Loss-of-function mutations in SMARCE1 cause an inherited disorder of multiple spinal meningiomas von Smith, Miriam J, O'Sullivan, James, Bhaskar, Sanjeev S, Hadfield, Kristen D, Poke, Gemma, Caird, John, Sharif, Saba, Eccles, Diana, Fitzpatrick, David, Rawluk, Daniel, du Plessis, Daniel, Newman, William G, Evans, D Gareth

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MiR-204 is responsible for inherited retinal dystrophy associated with ocular coloboma von Conte, Ivan, Kristen D. Hadfield, Sara Barbato, Sabrina Carrella, Mariateresa Pizzo, Rajeshwari S. Bhat, Annamaria Carissimo, Marianthi Karali, Louise F. Porter, Jill Urquhart, Sofie Hateley, James O’Sullivan, Forbes D. C. Manson, Stephan C. F. Neuhauss, Sandro Banfi, Graeme C. M. Black

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Impaired Tamoxifen Metabolism Reduces Survival in Familial Breast Cancer Patients von NEWMAN, William G, HADFIELD, Kristen D, LATIF, Ayshe, ROBERTS, Stephen A, SHENTON, Andrew, MCHAGUE, Christopher, LALLOO, Fiona, HOWELL, Sacha, EVANS, D. Gareth

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Polymorphisms of CYP19A1 and response to aromatase inhibitors in metastatic breast cancer patients von Ferraldeschi, Roberta, Arnedos, Monica, Hadfield, Kristen D., A’Hern, Roger, Drury, Suzie, Wardley, Andrew, Howell, Anthony, Evans, D. Gareth, Roberts, Stephen A., Smith, Ian, Newman, William G., Dowsett, Mitch

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EGFR and KRAS mutational analysis and their correlation to survival in pancreatic and periampullary cancer von Oliveira-Cunha, Melissa, Hadfield, Kristen D, Siriwardena, Ajith K, Newman, William

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Fundus Examination Pointing to the Diagnosis of Senior-Loken Syndrome von Sergouniotis, Panagiotis I, Hadfield, Kristen D, Black, Graeme C

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HtrA1 Inhibits Mineral Deposition by Osteoblasts: REQUIREMENT FOR THE PROTEASE AND PDZ DOMAINS von Hadfield, Kristen D, Rock, Claire Farrington, Inkson, Colette A, Dallas, Sarah L, Sudre, Laure, Wallis, Gillian A, Boot-Handford, Raymond P, Canfield, Ann E

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Breast cancer susceptibility variants alter risks in familial disease von Latif, Ayşe, Hadfield, Kristen D, Roberts, Stephen A, Shenton, Andrew, Lalloo, Fiona, Black, Graeme C M, Howell, Anthony, Evans, D Gareth, Newman, William G

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Involvement of SMARCB1 in Inherited Predisposition to Schwannoma, Meningioma and Rhabdoid Tumours von Smith, Miriam J, Hadfield, Kristen D, Newman, William G, Evans, D. Gareth

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Involvement of the SWI/SNF Complex in Familial Meningiomatosis von Smith, Miriam J, Sullivan, James O, Bhaskar, Sanjeev S, Hadfield, Kristen D, Poke, Gemma, Caird, John, Sharif, Saba, Eccles, Diana, Fitzpatrick, David, Rawluk, Daniel, du Plessis, Daniel, van Hoff, Jack, Newman, William G, Evans, D. Gareth

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Exacerbation of Hereditary Warfarin Resistance by Azathioprine von Pushpakom, Sudeep P., Gambhir, Nikki, Latif, Ayshe, Hadfield, Kristen D., Campbell, Simon, Newman, William G.

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Isolated unilateral vestibular schwannomas do not harbor HRAS mutations von Smith, Miriam J., Hadfield, Kristen D., Ramsden, Richard T., Rutherford, Scott A., King, Andrew T., Newman, William G., Evans, D. Gareth

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HtrA1 Inhibits Mineral Deposition by Osteoblasts von Hadfield, Kristen D., Rock, Claire Farrington, Inkson, Colette A., Dallas, Sarah L., Sudre, Laure, Wallis, Gillian A., Boot-Handford, Raymond P., Canfield, Ann E.

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SMARCB1 mutations are not a common cause of multiple meningiomas von Hadfield, K D, Smith, M J, Trump, D, Newman, W G, Evans, D G

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Urinary tract effects of HPSE2 mutations von Stuart, Helen M, Roberts, Neil A, Hilton, Emma N, McKenzie, Edward A, Daly, Sarah B, Hadfield, Kristen D, Rahal, Jeffery S, Gardiner, Natalie J, Tanley, Simon W, Lewis, Malcolm A, Sites, Emily, Angle, Brad, Alves, Cláudia, Lourenço, Teresa, Rodrigues, Márcia, Calado, Angelina, Amado, Marta, Guerreiro, Nancy, Serras, Inês, Beetz, Christian, Varga, Rita-Eva, Silay, Mesrur Selcuk, Darlow, John M, Dobson, Mark G, Barton, David E, Hunziker, Manuela, Puri, Prem, Feather, Sally A, Goodship, Judith A, Goodship, Timothy H J, Lambert, Heather J, Cordell, Heather J, Saggar, Anand, Kinali, Maria, Lorenz, Christian, Moeller, Kristina, Schaefer, Franz, Bayazit, Aysun K, Weber, Stefanie, Newman, William G, Woolf, Adrian S

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MiR-204 is responsible for inherited retinal dystrophy associated with ocular coloboma von Conte, Ivan, Hadfield, Kristen D, Barbato, Sara, Carrella, Sabrina, Pizzo, Mariateresa, Bhat, Rajeshwari S, Carissimo, Annamaria, Karali, Marianthi, Porter, Louise F, Urquhart, Jill, Hateley, Sofie, O'Sullivan, James, Manson, Forbes D C, Neuhauss, Stephan C F, Banfi, Sandro, Black, Graeme C M

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Abstract A35: SMARCE1 mutations cause inherited multiple spinal meningiomas von Smith, Miriam J., O'Sullivan, James, Bhaskar, Sanjeev S., Hadfield, Kristen D., Poke, Gemma, Caird, John, Sharif, Saba, Eccles, Diana, FitzPatrick, David, Rawluk, Daniel, Plessis, Daniel du, Newman, William G., Evans, D. Gareth

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HtrA1-a serine protease that regulates vascular calcification von Inkson, Colette A., Hadfield, Kristen D., Wilkinson, Fiona L., Wallis, Gillian A., Canfield, Ann E.

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Telomere-to-telomere assemblies of cattle and sheep Y-chromosomes uncover divergent structure and gene content von Olagunju, Temitayo A., Rosen, Benjamin D., Neibergs, Holly L., Becker, Gabrielle M., Davenport, Kimberly M., Elsik, Christine G., Hadfield, Tracy S., Koren, Sergey, Kuhn, Kristen L., Rhie, Arang, Shira, Katie A., Skibiel, Amy L., Stegemiller, Morgan R., Thorne, Jacob W., Villamediana, Patricia, Cockett, Noelle E., Murdoch, Brenda M., Smith, Timothy P. L.

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Polygalacturonase Gene Expression in Ripe Melon Fruit Supports a Role for Polygalacturonase in Ripening-Associated Pectin Disassembly von Kristen A. Hadfield, Jocelyn K. C. Rose, Yaver, Debbie S., Berka, Randy M., Bennett, Alan B.

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