Výsledky vyhledávání - Jaeyoon Chung
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Integrative brain transcriptome analysis links complement component 4 and HSPA2 to the APOE ε2 protective effect in Alzheimer disease Autor Rebecca Panitch, Junming Hu, Jaeyoon Chung, Congcong Zhu, Gaoyuan Meng, Weiming Xia, David A. Bennett, Kathryn L. Lunetta, Tsuneya Ikezu, Rhoda Au, Thor D. Stein, Lindsay A. Farrer, Gyungah Jun
Vydáno 2021Artigo -
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A rare missense variant of <i>CASP7</i> is associated with familial late‐onset Alzheimer's disease Autor Xiaoling Zhang, Congcong Zhu, Gary W. Beecham, Badri N. Vardarajan, Yiyi Ma, Daniel Lancour, John J. Farrell, Jaeyoon Chung, Richard Mayeux, Jonathan L. Haines, Gerard Schellenberg, Margaret Pericak‐Vance, Kathryn L. Lunetta, Lindsay A. Farrer
Vydáno 2018Artigo -
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Protein phosphatase 2A and complement component 4 are linked to the protective effect of <i>APOE</i> ɛ2 for Alzheimer's disease Autor Gyungah Jun, Yang You, Congcong Zhu, Gaoyuan Meng, Jaeyoon Chung, Rebecca Panitch, Junming Hu, Weiming Xia, David A. Bennett, Tatiana Foroud, Weixin Wang, Jonathan L. Haines, Richard Mayeux, Margaret A. Pericak‐Vance, Gerard D. Schellenberg, Rhoda Au, Kathryn L. Lunetta, Tsuneya Ikezu, Thor D. Stein, Lindsay A. Farrer
Vydáno 2022Artigo -
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<scp><i>PLXNA</i></scp><i>4</i> is associated with <scp>A</scp>lzheimer disease and modulates tau phosphorylation Autor Gyungah Jun, Hirohide Asai, Ella Zeldich, Elodie Drapeau, Ci-Di Chen, Jaeyoon Chung, Jong‐Ho Park, Se‐Hwa Kim, Vahram Haroutunian, Tatiana Foroud, Ryozo Kuwano, Jonathan L. Haines, Margaret A. Pericak‐Vance, Gerard D. Schellenberg, Kathryn L. Lunetta, Jong‐Won Kim, Joseph D. Buxbaum, Richard Mayeux, Tsuneya Ikezu, Carmela R. Abraham, Lindsay A. Farrer
Vydáno 2014Artigo -
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Association of Rare Coding Mutations With Alzheimer Disease and Other Dementias Among Adults of European Ancestry Autor Devanshi Patel, Jesse Mez, Badri N. Vardarajan, Lyndsay A. Staley, Jaeyoon Chung, Xiaoling Zhang, John J. Farrell, Michael J. Rynkiewicz, Lisa Cannon‐Albright, Craig C. Teerlink, Jeffery Stevens, Christopher Corcoran, Josue D. Gonzalez Murcia, Oscar L. López, Richard Mayeux, Jonathan L. Haines, Margaret A. Pericak‐Vance, Gerard D. Schellenberg, John Kauwe, Kathryn L. Lunetta, Lindsay A. Farrer
Vydáno 2019Artigo -
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Genome-wide association study of cerebral small vessel disease reveals established and novel loci Autor Jaeyoon Chung, Sandro Marini, Joanna Pera, Bo Norrving, Jordi Jiménez-Conde, Jaume Roquer, Israel Fernández‐Cadenas, David Tirschwell, Magdy Selim, Devin L. Brown, Scott Silliman, Bradford B. Worrall, James F. Meschia, Stacie L Demel, Steven M. Greenberg, Agnieszka Słowik, Cecilia M. Lindgren, Reinhold Schmidt, Matthew Traylor, Muralidharan Sargurupremraj, Steffen Tiedt, Rainer Malik, Stéphanie Debette, Martin Dichgans, Carl D. Langefeld, Daniel Woo, Jonathan Rosand, Christopher D. Anderson
