High throughput DNA sequence variant detection by conformation sensitive capillary electrophoresis and automated peak comparisonDAVIES, Helen; DICKS, Ed; STEVENS, Claire et al.Genomics (San Diego, Calif.). 2006, Vol 87, Num 3, pp 427-432, issn 0888-7543, 6 p.Article

The Y deletion gr/gr and susceptibility to testicular germ cell tumorNATHANSON, Katherine L; KANETSKY, Peter A; LOHYNSKA, Radka et al.American journal of human genetics. 2005, Vol 77, Num 6, pp 1034-1043, issn 0002-9297, 10 p.Article

Evaluation of fanconi Anemia genes in familial breast cancer predispositionSEAL, Sheila; BARFOOT, Rita; STRATTON, Michael R et al.Cancer research (Baltimore). 2003, Vol 63, Num 24, pp 8596-8599, issn 0008-5472, 4 p.Article

Predisposition gene identification in common cancers by exome sequencing: insights from familial breast cancerSNAPE, Katie; RUARK, Elise; RAHMAN, Nazneen et al.Breast cancer research and treatment. 2012, Vol 134, Num 1, pp 429-433, issn 0167-6806, 5 p.Article

Clinical significance of SF3B1 mutations in myelodysplastic syndromes and myelodysplastic/myeloproliferative neoplasmsMALCOVATI, Luca; PAPAEMMANUIL, Elli; GALLI, Anna et al.Blood. 2011, Vol 118, Num 24, pp 6239-6246, issn 0006-4971, 8 p.Article

Mutation and association analysis of GEN1 in breast cancer susceptibilityTURNBULL, Clare; HINES, Sarah; STRATTON, Michael R et al.Breast cancer research and treatment. 2010, Vol 124, Num 1, pp 283-288, issn 0167-6806, 6 p.Article

Hypomorphic Temperature-Sensitive Alleles of NSDHL Cause CK SyndromeMCLARREN, Keith W; SEVERSON, Tesa M; JIANGHONG AN et al.American journal of human genetics. 2010, Vol 87, Num 6, pp 905-914, issn 0002-9297, 10 p.Article

Arena Syndrome Is Caused by a Missense Mutation in PLP1STEVENSON, Roger E; TARPEY, Patrick; MAY, Melanie M et al.American journal of medical genetics. Part A. 2009, Vol 149, Num 5, pp 1081-1081, issn 1552-4825, 1 p.Article

Complex landscapes of somatic rearrangement in human breast cancer genomesSTEPHENS, Philip J; MCBRIDE, David J; GREENMAN, Chris D et al.Nature (London). 2009, Vol 462, Num 7276, pp 1005-1010, issn 0028-0836, 6 p.Article