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

Autor 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.
Vydáno 2012

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

Autor 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.
Vydáno 2013

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

Autor 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.
Vydáno 2009

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

Autor 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.
Vydáno 2010

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

Autor 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.
Vydáno 2011

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

Autor 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
Vydáno 2012

Variation Within DNA Repair Pathway Genes and Risk of Multiple Sclerosis

Autor 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.
Vydáno 2010

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

Autor 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.
Vydáno 2010

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

Autor 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.
Vydáno 2010

A non-synonymous SNP within membrane metalloendopeptidase-like 1 (MMEL1) is associated with multiple sclerosis

Autor Ban, Maria, McCauley, Jacob L., Zuvich, Rebecca, Baker, Amie, Bergamaschi, Laura, Cox, Mathew, Kemppinen, Anu, D’Alfonso, Sandra, Guerini, Franca R., Lechner-Scott, Jeannette, Dudbridge, Frank, Wason, James, Robertson, Neil P., De Jager, Philip L., Hafler, David A., Barcellos, Lisa F., Ivinson, Adrian J., Sexton, David, Oksenberg, Jorge R., Hauser, Stephen L., Pericak-Vance, Margaret A., Haines, Jonathan, Compston, Alastair, Sawcer, Stephen
Vydáno 2010

Quality Control Procedures for Genome Wide Association Studies

Autor 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.
Vydáno 2011

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

Autor 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.
Vydáno 2012

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

Autor 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.
Vydáno 2013

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

Autor 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.
Vydáno 2010

Enhancing the Power of Genetic Association Studies through the Use of Silver Standard Cases Derived from Electronic Medical Records

Autor 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.
Vydáno 2013

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

Autor 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.
Vydáno 2011

Variants Near FOXE1 Are Associated with Hypothyroidism and Other Thyroid Conditions: Using Electronic Medical Records for Genome- and Phenome-wide Studies

Autor 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
Vydáno 2011

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

Autor 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, Boneschi, Filippo Martinelli, 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, Fontenille, Claire, Foote, Simon, Franke, Andre, Galimberti, Daniela, Ghezzi, Angelo, Glessner, Joseph, Gomez, Refujia, Gout, Olivier, Graham, Colin, Grant, Struan F.A., Guerini, Franca Rosa, Hakonarson, Hakon, Hall, Per, Hamsten, Anders, Hartung, Hans-Peter, Heard, Rob N., Heath, Simon, Hobart, Jeremy, Hoshi, Muna, Infante-Duarte, Carmen, Ingram, Gillian, Ingram, Wendy, Islam, Talat, Jagodic, Maja, Kabesch, Michael, Kermode, Allan G., Kilpatrick, Trevor J., Kim, Cecilia, Klopp, Norman, Koivisto, Keijo, Larsson, Malin, Lathrop, Mark, Lechner-Scott, Jeannette S., Leone, Maurizio A., Leppä, Virpi, Liljedahl, Ulrika, Bomfim, Izaura Lima, Lincoln, Robin R., Link, Jenny, Liu, Jianjun, Lorentzen, Åslaug R., Lupoli, Sara, Macciardi, Fabio, Mack, Thomas, Marriott, Mark, Martinelli, Vittorio, Mason, Deborah, McCauley, Jacob L., Mentch, Frank, Mero, Inger-Lise, Mihalova, Tania, Montalban, Xavier, Mottershead, John, Myhr, Kjell-Morten, Naldi, Paola, Ollier, William, Page, Alison, Palotie, Aarno, Pelletier, Jean, Piccio, Laura, Pickersgill, Trevor, Piehl, Fredrik, Pobywajlo, Susan, Quach, Hong L., Ramsay, Patricia P., Reunanen, Mauri, Reynolds, Richard, Rioux, John D., Rodegher, Mariaemma, Roesner, Sabine, Rubio, Justin P., Rückert, Ina-Maria, Salvetti, Marco, Salvi, Erika, Santaniello, Adam, Schaefer, Catherine A., Schreiber, Stefan, Schulze, Christian, Scott, Rodney J., Sellebjerg, Finn, Selmaj, Krzysztof W., Sexton, David, Shen, Ling, Simms-Acuna, Brigid, Skidmore, Sheila, Sleiman, Patrick M.A., Smestad, Cathrine, Sørensen, Per Soelberg, Søndergaard, Helle Bach, Stankovich, Jim, Strange, Richard C., Sulonen, Anna-Maija, Sundqvist, Emilie, Syvänen, Ann-Christine, Taddeo, Francesca, Taylor, Bruce, Blackwell, Jenefer M., Tienari, Pentti, Bramon, Elvira, Tourbah, Ayman, Brown, Matthew A., Tronczynska, Ewa, Casas, Juan P., Tubridy, Niall, Corvin, Aiden, Vickery, Jane, Jankowski, Janusz, Villoslada, Pablo, Markus, Hugh S., Wang, Kai, Mathew, Christopher G., Wason, James, Palmer, Colin N.A., Wichmann, H-Erich, Plomin, Robert, Willoughby, Ernest, Rautanen, Anna, Winkelmann, Juliane, Wittig, Michael, Trembath, Richard C., Yaouanq, Jacqueline, Viswanathan, Ananth C., Zhang, Haitao, Wood, Nicholas W., Zuvich, Rebecca, Deloukas, Panos, Langford, Cordelia, Duncanson, Audrey, Oksenberg, Jorge R., Pericak-Vance, Margaret A., Haines, Jonathan L., Olsson, Tomas, Hillert, Jan, Ivinson, Adrian J., De Jager, Philip L., Peltonen, Leena, Stewart, Graeme J., Hafler, David A., Hauser, Stephen L., McVean, Gil, Donnelly, Peter, Compston, Alastair
Vydáno 2011

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

Autor 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
Vydáno 2014