Alpha-B Crystallin Gene ( CRYAB) Mutation Causes Dominant Congenital Posterior Polar Cataract in Humans von Berry, Vanita, Francis, Peter, Reddy, M. Ashwin, Collyer, Dean, Vithana, Eranga, MacKay, Ian, Dawson, Gary, Carey, Alisoun H., Moore, Anthony, Bhattacharya, Shomi S., Quinlan, Roy A.

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Inflammatory bowel disease is associated with a TNF polymorphism that affects an interaction between the OCT1 and NF-κB transcription factors von van Heel, David A., Udalova, Irina A., De Silva, Arjuna P., McGovern, Dermot P., Kinouchi, Yoshitaka, Hull, Jeremy, Lench, Nicholas J., Cardon, Lon R., Carey, Alisoun H., Jewell, Derek P., Kwiatkowski, Dominic

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Association of the TSHR gene with Graves' disease: the first disease specific locus von DECHAIRO, Bryan M, ZABANEH, Delilah, WIERSINGA, Wilmar M, HEGEDUS, Laszlo, BRIX, Thomas, ROBINSON, Bruce G, HUNT, Penny J, WEETMAN, Anthony P, CAREY, Alisoun H, GOUGH, Stephen C, COLLINS, Joanne, BRAND, Oliver, DAWSON, Gary J, GREEN, Angie P, MACKAY, Ian, FRANKLYN, Jayne A, CONNELL, John M, WASS, John A. H

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The IBD6 Crohn's disease locus demonstrates complex interactions with CARD15 and IBD5 disease-associated variants von van Heel, David A., Dechairo, Bryan M., Dawson, Gary, McGovern, Dermot P.B., Negoro, Kenichi, Carey, Alisoun H., Cardon, Lon R., Mackay, Ian, Jewell, Derek P., Lench, Nicholas J.

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Imprinting of a RING Zinc-Finger Encoding Gene in the Mouse Chromosome Region Homologous to the Prader-Willi Syndrome Genetic Region von Jong, Michelle T. C., Carey, Alisoun H., Caldwell, Kim A., Lau, Michel H., Handel, Mary Ann, Driscoll, Daniel J., Stewart, Colin L., Rinchik, Eugene M., Nicholls, Robert D.

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Differential Genetic Effects of ESR1 Gene Polymorphisms on Osteoporosis Outcomes von Ioannidis, John P. A, Ralston, Stuart H, Bennett, Simon T, Brandi, Maria Luisa, Grinberg, Daniel, Karassa, Fotini B, Langdahl, Bente, van Meurs, Joyce B. J, Mosekilde, Leif, Scollen, Serena, Albagha, Omar M. E, Bustamante, Mariona, Carey, Alisoun H, Dunning, Alison M, Enjuanes, Anna, van Leeuwen, Johannes P. T. M, Mavilia, Carmelo, Masi, Laura, McGuigan, Fiona E. A, Nogues, Xavier, Pols, Huibert A. P, Reid, David M, Schuit, Stephanie C. E, Sherlock, Rachael E, Uitterlinden, André G, GENOMOS Study, for the

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The Ancient Source of a Distinct Gene Family Encoding Proteins Featuring RING and C3H Zinc-Finger Motifs with Abundant Expression in Developing Brain and Nervous System von Gray, Todd A., Hernandez, Lidia, Carey, Alisoun H., Schaldach, Melanie A., Smithwick, Megan J., Rus, Kristina, Marshall Graves, Jennifer A., Stewart, Colin L., Nicholls, Robert D.

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Linkage disequilibrium mapping of the chromosome 12 ( IBD2) inflammatory bowel disease susceptibility locus in an enlarged cohort von Van Heel, David A., Lench, Nicholas, Cardon, Lon R., Carey, Alisoun H., Jewell, Derek P.

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Novel polymorphisms in the beta 7 integrin gene (ITGB7): Family based association studies in IBD von Van Heel, David A., Jewell, Derek P., Carey, Alisoun H.

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Correction: Large-Scale Evidence for the Effect of the COLIA1 Sp1 Polymorphism on Osteoporosis Outcomes: The GENOMOS Study von Ralston, Stuart H, Uitterlinden, André G, Luisa Brandi, Maria, Balcells, Susana, Langdahl, Bente L, Lips, Paul, Lorenc, Roman, Obermayer-Pietsch, Barbara, Scollen, Serena, Bustamante, Mariona, Bjerre Husted, Lise, Carey, Alisoun H, Diez-Perez, Adolfo, Dunning, Alison M, Falchetti, Alberto, Karczmarewicz, Elzbieta, Kruk, Marcin, van Leeuwen, Johannes P. T. M, van Meurs, Joyce B. J, Mangion, Jon, McGuigan, Fiona E. A, Mellibovsky, Leonardo, del Monte, Francesca, Pols, Huibert A. P, Reeve, Jonathan, Reid, David M, Renner, Wilfried, Rivadeneira, Fernando, van Schoor, Natasja M, Sherlock, Rachael E, Ioannidis, John P. A

