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

Genome-wide study of resistant hypertension identified from electronic health records

基于电子健康记录的难治性高血压全基因组研究

Dumitrescu, Logan; Ritchie, Marylyn D; Denny, Joshua C; El Rouby, Nihal M; McDonough, Caitrin W; Bradford, Yuki; Ramirez, Andrea H; Bielinski, Suzette J; Basford, Melissa A; Chai, High Seng; Peissig, Peggy; Carrell, David; Pathak, Jyotishman; Rasmussen, Luke V; Wang, Xiaoming; Pacheco, Jennifer A; Kho, Abel N; Hayes, M Geoffrey; Matsumoto, Martha; Smith, Maureen E; Li, Rongling; Cooper-DeHoff, Rhonda M; Kullo, Iftikhar J; Chute, Christopher G; Chisholm, Rex L; Jarvik, Gail P; Larson, Eric B; Carey, David; McCarty, Catherine A; Williams, Marc S; Roden, Dan M; Bottinger, Erwin; Johnson, Julie A; de Andrade, Mariza; Crawford, Dana C

Human whole genome genotype and transcriptome data for Alzheimer's and other neurodegenerative diseases

阿尔茨海默病和其他神经退行性疾病的人类全基因组基因型和转录组数据

Allen, Mariet; Carrasquillo, Minerva M; Funk, Cory; Heavner, Benjamin D; Zou, Fanggeng; Younkin, Curtis S; Burgess, Jeremy D; Chai, High-Seng; Crook, Julia; Eddy, James A; Li, Hongdong; Logsdon, Ben; Peters, Mette A; Dang, Kristen K; Wang, Xue; Serie, Daniel; Wang, Chen; Nguyen, Thuy; Lincoln, Sarah; Malphrus, Kimberly; Bisceglio, Gina; Li, Ma; Golde, Todd E; Mangravite, Lara M; Asmann, Yan; Price, Nathan D; Petersen, Ronald C; Graff-Radford, Neill R; Dickson, Dennis W; Younkin, Steven G; Ertekin-Taner, Nilüfer

Late-onset Alzheimer disease risk variants mark brain regulatory loci

晚发性阿尔茨海默病风险变异标记大脑调控位点

Allen, Mariet; Kachadoorian, Michaela; Carrasquillo, Minerva M; Karhade, Aditya; Manly, Lester; Burgess, Jeremy D; Wang, Chen; Serie, Daniel; Wang, Xue; Siuda, Joanna; Zou, Fanggeng; Chai, High Seng; Younkin, Curtis; Crook, Julia; Medway, Christopher; Nguyen, Thuy; Ma, Li; Malphrus, Kimberly; Lincoln, Sarah; Petersen, Ronald C; Graff-Radford, Neill R; Asmann, Yan W; Dickson, Dennis W; Younkin, Steven G; Ertekin-Taner, Nilüfer

Association of MAPT haplotypes with Alzheimer's disease risk and MAPT brain gene expression levels

MAPT单倍型与阿尔茨海默病风险及MAPT脑基因表达水平的关联

Allen, Mariet; Kachadoorian, Michaela; Quicksall, Zachary; Zou, Fanggeng; Chai, High Seng; Younkin, Curtis; Crook, Julia E; Pankratz, V Shane; Carrasquillo, Minerva M; Krishnan, Siddharth; Nguyen, Thuy; Ma, Li; Malphrus, Kimberly; Lincoln, Sarah; Bisceglio, Gina; Kolbert, Christopher P; Jen, Jin; Mukherjee, Shubhabrata; Kauwe, John K; Crane, Paul K; Haines, Jonathan L; Mayeux, Richard; Pericak-Vance, Margaret A; Farrer, Lindsay A; Schellenberg, Gerard D; Parisi, Joseph E; Petersen, Ronald C; Graff-Radford, Neill R; Dickson, Dennis W; Younkin, Steven G; Ertekin-Taner, Nilüfer

Concordance of changes in metabolic pathways based on plasma metabolomics and skeletal muscle transcriptomics in type 1 diabetes

