Comprehensive follow-up of the first genome-wide association study of multiple sclerosis identifies KIF21B and TMEM39A as susceptibility loci by McCauley, Jacob L., Zuvich, Rebecca L., Beecham, Ashley H., De Jager, Philip L., Konidari, Ioanna, Whitehead, Patrice L., Aubin, Cristin, Ban, Maria, Pobywajlo, Susan, Briskin, Rebeccah, Romano, Susan, Aggarwal, Neelum T., Piccio, Laura, McArdle, Wendy L., Strachan, David P., Evans, Denis, Cross, Anne H., Cree, Bruce, Rioux, John D., Barcellos, Lisa F., Ivinson, Adrian J., Compston, Alastair, Hafler, David A., Hauser, Stephen L., Oksenberg, Jorge R., Sawcer, Stephen J., Pericak-Vance, Margaret A., Haines, Jonathan L.

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Variation Within DNA Repair Pathway Genes and Risk of Multiple Sclerosis by Briggs, Farren B. S., Goldstein, Benjamin A., McCauley, Jacob L., Zuvich, Rebecca L., De Jager, Philip L., Rioux, John D., Ivinson, Adrian J., Compston, Alastair, Hafler, David A., Hauser, Stephen L., Oksenberg, Jorge R., Sawcer, Stephen J., Pericak-Vance, Margaret A., Haines, Jonathan L., Barcellos, Lisa F.

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Genome- and Phenome-Wide Analyses of Cardiac Conduction Identifies Markers of Arrhythmia Risk by RITCHIE, Marylyn D, DENNY, Joshua C, BRADFORD, Yuki, RASMUSSEN, Luke V, PATHAK, Jyotishman, CHUTE, Christopher G, KULLO, Iftikhar J, MCCARTY, Catherine A, CHISHOLM, Rex L, KHO, Abel N, CARLSON, Christopher S, LARSON, Eric B, ZUVICH, Rebecca L, JARVIK, Gail P, SOTOODEHNIA, Nona, MANOLIO, Teri A, RONGLING LI, MASYS, Daniel R, HAINES, Jonathan L, RODEN, Dan M, CRAWFORD, Dana C, SCHILDCROUT, Jonathan S, BASTARACHE, Lisa, RAMIREZ, Andrea H, MOSLEY, Jonathan D, PULLEY, Jill M, BASFORD, Melissa A

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High Density GWAS for LDL Cholesterol in African Americans Using Electronic Medical Records Reveals a Strong Protective Variant in APOE by Rasmussen-Torvik, Laura J., Pacheco, Jennifer A., Wilke, Russell A., Thompson, William K., Ritchie, Marylyn D., Kho, Abel N., Muthalagu, Arun, Hayes, M. Geoff, Armstrong, Loren L., Scheftner, Douglas A., Wilkins, John T., Zuvich, Rebecca L., Crosslin, David, Roden, Dan M., Denny, Joshua C., Jarvik, Gail P., Carlson, Christopher S., Kullo, Iftikhar J., Bielinski, Suzette J., McCarty, Catherine A., Li, Rongling, Manolio, Teri A., Crawford, Dana C., Chisholm, Rex L.

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Interrogating the complex role of chromosome 16p13.13 in multiple sclerosis susceptibility: independent genetic signals in the CIITA-CLEC16A-SOCS1 gene complex by Zuvich, Rebecca L., Bush, William S., McCauley, Jacob L., Beecham, Ashley H., De Jager, Philip L., Ivinson, Adrian J., Compston, Alastair, Hafler, David A., Hauser, Stephen L., Sawcer, Stephen J., Pericak-Vance, Margaret A., Barcellos, Lisa F., Mortlock, Douglas P., Haines, Jonathan L.

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Pitfalls of merging GWAS data: lessons learned in the eMERGE network and quality control procedures to maintain high data quality by Zuvich, Rebecca L., Armstrong, Loren L., Bielinski, Suzette J., Bradford, Yuki, Carlson, Christopher S., Crawford, Dana C., Crenshaw, Andrew T., de Andrade, Mariza, Doheny, Kimberly F., Haines, Jonathan L., Hayes, M. Geoffrey, Jarvik, Gail P., Jiang, Lan, Kullo, Iftikhar J., Li, Rongling, Ling, Hua, Manolio, Teri A., Matsumoto, Martha E., McCarty, Catherine A., McDavid, Andrew N., Mirel, Daniel B., Olson, Lana M., Paschall, Justin E., Pugh, Elizabeth W., Rasmussen, Luke V., Rasmussen-Torvik, Laura J., Turner, Stephen D., Wilke, Russell A., Ritchie, Marylyn D.

