Use of task-shifting to rapidly scale-up HIV treatment services: experiences from Lusaka, Zambia by Morris, Mary B, Chapula, Bushimbwa Tambatamba, Chi, Benjamin H, Mwango, Albert, Chi, Harmony F, Mwanza, Joyce, Manda, Handson, Bolton, Carolyn, Pankratz, Debra S, Stringer, Jeffrey S A, Reid, Stewart E

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Burnout and use of HIV services among health care workers in Lusaka District, Zambia: a cross-sectional study by Kruse, Gina R, Chapula, Bushimbwa Tambatamba, Ikeda, Scott, Nkhoma, Mavis, Quiterio, Nicole, Pankratz, Debra, Mataka, Kaluba, Chi, Benjamin H, Bond, Virginia, Reid, Stewart E

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A pilot randomized, placebo-controlled, double-blind study of omega-3 fatty acids to prevent paclitaxel-associated acute pain syndrome in breast cancer patients: Alliance A22_Pilot... by Tawfik, Bernard, Dayao, Zoneddy R., Brown-Glaberman, Ursa Abigail, Pankratz, V. Shane, Lafky, Jacqueline M., Loprinzi, Charles L., Barton, Debra L.

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The Otago Exercise Program compared to falls prevention education in Zuni elders: a randomized controlled trial by Waters, Debra L, Popp, Janet, Herman, Carla, Ghahate, Donica, Bobelu, Jeanette, Pankratz, Vernon S, Shah, Vallabh O

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Glutathione S-transferase omega genes in Alzheimer and Parkinson disease risk, age-at-diagnosis and brain gene expression: an association study with mechanistic implications by Allen, Mariet, Zou, Fanggeng, Chai, High Seng, Younkin, Curtis S, Miles, Richard, Nair, Asha A, Crook, Julia E, Pankratz, V Shane, Carrasquillo, Minerva M, Rowley, Christopher N, Nguyen, Thuy, Ma, Li, Malphrus, Kimberly G, Bisceglio, Gina, Ortolaza, Alexandra I, Palusak, Ryan, Middha, Sumit, Maharjan, Sooraj, Georgescu, Constantin, Schultz, Debra, Rakhshan, Fariborz, Kolbert, Christopher P, Jen, Jin, Sando, Sigrid B, Aasly, Jan O, Barcikowska, Maria, Uitti, Ryan J, Wszolek, Zbigniew K, Ross, Owen A, Petersen, Ronald C, Graff-Radford, Neill R, Dickson, Dennis W, Younkin, Steven G, Ertekin-Taner, Nilüfer

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A novel, microvascular evaluation method and device for early diagnosis of peripheral artery disease and chronic limb-threatening ischemia in individuals with diabetes by Matheson, Benjamin T., Osofsky, Robin B., Friedrichsen, Debra M., Brooks, Bill J., Giacolone, Joseph, Khotan, Mehdy, Shekarriz, Reza, Pankratz, Vernon Shane, Lew, Eric J., Clark, Ross M., Kanagy, Nancy L.

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Common variants associated with breast cancer in genome-wide association studies are modifiers of breast cancer risk in BRCA1 and BRCA2 mutation carriers by Wang, Xianshu, Pankratz, V. Shane, Fredericksen, Zachary, Tarrell, Robert, Karaus, Mary, McGuffog, Lesley, Pharaoh, Paul D.P., Ponder, Bruce A.J., Dunning, Alison M., Peock, Susan, Cook, Margaret, Oliver, Clare, Frost, Debra, Sinilnikova, Olga M., Stoppa-Lyonnet, Dominique, Mazoyer, Sylvie, Houdayer, Claude, Hogervorst, Frans B.L., Hooning, Maartje J., Ligtenberg, Marjolijn J., Spurdle, Amanda, Chenevix-Trench, Georgia, Schmutzler, Rita K., Wappenschmidt, Barbara, Engel, Christoph, Meindl, Alfons, Domchek, Susan M., Nathanson, Katherine L., Rebbeck, Timothy R., Singer, Christian F., Gschwantler-Kaulich, Daphne, Dressler, Catherina, Fink, Anneliese, Szabo, Csilla I., Zikan, Michal, Foretova, Lenka, Claes, Kathleen, Thomas, Gilles, Hoover, Robert N., Hunter, David J., Chanock, Stephen J., Easton, Douglas F., Antoniou, Antonis C., Couch, Fergus J.

