Canlyniadau Chwilio - April P Carson

Race‐Sex Differences in Statin Use and Low‐Density Lipoprotein Cholesterol Control Among People With Diabetes Mellitus in the Reasons for Geographic and Racial Differences in Strok... gan Christopher M. Gamboa, Lisandro D. Colantonio, Todd M. Brown, April P. Carson, Monika M. Safford

Cael y testun llawn

Association of functional and structural social support with medication adherence among individuals treated for coronary heart disease risk factors: Findings from the REasons for G... gan Favel L Mondesir, April P Carson, Raegan W Durant, Marquita W Lewis, Monika M Safford, Emily B Levitan

Cael y testun llawn

P‐Wave Indices and the Risks of Incident Atrial Fibrillation and Ischemic Stroke in Black Adults: The Jackson Heart Study gan Vidhushei Yogeswaran, Kerri L. Wiggins, Colleen M. Sitlani, Susan R. Heckbert, Hooman Kamel, Emelia J. Benjamin, Wondwosen Kassahun‐Yimer, Rizwan Kalani, Elsayed Z. Soliman, April P. Carson, James S. Floyd

Cael y testun llawn

Development and implementation of the Forge AHEAD Center: A collaborative research center addressing cardiometabolic disease through academic–community partnership in the Deep Sout... gan Gareth R. Dutton, Monica L. Baskin, Orlando M. Gutiérrez, Caroline E. Compretta, Michael J. Mugavero, April A. Agne, Lauren Hebert-Henderson, Trudi V. Horton, Rikki M. Tanner, April P. Carson, Peter T. Katzmarzyk, Timothy Turner, Tapan S. Mehta, Kara D. Denstel, Aseel El Zein, Michael E. Hall, Sharonda Hardy, Eboni Price-Haywood, Andrea L. Cherrington

Cael y testun llawn

Integrating whole genome and transcriptome sequencing to characterize the genetic architecture of isoform variation gan Chunyu Liu, Roby Joehanes, Jiantao Ma, Jiuyong Xie, Jian Yang, Mengyao Wang, Tianxiao Huan, Shih-Jen Hwang, Jia Wen, Quan Sun, Cumhur Y. Demirkale, Nancy L. Heard-Costa, Peter Orchard, April P. Carson, Jeffrey W. Haessler, Laura M. Raffield, Alex P. Reiner, Nora Franceschini, Paul L. Auer, Charles Kooperberg, Yun Li, George O’Connor, Joanne M. Murabito, Peter Munson, Daniel Levy

Cael y testun llawn

Epigenome-wide DNA methylation association study of CHIP provides insight into perturbed gene regulation gan Sara Kirmani, Tianxiao Huan, Joseph C. Van Amburg, Roby Joehanes, Md Mesbah Uddin, Ngoc Quynh H. Nguyen, Bing Yu, Jennifer A. Brody, Myriam Fornage, Jan Bressler, Nona Sotoodehnia, David A. Ong, Fabio Puddu, James S. Floyd, Christie M. Ballantyne, Bruce M. Psaty, Laura M. Raffield, Pradeep Natarajan, Karen N. Conneely, Joshua S. Weinstock, April P. Carson, Leslie A. Lange, Kendra Ferrier, Nancy L. Heard-Costa, Joanne Murabito, Alexander G. Bick, Daniel Levy

Cael y testun llawn

Association Between Whole Blood–Derived Mitochondrial DNA Copy Number, Low‐Density Lipoprotein Cholesterol, and Cardiovascular Disease Risk gan Xue Liu, Xianbang Sun, Yuankai Zhang, Wenqing Jiang, Meng Lai, Kerri L. Wiggins, Laura M. Raffield, Lawrence F. Bielak, Wei Zhao, Achilleas Pitsillides, Jeffrey Haessler, Yinan Zheng, Thomas W. Blackwell, Jie Yao, Xiuqing Guo, Yong Qian, Bharat Thyagarajan, Nathan Pankratz, Stephen S. Rich, Kent D. Taylor, Patricia A. Peyser, Susan R. Heckbert, Sudha Seshadri, Eric Boerwinkle, Megan L. Grove, Nicholas B. Larson, Jennifer A. Smith, Ramachandran S. Vasan, Annette L. Fitzpatrick, Myriam Fornage, Jun Ding, April P. Carson, Goncalo Abecasis, Josée Dupuis, Alexander Reiner, Charles Kooperberg, Lifang Hou, Bruce M. Psaty, James G. Wilson, Daniel Levy, Jerome I. Rotter, Joshua C. Bis, Claudia L. Satizabal, Dan E. Arking, Chunyu Liu