Vydáno 2019Artigo -
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Genome‐wide association and multi‐omics studies identify <i>MGMT</i> as a novel risk gene for Alzheimer's disease among women Autor Jaeyoon Chung, Anjali Das, Xinyu Sun, Débora R. Sobreira, Yuk Yee Leung, Catherine Igartua, Sahar V. Mozaffari, Yi‐Fan Chou, Sam Thiagalingam, Jesse Mez, Xiaoling Zhang, Gyungah Jun, Thor D. Stein, Brian W. Kunkle, Eden R. Martin, Margaret A. Pericak‐Vance, Richard Mayeux, Jonathan L. Haines, Gerard D. Schellenberg, Marcelo A. Nóbrega, Kathryn L. Lunetta, Jayant M. Pinto, Weixin Wang, Carole Ober, Lindsay A. Farrer
Vydáno 2022Artigo -
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Two novel loci, <i>COBL</i> and <i>SLC10A2</i>, for Alzheimer's disease in African Americans Autor Jesse Mez, Jaeyoon Chung, Gyungah Jun, Joshua Kriegel, Alexandra P. Bourlas, Richard Sherva, Mark W. Logue, Lisa L. Barnes, David A. Bennett, Joseph D. Buxbaum, Goldie S. Byrd, Paul K. Crane, Nilüfer Ertekin‐Taner, Denis A. Evans, M. Daniele Fallin, Tatiana Foroud, Alison Goate, Neill R. Graff‐Radford, Kathleen Hall, M. Ilyas Kamboh, Walter A. Kukull, Eric B. Larson, Jennifer J. Manly, Jonathan L. Haines, Richard Mayeux, Margaret A. Pericak‐Vance, Gerard D. Schellenberg, Kathryn L. Lunetta, Lindsay A. Farrer
Vydáno 2016Artigo -
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Association of <i>APOE</i> Genotypes and Chronic Traumatic Encephalopathy Autor Kathryn Atherton, Xudong Han, Jaeyoon Chung, Jonathan D. Cherry, Zachary Baucom, Nicole Saltiel, Evan Nair, Bobak Abdolmohammadi, Madeline Uretsky, Mohammed Muzamil Khan, Conor Shea, Shruti Durape, Brett Martin, Joseph Palmisano, Kurt Farrell, Christopher J. Nowinski, Victor E. Alvarez, Brigid Dwyer, Daniel H. Daneshvar, Douglas I. Katz, Lee E. Goldstein, Robert C. Cantu, Neil W. Kowall, Michael L. Alosco, Bertrand R. Huber, Yorghos Tripodis, John F. Crary, Lindsay A. Farrer, Robert A. Stern, Thor D. Stein, Ann C. McKee, Jesse Mez
Vydáno 2022Artigo -
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Genetically Elevated <scp>LDL</scp> Associates with Lower Risk of Intracerebral Hemorrhage Autor Guido J. Falcone, Elayna Kirsch, Julián Acosta, Rommell B. Noche, Audrey C. Leasure, Sandro Marini, Jaeyoon Chung, Magdy Selim, James F. Meschia, Devin L. Brown, Bradford B. Worrall, David Tirschwell, Jeremiasz Jagiełła, Helena Schmidt, Jordi Jiménez-Conde, Israel Fernández‐Cadenas, Cecilia M. Lindgren, Agnieszka Słowik, Dipender Gill, Michael V. Holmes, Chia‐Ling Phuah, Nils Petersen, Charles N. Matouk, Murat Günel, Lauren Sansing, Derrick Bennett, Zhengming Chen, Luan L. Sun, Robert Clarke, Robin Walters, Thomas M. Gill, Alessandro Biffi, Sekar Kathiresan, Carl D. Langefeld, Daniel Woo, Jonathan Rosand, Kevin N. Sheth, Christopher D. Anderson