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Identification of a BRCA2-specific modifier locus at 6p24 related to breast cancer risk by Gaudet, Mia M, Kuchenbaecker, Karoline B, Vijai, Joseph, Klein, Robert J, Kirchhoff, Tomas, McGuffog, Lesley, Barrowdale, Daniel, Dunning, Alison M, Lee, Andrew, Dennis, Joe, Healey, Sue, Dicks, Ed, Soucy, Penny, Sinilnikova, Olga M, Pankratz, Vernon S, Wang, Xianshu, Eldridge, Ronald C, Tessier, Daniel C, Vincent, Daniel, Bacot, Francois, Hogervorst, Frans B L, Peock, Susan, Stoppa-Lyonnet, Dominique, Peterlongo, Paolo, Schmutzler, Rita K, Nathanson, Katherine L, Piedmonte, Marion, Singer, Christian F, Thomassen, Mads, Hansen, Thomas v O, Neuhausen, Susan L, Blanco, Ignacio, Greene, Mark H, Garber, Judith, Weitzel, Jeffrey N, Andrulis, Irene L, Goldgar, David E, D'Andrea, Emma, Caldes, Trinidad, Nevanlinna, Heli, Osorio, Ana, van Rensburg, Elizabeth J, Arason, Adalgeir, Rennert, Gad, van den Ouweland, Ans M W, van der Hout, Annemarie H, Kets, Carolien M, Aalfs, Cora M, Wijnen, Juul T, Ausems, Margreet G E M, Frost, Debra, Ellis, Steve, Fineberg, Elena, Platte, Radka, Evans, D Gareth, Jacobs, Chris, Adlard, Julian, Tischkowitz, Marc, Porteous, Mary E, Damiola, Francesca, Golmard, Lisa, Barjhoux, Laure, Longy, Michel, Belotti, Muriel, Ferrer, Sandra Fert, Mazoyer, Sylvie, Spurdle, Amanda B, Manoukian, Siranoush, Barile, Monica, Genuardi, Maurizio, Arnold, Norbert, Meindl, Alfons, Sutter, Christian, Wappenschmidt, Barbara, Domchek, Susan M, Pfeiler, Georg, Friedman, Eitan, Jensen, Uffe Birk, Robson, Mark, Shah, Sohela, Lazaro, Conxi, Mai, Phuong L, Benitez, Javier, Southey, Melissa C, Schmidt, Marjanka K, Fasching, Peter A, Peto, Julian, Humphreys, Manjeet K, Wang, Qin, Michailidou, Kyriaki, Sawyer, Elinor J, Burwinkel, Barbara, Guénel, Pascal, Bojesen, Stig E, Milne, Roger L, Brenner, Hermann, Lochmann, Magdalena, Aittomäki, Kristiina, Dörk, Thilo, Margolin, Sara

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Abstract B134: The art of science: Painting a new image of genomic research in the indigenous communities of the Southwest by Jaffe, Shoshana Adler, Jacobson, Kendal, Rodman, Joseph, Blair, Cindy, MacKenzie, Debra, Quetawki, Mallery, Ginossar, Tamar, Pankratz, V. Shane, Sussman, Andrew, Brown-Glabermen, Ursa, Trent, Jeffrey, Willman, Cheryl, Mishra, Shiraz I.

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Presence of an APOE4 allele results in significantly earlier onset of Parkinson's disease and a higher risk with dementia by Pankratz, Nathan, Byder, Lisa, Halter, Cheryl, Rudolph, Alice, Shults, Clifford W., Conneally, P. Michael, Foroud, Tatiana, Nichols, William C.

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Significant Linkage of Parkinson Disease to Chromosome 2q36-37 by Pankratz, Nathan, Nichols, William C., Uniacke, Sean K., Halter, Cheryl, Rudolph, Alice, Shults, Cliff, Conneally, P. Michael, Foroud, Tatiana

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Genome Screen to Identify Susceptibility Genes for Parkinson Disease in a Sample without parkin Mutations by Pankratz, Nathan, Nichols, William C., Uniacke, Sean K., Halter, Cheryl, Rudolph, Alice, Shults, Cliff, Conneally, P. Michael, Foroud, Tatiana

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Genome-wide linkage analysis and evidence of gene-by-gene interactions in a sample of 362 multiplex Parkinson disease families by Pankratz, Nathan, Nichols, William C., Uniacke, Sean K., Halter, Cheryl, Murrell, Jill, Rudolph, Alice, Shults, Clifford W., Conneally, P. Michael, Foroud, Tatiana