Cael y testun llawn

Epigenome-wide association study of nuclear DNA methylation in relation to mitochondrial heteroplasmy gan Meng Lai, Kyeezu Kim, Yinan Zheng, Christina A. Castellani, Scott M. Ratliff, Mengyao Wang, Xue Liu, Jeffrey Haessler, Tianxiao Huan, Kwadwo Bonsu, Charles Newcomb, Kyler McKessy, Lawrence F. Bielak, Wei Zhao, Roby Joehanes, Jiantao Ma, Xiuqing Guo, JoAnn E. Manson, Megan L. Grove, Jan Bressler, Kent D. Taylor, Tuuli Lappalainen, Silva Kasela, Thomas W. Blackwell, Nicole J. Lake, Jessica D. Faul, Kendra R. Ferrier, Stephen C. Ekker, Lifang Hou, Charles Kooperberg, Alexander P. Reiner, Kai Zhang, Patricia A. Peyser, Myriam Fornage, Eric Boerwinkle, Laura M. Raffield, April P. Carson, Stephen S. Rich, Yongmei Liu, Daniel Levy, Jerome I. Rotter, Jennifer A. Smith, Dan E. Arking, Chunyu Liu, NHLBI Trans-Omics for Precision Medicine (TOPMed) mtDNA Working Group

Cael y testun llawn

Publisher Correction: Whole genome sequence analysis of pulmonary function and COPD in 44,287 multi-ancestry participants gan Wonji Kim, Xiaowei Hu, Kangjin Kim, Sung Chun, Peter Orchard, Dandi Qiao, Ingo Ruczinski, Aabida Saferali, Francois Aguet, Lucinda Antonacci-Fulton, Pallavi P. Balte, Traci M. Bartz, Wardatul Jannat Anamika, Xiaobo Zhou, JunYi Duan, Jennifer A. Brody, Brian E. Cade, Martha L. Daviglus, Harshavadran Doddapaneni, Shannon Dugan-Perez, Susan K. Dutcher, Christian D. Frazar, Stacey B. Gabriel, Sina A. Gharib, Namrata Gupta, Brian D. Hobbs, Silva Kasela, Laura R. Loehr, Ginger A. Metcalf, Donna M. Muzny, Elizabeth C. Oelsner, Laura J. Rasmussen-Torvik, Colleen M. Sitlani, Joshua Smith, Tamar Sofer, Hanfei Xu, Bing Yu, David Zhang, John Ziniti, R. Graham Barr, April P. Carson, Myriam Fornage, Lifang Hou, Ravi Kalhan, Robert Kaplan, Tuuli Lappalainen, Stephanie J. London, Alanna C. Morrison, George T. O’Connor, Bruce M. Psaty, Laura M. Raffield, Susan Redline, Stephen S. Rich, Jerome I. Rotter, Edwin K. Silverman, Ani Manichaikul, Michael H. Cho

Cael y testun llawn

Whole genome sequence analysis of pulmonary function and COPD in 44,287 multi-ancestry participants gan Wonji Kim, Xiaowei Hu, Kangjin Kim, Sung Chun, Peter Orchard, Dandi Qiao, Ingo Ruczinski, Aabida Saferali, Francois Aguet, Lucinda Antonacci-Fulton, Pallavi P. Balte, Traci M. Bartz, Wardatul Jannat Anamika, Xiaobo Zhou, JunYi Duan, Jennifer A. Brody, Brian E. Cade, Martha L. Daviglus, Harshavadran Doddapaneni, Shannon Dugan-Perez, Susan K. Dutcher, Christian D. Frazar, Stacey B. Gabriel, Sina A. Gharib, Namrata Gupta, Brian D. Hobbs, Silva Kasela, Laura R. Loehr, Ginger A. Metcalf, Donna M. Muzny, Elizabeth C. Oelsner, Laura J. Rasmussen-Torvik, Colleen M. Sitlani, Joshua Smith, Tamar Sofer, Hanfei Xu, Bing Yu, David Zhang, John Ziniti, R. Graham Barr, April P. Carson, Myriam Fornage, Lifang Hou, Ravi Kalhan, Robert Kaplan, Tuuli Lappalainen, Stephanie J. London, Alanna C. Morrison, George T. O’Connor, Bruce M. Psaty, Laura M. Raffield, Susan Redline, Stephen S. Rich, Jerome I. Rotter, Edwin K. Silverman, Ani Manichaikul, Michael H. Cho

