Observations and Reflections on the Evolution of Crime-Related Higher Education by Foster, J. Price, Magers, Jeffrey S., Mullikin, Jessica

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Somatic mutational landscape of AML with inv(16) or t(8;21) identifies patterns of clonal evolution in relapse leukemia by Sood, R, Hansen, N F, Donovan, F X, Carrington, B, Bucci, D, Maskeri, B, Young, A, Trivedi, N S, Kohlschmidt, J, Stone, R M, Caligiuri, M A, Chandrasekharappa, S C, Marcucci, G, Mullikin, J C, Bloomfield, C D, Liu, P

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Sequencing of candidate chromosome instability genes in endometrial cancers reveals somatic mutations in ESCO1, CHTF18, and MRE11A by Price, Jessica C, Pollock, Lana M, Rudd, Meghan L, Fogoros, Sarah K, Mohamed, Hassan, Hanigan, Christin L, Le Gallo, Matthieu, Zhang, Suiyuan, Cruz, Pedro, Cherukuri, Praveen F, Hansen, Nancy F, McManus, Kirk J, Godwin, Andrew K, Sgroi, Dennis C, Mullikin, James C, Merino, Maria J, Hieter, Philip, Bell, Daphne W

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Predisposition to cancer caused by genetic and functional defects of mammalian Atad5 by Bell, Daphne W, Sikdar, Nilabja, Lee, Kyoo-Young, Price, Jessica C, Chatterjee, Raghunath, Park, Hee-Dong, Fox, Jennifer, Ishiai, Masamichi, Rudd, Meghan L, Pollock, Lana M, Fogoros, Sarah K, Mohamed, Hassan, Hanigan, Christin L, Zhang, Suiyuan, Cruz, Pedro, Renaud, Gabriel, Hansen, Nancy F, Cherukuri, Praveen F, Borate, Bhavesh, McManus, Kirk J, Stoepel, Jan, Sipahimalani, Payal, Godwin, Andrew K, Sgroi, Dennis C, Merino, Maria J, Elliot, Gene, Elkahloun, Abdel, Vinson, Charles, Takata, Minoru, Mullikin, James C, Wolfsberg, Tyra G, Hieter, Philip, Lim, Dae-Sik, Myung, Kyungjae

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Great ape genetic diversity and population history by Prado-Martinez, Javier, Sudmant, Peter H., Kidd, Jeffrey M., Li, Heng, Kelley, Joanna L., Lorente-Galdos, Belen, Veeramah, Krishna R., Woerner, August E., O’Connor, Timothy D., Santpere, Gabriel, Cagan, Alexander, Theunert, Christoph, Casals, Ferran, Laayouni, Hafid, Munch, Kasper, Hobolth, Asger, Halager, Anders E., Malig, Maika, Hernandez-Rodriguez, Jessica, Hernando-Herraez, Irene, Prüfer, Kay, Pybus, Marc, Johnstone, Laurel, Lachmann, Michael, Alkan, Can, Twigg, Dorina, Petit, Natalia, Baker, Carl, Hormozdiari, Fereydoun, Fernandez-Callejo, Marcos, Dabad, Marc, Wilson, Michael L., Stevison, Laurie, Camprubí, Cristina, Carvalho, Tiago, Ruiz-Herrera, Aurora, Vives, Laura, Mele, Marta, Abello, Teresa, Kondova, Ivanela, Bontrop, Ronald E., Pusey, Anne, Lankester, Felix, Kiyang, John A., Bergl, Richard A., Lonsdorf, Elizabeth, Myers, Simon, Ventura, Mario, Gagneux, Pascal, Comas, David, Siegismund, Hans, Blanc, Julie, Agueda-Calpena, Lidia, Gut, Marta, Fulton, Lucinda, Tishkoff, Sarah A., Mullikin, James C., Wilson, Richard K., Gut, Ivo G., Gonder, Mary Katherine, Ryder, Oliver A., Hahn, Beatrice H., Navarro, Arcadi, Akey, Joshua M., Bertranpetit, Jaume, Reich, David, Mailund, Thomas, Schierup, Mikkel H., Hvilsom, Christina, Andrés, Aida M., Wall, Jeffrey D., Bustamante, Carlos D., Hammer, Michael F., Eichler, Evan E., Marques-Bonet, Tomas

