Resultats de la cerca - Ron Do

Trans-ancestral rare variant association study with machine learning-based phenotyping for metabolic dysfunction-associated steatotic liver disease per Robert Chen, Ben Omega Petrazzini, Áine Duffy, Ghislain Rocheleau, Daniel Jordan, Meena Bansal, Ron Do

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Genetically supported drug target prioritization for rare diseases per Robert Chen, Áine Duffy, Matthew Mort, David N. Cooper, Ghislain Rocheleau, Daniel M. Jordan, Ron Do

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Deoxynucleotides can replace dideoxynucleotides in minisequencing by arrayed primer extension per Scott J. Tebbutt, Gareth D. Mercer, Ron Do, Ben W. Tripp, Alyson W.M. Wong, Jian Ruan

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An atlas of associations between 14 micronutrients and 22 cancer outcomes: Mendelian randomization analyses per Jong Yeob Kim, Minku Song, Min Seo Kim, Pradeep Natarajan, Ron Do, Woojae Myung, Hong-Hee Won

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Ensemble and consensus approaches to prediction of recessive inheritance for missense variants in human disease per Ben O. Petrazzini, Daniel J. Balick, Iain S. Forrest, Judy Cho, Ghislain Rocheleau, Daniel M. Jordan, Ron Do

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A tissue-level phenome-wide network map of colocalized genes and phenotypes in the UK Biobank per Ghislain Rocheleau, Iain S. Forrest, Áine Duffy, Shantanu Bafna, Amanda Dobbyn, Marie Verbanck, Hong-Hee Won, Daniel M. Jordan, Ron Do

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No causal effects of serum urate levels on the risk of chronic kidney disease: A Mendelian randomization study. per Daniel M Jordan, Hyon K Choi, Marie Verbanck, Ruth Topless, Hong-Hee Won, Girish Nadkarni, Tony R Merriman, Ron Do

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Genetic analyses of eight complex diseases using predicted continuous representations of disease per Robert Chen, Ghislain Rocheleau, Ben Omega Petrazzini, Iain S. Forrest, Joshua K. Park, Áine Duffy, Ha My T. Vy, Daniel Jordan, Ron Do

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Machine Learning Identifies Plasma Metabolites Associated With Heart Failure in Underrepresented Populations With the TTR V122I Variant per Joshua K. Park, Ben O. Petrazzini, Aparna Saha, Akhil Vaid, Ha My T. Vy, Carla Márquez‐Luna, Lili Chan, Girish N. Nadkarni, Ron Do

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Associations between pathophysiological traits and symptom development in retrospective analysis of V30M and V122I transthyretin amyloidosis per Sameer U. Kini, Ha My Thi Vy, Madhav Subramanian, Parasuram M. Krishnamoorthy, Son Q. Duong, Ghislain Rocheleau, Jagat Narula, Ron Do, Girish N. Nadkarni

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Development of a genetic priority score to predict drug side effects using human genetic evidence per Áine Duffy, Robert Chen, David Stein, Joshua K. Park, Matthew Mort, Marie Verbanck, Avner Schlessinger, Yuval Itan, David N. Cooper, Daniel M. Jordan, Ghislain Rocheleau, Ron Do

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Multimodal fusion learning for long QT syndrome pathogenic genotypes in a racially diverse population per Joy Jiang, Ha My Thi Vy, Alexander Charney, Patricia Kovatch, Vivek Reddy, Pushkala Jayaraman, Ron Do, Rohan Khera, Sumeet Chugh, Deepak L. Bhatt, Akhil Vaid, Joshua Lampert, Girish Nitin Nadkarni

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Expanding drug targets for 112 chronic diseases using a machine learning-assisted genetic priority score per Robert Chen, Áine Duffy, Ben O. Petrazzini, Ha My Vy, David Stein, Matthew Mort, Joshua K. Park, Avner Schlessinger, Yuval Itan, David N. Cooper, Daniel M. Jordan, Ghislain Rocheleau, Ron Do

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Quantitative Prediction of Right Ventricular Size and Function From the ECG per Son Q. Duong, Akhil Vaid, Vy Thi Ha My, Liam R. Butler, Joshua Lampert, Robert H. Pass, Alexander W. Charney, Jagat Narula, Rohan Khera, Ankit Sakhuja, Hayit Greenspan, Bruce D. Gelb, Ron Do, Girish N. Nadkarni