Cael y testun llawn

Co-occurring clonal hematopoiesis exhibits strong selection and high leukemia risk gan Kara M. Barnao, Aubrey K. Hubbard, Irenaeus C. C. Chan, Weiyin Zhou, Yasminka A. Jakubek, Giulio Genovese, Wendy S. W. Wong, Rebecca L. Kelly, Corey D. Young, Derek W. Brown, Wen-Yi Huang, Neal D. Freedman, Kristine Jones, Amy Hutchinson, Belynda Hicks, Duc Tran, Donna Arnett, Kathleen C. Barnes, Joshua C. Bis, Eric Boerwinkle, Jennifer A. Brody, April P. Carson, Daniel I. Chasman, Michael H. Cho, Pinkal Desai, Margaret F. Doyle, Myriam Fornage, Xiuqing Guo, Nancy Heard-Costa, Marguerite Ryan Irvin, Andrew D. Johnson, Sharon L. R. Kardia, Charles Kooperberg, Daniel Levy, Joshua P. Lewis, Yun Li, Ruth J. F. Loos, Taralynn M. Mack, Rasika A. Mathias, Braxton D. Mitchell, Kari E. North, Nathan Pankratz, Patricia A. Peyser, Michael H. Preuss, Bruce M. Psaty, Laura M. Raffield, Susan Redline, Stephen S. Rich, Jerome I. Rotter, Edwin K. Silverman, Albert V. Smith, Jennifer A. Smith, Adrienne Stilp, Yin Cao, Paul Scheet, Alexander P. Reiner, Alexander G. Bick, Stephen J. Chanock, Paul L. Auer, Kelly L. Bolton, Mitchell J. Machiela

Cael y testun llawn

Whole-genome sequencing in 333,100 individuals reveals rare non-coding single variant and aggregate associations with height gan Gareth Hawkes, Robin N. Beaumont, Zilin Li, Ravi Mandla, Xihao Li, Christine M. Albert, Donna K. Arnett, Allison E. Ashley-Koch, Aneel A. Ashrani, Kathleen C. Barnes, Eric Boerwinkle, Jennifer A. Brody, April P. Carson, Nathalie Chami, Yii-Der Ida Chen, Mina K. Chung, Joanne E. Curran, Dawood Darbar, Patrick T. Ellinor, Myrian Fornage, Victor R. Gordeuk, Xiuqing Guo, Jiang He, Chii-Min Hwu, Rita R. Kalyani, Robert Kaplan, Sharon L. R. Kardia, Charles Kooperberg, Ruth J. F. Loos, Steven A. Lubitz, Ryan L. Minster, Take Naseri, Satupa’itea Viali, Braxton D. Mitchell, Joanne M. Murabito, Nicholette D. Palmer, Bruce M. Psaty, Susan Redline, M. Benjamin Shoemaker, Edwin K. Silverman, Marilyn J. Telen, Scott T. Weiss, Lisa R. Yanek, Hufeng Zhou, NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, Ching-Ti Liu, Kari E. North, Anne E. Justice, Jonathan M. Locke, Nick Owens, Anna Murray, Kashyap Patel, Timothy M. Frayling, Caroline F. Wright, Andrew R. Wood, Xihong Lin, Alisa Manning, Michael N. Weedon

Cael y testun llawn

Rare damaging CCR2 variants are associated with lower lifetime cardiovascular risk gan Marios K. Georgakis, Rainer Malik, Omar El Bounkari, Natalie R. Hasbani, Jiang Li, Jennifer E. Huffman, Gabrielle Shakt, Reinier W. P. Tack, Tamara N. Kimball, Yaw Asare, Alanna C. Morrison, Noah L. Tsao, Renae Judy, Braxton D. Mitchell, Huichun Xu, May E. Montasser, Ron Do, Eimear E. Kenny, Ruth J. F. Loos, James G. Terry, John Jeffrey Carr, Joshua C. Bis, Bruce M. Psaty, W. T. Longstreth, Kendra A. Young, Sharon M. Lutz, Michael H. Cho, Jai Broome, Alyna T. Khan, Fei Fei Wang, Nancy Heard-Costa, Sudha Seshadri, Ramachandran S. Vasan, Nicholette D. Palmer, Barry I. Freedman, Donald W. Bowden, Lisa R. Yanek, Brian G. Kral, Lewis C. Becker, Patricia A. Peyser, Lawrence F. Bielak, Farah Ammous, April P. Carson, Michael E. Hall, Laura M. Raffield, Stephen S. Rich, Wendy S. Post, Russel P. Tracy, Kent D. Taylor, Xiuqing Guo, Michael C. Mahaney, Joanne E. Curran, John Blangero, Shoa L. Clarke, Jeffrey W. Haessler, Yao Hu, Themistocles L. Assimes, Charles Kooperberg, Jürgen Bernhagen, Christopher D. Anderson, Scott M. Damrauer, Ramin Zand, Jerome I. Rotter, Paul S. de Vries, Martin Dichgans

