Association of low-frequency and rare coding variants with information processing speed

por Bressler, Jan, Davies, Gail, Smith, Albert V., Saba, Yasaman, Bis, Joshua C., Jian, Xueqiu, Hayward, Caroline, Yanek, Lisa, Smith, Jennifer A., Mirza, Saira S., Wang, Ruiqi, Adams, Hieab H. H., Becker, Diane, Boerwinkle, Eric, Campbell, Archie, Cox, Simon R., Eiriksdottir, Gudny, Fawns-Ritchie, Chloe, Gottesman, Rebecca F., Grove, Megan L., Guo, Xiuqing, Hofer, Edith, Kardia, Sharon L. R., Knol, Maria J., Koini, Marisa, Lopez, Oscar L., Marioni, Riccardo E., Nyquist, Paul, Pattie, Alison, Polasek, Ozren, Porteous, David J., Rudan, Igor, Satizabal, Claudia L., Schmidt, Helena, Schmidt, Reinhold, Sidney, Stephen, Simino, Jeannette, Smith, Blair H., Turner, Stephen T., van der Lee, Sven J., Ware, Erin B., Whitmer, Rachel A., Yaffe, Kristine, Yang, Qiong, Zhao, Wei, Gudnason, Vilmundur, Launer, Lenore J., Fitzpatrick, Annette L., Psaty, Bruce M., Fornage, Myriam, Arfan Ikram, M., van Duijn, Cornelia M., Seshadri, Sudha, Mosley, Thomas H., Deary, Ian J.
Publicado 2021

Correction: Association of low-frequency and rare coding variants with information processing speed

por Bressler, Jan, Davies, Gail, Smith, Albert V., Saba, Yasaman, Bis, Joshua C., Jian, Xueqiu, Hayward, Caroline, Yanek, Lisa, Smith, Jennifer A., Mirza, Saira S., Wang, Ruiqi, Adams, Hieab H. H., Becker, Diane, Boerwinkle, Eric, Campbell, Archie, Cox, Simon R., Eiriksdottir, Gudny, Fawns-Ritchie, Chloe, Gottesman, Rebecca F., Grove, Megan L., Guo, Xiuqing, Hofer, Edith, Kardia, Sharon L. R., Knol, Maria J., Koini, Marisa, Lopez, Oscar L., Marioni, Riccardo E., Nyquist, Paul, Pattie, Alison, Polasek, Ozren, Porteous, David J., Rudan, Igor, Satizabal, Claudia L., Schmidt, Helena, Schmidt, Reinhold, Sidney, Stephen, Simino, Jeannette, Smith, Blair H., Turner, Stephen T., van der Lee, Sven J., Ware, Erin B., Whitmer, Rachel A., Yaffe, Kristine, Yang, Qiong, Zhao, Wei, Gudnason, Vilmundur, Launer, Lenore J., Fitzpatrick, Annette L., Psaty, Bruce M., Fornage, Myriam, Arfan Ikram, M., van Duijn, Cornelia M., Seshadri, Sudha, Mosley, Thomas H., Deary, Ian J.
Publicado 2022

Carriers of rare damaging CCR2 genetic variants are at lower risk of atherosclerotic disease

por Georgakis, Marios K., Malik, Rainer, Hasbani, Natalie R., Shakt, Gabrielle, Morrison, Alanna C., Tsao, Noah L., Judy, Renae, Mitchell, Braxton D., Xu, Huichun, Montasser, May E., Do, Ron, Kenny, Eimear E., Loos, Ruth J.F., Terry, James G., Carr, John Jeffrey, Bis, Joshua C., Psaty, Bruce M., Longstreth, W. T., Young, Kendra A, Lutz, Sharon M, Cho, Michael H, Broome, Jai, Khan, Alyna T., Wang, Fei Fei, Heard-Costa, Nancy, Seshadri, Sudha, Vasan, Ramachandran S., Palmer, Nicholette D., Freedman, Barry I., Bowden, Donald W., Yanek, Lisa R., Kral, Brian G., Becker, Lewis C., Peyser, Patricia A., Bielak, Lawrence F., Ammous, Farah, Carson, April P., Hall, Michael E., Raffield, Laura M., Rich, Stephen S., Post, Wendy S., Tracy, Russel P., Taylor, Kent D., Guo, Xiuqing, Mahaney, Michael C., Curran, Joanne E., Blangero, John, Clarke, Shoa L., Haessler, Jeffrey W., Hu, Yao, Assimes, Themistocles L., Kooperberg, Charles, Damrauer, Scott M., Rotter, Jerome I., de Vries, Paul S., Dichgans, Martin
Publicado 2023

