Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility von Landi, Maria Teresa, MacGregor, Stuart, Machiela, Mitchell J., Stratigos, Alexander J., Ghiorzo, Paola, Brossard, Myriam, Calista, Donato, Zhang, Tongwu, Rodolfo, Monica, Trower, Adam J., Martinez, Jacobo, Hadjisavvas, Andreas, Stefanaki, Irene, Scolyer, Richard, Yang, Rose, Pastorino, Lorenza, Cattaneo, Laura, Zawistowski, Matthew, Gimenez-Xavier, Pol, Rodriguez, Arantxa, Elefanti, Lisa, Rivoltini, Licia, Del Regno, Laura, Massi, Daniela, Mandala, Mario, Amos, Christopher I., Andresen, Per A., Avril, Marie-Françoise, Azizi, Esther, Soyer, H. Peter, Bataille, Veronique, Bowdler, Lisa M., Burdon, Kathryn P., Chen, Wei V., Craig, Jamie E., Fang, Shenying, Friedman, Eitan, Simi, Sarah, Galan, Pilar, Gillanders, Elizabeth M., Gordon, Scott, Green, Adele, Hansson, Johan, Harland, Mark, Helsing, Per, Henders, Anjali, Hočevar, Marko, Hunter, David, Ingvar, Christian, Lang, Julie, Lathrop, G. Mark, Li, Xin, Lubiński, Jan, Malvehy, Josep, Molven, Anders, Moses, Eric K., Nyholt, Dale R., Olsson, Håkan, Orr, Nicholas, Radford-Smith, Graham L., Randerson-Moor, Juliette, Rowe, Casey, Schadendorf, Dirk, Simms, Lisa A., Smithers, Mark, Song, Fengju, Visconti, Alessia, Wallace, Leanne, Wheeler, Lawrie, Sturm, Richard A., Hutchinson, Amy, Jones, Kristine, Malasky, Michael, Vogt, Aurelie, Zhou, Weiyin, Elder, David E., Han, Jiali, Hicks, Belynda, Hayward, Nicholas K., Brummett, Chad, Montgomery, Grant W., Olsen, Catherine M., Hayward, Caroline, Dunning, Alison M., Martin, Nicholas G., Mann, Graham J., Long, Georgina, Pharoah, Paul D. P., Barrett, Jennifer H., Abecasis, Goncalo, Whiteman, David C., Gogas, Helen, Tucker, Margaret A., Newton-Bishop, Julia A., Peris, Ketty, Chanock, Stephen J., Nagore, Eduardo, Shi, Jianxin, Iles, Mark M., Law, Matthew H.

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Multiple rare variants in high-risk pancreatic cancer-related genes may increase risk for pancreatic cancer in a subset of patients with and without germline CDKN2A mutations von Yang, Xiaohong R., Rotunno, Melissa, Xiao, Yanzi, Ingvar, Christian, Helgadottir, Hildur, Pastorino, Lorenza, van Doorn, Remco, Bennett, Hunter, Graham, Cole, Sampson, Joshua N., Malasky, Michael, Vogt, Aurelie, Zhu, Bin, Bianchi-Scarra, Giovanna, Bruno, William, Queirolo, Paola, Fornarini, Giuseppe, Hansson, Johan, Tuominen, Rainer, Burdett, Laurie, Hicks, Belynda, Hutchinson, Amy, Jones, Kristine, Yeager, Meredith, Chanock, Stephen J., Landi, Maria Teresa, Höiom, Veronica, Olsson, Håkan, Gruis, Nelleke, Ghiorzo, Paola, Tucker, Margaret A., Goldstein, Alisa M.

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Genome-Wide Association Study Implicates PARD3B-Based AIDS Restriction von Troyer, Jennifer L., Nelson, George W., Lautenberger, James A., Chinn, Leslie, McIntosh, Carl, Johnson, Randall C., Sezgin, Efe, Kessing, Bailey, Malasky, Michael, Hendrickson, Sher L., Li, Guan, Pontius, Joan, Tang, Minzhong, An, Ping, Winkler, Cheryl A., Limou, Sophie, Le Clerc, Sigrid, Delaneau, Olivier, Zagury, Jean-François, Schuitemaker, Hanneke, van Manen, Daniëlle, Bream, Jay H., Gomperts, Edward D., Buchbinder, Susan, Goedert, James J., Kirk, Gregory D., O'Brien, Stephen J.