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Genetic regulatory signatures underlying islet gene expression and type 2 diabetes by Varshney, Arushi, Scott, Laura J., Welch, Ryan P., Erdos, Michael R., Chines, Peter S., Narisu, Narisu, Albanus, Ricardo D’O., Orchard, Peter, Wolford, Brooke N., Kursawe, Romy, Vadlamudi, Swarooparani, Cannon, Maren E., Didion, John P., Hensley, John, Kirilusha, Anthony, Bonnycastle, Lori L., Taylor, D. Leland, Watanabe, Richard, Mohlke, Karen L., Boehnke, Michael, Collins, Francis S., Parker, Stephen C. J., Stitzel, Michael L.

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Gene-Specific Substitution Profiles Describe the Types and Frequencies of Amino Acid Changes during Antibody Somatic Hypermutation by Sheng, Zizhang, Schramm, Chaim A, Kong, Rui, Mullikin, James C, Mascola, John R, Kwong, Peter D, Shapiro, Lawrence

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HLA and autoantibodies define scleroderma subtypes and risk in African and European Americans and suggest a role for molecular mimicry by Gourh, Pravitt, Safran, Sarah A., Alexander, Theresa, Boyden, Steven E., Morgan, Nadia D., Shah, Ami A., Mayes, Maureen D., Doumatey, Ayo, Bentley, Amy R., Shriner, Daniel, Domsic, Robyn T., Medsger, Thomas A., Ramos, Paula S., Silver, Richard M., Steen, Virginia D., Varga, John, Hsu, Vivien, Saketkoo, Lesley Ann, Schiopu, Elena, Khanna, Dinesh, Gordon, Jessica K., Kron, Brynn, Criswell, Lindsey A., Gladue, Heather, Derk, Chris T., Bernstein, Elana J., Bridges, S. Louis, Shanmugam, Victoria K., Kolstad, Kathleen D., Chung, Lorinda, Kafaja, Suzanne, Jan, Reem, Trojanowski, Marcin, Goldberg, Avram, Korman, Benjamin D., Steinbacha, Peter J., Chandrasekharappab, Settara C., Mullikinc, James C., Adeyemo, Adebowale, Rotimi, Charles, Wigley, Fredrick M., Kastner, Daniel L., Boin, Francesco, Remmers, Elaine F.

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Exome‐wide assessment of isolated biliary atresia: A report from the National Birth Defects Prevention Study using child–parent trios and a case–control design to identify novel ra... by Sok, Pagna, Sabo, Aniko, Almli, Lynn M., Jenkins, Mary M., Nembhard, Wendy N., Agopian, A. J., Bamshad, Michael J., Blue, Elizabeth E., Brody, Lawrence C., Brown, Austin L., Browne, Marilyn L., Canfield, Mark A., Carmichael, Suzan L., Chong, Jessica X., Dugan‐Perez, Shannon, Feldkamp, Marcia L., Finnell, Richard H., Gibbs, Richard A., Kay, Denise M., Lei, Yunping, Meng, Qingchang, Moore, Cynthia A., Mullikin, James C., Muzny, Donna, Olshan, Andrew F., Pangilinan, Faith, Reefhuis, Jennita, Romitti, Paul A., Schraw, Jeremy M., Shaw, Gary M., Werler, Martha M., Harpavat, Sanjiv, Lupo, Philip J.