Drug-Gene Interactions of Antihypertensive Medications and Risk of Incident Cardiovascular Disease: A Pharmacogenomics Study from the CHARGE Consortium

por Bis, Joshua C., Sitlani, Colleen, Irvin, Ryan, Avery, Christy L., Smith, Albert Vernon, Sun, Fangui, Evans, Daniel S., Musani, Solomon K., Li, Xiaohui, Trompet, Stella, Krijthe, Bouwe P., Harris, Tamara B., Quibrera, P. Miguel, Brody, Jennifer A., Demissie, Serkalem, Davis, Barry R., Wiggins, Kerri L., Tranah, Gregory J., Lange, Leslie A., Sotoodehnia, Nona, Stott, David J., Franco, Oscar H., Launer, Lenore J., Stürmer, Til, Taylor, Kent D., Cupples, L. Adrienne, Eckfeldt, John H., Smith, Nicholas L., Liu, Yongmei, Wilson, James G., Heckbert, Susan R., Buckley, Brendan M., Ikram, M. Arfan, Boerwinkle, Eric, Chen, Yii-Der Ida, de Craen, Anton J. M., Uitterlinden, Andre G., Rotter, Jerome I., Ford, Ian, Hofman, Albert, Sattar, Naveed, Slagboom, P. Eline, Westendorp, Rudi G. J., Gudnason, Vilmundur, Vasan, Ramachandran S., Lumley, Thomas, Cummings, Steven R., Taylor, Herman A., Post, Wendy, Jukema, J. Wouter, Stricker, Bruno H., Whitsel, Eric A., Psaty, Bruce M., Arnett, Donna
Publicado 2015

Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium

por Ganesh, Santhi K., Zakai, Neil A., van Rooij, Frank J A., Soranzo, Nicole, Smith, Albert V., Nalls, Michael A., Chen, Ming-Huei, Kottgen, Anna, Glazer, Nicole L., Dehghan, Abbas, Kuhnel, Brigitte, Aspelund, Thor, Yang, Qiong, Tanaka, Toshiko, Jaffe, Andrew, Bis, Joshua C M., Verwoert, Germaine C., Teumer, Alexander, Fox, Caroline S., Guralnik, Jack M., Ehret, Georg B., Rice, Kenneth, Felix, Janine F., Rendon, Augusto, Eiriksdottir, Gudny, Levy, Daniel, Patel, Kushang V., Boerwinkle, Eric, Rotter, Jerome I., Hofman, Albert, Sambrook, Jennifer G., Hernandez, Dena, Zheng, Gang, Bandinelli, Stefania, Singleton, Andrew B., Coresh, Josef, Lumley, Thomas, Uitterlinden, André G., vanGils, Janine M., Launer, Lenore J., Cupples, L. Adrienne, Oostra, Ben A., Zwaginga, Jaap-Jan, Ouwehand, Willem H., Thein, Swee-Lay, Meisinger, Christa, Deloukas, Panos, Nauck, Matthias, Spector, Tim, Gieger, Christian, Gudnason, Vilmundur, van Duijn, Cornelia M., Psaty, Bruce M., Ferrucci, Luigi, Chakravarti, Aravinda, Greinacher, Andreas, O’Donnell, Christopher J., Witteman, Jacqueline C M., Furth, Susan, Cushman, Mary, Harris, Tamara B., Lin, Jing-Ping
Publicado 2009

Genetic variation at 16q24.2 is associated with small vessel stroke

por Traylor, Matthew, Malik, Rainer, Nalls, Mike A., Cotlarciuc, Ioana, Radmanesh, Farid, Thorleifsson, Gudmar, Hanscombe, Ken B., Langefeld, Carl, Saleheen, Danish, Rost, Natalia S., Yet, Idil, Spector, Tim D., Bell, Jordana T., Hannon, Eilis, Mill, Jonathan, Chauhan, Ganesh, Debette, Stephanie, Bis, Joshua C., Longstreth, W.T., Ikram, M. Arfan, Launer, Lenore J., Seshadri, Sudha, Hamilton‐Bruce, Monica Anne, Jimenez‐Conde, Jordi, Cole, John W., Schmidt, Reinhold, Słowik, Agnieszka, Lemmens, Robin, Lindgren, Arne, Melander, Olle, Grewal, Raji P., Sacco, Ralph L., Rundek, Tatjana, Rexrode, Kathryn, Arnett, Donna K., Johnson, Julie A., Benavente, Oscar R., Wasssertheil‐Smoller, Sylvia, Lee, Jin‐Moo, Pulit, Sara L., Wong, Quenna, Rich, Stephen S., de Bakker, Paul I.W., McArdle, Patrick F., Woo, Daniel, Anderson, Christopher D., Xu, Huichun, Heitsch, Laura, Fornage, Myriam, Jern, Christina, Stefansson, Kari, Thorsteinsdottir, Unnur, Gretarsdottir, Solveig, Lewis, Cathryn M., Sharma, Pankaj, Sudlow, Cathie L.M., Rothwell, Peter M., Boncoraglio, Giorgio B., Thijs, Vincent, Levi, Chris, Meschia, James F., Rosand, Jonathan, Kittner, Steven J., Mitchell, Braxton D., Dichgans, Martin, Worrall, Bradford B., Markus, Hugh S.
Publicado 2017

