SNP-SNP interactions dominate the genetic architecture of candidate genes associated with left ventricular mass in african-americans of the GENOA study

by Mosley Thomas H, Chu Jian, Meyers Kristin J, Kardia Sharon LR
Published 2010-11-01

Investigating the complex genetic architecture of ankle-brachial index, a measure of peripheral arterial disease, in non-Hispanic whites

by Turner Stephen T, Boerwinkle Eric, Greene M Todd, Kardia Sharon LR, Kullo Iftikhar J
Published 2008-05-01

Interactions between the <it>adducin 2 </it>gene and antihypertensive drug therapies in determining blood pressure in people with hypertension

by Barkley Ruth, Hamon Sara C, Sun Yan V, Kardia Sharon LR, Boerwinkle Eric, Turner Stephen T
Published 2007-09-01

Software comparison for evaluating genomic copy number variation for Affymetrix 6.0 SNP array platform

by Kardia Sharon LR, Maharjan Sooraj, Atkinson Elizabeth J, Eckel-Passow Jeanette E, de Andrade Mariza
Published 2011-05-01

Complexity in the genetic architecture of leukoaraiosis in hypertensive sibships from the GENOA Study

by Jack Clifford R, Mosley Thomas H, Kelly Reagan J, Fornage Myriam, Sun Yan V, Turner Stephen T, Smith Jennifer A, Kullo Iftikhar J, Kardia Sharon LR
Published 2009-04-01

Sex difference in the association of metabolic syndrome with high sensitivity C-reactive protein in a Taiwanese population

by Lin Wen-Yuan, Liu Chiu-Shong, Kardia Sharon LR, Li Chia-Ing, Lai Ming-May, Lee Yih-Dar, Chang Pei-Chia, Lin Cheng-Chieh, Li Tsai-Chung
Published 2010-07-01

Metabolic syndrome is associated with change in subclinical arterial stiffness - A community-based Taichung Community Health Study

by Lin Wen-Yuan, Liu Chiu-Shong, Kardia Sharon LR, Li Chia-Ing, Lin Chih-Hsueh, Lee Yi-Dar, Sung Fung-Chang, Li Tsai-Chung, Lin Cheng-Chieh
Published 2011-10-01

Multiple interactions between the alpha_2C- and beta₁-adrenergic receptors influence heart failure survival

by Case Karen L, Hahn Harvey S, Grabowski Gregory A, Aronow Bruce J, Keddache Mehdi A, Kelly Reagan J, Kardia Sharon LR, Wagoner Lynne E, Dorn Gerald W, Liggett Stephen B
Published 2008-10-01

Joint relationship between renal function and proteinuria on mortality of patients with type 2 diabetes: The Taichung Diabetes Study

by Lin Cheng-Chieh, Chen Ching-Chu, Kung Pei-Tseng, Li Chia-Ing, Yang Sing-Yu, Liu Chiu-Shong, Lin Wen-Yuan, Lee Cheng-Chun, Li Tsai-Chung, Kardia Sharon LR
Published 2012-10-01

The relationship of high sensitivity C-reactive protein to percent body fat mass, body mass index, waist-to-hip ratio, and waist circumference in a Taiwanese population

by Lin Wen-Yuan, Lai Ming-May, Liu Chiu-Shong, Li Chia-Ing, Kardia Sharon LR, Lin Cheng-Chieh, Chang Pei-Chia, Lee Yih-Dar, Chen Ching-Chu, Lin Chih-Hsueh, Yang Chuan-Wei, Hsiao Chih-Yi, Chen Walter, Li Tsai-Chung
Published 2010-09-01

Smoking-by-genotype interaction in type 2 diabetes risk and fasting glucose.

