Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Timothy S. Chang"'
Autor:
Mingzhou Fu, Leopoldo Valiente-Banuet, Satpal S. Wadhwa, Bogdan Pasaniuc, Keith Vossel, Timothy S. Chang
Publikováno v:
Communications Biology, Vol 7, Iss 1, Pp 1-12 (2024)
Abstract Genetic risk modeling for dementia offers significant benefits, but studies based on real-world data, particularly for underrepresented populations, are limited. We employ an Elastic Net model for dementia risk prediction using single-nucleo
Externí odkaz:
https://doaj.org/article/22d8480a8e0f4fb7ab808b03c846063b
Autor:
Hui Wang, Timothy S. Chang, Beth A. Dombroski, Po-Liang Cheng, Vishakha Patil, Leopoldo Valiente-Banuet, Kurt Farrell, Catriona Mclean, Laura Molina-Porcel, Alex Rajput, Peter Paul De Deyn, Nathalie Le Bastard, Marla Gearing, Laura Donker Kaat, John C. Van Swieten, Elise Dopper, Bernardino F. Ghetti, Kathy L. Newell, Claire Troakes, Justo G. de Yébenes, Alberto Rábano-Gutierrez, Tina Meller, Wolfgang H. Oertel, Gesine Respondek, Maria Stamelou, Thomas Arzberger, Sigrun Roeber, Ulrich Müller, Franziska Hopfner, Pau Pastor, Alexis Brice, Alexandra Durr, Isabelle Le Ber, Thomas G. Beach, Geidy E. Serrano, Lili-Naz Hazrati, Irene Litvan, Rosa Rademakers, Owen A. Ross, Douglas Galasko, Adam L. Boxer, Bruce L. Miller, Willian W. Seeley, Vivanna M. Van Deerlin, Edward B. Lee, Charles L. White, Huw Morris, Rohan de Silva, John F. Crary, Alison M. Goate, Jeffrey S. Friedman, Yuk Yee Leung, Giovanni Coppola, Adam C. Naj, Li-San Wang, P. S. P. genetics study group, Clifton Dalgard, Dennis W. Dickson, Günter U. Höglinger, Gerard D. Schellenberg, Daniel H. Geschwind, Wan-Ping Lee
Publikováno v:
Molecular Neurodegeneration, Vol 19, Iss 1, Pp 1-16 (2024)
Abstract Background Progressive supranuclear palsy (PSP) is a rare neurodegenerative disease characterized by the accumulation of aggregated tau proteins in astrocytes, neurons, and oligodendrocytes. Previous genome-wide association studies for PSP w
Externí odkaz:
https://doaj.org/article/855cdef1a9b046af9ac1a7a118950c99
Autor:
Mingzhou Fu, UCLA Precision Health Data Discovery Repository Working Group, UCLA Precision Health ATLAS Working Group, Timothy S. Chang, Anna L. Antonio, Maryam Ariannejad, Angela M. Badillo, Brunilda Balliu, Yael Berkovich, Michael Broudy, Tony Dang, Chris Denny, Eleazar Eskin, Eran Halperin, Brian L. Hill, Ankur Jain, Vivek Katakwar, Clara Lajonchere, Clara Magyar, Sheila Minton, Ghouse Mohammed, Ariff Muhamed, Pabba Pavan, Michael A. Pfeffer, Nadav Rakocz, Akos Rudas, Rey Salonga, Timothy J. Sanders, Paul Tung, Vu Vu, Ailsa Zheng, Ruth Jhnson, Yi Ding, Alec Chiu, Jae-Hoon Sul, Sriram Sankraraman, Bogdan Pasaniuc
Publikováno v:
Frontiers in Aging Neuroscience, Vol 14 (2022)
Alzheimer’s disease (AD) is the most common form of dementia and a growing public health burden in the United States. Significant progress has been made in identifying genetic risk for AD, but limited studies have investigated how AD genetic risk m
Externí odkaz:
https://doaj.org/article/d7c346ab263a4b27a45f08b832a88996
Autor:
Timothy S. Chang, Yi Ding, Malika K. Freund, Ruth Johnson, Tommer Schwarz, Julie M. Yabu, Chad Hazlett, Jeffrey N. Chiang, David A. Wulf, Daniel H. Geschwind, Manish J. Butte, Bogdan Pasaniuc, Anna L. Antonio, Maryam Ariannejad, Angela M. Badillo, Brunilda Balliu, Yael Berkovich, Michael Broudy, Tony Dang, Chris Denny, Eleazar Eskin, Eran Halperin, Brian L. Hill, Ankur Jain, Vivek Katakwar, Clara Lajonchere, Clara Magyar, Sheila Minton, Ghouse Mohammed, Ariff Muhamed, Pabba Pavan, Michael A. Pfeffer, Nadav Rakocz, Akos Rudas, Rey Salonga, Timothy J. Sanders, Paul Tung, Vu Vu, Ailsa Zheng
Publikováno v:
iScience, Vol 24, Iss 3, Pp 102188- (2021)
Summary: Coronavirus disease 2019 (COVID-19) has exposed health care disparities in minority groups including Hispanics/Latinxs (HL). Studies of COVID-19 risk factors for HL have relied on county-level data. We investigated COVID-19 risk factors in H
Externí odkaz:
