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Michael Stratton

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

Research Profile (preview)

Disorders

Concepts & Ideas

Physiology

Chemicals & Drugs

Genes & Molecular Sequences

BRCA1 Genes

Procedures

Living Beings

Heterozygote

Anatomy

Chromosomes, Human, Pair 17

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Publications

TOP 3
Rapley Elizabeth A; Turnbull Clare; Al Olama Ali Amin; Dermitzakis Emmanouil T; Linger Rachel; Huddart Robert A; Renwick Anthony; Hughes Deborah; Hines Sarah; Seal Sheila; Morrison Jonathan; Nsengimana Jeremie; Deloukas Panagiotis; Rahman Nazneen; Bishop D Timothy; Easton Douglas F; Stratton Michael R
A genome-wide association study of testicular germ cell tumor.
Stevenson Roger E; Tarpey Patrick; May Melanie M; Stratton Michael R; Schwartz Charles E
Arena syndrome is caused by a missense mutation in PLP1.
Stratton Michael R; Campbell Peter J; Futreal P Andrew
The cancer genome.

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All Publications

2009: Rapley Elizabeth A; Turnbull Clare; Al Olama Ali Amin; Dermitzakis Emmanouil T; Linger Rachel; Huddart Robert A; Renwick Anthony; Hughes Deborah; Hines Sarah; Seal Sheila; Morrison Jonathan; Nsengimana Jeremie; Deloukas Panagiotis; Rahman Nazneen; Bishop D Timothy; Easton Douglas F; Stratton Michael R
A genome-wide association study of testicular germ cell tumor.
Nature genetics 2009;41(7):807-10.
2009: Stevenson Roger E; Tarpey Patrick; May Melanie M; Stratton Michael R; Schwartz Charles E
Arena syndrome is caused by a missense mutation in PLP1.
American journal of medical genetics. Part A 2009;149A(5):1081.
2009: Stratton Michael R; Campbell Peter J; Futreal P Andrew
The cancer genome.
Nature 2009;458(7239):719-24.
2009: Raymond F Lucy; Whibley Annabel; Stratton Michael R; Gecz Jozef
Lessons learnt from large-scale exon re-sequencing of the X chromosome.
Human molecular genetics 2009;18(R1):R60-4.
2009: Mahoney C L; Choudhury B; Davies H; Edkins S; Greenman C; Haaften G van; Mironenko T; Santarius T; Stevens C; Stratton M R; Futreal P A
LKB1/KRAS mutant lung cancers constitute a genetic subset of NSCLC with increased sensitivity to MAPK and mTOR signalling inhibition.
British journal of cancer 2009;100(2):370-5.
2009: Mai Phuong L; Chen Bingshu E; Tucker Kathy; Friedlander Michael; Phillips Kelly-Anne; Hogg David; Jewett Michael A S; Bodrogi Istvan; Geczi Lajos; Olah Edith; Heimdal Ketil; Fosså Sophie D; Nathanson Katherine L; Korde Larissa; Easton Douglas F; Dudakia Darshna; Huddart Robert; Stratton Michael R; Bishop D Timothy; Rapley Elizabeth A; Greene Mark H
Younger age-at-diagnosis for familial malignant testicular germ cell tumor.
Familial cancer 2009;8(4):451-6.
2008: Campbell Peter J; Pleasance Erin D; Stephens Philip J; Dicks Ed; Rance Richard; Goodhead Ian; Follows George A; Green Anthony R; Futreal P Andy; Stratton Michael R
Subclonal phylogenetic structures in cancer revealed by ultra-deep sequencing.
Proceedings of the National Academy of Sciences of the United States of America 2008;105(35):13081-6.
2008: Campbell Peter J; Stephens Philip J; Pleasance Erin D; O'Meara Sarah; Li Heng; Santarius Thomas; Stebbings Lucy A; Leroy Catherine; Edkins Sarah; Hardy Claire; Teague Jon W; Menzies Andrew; Goodhead Ian; Turner Daniel J; Clee Christopher M; Quail Michael A; Cox Antony; Brown Clive; Durbin Richard; Hurles Matthew E; Edwards Paul A W; Bignell Graham R; Stratton Michael R; Futreal P Andrew
Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing.
Nature genetics 2008;40(6):722-9.
2008: Forbes S A; Bhamra G; Bamford S; Dawson E; Kok C; Clements J; Menzies A; Teague J W; Futreal P A; Stratton M R
The Catalogue of Somatic Mutations in Cancer (COSMIC).
Current protocols in human genetics / editorial board, Jonathan L. Haines ... [et al.] 2008;Chapter 10():Unit 10.11.
2008: Gilfillan Gregor D; Selmer Kaja K; Roxrud Ingrid; Smith Raffaella; Kyllerman Mårten; Eiklid Kristin; Kroken Mette; Mattingsdal Morten; Egeland Thore; Stenmark Harald; Sjøholm Hans; Server Andres; Samuelsson Lena; Christianson Arnold; Tarpey Patrick; Whibley Annabel; Stratton Michael R; Futreal P Andrew; Teague Jon; Edkins Sarah; Gecz Jozef; Turner Gillian; Raymond F Lucy; Schwartz Charles; Stevenson Roger E; Undlien Dag E; Strømme Petter
