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

Citations per year for Li-San Wang1989: 1 citations1996: 1 citations2000: 9 citations2001: 21 citations2002: 33 citations2003: 20 citations2004: 22 citations2005: 51 citations2006: 51 citations2007: 54 citations2008: 34 citations2009: 45 citations2010: 93 citations2011: 152 citations2012: 238 citations2013: 330 citations2014: 361 citations2015: 405 citations2016: 419 citations2017: 432 citations2018: 414 citations2019: 952 citations2020: 977 citations2021: 1,009 citations2022: 741 citations2023: 670 citations2024: 850 citations2025: 423 citations2026: 14 citations1990–1995: no citations, so these years are not shown1997–1999: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 4,259 citing papers, 30.5% of this breakdownChina: 1,049 citing papers, 7.5% of this breakdownUnited Kingdom: 1,037 citing papers, 7.4% of this breakdownGermany: 720 citing papers, 5.2% of this breakdownCanada: 615 citing papers, 4.4% of this breakdownFrance: 483 citing papers, 3.5% of this breakdownItaly: 453 citing papers, 3.3% of this breakdownAustralia: 418 citing papers, 3% of this breakdownNetherlands: 414 citing papers, 3% of this breakdownSpain: 381 citing papers, 2.7% of this breakdownSweden: 306 citing papers, 2.2% of this breakdownJapan: 298 citing papers, 2.1% of this breakdown
0%30.5%Other 25.2%

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

All papers

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  1. Synaptic, transcriptional and chromatin genes disrupted in autism

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  2. Enhancing CD8 T-cell memory by modulating fatty acid metabolism

    Authors: , , , , , , , - Nature 2009 cited by 1,567

  3. Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  4. An integrated multi-omics approach identifies epigenetic alterations associated with Alzheimer’s disease

    Authors: , , , , , , , , , , , , , , , - Nature Genetics 2020 cited by 377

  5. Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer’s disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  6. Exceptionally low likelihood of Alzheimer’s dementia in APOE2 homozygotes from a 5,000-person neuropathological study

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  7. Apolipoprotein E Genotype and Sex Risk Factors for Alzheimer Disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , - JAMA Neurology 2017 cited by 665

  8. Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  9. Novel Alzheimer Disease Risk Loci and Pathways in African American Individuals Using the African Genome Resources Panel

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  10. Dysregulation of the epigenetic landscape of normal aging in Alzheimer’s disease

    Authors: , , , , , , , , , , , , , , - Nature Neuroscience 2018 cited by 380

  11. Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  12. Patterns and rates of exonic de novo mutations in autism spectrum disorders

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  13. Variants in the ATP-Binding Cassette Transporter (ABCA7), Apolipoprotein E ϵ4, and the Risk of Late-Onset Alzheimer Disease in African Americans

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  14. Genetic variants and functional pathways associated with resilience to Alzheimer’s disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  15. Sex differences in the genetic architecture of cognitive resilience to Alzheimer’s disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  16. PASTA: Ultra-Large Multiple Sequence Alignment for Nucleotide and Amino-Acid Sequences

    Authors: , , , , , - Journal of Computational Biology, J. Comput. Biol. 2014 cited by 463

  17. Changes in the Transcriptome of Human Astrocytes Accompanying Oxidative Stress-Induced Senescence

    Authors: , , , , , , , , , , , , , , - Frontiers in Aging Neuroscience 2016 cited by 111

  18. Replication of progressive supranuclear palsy genome-wide association study identifies SLCO1A2 and DUSP10 as new susceptibility loci

    Authors: , , , , , , , , , , , , , , , - Molecular Neurodegeneration 2018 cited by 102

  19. Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  20. Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  21. Associations of Sex, Race, and Apolipoprotein E Alleles With Multiple Domains of Cognition Among Older Adults

