Li-San Wang
Active 2000–2025
- Also published as
- Li‐San Wang · Li San Wang · Li-san Wang
- 113
- Papers
- 21,052
- Citations
- 56
- h-index
- 94
- i10-index
Citations
Citation sources
Countries
Institutions
Fields
- Biochemistry, Genetics and Molecular Biology41.4%
- Medicine29.8%
- Neuroscience15.8%
- Immunology and Microbiology5.9%
- Agricultural and Biological Sciences1.6%
- Computer Science1.5%
- Other4%
Topics
- Alzheimer's disease research and treatments7.6%
- Genetics and Neurodevelopmental Disorders4.2%
- Autism Spectrum Disorder Research3.3%
- Neuroinflammation and Neurodegeneration Mechanisms3%
- Dementia and Cognitive Impairment Research2.8%
- Genomics and Phylogenetic Studies2.5%
- Other76.6%
Coauthors
- Otto Valladares27
- Yuk Yee Leung26
- Gerard D. Schellenberg16
- Pavel P. Kuksa14
- Tandy J. Warnow13
- Wan‐Ping Lee11
- Brian D. Gregory10
- Lindsay A. Farrer10
- Paul K. Crane10
- Prabhakaran Gangadharan10
- William S. Bush10
- Adam C. Naj9
- Alexandre Amlie‐Wolf9
- Liming Qu9
- Živadin Katanić9
- Amanda B Kuzma8
- Badri N. Vardarajan8
- Brian W. Kunkle8
- Jonathan L. Haines8
- Amanda Kuzma7
- Bernard M. E. Moret7
- Beth A. Dombroski7
- Emily Greenfest‐Allen7
- Eric B. Larson7
All papers
- Synaptic, transcriptional and chromatin genes disrupted in autism
Authors: The DDD Study, Silvia De Rubeis, Homozygosity Mapping Collaborative for Autism, Xin He, Arthur P. Goldberg, Christopher S. Poultney, Kaitlin E. Samocha, A. Ercüment Çiçek, Yan Kou, Li Liu, Menachem Fromer, Susan L. Walker, Tarjinder Singh, Lambertus Klei, Jack A. Kosmicki, Shih‐Chen Fu, Branko Aleksić, Monica Biscaldi, Patrick Bolton, Jessica M. Brownfeld, Jinlu Cai, Nicholas G. Campbell, Ãngel Carracedo, Maria H. Chahrour, Andreas G. Chiocchetti, Hilary Coon, Emily L. Crawford, Lucy Crooks, Sarah Curran, Géraldine Dawson, Eftichia Duketis, Bridget A. Fernandez, Louise Gallagher, Evan Geller, Stephen J. Guter, R. Sean Hill, Iuliana Ionita‐Laza, Patricia González, Helena Kilpinen, Sabine M. Klauck, A lexander Kolevzon, Irene Lee, Jing Lei, Terho Lehtimäki, Chiao‐Feng Lin, Avi Ma’ayan, Christian R. Marshall, Alison McInnes, Benjamin M. Neale, Michael J. Owen, Norio Ozaki, Mara Parellada, Jeremy Parr, Shaun Purcell, Kaija Puura, Deepthi Rajagopalan, Karola Rehnström, Abraham Reichenberg, Aniko Sabo, Michael Sachse, Stephan Sanders, Chad Schafer, Martin Schulte‐Rüther, David Skuse, Christine Stevens, Péter Szatmári, Kristiina Tammimies, Otto Valladares, Annette Voran, Li‐San Wang, Lauren A. Weiss, A. Jeremy Willsey, Timothy W. Yu, Ryan K. C. Yuen, Edwin H. Cook, Christine M. Freitag, Michael Gill, Christina M. Hultman, Thomas Lehner, Aarno Palotie, Gerard D. Schellenberg, Pamela Sklar, Matthew W. State, James S. Sutcliffe, Christopher A. Walsh, Stephen W. Scherer, Michael E. Zwick, Jeffrey C. Barrett, David J. Cutler, Kathryn Roeder, Bernie Devlin, Mark J. Daly, Joseph D. Buxbaum - Nature 2014 cited by 2,974
- Enhancing CD8 T-cell memory by modulating fatty acid metabolism