SLC9A6 mutations cause X-linked mental retardation, microcephaly, epilepsy, and ataxia, a phenotype mimicking Angelman syndrome.
American journal of human genetics 2008;82(4):1003-10.
2008: Stratton Michael R; Rahman Nazneen
The emerging landscape of breast cancer susceptibility.
Nature genetics 2008;40(1):17-22.
2007: Coffey J; Huddart R A; Elliott F; Sohaib S A; Parker E; Dudakia D; Pugh J L; Easton D F; Bishop D T; Stratton M R; Rapley E A
Testicular microlithiasis as a familial risk factor for testicular germ cell tumour.
British journal of cancer 2007;97(12):1701-6.
2007: Bignell Graham R; Santarius Thomas; Pole Jessica C M; Butler Adam P; Perry Janet; Pleasance Erin; Greenman Chris; Menzies Andrew; Taylor Sheila; Edkins Sarah; Campbell Peter; Quail Michael; Plumb Bob; Matthews Lucy; McLay Kirsten; Edwards Paul A W; Rogers Jane; Wooster Richard; Futreal P Andrew; Stratton Michael R
Architectures of somatic genomic rearrangement in human cancer amplicons at sequence-level resolution.
Genome research 2007;17(9):1296-303.
2007: Dicks E; Teague J W; Stephens P; Raine K; Yates A; Mattocks C; Tarpey P; Butler A; Menzies A; Richardson D; Jenkinson A; Davies H; Edkins S; Forbes S; Gray K; Greenman C; Shepherd R; Stratton M R; Futreal P A; Wooster R
AutoCSA, an algorithm for high throughput DNA sequence variant detection in cancer genomes.
Bioinformatics (Oxford, England) 2007;23(13):1689-91.
2007: Schwartz Charles E; Tarpey Patrick S; Lubs Herbert A; Verloes Alain; May Melanie M; Risheg Hiba; Friez Michael J; Futreal P Andrew; Edkins Sarah; Teague Jon; Briault Sylvain; Skinner Cindy; Bauer-Carlin Astrid; Simensen Richard J; Joseph Sumy M; Jones Julie R; Gecz Josef; Stratton Michael R; Raymond F Lucy; Stevenson Roger E
The original Lujan syndrome family has a novel missense mutation (p.N1007S) in the MED12 gene.
Journal of medical genetics 2007;44(7):472-7.
2007: Scott Linda M; Tong Wei; Levine Ross L; Scott Mike A; Beer Philip A; Stratton Michael R; Futreal P Andrew; Erber Wendy N; McMullin Mary Frances; Harrison Claire N; Warren Alan J; Gilliland D Gary; Lodish Harvey F; Green Anthony R
JAK2 exon 12 mutations in polycythemia vera and idiopathic erythrocytosis.
The New England journal of medicine 2007;356(5):459-68.
2007: Tarpey Patrick; Pemberton Trevor J; Stockton David W; Das Parimal; Ninis Vasiliki; Edkins Sarah; Andrew Futreal P; Wooster Richard; Kamath Sushanth; Nayak Rabindra; Stratton Michael R; Patel Pragna I
A novel Gln358Glu mutation in ectodysplasin A associated with X-linked dominant incisor hypodontia.
American journal of medical genetics. Part A 2007;143(4):390-4.
2007: Rahman Nazneen; Seal Sheila; Thompson Deborah; Kelly Patrick; Renwick Anthony; Elliott Anna; Reid Sarah; Spanova Katarina; Barfoot Rita; Chagtai Tasnim; Jayatilake Hiran; McGuffog Lesley; Hanks Sandra; Evans D Gareth; Eccles Diana; Easton Douglas F; Stratton Michael R
PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene.
Nature genetics 2007;39(2):165-7.
2007: Linger R; Dudakia D; Huddart R; Easton D; Bishop D T; Stratton M R; Rapley E A
A physical analysis of the Y chromosome shows no additional deletions, other than Gr/Gr, associated with testicular germ cell tumour.
British journal of cancer 2007;96(2):357-61.
2006: Seal Sheila; Thompson Deborah; Renwick Anthony; Elliott Anna; Kelly Patrick; Barfoot Rita; Chagtai Tasnim; Jayatilake Hiran; Ahmed Munaza; Spanova Katarina; North Bernard; McGuffog Lesley; Evans D Gareth; Eccles Diana; Easton Douglas F; Stratton Michael R; Rahman Nazneen
Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles.
Nature genetics 2006;38(11):1239-41.
2006: Edkins Sarah; O'Meara Sarah; Parker Adrian; Stevens Claire; Reis Marcelo; Jones Siân; Greenman Chris; Davies Helen; Dalgliesh Gillian; Forbes Simon; Hunter Chris; Smith Raffaella; Stephens Philip; Goldstraw Peter; Nicholson Andrew; Chan Tsun Leung; Velculescu Victor E; Yuen Siu Tsan; Leung Suet Yi; Stratton Michael R; Futreal P Andrew