https://doaj.org/article/36d513b91c8c4d7b9d8869b017756eb7
Autor:
Jessica E. Rexach, Damon Polioudakis, Anna Yin, Vivek Swarup, Timothy S. Chang, Tam Nguyen, Arjun Sarkar, Lawrence Chen, Jerry Huang, Li-Chun Lin, William Seeley, John Q. Trojanowski, Dheeraj Malhotra, Daniel H. Geschwind
Publikováno v:
Cell Reports, Vol 33, Iss 7, Pp 108398- (2020)
Summary: To understand how neural-immune-associated genes and pathways contribute to neurodegenerative disease pathophysiology, we performed a systematic functional genomic analysis in purified microglia and bulk tissue from mouse and human AD, FTD,
Externí odkaz:
https://doaj.org/article/37aa7e68692a4664bc402acdec6fd6ab
Autor:
Timothy S Chang, Matilde Cirnigliaro, Stephanie A Arteaga, Laura Pérez-Cano, Elizabeth K Ruzzo, Aaron Gordon, Lucy Bicks, Jae-Yoon Jung, Jennifer K Lowe, Dennis P Wall, Daniel H Geschwind
Autism Spectrum Disorder (ASD) has a complex genetic architecture involving contributions from de novo and inherited variation. Few studies have been designed to address the role of rare inherited variation, or its interaction with polygenic risk in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1d974e59b7402660c1def72bdd8c18d2
https://doi.org/10.1101/2022.04.05.22273459
https://doi.org/10.1101/2022.04.05.22273459
Publikováno v:
Journal of Biomedical Informatics. 139:104307
Autor:
Tara E. Tracy, Jesus Madero-Pérez, Danielle L. Swaney, Timothy S. Chang, Michelle Moritz, Csaba Konrad, Michael E. Ward, Erica Stevenson, Ruth Hüttenhain, Grant Kauwe, Maria Mercedes, Lauren Sweetland-Martin, Xu Chen, Sue-Ann Mok, Man Ying Wong, Maria Telpoukhovskaia, Sang-Won Min, Chao Wang, Peter Dongmin Sohn, Jordie Martin, Yungui Zhou, Wenjie Luo, John Q. Trojanowski, Virginia M.Y. Lee, Shiaoching Gong, Giovanni Manfredi, Giovanni Coppola, Nevan J. Krogan, Daniel H. Geschwind, Li Gan
Publikováno v:
Cell, vol 185, iss 4
Tau (MAPT) drives neuronal dysfunction in Alzheimer disease (AD) and other tauopathies. To dissect the underlying mechanisms, we combined an engineered ascorbic acid peroxidase (APEX) approach with quantitative affinity purification mass spectrometry
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe7c2ab524e7117a3fe6db828aa20a56
https://escholarship.org/uc/item/9tw4v44t
https://escholarship.org/uc/item/9tw4v44t
Autor:
Tianyun Wang, Jessica Wright, Natalia Volfovsky, Simon Xuming Xu, Brian J. O'Roak, Christopher Fleisch, Leo Brueggeman, LeeAnne Green Snyder, Evan E. Eichler, Sarah D. Barns, Olena Marchenko, Wendy K. Chung, Shwetha C. Murali, Joseph U. Obiajulu, Xueya Zhou, Jacob B. Hall, William T. Harvey, Jacob J. Michaelson, Timothy S. Chang, Daniel H. Geschwind, Irina Astrovskaya, Pamela Feliciano, Bing Han, Andrew Nishida, Chang Shu, Taylor R. Thomas, Yufeng Shen, Tychele N. Turner
Despite the known heritable nature of autism spectrum disorder (ASD), studies have primarily identified risk genes with de novo variants (DNVs). To capture the full spectrum of ASD genetic risk, we performed a two-stage analysis of rare de novo and i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::57bbda70b96aededbabea20ebf74af08
https://doi.org/10.1101/2021.10.08.21264256
https://doi.org/10.1101/2021.10.08.21264256
Autor:
Xueya, Zhou, Pamela, Feliciano, Chang, Shu, Tianyun, Wang, Irina, Astrovskaya, Jacob B, Hall, Joseph U, Obiajulu, Jessica R, Wright, Shwetha C, Murali, Simon Xuming, Xu, Leo, Brueggeman, Taylor R, Thomas, Olena, Marchenko, Christopher, Fleisch, Sarah D, Barns, LeeAnne Green, Snyder, Bing, Han, Timothy S, Chang, Tychele N, Turner, William T, Harvey, Andrew, Nishida, Brian J, O'Roak, Daniel H, Geschwind, Jacob J, Michaelson, Natalia, Volfovsky, Evan E, Eichler, Yufeng, Shen, Zachary E, Warren
Publikováno v:
Nature genetics. 54(9)
To capture the full spectrum of genetic risk for autism, we performed a two-stage analysis of rare de novo and inherited coding variants in 42,607 autism cases, including 35,130 new cases recruited online by SPARK. We identified 60 genes with exome-w