Authors: Erika L. Pearce, Matthew C. Walsh, Pedro J. Cejas, Gretchen M. Harms, Hao Shen, Li‐San Wang, Russell G. Jones, Yongwon Choi - Nature 2009 cited by 1,567
- Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease
Authors: Adam C. Naj, Gyungah Jun, Gary W. Beecham, Li‐San Wang, Badri N. Vardarajan, Jacqueline L. Buros, Paul J. Gallins, Joseph D. Buxbaum, Gail P. Jarvik, Paul K. Crane, Eric B. Larson, Thomas D. Bird, Bradley F. Boeve, Neill R. Graff‐Radford, Philip L. De Jager, Denis A. Evans, Julie A. Schneider, Minerva M. Carrasquillo, Nilüfer Ertekin‐Taner, Steven G. Younkin, Carlos Cruchaga, John Kauwe, Petra Nowotny, Patricia Kramer, John Hardy, Matthew J. Huentelman, Amanda Myers, M. Michael Barmada, F. Yesim Demirci, Clinton T. Baldwin, Robert C. Green, Ekaterina Rogaeva, Peter St George‐Hyslop, Steven E. Arnold, Robert C. Barber, Thomas G. Beach, Eileen H. Bigio, James D. Bowen, Adam Boxer, James R. Burke, Nigel J. Cairns, Chris Carlson, Regina M. Carney, Steven L. Carroll, Helena C. Chui, David G. Clark, Jason J. Corneveaux, Carl W. Cotman, Jeffrey L. Cummings, Charles DeCarli, Steven T. DeKosky, Ramon Diaz‐Arrastia, Malcolm Dick, Dennis W. Dickson, William G. Ellis, Kelley M. Faber, Kenneth B. Fallon, Martin R. Farlow, Steven H. Ferris, Matthew P. Frosch, Douglas Galasko, Mary Ganguli, Marla Gearing, Daniel H. Geschwind, Bernardino Ghetti, John R. Gilbert, Sid Gilman, Bruno Giordani, Jonathan D. Glass, John H. Growdon, Ronald L. Hamilton, Lindy E. Harrell, Elizabeth Head, Lawrence S. Honig, Christine M. Hulette, Bradley T. Hyman, Gregory A. Jicha, Lee‐Way Jin, Nancy Johnson, Jason Karlawish, Anna Karydas, Jeffrey Kaye, Ronald Kim, Edward H. Koo, Neil W. Kowall, James J. Lah, Allan I. Levey, Andrew P. Lieberman, Oscar L. López, Wendy J. Mack, Daniel Marson, Frank Martiniuk, Deborah C. Mash, Eliezer Masliah, Wayne C. McCormick, Susan M. McCurry, Andrew McDavid, Ann C. McKee, Marsel Mesulam, Bruce L. Miller and 55 more - Nature Genetics 2011 cited by 2,014
- An integrated multi-omics approach identifies epigenetic alterations associated with Alzheimer’s disease
Authors: Raffaella Nativio, Yemin Lan, Greg Donahue, Simone Sidoli, Amit Berson, Ananth Srinivasan, Oksana Shcherbakova, Alexandre Amlie‐Wolf, Ji Nie, Xiaolong Cui, Chuan He, Li-San Wang, Benjamin A. García, John Q. Trojanowski, Nancy M. Bonini, Shelley L. Berger - Nature Genetics 2020 cited by 377
- Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer’s disease
Authors: Henne Holstege, Marc Hulsman, Camille Charbonnier, Benjamin Grenier‐Boley, Olivier Quenez, Detelina Grozeva, Jeroen van Rooij, Rebecca Sims, Shahzad Ahmad, Najaf Amin, Penny J. Norsworthy, Oriol Dols‐Icardo, Holger Hummerich, Amit Kawalia, Philippe Amouyel, Gary W. Beecham, Claudine Berr, Joshua C. Bis, Anne Boland, Paola Bossù, Femke H. Bouwman, José Brás, Dominique Campion, J. Nicholas Cochran, Antonio Daniele, Jean‐François Dartigues, Stéphanie Debette, Jean-François Deleuze, Nicola Denning, Anita L. DeStefano, Lindsay A. Farrer, María Victoria Fernández, Nick C. Fox, Daniela Galimberti, Emmanuelle Génin, Johan