日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Rare coding variants from ADSP R5 whole-genome sequencing implicate novel genes in Alzheimer's disease

来自 ADSP R5 全基因组测序的罕见编码变异揭示了与阿尔茨海默病相关的新基因

Lee, Wan-Ping; Wang, Hui; Leung, Yuk Yee; Cheng, Po-Liang; Zheng, Wendi; Valladares, Otto; Chung, Wei-Hsuan; Kuzma, Amanda; Naj, Adam; Vardarajan, Badri; Grsiwold, Anthony; Haines, Jonathan; Wang, Li-San; Schellenberg, Gerard

Structural variation detection and association analysis of whole-genome-sequence data from 16,543 Alzheimer's disease sequencing project subjects

对来自16,543名阿尔茨海默病测序项目受试者的全基因组测序数据进行结构变异检测和关联分析

Wang, Hui; Dombroski, Beth A; Cheng, Po-Liang; Tucci, Albert; Si, Ya-Qin; Farrell, John J; Tzeng, Jung-Ying; Leung, Yuk Yee; Malamon, John S; Wang, Li-San; Vardarajan, Badri N; Farrer, Lindsay A; Schellenberg, Gerard D; Lee, Wan-Ping

Alzheimer's Disease Sequencing Project release 4 whole genome sequencing dataset

阿尔茨海默病测序项目第四版全基因组测序数据集

Leung, Yuk Yee; Lee, Wan-Ping; Kuzma, Amanda B; Nicaretta, Heather; Valladares, Otto; Gangadharan, Prabhakaran; Qu, Liming; Zhao, Yi; Ren, Youli; Cheng, Po-Liang; Kuksa, Pavel P; Wang, Hui; White, Heather; Katanic, Zivadin; Bass, Lauren; Saravanan, Naveen; Greenfest-Allen, Emily; Kirsch, Maureen; Cantwell, Laura; Iqbal, Taha; Wheeler, Nicholas R; Farrell, John J; Zhu, Congcong; Turner, Shannon L; Gunasekaran, Tamil I; Mena, Pedro R; Jin, Yumi; Carter, Luke; Zhang, Xiaoling; Vardarajan, Badri N; Toga, Arthur; Cuccaro, Michael; Hohman, Timothy J; Bush, William S; Naj, Adam C; Martin, Eden; Dalgard, Clifton L; Kunkle, Brian W; Farrer, Lindsay A; Mayeux, Richard P; Haines, Jonathan L; Pericak-Vance, Margaret A; Schellenberg, Gerard D; Wang, Li-San

Copy Number Variation and Haplotype Analysis of 17q21.31 Reveals Increased Risk Associated with Progressive Supranuclear Palsy and Gene Expression Changes in Neuronal Cells

17q21.31拷贝数变异和单倍型分析揭示了进行性核上性麻痹风险增加以及神经元细胞基因表达变化。

Wang, Hui; Chang, Timothy S; Dombroski, Beth A; Cheng, Po-Liang; Si, Ya-Qin; Tucci, Albert; Patil, Vishakha; Valiente-Banuet, Leopoldo; Li, Chong; Farrell, Kurt; Mclean, Catriona; Molina-Porcel, Laura; Rajput, Alex; De Deyn, Peter Paul; Le Bastard, Nathalie; Gearing, Marla; Donker Kaat, Laura; Van Swieten, John C; Dopper, Elise; Ghetti, Bernardino F; Newell, Kathy L; Troakes, Claire; de Yébenes, Justo G; Rábano-Gutierrez, Alberto; Meller, Tina; Oertel, Wolfgang H; Respondek, Gesine; Stamelou, Maria; Arzberger, Thomas; Roeber, Sigrun; Müller, Ulrich; Hopfner, Franziska; Pastor, Pau; Brice, Alexis; Durr, Alexandra; Le Ber, Isabelle; Beach, Thomas G; Serrano, Geidy E; Hazrati, Lili-Naz; Litvan, Irene; Rademakers, Rosa; Ross, Owen A; Galasko, Douglas; Boxer, Adam L; Miller, Bruce L; Seeley, Willian W; Van Deerlin, Vivianna M; Lee, Edward B; White, Charles L 3rd; Morris, Huw R; de Silva, Rohan; Crary, John F; Goate, Alison M; Friedman, Jeffrey S; Compta, Yaroslau; Leung, Yuk Yee; Coppola, Giovanni; Naj, Adam C; Wang, Li-San; Dalgard, Clifton; Dickson, Dennis W; Höglinger, Günter U; Tzeng, Jung-Ying; Geschwind, Daniel H; Schellenberg, Gerard D; Lee, Wan-Ping

A specialized reference panel with structural variants integration for improving genotype imputation in Alzheimer disease and related dementias

整合了结构变异的专用参考面板,用于改进阿尔茨海默病及相关痴呆症的基因型推断。

Cheng, Po-Liang; Wang, Hui; Dombroski, Beth A; Farrell, John J; Horng, Iris; Chung, Tingting; Tosto, Giuseppe; Kunkle, Brian W; Bush, William S; Vardarajan, Badri; Schellenberg, Gerard D; Lee, Wan-Ping

Distinct genomic features and mutational signatures of nucleotide excision repair and mismatch repair in thymoma

胸腺瘤中核苷酸切除修复和错配修复的独特基因组特征和突变特征

Cheng, Po-Liang; Wang, Wei-Jan; Chuang, Cheng-Yen; Lin, Chih-Hung; Huang, Chih-Yang; Hsiao, Tzu-Hung; Hsu, Chung-Ping

Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy

全基因组测序分析揭示了与进行性核上性麻痹相关的新的易感基因位点和结构变异

Wang, Hui; Chang, Timothy S; Dombroski, Beth A; Cheng, Po-Liang; Patil, Vishakha; Valiente-Banuet, Leopoldo; Farrell, Kurt; Mclean, Catriona; Molina-Porcel, Laura; Rajput, Alex; De Deyn, Peter Paul; Le Bastard, Nathalie; Gearing, Marla; Kaat, Laura Donker; Van Swieten, John C; Dopper, Elise; Ghetti, Bernardino F; Newell, Kathy L; Troakes, Claire; de Yébenes, Justo G; Rábano-Gutierrez, Alberto; Meller, Tina; Oertel, Wolfgang H; Respondek, Gesine; Stamelou, Maria; Arzberger, Thomas; Roeber, Sigrun; Müller, Ulrich; Hopfner, Franziska; Pastor, Pau; Brice, Alexis; Durr, Alexandra; Le Ber, Isabelle; Beach, Thomas G; Serrano, Geidy E; Hazrati, Lili-Naz; Litvan, Irene; Rademakers, Rosa; Ross, Owen A; Galasko, Douglas; Boxer, Adam L; Miller, Bruce L; Seeley, Willian W; Van Deerlin, Vivanna M; Lee, Edward B; White, Charles L 3rd; Morris, Huw; de Silva, Rohan; Crary, John F; Goate, Alison M; Friedman, Jeffrey S; Leung, Yuk Yee; Coppola, Giovanni; Naj, Adam C; Wang, Li-San; Dalgard, Clifton; Dickson, Dennis W; Höglinger, Günter U; Schellenberg, Gerard D; Geschwind, Daniel H; Lee, Wan-Ping

Correction: Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy

更正:全基因组测序分析揭示了与进行性核上性麻痹相关的新的易感基因位点和结构变异

Wang, Hui; Chang, Timothy S; Dombroski, Beth A; Cheng, Po-Liang; Patil, Vishakha; Valiente-Banuet, Leopoldo; Farrell, Kurt; Mclean, Catriona; Molina-Porcel, Laura; Rajput, Alex; De Deyn, Peter Paul; Le Bastard, Nathalie; Gearing, Marla; Kaat, Laura Donker; Van Swieten, John C; Dopper, Elise; Ghetti, Bernardino F; Newell, Kathy L; Troakes, Claire; de Yébenes, Justo G; Rábano-Gutierrez, Alberto; Meller, Tina; Oertel, Wolfgang H; Respondek, Gesine; Stamelou, Maria; Arzberger, Thomas; Roeber, Sigrun; Müller, Ulrich; Hopfner, Franziska; Pastor, Pau; Brice, Alexis; Durr, Alexandra; Le Ber, Isabelle; Beach, Thomas G; Serrano, Geidy E; Hazrati, Lili-Naz; Litvan, Irene; Rademakers, Rosa; Ross, Owen A; Galasko, Douglas; Boxer, Adam L; Miller, Bruce L; Seeley, Willian W; Van Deerlin, Vivanna M; Lee, Edward B; White, Charles L 3rd; Morris, Huw; de Silva, Rohan; Crary, John F; Goate, Alison M; Friedman, Jeffrey S; Leung, Yuk Yee; Coppola, Giovanni; Naj, Adam C; Wang, Li-San; Dalgard, Clifton; Dickson, Dennis W; Höglinger, Günter U; Schellenberg, Gerard D; Geschwind, Daniel H; Lee, Wan-Ping

Association of common and rare variants with Alzheimer's disease in more than 13,000 diverse individuals with whole-genome sequencing from the Alzheimer's Disease Sequencing Project.

通过阿尔茨海默病测序项目对超过 13,000 名不同个体进行全基因组测序,研究常见和罕见变异与阿尔茨海默病的关联

Lee Wan-Ping, Choi Seung Hoan, Shea Margaret G, Cheng Po-Liang, Dombroski Beth A, Pitsillides Achilleas N, Heard-Costa Nancy L, Wang Hui, Bulekova Katia, Kuzma Amanda B, Leung Yuk Yee, Farrell John J, Lin Honghuang, Kunkle Brian W, Naj Adam, Blue Elizabeth E, Nusetor Frederick, Wang Dongyu, Boerwinkle Eric, Bush William S, Zhang Xiaoling, De Jager Philip L, Dupuis Josée, Farrer Lindsay A, Fornage Myriam, Martin Eden, Pericak-Vance Margaret, Seshadri Sudha, Wijsman Ellen M, Wang Li-San, Schellenberg Gerard D, Destefano Anita L, Haines Jonathan L, Peloso Gina M

Myeloperoxidase and Thyrotropin-Releasing Hormone Within Leukaemia Stem Cells Increased Chemosensitivity in Acute Myeloid Leukaemia

白血病干细胞内的髓过氧化物酶和促甲状腺激素释放激素可增强急性髓系白血病的化疗敏感性

Chen, Chung-Hsing; Chen, Tsung-Chih; Wu, Ting-Shuan; Hsiao, Tzu-Hung; Chen, Jo-Mei Maureen; Huang, Chi-Ying F; Cheng, Po-Liang; Tsai, Jia-Rung; Teng, Chieh-Lin Jerry