Vydáno 2020Artigo -
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Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project Autor Yao Hu, Jeffrey Haessler, Regina Manansala, Kerri L. Wiggins, Arden Moscati, Alexa Beiser, Nancy L. Heard‐Costa, Chloé Sarnowski, Laura M. Raffield, Jaeyoon Chung, Sandro Marini, Christopher D. Anderson, Jonathan Rosand, Huichun Xu, Xiao Sun, Tanika N. Kelly, Quenna Wong, Leslie A. Lange, Jerome I. Rotter, Adolfo Correa, Ramachandran S. Vasan, Sudha Seshadri, Stephen S. Rich, Ron Do, Ruth J. F. Loos, W.T. Longstreth, Joshua C. Bis, Bruce M. Psaty, David Tirschwell, Themistocles L. Assimes, Brian Silver, Simin Liu, Rebecca D. Jackson, Sylvia Wassertheil‐Smoller, Braxton D. Mitchell, Myriam Fornage, Paul L. Auer, Alex P. Reiner, Charles Kooperberg
Vydáno 2021Artigo -
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Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation Autor Joshua C. Bis, Xueqiu Jian, Brian W. Kunkle, Yuning Chen, Kara L. Hamilton‐Nelson, William S. Bush, William Salerno, Daniel Lancour, Yiyi Ma, Alan E. Renton, Edoardo Marcora, John Farrell, Yi Zhao, Liming Qu, Shahzad Ahmad, Najaf Amin, Philippe Amouyel, Gary W. Beecham, Jennifer E. Below, Dominique Campion, Laura Cantwell, Camille Charbonnier, Jaeyoon Chung, Paul K. Crane, Carlos Cruchaga, L. Adrienne Cupples, Jean‐François Dartigues, Stéphanie Debette, Jean‐François Deleuze, Lucinda A. Fulton, Stacey Gabriel, Emmanuelle Génin, Richard A. Gibbs, Alison Goate, Benjamin Grenier‐Boley, Namrata Gupta, Jonathan L. Haines, Aki S. Havulinna, Seppo Helisalmi, Mikko Hiltunen, Daniel P. Howrigan, M. Arfan Ikram, Jaakko Kaprio, Jan Konrad, Amanda Kuzma, Eric S. Lander, Mark Lathrop, Terho Lehtimäki, Honghuang Lin, Kari Mattila, Richard Mayeux, Donna M. Muzny, Waleed Nasser, Benjamin M. Neale, Kwangsik Nho, Gaël Nicolas, Devanshi Patel, Margaret A. Pericak‐Vance, Markus Perola, Bruce M. Psaty, Olivier Quenez, Farid Rajabli, Richard Redon, Christiane Reitz, Anne M. Remes, Veikko Salomaa, Chloé Sarnowski, Helena Schmidt, Michael A. Schmidt, Reinhold Schmidt, Hilkka Soininen, Timothy Thornton, Giuseppe Tosto, Christophe Tzourio, Sven J. van der Lee, Cornelia M. van Duijn, Otto Valladares, Badri N. Vardarajan, Li-San Wang, Weixin Wang, Ellen M. Wijsman, Richard K. Wilson, Daniela Witten, Kim C. Worley, Xiaoling Zhang, Céline Bellenguez, Jean‐Charles Lambert, Mitja I. Kurki, Aarno Palotie, Mark J. Daly, Eric Boerwinkle, Kathryn L. Lunetta, Anita L. DeStefano, Josée Dupuis, Eden R. Martin, Gerard D. Schellenberg, Sudha Seshadri, Adam C. Naj, Myriam Fornage, Lindsay A. Farrer
Vydáno 2018Artigo -
