A second case of intrauterine growth retardation and primary hypospadias associated with a trisomy 22 placenta but with biparental inheritance of chromosome 22 in the fetusBRYAN, Jennifer; PETERS, Michelle; PRITCHARD, Gary et al.Prenatal diagnosis. 2002, Vol 22, Num 2, pp 137-140, issn 0197-3851Article

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Gene expression profiling of formalin-fixed, paraffin-embedded familial breast tumours using the whole genome-DASL assayWADDELL, Nic; COCCIARDI, Sibylle; LAKHANI, Sunil R et al.Journal of pathology (Print). 2010, Vol 221, Num 4, pp 452-460, issn 0022-3417, 9 p.Article

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A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor―negative breast cancer in the general populationANTONIOU, Antonis C; XIANSHU WANG; GHOUSSAINI, Maya et al.Nature genetics. 2010, Vol 42, Num 10, pp 885-892, issn 1061-4036, 8 p.Article

Analysis of the transcription regulator, CNOT7, as a candidate chromosome 8 tumor suppressor gene in colorectal cancerFLANAGAN, James; HEALEY, Sue; YOUNG, Joanne et al.International journal of cancer. 2003, Vol 106, Num 4, pp 505-509, issn 0020-7136, 5 p.Article

A Nonsynonymous Polymorphism in IRS1 Modifies Risk of Developing Breast and Ovarian Cancers in BRCA1 and Ovarian Cancer in BRCA2 Mutation CarriersDING, Yuan C; MCGUFFOG, Lesley; KRISTOFFERSSON, Ulf et al.Cancer epidemiology, biomarkers & prevention. 2012, Vol 21, Num 8, pp 1362-1370, issn 1055-9965, 9 p.Article

Association Between BRCA1 and BRCA2 Mutations and Survival in Women With Invasive Epithelial Ovarian CancerBOLTON, Kelly L; CHENEVIX-TRENCH, Georgia; HEALEY, Sue et al.JAMA, the journal of the American Medical Association. 2012, Vol 307, Num 4, pp 382-390, issn 0098-7484, 9 p.Article

Common alleles at 6q25.1 and 1 p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriersANTONIOU, Antonis C; KARTSONAKI, Christiana; ZAFFARONI, Daniela et al.Human molecular genetics (Print). 2011, Vol 20, Num 16, pp 3304-3321, issn 0964-6906, 18 p.Article

BRCA1 R 1699Q variant displaying ambiguous functional abrogation confers intermediate breast and ovarian cancer riskSPURDLE, Amanda B; WHILEY, Phillip J; KATTENTIDT-MOURAVIEVA, Anna A et al.Journal of medical genetics. 2012, Vol 49, Num 8, pp 525-532, issn 0022-2593, 8 p.Article

Common Genetic Variation at BARD1 Is Not Associated with Breast Cancer Risk in BRCA1 or BRCA2 Mutation CarriersSPURDLE, Amanda B; MARQUART, Louise; GSCHWANTLER-KAULICH, Daphne et al.Cancer epidemiology, biomarkers & prevention. 2011, Vol 20, Num 5, pp 1032-1038, issn 1055-9965, 7 p.Article

Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriersIM, Kate M; KIRCHHOFF, Tomas; GUIDUCCI, Candace et al.Human genetics. 2011, Vol 130, Num 5, pp 685-699, issn 0340-6717, 15 p.Article

Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriersANTONIOU, Antonis C; SINILNIKOVA, Olga M; NEUHAUSEN, Susan L et al.Human molecular genetics (Print). 2009, Vol 18, Num 22, pp 4442-4456, issn 0964-6906, 15 p.Article

Common Variants at the 19p13.1 and ZNF365 Loci Are Associated with ER Subtypes of Breast Cancer and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation CarriersCOUCH, Fergus J; GAUDET, Mia M; MCGUFFOG, Lesley et al.Cancer epidemiology, biomarkers & prevention. 2012, Vol 21, Num 4, pp 645-657, issn 1055-9965, 13 p.Article

Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriersCOX, David G; SIMARD, Jacques; SZABO, Csilla et al.Human molecular genetics (Print). 2011, Vol 20, Num 23, pp 4732-4747, issn 0964-6906, 16 p.Article

Rare, Evolutionarily Unlikely Missense Substitutions in ATM Confer Increased Risk of Breast CancerTAVTIGIAN, Sean V; OEFNER, Peter J; FEUCHTINGER, Corinna et al.American journal of human genetics. 2009, Vol 85, Num 4, pp 427-446, issn 0002-9297, 20 p.Article

Cognition and the temporal arts: Investigating audience response to dance using PDAs that record continuous data during live performanceSTEVENS, Catherine J; SCHUBERT, Emery; HASZARD MORRIS, Rua et al.International journal of human-computer studies. 2009, Vol 67, Num 9, pp 800-813, issn 1071-5819, 14 p.Article

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Genetic Variation at 9p22.2 and Ovarian Cancer Risk for BRCA1 and BRCA2 Mutation CarriersRAMUS, Susan J; KARTSONAKI, Christiana; XIANSHU WANG et al.Journal of the National Cancer Institute. 2011, Vol 103, Num 2, pp 105-116, issn 0027-8874, 12 p.Article

A genome wide linkage scan for dizygotic twinning in 525 families of mothers of dizygotic twinsPAINTER, Jodie N; WILLEMSEN, Gonneke; MARTIN, Nicholas G et al.Human reproduction (Oxford. Print). 2010, Vol 25, Num 6, pp 1569-1580, issn 0268-1161, 12 p.Article

Common Breast Cancer Susceptibility Alleles and the Risk of Breast Cancer for BRCA1 and BRCA2 Mutation Carriers: Implications for Risk PredictionANTONIOU, Antonis C; BEESLEY, Jonathan; ISAACS, Claudine et al.Cancer research (Chicago, Ill.). 2010, Vol 70, Num 23, pp 9742-9754, issn 0008-5472, 13 p.Article

Clinical Classification of BRCA1 and BRCA2 DNA Sequence Variants : The Value of Cytokeratin Profiles and Evolutionary Analysis-A Report From the kConFab InvestigatorsSPURDLE, Amanda B; LAKHANI, Sunil R; TAVTIGIAN, Sean V et al.Journal of clinical oncology. 2008, Vol 26, Num 10, pp 1657-1663, issn 0732-183X, 7 p.Article

Common Breast Cancer-Predisposition Alleles Are Associated with Breast Cancer Risk in BRCA1 and BRCA2 Mutation CarriersANTONIOU, Antonis C; SPURDLE, Amanda B; HOFMANN, Wera et al.American journal of human genetics. 2008, Vol 82, Num 4, pp 937-948, issn 0002-9297, 12 p.Article

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Human twinning is not linked to the region of chromosome 4 syntenic with the sheep twinning gene FecBDUFFY, David L; MONTGOMERY, Grant W; HALL, Jeff et al.American journal of medical genetics. 2001, Vol 100, Num 3, pp 182-186, issn 0148-7299Article