Recurrent KRAS codon 146 mutations in human colorectal cancer.
Cancer biology & therapy 2006;5(8):928-32.
2006: Renwick Anthony; Thompson Deborah; Seal Sheila; Kelly Patrick; Chagtai Tasnim; Ahmed Munaza; North Bernard; Jayatilake Hiran; Barfoot Rita; Spanova Katarina; McGuffog Lesley; Evans D Gareth; Eccles Diana; Easton Douglas F; Stratton Michael R; Rahman Nazneen
ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles.
Nature genetics 2006;38(8):873-5.
2006: Greenman Chris; Wooster Richard; Futreal P Andrew; Stratton Michael R; Easton Douglas F
Statistical analysis of pathogenicity of somatic mutations in cancer.
Genetics 2006;173(4):2187-98.
2006: Tommiska Johanna; Seal Sheila; Renwick Anthony; Barfoot Rita; Baskcomb Linda; Jayatilake Hiran; Bartkova Jirina; Tallila Jonna; Kaare Milja; Tamminen Anitta; Heikkilä Päivi; Evans D Gareth; Eccles Diana; Aittomäki Kristiina; Blomqvist Carl; Bartek Jiri; Stratton Michael R; Nevanlinna Heli; Rahman Nazneen
Evaluation of RAD50 in familial breast cancer predisposition.
International journal of cancer. Journal international du cancer 2006;118(11):2911-6.
2006: Davies Helen; Dicks Ed; Stephens Philip; Cox Charles; Teague Jon; Greenman Chris; Bignell Graham; O'meara Sarah; Edkins Sarah; Parker Adrian; Stevens Claire; Menzies Andrew; Blow Matt; Bottomley Bill; Dronsfield Mark; Futreal P Andrew; Stratton Michael R; Wooster Richard
High throughput DNA sequence variant detection by conformation sensitive capillary electrophoresis and automated peak comparison.
Genomics 2006;87(3):427-32.
2006: Forbes S; Clements J; Dawson E; Bamford S; Webb T; Dogan A; Flanagan A; Teague J; Wooster R; Futreal P A; Stratton M R
COSMIC 2005.
British journal of cancer 2006;94(2):318-22.
2006: Blow Matthew J; Grocock Russell J; van Dongen Stijn; Enright Anton J; Dicks Ed; Futreal P Andrew; Wooster Richard; Stratton Michael R
RNA editing of human microRNAs.
Genome biology 2006;7(4):R27.
2005: Scott Linda M; Campbell Peter J; Baxter E Joanna; Todd Tony; Stephens Philip; Edkins Sarah; Wooster Richard; Stratton Michael R; Futreal P Andrew; Green Anthony R
The V617F JAK2 mutation is uncommon in cancers and in myeloid malignancies other than the classic myeloproliferative disorders.
Blood 2005;106(8):2920-1.
2005: Cox Charles; Bignell Graham; Greenman Chris; Stabenau Arne; Warren William; Stephens Philip; Davies Helen; Watt Stephen; Teague Jon; Edkins Sara; Birney Ewan; Easton Douglas F; Wooster Richard; Futreal P Andrew; Stratton Michael R
A survey of homozygous deletions in human cancer genomes.
Proceedings of the National Academy of Sciences of the United States of America 2005;102(12):4542-7.
2005: Reid S; Renwick A; Seal S; Baskcomb L; Barfoot R; Jayatilake H; Pritchard-Jones K; Stratton M R; Ridolfi-Lüthy A; Rahman N;
Biallelic BRCA2 mutations are associated with multiple malignancies in childhood including familial Wilms tumour.
Journal of medical genetics 2005;42(2):147-51.
2005: Futreal P A; Wooster R; Stratton M R
Somatic mutations in human cancer: insights from resequencing the protein kinase gene family.
Cold Spring Harbor symposia on quantitative biology 2005;70():43-9.
2004: Blow Matthew; Futreal P Andrew; Wooster Richard; Stratton Michael R
A survey of RNA editing in human brain.
Genome research 2004;14(12):2379-87.
2004: Stratton Michael R; Wooster Richard W; Futreal P Andrew
The BRAF gene is frequently mutated in malignant melanoma.
Journal of drugs in dermatology : JDD 2004;3(5):573-5.
2004: Bamford S; Dawson E; Forbes S; Clements J; Pettett R; Dogan A; Flanagan A; Teague J; Futreal P A; Stratton M R; Wooster R
The COSMIC (Catalogue of Somatic Mutations in Cancer) database and website.
British journal of cancer 2004;91(2):355-8.
2004: Huang Jing; Wei Wen; Zhang Jane; Liu Guoying; Bignell Graham R; Stratton Michael R; Futreal P Andrew; Wooster Richard; Jones Keith W; Shapero Michael H
Whole genome DNA copy number changes identified by high density oligonucleotide arrays.
Human genomics 2004;1(4):287-99.
2004: Futreal P Andrew; Coin Lachlan; Marshall Mhairi; Down Thomas; Hubbard Timothy; Wooster Richard; Rahman Nazneen; Stratton Michael R
