Torthaí cuardaigh - Wan‐Ping Lee
- 1 - 20 toradh as 24 á dtaispeáint
- Téigh chuig an gcéad leathanach eile
-
1
SSW Library: An SIMD Smith-Waterman C/C++ Library for Use in Genomic Applications de réir Mengyao Zhao, Wan-Ping Lee, Erik Garrison, Gábor Marth
Foilsithe / Cruthaithe 2013Artigo -
2
One reference genome is not enough de réir Xiaofei Yang, Wan‐Ping Lee, Kai Ye, Charles Lee
Foilsithe / Cruthaithe 2019Artigo -
3
The role of structural variations in Alzheimer’s disease and other neurodegenerative diseases de réir Hui Wang, Li‐San Wang, Gerard D. Schellenberg, Wan‐Ping Lee
Foilsithe / Cruthaithe 2023Revisão -
4
MOSAIK: A Hash-Based Algorithm for Accurate Next-Generation Sequencing Short-Read Mapping de réir Wan-Ping Lee, Michael P. Strömberg, Alistair Ward, Chip Stewart, Erik Garrison, Gábor Marth
Foilsithe / Cruthaithe 2014Artigo -
5
Polygenic Risk Scores in Alzheimer’s Disease Genetics: Methodology, Applications, Inclusion, and Diversity de réir Kaylyn Clark, Yuk Yee Leung, Wan‐Ping Lee, Benjamin F. Voight, Li‐San Wang
Foilsithe / Cruthaithe 2022Revisão -
6
Polygenic burden of short tandem repeat expansions promotes risk for Alzheimer’s disease de réir Michael H. Guo, Wan‐Ping Lee, Badri N. Vardarajan, Gerard D. Schellenberg, Jennifer E. Phillips‐Cremins
Foilsithe / Cruthaithe 2025Artigo -
7
Tangram: a comprehensive toolbox for mobile element insertion detection de réir Jiantao Wu, Wan-Ping Lee, Alistair Ward, Jerilyn A. Walker, Miriam K. Konkel, Mark A. Batzer, Gábor Marth
Foilsithe / Cruthaithe 2014Artigo -
8
Persistence and clinical consequences of post-traumatic and dissociative symptoms in people with depressive symptoms: a one-year follow-up study de réir Hong Wang Fung, Anson Kai Chun Chau, Suet Lin Hung, Stanley Kam Ki Lam, Wai Tong Chien, Vincent Wan Ping Lee
Foilsithe / Cruthaithe 2023Artigo -
9
Structural variation detection and association analysis of whole‐genome‐sequence data from 16,543 Alzheimer's disease sequencing project subjects de réir 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
Foilsithe / Cruthaithe 2025Artigo -
10
NIAGADS Alzheimer's GenomicsDB: A resource for exploring Alzheimer's disease genetic and genomic knowledge de réir 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
Foilsithe / Cruthaithe 2023Artigo -
11
FusorSV: an algorithm for optimally combining data from multiple structural variation detection methods de réir 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
Foilsithe / Cruthaithe 2018Artigo -
12
A Comprehensive Map of Mobile Element Insertion Polymorphisms in Humans de réir 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
Foilsithe / Cruthaithe 2011Artigo -
13
Expectations and blind spots for structural variation detection from long-read assemblies and short-read genome sequencing technologies de réir 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
Foilsithe / Cruthaithe 2021Artigo -
14
Fast and accurate genomic analyses using genome graphs de réir 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
Foilsithe / Cruthaithe 2019Artigo -
15
Extended genome‐wide association study employing the African genome resources panel identifies novel susceptibility loci for Alzheimer's disease in individuals of African ancestry... de réir 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
Foilsithe / Cruthaithe 2024Revisão -
16
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... de réir 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
Foilsithe / Cruthaithe 2024Artigo -
17
Alzheimer's Disease Sequencing Project release 4 whole genome sequencing dataset de réir 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
Foilsithe / Cruthaithe 2025Artigo -
18
Genetic, transcriptomic, histological, and biochemical analysis of progressive supranuclear palsy implicates glial activation and novel risk genes de réir 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
Foilsithe / Cruthaithe 2024Artigo -
19
Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy de réir 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
Foilsithe / Cruthaithe 2024Artigo -
20
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... de réir 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
Foilsithe / Cruthaithe 2025Artigo
Uirlisí cuardaigh:
Ábhair a bhaineann le hábhar
Biology
Gene
Genetics
Genome
Genotype
Single-nucleotide polymorphism
Computational biology
Medicine
Disease
Structural variation
Computer science
Genetic association
Genome-wide association study
Human genome
Pathology
Reference genome
1000 Genomes Project
Haplotype
Genomics
Population
Allele
Alzheimer's disease
Copy-number variation
DNA sequencing
Indel
Atrophy
Environmental health
Genetic architecture
Programming language
Progressive supranuclear palsy