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Exome sequencing identifies genetic variants in anophthalmia and microphthalmia by Li, Jingjing, Yang, Wei, Wang, Yuejun Jessie, Ma, Chen, Curry, Cynthia J., McGoldrick, Daniel, Nickerson, Deborah A., Chong, Jessica X., Blue, Elizabeth E., Mullikin, James C., Reefhuis, Jennita, Nembhard, Wendy N., Romitti, Paul A., Werler, Martha M., Browne, Marilyn L., Olshan, Andrew F., Finnell, Richard H., Feldkamp, Marcia L., Pangilinan, Faith, Almli, Lynn M., Bamshad, Mike J., Brody, Lawrence C., Jenkins, Mary M., Shaw, Gary M.

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Mutational analysis of the tyrosine kinome in serous and clear cell endometrial cancer uncovers rare somatic mutations in TNK2 and DDR1 by Rudd, Meghan L, Mohamed, Hassan, Price, Jessica C, O'Hara, Andrea J, Le Gallo, Matthieu, Urick, Mary Ellen, Cruz, Pedro, Zhang, Suiyuan, Hansen, Nancy F, Godwin, Andrew K, Sgroi, Dennis C, Wolfsberg, Tyra G, Mullikin, James C, Merino, Maria J, Bell, Daphne W

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Brief Report: Whole‐Exome Sequencing to Identify Rare Variants and Gene Networks That Increase Susceptibility to Scleroderma in African Americans by Gourh, Pravitt, Remmers, Elaine F., Boyden, Steven E., Alexander, Theresa, Morgan, Nadia D., Shah, Ami A., Mayes, Maureen D., Doumatey, Ayo, Bentley, Amy R., Shriner, Daniel, Domsic, Robyn T., Medsger, Thomas A., Steen, Virginia D., Ramos, Paula S., Silver, Richard M., Korman, Benjamin, Varga, John, Schiopu, Elena, Khanna, Dinesh, Hsu, Vivien, Gordon, Jessica K., Saketkoo, Lesley Ann, Gladue, Heather, Kron, Brynn, Criswell, Lindsey A., Derk, Chris T., Bridges, S. Louis, Shanmugam, Victoria K., Kolstad, Kathleen D., Chung, Lorinda, Jan, Reem, Bernstein, Elana J., Goldberg, Avram, Trojanowski, Marcin, Kafaja, Suzanne, Maksimowicz‐McKinnon, Kathleen M., Mullikin, James C., Adeyemo, Adebowale, Rotimi, Charles, Boin, Francesco, Kastner, Daniel L., Wigley, Fredrick M.

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The aesthetics of space and state formation in post-2000 Rwanda by Mullikin, Justin Dodd, Ansoms, An, Marter-Kenyon, Jessica, Cottyn, Ine, Legrand, Vincent, Niyonkuru, René-Claude, Nyenyezi Bisoka, Aymar

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The Time Scale of Recombination Rate Evolution in Great Apes by Stevison, Laurie S, Woerner, August E, Kidd, Jeffrey M, Kelley, Joanna L, Veeramah, Krishna R, McManus, Kimberly F, Bustamante, Carlos D, Hammer, Michael F, Wall, Jeffrey D

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Hypoxia‐induced HIF1α targets in melanocytes reveal a molecular profile associated with poor melanoma prognosis by Loftus, Stacie K., Baxter, Laura L., Cronin, Julia C., Fufa, Temesgen D., Pavan, William J., Barnabas, Beatrice B., Bouffard, Gerard G., Brooks, Shelise Y., Coleman, Holly, Dekhtyar, Lyudmila, Guan, Xiaobin, Han, Joel, Ho, Shi‐ling, Legaspi, Richelle, Maduro, Quino L., Masiello, Catherine A., McDowell, Jennifer C., Montemayor, Casandra, Mullikin, James C., Park, Morgan, Riebow, Nancy L., Rosarda, Jessica, Schandler, Karen, Schmidt, Brian, Sison, Christina, Smith, Raymond, Stantripop, Sirintorn, Thomas, James W., Thomas, Pamela J., Vemulapalli, Meghana, Young, Alice C.