Large-scale pharmacogenomic study of sulfonylureas and the QT, JT, and QRS intervals: CHARGE Pharmacogenomics Working Group

por Floyd, James S, Sitlani, Colleen M, Avery, Christy L, Noordam, Raymond, Li, Xiaohui, Smith, Albert V, Gogarten, Stephanie M, Li, Jin, Broer, Linda, Evans, Daniel S, Trompet, Stella, Brody, Jennifer A, Stewart, James D, Eicher, John D, Seyerle, Amanda A, Roach, Jeffrey, Lange, Leslie A, Lin, Henry J, Kors, Jan A, Harris, Tamara B, Li-Gao, Ruifang, Sattar, Naveed, Cummings, Steven R, Wiggins, Kerri L, Napier, Melanie D, Stürmer, Til, Bis, Joshua C, Kerr, Kathleen F, Uitterlinden, André G, Taylor, Kent D, Stott, David J, de Mutsert, Renée, Launer, Lenore J, Busch, Evan L, Méndez-Giráldez, Raúl, Sotoodehnia, Nona, Soliman, Elsayed Z, Li, Yun, Duan, Qing, Rosendaal, Frits R, Slagboom, P Eline, Wilhelmsen, Kirk C, Reiner, Alexander P, Chen, Yii-Der I, Heckbert, Susan R, Kaplan, Robert C, Rice, Kenneth M, Jukema, J Wouter, Johnson, Andrew D, Liu, Yongmei, Mook-Kanamori, Dennis O, Gudnason, Vilmundur, Wilson, James G, Rotter, Jerome I, Laurie, Cathy C, Psaty, Bruce M, Whitsel, Eric A, Cupples, L Adrienne, Stricker, Bruno H
Publicado 2016

A genome-wide association study identifies genetic loci associated with specific lobar brain volumes

por van der Lee, Sven J., Knol, Maria J., Chauhan, Ganesh, Satizabal, Claudia L., Smith, Albert Vernon, Hofer, Edith, Bis, Joshua C., Hibar, Derrek P., Hilal, Saima, van den Akker, Erik B., Arfanakis, Konstantinos, Bernard, Manon, Yanek, Lisa R., Amin, Najaf, Crivello, Fabrice, Cheung, Josh W., Harris, Tamara B., Saba, Yasaman, Lopez, Oscar L., Li, Shuo, van der Grond, Jeroen, Yu, Lei, Paus, Tomas, Roshchupkin, Gennady V., Amouyel, Philippe, Jahanshad, Neda, Taylor, Kent D., Yang, Qiong, Mathias, Rasika A., Boehringer, Stefan, Mazoyer, Bernard, Rice, Ken, Cheng, Ching Yu, Maillard, Pauline, van Heemst, Diana, Wong, Tien Yin, Niessen, Wiro J., Beiser, Alexa S., Beekman, Marian, Zhao, Wanting, Nyquist, Paul A., Chen, Christopher, Launer, Lenore J., Psaty, Bruce M., Ikram, M. Kamran, Vernooij, Meike W., Schmidt, Helena, Pausova, Zdenka, Becker, Diane M., De Jager, Philip L., Thompson, Paul M., van Duijn, Cornelia M., Bennett, David A., Slagboom, P. Eline, Schmidt, Reinhold, Longstreth, W. T., Ikram, M. Arfan, Seshadri, Sudha, Debette, Stéphanie, Gudnason, Vilmundur, Adams, Hieab H. H., DeCarli, Charles
Publicado 2019

Gene-mapping study of extremes of cerebral small vessel disease reveals TRIM47 as a strong candidate

