Inhibition of electron-transfer reactions at the mercury/acetonitrile interface by adsorbed lithium ions by COMPTON, R. G, NORTHING, R. J, QUARRELL, R. E. L

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Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study by Lord, Jenny, McMullan, Dominic J, Eberhardt, Ruth Y, Rinck, Gabriele, Hamilton, Susan J, Quinlan-Jones, Elizabeth, Prigmore, Elena, Carey, Georgina K, Mellis, Rhiannon, Robart, Sarah, Berry, Ian R, Chandler, Kate E, Cilliers, Deirdre, Cresswell, Lara, Edwards, Sandra L, Gardiner, Carol, Henderson, Alex, Holden, Simon T, Homfray, Tessa, Lester, Tracy, Newbury-Ecob, Ruth, Prescott, Katrina, Quarrell, Oliver W, Ramsden, Simon C, Roberts, Eileen, Tapon, Dagmar, Tooley, Madeleine J, Vasudevan, Pradeep C, Weber, Astrid P, Wellesley, Diana G, Westwood, Paul, White, Helen, Parker, Michael, Williams, Denise, Jenkins, Lucy, Scott, Richard H, Kilby, Mark D, Chitty, Lyn S, Hurles, Matthew E, Maher, Eamonn R, Bateman, Mark, Best, Sunayna K, Campbell, Carolyn, Carey, Georgina, Chitty, Lyn S, Cilliers, Deirdre, Cohen, Kelly, Collingwood, Emma, Constantinou, Panayiotis, Cresswell, Lara, Delmege, Catherine, Edwards, Sandra L, Ellis, Richard, Evans, Jerry, Everett, Thomas, Pinto, Clare F, Forrester, Natalie, Fowler, Emma, Gardiner, Carol, Hamilton, Susan, Healey, Karen, Henderson, Alex, Holden, Simon T, Homfray, Tessa, Hudson, Rebecca, Hurles, Matthew E, Jenkins, Lucy, Keelagher, Rebecca, Kilby, Mark D, Lester, Tracey, Lewis, Rebecca, Lord, Jenny, Maher, Eamonn R, Marton, Tamas, McMullan, Dominic J, Mehta, Sarju, Mellis, Rhiannon, Newbury-Ecob, Ruth, Park, Soo-Mi, Parker, Michael, Prescott, Katrina, Prigmore, Elena, Quarrell, Oliver W, Quinlan-Jones, Elizabeth, Ramsden, Simon C, Rinck, Gabriele, Robart, Sarah, Roberts, Eileen, Rowland, Jayne, Steer, James, Tapon, Dagmar, Taylor, Emma J, Tooley, Madeleine J, Vasudevan, Pradeep C, Weber, Astrid P, Wellesley, Diana G, Westwood, Paul, White, Helen, Williams, Denise, Wilson, Elizabeth

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A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants by Chawner, Samuel J.R.A, Doherty, Joanne L, Anney, Richard J. L, Antshel, Kevin M, Bearden, Carrie E, Bernier, Raphael, Chung, Wendy K, Clements, Caitlin C, Curran, Sarah R, Cuturilo, Goran, Fiksinski, Ania M, Gallagher, Louise, Goin-Kochel, Robin P, Gur, Raquel E, Hanson, Ellen, Jacquemont, Sebastien, Kates, Wendy R, Kushan, Leila, Maillard, Anne M, McDonald-McGinn, Donna M, Mihaljevic, Marina, Miller, Judith S, Moss, Hayley, Pejovic-Milovancevic, Milica, Schultz, Robert T, Green-Snyder, LeeAnne, Vorstman, Jacob A, Wenger, Tara L, Hall, Jeremy, Owen, Michael J, van den Bree, Marianne B.M

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Clinical studies on submicroscopic subtelomeric rearrangements: a checklist by de Vries, B B A, White, S M, Knight, S J L, Regan, R, Homfray, T, Young, I D, Super, M, McKeown, C, Splitt, M, Quarrell, O W J, Trainer, A H, Niermeijer, M F, Malcolm, S, Flint, J, Hurst, J A, Winter, R M

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MRI breast screening in high-risk women: cancer detection and survival analysis by Gareth, Evans D., Nisha, Kesavan, Yit, Lim, Soujanye, Gadde, Emma, Hurley, Massat, Nathalie J., Maxwell, Anthony J., Sarah, Ingham, Rosalind, Eeles, Leach, Martin O., Anthony, Howell, Stephen, Duffy

