Analysis of genetically determined gene expression suggests role of inflammatory processes in exfoliation syndrome by Hirbo, Jibril B, Pasutto, Francesca, Gamazon, Eric R, Evans, Patrick, Pawar, Priyanka, Berner, Daniel, Sealock, Julia, Tao, Ran, Straub, Peter S, Konkashbaev, Anuar I, Breyer, Max A, Schlötzer-Schrehardt, Ursula, Reis, André, Brantley, Jr, Milam A, Khor, Chiea C, Joos, Karen M, Cox, Nancy J

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GRIK5 Genetically Regulated Expression Associated with Eye and Vascular Phenomes: Discovery through Iteration among Biobanks, Electronic Health Records, and Zebrafish by Unlu, Gokhan, Gamazon, Eric R., Qi, Xinzi, Levic, Daniel S., Bastarache, Lisa, Denny, Joshua C., Roden, Dan M., Mayzus, Ilya, Breyer, Max, Zhong, Xue, Konkashbaev, Anuar I., Rzhetsky, Andrey, Knapik, Ela W., Cox, Nancy J.

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Cross-Disorder Genome-Wide Analyses Suggest a Complex Genetic Relationship Between Tourette’s Syndrome and OCD by Yu, Dongmei, Davis, Lea K., Gamazon, Eric R., Derks, Eske M., Evans, Patrick, Crane, Jacquelyn, Osiecki, Lisa, Gerber, Gloria, Haddad, Stephen, McGrath, Lauren M., Mayerfeld, Catherine, Arepalli, Sampath, Barlassina, Cristina, Barr, Cathy L., Black, Donald W., Bloch, Michael H., Brentani, Helena, Camarena, Beatriz, Campbell, Desmond D., Cavallini, Maria C., Chavira, Denise A., Cook, Edwin H., Cookson, M.R., Cullen, Bernadette, Denys, Damiaan, Dion, Yves, Eapen, Valsama, Egberts, Karin, Fernandez, Thomas, Fournier, Eduardo, Garrido, Helena, Geller, Daniel, Girard, Simon L., Grabe, Hans J., Greenberg, Benjamin D., Heiman, Gary A., Hemmings, Sian M.J., Herrera, Luis D., Hezel, Dianne M., Jankovic, Joseph, Kremeyer, Barbara, Lanzagorta, Nuria, Lowe, Thomas L., Lupoli, Sara, Macciardi, Fabio, Maier, Wolfgang, Manunta, Paolo, Marconi, Maurizio, McCracken, James T., Mesa Restrepo, Sandra C., Moessner, Rainald, Moorjani, Priya, Morgan, Jubel, Muller, Heike, Murphy, Dennis L., Naarden, Allan L., Nurmi, Erika, Ochoa, William Cornejo, Pato, Carlos N., Piacentini, John, Pittenger, Christopher, Rauch, Scott L., Renner, Tobias, Reus, Victor I., Riddle, Mark A., Romero, Roxana, Rosenberg, David, Ruhrmann, Stephan, Sabatti, Chiara, Salvi, Erika, Samuels, Jack, Sandor, Paul, Sheppard, Brooke, Singer, Harvey S., Stein, Dan J., Strengman, Eric, Tischfield, Jay A., Turiel, Maurizio, Vallada, Homero, Veenstra-VanderWeele, Jeremy, Walitza, Susanne, Wang, Ying, Weale, Mike, Weiss, Robert, Wendland, Jens R., Westenberg, Herman G.M., Shugart, Yin Yao, Hounie, Ana G., Wagner, Michael, Ruiz-Linares, Andres, Cath, Danielle C., Posthuma, Danielle, Heutink, Peter, Hanna, Gregory L., Conti, David V., Arnold, Paul D., Freimer, Nelson B., Stewart, S. Evelyn, Knowles, James A., Pauls, David L.