Cael y testun llawn

Unveiling the Genetic Landscape of Coronary Artery Disease Through Common and Rare Structural Variants gan Kruthika R. Iyer, Shoa L. Clarke, Rodrigo Guarischi‐Sousa, Ketrin Gjoni, Adam S. Heath, Erica P. Young, Nathan O. Stitziel, Cecelia Laurie, Jai G. Broome, Alyna T. Khan, Joshua P. Lewis, Huichun Xu, May E. Montasser, Kellan E. Ashley, Natalie R. Hasbani, Eric Boerwinkle, Alanna C. Morrison, Nathalie Chami, Ron Do, Ghislain Rocheleau, Donald M. Lloyd‐Jones, Rozenn N. Lemaitre, Joshua C. Bis, James S. Floyd, Gregory L. Kinney, Donald W. Bowden, Nicholette D. Palmer, Emelia J. Benjamin, Matthew Nayor, Lisa R. Yanek, Brian G. Kral, Lewis C. Becker, Sharon L. R. Kardia, Jennifer A. Smith, Lawrence F. Bielak, Arnita F. Norwood, Yuan‐I Min, April P. Carson, Wendy S. Post, Stephen S. Rich, David Herrington, Xiuqing Guo, Kent D. Taylor, JoAnn E. Manson, Nora Franceschini, Katherine S. Pollard, Braxton D. Mitchell, Ruth J. F. Loos, Myriam Fornage, Lifang Hou, Bruce M. Psaty, Kendra A. Young, Elizabeth A. Regan, Barry I. Freedman, Ramachandran S. Vasan, Daniel Levy, Rasika A. Mathias, Patricia A. Peyser, Laura M. Raffield, Charles Kooperberg, Alex P. Reiner, Jerome I. Rotter, Goo Jun, Paul S. de Vries, Themistocles L. Assimes

Cael y testun llawn

Whole genome sequencing analysis of body mass index identifies novel African ancestry-specific risk allele gan Xinruo Zhang, Jennifer A. Brody, Mariaelisa Graff, Heather M. Highland, Nathalie Chami, Hanfei Xu, Zhe Wang, Kendra R. Ferrier, Geetha Chittoor, Navya Shilpa Josyula, Mariah Meyer, Shreyash Gupta, Xihao Li, Zilin Li, Matthew A. Allison, Diane M. Becker, Lawrence F. Bielak, Joshua C. Bis, Meher Preethi Boorgula, Donald W. Bowden, Jai G. Broome, Erin J. Buth, Christopher S. Carlson, Kyong-Mi Chang, Sameer Chavan, Yen-Feng Chiu, Lee-Ming Chuang, Matthew P. Conomos, Dawn L. DeMeo, Mengmeng Du, Ravindranath Duggirala, Celeste Eng, Alison E. Fohner, Barry I. Freedman, Melanie E. Garrett, Xiuqing Guo, Chris Haiman, Benjamin D. Heavner, Bertha Hidalgo, James E. Hixson, Yuk-Lam Ho, Brian D. Hobbs, Donglei Hu, Qin Hui, Chii-Min Hwu, Rebecca D. Jackson, Deepti Jain, Rita R. Kalyani, Sharon L. R. Kardia, Tanika N. Kelly, Ethan M. Lange, Michael LeNoir, Changwei Li, Loic Le Marchand, Merry-Lynn N. McDonald, Caitlin P. McHugh, Alanna C. Morrison, Take Naseri, NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, Jeffrey O’Connell, Christopher J. O’Donnell, Nicholette D. Palmer, James S. Pankow, James A. Perry, Ulrike Peters, Michael H. Preuss, D. C. Rao, Elizabeth A. Regan, Sefuiva M. Reupena, Dan M. Roden, Jose Rodriguez-Santana, Colleen M. Sitlani, Jennifer A. Smith, Hemant K. Tiwari, Ramachandran S. Vasan, Zeyuan Wang, Daniel E. Weeks, Jennifer Wessel, Kerri L. Wiggins, Lynne R. Wilkens, Peter W. F. Wilson, Lisa R. Yanek, Zachary T. Yoneda, Wei Zhao, Sebastian Zöllner, Donna K. Arnett, Allison E. Ashley-Koch, Kathleen C. Barnes, John Blangero, Eric Boerwinkle, Esteban G. Burchard, April P. Carson, Daniel I. Chasman, Yii-Der Ida Chen, Joanne E. Curran, Myriam Fornage, Victor R. Gordeuk, Jiang He, Susan R. Heckbert, Lifang Hou, Marguerite R. Irvin, Charles Kooperberg, Ryan L. Minster, Braxton D. Mitchell, Mehdi Nouraie, Bruce M. Psaty, Laura M. Raffield, Alexander P. Reiner, Stephen S. Rich, Jerome I. Rotter, M. Benjamin Shoemaker, Nicholas L. Smith, Kent D. Taylor, Marilyn J. Telen, Scott T. Weiss, Yingze Zhang, Nancy Heard-Costa, Yan V. Sun, Xihong Lin, L. Adrienne Cupples, Leslie A. Lange, Ching-Ti Liu, Ruth J. F. Loos, Kari E. North, Anne E. Justice

Cael y testun llawn