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Timothy J. Hohman, Logan Dumitrescu, Erin L. Abner, Perrie M. Adams, Alyssa Aguirre, Marilyn Albert, Roger L. Albin, Mariet Allen, Lisa Alvarez, Liana G. Apostolova, Steven E. Arnold, Sanjay Asthana, Craig Atwood, Gayle Ayres, Robert C. Barber, Lisa L. Barnes, Sandra Barral, Jackie Bartlett, Thomas G. Beach, James T. Becker, Gary W. Beecham, Penelope Benchek, David A. Bennett, John Bertelson, Sarah Biber, Thomas D. Bird, Deborah Blacker, Bradley F. Boeve, James D. Bowen, Adam Boxer, James Brewer, James R. Burke, Jeffery Burns, William S. Bush, Joseph D. Buxbaum, Goldie S. Byrd, Laura B. Cantwell, Chuanhai Cao, Cynthia M. Carlsson, Minerva M. Carrasquillo, Kwun Chuen Gary Chan, Scott Chase, Yen‐Chi Chen, Marie-Franciose Chesselet, Nathaniel A. Chin, Helena C. Chui, Jaeyoon Chung, Suzanne Craft, Paul K. Crane, Carlos Cruchaga, Michael L. Cuccaro, Jessica E. Culhane, C. Munro Cullum, Eveleen Darby, Bárbara Davis, Charles DeCarli, John C. DeToledo, Dennis W. Dickson, Nic Dobbins, Ranjan Duara, Nilüfer Ertekin‐Taner, Denis A. Evans, Kelley Faber, Thomas Fairchild, M. Daniele Fallin, Kenneth B. Fallon, David W. Fardo, Martin R. Farlow, John J. Farrell, Lindsay A. Farrer and 273 more - JAMA Neurology 2023 cited by 56

  22. SORL1 Is Genetically Associated with Late-Onset Alzheimer’s Disease in Japanese, Koreans and Caucasians

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Yoshikatsu Fujisawa, Ken Sasaki, Ken Watanabe, Kenji Nakashima, Katsuya Urakami, Terumi Ooya, Mitsuo Takahashi, Takefumi Yuzuriha, Kayoko Serikawa, Seishi Yoshimoto, Ryuji Nakagawa, Jong‐Won Kim, Chang‐Seok Ki, Hong‐Hee Won, Duk L. Na, Sang Won Seo, Inhee Mook‐Jung, Peter St George‐Hyslop, Richard Mayeux, Jonathan L. Haines, Margaret A. Pericak‐Vance, Makiko Yoshida, Nao Nishida, Katsushi Tokunaga, Ken Yamamoto, Shoji Tsuji, Ichiro Kanazawa, Yasuo Ihara, Gerard D. Schellenberg, Lindsay A. Farrer, Ryozo Kuwano - PLoS ONE 2013 cited by 200

  23. VCPA: genomic variant calling pipeline and data management tool for Alzheimer's Disease Sequencing Project

    Authors: , , , , , , , , , , - Bioinformatics, Bioinform. 2018 cited by 57

  24. Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Carol F. Lippa, Eileen H. Bigio, Ian R. Mackenzie, Elizabeth Finger, Andrew Kertesz, Richard J. Caselli, Marla Gearing, Jorge L. Juncos, Bernardino Ghetti, Salvatore Spina, Yvette Bordelon, Wallace W. Tourtellotte, Matthew P. Frosch, Jean Paul Vonsattel, Chris Zarow, Thomas G. Beach, Roger L. Albin, Andrew P. Lieberman, Virginia M. Lee, John Q. Trojanowski, Vivianna M. Van Deerlin, Thomas D. Bird, Douglas Galasko, Eliezer Masliah, Charles L. White, Juan C. Troncoso, Didier Hannequin, Adam L. Boxer, Michael D. Geschwind, Satish Kumar, Eva‐Maria Mandelkow, Zbigniew K. Wszołek, Ryan J. Uitti, Dennis W. Dickson, Jonathan L. Haines, Richard Mayeux, Margaret A. Pericak‐Vance, Lindsay A. Farrer, Owen A. Ross, Rosa Rademakers, Gerard D. Schellenberg, Bruce L. Miller, Eckhard Mandelkow, Daniel H. Geschwind - Human Molecular Genetics 2012 cited by 236