BRCA1 and BRCA2 genetic testing—pitfalls and recommendations for managing variants of uncertain clinical significance

by Eccles, D.M., Mitchell, G., Monteiro, A.N.A., Schmutzler, R., Couch, F.J., Spurdle, A.B., Gómez-García, E.B., Driessen, R., Lindor, N.M., Blok, M.J., Moller, P., de la Hoya, M., Pal, T., Domchek, S., Nathanson, K., Van Asperen, C., Diez, O., Rheim, K., Stoppa-Lyonnet, D., Parsons, M., Goldgar, D.
Published in Annals of oncology

Impact of weight change and weight cycling on risk of different subtypes of endometrial cancer

by Nagle, C.M, Marquart, L, Bain, C.J, O’Brien, S, Lahmann, P.H, Quinn, M, Oehler, M.K, Obermair, A, Spurdle, A.B, Webb, P.M
Published in European journal of cancer (1990)

The association between diabetes, comorbidities, body mass index and all-cause and cause-specific mortality among women with endometrial cancer

by Nagle, C.M., Crosbie, E.J., Brand, A., Obermair, A., Oehler, M.K., Quinn, M., Leung, Y., Spurdle, A.B., Webb, P.M.
Published in Gynecologic oncology

Whole-genome sequencing reveals clinically relevant insights into the aetiology of familial breast cancers

by Nones, K., Johnson, J., Newell, F., Patch, A.M., Thorne, H., Kazakoff, S.H., de Luca, X.M., Parsons, M.T., Ferguson, K., Reid, L.E., McCart Reed, A.E., Srihari, S., Lakis, V., Davidson, A.L., Mukhopadhyay, P., Holmes, O., Xu, Q., Wood, S., Leonard, C., Beesley, J., Harris, J.M., Barnes, D., Degasperi, A., Ragan, M.A., Spurdle, A.B., Khanna, K.K., Lakhani, S.R., Pearson, J.V., Nik-Zainal, S., Chenevix-Trench, G., Waddell, N., Simpson, P.T.
Published in Annals of oncology

Use of aspirin, other nonsteroidal anti-inflammatory drugs and acetaminophen and risk of endometrial cancer: the Epidemiology of Endometrial Cancer Consortium

by Webb, P.M., Na, R., Weiderpass, E., Adami, H.O., Anderson, K.E., Bertrand, K.A., Botteri, E., Brasky, T.M., Brinton, L.A., Chen, C., Doherty, J.A., Lu, L., McCann, S.E., Moysich, K.B., Olson, S., Petruzella, S., Palmer, J.R., Prizment, A.E., Schairer, C., Setiawan, V.W., Spurdle, A.B., Trabert, B., Wentzensen, N., Wilkens, L., Yang, H.P., Yu, H., Risch, H.A., Jordan, S.J.
Published in Annals of oncology

Identification of a novel prostate cancer susceptibility variant in the KLK3 gene transcript

by Kote-Jarai, Z., Amin Al Olama, A., Leongamornlert, D., Tymrakiewicz, M., Saunders, E., Guy, M., Giles, G. G., Severi, G., Southey, M., Hopper, J. L., Sit, K. C., Harris, J. M., Batra, J., Spurdle, A. B., Clements, J. A., Hamdy, F., Neal, D., Donovan, J., Muir, K., Pharoah, P. D. P., Chanock, S. J., Brown, N., Benlloch, S., Castro, E., Mahmud, N., O’Brien, L., Hall, A., Sawyer, E., Wilkinson, R., Easton, D. F., Eeles, R. A.
Published in Human genetics

RAD51 135G→C Modifies Breast Cancer Risk among BRCA2 Mutation Carriers: Results from a Combined Analysis of 19 Studies

by Antoniou, Antonis C., Sinilnikova, Olga M., Simard, Jacques, Léoné, Mélanie, Dumont, Martine, Neuhausen, Susan L., Struewing, Jeffery P., Stoppa-Lyonnet, Dominique, Barjhoux, Laure, Hughes, David J., Coupier, Isabelle, Belotti, Muriel, Lasset, Christine, Bonadona, Valérie, Bignon, Yves-Jean, Rebbeck, Timothy R., Wagner, Theresa, Lynch, Henry T., Domchek, Susan M., Nathanson, Katherine L., Garber, Judy E., Weitzel, Jeffrey, Narod, Steven A., Tomlinson, Gail, Olopade, Olufunmilayo I., Godwin, Andrew, Isaacs, Claudine, Jakubowska, Anna, Lubinski, Jan, Gronwald, Jacek, Górski, Bohdan, Byrski, Tomasz, Huzarski, Tomasz, Peock, Susan, Cook, Margaret, Baynes, Caroline, Murray, Alexandra, Rogers, Mark, Daly, Peter A., Dorkins, Huw, Schmutzler, Rita K., Versmold, Beatrix, Engel, Christoph, Meindl, Alfons, Arnold, Norbert, Niederacher, Dieter, Deissler, Helmut, Spurdle, Amanda B., Chen, Xiaoqing, Waddell, Nicola, Cloonan, Nicole, Kirchhoff, Tomas, Offit, Kenneth, Friedman, Eitan, Kaufmann, Bella, Laitman, Yael, Galore, Gilli, Rennert, Gad, Lejbkowicz, Flavio, Raskin, Leon, Andrulis, Irene L., Ilyushik, Eduard, Ozcelik, Hilmi, Devilee, Peter, Vreeswijk, Maaike P.G., Greene, Mark H., Prindiville, Sheila A., Osorio, Ana, Benítez, Javier, Zikan, Michal, Szabo, Csilla I., Kilpivaara, Outi, Nevanlinna, Heli, Hamann, Ute, Durocher, Francine, Arason, Adalgeir, Couch, Fergus J., Easton, Douglas F., Chenevix-Trench, Georgia
Published in American journal of human genetics