J. P. Gille, Yann Le Guen, Rita Guerreiro, Jonathan L. Haines, Clive Holmes, M. Arfan Ikram, M. Kamran Ikram, Iris E. Jansen, Robert Kraaij, M Lathrop, Afina W. Lemstra, Alberto Lleó, Lauren Luckcuck, Marcel M. A. M. Mannens, Iain Marshall, Eden R. Martin, Carlo Masullo, Richard Mayeux, Patrizia Mecocci, Alun Meggy, Merel O. Mol, Kevin Morgan, R Myers, Benedetta Nacmias, Adam C. Naj, Valerio Napolioni, Florence Pasquier, Pau Pástor, Margaret A. Pericak‐Vance, Rachel Raybould, Richard Redon, Marcel Reinders, Anne‐Claire Richard, Steffi G. Riedel‐Heller, Fernando Rivadeneira, Stéphane Rousseau, Natalie S. Ryan, Salha Saad, Pascual Sánchez‐Juan, Gerard D. Schellenberg, Philip Scheltens, Jonathan M. Schott, Davide Seripa, Sudha Seshadri, Daoud Sie, Erik A. Sistermans, Sandro Sorbi, Resie van Spaendonk, Gianfranco Spalletta, Niccoló Tesi, Betty M. Tijms, André G. Uitterlinden, Sven J. van der Lee, Pieter Jelle Visser, Michael Wagner, David Wallon, Li-San Wang, Aline Zaréa, Jordi Clarimón, John C. van Swieten, Michael D. Greicius, Jennifer S. Yokoyama, Carlos Cruchaga, John Hardy, Alfredo Ramı́rez and 7 more - Nature Genetics 2022 cited by 219
- Exceptionally low likelihood of Alzheimer’s dementia in APOE2 homozygotes from a 5,000-person neuropathological study
Authors: Eric M. Reiman, Joseph F. Arboleda‐Velásquez, Yakeel T. Quiroz, Matthew J. Huentelman, Thomas G. Beach, Richard J. Caselli, Yinghua Chen, Yi Su, Amanda Myers, John Hardy, Jean Paul Vonsattel, Steven G. Younkin, David Bennett, Philip L. De Jager, Eric B. Larson, Paul K. Crane, C. Dirk Keene, M. Ilyas Kamboh, Julia Kofler, Linda Duque, John R. Gilbert, Harry E. Gwirtsman, Joseph D. Buxbaum, Dennis W. Dickson, Matthew P. Frosch, Bernardino Ghetti, Kathryn L. Lunetta, Li-San Wang, Bradley T. Hyman, Walter A. Kukull, Tatiana M. Foroud, Jonathan L. Haines, Richard Mayeux, Margaret A. Pericak‐Vance, Julie A. Schneider, John Q. Trojanowski, Lindsay A. Farrer, Gerard D. Schellenberg, Gary W. Beecham, Thomas J. Montine, Gyungah Jun, Erin L. Abner, Perrie M. Adams, Marilyn S. Albert, Roger L. Albin, Liana G. Apostolova, Steven E. Arnold, Sanjay Asthana, Craig Atwood, Clinton T. Baldwin, Robert C. Barber, Lisa L. Barnes, Sandra Barral, James T. Becker, Duane Beekly, Eileen H. Bigio, Thomas D. Bird, Deborah Blacker, Bradley F. Boeve, James D. Bowen, Adam Boxer, James R. Burke, Jeffrey M. Burns, Nigel J. Cairns, Laura B. Cantwell, Chuanhai Cao, Chris Carlson, Cynthia M. Carlsson, Regina M. Carney, Minerva M. Carrasquillo, Helena C. Chui, David H. Cribbs, Elizabeth Crocco, Carlos Cruchaga, Charles DeCarli, Malcolm Dick, Rachelle S. Doody, Ranjan Duara, Nilüfer Ertekin‐Taner, Denis A. Evans, Kelley Faber, Thomas Fairchild, Kenneth B. Fallon, David W. Fardo, Martin R. Farlow, Steven H. Ferris, Douglas Galasko, Marla Gearing, Daniel H. Geschwind, Valentina Ghisays, Alison Goate, Neill R. Graff‐Radford, Robert C. Green, John H. Growdon, Håkon Håkonarson, Ronald L. Hamilton, Kara L. Hamilton‐Nelson, Lindy E. Harrell, Lawrence S. Honig, Ryan M. Huebinger and 92 more - Nature Communications 2020 cited by 490
