Evaluation of two population screening programmes for BRCA1/2 founder mutations in the Australian Jewish community: a protocol paper by Cousens, Nicole E, Tiller, Jane, Meiser, Bettina, Barlow-Stewart, Kristine, Rowley, Simone, Ko, Yi-An, Mahale, Sakshi, Campbell, Ian G, Kaur, Rajneesh, Bankier, Agnes, Burnett, Leslie, Jacobs, Chris, James, Paul A, Trainer, Alison, Neil, Suzanne, Delatycki, Martin B, Andrews, Lesley

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Tay Sachs disease in Australia: reduced disease incidence despite stable carrier frequency in Australian Jews by Lew, Raelia M, Proos, Anne L, Burnett, Leslie, Delatycki, Martin, Bankier, Agnes, Fietz, Michael J

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Population-based carrier screening for cystic fibrosis in Victoria: The first three years experience by MASSIE, John, PETROU, Vicki, FORBES, Robyn, CURNOW, Lisette, IOANNOU, Liane, DUSART, Desiree, BANKIER, Agnes, DELATYCKI, Martin

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Screening couples for cystic fibrosis carrier status: why are we waiting? by Massie, R John, Delatycki, Martin B, Bankier, Agnes

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Assessing associations between the AURKA-HMMR-TPX2-TUBG1 functional module and breast cancer risk in BRCA1/2 mutation carriers by Blanco, Ignacio, Kuchenbaecker, Karoline, Cuadras, Daniel, Wang, Xianshu, Barrowdale, Daniel, de Garibay, Gorka Ruiz, Librado, Pablo, Sánchez-Gracia, Alejandro, Rozas, Julio, Bonifaci, Núria, McGuffog, Lesley, Pankratz, Vernon S, Islam, Abul, Mateo, Francesca, Berenguer, Antoni, Petit, Anna, Català, Isabel, Brunet, Joan, Feliubadaló, Lidia, Tornero, Eva, Benítez, Javier, Osorio, Ana, Ramón y Cajal, Teresa, Nevanlinna, Heli, Aittomäki, Kristiina, Arun, Banu K, Toland, Amanda E, Karlan, Beth Y, Walsh, Christine, Lester, Jenny, Greene, Mark H, Mai, Phuong L, Nussbaum, Robert L, Andrulis, Irene L, Domchek, Susan M, Nathanson, Katherine L, Rebbeck, Timothy R, Barkardottir, Rosa B, Jakubowska, Anna, Lubinski, Jan, Durda, Katarzyna, Jaworska-Bieniek, Katarzyna, Claes, Kathleen, Van Maerken, Tom, Díez, Orland, Hansen, Thomas V, Jønson, Lars, Gerdes, Anne-Marie, Ejlertsen, Bent, de la Hoya, Miguel, Caldés, Trinidad, Dunning, Alison M, Oliver, Clare, Fineberg, Elena, Cook, Margaret, Peock, Susan, McCann, Emma, Murray, Alex, Jacobs, Chris, Pichert, Gabriella, Lalloo, Fiona, Chu, Carol, Dorkins, Huw, Paterson, Joan, Ong, Kai-Ren, Teixeira, Manuel R, Hogervorst, Frans B L, van der Hout, Annemarie H, Seynaeve, Caroline, van der Luijt, Rob B, Ligtenberg, Marjolijn J L, Devilee, Peter, Wijnen, Juul T, Rookus, Matti A, Meijers-Heijboer, Hanne E J, Blok, Marinus J, van den Ouweland, Ans M W, Aalfs, Cora M, Rodriguez, Gustavo C, Phillips, Kelly-Anne A, Piedmonte, Marion, Nerenstone, Stacy R, Bae-Jump, Victoria L, O'Malley, David M, Ratner, Elena S, Schmutzler, Rita K, Wappenschmidt, Barbara, Rhiem, Kerstin, Engel, Christoph, Meindl, Alfons, Ditsch, Nina, Arnold, Norbert, Plendl, Hansjoerg J, Niederacher, Dieter, Sutter, Christian, Wang-Gohrke, Shan, Steinemann, Doris, Preisler-Adams, Sabine, Kast, Karin, Varon-Mateeva, Raymonda