by Wu, Peitao, Rybin, Denis, Bielak, Lawrence F, Feitosa, Mary F, Franceschini, Nora, Li, Yize, Lu, Yingchang, Marten, Jonathan, Musani, Solomon K, Noordam, Raymond, Raghavan, Sridharan, Rose, Lynda M, Schwander, Karen, Smith, Albert V, Tajuddin, Salman M, Vojinovic, Dina, Amin, Najaf, Arnett, Donna K, Bottinger, Erwin P, Demirkan, Ayse, Florez, Jose C, Ghanbari, Mohsen, Harris, Tamara B, Launer, Lenore J, Liu, Jingmin, Liu, Jun, Mook-Kanamori, Dennis O, Murray, Alison D, Nalls, Mike A, Peyser, Patricia A, Uitterlinden, André G, Voortman, Trudy, Bouchard, Claude, Chasman, Daniel, Correa, Adolfo, de Mutsert, Renée, Evans, Michele K, Gudnason, Vilmundur, Hayward, Caroline, Kao, Linda, Kardia, Sharon LR, Kooperberg, Charles, Loos, Ruth JF, Province, Michael M, Rankinen, Tuomo, Redline, Susan, Ridker, Paul M, Rotter, Jerome I, Siscovick, David, Smith, Blair H, van Duijn, Cornelia, Zonderman, Alan B, Rao, DC, Wilson, James G, Dupuis, Josée, Meigs, James B, Liu, Ching-Ti, Vassy, Jason L
Published 2020

Author Correction: Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function.

by Davies, Gail, Lam, Max, Harris, Sarah E, Trampush, Joey W, Luciano, Michelle, Hill, W David, Hagenaars, Saskia P, Ritchie, Stuart J, Marioni, Riccardo E, Fawns-Ritchie, Chloe, Liewald, David CM, Okely, Judith A, Ahola-Olli, Ari V, Barnes, Catriona LK, Bertram, Lars, Bis, Joshua C, Burdick, Katherine E, Christoforou, Andrea, DeRosse, Pamela, Djurovic, Srdjan, Espeseth, Thomas, Giakoumaki, Stella, Giddaluru, Sudheer, Gustavson, Daniel E, Hayward, Caroline, Hofer, Edith, Ikram, M Arfan, Karlsson, Robert, Knowles, Emma, Lahti, Jari, Leber, Markus, Li, Shuo, Mather, Karen A, Melle, Ingrid, Morris, Derek, Oldmeadow, Christopher, Palviainen, Teemu, Payton, Antony, Pazoki, Raha, Petrovic, Katja, Reynolds, Chandra A, Sargurupremraj, Muralidharan, Scholz, Markus, Smith, Jennifer A, Smith, Albert V, Terzikhan, Natalie, Thalamuthu, Anbupalam, Trompet, Stella, van der Lee, Sven J, Ware, Erin B, Windham, B Gwen, Wright, Margaret J, Yang, Jingyun, Yu, Jin, Ames, David, Amin, Najaf, Amouyel, Philippe, Andreassen, Ole A, Armstrong, Nicola J, Assareh, Amelia A, Attia, John R, Attix, Deborah, Avramopoulos, Dimitrios, Bennett, David A, Böhmer, Anne C, Boyle, Patricia A, Brodaty, Henry, Campbell, Harry, Cannon, Tyrone D, Cirulli, Elizabeth T, Congdon, Eliza, Conley, Emily Drabant, Corley, Janie, Cox, Simon R, Dale, Anders M, Dehghan, Abbas, Dick, Danielle, Dickinson, Dwight, Eriksson, Johan G, Evangelou, Evangelos, Faul, Jessica D, Ford, Ian, Freimer, Nelson A, Gao, He, Giegling, Ina, Gillespie, Nathan A, Gordon, Scott D, Gottesman, Rebecca F, Griswold, Michael E, Gudnason, Vilmundur, Harris, Tamara B, Hartmann, Annette M, Hatzimanolis, Alex, Heiss, Gerardo, Holliday, Elizabeth G, Joshi, Peter K, Kähönen, Mika, Kardia, Sharon LR, Karlsson, Ida, Kleineidam, Luca
Published 2019