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Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers by Im, Kate M., Kirchhoff, Tomas, Wang, Xianshu, Green, Todd, Chow, Clement Y., Korn, Joshua, Gaudet, Mia M., Fredericksen, Zachary, Shane Pankratz, V., Guiducci, Candace, Crenshaw, Andrew, McGuffog, Lesley, Kartsonaki, Christiana, Morrison, Jonathan, Healey, Sue, Sinilnikova, Olga M., Mai, Phuong L., Greene, Mark H., Piedmonte, Marion, Rubinstein, Wendy S., Hogervorst, Frans B., Rookus, Matti A., Collée, J. Margriet, Hoogerbrugge, Nicoline, Meijers-Heijboer, Hanne E. J., Van Roozendaal, Cees E., Perez-Segura, Pedro, Jakubowska, Anna, Huzarski, Tomasz, Blecharz, Paweł, Nevanlinna, Heli, Aittomäki, Kristiina, Lazaro, Conxi, Blanco, Ignacio, Barkardottir, Rosa B., D’Andrea, Emma, Devilee, Peter, Olopade, Olufunmilayo I., Peissel, Bernard, Bonanni, Bernardo, Peterlongo, Paolo, Singer, Christian F., Rennert, Gad, Lejbkowicz, Flavio, Andrulis, Irene L., Ozcelik, Hilmi, Toland, Amanda Ewart, Caligo, Maria Adelaide, Beattie, Mary S., Chan, Salina, Domchek, Susan M., Nathanson, Katherine L., Rebbeck, Timothy R., Phelan, Catherine, Narod, Steven, John, Esther M., Hopper, John L., Buys, Saundra S., Southey, Melissa C., Terry, Mary-Beth, Tung, Nadine, Hansen, Thomas v. O., Benitez, Javier, Weitzel, Jeffrey N., Garber, Judy, Hamann, Ute, Peock, Susan, Cook, Margaret, Oliver, Clare T., Frost, Debra, Eeles, Ros, Izatt, Louise, Paterson, Joan, Brewer, Carole, Hodgson, Shirley, Porteous, Mary, Walker, Lisa, Rogers, Mark T., Side, Lucy E., Godwin, Andrew K., Wappenschmidt, Barbara, Laitman, Yael, Deissler, Helmut, Varon-Mateeva, Raymonda, Preisler-Adams, Sabine, Kast, Karin, Venat-Bouvet, Laurence, Stoppa-Lyonnet, Dominique, Chenevix-Trench, Georgia, Easton, Douglas F., Klein, Robert J., Daly, Mark J., Friedman, Eitan, Dean, Michael, Clark, Andrew G., Altshuler, David M., Antoniou, Antonis C., Couch, Fergus J., Offit, Kenneth, Gold, Bert

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Evidence for SMAD3 as a modifier of breast cancer risk in BRCA2 mutation carriers by Walker, Logan C, Fredericksen, Zachary S, Wang, Xianshu, Tarrell, Robert, Pankratz, Vernon S, Lindor, Noralane M, Beesley, Jonathan, Healey, Sue, Chen, Xiaoqing, Stoppa-Lyonnet, Dominique, Tirapo, Carole, Giraud, Sophie, Mazoyer, Sylvie, Muller, Danièle, Fricker, Jean-Pierre, Delnatte, Capucine, Schmutzler, Rita K, Wappenschmidt, Barbara, Engel, Christoph, Schönbuchner, Ines, Deissler, Helmut, Meindl, Alfons, Hogervorst, Frans B, Verheus, Martijn, Hooning, Maartje J, van den Ouweland, Ans Mw, Nelen, Marcel R, Ausems, Margreet Gem, Aalfs, Cora M, van Asperen, Christi J, Devilee, Peter, Gerrits, Monique M, Waisfisz, Quinten, Szabo, Csilla I, Easton, Douglas F, Peock, Susan, Cook, Margaret, Oliver, Clare T, Frost, Debra, Harrington, Patricia, Evans, D Gareth, Lalloo, Fiona, Eeles, Ros, Izatt, Louise, Chu, Carol, Davidson, Rosemarie, Eccles, Diana, Ong, Kai-Ren, Cook, Jackie, Rebbeck, Tim, Nathanson, Katherine L, Domchek, Susan M, Singer, Christian F, Gschwantler-Kaulich, Daphne, Dressler, Anne-Catharina, Pfeiler, Georg, Godwin, Andrew K, Heikkinen, Tuomas, Nevanlinna, Heli, Agnarsson, Bjarni A, Caligo, Maria Adelaide, Olsson, Håkan, Kristoffersson, Ulf, Liljegren, Annelie, Arver, Brita, Karlsson, Per, Melin, Beatrice, Sinilnikova, Olga M, McGuffog, Lesley, Antoniou, Antonis C, Chenevix-Trench, Georgia, Spurdle, Amanda B, Couch, Fergus J

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Evaluation of the role of Nurr1 in a large sample of familial Parkinson's disease by Nichols, William C., Uniacke, Sean K., Pankratz, Nathan, Reed, Terry, Simon, David K., Halter, Cheryl, Rudolph, Alice, Shults, Clifford W., Conneally, P. Michael, Foroud, Tatiana

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