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Microdeletions within 22q11 associated with sporadic and familial DiGeorge syndrome von Scambler, Peter J., Carey, Alisoun H., Wyse, Richard K.H., Roach, Sherry, Dumanski, Jan P., Nordenskjold, Magnus, Williamson, Robert

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Large-scale evidence for the effect of the COL1A1 Sp1 polymorphism on osteoporosis outcomes: the GENOMOS study von Ralston, Stuart H, Uitterlinden, André G, Brandi, Maria Luisa, Balcells Comas, Susana, Langdahl, Bente L, Lips, Paul, Lorenc, Roman, Obermayer-Pietsch, Barbara, Scollen, Serena, Bustamante Pineda, Mariona, Bjerre Husted, Lise, Carey, Alisoun H, Diez Pérez, Adolfo, Dunning, Alison M, Falchetti, Alberto, Karczmarewicz, Elzbieta, Kruk, Marcin

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Large-scale evidence for the effect of the COL1A1 Sp1 polymorphism on osteoporosis outcomes: the GENOMOS study von Ralston, Stuart H, Uitterlinden, André G, Brandi, Maria Luisa, Balcells Comas, Susana, Langdahl, Bente L, Lips, Paul, Lorenc, Roman, Obermayer-Pietsch, Barbara, Scollen, Serena, Bustamante Pineda, Mariona, Bjerre Husted, Lise, Carey, Alisoun H, Díez Pérez, Adolfo, Dunning, Alison M, Falchetti, Alberto, Karczmarewicz, Elzbieta, Kruk, Marcin

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Correction: large-scale evidence for the effect of the COLIA1 Sp1 polymorphism on osteoporosis outcomes: the GENOMOS study von Ralston, Stuart H, Uitterlinden, Andre G, Brandi, Maria Luisa, Balcells, Susana, Langdahl, Bente L, Lips, Paul, Lorenc, Roman, Obermayer-Pietsch, Barbara, Scollen, Serena, Bustamante, Mariona, Husted, Lise Bjerre, Carey, Alisoun H, Diez-Perez, Adolfo, Dunning, Alison M, Falchetti, Alberto, Karczmarewicz, Elzbieta, Kruk, Marcin, van Leeuwen, Johannes P.T.M, van Meurs, Joyce B.J, Mangion, Jon, McGuigan, Fiona E.A, Mellibovsky, Leonardo, del Monte, Francesca, Pols, Huibert A.P, Reeve, Jonathan, Reid, David M, Renner, Wilfried, Rivadeneira, Fernando, van Schoor, Natasja M, Sherlock, Rachael E, Ioannidis, John P.A

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Inflammatory bowel disease: progress toward a gene von van Heel, D A, Satsangi, J, Carey, A H, Jewell, D P

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Correction: Large-Scale Evidence for the Effect of the Sp1 Polymorphism on Osteoporosis Outcomes: The GENOMOS Study von Stuart H Ralston, André G Uitterlinden, Maria Luisa Brandi, Susana Balcells, Bente L Langdahl, Paul Lips, Roman Lorenc, Barbara Obermayer-Pietsch, Serena Scollen, Mariona Bustamante, Lise Bjerre Husted, Alisoun H Carey, Adolfo Diez-Perez, Alison M Dunning, Alberto Falchetti, Elzbieta Karczmarewicz, Marcin Kruk, Johannes P. T. M van Leeuwen, Joyce B. J van Meurs, Jon Mangion, Fiona E. A McGuigan, Leonardo Mellibovsky, Francesca del Monte, Huibert A. P Pols, Jonathan Reeve, David M Reid, Wilfried Renner, Fernando Rivadeneira, Natasja M van Schoor, Rachael E Sherlock, John P. A Ioannidis

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Fine mapping of the IBD1 locus did not identify Crohn disease-associated NOD2 variants: Implications for complex disease genetics von van Heel, David A., McGovern, Dermot P.B., Cardon, Lon R., Dechairo, Bryan M., Lench, Nicholas J., Carey, Alisoun H., Jewell, Derek P.

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Reply to Veromann von Berry, Vanita, Francis, Peter, Reddy, M. Ashwin, Collyer, Dean, Vithana, Eranga, MacKay, Ian, Dawson, Gary, Carey, Alisoun H., Moore, Anthony, Bhattacharya, Shomi S., Quinlan, Roy A.

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Target identification and validation through genetics von Allen, Maxine J., Carey, Alisoun H.

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Family based association studies of STAT6, a positional candidate gene for IBD von Dimon, Claire, Allen, Maxine, Van Heel, David A., Mackay, Ian, Lench, Nicholas J., Jewell, Derek P., Carey, Alisoun H.

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