检索结果 - Wan‐Ping Lee
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One reference genome is not enough 由 Xiaofei Yang, Wan‐Ping Lee, Kai Ye, Charles Lee
出版 2019Artigo -
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Structural variation detection and association analysis of whole‐genome‐sequence data from 16,543 Alzheimer's disease sequencing project subjects 由 Hui Wang, Beth A. Dombroski, Po‐Liang Cheng, Albert Tucci, Yaqin Si, John Farrell, Jung‐Ying Tzeng, Yuk Yee Leung, John Malamon, Li‐San Wang, Richard Mayeux, Lindsay A. Farrer, Gerard D. Schellenberg, Wan‐Ping Lee
出版 2025Artigo -
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NIAGADS Alzheimer's GenomicsDB: A resource for exploring Alzheimer's disease genetic and genomic knowledge 由 Emily Greenfest‐Allen, Otto Valladares, Pavel P. Kuksa, Prabhakaran Gangadharan, Wan‐Ping Lee, Jeffrey Cifello, Živadin Katanić, Amanda B Kuzma, Nicholas R. Wheeler, William S. Bush, Yuk Yee Leung, Gerard D. Schellenberg, Christian J. Stoeckert, Li‐San Wang
出版 2023Artigo -
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FusorSV: an algorithm for optimally combining data from multiple structural variation detection methods 由 Timothy Becker, Wan‐Ping Lee, Joseph F. Leone, Qihui Zhu, Chengsheng Zhang, Silvia Liu, Jack Sargent, Kritika Shanker, Adam Mil-Homens, Eliza Cerveira, Mallory Ryan, Jane Cha, Fábio C. P. Navarro, Timur R. Galeev, Mark Gerstein, Ryan E. Mills, Dong‐Guk Shin, Charles Lee, Ankit Malhotra
出版 2018Artigo -
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A Comprehensive Map of Mobile Element Insertion Polymorphisms in Humans 由 Chip Stewart, Deniz Kural, Michael P. Strömberg, Jerilyn A. Walker, Miriam K. Konkel, Adrian M. Stütz, Alexander E. Urban, Fabian Grubert, Hugo Y. K. Lam, Wan-Ping Lee, Michele Busby, Amit Indap, Erik Garrison, Chad D. Huff, Jinchuan Xing, M Snyder, Lynn B. Jorde, Mark A. Batzer, Jan O. Korbel, Gábor Marth
出版 2011Artigo -
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Expectations and blind spots for structural variation detection from long-read assemblies and short-read genome sequencing technologies 由 Xuefang Zhao, Ryan L. Collins, Wan‐Ping Lee, Alexandra M. Weber, Yukyung Jun, Qihui Zhu, Ben Weisburd, Yongqing Huang, Peter A. Audano, Harold Wang, Mark Walker, Chelsea Lowther, Jack Fu, Mark Gerstein, Scott E. Devine, Tobias Marschall, Jan O. Korbel, Evan E. Eichler, Mark Chaisson, Charles Lee, Ryan E. Mills, Harrison Brand, Michael E. Talkowski
出版 2021Artigo -
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Fast and accurate genomic analyses using genome graphs 由 Goran Rakočević, Vladimir Semenyuk, Wan‐Ping Lee, James Spencer, John Browning, Ivan J. Johnson, V. Arsenijevic, Jelena Nadj, Kaushik Ghose, Maria Suciu, Sun‐Gou Ji, Gülfem Demir, Lizao Li, Berke Ç. Toptaş, Alexey Dolgoborodov, Björn Pollex, Iosif Spulber, Irina Glotova, Péter Kómár, A. L. Stachyra, Yilong Li, Miloš A. Popović, Morten Källberg, Amit Jain, Deniz Kural
出版 2019Artigo -
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Extended genome‐wide association study employing the African genome resources panel identifies novel susceptibility loci for Alzheimer's disease in individuals of African ancestry... 由 Nicholas R. Ray, Brian W. Kunkle, Kara L. Hamilton‐Nelson, Jiji T. Kurup, Farid Rajabli, Min Qiao, Badri N. Vardarajan, Mehmet İlyas Coşacak, Çağhan Kızıl, Melissa Jean‐Francois, Michael L. Cuccaro, Dolly Reyes‐Dumeyer, Laura Cantwell, Amanda Kuzma, Jeffery M. Vance, Sujuan Gao, Hugh C. Hendrie, Olusegun Baiyewu, Adesola Ogunniyi, Rufus Akinyemi, Wan‐Ping Lee, Eden R. Martin, Li‐San Wang, Gary W. Beecham, William S. Bush, Wanying Xu, Fulai Jin, Liyong Wang, Lindsay A. Farrer, Jonathan L. Haines, Goldie S. Byrd, Gerard D. Schellenberg, Richard Mayeux, Margaret A. Pericak‐Vance, Christiane Reitz
出版 2024Revisão -
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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 Projec... 由 Wan‐Ping Lee, Seung Hoan Choi, Margaret G. Shea, Po‐Liang Cheng, Beth A. Dombroski, Achilleas Pitsillides, Nancy L. Heard‐Costa, Hui Wang, Katia Bulekova, Amanda B Kuzma, Yuk Yee Leung, John J. Farrell, Honghuang Lin, Brian W. Kunkle, Adam C. Naj, Elizabeth Blue, Frederick Nusetor, Dongyu Wang, Eric Boerwinkle, William S. Bush, Xiaoling Zhang, Philip L. De Jager, Josée Dupuis, Lindsay A. Farrer, Myriam Fornage, Eden R. Martin, Margaret Pericak‐Vance, Sudha Seshadri, Ellen M. Wijsman, Li‐San Wang, Gerard D. Schellenberg, Anita L. DeStefano, Jonathan L. Haines, Gina M. Peloso