por Mishra, Aniket, Duplaà, Cécile, Vojinovic, Dina, Suzuki, Hideaki, Sargurupremraj, Muralidharan, Zilhão, Nuno R, Li, Shuo, Bartz, Traci M, Jian, Xueqiu, Zhao, Wei, Hofer, Edith, Wittfeld, Katharina, Harris, Sarah E, van der Auwera-Palitschka, Sandra, Luciano, Michelle, Bis, Joshua C, Adams, Hieab H H, Satizabal, Claudia L, Gottesman, Rebecca F, Gampawar, Piyush G, Bülow, Robin, Weiss, Stefan, Yu, Miao, Bastin, Mark E, Lopez, Oscar L, Vernooij, Meike W, Beiser, Alexa S, Völker, Uwe, Kacprowski, Tim, Soumare, Aicha, Smith, Jennifer A, Knopman, David S, Morris, Zoe, Zhu, Yicheng, Rotter, Jerome I, Dufouil, Carole, Valdés Hernández, Maria, Muñoz Maniega, Susana, Lathrop, Mark, Boerwinkle, Erik, Schmidt, Reinhold, Ihara, Masafumi, Mazoyer, Bernard, Yang, Qiong, Joutel, Anne, Tournier-Lasserve, Elizabeth, Launer, Lenore J, Deary, Ian J, Mosley, Thomas H, Amouyel, Philippe, DeCarli, Charles S, Psaty, Bruce M, Tzourio, Christophe, Kardia, Sharon L R, Grabe, Hans J, Teumer, Alexander, van Duijn, Cornelia M, Schmidt, Helena, Wardlaw, Joanna M, Ikram, M Arfan, Fornage, Myriam, Gudnason, Vilmundur, Seshadri, Sudha, Matthews, Paul M, Longstreth, William T, Couffinhal, Thierry, Debette, Stephanie
Publicado 2022

A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studies

por Li, Xihao, Chen, Han, Selvaraj, Margaret Sunitha, Van Buren, Eric, Zhou, Hufeng, Wang, Yuxuan, Sun, Ryan, McCaw, Zachary R., Yu, Zhi, Arnett, Donna K., Bis, Joshua C., Blangero, John, Boerwinkle, Eric, Bowden, Donald W., Brody, Jennifer A., Cade, Brian E., Carson, April P., Carlson, Jenna C., Chami, Nathalie, Chen, Yii-Der Ida, Curran, Joanne E., de Vries, Paul S., Fornage, Myriam, Franceschini, Nora, Freedman, Barry I., Gu, Charles, Heard-Costa, Nancy L., He, Jiang, Hou, Lifang, Hung, Yi-Jen, Irvin, Marguerite R., Kaplan, Robert C., Kardia, Sharon L.R., Kelly, Tanika, Konigsberg, Iain, Kooperberg, Charles, Kral, Brian G., Li, Changwei, Loos, Ruth J.F., Mahaney, Michael C., Martin, Lisa W., Mathias, Rasika A., Minster, Ryan L., Mitchell, Braxton D., Montasser, May E., Morrison, Alanna C., Palmer, Nicholette D., Peyser, Patricia A., Psaty, Bruce M., Raffield, Laura M., Redline, Susan, Reiner, Alexander P., Rich, Stephen S., Sitlani, Colleen M., Smith, Jennifer A., Taylor, Kent D., Tiwari, Hemant, Vasan, Ramachandran S., Wang, Zhe, Yanek, Lisa R., Yu, Bing, Rice, Kenneth M., Rotter, Jerome I., Peloso, Gina M., Natarajan, Pradeep, Li, Zilin, Liu, Zhonghua, Lin, Xihong
Publicado 2023

Genome-wide association study of PR interval

por Pfeufer, Arne, van Noord, Charlotte, Marciante, Kristin D., Arking, Dan E., Larson, Martin G., Smith, Albert Vernon, Tarasov, Kirill V., Müller, Martina, Sotoodehnia, Nona, Sinner, Moritz F., Verwoert, Germaine C., Li, Man, Kao, W.H. Linda, Köttgen, Anna, Coresh, Josef, Bis, Joshua C., Psaty, Bruce M., Rice, Kenneth, Rotter, Jerome I., Rivadeneira, Fernando, Hofman, Albert, Kors, Jan A., Stricker, Bruno H.C., Uitterlinden, André G., van Duijn, Cornelia M., Beckmann, Britt M., Sauter, Wiebke, Gieger, Christian, Lubitz, Steven A., Newton-Cheh, Christopher, Wang, Thomas J., Magnani, Jared W., Schnabel, Renate B., Chung, Mina K., Barnard, John, Smith, Jonathan D., Van Wagoner, David R., Vasan, Ramachandran S., Aspelund, Thor, Eiriksdottir, Gudny, Harris, Tamara B., Launer, Lenore J., Najjar, Samer S., Lakatta, Edward, Schlessinger, David, Uda, Manuela, Abecasis, Gonçalo R., Müller-Myhsok, Bertram, Ehret, Georg B., Boerwinkle, Eric, Chakravarti, Aravinda, Soliman, Elsayed Z., Lunetta, Kathryn L., Perz, Siegfried, Wichmann, H.-Erich, Meitinger, Thomas, Levy, Daniel, Gudnason, Vilmundur, Ellinor, Patrick T., Sanna, Serena, Kääb, Stefan, Witteman, Jacqueline C.M., Alonso, Alvaro, Benjamin, Emelia J., Heckbert, Susan R.
Publicado 2010

