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David W. Fardo

University of Kentucky

51H指数
277论文数
1.6W被引数
收录论文 114
发表时间
Distinct single-nucleus RNA-seq changes among non-neuronal cells in ADNC, LATE-NC, and mixed pathologies阿尔茨海默病神经炎性斑块、LATE神经炎性斑块以及混合病理中非神经元细胞的单核RNA测序变化差异
err2026-09-24
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errOAAI
errQi Qiao; Yuriko Katsumata; Hsin-Yu Lai; Kevin Z. Lin; Steven A. Claas; Mariano I. Gabitto; Josh M. Morganti; Peter T. Nelson; Shubhabrata Mukherjee; David W. Fardo
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ABCC9/SUR2 has a Complex Expression Pattern in Human Brain Gliovascular Unit Cells, Including AstrocytesABCC9/SUR2在人脑神经胶质-血管单元细胞中具有复杂的表达模式,包括星形胶质细胞
err2026-09-19
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errOAAI
errYuriko Katsumata; Josh M. Morganti; Andrew Liao; Wei Zhou; Yu Zhong; Shuling Fister; Kai Saito; Qi Qiao; Sergei Artiushin; Angela Wei; Gao Jian; Colin G. Nichols; Tiffany L. Lee; Dana M. Niedowicz; Ryan K. Shahidehpour; Christopher M. Norris; Colin B. Rogers; David W. Fardo; Junyue Cao; Peter T. Nelson
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Locus coeruleus TDP-43 pathology in a community-based cohort: Clinical and pathological correlates蓝斑TDP-43病理学在基于社区队列中的临床与病理学相关性
err2026-08-01
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errOAAI
errAllison M Neltner; Ryan K Shahidehpour, PhD; Megan E Hall, MS; Xiaotong Ning, MS; Shuling Fister, MS; Hannah Kang; Sonya Anderson, BA; Gregory A Jicha, MD, PhD; Tiffany L Lee, BA; Erin L Abner, MPH, PhD; David W Fardo, PhD; Peter T Nelson, MD, PhD
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Data-driven thresholds for standardized classification of severe Alzheimer's disease neuropathology using digital neuropathology基于数字神经病理学的阿尔茨海默病严重神经病理学标准化分类的数据驱动阈值
err2026-04-26
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errRyan K. Shahidehpour; Allison M. Neltner; Mitchell A. Klusty; Cole Corbett; Angelique D. Gonzalez; David A. Gutman; David W. Fardo; Adam D. Bachstetter; Cody Bumgardner; Margaret E. Flanagan; Peter T. Nelson
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Clonal expansion of cytotoxic CD8⁺ T cells in lecanemab-associated ARIAlecanemab相关咏叹调中细胞毒性CD8 + T细胞的克隆扩增
err2026-01-30
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errOAAI
errLance A. Johnson; Kai Saito; Akhil V. Pallerla; Jessica L. Funnell; Ashley R. Ezzo; Chelsea M. Song; Douglas A. Harrison; Noah J. Norton; Lauren C. Moore; Linda J. Van Eldik; David W. Fardo; Greg E. Cooper; Josh M. Morganti
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Reply to: a quantitative trait locus for reduced microglial APOE expression associates with reduced cerebral amyloid angiopathy回复: 减少小胶质细胞APOE表达的定量性状位点与减少的脑淀粉样血管病有关
err2026-01-26
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PREAI
errLincoln M. P. Shade; Qi Qiao; Yuriko Katsumata; Shubhabrata Mukherjee; Jai G. Broome; Lance A. Johnson; Mark T. W. Ebbert; Peter T. Nelson; David W. Fardo
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Associations between multiallelic genetic variants and ADRD-related proteinopathy多等位基因遗传变异与ADRD相关蛋白病的关联
err2025-12-24
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errOAAI
errYuriko Katsumata; Khine Zin Aung; Xian Wu; Inori Tsuchiya; Lincoln MP Shade; Erin L. Abner; Peter T Nelson; David W. Fardo
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Genetic association analyses of cognitive performance across multi-ancestry older adults: Application of Tobit models多祖先老年人群认知表现遗传关联分析:Tobit模型的应用
err2025-10-23
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PREAI
errXian Wu; Inori Tsuchiya; Khine Zin Aung; Qi Qiao; David W Fardo; Peter T Nelson; Erin L Abner; Bryan D James; Christopher M Norris; Yuriko Katsumata
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Clonal hematopoiesis of indeterminate potential and the risk of cognitive impairment in the Women's Health Initiative Memory Study克隆性中性粒细胞发育潜能与女性健康倡议记忆研究中的认知障碍风险
err2025-09-30
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errJakubek, Yasminka A.; Smith, Aaron P.; Leng, Xiaoyan I.; Hall, Megan E.; Ezzat, Daniel; Pershad, Yash; Collins, Jason M.; Uddin, Md Mesbah; Fardo, David W.; Natarajan, Pradeep; Bick, Alexander G.; Kitzman, Jacob O.; Honigberg, Michael C.; Hayden, Kathleen M.; Manson, JoAnn E.; Jaiswal, Siddhartha; Whitsel, Eric A.; Reiner, Alexander P.