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Dating the Origin of the CCR5-Δ 32 AIDS-Resistance Allele by the Coalescence of Haplotypes von Stephens, J. Claiborne, Reich, David E., Goldstein, David B., Shin, Hyoung Doo, Smith, Michael W., Carrington, Mary, Winkler, Cheryl, Huttley, Gavin A., Allikmets, Rando, Schriml, Lynn, Gerrard, Bernard, Malasky, Michael, Ramos, Maria D., Morlot, Susanne, Tzetis, Maria, Oddoux, Carole, di Giovine, Francesco S., Nasioulas, Georgios, Chandler, David, Aseev, Michael, Hanson, Matthew, Kalaydjieva, Luba, Glavac, Damjan, Gasparini, Paolo, Kanavakis, E., Claustres, Mireille, Kambouris, Marios, Ostrer, Harry, Duff, Gordon, Baranov, Vladislav, Sibul, Hiljar, Metspalu, Andres, Goldman, David, Martin, Nick, Duffy, David, Schmidtke, Jorg, Estivill, Xavier, O'Brien, Stephen J., Dean, Michael

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High-density map of short tandem repeats across the human major histocompatibility complex von Cullen, Michael, Malasky, Michael, Harding, Anita, Carrington, Mary

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Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility von Landi, MT, MacGregor, S, Machiela, MJ, Stratigos, AJ, Ghiorzo, P, Calista, D, Fargnoli, MC, Rodolfo, M, Trower, AJ, Martinez, J, Hadjisavvas, A, Song, L, Scolyer, R, Yang, R, Goldstein, AM, Pastorino, L, Queirolo, P, Pellegrini, C, Zawistowski, M, Gimenez-Xavier, P, Manoukian, S, Rivoltini, L, Smith, BH, Mandala, M, Amos, CI, Azizi, E, Soyer, HP, Bataille, V, Chen, WV, Codd, V, Craig, JE, Friedman, E, Simi, S, Galan, P, Garcia-Casado, Z, Gillanders, EM, Green, A, Gruis, NA, Hansson, J, Harland, M, Harris, J, Helsing, P, Hunter, D, Ingvar, C, Lee, JE, Mackie, RM, Malvehy, J, McAloney, K, Mohamdi, H, Molven, A, Moses, EK, Neale, RE, Nyholt, DR, Orr, N, Radford-Smith, GL, Randerson-Moor, J, Samani, NJ, Sanna, M, Schulze, H-J, Swerdlow, AJ, van der Stoep, N, Kukutsch, NA, Visconti, A, Ward, SV, Wheeler, L, Hutchinson, A, Vogt, A, Zhou, W, Pooley, KA, Elder, DE, Han, J, Hayward, NK, Kanetsky, PA, Brummett, C, Montgomery, GW, Olsen, CM, Hayward, C, Martin, NG, Evangelou, E, Mann, GJ, Pharoah, PDP, Easton, DF, Barrett, JH, Cust, AE, Abecasis, G, Duffy, DL, Whiteman, DC, Gogas, H, De Nicolo, A, Tucker, MA, Newton-Bishop, JA, ATHENS Melanoma Study Group, 23andMe, The SDH Study Group, IBD Investigators, Essen-Heidelberg Investigators, AMFS Investigators, Demenais, F, Puig, S, Shi, J

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Stratified testing for HLA matching: Selection of identical sib pairs using microsatellite loci across HLA von Wade, JA, Ng, CM, Harding, A, Malasky, M, Carrington, M

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Dating the origin of the CCR5-Delta32 AIDS-resistance allele by the coalescence of haplotypes von Stephens, J C, Reich, D E, Goldstein, D B, Shin, H D, Smith, M W, Carrington, M, Winkler, C, Huttley, G A, Allikmets, R, Schriml, L, Gerrard, B, Malasky, M, Ramos, M D, Morlot, S, Tzetis, M, Oddoux, C, di Giovine, F S, Nasioulas, G, Chandler, D, Aseev, M, Hanson, M, Kalaydjieva, L, Glavac, D, Gasparini, P, Kanavakis, E, Claustres, M, Kambouris, M, Ostrer, H, Duff, G, Baranov, V, Sibul, H, Metspalu, A, Goldman, D, Martin, N, Duffy, D, Schmidtke, J, Estivill, X, O'Brien, S J, Dean, M

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Dating the origin of the CCR5-Δ32 AIDS-resistance allele by the coalescence of haplotypes von STEPHENS, J. C, REICH, D. E, GERRARD, B, MALASKY, M, RAMOS, M. D, MORLOT, S, TZETIS, M, ODDOUX, C, DI GIOVINE, F. S, NASIOULAS, G, CHANDLER, D, ASEEV, M, GOLDSTEIN, D. B, HANSON, M, KALAYDJIEVA, L, GLAVAC, D, GASPARINI, P, KANAVAKIS, E, CLAUSTRES, M, KAMBOURIS, M, OSTRER, H, DUFF, G, BARANOV, V, HYOUNG DOO SHIN, SIBUL, H, METSPALU, A, GOLDMAN, D, MARTIN, N, DUFFY, D, SCHMIDTKE, J, ESTIVILL, X, O'BRIEN, S. J, DEAN, M, SMITH, M. W, CARRINGTON, M, WINKLER, C, HUTTLEY, G. A, ALLIKMETS, R, SCHRIML, L

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Genetic Associations of Variants in Genes Encoding HIV-Dependency Factors Required for HIV-1 Infection von Chinn, Leslie W., Tang, Minzhong, Kessing, Bailey D., Lautenberger, James A., Troyer, Jennifer L., Malasky, Michael J., McIntosh, Carl, Kirk, Gregory D., Wolinsky, Steven M., Buchbinder, Susan P., Gomperts, Edward D., Goedert, James J., O'Brien, Stephen J.