- Apolipoprotein E Genotype and Sex Risk Factors for Alzheimer Disease
Authors: Scott Neu, Judy Pa, Walter A. Kukull, Duane Beekly, Amanda Kuzma, Prabhakaran Gangadharan, Li-San Wang, Klaus Romero, Stephen P. Arnerić, Alberto Redolfi, Daniele Orlandi, Giovanni B. Frisoni, Rhoda Au, Sherral Devine, Sanford Auerbach, Ana Espinosa, Merçé Boada, Agustı́n Ruiz, Sterling C. Johnson, Rebecca L. Koscik, Jiun‐Jie Wang, Wen‐Chuin Hsu, Yao-Liang Chen, Arthur W. Toga - JAMA Neurology 2017 cited by 665
- Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions
Authors: Vivianna M. Van Deerlin, Patrick Sleiman, Maria Martinez‐Lage, Alice Chen‐Plotkin, Li-San Wang, Neill R. Graff‐Radford, Dennis W. Dickson, Rosa Rademakers, Bradley F. Boeve, Murray Grossman, Steven E. Arnold, David Mann, Stuart Pickering‐Brown, Harro Seelaar, Peter Heutink, John C. van Swieten, Jill R. Murrell, Bernardino Ghetti, Salvatore Spina, Jordan Grafman, John R. Hodges, Maria Grazia Spillantini, Sid Gilman, Andrew P. Lieberman, Jeffrey Kaye, Randall L. Woltjer, Eileen H. Bigio, Marsel Mesulam, Safa Al‐Sarraj, Claire Troakes, Roger N. Rosenberg, Charles L. White, Isidró Ferrer, Albert Lladó, Manuela Neumann, Hans A. Kretzschmar, Christine M. Hulette, Kathleen A. Welsh‐Bohmer, Bruce L. Miller, Ainhoa Alzualde, Adolfo López de Munain, Ann C. McKee, Marla Gearing, Allan I. Levey, James J. Lah, John Hardy, Jonathan D. Rohrer, Tammaryn Lashley, Ian R. Mackenzie, Howard Feldman, Ronald L. Hamilton, Steven T. DeKosky, Julie van der Zee, Samir Kumar‐Singh, Christine Van Broeckhoven, Richard Mayeux, Jean Paul Vonsattel, Juan C. Troncoso, Jillian J. Kril, John B. Kwok, Glenda M. Halliday, Thomas D. Bird, Paul G. Ince, Pamela J. Shaw, Nigel J. Cairns, John C. Morris, Catriona McLean, Charles DeCarli, William G. Ellis, Stefanie H. Freeman, Matthew P. Frosch, John H. Growdon, Daniel P. Perl, Mary Sano, David A. Bennett, Julie A. Schneider, Thomas G. Beach, Eric M. Reiman, Bryan K. Woodruff, Jeffrey L. Cummings, Harry V. Vinters, Carol A. Miller, Helena C. Chui, Irina Alafuzoff, Päivi Hartikainen, Danielle Seilhean, Douglas Galasko, Eliezer Masliah, Carl W. Cotman, MJ Tuñón, Mònica Martínez, David G. Muñoz, Steven L. Carroll, Daniel Marson, Peter Riederer, Nenad Bogdanović, Gerard D Schellenberg, Håkon Håkonarson, John Q. Trojanowski, Virginia M.‐Y. Lee - Nature Genetics 2010 cited by 609
- Novel Alzheimer Disease Risk Loci and Pathways in African American Individuals Using the African Genome Resources Panel
Authors: Brian W. Kunkle, Michael A. Schmidt, Hans‐Ulrich Klein, Adam C. Naj, Kara L. Hamilton‐Nelson, Eric B. Larson, Denis A. Evans, Phil L. De Jager, Paul K. Crane, Joseph D. Buxbaum, Nilüfer Ertekin‐Taner, Lisa L. Barnes, M. Daniele Fallin, Jennifer J. Manly, Rodney C.P. Go, Thomas O. Obisesan, M. Ilyas Kamboh, David A. Bennett, Kathleen Hall, Alison Goate, Tatiana M. Foroud, Eden R. Martin, Li‐San Wang, Goldie S. Byrd, Lindsay A. Farrer, Jonathan L. Haines, Gerard D. Schellenberg, Richard