Genome-Wide Association Study for Incident Myocardial Infarction and Coronary Heart Disease in Prospective Cohort Studies: The CHARGE Consortium

por Dehghan, Abbas, Bis, Joshua C., White, Charles C., Smith, Albert Vernon, Morrison, Alanna C., Cupples, L. Adrienne, Trompet, Stella, Chasman, Daniel I., Lumley, Thomas, Völker, Uwe, Buckley, Brendan M., Ding, Jingzhong, Jensen, Majken K., Folsom, Aaron R., Kritchevsky, Stephen B., Girman, Cynthia J., Ford, Ian, Dörr, Marcus, Salomaa, Veikko, Uitterlinden, André G., Eiriksdottir, Gudny, Vasan, Ramachandran S., Franceschini, Nora, Carty, Cara L., Virtamo, Jarmo, Demissie, Serkalem, Amouyel, Philippe, Arveiler, Dominique, Heckbert, Susan R., Ferrières, Jean, Ducimetière, Pierre, Smith, Nicholas L., Wang, Ying A., Siscovick, David S., Rice, Kenneth M., Wiklund, Per-Gunnar, Taylor, Kent D., Evans, Alun, Kee, Frank, Rotter, Jerome I., Karvanen, Juha, Kuulasmaa, Kari, Heiss, Gerardo, Kraft, Peter, Launer, Lenore J., Hofman, Albert, Markus, Marcello R. P., Rose, Lynda M., Silander, Kaisa, Wagner, Peter, Benjamin, Emelia J., Lohman, Kurt, Stott, David J., Rivadeneira, Fernando, Harris, Tamara B., Levy, Daniel, Liu, Yongmei, Rimm, Eric B., Jukema, J. Wouter, Völzke, Henry, Ridker, Paul M., Blankenberg, Stefan, Franco, Oscar H., Gudnason, Vilmundur, Psaty, Bruce M., Boerwinkle, Eric, O'Donnell, Christopher J.
Publicado 2016

Genetic Interactions with Age, Sex, Body Mass Index, and Hypertension in Relation to Atrial Fibrillation: The AFGen Consortium

por Weng, Lu-Chen, Lunetta, Kathryn L., Müller-Nurasyid, Martina, Smith, Albert Vernon, Thériault, Sébastien, Weeke, Peter E., Barnard, John, Bis, Joshua C., Lyytikäinen, Leo-Pekka, Kleber, Marcus E., Martinsson, Andreas, Lin, Henry J., Rienstra, Michiel, Trompet, Stella, Krijthe, Bouwe P., Dörr, Marcus, Klarin, Derek, Chasman, Daniel I., Sinner, Moritz F., Waldenberger, Melanie, Launer, Lenore J., Harris, Tamara B., Soliman, Elsayed Z., Alonso, Alvaro, Paré, Guillaume, Teixeira, Pedro L., Denny, Joshua C., Shoemaker, M. Benjamin, Van Wagoner, David R., Smith, Jonathan D., Psaty, Bruce M., Sotoodehnia, Nona, Taylor, Kent D., Kähönen, Mika, Nikus, Kjell, Delgado, Graciela E., Melander, Olle, Engström, Gunnar, Yao, Jie, Guo, Xiuqing, Christophersen, Ingrid E., Ellinor, Patrick T., Geelhoed, Bastiaan, Verweij, Niek, Macfarlane, Peter, Ford, Ian, Heeringa, Jan, Franco, Oscar H., Uitterlinden, André G., Völker, Uwe, Teumer, Alexander, Rose, Lynda M., Kääb, Stefan, Gudnason, Vilmundur, Arking, Dan E., Conen, David, Roden, Dan M., Chung, Mina K., Heckbert, Susan R., Benjamin, Emelia J., Lehtimäki, Terho, März, Winfried, Smith, J. Gustav, Rotter, Jerome I., van der Harst, Pim, Jukema, J. Wouter, Stricker, Bruno H., Felix, Stephan B., Albert, Christine M., Lubitz, Steven A.
Publicado 2017

