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

Donor-specific assemblies enhance somatic structural variant detection in complex genomic regions

供体特异性组装可增强复杂基因组区域中体细胞结构变异的检测

Mack, Taralynn; Lin, Jiadong; Ren, Luyao; Sohn, Min-Hwan; Minkina, Anna; Kwon, Youngjun; Yoo, DongAhn; Sui, Yang; Munson, Katherine M; Hoekzema, Kendra; Mastrorosa, F Kumara; Sorensen, Melanie; Ayllon, Marcelo; Sun, Kaitlyn A; Koundiya, Nidhi; Ou, Jeffrey; Noyes, Michelle D; Sedeño-Cortés, Adriana; Leonardson, Amy; Jacques, Caitlin N; Oliviera, Chris; Frazar, Christian D; Zakarian, Christina; Jensen, Dana M; Swanson, Elliot G; Ryke, Erica; Kolar, J Thomas; Ranchalis, Jane; Sutherlin, Lila; Vollger, Mitchell R; Loy, Kelsey; Pham, Meranda M; Huang, Meng-Fan; Au, Natalie Yt; Nielsen, Patrick M; McGee, Sean R; Neph, Shane; Bohaczuk, Stephanie; Shaffer, Tristan; Freeman, Vea; Mao, Yizi; Stillman, Benjamin Cohen; Richardson, Matthew; Smith, Joshua D; Weiss, Jeffrey M; Parmalee, Nancy L; Wei, Chia-Lin; Bennett, James T; Stergachis, Andrew B; Eichler, Evan E

Mapping single-cell diploid chromatin fiber architectures using DAF-seq

利用DAF-seq技术绘制单细胞二倍体染色质纤维结构图谱

Swanson, Elliott G; Mao, Yizi; Mallory, Benjamin J; Vollger, Mitchell R; Bohaczuk, Stephanie C; Oliveira, Christopher B; Lyon, Daniel B; Ranchalis, Jane; Parmalee, Nancy L; Cohen, Barak A; Bennett, James T; Stergachis, Andrew B

A telomere-to-telomere map of somatic mutation burden and functional impact in cancer

癌症中体细胞突变负荷和功能影响的端粒到端粒图谱

Sohn, Min-Hwan; Dubocanin, Danilo; Vollger, Mitchell R; Kwon, Youngjun; Minkina, Anna; Munson, Katherine M; Hart, Samuel Fm; Ranchalis, Jane E; Parmalee, Nancy L; Sedeño-Cortés, Adriana E; Ou, Jeffrey; Au, Natalie Yt; Bohaczuk, Stephanie; Carroll, Brianne; Frazar, Christian D; Harvey, William T; Hoekzema, Kendra; Huang, Meng-Fan; Jacques, Caitlin N; Jensen, Dana M; Kolar, J Thomas; Lee, Rosa; Lin, Jiadong; Loy, Kelsey; Mack, Taralynn; Mao, Yizi; Pham, Meranda M; Ryke, Erica; Smith, Joshua D; Sutherlin, Lila; Swanson, Elliott G; Weiss, Jeffrey M; Wg, SMaHT Assembly; Carvalho, Claudia; Coorens, Tim Hh; Harris, Kelley; Wei, Chia-Lin; Eichler, Evan E; Altemose, Nicolas; Bennett, James T; Stergachis, Andrew B

Comprehensive benchmarking of somatic single-nucleotide variant and indel detection at ultra-low allele fractions using short- and long-read data

利用短读长和长读长数据对超低等位基因频率下的体细胞单核苷酸变异和插入缺失检测进行全面基准测试

Jiny Ha, Yoo-Jin; Maziec, Dominika; Markowski, Julia; Georges, Stephanie J; Parmalee, Nancy L; Berselli, Michele; Coorens, Tim H H; Dong, Shihua; Gardiner, Stephanie; Kalra, Divya; Li, Daofeng; Miao, Benpeng; Musunuri, Rajeeva; Xue, Liying; Yu, Zhi; Walker, Kimberly; Anderson, Lisa; Au, Natalie Y T; Cibulskis, Carrie; Doddapaneni, Harsha; Grochowski, Christopher M; Jensen, Dana M; Lindsay, Tina; Loy, Kelsey; Narayan, Azeet; Narzisi, Giuseppe; Ou, Jeffrey; Pham, Meranda M; Runnels, Alexi M; Stergachis, Andrew B; Sutherlin, Lila M; Wang, Ting; Jin, Hu; Feng, William C; Zhang, Yuwei; Veit, Alexander D; TaeHee Kim, Clara; Chun, Hye-Jung E; Ardlie, Kristin; Fulton, Robert S; Germer, Soren; Gibbs, Richard; Marth, Gabor T; Bennett, James T; Park, Peter J

A haplotype-resolved view of human gene regulation.

基于单倍型解析的人类基因调控观点

Vollger Mitchell R, Swanson Elliott G, Neph Shane J, Ranchalis Jane, Munson Katherine M, Ho Ching-Huang, Cheng Y H Hank, Sedeño-Cortés Adriana E, Fondrie William E, Bohaczuk Stephanie C, Dippel Maxwell A, Mao Yizi, Parmalee Nancy L, Mallory Benjamin J, Harvey William T, Kwon Younjun, Garcia Gage H, Hoekzema Kendra, Meyer Jeffrey G, Cicek Mine, Eichler Evan E, Noble William S, Witten Daniela M, Bennett James T, Ray John P, Stergachis Andrew B

Analysis of recent shared ancestry in a familial cohort identifies coding and noncoding autism spectrum disorder variants

对家族队列中近期共同祖先的分析,识别出编码和非编码自闭症谱系障碍的变异。

Tuncay, Islam Oguz; Parmalee, Nancy L; Khalil, Raida; Kaur, Kiran; Kumar, Ashwani; Jimale, Mohamed; Howe, Jennifer L; Goodspeed, Kimberly; Evans, Patricia; Alzghoul, Loai; Xing, Chao; Scherer, Stephen W; Chahrour, Maria H

Huntington's disease genotype suppresses global manganese-responsive processes in pre-manifest and manifest YAC128 mice

亨廷顿氏病基因型抑制了 YAC128 小鼠在发病前和发病时的总体锰反应过程

Anna C Pfalzer, Jordyn M Wilcox, Simona G Codreanu, Melissa Totten, Terry J V Bichell, Timothy Halbesma, Preethi Umashanker, Kevin L Yang, Nancy L Parmalee, Stacy D Sherrod, Keith M Erikson, Fiona E Harrison, John A McLean, Michael Aschner, Aaron B Bowman

Microglia Activation and Gene Expression Alteration of Neurotrophins in the Hippocampus Following Early-Life Exposure to E-Cigarette Aerosols in a Murine Model

小鼠模型中早期接触电子香烟气溶胶后海马中小胶质细胞的激活和神经营养因子基因表达的改变

Judith T Zelikoff, Nancy L Parmalee, Kevin Corbett, Terry Gordon, Catherine B Klein, Michael Aschner

Metals and Circadian Rhythms

金属与昼夜节律

Parmalee, Nancy L; Aschner, Michael

Untangling the Manganese-α-Synuclein Web

解开锰-α-突触核蛋白网络

Peres, Tanara Vieira; Parmalee, Nancy L; Martinez-Finley, Ebany J; Aschner, Michael