A census of human cancer genes.
Nature reviews. Cancer 2004;4(3):177-83.
2004: Bignell Graham R; Huang Jing; Greshock Joel; Watt Stephen; Butler Adam; West Sofie; Grigorova Mira; Jones Keith W; Wei Wen; Stratton Michael R; Futreal P Andrew; Weber Barbara; Shapero Michael H; Wooster Richard
High-resolution analysis of DNA copy number using oligonucleotide microarrays.
Genome research 2004;14(2):287-95.
2004: Zhao Wei; Chan Tsun Leung; Chu Kent-Man; Chan Annie S; Stratton Michael R; Yuen Siu Tsan; Leung Suet Yi
Mutations of BRAF and KRAS in gastric cancer and their association with microsatellite instability.
International journal of cancer. Journal international du cancer 2004;108(1):167-9.
2003: Seal Sheila; Barfoot Rita; Jayatilake Hiran; Smith Paula; Renwick Anthony; Bascombe Linda; McGuffog Lesley; Evans D Gareth; Eccles Diana; Easton Douglas F; Stratton Michael R; Rahman Nazneen;
Evaluation of Fanconi Anemia genes in familial breast cancer predisposition.
Cancer research 2003;63(24):8596-9.
2003: Schutte Mieke; Seal Sheila; Barfoot Rita; Meijers-Heijboer Hanne; Wasielewski Marijke; Evans D Gareth; Eccles Diana; Meijers Carel; Lohman Frans; Klijn Jan; van den Ouweland Ans; Futreal P Andrew; Nathanson Katherine L; Weber Barbara L; Easton Douglas F; Stratton Michael R; Rahman Nazneen;
Variants in CHEK2 other than 1100delC do not make a major contribution to breast cancer susceptibility.
American journal of human genetics 2003;72(4):1023-8.
2003: Rapley Elizabeth A; Crockford Gillian P; Easton Douglas F; Stratton Michael R; Bishop D Timothy;
Localisation of susceptibility genes for familial testicular germ cell tumour.
APMIS : acta pathologica, microbiologica, et immunologica Scandinavica 2003;111(1):128-33; discussion 33-5.
2002: Brose Marcia S; Volpe Patricia; Feldman Michael; Kumar Madhu; Rishi Irum; Gerrero Renee; Einhorn Eugene; Herlyn Meenhard; Minna John; Nicholson Andrew; Roth Jack A; Albelda Steven M; Davies Helen; Cox Charles; Brignell Graham; Stephens Philip; Futreal P Andrew; Wooster Richard; Stratton Michael R; Weber Barbara L
BRAF and RAS mutations in human lung cancer and melanoma.
Cancer research 2002;62(23):6997-7000.
2002: Yuen Siu T; Davies Helen; Chan Tsun L; Ho Judy W; Bignell Graham R; Cox Charles; Stephens Philip; Edkins Sarah; Tsui Wendy W; Chan Annie S; Futreal P Andrew; Stratton Michael R; Wooster Richard; Leung Suet Y
Similarity of the phenotypic patterns associated with BRAF and KRAS mutations in colorectal neoplasia.
Cancer research 2002;62(22):6451-5.
2002: Meitz J C; Edwards S M; Easton D F; Murkin A; Ardern-Jones A; Jackson R A; Williams S; Dearnaley D P; Stratton M R; Houlston R S; Eeles R A;
HPC2/ELAC2 polymorphisms and prostate cancer risk: analysis by age of onset of disease.
British journal of cancer 2002;87(8):905-8.
2002: Shih Helen A; Couch Fergus J; Nathanson Katherine L; Blackwood M Anne; Rebbeck Timothy R; Armstrong Katrina A; Calzone Kathleen; Stopfer Jill; Seal Sheila; Stratton Michael R; Weber Barbara L
BRCA1 and BRCA2 mutation frequency in women evaluated in a breast cancer risk evaluation clinic.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2002;20(4):994-9.
2002: Antoniou A C; Pharoah P D P; McMullan G; Day N E; Stratton M R; Peto J; Ponder B J; Easton D F
A comprehensive model for familial breast cancer incorporating BRCA1, BRCA2 and other genes.
British journal of cancer 2002;86(1):76-83.
2001: Rapley E A; Hargrave D; Persinguhe N; Barfoot R; Moore I; Radford M; Stratton M R; Rahman N; Pritchard-Jones K
Case of interstitial 12q deletion in association with Wilms tumor.
American journal of medical genetics 2001;104(3):246-9.
2001: Bevan S; Pal T; Greenberg C R; Green H; Wixey J; Bignell G; Narod S A; Foulkes W D; Stratton M R; Houlston R S
A comprehensive analysis of MNG1, TCO1, fPTC, PTEN, TSHR, and TRKA in familial nonmedullary thyroid cancer: confirmation of linkage to TCO1.
The Journal of clinical endocrinology and metabolism 2001;86(8):3701-4.
2001: Stone J G; Coleman G; Gusterson B; Marossy A; Lakhani S R; Ward A; Nash A; McKinna A; A'Hern R; Stratton M R; Houlston R S