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MicroRNA related polymorphisms and breast cancer risk by Khan, Sofia, Greco, Dario, Michailidou, Kyriaki, Milne, Roger L, Muranen, Taru A, Heikkinen, Tuomas, Aaltonen, Kirsimari, Dennis, Joe, Bolla, Manjeet K, Liu, Jianjun, Hall, Per, Irwanto, Astrid, Humphreys, Keith, Li, Jingmei, Czene, Kamila, Chang-Claude, Jenny, Hein, Rebecca, Rudolph, Anja, Seibold, Petra, Flesch-Janys, Dieter, Fletcher, Olivia, Peto, Julian, dos Santos Silva, Isabel, Johnson, Nichola, Gibson, Lorna, Aitken, Zoe, Hopper, John L, Tsimiklis, Helen, Bui, Minh, Makalic, Enes, Schmidt, Daniel F, Southey, Melissa C, Apicella, Carmel, Stone, Jennifer, Waisfisz, Quinten, Meijers-Heijboer, Hanne, Adank, Muriel A, van der Luijt, Rob B, Meindl, Alfons, Schmutzler, Rita K, Müller-Myhsok, Bertram, Lichtner, Peter, Turnbull, Clare, Rahman, Nazneen, Chanock, Stephen J, Hunter, David J, Cox, Angela, Cross, Simon S, Reed, Malcolm W R, Schmidt, Marjanka K, Broeks, Annegien, Van't Veer, Laura J, Hogervorst, Frans B, Fasching, Peter A, Schrauder, Michael G, Ekici, Arif B, Beckmann, Matthias W, Bojesen, Stig E, Nordestgaard, Børge G, Nielsen, Sune F, Flyger, Henrik, Benitez, Javier, Zamora, Pilar M, Perez, Jose I A, Haiman, Christopher A, Henderson, Brian E, Schumacher, Fredrick, Le Marchand, Loic, Pharoah, Paul D P, Dunning, Alison M, Shah, Mitul, Luben, Robert, Brown, Judith, Couch, Fergus J, Wang, Xianshu, Vachon, Celine, Olson, Janet E, Lambrechts, Diether, Moisse, Matthieu, Paridaens, Robert, Christiaens, Marie-Rose, Guénel, Pascal, Truong, Thérèse, Laurent-Puig, Pierre, Mulot, Claire, Marme, Frederick, Burwinkel, Barbara, Schneeweiss, Andreas, Sohn, Christof, Sawyer, Elinor J, Tomlinson, Ian, Kerin, Michael J, Miller, Nicola, Andrulis, Irene L, Knight, Julia A, Tchatchou, Sandrine, Mulligan, Anna Marie, Dörk, Thilo, Bogdanova, Natalia V, Antonenkova, Natalia N

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Ashkenazi Jewish population screening for Tay-Sachs disease: The International and Australian experience by Lew, Raelia M, Burnett, Leslie, Proos, Anné L, Barlow-Stewart, Kristine, Delatycki, Martin B, Bankier, Agnes, Aizenberg, Harry, Field, Michael J, Berman, Yemima, Fleischer, Ronald, Fietz, Michael

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A shkenazi J ewish population screening for T ay– S achs disease: The International and A ustralian experience by Lew, Raelia M, Burnett, Leslie, Proos, Anné L, Barlow‐Stewart, Kristine, Delatycki, Martin B, Bankier, Agnes, Aizenberg, Harry, Field, Michael J, Berman, Yemima, Fleischer, Ronald, Fietz, Michael