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Partitioning the Heritability of Tourette Syndrome and Obsessive Compulsive Disorder Reveals Differences in Genetic Architecture: e1003864 by Davis, Lea K, Yu, Dongmei, Keenan, Clare L, Gamazon, Eric R, Konkashbaev, Anuar I, Derks, Eske M, Yang, Jian, Lee, S Hong, Barr, Cathy L, Bellodi, Laura, Benarroch, tu, Berrio, Gabriel Bedoya, Bienvenu, Oscar J, Bloch, Michael H, Bruun, Ruth D, Budman, Cathy L, Camarena, Beatriz, Cappi, Carolina, Silgado, Julio CCardona, Cath, Danielle C, Cavallini, Maria C, Chouinard, Sylvain, Conti, David V, Cook, Edwin H, Coric, Vladimir, Cullen, Bernadette A, Deforce, Dieter, Delorme, Richard, Dion, Yves, Edlund, Christopher K, Egberts, Karin, Falkai, Peter, Fernandez, Thomas V, Geller, Daniel, Girard, Simon L, Grados, Marco A, Haddad, Stephen, Heiman, Gary A, Hemmings, Sian MJ, Hounie, Ana G, Jankovic, Joseph, Jenike, Michael A, Kennedy, James L, King, Robert A, Kremeyer, Barbara, Kurlan, Roger, Lennertz, Leonhard, Liu, Chunyu, Lochner, Christine, Macciardi, Fabio, McCracken, James T, McGrath, Lauren M, Restrepo, Sandra CMesa, Moessner, Rainald, Morgan, Jubel, Muller, Heike, Ochoa, William Cornejo, Ophoff, Roel A, Osiecki, Lisa, Pakstis, Andrew J, Pato, Michele T, Pato, Carlos N, Piacentini, John, Pittenger, Christopher, Rauch, Scott L, Renner, Tobias J, Reus, Victor I, Richter, Margaret A, Riddle, Mark A, Robertson, Mary M, Rosàrio, Maria C, Rosenberg, David, Rouleau, Guy A, Ruhrmann, Stephan, Ruiz-Linares, Andres, Sampaio, Aline S, Samuels, Jack, Sheppard, Brooke, Smit, Jan H, Tischfield, Jay A, Duarte, Ana VValencia, Vallada, Homero, Veenstra-VanderWeele, Jeremy, Walitza, Susanne, Wang, Ying, Westenberg, Herman GM, Shugart, Yin Yao, Miguel, Euripedes C, McMahon, William, Nicolini, Humberto, Posthuma, Danielle, Hanna, Gregory L, Arnold, Paul D, Nestadt, Gerald, Freimer, Nelson B, Wray, Naomi R, Stewart, S Evelyn, Knowles, James A, Cox, Nancy J, Scharf, Jeremiah M

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SCAN: SNP and copy number annotation by Gamazon, Eric R., Zhang, Wei, Konkashbaev, Anuar, Duan, Shiwei, Kistner, Emily O., Nicolae, Dan L., Dolan, M. Eileen, Cox, Nancy J.

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Evidence of selection on splicing-associated loci in human populations and relevance to disease loci mapping by Gamazon, Eric R., Konkashbaev, Anuar, Derks, Eske M., Cox, Nancy J., Lee, Younghee

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Genetic variants associated with warfarin dose in African-American individuals: a genome-wide association study by Perera, Minoli A, PharmD, Cavallari, Larisa H, PharmD, Limdi, Nita A, PharmD, Gamazon, Eric R, MS, Konkashbaev, Anuar, MS, Daneshjou, Roxana, BS, Pluzhnikov, Anna, PhD, Crawford, Dana C, PhD, Wang, Jelai, BS, Liu, Nianjun, PhD, Tatonetti, Nicholas, PhD, Bourgeois, Stephane, MS, Takahashi, Harumi, Prof, Bradford, Yukiko, MS, Burkley, Benjamin M, MS, Desnick, Robert J, Prof, Halperin, Jonathan L, Prof, Khalifa, Sherief I, Prof, Langaee, Taimour Y, PhD, Lubitz, Steven A, MD, Nutescu, Edith A, Prof, Oetjens, Matthew, BS, Shahin, Mohamed H, MS, Patel, Shitalben R, MS, Sagreiya, Hersh, MD, Tector, Matthew, PhD, Weck, Karen E, Prof, Rieder, Mark J, PhD, Scott, Stuart A, PhD, Wu, Alan HB, PhD, Burmester, James K, PhD, Wadelius, Mia, MD, Deloukas, Panos, PhD, Wagner, Michael J, PhD, Mushiroda, Taisei, PhD, Kubo, Michiaki, MD, Roden, Dan M, Prof, Cox, Nancy J, Prof, Altman, Russ B, Prof, Klein, Teri E, PhD, Nakamura, Yusuke, Prof, Johnson, Julie A, Prof