Correction: The complex genetics of gait speed: genome-wide meta-analysis approach

by Ben-Avraham, Dan, Karasik, David, Verghese, Joe, Lunetta, Kathryn L., Smith, Jennifer A., Eicher, John D., Vered, Rotem, Deelen, Joris, Arnold, Alice M., Buchman, Aron S., Tanaka, Toshiko, Faul, Jessica D., Nethander, Maria, Fornage, Myriam, Adams, Hieab H., Matteini, Amy M., Callisaya, Michele L., Smith, Albert V., Yu, Lei, De Jager, Philip L., Evans, Denis A., Gudnason, Vilmundur, Hofman, Albert, Pattie, Alison, Corley, Janie, Launer, Lenore J., Knopman, Davis S., Parimi, Neeta, Turner, Stephen T., Bandinelli, Stefania, Beekman, Marian, Gutman, Danielle, Sharvit, Lital, Mooijaart, Simon P., Liewald, David C., Houwing-Duistermaat, Jeanine J., Ohlsson, Claes, Moed, Matthijs, Verlinden, Vincent J., Mellström, Dan, van der Geest, Jos N., Karlsson, Magnus, Hernandez, Dena, McWhirter, Rebekah, Liu, Yongmei, Thomson, Russell, Tranah, Gregory J., Uitterlinden, Andre G., Weir, David R., Zhao, Wei, Starr, John M., Johnson, Andrew D., Ikram, M. Arfan, Bennett, David A., Cummings, Steven R., Deary, Ian J., Harris, Tamara B., Kardia, Sharon L. R., Mosley, Thomas H., Srikanth, Velandai K., Windham, Beverly G., Newman, Ann B., Walston, Jeremy D., Davies, Gail, Evans, Daniel S., Slagboom, Eline P., Ferrucci, Luigi, Kiel, Douglas P., Murabito, Joanne M., Atzmon, Gil
Published 2017

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

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

Comparison of smoking-related DNA methylation between newborns from prenatal exposure and adults from personal smoking.

by Sikdar, Sinjini, Joehanes, Roby, Joubert, Bonnie R, Xu, Cheng-Jian, Vives-Usano, Marta, Rezwan, Faisal I, Felix, Janine F, Ward, James M, Guan, Weihua, Richmond, Rebecca C, Brody, Jennifer A, Küpers, Leanne K, Baïz, Nour, Håberg, Siri E, Smith, Jennifer A, Reese, Sarah E, Aslibekyan, Stella, Hoyo, Cathrine, Dhingra, Radhika, Markunas, Christina A, Xu, Tao, Reynolds, Lindsay M, Just, Allan C, Mandaviya, Pooja R, Ghantous, Akram, Bennett, Brian D, Wang, Tianyuan, Consortium, The Bios, Bakulski, Kelly M, Melen, Erik, Zhao, Shanshan, Jin, Jianping, Herceg, Zdenko, Meurs, Joyce van, Taylor, Jack A, Baccarelli, Andrea A, Murphy, Susan K, Liu, Yongmei, Munthe-Kaas, Monica Cheng, Deary, Ian J, Nystad, Wenche, Waldenberger, Melanie, Annesi-Maesano, Isabella, Conneely, Karen, Jaddoe, Vincent Wv, Arnett, Donna, Snieder, Harold, Kardia, Sharon Lr, Relton, Caroline L, Ong, Ken K, Ewart, Susan, Moreno-Macias, Hortensia, Romieu, Isabelle, Sotoodehnia, Nona, Fornage, Myriam, Motsinger-Reif, Alison, Koppelman, Gerard H, Bustamante, Mariona, Levy, Daniel, London, Stephanie J
Published 2019

A meta-analysis of genome-wide association studies identifies multiple longevity genes.