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Common Breast Cancer Susceptibility Alleles and the Risk of Breast Cancer for BRCA1 and BRCA2 Mutation Carriers: Implications for Risk Prediction by ANTONIOU, Antonis C, BEESLEY, Jonathan, ISAACS, Claudine, GANZ, Patricia A, TOMLINSON, Gail, OLOPADE, Olufunmilayo I, COUCH, Fergus J, XIANSHU WANG, LINDOR, Noralane M, PANKRATZ, Vernon S, RADICE, Paolo, MANOUKIAN, Siranoush, MCGUFFOG, Lesley, PEISSEL, Bernard, ZAFFARONI, Daniela, BARILE, Monica, VIEL, Alessandra, ALLAVENA, Anna, DALL' OLIO, Valentina, PETERLONGO, Paolo, SZABO, Csilla I, ZIKAN, Michal, CLAES, Kathleen, SINILNIKOVA, Olga M, POPPE, Bruce, FORETOVA, Lenka, MAI, Phuong L, GREENE, Mark H, RENNERT, Gad, LEJBKOWICZ, Flavio, GLENDON, Gord, OZCELIK, Hilmi, ANDRULIS, Irene L, THOMASSEN, Mads, HEALEY, Sue, GERDES, Anne-Marie, SUNDE, Lone, CRUGER, Dorthe, JENSEN, Uffe Birk, CALIGO, Maria, FRIEDMAN, Eitan, KAUFMAN, Bella, LAITMAN, Yael, MILGROM, Roni, DUBROVSKY, Maya, NEUHAUSEN, Susan L, COHEN, Shimrit, BORG, Ake, JERNSTRÖM, Helena, LINDBLOM, Annika, RANTALA, Johanna, STENMARK-ASKMALM, Marie, MELIN, Beatrice, NATHANSON, Kate, DOMCHEK, Susan, JAKUBOWSKA, Ania, YUAN CHUN DING, REBBECK, Timothy R, WEITZEL, Jeffrey N, LYNCH, Henry T

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Subtelomeric deletions of chromosome 9q: A novel microdeletion syndrome by Stewart, Douglas R., Huang, Alina, Faravelli, Francesca, Anderlid, Britt-Marie, Medne, Livija, Ciprero, Karen, Kaur, Maninder, Rossi, Elena, Tenconi, Romano, Nordenskjöld, Magnus, Gripp, Karen W., Nicholson, Linda, Meschino, Wendy S., Capua, Esther, Quarrell, Oliver W.J., Flint, Jonathon, Irons, Mira, Giampietro, Philip F., Schowalter, David B., Zaleski, Christina A., Malacarne, Michela, Zackai, Elaine H., Spinner, Nancy B., Krantz, Ian D.

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Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers by Antoniou, Antonis C., Sinilnikova, Olga M., McGuffog, Lesley, Healey, Sue, Nevanlinna, Heli, Chen, Xiaoqing, Neuhausen, Susan L., Ding, Yuan C., Couch, Fergus J., Wang, Xianshu, Fredericksen, Zachary, Peterlongo, Paolo, Peissel, Bernard, Viel, Alessandra, Radice, Paolo, Szabo, Csilla I., Foretova, Lenka, Zikan, Michal, Claes, Kathleen, Greene, Mark H., Mai, Phuong L., Ozcelik, Hilmi, Thomassen, Mads, Sunde, Lone, Caligo, Maria A., Laitman, Yael, Kontorovich, Tair, Kaufman, Bella, Dagan, Efrat, Baruch, Ruth Gershoni, Harbst, Katja, Barbany-Bustinza, Gisela, Rantala, Johanna, Domchek, Susan M., Nathanson, Katherine L., Osorio, Ana, Blanco, Ignacio, Lasa, Adriana, Hamann, Ute, Rookus, Matti A., Collee, J. Margriet, Devilee, Peter, van der Luijt, Rob B., Waisfisz, Quinten, Wijnen, Juul, van Roozendaal, Cornelis E.P., Peock, Susan, Cook, Margaret, Frost, Debra, Oliver, Clare, Platte, Radka, Evans, D. Gareth, Eeles, Rosalind, Izatt, Louise, Eccles, Diana, Cole, Trevor, Hodgson, Shirley, Buecher, Bruno, Léoné, Mélanie, Remenieras, Audrey, Caron, Olivier, Lenoir, Gilbert M., Sevenet, Nicolas, Longy, Michel, Ferrer, Sandra Fert, Prieur, Fabienne, Goldgar, David, Miron, Alexander, John, Esther M., Daly, Mary B., Hopper, John L., Gschwantler-Kaulich, Daphne, Staudigl, Christine, Hansen, Thomas v. O., Barkardottir, Rosa Bjork, Kirchhoff, Tomas, Pal, Prodipto, Kosarin, Kristi, Offit, Kenneth, Piedmonte, Marion, Rodriguez, Gustavo C., Wakeley, Katie, Boggess, John F., Schwartz, Peter E., Montagna, Marco, Imyanitov, Evgeny N., Allavena, Anna, Schmutzler, Rita K., Versmold, Beatrix, Engel, Christoph, Ditsch, Nina, Niederacher, Dieter, Deißler, Helmut, Fiebig, Britta, Suttner, Christian, Schönbuchner, Ines, Gadzicki, Dorothea, Caldes, Trinidad, Pooley, Karen A., Chenevix-Trench, Georgia