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Cell-type-specific meQTLs extend melanoma GWAS annotation beyond eQTLs and inform melanocyte gene-regulatory mechanisms von Zhang, Tongwu, Choi, Jiyeon, Dilshat, Ramile, Einarsdóttir, Berglind Ósk, Kovacs, Michael A., Xu, Mai, Malasky, Michael, Chowdhury, Salma, Jones, Kristine, Bishop, D. Timothy, Goldstein, Alisa M., Iles, Mark M., Landi, Maria Teresa, Law, Matthew H., Shi, Jianxin, Steingrímsson, Eiríkur, Brown, Kevin M.

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Simulation-Based Training for Pulmonary and Critical Care Fellows in Urgent Endotracheal Intubation: Does Skill Transfer to the Clinical Arena? von Shah, Ronak, MD, Makaryus, Mina, Feldman, Matthew, Mayo-Malasky, Perry, BA, Narasimhan, Mangala, DO, Mayo, Paul, MD, Singas, Effie, MD

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Armrest for automotive seats von MALASKY PAUL M, NEALE COLIN G

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Hoyeraal-Hreidarsson syndrome caused by a germline mutation in the TEL patch of the telomere protein TPP1 von Kocak, Hande, Ballew, Bari J, Bisht, Kamlesh, Eggebeen, Rebecca, Hicks, Belynda D, Suman, Shalabh, O'Neil, Adri, Giri, Neelam, Maillard, Ivan, Alter, Blanche P, Keegan, Catherine E, Nandakumar, Jayakrishnan, Savage, Sharon A

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D34 INNOVATIONS IN PROFESSIONAL EDUCATION TO IMPROVE QUALITY OF CARE: Standardization Of urgent Endotracheal Intubation Using Simulation Training And Checklist Approach To Train Pu... von Makaryus, M, Mayo-Malasky, P, Koenig, S, Narasimhan, M, Lakticova, V, Singas, E, Mayo, P H

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A High-Density Admixture Map for Disease Gene Discovery in African Americans von Smith, Michael W., Patterson, Nick, Lautenberger, James A., Truelove, Ann L., McDonald, Gavin J., Waliszewska, Alicja, Kessing, Bailey D., Malasky, Michael J., Scafe, Charles, Le, Ernest, De Jager, Philip L., Mignault, Andre A., Yi, Zeng, de Thé, Guy, Essex, Myron, Sankalé, Jean-Louis, Moore, Jason H., Poku, Kwabena, Phair, John P., Goedert, James J., Vlahov, David, Williams, Scott M., Tishkoff, Sarah A., Winkler, Cheryl A., De La Vega, Francisco M., Woodage, Trevor, Sninsky, John J., Hafler, David A., Altshuler, David, Gilbert, Dennis A., O’Brien, Stephen J., Reich, David

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Hoyeraal-Hreidarsson Syndrome due to PARN Mutations: Fourteen Years of Follow-Up von Burris, Ashley M., DO, Ballew, Bari J., PhD, Kentosh, Joshua B., DO, Turner, Clesson E., MD, Norton, Scott A., MD, MPH, Giri, Neelam, MD, Alter, Blanche P., MD, MPH, Nellan, Anandani, MD, Gamper, Christopher, MD, PhD, Hartman, Kip R., MD, Savage, Sharon A., MD

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Juvenile myelomonocytic leukemia due to a germline CBL Y371C mutation: 35-year follow-up of a large family von Pathak, Anand, Pemov, Alexander, McMaster, Mary L., Dewan, Ramita, Ravichandran, Sarangan, Pak, Evgenia, Dutra, Amalia, Lee, Hyo Jung, Vogt, Aurelie, Zhang, Xijun, Yeager, Meredith, Anderson, Stacie, Kirby, Martha, Caporaso, Neil, Greene, Mark H., Goldin, Lynn R., Stewart, Douglas R.

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Novel FANCI mutations in Fanconi anemia with VACTERL association von Savage, Sharon A., Ballew, Bari J., Giri, Neelam, Chandrasekharappa, Settara C., Ameziane, Najim, de Winter, Johan, Alter, Blanche P.

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224 EXCESSIVE TIME TO TREATMENT DELAY IN RURAL NATIVE AMERICANS PRESENTING WITH ACUTE MYOCARDIAL INFARCTION: TEMPORAL TRENDS 1999-2006 von Duarte, A. C., June-Tsosie, A., Sewell, J. L., Malasky, B. R., Ranger-Moore, J., Cudilo, E., Sanderson, P., Freund, N. S., Galloway, J. M., Brody, E. A.

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