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New insights into the genetic etiology of Alzheimer’s disease and related dementias Autor Céline Bellenguez, Fahri Küçükali, Iris E. Jansen, Luca Kleineidam, Sonia Moreno‐Grau, Najaf Amin, Adam C. Naj, Rafael Campos‐Martin, Benjamin Grenier‐Boley, Víctor Andrade, Peter Holmans, Anne Boland, Vincent Damotte, Sven J. van der Lee, Marcos R. Costa, Teemu Kuulasmaa, Qiong Yang, Itziar de Rojas, Joshua C. Bis, Amber Yaqub, Ivana Nedeljković, Julien Chapuis, Shahzad Ahmad, Vilmantas Giedraitis, Dag Aarsland, Pablo García‐González, Carla Abdelnour, Emilio Alarcón‐Martín, Daniel Alcolea, Montserrat Alegret, Ignacio Álvarez, Victoria Álvarez, Nicola J. Armstrong, Anthoula Tsolaki, Carmen Antúnez, Ildebrando Appollonio, Marina Arcaro, Silvana Archetti, Alfonso Arias Pastor, Beatrice Arosio, Lavinia Athanasiu, Henri Bailly, Nerisa Banaj, Miquel Baquero, Sandra Barral, Alexa Beiser, Ana Belén Pastor, Jennifer E. Below, Penelope Benchek, Luisa Benussi, Claudine Berr, Céline Besse, Valentina Bessi, Giuliano Binetti, Alessandra Bizarro, Rafael Blesa, Merçé Boada, Eric Boerwinkle, Barbara Borroni, Silvia Boschi, Paola Bossù, Geir Bråthen, Jan Bressler, Catherine Bresner, Henry Brodaty, Keeley J. Brookes, Luis Ignacio Brusco, Dolores Buiza‐Rueda, Katharina Bürger, Vanessa Burholt, William S. Bush, Miguel Calero, Laura B. Cantwell, Geneviève Chêne, Jaeyoon Chung, Michael L. Cuccaro, Ãngel Carracedo, Roberta Cecchetti, Laura Cervera‐Carles, Camille Charbonnier, Hung‐Hsin Chen, Caterina Chillotti, Simona Ciccone, Jurgen A.H.R. Claassen, Christopher Clark, Elisa Conti, Anaïs Corma‐Gómez, Emanuele Maria Costantini, Carlo Custodero, Delphine Daian, Carolina Dalmasso, Antonio Daniele, Efthimios Dardiotis, Jean‐François Dartigues, Peter Paul De Deyn, Kátia de Paiva Lopes, Lot D. de Witte, Stéphanie Debette, Jürgen Deckert, Teodoro del Ser
Vydáno 2022Artigo -
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A novel Alzheimer disease locus located near the gene encoding tau protein Autor Gyungah Jun, Carla A. Ibrahim‐Verbaas, Maria Vronskaya, Jean‐Charles Lambert, Jaeyoon Chung, Adam C. Naj, Brian W. Kunkle, Li‐Shun Wang, Joshua C. Bis, Céline Bellenguez, Denise Harold, Kathryn L. Lunetta, Anita L. DeStefano, Benjamin Grenier‐Boley, Rebecca Sims, Gary W. Beecham, Albert V. Smith, Vincent Chouraki, Kara L. Hamilton‐Nelson, M. Arfan Ikram, Nathalie Fiévet, Nicola Denning, Eden R. Martin, Helena Schmidt, Yoichiro Kamatani, Melanie Dunstan, Otto Valladares, Agustín Ruiz Laza, Diana Zélénika, Alfredo Ramı́rez, Tatiana Foroud, Sung‐Hyuk Choi, Anne Boland, Tim Becker, Walter A. Kukull, Sven J. van der Lee, Florence Pasquier, Carlos Cruchaga, Duane Beekly, Annette L. Fitzpatrick, Olivier Hanon, Michael Gill, Robert C. Barber, Vilmundur Guðnason, Dominique Campion, Seth Love, David A. Bennett, Najaf Amin, Claudine Berr, Magda Tsolaki, Joseph D. Buxbaum, Oscar L. López, Vincent Deramecourt, Nick C. Fox, Laura B. Cantwell, Lluís Tárraga, Carole Dufouil, John Hardy, Paul K. Crane, Gudny Eiriksdottir, Didier Hannequin, Robert Clarke, Denis A. Evans, Thomas H. Mosley, Luc Letenneur, Carol