Mayeux, Margaret A. Pericak‐Vance, Christiane Reitz, Erin L. Abner, M. Adams Perrie, L. Albin Roger, G Apostolova Liana, Eschrich Steven, S Craig, T. Baldwin Clinton, C. Barber Robert, Sandra Barral, Gunther Thomas, T. James, W. Beecham Gary, H. Bigio Eileen, D. Thomas, Deborah Blacker, F. Boeve Bradley, D. Bowen James, Adam Boxer, R. Burke James, Morris Jeffrey, J Cairns Nigel, Chuanhai Cao, M. Carlsson Cynthia, M. Carney Regina, M. Carrasquillo Minerva, Hugh-Jones David, Carlos Cruchaga, Malcom Dick, Dennis, W. Dickson, Rachelle S. Doody, Ranjan Duara, M. Faber Kelley, Jaya Thomas, B. Kenneth, W. Fardo David, Roger Martin, Steven H. Ferris, P. Frosch Matthew, R. Galasko Douglas, Marla Gearing, Hervé Daniel, Bernardino Ghetti, John, R. Gilbert, C. Green Robert, Harding John, Håkon Håkonarson, L. Hamilton Ronald, John Hardy, E. Harrell Lindy, Steve Lawrence, Mary Ryan, J. Huentelman Matthew, M Hulette Christine, P. Jarvik Gail, Lee‐Way Jin, Anna Karydas, J. Katz Mindy, S. John, C. Dirk Keene, Ronald Kim, H. Kramer Joel, J. Lah James, Yuk Yee Leung, Ge Li, Peter Andrew, B. Richard, G. Lyketsos Constantine, John Malamon, Chammiran Daniel, Frank Martiniuk and 106 more - JAMA Neurology 2020 cited by 275
- Dysregulation of the epigenetic landscape of normal aging in Alzheimer’s disease
Authors: Raffaella Nativio, Greg Donahue, Amit Berson, Yemin Lan, Alexandre Amlie‐Wolf, Ferit Tüzer, Jon B. Toledo, Sager J. Gosai, Brian D. Gregory, Claudio Torres, John Q. Trojanowski, Li‐San Wang, F. Brad Johnson, Nancy M. Bonini, Shelley L. Berger - Nature Neuroscience 2018 cited by 380
- Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy
Authors: PSP Genetics Study Group, Günter U. Höglinger, Nadine M Melhem, Dennis W. Dickson, Patrick Sleiman, Li-San Wang, Lambertus Klei, Rosa Rademakers, Rohan de Silva, Irene Litvan, David E. Riley, John C. van Swieten, Peter Heutink, Zbigniew K. Wszołek, Ryan J. Uitti, Jana Vandrovcová, Howard I. Hurtig, Owen A. Ross, Walter Maetzler, Stefano Goldwurm, Eduardo Tolosa, Barbara Borroni, Pau Pástor, Laura B. Cantwell, Mi Ryung Han, Allissa Dillman, Marcel P. van der Brug, J. Raphael Gibbs, Mark Cookson, Dena G. Hernandez, Andrew Singleton, Matthew J. Farrer, Chang-En Yu, Lawrence I. Golbe, Tamás Révész, John Hardy, Andrew J. Lees, Bernie Devlin, Håkon Håkonarson, Ulrich Müller, Gerard D Schellenberg - Nature Genetics 2011 cited by 632
- Patterns and rates of exonic de novo mutations in autism spectrum disorders
Authors: Benjamin M. Neale, Yan Kou, Li Liu, Avi Ma’ayan, Kaitlin E. Samocha, Aniko Sabo, Chiao‐Feng Lin, Christine Stevens, Li-San Wang, Vladimir Makarov, Paz Polak, Seungtai Yoon, Jared Maguire, Emily L. Crawford, Nicholas G. Campbell, Evan Geller, Otto Valladares, Chad Schafer, Han Liu, Tuo Zhao, Guiqing Cai, Jayon Lihm, Ruth Dannenfelser, Omar Jabado, Zuleyma Peralta, Uma Nagaswamy, Donna M. Muzny, Jeffrey G. Reid, Irene Newsham, Yuanqing Wu, Lora Lewis, Yi Han, Benjamin F. Voight, Elaine T. Lim, Elizabeth J. Rossin, Andrew Kirby, Jason Flannick, Menachem Fromer, Khalid Shakir, Tim Fennell, Kiran Garimella, Eric Banks, Ryan Poplin, Stacey Gabriel, Mark A. DePristo, Jack R. Wimbish, Braden Boone, Shawn Levy, Catalina Betancur, Shamil Sunyaev, Eric Boerwinkle, Joseph D. Buxbaum, Edwin H. Cook, Bernie Devlin, Richard A. Gibbs, Kathryn Roeder, Gerard D. Schellenberg, James S. Sutcliffe, Mark J. Daly - Nature 2012 cited by 1,808