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Ethnic variation of TET2 SNP rs2454206 and association with clinical outcome in childhood AML: a report from the Children’s Oncology Group by Kutny, M A, Alonzo, T A, Gamazon, E R, Gerbing, R B, Geraghty, D, Lange, B, Heerema, N A, Sung, L, Aplenc, R, Franklin, J, Raimondi, S C, Hirsch, B A, Konkashbaev, A, Cox, N J, Onel, K, Gamis, A S, Meshinchi, S

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The neutrophil alloantigen HNA-3a (5b) is located on choline transporter-like protein 2 and appears to be encoded by an R>Q154 amino acid substitution by Curtis, Brian R., Cox, Nancy J., Sullivan, Mia J., Konkashbaev, Anuar, Bowens, Krista, Hansen, Kirk, Aster, Richard H.

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Integrating Cell-Based and Clinical Genome-Wide Studies to Identify Genetic Variants Contributing to Treatment Failure in Neuroblastoma Patients by Pinto, N, Gamazon, E R, Antao, N, Myers, J, Stark, A L, Konkashbaev, A, Im, H K, Diskin, S J, London, W B, Ludeman, S M, Maris, J M, Cox, N J, Cohn, S L, Dolan, M E

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Spoiling the Whole Bunch: Quality Control Aimed at Preserving the Integrity of High-Throughput Genotyping by Pluzhnikov, Anna, Below, Jennifer E., Konkashbaev, Anuar, Tikhomirov, Anna, Kistner-Griffin, Emily, Roe, Cheryl A., Nicolae, Dan L., Cox, Nancy J.

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Trans-population Analysis of Genetic Mechanisms of Ethnic Disparities in Neuroblastoma Survival by GAMAZON, Eric R, PINTO, Navin, KONKASHBAEV, Anuar, IM, Hae Kyung, DISKIN, Sharon J, LONDON, Wendy B, MARIS, John M, DOLAN, M. Eileen, COX, Nancy J, COHN, Susan L

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SCAN database: facilitating integrative analyses of cytosine modification and expression QTL by Zhang, Wei, Gamazon, Eric R, Zhang, Xu, Konkashbaev, Anuar, Liu, Cong, Szilágyi, Keely L, Dolan, M Eileen, Cox, Nancy J

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Abstract 2486: African ancestry is associated with high-risk disease and event-free survival in children with neuroblastoma by Pinto, Navin, Gamazon, Eric R., Im, Hae Kyung, Konkashbaev, Anuar, Cox, Nancy J., Dolan, Mary Eileen, Diskin, Sharon J., London, Wendy B., Maris, John M., Cohn, Susan L.

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Abstract B11: Replication of previously identified breast cancer susceptibility loci in a breast cancer case-control study on women of African ancestry by Zheng, Yonglan, Huo, Dezheng, Ogundiran, Temidayo O., Falusi, Adeyinka G., Ojengbede, Oladosu, Adebamowo, Clement, Blot, William J., Zheng, Wei, Cai, Qiuyin, Signorello, Lisa B., Nathanson, Katherine L., Domchek, Susan M., Rebbeck, Timothy R., Simon, Michael S., Hennis, Anselm J.M., Nemesure, Barbara, Wu, Suh-Yuh, Leske, Maria Cristina, Ambs, Stefan, Odetunde, Abayomi, Anetor, Imaria, Akinleye, Stella, Niu, Qun, Zhang, Jing, Pluzhnikov, Anna, Konkashbaev, Anuar, Chen, Lin, Gamazon, Eric R., Lee, Younghee, Cox, Nancy J., Olopade, Olufunmilayo O.

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Abstract A46: Genomic ancestry is associated with risk group and survival in children with neuroblastoma by Pinto, Navin R., Gamazon, Eric R., Konkashbaev, Anuar, Cox, Nancy J., Dolan, M. Eileen, Diskin, Sharon J., London, Wendy B., Devoto, Marcella, Maris, John M., Cohn, Susan L.

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The Neutrophil Alloantigen HNA-3a (5b) Is Encoded by an Amino Acid Substitution in Choline Transporter-Like Protein 2 (CTL2) by Curtis, Brian R, Nancy, Cox J, Sullivan, Mia J, Konkashbaev, Anuar, Bowens, Krista, Hansen, Kirk C, Aster, Richard H.

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On Single-Array Genotype Calling Algorithms by Tikhomirov, A., Konkashbaev, A., Nicolae, D.L.

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