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Genetic variation in the IL7RA/IL7 pathway increases multiple sclerosis susceptibility by Zuvich, Rebecca L, McCauley, Jacob L, Oksenberg, Jorge R, Sawcer, Stephen J, De Jager, Philip L, Aubin, Cristin, Cross, Anne H, Piccio, Laura, Aggarwal, Neelum T, Evans, Denis, Hafler, David A, Compston, Alastair, Hauser, Stephen L, Pericak-Vance, Margaret A, Haines, Jonathan L

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CIITA variation in the presence of HLA-DRB11501 increases risk for multiple sclerosis by Bronson, Paola G., Caillier, Stacy, Ramsay, Patricia P., McCauley, Jacob L., Zuvich, Rebecca L., De Jager, Philip L., Rioux, John D., Ivinson, Adrian J., Compston, Alastair, Hafler, David A., Sawcer, Stephen J., Pericak-Vance, Margaret A., Haines, Jonathan L., Hauser, Stephen L., Oksenberg, Jorge R., Barcellos, Lisa F.

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Evidence for CRHR1 in multiple sclerosis using supervised machine learning and meta-analysis in 12 566 individuals by Briggs, Farren B.S., Bartlett, Selena E., Goldstein, Benjamin A., Wang, Joanne, McCauley, Jacob L., Zuvich, Rebecca L., De Jager, Philip L., Rioux, John D., Ivinson, Adrian J., Compston, Alastair, Hafler, David A., Hauser, Stephen L., Oksenberg, Jorge R., Sawcer, Stephen J., Pericak-Vance, Margaret A., Haines, Jonathan L., Barcellos, Lisa F.

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Genome- and Phenome-Wide Analysis of Cardiac Conduction Identifies Markers of Arrhythmia Risk by Ritchie, Marylyn D., Denny, Joshua C., Zuvich, Rebecca L., Crawford, Dana C., Schildcrout, Jonathan S., Bastarache, Lisa, Ramirez, Andrea H., Mosley, Jonathan D., Pulley, Jill M., Basford, Melissa A., Bradford, Yuki, Rasmussen, Luke V., Pathak, Jyotishman, Chute, Christopher G., Kullo, Iftikhar J., McCarty, Catherine A., Chisholm, Rex L., Kho, Abel N., Carlson, Christopher S., Larson, Eric B., Jarvik, Gail P., Sotoodehnia, Nona, Manolio, Teri A., Li, Rongling, Masys, Daniel R., Haines, Jonathan L., Roden, Dan M.

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CIITA variation in the presence of HLA-DRB1 1501 increases risk for multiple sclerosis by BRONSON, Paola G, CAILLIER, Stacy, SAWCER, Stephen J, PERICAK-VANCE, Margaret A, HAINES, Jonathan L, HAUSER, Stephen L, OKSENBERG, Jorge R, BARCELLOS, Lisa F, RAMSAY, Patricia P, MCCAULEY, Jacob L, ZUVICH, Rebecca L, DE JAGER, Philip L, RIOUX, John D, IVINSON, Adrian J, COMPSTON, Alastair, HAFLER, David A