- Variants in the ATP-Binding Cassette Transporter (ABCA7), Apolipoprotein E ϵ4, and the Risk of Late-Onset Alzheimer Disease in African Americans
Authors: Christiane Reitz, Gyungah Jun, Adam C. Naj, Ruchita Rajbhandary, Badri N. Vardarajan, Li San Wang, Otto Valladares, Chiao‐Feng Lin, Eric B. Larson, Neill R. Graff‐Radford, Denis A. Evans, Philip L. De Jager, Paul K. Crane, Joseph D. Buxbaum, Jill R. Murrell, Towfique Raj, Nilüfer Ertekin‐Taner, Mark W. Logue, Clinton T. Baldwin, Robert C. Green, Lisa L. Barnes, Laura B. Cantwell, M. Daniele Fallin, Rodney C.P. Go, Patrick Griffith, Thomas O. Obisesan, Jennifer J. Manly, Kathryn L. Lunetta, M. Ilyas Kamboh, Oscar L. López, David A. Bennett, Hugh C. Hendrie, Kathleen Hall, Alison Goate, Goldie S. Byrd, Walter A. Kukull, Tatiana Foroud, Jonathan L. Haines, Lindsay A. Farrer, Margaret A. Pericak‐Vance, Gerard D. Schellenberg, Richard Mayeux - JAMA 2013 cited by 457
- Genetic variants and functional pathways associated with resilience to Alzheimer’s disease
Authors: Logan Dumitrescu, Emily R. Mahoney, Shubhabrata Mukherjee, Michael L. Lee, William S. Bush, Corinne D. Engelman, Qiongshi Lu, David W. Fardo, Emily H. Trittschuh, Jesse Mez, Catherine C. Kaczorowski, Hector Hernandez Saucedo, Keith F. Widaman, Rachel F. Buckley, Michael J Properzi, Elizabeth C. Mormino, Hyun‐Sik Yang, Tessa Harrison, Trey Hedden, Kwangsik Nho, Shea J. Andrews, Doug Tommet, Niran Hadad, R. Elizabeth Sanders, Douglas M. Ruderfer, Katherine A. Gifford, Annah M. Moore, Francis E. Cambronero, Xiaoyuan Zhong, Neha Raghavan, Badri N. Vardarajan, The Alzheimer’s Disease Neuroimaging Initiative (ADNI), Margaret A. Pericak‐Vance, Lindsay A. Farrer, Li‐San Wang, Carlos Cruchaga, Gerard D. Schellenberg, Nancy J. Cox, Jonathan L. Haines, C. Dirk Keene, Andrew J. Saykin, Eric B. Larson, Reisa A. Sperling, Richard Mayeux, David A. Bennett, Julie A. Schneider, Paul K. Crane, Angela L. Jefferson, Timothy J. Hohman - Brain 2020 cited by 142
- Sex differences in the genetic architecture of cognitive resilience to Alzheimer’s disease
Authors: Jaclyn M. Eissman, Logan Dumitrescu, Emily R. Mahoney, Alexandra N. Smith, Shubhabrata Mukherjee, Michael L. Lee, Phoebe Scollard, Seo Eun Choi, William S. Bush, Corinne D. Engelman, Qiongshi Lu, David W. Fardo, Emily H. Trittschuh, Jesse Mez, Catherine C. Kaczorowski, Hector Hernandez Saucedo, Keith F. Widaman, Rachel F. Buckley, Michael J Properzi, Elizabeth C. Mormino, Hyun Sik Yang, Theresa M. Harrison, Trey Hedden, Kwangsik Nho, Shea J. Andrews, Douglas Tommet, Niran Hadad, R. Elizabeth Sanders, Douglas M. Ruderfer, Katherine A. Gifford, Xiaoyuan Zhong, Neha Raghavan, Badri N. Vardarajan, The Alzheimer’s Disease Neuroimaging Initiative (ADNI), A4 Study Team, Margaret A. Pericak‐Vance, Lindsay A. Farrer, Li San Wang, Carlos Cruchaga, Gerard D. Schellenberg, Nancy J. Cox, Jonathan L. Haines, C. Dirk Keene, Andrew J. Saykin, Eric B. Larson, Reisa A. Sperling, Richard Mayeux, Michael L. Cuccaro, David A. Bennett, Julie A. Schneider, Paul K. Crane, Angela L. Jefferson, Timothy J. Hohman - Brain 2022 cited by 101