by Deelen, Joris, Evans, Daniel S, Arking, Dan E, Tesi, Niccolò, Nygaard, Marianne, Liu, Xiaomin, Wojczynski, Mary K, Biggs, Mary L, van der Spek, Ashley, Atzmon, Gil, Ware, Erin B, Sarnowski, Chloé, Smith, Albert V, Seppälä, Ilkka, Cordell, Heather J, Dose, Janina, Amin, Najaf, Arnold, Alice M, Ayers, Kristin L, Barzilai, Nir, Becker, Elizabeth J, Beekman, Marian, Blanché, Hélène, Christensen, Kaare, Christiansen, Lene, Collerton, Joanna C, Cubaynes, Sarah, Cummings, Steven R, Davies, Karen, Debrabant, Birgit, Deleuze, Jean-François, Duncan, Rachel, Faul, Jessica D, Franceschi, Claudio, Galan, Pilar, Gudnason, Vilmundur, Harris, Tamara B, Huisman, Martijn, Hurme, Mikko A, Jagger, Carol, Jansen, Iris, Jylhä, Marja, Kähönen, Mika, Karasik, David, Kardia, Sharon LR, Kingston, Andrew, Kirkwood, Thomas BL, Launer, Lenore J, Lehtimäki, Terho, Lieb, Wolfgang, Lyytikäinen, Leo-Pekka, Martin-Ruiz, Carmen, Min, Junxia, Nebel, Almut, Newman, Anne B, Nie, Chao, Nohr, Ellen A, Orwoll, Eric S, Perls, Thomas T, Province, Michael A, Psaty, Bruce M, Raitakari, Olli T, Reinders, Marcel JT, Robine, Jean-Marie, Rotter, Jerome I, Sebastiani, Paola, Smith, Jennifer, Sørensen, Thorkild IA, Taylor, Kent D, Uitterlinden, André G, van der Flier, Wiesje, van der Lee, Sven J, van Duijn, Cornelia M, van Heemst, Diana, Vaupel, James W, Weir, David, Ye, Kenny, Zeng, Yi, Zheng, Wanlin, Holstege, Henne, Kiel, Douglas P, Lunetta, Kathryn L, Slagboom, P Eline, Murabito, Joanne M
Published 2019

The Scientific Foundation for Personal Genomics: Recommendations from a National Institutes of Health–Centers for Disease Control and Prevention Multidisciplinary Workshop

by Khoury, Muin J., McBride, Colleen M., Schully, Sheri D., Ioannidis, John P. A., Feero, W. Gregory, Janssens, A. Cecile J. W., Gwinn, Marta, Simons-Morton, Denise G., Bernhardt, Jay M., Cargill, Michele, Chanock, Stephen J., Church, George, Coates, Ralph J., Collins, Francis S., Croyle, Robert T., Davis, Barry R., Downing, Gregory J., DuRoss, Amy, Friedman, Susan, Gail, Mitchell H., Ginsburg, Geoffrey S., Green, Robert, Greene, Mark H., Greenland, Philip, Gulcher, Jeffrey R., Hsu, Andro, Hudson, Kathy L., Kardia, Sharon LR, Kimmel, Paul L., Lauer, Michael S., Miller, Amy M., Offit, Kenneth, Ransohoff, David F., Roberts, J. Scott, Rasooly, Rebekah S., Stefansson, Kari, Terry, Sharon F., Teutsch, Steven M., Trepanier, Angela, Wanke, Kay L., Witte, John S., Xu, Jianfeng
Published 2021

Genetic diversity is a predictor of mortality in humans

by Bihlmeyer, Nathan A, Brody, Jennifer A, Smith, Albert Vernon, Lunetta, Kathryn L, Nalls, Mike, Smith, Jennifer A, Tanaka, Toshiko, Davies, Gail, Yu, Lei, Mirza, Saira Saeed, Teumer, Alexander, Coresh, Josef, Pankow, James S, Franceschini, Nora, Scaria, Anish, Oshima, Junko, Psaty, Bruce M, Gudnason, Vilmundur, Eiriksdottir, Gudny, Harris, Tamara B, Li, Hanyue, Karasik, David, Kiel, Douglas P, Garcia, Melissa, Liu, Yongmei, Faul, Jessica D, Kardia, Sharon LR, Zhao, Wei, Ferrucci, Luigi, Allerhand, Michael, Liewald, David C, Redmond, Paul, Starr, John M, De Jager, Philip L, Evans, Denis A, Direk, Nese, Ikram, Mohammed Arfan, Uitterlinden, André, Homuth, Georg, Lorbeer, Roberto, Grabe, Hans J, Launer, Lenore, Murabito, Joanne M, Singleton, Andrew B, Weir, David R, Bandinelli, Stefania, Deary, Ian J, Bennett, David A, Tiemeier, Henning, Kocher, Thomas, Lumley, Thomas, Arking, Dan E
Published 2015