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Association of genetic scores related to insulin resistance with neurological outcomes in ancestrally diverse cohorts from the Trans-Omics for Precision Medicine (TOPMed) program与胰岛素抵抗相关的遗传评分与 ancestry 多样化队列中神经病学结局的关联:来自精准医学跨组学计划 (TOPMed) 的数据
err2025-09-24
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errOAAI
errChloé Sarnowski; Yixin Zhang; Farah Ammous; Lincoln M. P. Shade; Daniel DiCorpo; Xueqiu Jian; Donna K. Arnett; Thomas R. Austin; Alexa Beiser; Joshua C. Bis; John Blangero; Eric Boerwinkle; Jan Bressler; Joanne E. Curran; Charles S. DeCarli; Harsha Doddapaneni; Josée Dupuis; David W. Fardo; Jose C. Florez; Stacey Gabriel; Richard A. Gibbs; David C. Glahn; Namrata Gupta; Hector M. González; Kevin A. González; Konstantinos Hatzikotoulas; Kathleen M. Hayden; Susan R. Heckbert; Bertha Hidalgo; Alicia Huerta-Chagoya; Timothy M. Hughes; Sharon L. R. Kardia; Charles L. Kooperberg; Lenore J. Launer; W. T. Longstreth; Ravi Mandla; Rasika A. Mathias; Andrew P. Morris; Thomas H. Mosley; Ilya M. Nasrallah; Paul Nyquist; Bruce M. Psaty; Qibin Qi; Laura M. Raffield; Nigel W. Rayner; Alexander P. Reiner; Claudia L. Satizabal; Elizabeth Selvin; Magdalena D. R. Sevilla-Gonzalez; Albert V. Smith; Jennifer A. Smith; Kirk Smith; Beverly M. Snively; Lorraine Southam; Tamar Sofer; Ken Suzuki; Henry J. Taylor; Miriam S. Udler; Karine A. Viaud-Martinez; Sylvia Wassertheil-Smoller; Alexis C. Wood; Lisa R. Yanek; Xianyong Yin; Alisa K. Manning; Jerome I. Rotter; Stephen S. Rich; James B. Meigs; Myriam Fornage; Sudha Seshadri; Alanna C. Morrison
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Machine learning approaches to predicting medication nonadherence: a scoping review机器学习方法预测用药不依从性:一项范围综述
err2025-08-14
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PREAI
errChristian Rhudy; Jacob Johnson; Courtney Perry; Cody Bumgardner; Michael J. Wesley; David Fardo; Terrence Barrett; Jeffery Talbert
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Genetically proxied blood pressure, vascular brain injury, and Alzheimer's disease pathology基因代理的血压,血管性脑损伤和阿尔茨海默氏病病理
err2025-07-19
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errOAAI
errIyas Daghlas; Michelle R. Caunca; Lincoln M. P. Shade; Malik Nassan; Kristine Yaffe; David W. Fardo; Dipender Gill
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Author Correction: GWAS of multiple neuropathology endophenotypes identifies new risk loci and provides insights into the genetic risk of dementia作者更正:对多种神经病理内表型的全基因组关联研究识别出新的风险位点,并提供了对痴呆遗传风险的见解。
err2025-06-17
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errLincoln M. P. Shade; Yuriko Katsumata; Erin L. Abner; Khine Zin Aung; Steven A. Claas; Qi Qiao; Bernardo Aguzzoli Heberle; J. Anthony Brandon; Madeline L. Page; Timothy J. Hohman; Shubhabrata Mukherjee; Richard P. Mayeux; Lindsay A. Farrer; Gerard D. Schellenberg; Jonathan L. Haines; Walter A. Kukull; Kwangsik Nho; Andrew J. Saykin; David A. Bennett; Julie A. Schneider; Mark T. W. Ebbert; Peter T. Nelson; David W. Fardo
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Publisher Correction: GWAS of multiple neuropathology endophenotypes identifies new risk loci and provides insights into the genetic risk of dementia出版商更正:多神经病理内表型全基因组关联研究识别了新的风险位点,并提供了对痴呆遗传风险的见解。
err2025-06-17
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errOAAI