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Mutations in ZDHHC9, Which Encodes a Palmitoyltransferase of NRAS and HRAS, Cause X-Linked Mental Retardation Associated with a Marfanoid Habitus by Raymond, F. Lucy, Tarpey, Patrick S., Edkins, Sarah, Tofts, Calli, O’Meara, Sarah, Teague, Jon, Butler, Adam, Stevens, Claire, Barthorpe, Syd, Buck, Gemma, Cole, Jennifer, Dicks, Ed, Gray, Kristian, Halliday, Kelly, Hills, Katy, Hinton, Jonathon, Jones, David, Menzies, Andrew, Perry, Janet, Raine, Keiran, Shepherd, Rebecca, Small, Alexandra, Varian, Jennifer, Widaa, Sara, Mallya, Uma, Moon, Jenny, Luo, Ying, Shaw, Marie, Boyle, Jackie, Kerr, Bronwyn, Turner, Gillian, Quarrell, Oliver, Cole, Trevor, Easton, Douglas F., Wooster, Richard, Bobrow, Martin, Schwartz, Charles E., Gecz, Jozef, Stratton, Michael R., Futreal, P. Andrew

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Association of PHB 1630 C>T and MTHFR 677 C>T polymorphisms with breast and ovarian cancer risk in BRCA1/2 mutation carriers: results from a multicenter study by Jakubowska, A, Rozkrut, D, Hamann, U, Scott, R J, McGuffog, L, Healy, S, Sinilnikova, O M, Rennert, G, Lejbkowicz, F, Flugelman, A, Andrulis, I L, Glendon, G, Ozcelik, H, Thomassen, M, Paligo, M, Kantala, J, Aroer, B, von Wachenfeldt, A, Loman, N, Herbst, K, Kristoffersson, U, Rosenquist, R, Karlsson, P, Stenmark-Askmalm, M, Melin, B, Nathanson, K L, Domchek, S M, Byrski, T, Huzarski, T, Gronwald, J, Menkiszak, J, Cybulski, C, Serrano, P, Cajal, T R, Tsitlaidou, M, Benítez, J, Rookus, M, Kluijt, I, Boessenkool-Pape, J L, Meijers-Heijboer, H E J, Oosterwijk, J C, van Asperen, C J, Nelen, M R, van den Ouweland, A M W, Seynaeve, C, Easton, D F, Frost, D, Platte, R, Ellis, S D, Fineberg, E, Evans, D G, Lalloo, F, Eeles, R, Jacobs, C, Adlard, J, Davidson, R, Eccles, D, Cole, T, Cook, J, Godwin, A, Bove, B, Stoppa-Lyonnet, D, Caux-Moncoutier, V, Belotti, M, Tirapo, C, Barjhoux, L, Pujol, P, Coupier, I, Peyrat, J-P, Vennin, P, Fricker, J-P, Venat-Bouvet, L, Johannsson, O Th, Isaacs, C, Schmutzler, R, Wappenschmidt, B, Meindl, A, Arnold, N, Varon-Mateeva, R, Niederacher, D, Sutter, C, Deissler, H, Preisler-Adams, S, Simard, J, Durocher, F, Beesley, J, Chen, X, Rebbeck, T, Couch, F, Wang, X, Lindor, N, Fredericksen, Z, Pankratz, V S, Peterlongo, P, Bonanni, B, Fortuzzi, S, Peissel, B, Szabo, C, Mai, P L, Loud, J T

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Familial visceral neuropathy: A defined entity? by Roper, E.C., Gibson, A., McAlindon, M.E., Williams, L.H.P., Cook, J.A., Kandler, R.H., Quarrell, O.W.J.

