Genome-wide association and meta-analysis in populations from Starr County, Texas, and Mexico City identify type 2 diabetes susceptibility loci and enrichment for expression quanti... by Below, J. E., Gamazon, E. R., Morrison, J. V., Konkashbaev, A., Pluzhnikov, A., McKeigue, P. M., Parra, E. J., Elbein, S. C., Hallman, D. M., Nicolae, D. L., Bell, G. I., Cruz, M., Cox, N. J., Hanis, C. L.

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Transcriptomic variation of pharmacogenes in multiple human tissues and lymphoblastoid cell lines by Chhibber, A, French, C E, Yee, S W, Gamazon, E R, Theusch, E, Qin, X, Webb, A, Papp, A C, Wang, A, Simmons, C Q, Konkashbaev, A, Chaudhry, A S, Mitchel, K, Stryke, D, Ferrin, T E, Weiss, S T, Kroetz, D L, Sadee, W, Nickerson, D A, Krauss, R M, George, A L, Schuetz, E G, Medina, M W, Cox, N J, Scherer, S E, Giacomini, K M, Brenner, S E

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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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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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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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An assessment of disruption erosion in the ITER environment by Hassanein, A

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

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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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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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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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Integrated simulation of plasma surface interaction during edge localized modes and disruptions: Self-consistent approach by Hassanein, A., Sizyuk, T., Konkashbaev, I.

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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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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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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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Comprehensive physical models and simulation package for plasma/material interactions during plasma instabilities by Hassanein, A, Konkashbaev, I

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Comprehensive modeling of ELMs and their effect on plasma-facing surfaces during normal tokamak operation by Hassanein, A., Konkashbaev, I.

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Triggers for RF breakdown by Norem, J., Insepov, Z., Konkashbaev, I.

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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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