- PASTA: Ultra-Large Multiple Sequence Alignment for Nucleotide and Amino-Acid Sequences
Authors: Siavash Mirarab, Nam Nguyen, Sheng Guo, Li-San Wang, Junhyong Kim, Tandy J. Warnow - Journal of Computational Biology, J. Comput. Biol. 2014 cited by 463
- Changes in the Transcriptome of Human Astrocytes Accompanying Oxidative Stress-Induced Senescence
Authors: Elizabeth P. Crowe, Ferit Tüzer, Brian D. Gregory, Greg Donahue, Sager J. Gosai, Justin Cohen, Yuk Yee Leung, Emre C. Yetkin, Raffaella Nativio, Li‐San Wang, Christian Sell, Nancy M. Bonini, Shelley L. Berger, F. Brad Johnson, Claudio Torres - Frontiers in Aging Neuroscience 2016 cited by 111
- Replication of progressive supranuclear palsy genome-wide association study identifies SLCO1A2 and DUSP10 as new susceptibility loci
Authors: Mónica Sánchez-Contreras, Naomi Kouri, Casey Cook, Daniel Serie, Michael G. Heckman, NiCole A. Finch, Richard J. Caselli, Ryan J. Uitti, Zbigniew K. Wszołek, Neill R. Graff‐Radford, Leonard Petrucelli, Li-San Wang, Gerard D. Schellenberg, Dennis W. Dickson, Rosa Rademakers, Owen A. Ross - Molecular Neurodegeneration 2018 cited by 102
- Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy
Authors: Naomi Kouri, Owen A. Ross, Beth A. Dombroski, Curtis Younkin, Daniel Serie, Alexandra I. Soto‐Ortolaza, Matthew Baker, Ni Cole A. Finch, Hyejin Yoon, Jungsu Kim, Shinsuke Fujioka, Catriona McLean, Bernardino Ghetti, Salvatore Spina, Laura B. Cantwell, Martin R. Farlow, Jordan Grafman, Edward D. Huey, Mi Ryung Han, Sherry Beecher, Evan Geller, Hans A. Kretzschmar, Sigrun Roeber, Marla Gearing, Jorge L. Juncos, Jean Paul Vonsattel, Vivianna M. Van Deerlin, Murray Grossman, Howard I. Hurtig, Owen A. Ross, Steven E. Arnold, John Q. Trojanowski, Virginia M. Lee, Gregor K. Wenning, Charles L. White, Günter U. Höglinger, Ulrich Müller, Bernie Devlin, Lawrence I. Golbe, Julia E. Crook, Joseph E. Parisi, Bradley F. Boeve, Keith A. Josephs, Zbigniew K. Wszołek, Ryan J. Uitti, Neill R. Graff‐Radford, Irene Litvan, Steven G. Younkin, Li-San Wang, Nilüfer Ertekin‐Taner, Rosa Rademakers, Hakon Hakonarsen, Gerard D. Schellenberg, Dennis W. Dickson - Nature Communications 2015 cited by 241
- Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation
Authors: 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, Alzheimer’s Disease Sequencing Project, 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 and 1 more - Molecular Psychiatry 2018 cited by 266
- Associations of Sex, Race, and Apolipoprotein E Alleles With Multiple Domains of Cognition Among Older Adults
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