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Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study by Johnson, Nichola, Dudbridge, Frank, Orr, Nick, Gibson, Lorna, Jones, Michael E, Schoemaker, Minouk J, Folkerd, Elizabeth J, Haynes, Ben P, Hopper, John L, Southey, Melissa C, Dite, Gillian S, Apicella, Carmel, Schmidt, Marjanka K, Broeks, Annegien, Van't Veer, Laura J, Atsma, Femke, Muir, Kenneth, Lophatananon, Artitaya, Fasching, Peter A, Beckmann, Matthias W, Ekici, Arif B, Renner, Stefan P, Sawyer, Elinor, Tomlinson, Ian, Kerin, Michael, Miller, Nicola, Burwinkel, Barbara, Marme, Frederik, Schneeweiss, Andreas, Sohn, Christof, Guénel, Pascal, Truong, Therese, Cordina, Emilie, Menegaux, Florence, Bojesen, Stig E, Nordestgaard, Børge G, Flyger, Henrik, Milne, Roger, Zamora, M Pilar, Arias Perez, Jose Ignacio, Benitez, Javier, Bernstein, Leslie, Anton-Culver, Hoda, Ziogas, Argyrios, Clarke Dur, Christina, Brenner, Hermann, Müller, Heiko, Arndt, Volker, Dieffenbach, Aida Karina, Meindl, Alfons, Heil, Joerg, Bartram, Claus R, Schmutzler, Rita K, Brauch, Hiltrud, Justenhoven, Christina, Ko, Yon-Dschun, Nevanlinna, Heli, Muranen, Taru A, Aittomäki, Kristiina, Blomqvist, Carl, Matsuo, Keitaro, Dörk, Thilo, Bogdanova, Natalia V, Antonenkova, Natalia N, Lindblom, Annika, Mannermaa, Arto, Kataja, Vesa, Kosma, Veli-Matti, Hartikainen, Jaana M, Chenevix-Trench, Georgia, Beesley, Jonathan, Wu, Anna H, Van den Berg, David, Tseng, Chiu-Chen, Lambrechts, Diether, Smeets, Dominiek, Neven, Patrick, Wildiers, Hans, Chang-Claude, Jenny, Rudolph, Anja, Nickels, Stefan, Flesch-Janys, Dieter, Radice, Paolo, Peterlongo, Paolo, Bonanni, Bernardo, Pensotti, Valeria, Couch, Fergus J, Olson, Janet E, Wang, Xianshu, Fredericksen, Zachary, Pankratz, Vernon S, Giles, Graham G, Severi, Gianluca, Baglietto, Laura, Haiman, Chris, Simard, Jacques, Goldberg, Mark S, Labrèche, France, Dumont, Martine, Soucy, Penny

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LETTER OF RESPONSE TO EDITORIAL BY R WILLIAMSON (SEPTEMBER 2003) by Bankier, Agnes

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High school Tay–Sachs disease carrier screening: 5 to 11-year follow-up by Curd, Helen, Lewis, Sharon, Macciocca, Ivan, Sahhar, Margaret, Petrou, Vicki, Bankier, Agnes, Lieberman, Sari, Levy-Lahad, Ephrat, Delatycki, Martin B.

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Two cases of trisomy 16 mosaicism ascertained postnatally by Rieubland, Claudine, Francis, David, Houben, Leonie, Corrie, Sylvea, Bankier, Agnes, White, Susan M.

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Community-wide screening for cystic fibrosis carriers could replace newborn screening for the diagnosis of cystic fibrosis by Massie, John, Forbes, Robin, DuSart, Desiree, Bankier, Agnes, Delatycki, Martin B

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A new disorder of hyaluronan metabolism associated generalized folding and thickening of the skin by Ramsden, C.Andrew, Bankier, Agnes, Brown, Tracey J, Cowen, Peter S.J, Frost, Gregory I, McCallum, Dugald D, Studdert, Virginia P, Fraser, J.Robert E

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Focal Segmental Glomerulosclerosis in Patients with Mandibuloacral Dysplasia Owing to ZMPSTE24 Deficiency by Agarwal, Anil K., Zhou, Xin J., Hall, Roger K., Nicholls, Kathy, Bankier, Agnes, Van Esch, Hilde, Fryns, Jean-Pierre, Garg, Abhimanyu

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Issues and concerns of couples presenting for preimplantation genetic diagnosis (PGD) by Katz, Mandy G., Fitzgerald, Lara, Bankier, Agnes, Savulescu, Julian, Cram, David S.

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Menkes disease by Bankier, A

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Consumer contribution to the delivery of genetic health services by Nisselle, Amy, Forbes, Robin, Bankier, Agnes, Hughes, Eilís, Aitken, MaryAnne

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Solitary median maxillary central incisor, short stature, choanal atresia/midnasal stenosis (SMMCI) syndrome by Hall, Roger K, Bankier, Agnes, Aldred, Michael J, Kan, Karen, Lucas, James O, Perks, A.Graeme B

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ANNOTATION: Community-wide screening for cystic fibrosis carriers could replace newborn screening for the diagnosis of cystic fibrosis by Massie, John, bes, Robin, duSart, Desiree, Bankier, Agnes, Delatycki, Martin B

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