Genetics of the thrombomodulin-endothelial cell protein C receptor system and the risk of early-onset ischemic stroke

por Cole, John W., Xu, Huichun, Ryan, Kathleen, Jaworek, Thomas, Dueker, Nicole, McArdle, Patrick, Gaynor, Brady, Cheng, Yu-Ching, O'Connell, Jeffrey, Bevan, Steve, Malik, Rainer, Ahmed, Naveed Uddin, Amouyel, Philippe, Anjum, Sheraz, Bis, Joshua C., Crosslin, David, Danesh, John, Engelter, Stefan T., Fornage, Myriam, Frossard, Philippe, Gieger, Christian, Giese, Anne-Katrin, Grond-Ginsbach, Caspar, Ho, Weang Kee, Holliday, Elizabeth, Hopewell, Jemma, Hussain, M., Iqbal, W., Jabeen, S., Jannes, Jim, Kamal, Ayeesha, Kamatani, Yoichiro, Kanse, Sandip, Kloss, Manja, Lathrop, Mark, Leys, Didier, Lindgren, Arne, Longstreth, W. T., Mahmood, Khalid, Meisinger, Christa, Metso, Tiina M., Mosley, Thomas, Müller-Nurasyid, Martina, Norrving, Bo, Parati, Eugenio, Peters, Annette, Pezzini, Alessandro, Quereshi, I., Rasheed, Asif, Rauf, A., Salam, T., Shen, Jess, Słowik, Agnieszka, Stanne, Tara, Strauch, Konstantin, Tatlisumak, Turgut, Thijs, Vincent N., Tiedt, Steffen, Traylor, Matthew, Waldenberger, Melanie, Walters, Matthew, Zhao, Wei, Boncoraglio, Giorgio, Debette, Stéphanie, Jern, Christina, Levi, Christopher, Markus, Hugh, Meschia, James, Rolfs, Arndt, Rothwell, Peter, Saleheen, Danish, Seshadri, Sudha, Sharma, Pankaj, Sudlow, Cathie, Worrall, Bradford, Stine, O. Colin, Kittner, Steven J., Mitchell, Braxton D.
Publicado 2018

Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study

por Wang, Yuxuan, Selvaraj, Margaret Sunitha, Li, Xihao, Li, Zilin, Holdcraft, Jacob A., Arnett, Donna K., Bis, Joshua C., Blangero, John, Boerwinkle, Eric, Bowden, Donald W., Cade, Brian E., Carlson, Jenna C., Carson, April P., Chen, Yii-Der Ida, Curran, Joanne E., de Vries, Paul S., Dutcher, Susan K., Ellinor, Patrick T., Floyd, James S., Fornage, Myriam, Freedman, Barry I., Gabriel, Stacey, Germer, Soren, Gibbs, Richard A., Guo, Xiuqing, He, Jiang, Heard-Costa, Nancy, Hildalgo, Bertha, Hou, Lifang, Irvin, Marguerite R., Joehanes, Roby, Kaplan, Robert C., Kardia, Sharon LR., Kelly, Tanika N., Kim, Ryan, Kooperberg, Charles, Kral, Brian G., Levy, Daniel, Li, Changwei, Liu, Chunyu, Lloyd-Jone, Don, Loos, Ruth JF., Mahaney, Michael C., Martin, Lisa W., Mathias, Rasika A., Minster, Ryan L., Mitchell, Braxton D., Montasser, May E., Morrison, Alanna C., Murabito, Joanne M., Naseri, Take, O’Connell, Jeffrey R., Palmer, Nicholette D., Preuss, Michael H., Psaty, Bruce M., Raffield, Laura M., Rao, Dabeeru C., Redline, Susan, Reiner, Alexander P., Rich, Stephen S., Ruepena, Muagututi’a Sefuiva, Sheu, Wayne H-H., Smith, Jennifer A., Smith, Albert, Tiwari, Hemant K., Tsai, Michael Y., Viaud-Martinez, Karine A., Wang, Zhe, Yanek, Lisa R., Zhao, Wei, Rotter, Jerome I., Lin, Xihong, Natarajan, Pradeep, Peloso, Gina M.
Publicado 2023

Cystatin C and Cardiovascular Disease: A Mendelian Randomization Study

por van der Laan, Sander W., Fall, Tove, Soumaré, Aicha, Teumer, Alexander, Sedaghat, Sanaz, Baumert, Jens, Zabaneh, Delilah, van Setten, Jessica, Isgum, Ivana, Galesloot, Tessel E., Arpegård, Johannes, Amouyel, Philippe, Trompet, Stella, Waldenberger, Melanie, Dörr, Marcus, Magnusson, Patrik K., Giedraitis, Vilmantas, Larsson, Anders, Morris, Andrew P., Felix, Janine F., Morrison, Alanna C., Franceschini, Nora, Bis, Joshua C., Kavousi, Maryam, O’Donnell, Christopher, Drenos, Fotios, Tragante, Vinicius, Munroe, Patricia B., Malik, Rainer, Dichgans, Martin, Worrall, Bradford B., Erdmann, Jeanette, Nelson, Christopher P., Samani, Nilesh J., Schunkert, Heribert, Marchini, Jonathan, Patel, Riyaz S., Hingorani, Aroon D., Lind, Lars, Pedersen, Nancy L., de Graaf, Jacqueline, Kiemeney, Lambertus A.L.M., Baumeister, Sebastian E., Franco, Oscar H., Hofman, Albert, Uitterlinden, André G., Koenig, Wolfgang, Meisinger, Christa, Peters, Annette, Thorand, Barbara, Jukema, J. Wouter, Eriksen, Bjørn Odvar, Toft, Ingrid, Wilsgaard, Tom, Onland-Moret, N. Charlotte, van der Schouw, Yvonne T., Debette, Stéphanie, Kumari, Meena, Svensson, Per, van der Harst, Pim, Kivimaki, Mika, Keating, Brendan J., Sattar, Naveed, Dehghan, Abbas, Reiner, Alex P., Ingelsson, Erik, den Ruijter, Hester M., de Bakker, Paul I.W., Pasterkamp, Gerard, Ärnlöv, Johan, Holmes, Michael V., Asselbergs, Folkert W.
Publicado 2016