Rare variants in fox-1 homolog A (RBFOX1) are associated with lower blood pressure

by He, Karen Y., Wang, Heming, Cade, Brian E., Nandakumar, Priyanka, Giri, Ayush, Ware, Erin B., Haessler, Jeffrey, Liang, Jingjing, Smith, Jennifer A., Franceschini, Nora, Le, Thu H., Kooperberg, Charles, Edwards, Todd L., Kardia, Sharon L. R., Lin, Xihong, Chakravarti, Aravinda, Redline, Susan, Zhu, Xiaofeng
Published 2017

Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential.

by Nakao, Tetsushi, Bick, Alexander G, Taub, Margaret A, Zekavat, Seyedeh M, Uddin, Md M, Niroula, Abhishek, Carty, Cara L, Lane, John, Honigberg, Michael C, Weinstock, Joshua S, Pampana, Akhil, Gibson, Christopher J, Griffin, Gabriel K, Clarke, Shoa L, Bhattacharya, Romit, Assimes, Themistocles L, Emery, Leslie S, Stilp, Adrienne M, Wong, Quenna, Broome, Jai, Laurie, Cecelia A, Khan, Alyna T, Smith, Albert V, Blackwell, Thomas W, Codd, Veryan, Nelson, Christopher P, Yoneda, Zachary T, Peralta, Juan M, Bowden, Donald W, Irvin, Marguerite R, Boorgula, Meher, Zhao, Wei, Yanek, Lisa R, Wiggins, Kerri L, Hixson, James E, Gu, C Charles, Peloso, Gina M, Roden, Dan M, Reupena, Muagututi'a S, Hwu, Chii-Min, DeMeo, Dawn L, North, Kari E, Kelly, Shannon, Musani, Solomon K, Bis, Joshua C, Lloyd-Jones, Donald M, Johnsen, Jill M, Preuss, Michael, Tracy, Russell P, Peyser, Patricia A, Qiao, Dandi, Desai, Pinkal, Curran, Joanne E, Freedman, Barry I, Tiwari, Hemant K, Chavan, Sameer, Smith, Jennifer A, Smith, Nicholas L, Kelly, Tanika N, Hidalgo, Bertha, Cupples, L Adrienne, Weeks, Daniel E, Hawley, Nicola L, Minster, Ryan L, Samoan Obesity, Lifestyle and Genetic Adaptations Study (OLaGA) Group, Deka, Ranjan, Naseri, Take T, de Las Fuentes, Lisa, Raffield, Laura M, Morrison, Alanna C, Vries, Paul S, Ballantyne, Christie M, Kenny, Eimear E, Rich, Stephen S, Whitsel, Eric A, Cho, Michael H, Shoemaker, M Benjamin, Pace, Betty S, Blangero, John, Palmer, Nicholette D, Mitchell, Braxton D, Shuldiner, Alan R, Barnes, Kathleen C, Redline, Susan, Kardia, Sharon LR, Abecasis, Gonçalo R, Becker, Lewis C, Heckbert, Susan R, He, Jiang, Post, Wendy, Arnett, Donna K, Vasan, Ramachandran S, Darbar, Dawood, Weiss, Scott T, McGarvey, Stephen T, de Andrade, Mariza, Chen, Yii-Der Ida, Kaplan, Robert C, Meyers, Deborah A, Custer, Brian S
Published 2022