出版 2024Artigo -
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Alzheimer's Disease Sequencing Project release 4 whole genome sequencing dataset 由 Yuk Yee Leung, Wan‐Ping Lee, Amanda Kuzma, Heather Nicaretta, Otto Valladares, Prabhakaran Gangadharan, Liming Qu, Yi Zhao, Youli Ren, Po‐Liang Cheng, Pavel P. Kuksa, Hui Wang, Heather White, Živadin Katanić, Lauren Bass, Naveen Saravanan, Emily Greenfest‐Allen, Maureen Kirsch, Laura B. Cantwell, Taha Iqbal, Nicholas R. Wheeler, John Farrell, Congcong Zhu, F. S. Turner, Tamil Iniyan Gunasekaran, Pedro Mena, Yumi Jin, Luke Carter, Xiaoling Zhang, Badri N. Vardarajan, Arthur W. Toga, Michael L. Cuccaro, Timothy J. Hohman, William S. Bush, Adam C. Naj, Eden R. Martin, Clifton L. Dalgard, Brian W. Kunkle, Lindsay A. Farrer, Richard Mayeux, Jonathan L. Haines, Margaret A. Pericak‐Vance, Gerard D. Schellenberg, Li‐San Wang
出版 2025Artigo -
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Genetic, transcriptomic, histological, and biochemical analysis of progressive supranuclear palsy implicates glial activation and novel risk genes 由 Kurt Farrell, Jack Humphrey, Timothy S. Chang, Yi Zhao, Yuk Yee Leung, Pavel P. Kuksa, Vishakha Patil, Wan‐Ping Lee, Amanda B Kuzma, Otto Valladares, Laura B. Cantwell, Hui Wang, Ashvin Ravi, Claudia De Sanctis, Natalia Han, Thomas D. Christie, Robina Afzal, Shrishtee Kandoi, Kristen Whitney, Margaret M. Krassner, Hadley W. Ressler, SoongHo Kim, Diana K. Dangoor, Megan A. Iida, Alicia Casella, Ruth H. Walker, Melissa J. Nirenberg, Alan E. Renton, Bergan Babrowicz, Giovanni Coppola, Towfique Raj, Günter U. Höglinger, Ulrich Müller, Lawrence I. Golbe, Huw R. Morris, John Hardy, Tamás Révész, Thomas T. Warner, Zane Jaunmuktane, Kin Y. Mok, Rosa Rademakers, Dennis W. Dickson, Owen A. Ross, Li‐San Wang, Alison Goate, Daniela Berg, Daniel H. Geschwind, John F. Crary, Adam C. Naj
出版 2024Artigo -
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Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy 由 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 G.P. Dopper, Bernardino Ghetti, Kathy L. Newell, Claire Troakes, Justo Garcı́a de Yébenes, Alberto Rábano‐Gutierrez, Tina Meller, Wolfgang H. Oertel, Gesine Respondek, María Stamelou, Thomas Arzberger, Sigrun Roeber, Ulrich Müller, Franziska Hopfner, Pau Pástor, Alexis Brice, Alexandra Dürr, 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 R. Morris, Rohan de Silva, John F. Crary, Alison Goate, Jeffrey S. Friedman, Yuk Yee Leung, Giovanni Coppola, Adam C. Naj, Li-San Wang, Clifton L. Dalgard, Dennis W. Dickson, Günter U. Höglinger, Gerard D. Schellenberg, Daniel H. Geschwind, Wan‐Ping Lee
出版 2024Artigo -
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Copy Number Variation and Haplotype Analysis of <scp>17q21.31</scp> Reveals Increased Risk Associated with Progressive Supranuclear Palsy and Gene Expression Changes in Neuronal Ce... 由 Hui Wang, Timothy S. Chang, Beth A. Dombroski, Po‐Liang Cheng, Yaqin Si, Albert Tucci, Vishakha Patil, Leopoldo Valiente‐Banuet, Chong Li, 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 G.P. Dopper, Bernardino Ghetti, Kathy L. Newell, Claire Troakes, Onintza Sagredo, Alberto Rábano‐Gutierrez, Tina Meller, Wolfgang H. Oertel, Gesine Respondek, María Stamelou, Thomas Arzberger, Sigrun Roeber, Ulrich Müller, Franziska Hopfner, Pau Pástor, Alexis Brice, Alexandra Dürr, 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, Vivianna M. Van Deerlin, Edward B. Lee, Charles L. White, Huw R. Morris, Rohan de Silva, John F. Crary, Alison Goate, Jeffrey S. Friedman, Yaroslau Compta, Yuk Yee Leung, Giovanni Coppola, Adam C. Naj, Li‐San Wang, Clifton L. Dalgard, Dennis W. Dickson, Günter U. Höglinger, Jung‐Ying Tzeng, Daniel H. Geschwind, Gerard D. Schellenberg, Wan‐Ping Lee
出版 2025Artigo
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Biology
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Single-nucleotide polymorphism
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Structural variation
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Genome-wide association study
Human genome
Pathology
Reference genome
1000 Genomes Project
Haplotype
Genomics
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Alzheimer's disease
Copy-number variation
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Indel
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Environmental health
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Progressive supranuclear palsy