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Association of the Variants CASP8 D302H and CASP10 V410I with Breast and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers by ENGEL, Christoph, VERSMOLD, Beatrix, GARETH EVANS, D, EELES, Rosalind, PATERSON, Joan, BREWER, Carole, MCGUFFOG, Lesley, ANTONIOU, Antonis C, STOPPA-LYONNET, Dominique, SINILNIKOVA, Olga M, BARJHOUX, Laure, FRENAY, Marc, WAPPENSCHMIDT, Barbara, MICHEL, Cécile, LEROUX, Dominique, DREYFUS, Helene, TOULAS, Christine, GLADIEFF, Laurence, UHRHAMMER, Nancy, BIGNON, Yves-Jean, MEINDL, Alfons, ARNOLD, Norbert, VARON-MATEEVA, Raymonda, SIMARD, Jacques, NIEDERACHER, Dieter, PREISLER-ADAMS, Sabine, KAST, Karin, DEISSLER, Helmut, SUTTER, Christian, GADZICKI, Dorothea, CHENEVIX-TRENCH, Georgia, SPURDLE, Amanda B, XIAOQING CHEN, BEESLEY, Jonathan, EASTON, Douglas F, OLSSON, Håkan, KRISTOFFERSSON, Ulf, EHRENCRONA, Hans, LILJEGREN, Annelie, VAN DER LUIJT, Rob B, VAN OS, Theo A, VAN LEEUWEN, Flora E, DOMCHEK, Susan M, REBBECK, Timothy R, NATHANSON, Katherine L, PEOCK, Susan, OSORIO, Ana, RAMON Y CAJAL, Teresa, KONSTANTOPOULOU, Irene, BENITEZ, Javier, FRIEDMAN, Eitan, KAUFMAN, Bella, LAITMAN, Yael, MAI, Phuong L, GREENE, Mark H, NEVANLINNA, Heli, COOK, Margaret, OLIVER, Clare, FROST, Debra, MAYES, Rebecca

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No association of TGFB1 L10P genotypes and breast cancer risk in BRCA1 and BRCA2 mutation carriers: a multi-center cohort study by Rebbeck, Timothy R., Antoniou, Antonis C., Llopis, Trinidad Caldes, Nevanlinna, Heli, Aittomäki, Kristiina, Simard, Jacques, Spurdle, Amanda B., Couch, Fergus J., Pereira, Lutecia H. Mateus, Greene, Mark H., Andrulis, Irene L., Pasche, Boris, Kaklamani, Virginia, Hamann, Ute, Szabo, Csilla, Peock, Susan, Cook, Margaret, Harrington, Patricia A., Donaldson, Alan, Male, Allison M., Gardiner, Carol Anne, Gregory, Helen, Side, Lucy E., Robinson, Anne C., Emmerson, Louise, Ellis, Ian, Peyrat, Jean-Philippe, Fournier, Joëlle, Vennin, Philippe, Adenis, Claude, Muller, Danièle, Fricker, Jean-Pierre, Longy, Michel, Sinilnikova, Olga M., Stoppa-Lyonnet, Dominique, Schmutzler, Rita K., Versmold, Beatrix, Engel, Christoph, Meindl, Alfons, Kast, Karin, Schaefer, Dieter, Froster, Ursula G., Chenevix-Trench, Georgia, Easton, Douglas F.

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Comparison between radiological and artificial neural network diagnosis in clinical screening by Degenhard, A, Tanner, C, Hayes, C, Hawkes, D J, Leach, M O, Study, the UK MRI Breast Screening

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General discussion by Thomson, G. P., Ornstein, L. S., Finch, G. I., Quarrell, A. G., Tronstad, L., Kohlschütter, V., Darbyshire, J. A., Cooper, E. R., Andrade, E. N. da C.

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General discussion by Thomson, G. P., Ornstein, L. S., Finch, G. I., Rideal, E. K., Tillman, J. R., Tronstad, L., Cosslett, V. E., Beeching, R., Kirchner, F., Vernon, W. H. J., Thomson, Laschkarew, W. E., Ditchburn, R. W., Quarrell, A. G., Adam, N. K., Lees, C. S., Darbyshire, J. A., Hopkins

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