Contribution of germline MLH1 and MSH2 mutations to lobular carcinoma in situ of the breast.
Cancer letters 2001;167(2):171-4.
2001: Martin A M; Blackwood M A; Antin-Ozerkis D; Shih H A; Calzone K; Colligon T A; Seal S; Collins N; Stratton M R; Weber B L; Nathanson K L
Germline mutations in BRCA1 and BRCA2 in breast-ovarian families from a breast cancer risk evaluation clinic.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2001;19(8):2247-53.
2001: Futreal P A; Kasprzyk A; Birney E; Mullikin J C; Wooster R; Stratton M R
Cancer and genomics.
Nature 2001;409(6822):850-2.
2000: Shih H A; Nathanson K L; Seal S; Collins N; Stratton M R; Rebbeck T R; Weber B L
BRCA1 and BRCA2 mutations in breast cancer families with multiple primary cancers.
Clinical cancer research : an official journal of the American Association for Cancer Research 2000;6(11):4259-64.
2000: Mangion J; Edkins S; Goss A N; Stratton M R; Flanagan A M
Familial craniofacial fibrous dysplasia: absence of linkage to GNAS1 and the gene for cherubism.
Journal of medical genetics 2000;37(11):E37.
2000: Gayther S A; de Foy K A; Harrington P; Pharoah P; Dunsmuir W D; Edwards S M; Gillett C; Ardern-Jones A; Dearnaley D P; Easton D F; Ford D; Shearer R J; Kirby R S; Dowe A L; Kelly J; Stratton M R; Ponder B A; Barnes D; Eeles R A
The frequency of germ-line mutations in the breast cancer predisposition genes BRCA1 and BRCA2 in familial prostate cancer. The Cancer Research Campaign/British Prostate Group United Kingdom Familial Prostate Cancer Study Collaborators.
Cancer research 2000;60(16):4513-8.
2000: Rahman N; Teare M D; Seal S; Renard H; Mangion J; Cour C; Thompson D; Shugart Y; Eccles D; Devilee P; Meijers H; Nathanson K L; Neuhausen S L; Weber B; Chang-Claude J; Easton D F; Goldgar D; Stratton M R
Absence of evidence for a familial breast cancer susceptibility gene at chromosome 8p12-p22.
Oncogene 2000;19(36):4170-3.
2000: Rapley E A; Barfoot R; Bonaïti-Pellié C; Chompret A; Foulkes W; Perusinghe N; Reeve A; Royer-Pokora B; Schumacher V; Shelling A; Skeen J; de Tourreil S; Weirich A; Pritchard-Jones K; Stratton M R; Rahman N
Evidence for susceptibility genes to familial Wilms tumour in addition to WT1, FWT1 and FWT2.
British journal of cancer 2000;83(2):177-83.
2000: Rahman N; Arbour L; Houlston R; Bonaïti-Pellié C; Abidi F; Tranchemontagne J; Ford D; Narod S; Pritchard-Jones K; Foulkes W D; Schwartz C; Stratton M R
Penetrance of mutations in the familial Wilms tumor gene FWT1.
Journal of the National Cancer Institute 2000;92(8):650-2.
2000: Lakhani S R; Gusterson B A; Jacquemier J; Sloane J P; Anderson T J; van de Vijver M J; Venter D; Freeman A; Antoniou A; McGuffog L; Smyth E; Steel C M; Haites N; Scott R J; Goldgar D; Neuhausen S; Daly P A; Ormiston W; McManus R; Scherneck S; Ponder B A; Futreal P A; Peto J; Stoppa-Lyonnet D; Bignon Y J; Stratton M R
The pathology of familial breast cancer: histological features of cancers in families not attributable to mutations in BRCA1 or BRCA2.
Clinical cancer research : an official journal of the American Association for Cancer Research 2000;6(3):782-9.
2000: Rahman N; Stone J G; Coleman G; Gusterson B; Seal S; Marossy A; Lakhani S R; Ward A; Nash A; McKinna A; A'Hern R; Stratton M R; Houlston R S
Lobular carcinoma in situ of the breast is not caused by constitutional mutations in the E-cadherin gene.
British journal of cancer 2000;82(3):568-70.
2000: Rapley E A; Crockford G P; Teare D; Biggs P; Seal S; Barfoot R; Edwards S; Hamoudi R; Heimdal K; Fossâ S D; Tucker K; Donald J; Collins F; Friedlander M; Hogg D; Goss P; Heidenreich A; Ormiston W; Daly P A; Forman D; Oliver T D; Leahy M; Huddart R; Cooper C S; Bodmer J G; Easton D F; Stratton M R; Bishop D T
Localization to Xq27 of a susceptibility gene for testicular germ-cell tumours.
Nature genetics 2000;24(2):197-200.
1999: Lakhani S R; Chaggar R; Davies S; Jones C; Collins N; Odel C; Stratton M R; O'Hare M J
Genetic alterations in 'normal' luminal and myoepithelial cells of the breast.
The Journal of pathology 1999;189(4):496-503.
1999: Mao X; Barfoot R; Hamoudi R A; Easton D F; Flanagan A M; Stratton M R