errLincoln M. P. Shade; Yuriko Katsumata; Erin L. Abner; Khine Zin Aung; Steven A. Claas; Qi Qiao; Bernardo Aguzzoli Heberle; J. Anthony Brandon; Madeline L. Page; Timothy J. Hohman; Shubhabrata Mukherjee; Richard P. Mayeux; Lindsay A. Farrer; Gerard D. Schellenberg; Jonathan L. Haines; Walter A. Kukull; Kwangsik Nho; Andrew J. Saykin; David A. Bennett; Julie A. Schneider; Mark T. W. Ebbert; Peter T. Nelson; David W. Fardo
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Novel modelling approaches to elucidate the genetic architecture of resilience to Alzheimer's disease新颖的建模方法以阐明对阿尔茨海默病的遗传抗性机制
errBRAIN
IF11.7
err2025-05-01
err0
PREAI
errPhillips, Jared M.; Dumitrescu, Logan C.; Archer, Derek B.; Regelson, Alexandra N.; Mukherjee, Shubhabrata; Lee, Michael L.; Choi, Seo-Eun; Scollard, Phoebe; Trittschuh, Emily H.; Kukull, Walter A.; Biber, Sarah; Mez, Jesse; Mahoney, Emily R.; Clifton, Michelle; Libby, Julia B.; Walters, Skylar; Bush, William S.; Engelman, Corinne D.; Lu, Qiongshi; Fardo, David W.; Widaman, Keith F.; Buckley, Rachel F.; Mormino, Elizabeth C.; Sanders, R. Elizabeth; Clark, Lindsay R.; Gifford, Katherine A.; Vardarajan, Badri; Cuccaro, Michael L.; Pericak-Vance, Margaret A.; Farrer, Lindsay A.; Wang, Li-San; Schellenberg, Gerard D.; Haines, Jonathan L.; Jefferson, Angela L.; Johnson, Sterling C.; Albert, Marilyn S.; Keene, C. Dirk; Saykin, Andrew J.; Risacher, Shannon L.; Larson, Eric B.; Sperling, Reisa A.; Mayeux, Richard; Goate, Alison M.; Renton, Alan E.; Marcora, Edoardo; Fulton-Howard, Brian; Patel, Tulsi; Bennett, David A.; Schneider, Julie A.; Barnes, Lisa L.; Cruchaga, Carlos; Hassenstab, Jason; Belloy, Michael E.; Andrews, Shea J.; Resnick, Susan M.; Bilgel, Murat; An, Yang; Beason-Held, Lori L.; Walker, Keenan A.; Duggan, Michael R.; Klinedinst, Brandon S.; Crane, Paul K.; Hohman, Timothy J.
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LATE-NC Stage 3: a diagnostic rubric to differentiate severe LATE-NC from FTLD-TDPLATE-NC阶段3:一种用于区分严重LATE-NC与FTLD-TDP的诊断标准
err2025-04-28
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errOAAI
errShahidehpour, RK; Katsumata, Y; Dickson, DW; Ghayal, NB; Aung, KZ; Wu, X; Phe, P; Jicha, GA; Neltner, AM; Archer, JRC; Corrada, MM; Kawas, CH; Sajjadi, SA; Woodworth, DC; Bukhari, SA; Montine, TJ; Fardo, DW; Nelson, PT
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Genomic and phenotypic correlates of mosaic loss of chromosome Y in blood血液中嵌合体Y染色体缺失的基因组与表型相关性
err2025-02-01
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errOAAI
errJakubek, YA; Ma, XL; Stilp, AM; Yu, FL; Bacon, J; Wong, JW; Aguet, F; Ardlie, K; Arnett, DK; Barnes, K; Bis, JC; Blackwell, T; Becker, LC; Boerwinkle, E; Bowler, RP; Budoff, MJ; Carson, AP; Chen, JW; Cho, MH; Coresh, J; Cox, NJ; Vries, PSD; Demeo, DL; Fardo, DW; Fornage, M; Guo, XQ; Hall, ME; Heard-Costa, N; Hidalgo, B; Irvin, MR; Johnson, AD; Jorgenson, E; Kenny, EE; Kessler, MD; Levy, D; Li, Y; Lima, JAC; Liu, YM; Locke, AE; Loos, RJF; Machiela, MJ; Mathias, RA; Mitchell, BD; Murabito, JM; Mychaleckyj, JC; North, KE; Orchard, P; Parker, SCJ; Pershad, Y; Peyser, PA; Pratte, KA; Psaty, BM; Raffield, LM; Redline, S; Rich, SS; Rotter, JI; Shah, SJ; Smith, JA; Smith, AP; Smith, A; Taub, MA; Tiwari, HK; Tracy, R; Tuftin, B; Bick, AG; Sankaran, VG; Reiner, AP; Scheet, P; Auer, PL
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