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Large-scale cross-ancestry genome-wide meta-analysis of serum urate per Chamlee Cho, Beomsu Kim, Dan Say Kim, Mi Yeong Hwang, Injeong Shim, Minku Song, Yeong Chan Lee, Sang-Hyuk Jung, Sung Kweon Cho, Woong-Yang Park, Woojae Myung, Bong-Jo Kim, Ron Do, Hyon K. Choi, Tony R. Merriman, Young Jin Kim, Hong-Hee Won

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Pyruvate and related energetic metabolites modulate resilience against high genetic risk for glaucoma per Keva Li, Nicholas Tolman, Ayellet V Segrè, Kelsey V Stuart, Oana A Zeleznik, Neeru A Vallabh, Kuang Hu, Nazlee Zebardast, Akiko Hanyuda, Yoshihiko Raita, Christa Montgomery, Chi Zhang, Pirro G Hysi, Ron Do, Anthony P Khawaja, Janey L Wiggs, Jae H Kang, Simon WM John, Louis R Pasquale, UK Biobank Eye and Vision Consortium

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Rare variant contribution to the heritability of coronary artery disease per Ghislain Rocheleau, Shoa L. Clarke, Gaëlle Auguste, Natalie R. Hasbani, Alanna C. Morrison, Adam S. Heath, Lawrence F. Bielak, Kruthika R. Iyer, Erica P. Young, Nathan O. Stitziel, Goo Jun, Cecelia Laurie, Jai G. Broome, Alyna T. Khan, Donna K. Arnett, Lewis C. Becker, Joshua C. Bis, Eric Boerwinkle, Donald W. Bowden, April P. Carson, Patrick T. Ellinor, Myriam Fornage, Nora Franceschini, Barry I. Freedman, Nancy L. Heard-Costa, Lifang Hou, Yii-Der Ida Chen, Eimear E. Kenny, Charles Kooperberg, Brian G. Kral, Ruth J. F. Loos, Sharon M. Lutz, JoAnn E. Manson, Lisa W. Martin, Braxton D. Mitchell, Rami Nassir, Nicholette D. Palmer, Wendy S. Post, Michael H. Preuss, Bruce M. Psaty, Laura M. Raffield, Elizabeth A. Regan, Stephen S. Rich, Jennifer A. Smith, Kent D. Taylor, Lisa R. Yanek, Kendra A. Young, NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, Austin T. Hilliard, Catherine Tcheandjieu, Patricia A. Peyser, Ramachandran S. Vasan, Jerome I. Rotter, Clint L. Miller, Themistocles L. Assimes, Paul S. de Vries, Ron Do

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Rare damaging CCR2 variants are associated with lower lifetime cardiovascular risk per 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

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Unveiling the Genetic Landscape of Coronary Artery Disease Through Common and Rare Structural Variants per 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

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Genome-wide study investigating effector genes and polygenic prediction for kidney function in persons with ancestry from Africa and the Americas per Odessica Hughes, Amy R. Bentley, Charles E. Breeze, Francois Aguet, Xiaoguang Xu, Girish Nadkarni, Quan Sun, Bridget M. Lin, Thomas Gilliland, Mariah C. Meyer, Jiawen Du, Laura M. Raffield, Holly Kramer, Robert W. Morton, Mateus H. Gouveia, Elizabeth G. Atkinson, Adan Valladares-Salgado, Niels Wacher-Rodarte, Nicole D. Dueker, Xiuqing Guo, Yang Hai, Adebowale Adeyemo, Lyle G. Best, Jianwen Cai, Guanjie Chen, Michael Chong, Ayo Doumatey, James Eales, Mark O. Goodarzi, Eli Ipp, Marguerite Ryan Irvin, Minzhi Jiang, Alana C. Jones, Charles Kooperberg, Jose E. Krieger, Ethan M. Lange, Matthew B. Lanktree, James P. Lash, Paulo A. Lotufo, Ruth J.F. Loos, Vy Thi Ha My, Jesús Peralta-Romero, Lihong Qi, Leslie J. Raffel, Stephen S. Rich, Erik J. Rodriquez, Eduardo Tarazona-Santos, Kent D. Taylor, Jason G. Umans, Jia Wen, Bessie A. Young, Zhi Yu, Ying Zhang, Yii-Der Ida Chen, Tanja Rundek, Jerome I. Rotter, Miguel Cruz, Myriam Fornage, Maria Fernanda Lima-Costa, Alexandre C. Pereira, Guillaume Paré, Pradeep Natarajan, Shelley A. Cole, April P. Carson, Leslie A. Lange, Yun Li, Eliseo J. Perez-Stable, Ron Do, Fadi J. Charchar, Maciej Tomaszewski, Josyf C. Mychaleckyj, Charles Rotimi, Andrew P. Morris, Nora Franceschini

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