Brayne, Wolfgang Maier, Philip L. De Jager, Valur Emilsson, Dartigues Jf, Harald Hampel, M. Ilyas Kamboh, Renée F.A.G. de Bruijn, Christophe Tzourio, Pau Pástor, Eric B. Larson, Jerome I. Rotter, Michael O’Donovan, Thomas J. Montine, Michael A. Nalls, Simon Mead, Eric M. Reiman, Pálmi V. Jónsson, Clive Holmes, Peter St George‐Hyslop, Merçé Boada, Peter Passmore, Jens R. Wendland, R. Schmidt, Kevin Morgan, Ashley R. Winslow, John Powell, M Carasquillo, Steven G. Younkin, Jóhanna Jakobsdóttir, John Kauwe, Kirk C. Wilhelmsen, Dan Rujescu, Markus M. Nöthen, Albert Hofman
Vydáno 2015Artigo -
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Transethnic genome‐wide scan identifies novel Alzheimer's disease loci Autor Gyungah Jun, Jaeyoon Chung, Jesse Mez, Robert C. Barber, Gary W. Beecham, David A. Bennett, Joseph D. Buxbaum, Goldie S. Byrd, Minerva M. Carrasquillo, Paul K. Crane, Carlos Cruchaga, Philip L. De Jager, Nilüfer Ertekin‐Taner, Denis A. Evans, M. Danielle Fallin, Tatiana Foroud, Robert P. Friedland, Alison Goate, Neill R. Graff‐Radford, Hugh C. Hendrie, Kathleen Hall, Kara L. Hamilton‐Nelson, Rivka Inzelberg, M. Ilyas Kamboh, John S. K. Kauwe, Walter A. Kukull, Brian W. Kunkle, Ryozo Kuwano, Eric B. Larson, Mark W. Logue, Jennifer J. Manly, Eden R. Martin, Thomas J. Montine, Shubhabrata Mukherjee, Adam C. Naj, Eric M. Reiman, Christiane Reitz, Richard Sherva, Peter St George‐Hyslop, Timothy Thornton, Steven G. Younkin, Badri N. Vardarajan, Li‐San Wang, Jens R. Wendlund, Ashley R. Winslow, Perrie M. Adams, Marilyn S. Albert, Roger L. Albin, Liana G. Apostolova, Steven E. Arnold, Sanjay Asthana, Craig Atwood, Michjael M Barmada, Lisa L. Barnes, Thomas G. Beach, James T. Becker, Eileen H. Bigio, Thomas D. Bird, Deborah Blacker, Bradley F. Boeve, James D. Bowen, Adam Boxer, James R. Burke, Nigel J. Cairns, Chuanhai Cao, Chris Carlson, Cynthia M. Carlsson, Regina M. Carney, Minerva M. Carrasquillo, Steven L. Carroll, Helena C. Chui, David G. Clark, Jason J. Corneveaux, David H. Cribbs, Elizabeth Crocco, Carlos Cruchaga, Philip L. De Jager, Charles DeCarli, Steven T. DeKosky, F. Yesim Demirci, Malcolm Dick, Dennis W. Dickson, Rachelle S. Doody, Ranjan Duara, Nilüfer Ertekin‐Taner, Kelley Faber, Thomas Fairchild, Kenneth B. Fallon, Martin R. Farlow, Steven H. Ferris, Matthew P. Frosch, Douglas Galasko, Marla Gearing, Daniel H. Geschwind, Bernardino Ghetti, John R. Gilbert, Jonathan D. Glass, Neill R. Graff‐Radford, Robert C. Green, John H. Growdon
Vydáno 2017Artigo
Vyhledávací nástroje:
Související témata
Medicine
Biology
Genetics
Disease
Gene
Internal medicine
Genotype
Single-nucleotide polymorphism
Genome-wide association study
Genetic association
Alzheimer's disease
Apolipoprotein E
Locus (genetics)
Pathology
Allele
Bioinformatics
Neuroscience
Psychology
Endocrinology
Immune system
Mutation
Odds ratio
Phenotype
Quantitative trait locus
SNP
Cell biology
Cognition
Complement system
Dementia
Demography