53 Assessing interaction between established breast cancer genetic susceptibility loci and selected non-genetic risk factors using data from the Breast Cancer Association Consortiu...

by Milne, R.L, Gaudet, M.M, García-Closas, M, Pharoah, P.D.P, Couch, F.J, Fasching, P.A, Spurdle, A.B, Goode, E.L, Chang-Claude, J
Published in European journal of cancer supplements

Population-based estimates of breast cancer risks associated with ATM gene variants c.7271T>G and c.1066-6T>G (IVS10-6T>G) from the Breast Cancer Family Registry

by Bernstein, J.L., Teraoka, S., Southey, M.C., Jenkins, M.A., Andrulis, I.L., Knight, J.A., John, E.M., Lapinski, R., Wolitzer, A.L., Whittemore, A.S., West, D., Seminara, D., Olson, E.R., Spurdle, A.B., Chenevix-Trench, G., Giles, G.G., Hopper, J.L., Concannon, P.
Published in Human mutation

Common breast cancer predisposition alleles are associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers

by Sinilnikova, O.M, Antoniou, A.C, Spurdle, A.B, Healey, S, Schmutzler, R.K, Neuhausen, S.L, Couch, F.J, Stoppa-Lyonnet, D, Chenevix-Trench, G, Easton, D.F
Published in European journal of cancer supplements

Common Genetic Variation at BARD1 Is Not Associated with Breast Cancer Risk in BRCA1 or BRCA2 Mutation Carriers

by SPURDLE, Amanda B, MARQUART, Louise, GSCHWANTLER-KAULICH, Daphne, BLUM, Joanne L, TUNG, Nadine, WEITZEL, Jeff, LYNCH, Henry, GARBER, Judy, EASTON, Douglas F, PEOCK, Susan, COOK, Margaret, OLIVER, Clare T, MCGUFFOG, Lesley, FROST, Debra, CONROY, Don, GARETH EVANS, D, LALLOO, Fiona, EELES, Ros, IZATT, Louise, DAVIDSON, Rosemarie, CHU, Carol, ECCLES, Diana, SELKIRK, Christina G, HEALEY, Sue, DALY, Mary, ISAACS, Claudine, STOPPA-LYONNET, Dominique, SINILNIKOVA, Olga M, BUECHER, Bruno, BELOTTI, Muriel, MAZOYER, Sylvie, BARJHOUX, Laure, VERNY-PIERRE, Carole, LASSET, Christine, SINILNIKOVA, Olga, DREYFUS, Hélène, PUJOL, Pascal, COLLONGE-RAME, Marie-Agnès, ROOKUS, Matti A, VERHOEF, Senno, KRIEGE, Mieke, HOOGERBRUGGE, Nicoline, AUSEMS, Margreet G. E. M, VAN OS, Theo A, WIJNEN, Juul, FEI WAN, DEVILEE, Peter, MEIJERS-HEIJBOER, Hanne E. J, BLOK, Marinus J, HEIKKINEN, Tuomas, NEVANLINNA, Heli, JAKUBOWSKA, Anna, LUBINSKI, Jan, HUZARSKI, Tomasz, BYRSKI, Tomasz, DUROCHER, Francine, XIAOQING CHEN, BEESLEY, Jonathan, SINGER, Christian F, DRESSLER, Anne-Catharine
Published in Cancer epidemiology, biomarkers & prevention

The Y alu polymorphism in southern African populations and its relationship to other Y-specific polymorphisms

by SPURDLE, A. B, HAMMER, M. F, JENKINS, T
Published in American journal of human genetics

pDP1007, detects an X polymorphism with Hindlll in negroids at the ZFX locus

by Spurdle, A.B., Jenkins, T.
Published in Nucleic acids research

pDP1007, detects an X polymorphism with HindIII in negroids at the ZFX locus

by SPURDLE, A. B, JENKINS, T
Published in Nucleic acids research

New Taql allele detected by X-chromosome probe S21(DXS17)

by Stevens, G., Spurdle, A.B., Jenkins, Trefor
Published in Nucleic acids research

New TaqI allele detected by X-chromosome probe S21 (DXS17)

by STEVENS, G, SPURDLE, A. B, JENKINS, T
Published in Nucleic acids research