Mapping the Incidentalome: Estimating Incidental Findings Generated Through Clinical Pharmacogenomics Testing

Por Westbrook, Matthew J., Wright, M. Frances, Van Driest, Sara L., McGregor, Tracy L., Denny, Joshua C., Zuvich, Rebecca L., Clayton, Ellen Wright, Brothers, Kyle B.
Publicado em 2012

Genetic variants associated with angiotensin-converting enzyme inhibitor-associated angioedema

Por Pare, Guillaume, Kubo, Michiaki, Byrd, James B., McCarty, Catherine A., Woodard-Grice, Alencia, Teo, Koon K., Anand, Sonia S., Zuvich, Rebecca L., Bradford, Yuki, Ross, Stephanie, Nakamura, Yusuke, Ritchie, Marylyn, Brown, Nancy J.
Publicado em 2013

Follow-up examination of linkage and association to chromosome 1q43 in multiple sclerosis

Por McCauley, Jacob L., Zuvich, Rebecca L., Bradford, Yuki, Kenealy, Shannon J., Schnetz-Boutaud, Nathalie, Gregory, Simon G., Hauser, Stephen L., Oksenberg, Jorge R., Mortlock, Douglas P., Pericak-Vance, Margaret A., Haines, Jonathan L.
Publicado em 2009

Genetic Variation in the IL7RA/IL7 Pathway Increases Multiple Sclerosis Susceptibility

Por 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.
Publicado em 2010

Interrogating the complex role of chromosome 16p13.13 in multiple sclerosis susceptibility: independent genetic signals in the CIITA–CLEC16A–SOCS1 gene complex

Por 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.
Publicado em 2011

Predicting warfarin dosage in European–Americans and African–Americans using DNA samples linked to an electronic health record

Por Ramirez, Andrea H, Shi, Yaping, Schildcrout, Jonathan S, Delaney, Jessica T, Xu, Hua, Oetjens, Matthew T, Zuvich, Rebecca L, Basford, Melissa A, Bowton, Erica, Jiang, Min, Speltz, Peter, Zink, Raquel, Cowan, James, Pulley, Jill M, Ritchie, Marylyn D, Masys, Daniel R, Roden, Dan M, Crawford, Dana C, Denny, Joshua C
Publicado em 2012

Variation Within DNA Repair Pathway Genes and Risk of Multiple Sclerosis

Por 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.
Publicado em 2010

CIITA variation in the presence of HLA-DRB1*1501 increases risk for multiple sclerosis

Por 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.
Publicado em 2010

Evidence for CRHR1 in multiple sclerosis using supervised machine learning and meta-analysis in 12 566 individuals

Por 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.
Publicado em 2010

Quality Control Procedures for Genome Wide Association Studies

Por Turner, Stephen, Armstrong, Loren L., Bradford, Yuki, Carlson, Christopher S., Crawford, Dana C., Crenshaw, Andrew T., de Andrade, Mariza, Doheny, Kimberly F., Haines, Jonathan L., Hayes, Geoffrey, Jarvik, Gail, Jiang, Lan, Kullo, Iftikhar J., Li, Rongling, Ling, Hua, Manolio, Teri A., Matsumoto, Martha, McCarty, Catherine A., McDavid, Andrew N., Mirel, Daniel B., Paschall, Justin E., Pugh, Elizabeth W., Rasmussen, Luke V., Wilke, Russell A., Zuvich, Rebecca L., Ritchie, Marylyn D.
Publicado em 2011

High Density GWAS for LDL Cholesterol in African Americans Using Electronic Medical Records Reveals a Strong Protective Variant in APOE

Por 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.
Publicado em 2012

Genome- and Phenome-Wide Analysis of Cardiac Conduction Identifies Markers of Arrhythmia Risk

Por 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.
Publicado em 2013

Comprehensive follow-up of the first genome-wide association study of multiple sclerosis identifies KIF21B and TMEM39A as susceptibility loci

Por 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.
Publicado em 2010

Pitfalls of Merging GWAS Data: Lessons Learned in the eMERGE Network and Quality Control Procedures to Maintain High Data Quality