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Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis by Sawcer, Stephen, Hellenthal, Garrett, Pirinen, Matti, Spencer, Chris C A, Patsopoulos, Nikolaos A, Moutsianas, Loukas, Dilthey, Alexander, Su, Zhan, Freeman, Colin, Hunt, Sarah E, Edkins, Sarah, Gray, Emma, Booth, David R, Potter, Simon C, Goris, An, Band, Gavin, Oturai, Annette Bang, Strange, Amy, Saarela, Janna, Bellenguez, Céline, Fontaine, Bertrand, Gillman, Matthew, Hemmer, Bernhard, Gwilliam, Rhian, Zipp, Frauke, Jayakumar, Alagurevathi, Martin, Roland, Leslie, Stephen, Hawkins, Stanley, Giannoulatou, Eleni, D'alfonso, Sandra, Blackburn, Hannah, Martinelli Boneschi, Filippo, Liddle, Jennifer, Harbo, Hanne F, Perez, Marc L, Spurkland, Anne, Waller, Matthew J, Mycko, Marcin P, Ricketts, Michelle, Comabella, Manuel, Hammond, Naomi, Kockum, Ingrid, McCann, Owen T, Ban, Maria, Whittaker, Pamela, Kemppinen, Anu, Weston, Paul, Hawkins, Clive, Widaa, Sara, Zajicek, John, Dronov, Serge, Robertson, Neil, Bumpstead, Suzannah J, Barcellos, Lisa F, Ravindrarajah, Rathi, Abraham, Roby, Alfredsson, Lars, Ardlie, Kristin, Aubin, Cristin, Baker, Amie, Baker, Katharine, Baranzini, Sergio E, Bergamaschi, Laura, Bergamaschi, Roberto, Bernstein, Allan, Berthele, Achim, Boggild, Mike, Bradfield, Jonathan P, Brassat, David, Broadley, Simon A, Buck, Dorothea, Butzkueven, Helmut, Capra, Ruggero, Carroll, William M, Cavalla, Paola, Celius, Elisabeth G, Cepok, Sabine, Chiavacci, Rosetta, Clerget-Darpoux, Françoise, Clysters, Katleen, Comi, Giancarlo, Cossburn, Mark, Cournu-Rebeix, Isabelle, Cox, Mathew B, Cozen, Wendy, Cree, Bruce A C, Cross, Anne H, Cusi, Daniele, Daly, Mark J, Davis, Emma, de Bakker, Paul I W, Debouverie, Marc, D'hooghe, Marie Beatrice, Dixon, Katherine, Dobosi, Rita, Dubois, Bénédicte, Ellinghaus, David, Elovaara, Irina, Esposito, Federica

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Enhancing the power of genetic association studies through the use of silver standard cases derived from electronic medical records by McDavid, Andrew, Crane, Paul K, Newton, Katherine M, Crosslin, David R, McCormick, Wayne, Weston, Noah, Ehrlich, Kelly, Hart, Eugene, Harrison, Robert, Kukull, Walter A, Rottscheit, Carla, Peissig, Peggy, Stefanski, Elisha, McCarty, Catherine A, Zuvich, Rebecca Lynn, Ritchie, Marylyn D, Haines, Jonathan L, Denny, Joshua C, Schellenberg, Gerard D, de Andrade, Mariza, Kullo, Iftikhar, Li, Rongling, Mirel, Daniel, Crenshaw, Andrew, Bowen, James D, Li, Ge, Tsuang, Debby, McCurry, Susan, Teri, Linda, Larson, Eric B, Jarvik, Gail P, Carlson, Chris S

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Variants Near FOXE1 Are Associated with Hypothyroidism and Other Thyroid Conditions: Using Electronic Medical Records for Genome- and Phenome-wide Studies by Denny, Joshua C., Crawford, Dana C., Ritchie, Marylyn D., Bielinski, Suzette J., Basford, Melissa A., Bradford, Yuki, Chai, High Seng, Bastarache, Lisa, Zuvich, Rebecca, Peissig, Peggy, Carrell, David, Ramirez, Andrea H., Pathak, Jyotishman, Wilke, Russell A., Rasmussen, Luke, Wang, Xiaoming, Pacheco, Jennifer A., Kho, Abel N., Hayes, M. Geoffrey, Weston, Noah, Matsumoto, Martha, Kopp, Peter A., Newton, Katherine M., Jarvik, Gail P., Li, Rongling, Manolio, Teri A., Kullo, Iftikhar J., Chute, Christopher G., Chisholm, Rex L., Larson, Eric B., McCarty, Catherine A., Masys, Daniel R., Roden, Dan M., de Andrade, Mariza

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The National Patient-Centered Clinical Research Network (PCORnet) Bariatric Study Cohort: Rationale, Methods, and Baseline Characteristics by Toh, Sengwee, Rasmussen-Torvik, Laura J, Harmata, Emily E, Pardee, Roy, Saizan, Rosalinde, Malanga, Elisha, Sturtevant, Jessica L, Horgan, Casie E, Anau, Jane, Janning, Cheri D, Wellman, Robert D, Coley, R Yates, Cook, Andrea J, Courcoulas, Anita P, Coleman, Karen J, Williams, Neely A, McTigue, Kathleen M, Arterburn, David, McClay, James

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