基于血浆代谢组学和骨骼肌转录组学的1型糖尿病代谢通路变化的一致性

Dutta, Tumpa; Chai, High Seng; Ward, Lawrence E; Ghosh, Aditya; Persson, Xuan-Mai T; Ford, G Charles; Kudva, Yogish C; Sun, Zhifu; Asmann, Yan W; Kocher, Jean-Pierre A; Nair, K Sreekumaran

Brain expression genome-wide association study (eGWAS) identifies human disease-associated variants

脑表达全基因组关联研究(eGWAS)鉴定出与人类疾病相关的变异

Zou, Fanggeng; Chai, High Seng; Younkin, Curtis S; Allen, Mariet; Crook, Julia; Pankratz, V Shane; Carrasquillo, Minerva M; Rowley, Christopher N; Nair, Asha A; Middha, Sumit; Maharjan, Sooraj; Nguyen, Thuy; Ma, Li; Malphrus, Kimberly G; Palusak, Ryan; Lincoln, Sarah; Bisceglio, Gina; Georgescu, Constantin; Kouri, Naomi; Kolbert, Christopher P; Jen, Jin; Haines, Jonathan L; Mayeux, Richard; Pericak-Vance, Margaret A; Farrer, Lindsay A; Schellenberg, Gerard D; Petersen, Ronald C; Graff-Radford, Neill R; Dickson, Dennis W; Younkin, Steven G; Ertekin-Taner, Nilüfer

TREAT: a bioinformatics tool for variant annotations and visualizations in targeted and exome sequencing data

TREAT:一款用于靶向测序和外显子组测序数据中变异注释和可视化的生物信息学工具

Asmann, Yan W; Middha, Sumit; Hossain, Asif; Baheti, Saurabh; Li, Ying; Chai, High-Seng; Sun, Zhifu; Duffy, Patrick H; Hadad, Ahmed A; Nair, Asha; Liu, Xiaoyu; Zhang, Yuji; Klee, Eric W; Kalari, Krishna R; Kocher, Jean-Pierre A

Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies

FOXE1基因附近的变异与甲状腺功能减退症和其他甲状腺疾病相关:利用电子病历进行全基因组和全表型组研究

Denny, Joshua C; Crawford, Dana C; Ritchie, Marylyn D; Bielinski, Suzette J; Basford, Melissa A; Bradford, Yuki; Chai, High Seng; Bastarache, Lisa; Zuvich, Rebecca; Peissig, Peggy; Carrell, David; Ramirez, Andrea H; Pathak, Jyotishman; Wilke, Russell A; Rasmussen, Luke; Wang, Xiaoming; Pacheco, Jennifer A; Kho, Abel N; Hayes, M Geoffrey; Weston, Noah; Matsumoto, Martha; Kopp, Peter A; Newton, Katherine M; Jarvik, Gail P; Li, Rongling; Manolio, Teri A; Kullo, Iftikhar J; Chute, Christopher G; Chisholm, Rex L; Larson, Eric B; McCarty, Catherine A; Masys, Daniel R; Roden, Dan M; de Andrade, Mariza

Mayo Genome Consortia: a genotype-phenotype resource for genome-wide association studies with an application to the analysis of circulating bilirubin levels

梅奥基因组联盟:用于全基因组关联研究的基因型-表型资源,可应用于循环胆红素水平的分析

Bielinski, Suzette J; Chai, High Seng; Pathak, Jyotishman; Talwalkar, Jayant A; Limburg, Paul J; Gullerud, Rachel E; Sicotte, Hugues; Klee, Eric W; Ross, Jason L; Kocher, Jean-Pierre A; Kullo, Iftikhar J; Heit, John A; Petersen, Gloria M; de Andrade, Mariza; Chute, Christopher G

Batch effect correction for genome-wide methylation data with Illumina Infinium platform

利用Illumina Infinium平台对全基因组甲基化数据进行批次效应校正

Sun, Zhifu; Chai, High Seng; Wu, Yanhong; White, Wendy M; Donkena, Krishna V; Klein, Christopher J; Garovic, Vesna D; Therneau, Terry M; Kocher, Jean-Pierre A