Allelotype of uterine leiomyomas.
Cancer genetics and cytogenetics 1999;114(2):89-95.
1999: Mangion J; Rahman N; Mansour S; Brice G; Rosbotham J; Child A H; Murday V A; Mortimer P S; Barfoot R; Sigurdsson A; Edkins S; Sarfarazi M; Burnand K; Evans A L; Nunan T O; Stratton M R; Jeffery S
A gene for lymphedema-distichiasis maps to 16q24.3.
American journal of human genetics 1999;65(2):427-32.
1999: Mangion J; Rahman N; Edkins S; Barfoot R; Nguyen T; Sigurdsson A; Townend J V; Fitzpatrick D R; Flanagan A M; Stratton M R
The gene for cherubism maps to chromosome 4p16.3.
American journal of human genetics 1999;65(1):151-7.
1999: Peto J; Collins N; Barfoot R; Seal S; Warren W; Rahman N; Easton D F; Evans C; Deacon J; Stratton M R
Prevalence of BRCA1 and BRCA2 gene mutations in patients with early-onset breast cancer.
Journal of the National Cancer Institute 1999;91(11):943-9.
1999: Tomlinson I; Rahman N; Frayling I; Mangion J; Barfoot R; Hamoudi R; Seal S; Northover J; Thomas H J; Neale K; Hodgson S; Talbot I; Houlston R; Stratton M R
Inherited susceptibility to colorectal adenomas and carcinomas: evidence for a new predisposition gene on 15q14-q22.
Gastroenterology 1999;116(4):789-95.
1998: Rahman N; Abidi F; Ford D; Arbour L; Rapley E; Tonin P; Barton D; Batcup G; Berry J; Cotter F; Davison V; Gerrard M; Gray E; Grundy R; Hanafy M; King D; Lewis I; Ridolfi Luethy A; Madlensky L; Mann J; O'Meara A; Oakhill T; Skolnick M; Strong L; Stratton M R
Confirmation of FWT1 as a Wilms' tumour susceptibility gene and phenotypic characteristics of Wilms' tumour attributable to FWT1.
Human genetics 1998;103(5):547-56.
1998: Shayeghi M; Seal S; Regan J; Collins N; Barfoot R; Rahman N; Ashton A; Moohan M; Wooster R; Owen R; Bliss J M; Stratton M R; Yarnold J
Heterozygosity for mutations in the ataxia telangiectasia gene is not a major cause of radiotherapy complications in breast cancer patients.
British journal of cancer 1998;78(7):922-7.
1998: Roth S; Kristo P; Auranen A; Shayehgi M; Seal S; Collins N; Barfoot R; Rahman N; Klemi P J; Grénman S; Sarantaus L; Nevanlinna H; Butzow R; Ashworth A; Stratton M R; Aaltonen L A
A missense mutation in the BRCA2 gene in three siblings with ovarian cancer.
British journal of cancer 1998;77(8):1199-202.
1998: Bignell G R; Barfoot R; Seal S; Collins N; Warren W; Stratton M R
Low frequency of somatic mutations in the LKB1/Peutz-Jeghers syndrome gene in sporadic breast cancer.
Cancer research 1998;58(7):1384-6.
1998: Savelyeva L; Claas A; Gier S; Schlag P; Finke L; Mangion J; Stratton M R; Schwab M
An interstitial tandem duplication of 9p23-24 coexists with a mutation in the BRCA2 gene in the germ line of three brothers with breast cancer.
Cancer research 1998;58(5):863-6.
1998: Chang-Claude J; Dong J; Schmidt S; Shayeghi M; Komitowski D; Becher H; Stratton M R; Royer-Pokora B
Using gene carrier probability to select high risk families for identifying germline mutations in breast cancer susceptibility genes.
Journal of medical genetics 1998;35(2):116-21.
1998: Hemminki A; Markie D; Tomlinson I; Avizienyte E; Roth S; Loukola A; Bignell G; Warren W; Aminoff M; Höglund P; Järvinen H; Kristo P; Pelin K; Ridanpää M; Salovaara R; Toro T; Bodmer W; Olschwang S; Olsen A S; Stratton M R; de la Chapelle A; Aaltonen L A
A serine/threonine kinase gene defective in Peutz-Jeghers syndrome.
Nature 1998;391(6663):184-7.
1998: Rahman N; Stratton M R
The genetics of breast cancer susceptibility.
Annual review of genetics 1998;32():95-121.
1997: Bignell G R; Canzian F; Shayeghi M; Stark M; Shugart Y Y; Biggs P; Mangion J; Hamoudi R; Rosenblatt J; Buu P; Sun S; Stoffer S S; Goldgar D E; Romeo G; Houlston R S; Narod S A; Stratton M R; Foulkes W D
Familial nontoxic multinodular thyroid goiter locus maps to chromosome 14q but does not account for familial nonmedullary thyroid cancer.
American journal of human genetics 1997;61(5):1123-30.
1997: Easton D F; Steele L; Fields P; Ormiston W; Averill D; Daly P A; McManus R; Neuhausen S L; Ford D; Wooster R; Cannon-Albright L A; Stratton M R; Goldgar D E
Cancer risks in two large breast cancer families linked to BRCA2 on chromosome 13q12-13.