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Extreme selective sweeps independently targeted the X chromosomes of the great apes by Nam, Kiwoong, (남기웅), Munch, Kasper, Hobolth, Asger, Dutheil, Julien Yann, Veeramah, Krishna R., Woerner, August E., Hammer, Michael F., Mailund, Thomas, Schierup, Mikkel Heide

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Whole-Exome Sequencing to Identify Rare Variants and Gene Networks that Increase Susceptibility to Scleroderma in African Americans by Gourh, Pravitt, Remmers, Elaine F., Boyden, Steven E., Alexander, Theresa, Morgan, Nadia D., Shah, Ami A., Mayes, Maureen D., Doumatey, Ayo, Bentley, Amy R., Shriner, Daniel, Domsic, Robyn T., Medsger, Thomas A., Steen, Virginia D., Ramos, Paula S., Silver, Richard M., Korman, Benjamin, Varga, John, Schiopu, Elena, Khanna, Dinesh, Hsu, Vivien, Gordon, Jessica K., Saketkoo, Lesley Ann, Gladue, Heather, Kron, Brynn, Criswell, Lindsey A., Derk, Chris T., Bridges, S. Louis, Shanmugam, Victoria K., Kolstad, Kathleen D, Chung, Lorinda, Jan, Reem, Bernstein, Elana J, Goldberg, Avram, Trojanowski, Marcin, Kafaja, Suzanne, Maksimowicz-McKinnon, Kathleen M, Mullikin, James C., Adeyemo, Adebowale, Rotimi, Charles, Boin, Francesco, Kastner, Daniel L., Wigley, Fredrick M.

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Exome sequencing of family trios from the National Birth Defects Prevention Study: Tapping into a rich resource of genetic and environmental data by Jenkins, Mary M., Almli, Lynn M., Pangilinan, Faith, Chong, Jessica X., Blue, Elizabeth E., Shapira, Stuart K., White, Janson, McGoldrick, Daniel, Smith, Joshua D., Mullikin, James C., Bean, Christopher J., Nembhard, Wendy N., Lou, Xiang‐Yang, Shaw, Gary M., Romitti, Paul A., Keppler‐Noreuil, Kim, Yazdy, Mahsa M., Kay, Denise M., Carter, Tonia C., Olshan, Andrew F., Moore, Kristin J., Nascone‐Yoder, Nanette, Finnell, Richard H., Lupo, Philip J., Feldkamp, Marcia L., Nickerson, Deborah A., Bamshad, Michael J., Brody, Lawrence C., Reefhuis, Jennita

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Abstract 5312: Mutational analysis of the tyrosine kinome in serous and clear cell endometrial cancers by Rudd, Meghan L., Mohamed, Hassan, Price, Jessica C., Urick, Mary Ellen, O'Hara, Andrea J., Gallo, Matthieu Le, Cruz, Pedro, Zhang, Suiyuan, Mullikin, James, Merino, Maria J., Bell, Daphne W.

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Predisposition to Cancer Caused by Genetic and Functional Defects of Mammalian Atad5: e1002245 by Bell, Daphne W, Sikdar, Nilabja, Lee, Kyoo-young, Price, Jessica C, Chatterjee, Raghunath, Park, Hee-Dong, Fox, Jennifer, Ishiai, Masamichi, Rudd, Meghan L, Pollock, Lana M, Fogoros, Sarah K, Mohamed, Hassan, Hanigan, Christin L, Zhang, Suiyuan, Cruz, Pedro, Renaud, Gabriel, Hansen, Nancy F, Cherukuri, Praveen F, Borate, Bhavesh, McManus, Kirk J, Stoepel, Jan, Sipahimalani, Payal, Godwin, Andrew K, Sgroi, Dennis C, Merino, Maria J, Elliot, Gene, Elkahloun, Abdel, Vinson, Charles, Takata, Minoru, Mullikin, James C, Wolfsberg, Tyra G, Hieter, Philip, Lim, Dae-Sik, Myung, Kyungjae, Program, NISC ComparativeSequencing

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