Por 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.
Publicado em 2011

Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization

Por Arking, Dan E., Pulit, Sara L., Crotti, Lia, van der Harst, Pim, Munroe, Patricia B., Koopmann, Tamara T., Sotoodehnia, Nona, Rossin, Elizabeth J., Morley, Michael, Wang, Xinchen, Johnson, Andrew D., Lundby, Alicia, Gudbjartsson, Daníel F., Noseworthy, Peter A., Eijgelsheim, Mark, Bradford, Yuki, Tarasov, Kirill V., Dörr, Marcus, Müller-Nurasyid, Martina, Lahtinen, Annukka M., Nolte, Ilja M., Smith, Albert Vernon, Bis, Joshua C., Isaacs, Aaron, Newhouse, Stephen J., Evans, Daniel S., Post, Wendy S., Waggott, Daryl, Lyytikäinen, Leo-Pekka, Hicks, Andrew A., Eisele, Lewin, Ellinghaus, David, Hayward, Caroline, Navarro, Pau, Ulivi, Sheila, Tanaka, Toshiko, Tester, David J., Chatel, Stéphanie, Gustafsson, Stefan, Kumari, Meena, Morris, Richard W., Naluai, Åsa T., Padmanabhan, Sandosh, Kluttig, Alexander, Strohmer, Bernhard, Panayiotou, Andrie G., Torres, Maria, Knoflach, Michael, Hubacek, Jaroslav A., Slowikowski, Kamil, Raychaudhuri, Soumya, Kumar, Runjun D., Harris, Tamara B., Launer, Lenore J., Shuldiner, Alan R., Alonso, Alvaro, Bader, Joel S., Ehret, Georg, Huang, Hailiang, Kao, W.H. Linda, Strait, James B., Macfarlane, Peter W., Brown, Morris, Caulfield, Mark J., Samani, Nilesh J., Kronenberg, Florian, Willeit, Johann, Smith, J. Gustav, Greiser, Karin H., zu Schwabedissen, Henriette Meyer, Werdan, Karl, Carella, Massimo, Zelante, Leopoldo, Heckbert, Susan R., Psaty, Bruce M., Rotter, Jerome I., Kolcic, Ivana, Polašek, Ozren, Wright, Alan F., Griffin, Maura, Daly, Mark J., Arnar, David O., Hólm, Hilma, Thorsteinsdottir, Unnur, Denny, Joshua C., Roden, Dan M., Zuvich, Rebecca L., Emilsson, Valur, Plump, Andrew S., Larson, Martin G., O'Donnell, Christopher J., Yin, Xiaoyan, Bobbo, Marco, D'Adamo, Adamo P., Iorio, Annamaria, Sinagra, Gianfranco, Carracedo, Angel, Cummings, Steven R., Nalls, Michael A., Jula, Antti, Kontula, Kimmo K., Marjamaa, Annukka, Oikarinen, Lasse, Perola, Markus, Porthan, Kimmo, Erbel, Raimund, Hoffmann, Per, Jöckel, Karl-Heinz, Kälsch, Hagen, Nöthen, Markus M., consortium, HRGEN, den Hoed, Marcel, Loos, Ruth J.F., Thelle, Dag S., Gieger, Christian, Meitinger, Thomas, Perz, Siegfried, Peters, Annette, Prucha, Hanna, Sinner, Moritz F., Waldenberger, Melanie, de Boer, Rudolf A., Franke, Lude, van der Vleuten, Pieter A., Beckmann, Britt Maria, Martens, Eimo, Bardai, Abdennasser, Hofman, Nynke, Wilde, Arthur A.M., Behr, Elijah R., Dalageorgou, Chrysoula, Giudicessi, John R., Medeiros-Domingo, Argelia, Barc, Julien, Kyndt, Florence, Probst, Vincent, Ghidoni, Alice, Insolia, Roberto, Hamilton, Robert M., Scherer, Stephen W., Brandimarto, Jeffrey, Margulies, Kenneth, Moravec, Christine E., Fabiola Del, Greco M., Fuchsberger, Christian, O'Connell, Jeffrey R., Lee, Wai K., Watt, Graham C.M., Campbell, Harry, Wild, Sarah H., El Mokhtari, Nour E., Frey, Norbert, Asselbergs, Folkert W., Leach, Irene Mateo, Navis, Gerjan, van den Berg, Maarten P., van Veldhuisen, Dirk J., Kellis, Manolis, Krijthe, Bouwe P., Franco, Oscar H., Hofman, Albert, Kors, Jan A., Uitterlinden, André G., Witteman, Jacqueline C.M., Kedenko, Lyudmyla, Lamina, Claudia, Oostra, Ben A., Abecasis, Gonçalo R., Lakatta, Edward G., Mulas, Antonella, Orrú, Marco, Schlessinger, David, Uda, Manuela, Markus, Marcello R.P., Völker, Uwe, Snieder, Harold, Spector, Timothy D., Ärnlöv, Johan, Lind, Lars, Sundström, Johan, Syvänen, Ann-Christine, Kivimaki, Mika, Kähönen, Mika, Mononen, Nina, Raitakari, Olli T., Viikari, Jorma S., Adamkova, Vera, Kiechl, Stefan, Brion, Maria, Nicolaides, Andrew N., Paulweber, Bernhard, Haerting, Johannes, Dominiczak, Anna F., Nyberg, Fredrik, Whincup, Peter H., Hingorani, Aroon, Schott, Jean-Jacques, Bezzina, Connie R., Ingelsson, Erik, Ferrucci, Luigi, Gasparini, Paolo, Wilson, James F., Rudan, Igor, Franke, Andre, Mühleisen, Thomas W., Pramstaller, Peter P., Lehtimäki, Terho J., Paterson, Andrew D., Parsa, Afshin, Liu, Yongmei, van Duijn, Cornelia, Siscovick, David S., Gudnason, Vilmundur, Jamshidi, Yalda, Salomaa, Veikko, Felix, Stephan B., Sanna, Serena, Ritchie, Marylyn D., Stricker, Bruno H., Stefansson, Kari, Boyer, Laurie A., Cappola, Thomas P., Olsen, Jesper V., Lage, Kasper, Schwartz, Peter J., Kääb, Stefan, Chakravarti, Aravinda, Ackerman, Michael J., Pfeufer, Arne, de Bakker, Paul I.W., Newton-Cheh, Christopher
Publicado em 2014