American journal of human genetics 1997;61(1):120-8.
1997: Rahman N; Arbour L; Tonin P; Baruchel S; Pritchard-Jones K; Narod S A; Stratton M R
The familial Wilms' tumour susceptibility gene, FWT1, may not be a tumour suppressor gene.
Oncogene 1997;14(25):3099-102.
1997: Bignell G; Micklem G; Stratton M R; Ashworth A; Wooster R
The BRC repeats are conserved in mammalian BRCA2 proteins.
Human molecular genetics 1997;6(1):53-8.
1997: Gayther S A; Mangion J; Russell P; Seal S; Barfoot R; Ponder B A; Stratton M R; Easton D
Variation of risks of breast and ovarian cancer associated with different germline mutations of the BRCA2 gene.
Nature genetics 1997;15(1):103-5.
1997: Collins N; Wooster R; Stratton M R
Absence of methylation of CpG dinucleotides within the promoter of the breast cancer susceptibility gene BRCA2 in normal tissues and in breast and ovarian cancers.
British journal of cancer 1997;76(9):1150-6.
1996: Mazoyer S; Dunning A M; Serova O; Dearden J; Puget N; Healey C S; Gayther S A; Mangion J; Stratton M R; Lynch H T; Goldgar D E; Ponder B A; Lenoir G M
A polymorphic stop codon in BRCA2.
Nature genetics 1996;14(3):253-4.
1996: Rahman N; Arbour L; Tonin P; Renshaw J; Pelletier J; Baruchel S; Pritchard-Jones K; Stratton M R; Narod S A
Evidence for a familial Wilms' tumour gene (FWT1) on chromosome 17q12-q21.
Nature genetics 1996;13(4):461-3.
1996: Lancaster J M; Wooster R; Mangion J; Phelan C M; Cochran C; Gumbs C; Seal S; Barfoot R; Collins N; Bignell G; Patel S; Hamoudi R; Larsson C; Wiseman R W; Berchuck A; Iglehart J D; Marks J R; Ashworth A; Stratton M R; Futreal P A
BRCA2 mutations in primary breast and ovarian cancers.
Nature genetics 1996;13(2):238-40.
1996: Biggs P J; Chapman P; Lakhani S R; Burn J; Stratton M R
The cylindromatosis gene (cyld1) on chromosome 16q may be the only tumour suppressor gene involved in the development of cylindromas.
Oncogene 1996;12(6):1375-7.
1996: Phelan C M; Rebbeck T R; Weber B L; Devilee P; Ruttledge M H; Lynch H T; Lenoir G M; Stratton M R; Easton D F; Ponder B A; Cannon-Albright L; Larsson C; Goldgar D E; Narod S A
Ovarian cancer risk in BRCA1 carriers is modified by the HRAS1 variable number of tandem repeat (VNTR) locus.
Nature genetics 1996;12(3):309-11.
1996: Stratton M R; Wooster R
Hereditary predisposition to breast cancer.
Current opinion in genetics & development 1996;6(1):93-7.
1996: Lakhani S R; Slack D N; Hamoudi R A; Collins N; Stratton M R; Sloane J P
Detection of allelic imbalance indicates that a proportion of mammary hyperplasia of usual type are clonal, neoplastic proliferations.
Laboratory investigation; a journal of technical methods and pathology 1996;74(1):129-35.
1995: Biggs P J; Wooster R; Ford D; Chapman P; Mangion J; Quirk Y; Easton D F; Burn J; Stratton M R
Familial cylindromatosis (turban tumour syndrome) gene localised to chromosome 16q12-q13: evidence for its role as a tumour suppressor gene.
Nature genetics 1995;11(4):441-3.
1995: Gayther S A; Warren W; Mazoyer S; Russell P A; Harrington P A; Chiano M; Seal S; Hamoudi R; van Rensburg E J; Dunning A M; Love R; Evans G; Easton D; Clayton D; Stratton M R; Ponder B A
Germline mutations of the BRCA1 gene in breast and ovarian cancer families provide evidence for a genotype-phenotype correlation.
Nature genetics 1995;11(4):428-33.
1995: Cleton-Jansen A M; Collins N; Lakhani S R; Weissenbach J; Devilee P; Cornelisse C J; Stratton M R
Loss of heterozygosity in sporadic breast tumours at the BRCA2 locus on chromosome 13q12-q13.
British journal of cancer 1995;72(5):1241-4.
1995: Houlston R S; Stratton M R
Genetics of non-medullary thyroid cancer.
QJM : monthly journal of the Association of Physicians 1995;88(10):685-93.
1995: Lakhani S R; Collins N; Stratton M R; Sloane J P
Atypical ductal hyperplasia of the breast: clonal proliferation with loss of heterozygosity on chromosomes 16q and 17p.
Journal of clinical pathology 1995;48(7):611-5.
1995: Warren W; Biggs P J; el-Baz M; Ghoneim M A; Stratton M R; Venitt S
