J
Jason Lee
Researcher at Semel Institute for Neuroscience and Human Behavior
Publications - 3
Citations - 345
Jason Lee is an academic researcher from Semel Institute for Neuroscience and Human Behavior. The author has contributed to research in topics: Exome & Genome-wide association study. The author has an hindex of 3, co-authored 3 publications receiving 309 citations. Previous affiliations of Jason Lee include University of California, Los Angeles.
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Journal ArticleDOI
Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases
Giovanni Coppola,Subashchandrabose Chinnathambi,Jason Lee,Beth A. Dombroski,Matt Baker,Alexandra I. Soto-Ortolaza,Suzee E. Lee,Eric Klein,Alden Y. Huang,Renee L. Sears,Jessica Lane,Anna Karydas,Robert O. Kenet,Jacek Biernat,Li-San Wang,Carl W. Cotman,Charles DeCarli,Allan I. Levey,John M. Ringman,Mario F. Mendez,Helena C. Chui,Isabelle Le Ber,Isabelle Le Ber,Alexis Brice,Alexis Brice,Michelle K. Lupton,Elisavet Preza,Simon Lovestone,John Powell,Neill R. Graff-Radford,Ronald C. Petersen,Bradley F. Boeve,Carol F. Lippa,Eileen H. Bigio,Ian R. A. 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.-Y. 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. Wszolek,Ryan J. Uitti,Dennis W. Dickson,Jonathan L. Haines,Richard Mayeux,Margaret A. Pericak-Vance,Lindsay A. Farrer,Liana G. Apostolova,Steven E. Arnold,Clinton T. Baldwin,Robert Barber,M. Michael Barmada,Thomas G. Beach,Gary W. Beecham,Duane Beekly,David A. Bennett,Deborah Blacker,James D. Bowen,A. Boxer,James R. Burke,Jacqueline L. Buros,Joseph D. Buxbaum,Nigel J. Cairns,Laura B. Cantwell,Chuanhai Cao,Christopher S. Carlson,Regina M. Carney,Minerva M. Carrasquillo,Steven L. Carroll,David G. Clark,Jason J. Corneveaux,Paul K. Crane,Carlos Cruchaga,Jeffrey L. Cummings,Philip L. De Jager,Philip L. De Jager,Charles C. DeCarli,Steven T. DeKosky,F. Yesim Demirci,Ramon Diaz-Arrastia,Malcolm B. Dick,Ranjan Duara,William G. Ellis,Nilufer Ertekin-Taner,Denis A. Evans,Kelley Faber,Kenneth B. Fallon,Martin R. Farlow,Steven H. Ferris,Tatiana Foroud,Paul Gallins,Mary Ganguli,Daniel H. Geschwind,John R. Gilbert,Sid Gilman,Bruno Giordani,Jonathan D. Glass,Alison Goate,Neil Graff-Radford,Robert C. Green,John H. Growdon,Hakon Hakonarson,Ronald L. Hamilton,John Hardy,Lindy E. Harrell,Elizabeth Head,Lawrence S. Honig,Matthew J. Huentelman,Christine M. Hulette,Bradley T. Hyman,Gail P. Jarvik,Gregory A. Jicha,Lee-Way Jin,Nancy Johnson,Gyungah Jun,M. Ilyas Kamboh,Jason Karlawish,A. Karydas,John S. K. Kauwe,Jeffrey Kaye,Ronald C. Kim,Edward H. Koo,Neil W. Kowall,Patricia L. Kramer,Walter A. Kukull,James J. Lah,Eric B. Larson,Oscar L. Lopez,Kathryn L. Lunetta,Wendy J. Mack,Daniel C. Marson,Eden R. Martin,Frank Martiniuk,Deborah C. Mash,Wayne C. McCormick,Susan M. McCurry,Andrew McDavid,Ann C. McKee,M.-Marsel Mesulam,Bruce L. Miller,Carol A. Miller,Joshua W. Miller,Thomas J. Montine,John C. Morris,Amanda J. Myers,Adam C. Naj,Petra Nowotny,Joseph E. Parisi,Daniel P. Perl,Elaine R. Peskind,Wayne W. Poon,Huntington Potter,Joseph F. Quinn,Ashok Raj,Ruchita Rajbhandary,Murray A. Raskind,Eric M. Reiman,Barry Reisberg,Christiane Reitz,Erik D. Roberson,Ekaterina Rogaeva,Roger N. Rosenberg,Mary Sano,Andrew J. Saykin,Andrew J. Saykin,Julie A. Schneider,Lon S. Schneider,William W. Seeley,Michael L. Shelanski,Michael A. Slifer,Charles D. Smith,Joshua A. Sonnen,Peter St George-Hyslop,Peter St George-Hyslop,Robert S. Stern,Rudolph E. Tanzi,Debby W. Tsuang,Badri N. Vardarajan,Harry V. Vinters,Jean Paul G. Vonsattel,Sandra Weintraub,Kathleen A. Welsh-Bohmer,Jennifer Williamson,Randall L. Woltjer,Steven G. Younkin,Owen A. Ross,Rosa Rademakers,Gerard D. Schellenberg,Eckhard Mandelkow +211 more
TL;DR: These data provide the first genetic evidence and functional studies supporting the role of MAPT p.A152T as a rare risk factor for both FTD-s and AD and the concept that rare variants can increase the risk for relatively common, complex neurodegenerative diseases is suggested.
Journal ArticleDOI
Progranulin Mutations as Risk Factors for Alzheimer Disease
David C. Perry,Manja Lehmann,Jennifer S. Yokoyama,Anna Karydas,Jason Lee,Giovanni Coppola,Lea T. Grinberg,Daniel H. Geschwind,William W. Seeley,Bruce L. Miller,Howard J. Rosen,Gil D. Rabinovici +11 more
TL;DR: In addition to autosomal-dominant frontotemporal lobar degeneration, mutations in the progranulin gene may be a risk factor for AD clinical phenotypes and neuropathology.
Journal ArticleDOI
A multiancestral genome-wide exome array study of Alzheimer Disease, frontotemporal dementia, and progressive supranuclear palsy
Jason A. Chen,Qing Wang,Jeremy Davis-Turak,Yun Li,Anna Karydas,Sandy Chan Hsu,Renee L. Sears,Doxa Chatzopoulou,Alden Y. Huang,Kevin Wojta,Eric Klein,Jason Lee,Duane Beekly,Adam L. Boxer,Kelley Faber,Claudia M. Haase,Josh Miller,Wayne W. Poon,Ami Rosen,Howard J. Rosen,Anna Sapozhnikova,Jill S. Shapira,Arousiak Varpetian,Tatiana Foroud,Robert W. Levenson,Allan I. Levey,Walter A. Kukull,Mario F. Mendez,John M. Ringman,Helena C. Chui,Carl W. Cotman,Charles DeCarli,Bruce L. Miller,Daniel H. Geschwind,Giovanni Coppola +34 more
TL;DR: In this article, an exome array was applied to the multiancestral Genetic Investigation in Frontotemporal Dementia and Alzheimer's Disease (GIFT) Study cohort to determine the contribution of low-frequency coding variants to susceptibility to sporadic AD, PSP, and FTD.