A System for Phenotype Harmonization in the National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine (TOPMed) Program

por Stilp, Adrienne M, Emery, Leslie S, Broome, Jai G, Buth, Erin J, Khan, Alyna T, Laurie, Cecelia A, Wang, Fei Fei, Wong, Quenna, Chen, Dongquan, D’Augustine, Catherine M, Heard-Costa, Nancy L, Hohensee, Chancellor R, Johnson, William Craig, Juarez, Lucia D, Liu, Jingmin, Mutalik, Karen M, Raffield, Laura M, Wiggins, Kerri L, de Vries, Paul S, Kelly, Tanika N, Kooperberg, Charles, Natarajan, Pradeep, Peloso, Gina M, Peyser, Patricia A, Reiner, Alex P, Arnett, Donna K, Aslibekyan, Stella, Barnes, Kathleen C, Bielak, Lawrence F, Bis, Joshua C, Cade, Brian E, Chen, Ming-Huei, Correa, Adolfo, Cupples, L Adrienne, de Andrade, Mariza, Ellinor, Patrick T, Fornage, Myriam, Franceschini, Nora, Gan, Weiniu, Ganesh, Santhi K, Graffelman, Jan, Grove, Megan L, Guo, Xiuqing, Hawley, Nicola L, Hsu, Wan-Ling, Jackson, Rebecca D, Jaquish, Cashell E, Johnson, Andrew D, Kardia, Sharon L R, Kelly, Shannon, Lee, Jiwon, Mathias, Rasika A, McGarvey, Stephen T, Mitchell, Braxton D, Montasser, May E, Morrison, Alanna C, North, Kari E, Nouraie, Seyed Mehdi, Oelsner, Elizabeth C, Pankratz, Nathan, Rich, Stephen S, Rotter, Jerome I, Smith, Jennifer A, Taylor, Kent D, Vasan, Ramachandran S, Weeks, Daniel E, Weiss, Scott T, Wilson, Carla G, Yanek, Lisa R, Psaty, Bruce M, Heckbert, Susan R, Laurie, Cathy C
Publicado 2021

Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): a meta-analysis of genome-wide association studies

por Traylor, Matthew, Farrall, Martin, Holliday, Elizabeth G, Sudlow, Cathie, Hopewell, Jemma C, Cheng, Yu-Ching, Fornage, Myriam, Ikram, M Arfan, Malik, Rainer, Bevan, Steve, Thorsteinsdottir, Unnur, Nalls, Mike A, Longstreth, WT, Wiggins, Kerri L, Yadav, Sunaina, Parati, Eugenio A, DeStefano, Anita L, Worrall, Bradford B, Kittner, Steven J, Khan, Muhammad Saleem, Reiner, Alex P, Helgadottir, Anna, Achterberg, Sefanja, Fernandez-Cadenas, Israel, Abboud, Sherine, Schmidt, Reinhold, Walters, Matthew, Chen, Wei-Min, Ringelstein, E Bernd, O'Donnell, Martin, Ho, Weang Kee, Pera, Joanna, Lemmens, Robin, Norrving, Bo, Higgins, Peter, Benn, Marianne, Sale, Michele, Kuhlenbäumer, Gregor, Doney, Alexander S F, Vicente, Astrid M, Delavaran, Hossein, Algra, Ale, Davies, Gail, Oliveira, Sofia A, Palmer, Colin N A, Deary, Ian, Schmidt, Helena, Pandolfo, Massimo, Montaner, Joan, Carty, Cara, de Bakker, Paul I W, Kostulas, Konstantinos, Ferro, Jose M, van Zuydam, Natalie R, Valdimarsson, Einar, Nordestgaard, Børge G, Lindgren, Arne, Thijs, Vincent, Slowik, Agnieszka, Saleheen, Danish, Paré, Guillaume, Berger, Klaus, Thorleifsson, Gudmar, Hofman, Albert, Mosley, Thomas H, Mitchell, Braxton D, Furie, Karen, Clarke, Robert, Levi, Christopher, Seshadri, Sudha, Gschwendtner, Andreas, Boncoraglio, Giorgio B, Sharma, Pankaj, Bis, Joshua C, Gretarsdottir, Solveig, Psaty, Bruce M, Rothwell, Peter M, Rosand, Jonathan, Meschia, James F, Stefansson, Kari, Dichgans, Martin, Markus, Hugh S
Publicado 2012