Mutations in the p53 gene in schistosomal bladder cancer: a study of 92 tumours from Egyptian patients and a comparison between mutational spectra from schistosomal and non-schistosomal urothelial tumours.
Carcinogenesis 1995;16(5):1181-9.
1995: Stratton M R; Collins N; Lakhani S R; Sloane J P
Loss of heterozygosity in ductal carcinoma in situ of the breast.
The Journal of pathology 1995;175(2):195-201.
1995: Wooster R; Stratton M R
Breast cancer susceptibility: a complex disease unravels.
Trends in genetics : TIG 1995;11(1):3-5.
1995: Goldgar D E; Neuhausen S L; Steele L; Fields P; Ward J H; Tran T; Ngyuen K; Stratton M R; Easton D F
A 45-year follow-up of kindred 107 and the search for BRCA2.
Journal of the National Cancer Institute. Monographs 1995;(17):15-9.
1994: Stratton M R; Ford D; Neuhasen S; Seal S; Wooster R; Friedman L S; King M C; Egilsson V; Devilee P; McManus R
Familial male breast cancer is not linked to the BRCA1 locus on chromosome 17q.
Nature genetics 1994;7(1):103-7.
1994: Eeles R A; Stratton M R; Goldgar D E; Easton D F
The genetics of familial breast cancer and their practical implications.
European journal of cancer (Oxford, England : 1990) 1994;30A(9):1383-90.
1993: Stratton M R; Collins N; Lakhani S; Sloane J
Molecular analyses of in situ breast cancer.
European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation (ECP) 1993;2 Suppl 3():123.
1993: Wooster R; Ford D; Mangion J; Ponder B A; Peto J; Easton D F; Stratton M R
Absence of linkage to the ataxia telangiectasia locus in familial breast cancer.
Human genetics 1993;92(1):91-4.
1993: Biggs P J; Warren W; Venitt S; Stratton M R
Does a genotoxic carcinogen contribute to human breast cancer? The value of mutational spectra in unravelling the aetiology of cancer.
Mutagenesis 1993;8(4):275-83.
1993: Eeles R A; Warren W; Knee G; Bartek J; Averill D; Stratton M R; Blake P R; Tait D M; Lane D P; Easton D F
Constitutional mutation in exon 8 of the p53 gene in a patient with multiple primary tumours: molecular and immunohistochemical findings.
Oncogene 1993;8(5):1269-76.
1992: Wooster R; Mangion J; Eeles R; Smith S; Dowsett M; Averill D; Barrett-Lee P; Easton D F; Ponder B A; Stratton M R
A germline mutation in the androgen receptor gene in two brothers with breast cancer and Reifenstein syndrome.
Nature genetics 1992;2(2):132-4.
1991: Gill S; Stratton M R; Patterson H; Spurr N K; Fisher C; Gusterson B A; Cooper C S
Detection of transforming genes by transfection of DNA from primary soft-tissue tumours.
Oncogene 1991;6(9):1651-6.
1991: Stratton M R; Darling J; Cooper C S; Reeves B R
A case of cerebellar medulloblastoma with a single chromosome abnormality.
Cancer genetics and cytogenetics 1991;53(1):101-3.
1991: Cooper C S; Stratton M R
Soft tissue tumours: the genetic basis of development.
Carcinogenesis 1991;12(2):155-65.
1990: Patterson H; Mitchell P J; Cooper C S; Stratton M R
Dinucleotide repeat polymorphism at the SIS locus.
Nucleic acids research 1990;18(19):5917.
1990: Stratton M R; Moss S; Warren W; Patterson H; Clark J; Fisher C; Fletcher C D; Ball A; Thomas M; Gusterson B A
Mutation of the p53 gene in human soft tissue sarcomas: association with abnormalities of the RB1 gene.
Oncogene 1990;5(9):1297-301.
1989: Stratton M R; Fisher C; Gusterson B A; Cooper C S
Detection of point mutations in N-ras and K-ras genes of human embryonal rhabdomyosarcomas using oligonucleotide probes and the polymerase chain reaction.
Cancer research 1989;49(22):6324-7.
1989: Stratton M R; Darling J; Lantos P L; Cooper C S; Reeves B R
Cytogenetic abnormalities in human ependymomas.
International journal of cancer. Journal international du cancer 1989;44(4):579-81.
1989: Stratton M R; Williams S; Fisher C; Ball A; Westbury G; Gusterson B A; Fletcher C D; Knight J C; Fung Y K; Reeves B R
Structural alterations of the RB1 gene in human soft tissue tumours.
British journal of cancer 1989;60(2):202-5.
1989: Stratton M R; Darling J; Pilkington G J; Lantos P L; Reeves B R; Cooper C S
Characterization of the human cell line TE671.
Carcinogenesis 1989;10(5):899-905.
1989: Stratton M R; Reeves B R; Cooper C S
Misidentified cell.
Nature 1989;337(6205):311-2.

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