Genome of the Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels

por van Leeuwen, Elisabeth M., Karssen, Lennart C., Deelen, Joris, Isaacs, Aaron, Medina-Gomez, Carolina, Mbarek, Hamdi, Kanterakis, Alexandros, Trompet, Stella, Postmus, Iris, Verweij, Niek, van Enckevort, David J., Huffman, Jennifer E., White, Charles C., Feitosa, Mary F., Bartz, Traci M., Manichaikul, Ani, Joshi, Peter K., Peloso, Gina M., Deelen, Patrick, van Dijk, Freerk, Willemsen, Gonneke, de Geus, Eco J., Milaneschi, Yuri, Penninx, Brenda W.J.H., Francioli, Laurent C., Menelaou, Androniki, Pulit, Sara L., Rivadeneira, Fernando, Hofman, Albert, Oostra, Ben A., Franco, Oscar H., Leach, Irene Mateo, Beekman, Marian, de Craen, Anton J.M., Uh, Hae-Won, Trochet, Holly, Hocking, Lynne J., Porteous, David J., Sattar, Naveed, Packard, Chris J., Buckley, Brendan M., Brody, Jennifer A., Bis, Joshua C., Rotter, Jerome I., Mychaleckyj, Josyf C., Campbell, Harry, Duan, Qing, Lange, Leslie A., Wilson, James F., Hayward, Caroline, Polasek, Ozren, Vitart, Veronique, Rudan, Igor, Wright, Alan F., Rich, Stephen S., Psaty, Bruce M., Borecki, Ingrid B., Kearney, Patricia M., Stott, David J., Adrienne Cupples, L., Jukema, J. Wouter, van der Harst, Pim, Sijbrands, Eric J., Hottenga, Jouke-Jan, Uitterlinden, Andre G., Swertz, Morris A., van Ommen, Gert-Jan B., de Bakker, Paul I.W., Eline Slagboom, P., Boomsma, Dorret I., Wijmenga, Cisca, van Duijn, Cornelia M.
Publicado 2015

Pharmacogenomics Study of Thiazide Diuretics and QT Interval in Multi-Ethnic Populations: The Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE)

por Seyerle, Amanda A, Sitlani, Colleen M, Noordam, Raymond, Gogarten, Stephanie M, Li, Jin, Li, Xiaohui, Evans, Daniel S, Sun, Fangui, Laaksonen, Maarit A, Isaacs, Aaron, Kristiansson, Kati, Highland, Heather M, Stewart, James D, Harris, Tamara B, Trompet, Stella, Bis, Joshua C, Peloso, Gina M, Brody, Jennifer A, Broer, Linda, Busch, Evan L, Duan, Qing, Stilp, Adrienne M, O’Donnell, Christopher J, Macfarlane, Peter W, Floyd, James S, Kors, Jan A, Lin, Henry J, Li-Gao, Ruifang, Sofer, Tamar, Méndez-Giráldez, Raúl, Cummings, Steven R, Heckbert, Susan R, Hofman, Albert, Ford, Ian, Li, Yun, Launer, Lenore J, Porthan, Kimmo, Newton-Cheh, Christopher, Napier, Melanie D, Kerr, Kathleen F, Reiner, Alexander P, Rice, Kenneth M, Roach, Jeffrey, Buckley, Brendan M, Soliman, Elsayed Z, de Mutsert, Renée, Sotoodehnia, Nona, Uitterlinden, André G, North, Kari E, Lee, Craig R, Gudnason, Vilmundur, Stürmer, Til, Rosendaal, Frits R, Taylor, Kent D, Wiggins, Kerri L, Wilson, James G, Chen, Yii-Der I, Kaplan, Robert C, Wilhelmsen, Kirk, Cupples, L Adrienne, Salomaa, Veikko, van Duijn, Cornelia, Jukema, J Wouter, Liu, Yongmei, Mook-Kanamori, Dennis O, Lange, Leslie A, Vasan, Ramachandran S, Smith, Albert V, Stricker, Bruno H, Laurie, Cathy C, Rotter, Jerome I, Whitsel, Eric A, Psaty, Bruce M, Avery, Christy L
Publicado 2017