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

Global multi-ancestry genome-wide analyses identify genes and biological pathways associated with thyroid cancer and benign thyroid diseases

全球多族裔全基因组分析鉴定出与甲状腺癌和良性甲状腺疾病相关的基因和生物学通路

White, Samantha L; Brasher, Maizy S; Pattee, Jack; Zhou, Wei; Chapman, Sinéad; Jee, Yon Ho; Bell, Caitlin C; Jamil, Taylor L; Barrio, Martin; Arehart, Christopher H; Evans, Luke M; Hirbo, Jibril; Cox, Nancy J; Straub, Peter; Namba, Shinichi; Bertucci-Richter, Emily; Guare, Lindsay; Edris, Ahmed; Morris, Sam; Mulford, Ashley J; Zhang, Haoyu; Fennessy, Brian; Tobin, Martin D; Chen, Jing; Williams, Alexander T; John, Catherine; van Heel, David A; Mathur, Rohini; Finer, Sarah; Moksnes, Marta R; Brumpton, Ben M; Åsvold, Bjørn Olav; Peculis, Raitis; Rovite, Vita; Konrade, Ilze; Wang, Ying; Crooks, Kristy; Chavan, Sameer; Fisher, Matthew J; Rafaels, Nicholas; Lin, Meng; Shortt, Jonathan A; Sanders, Alan R; Whiteman, David C; MacGregor, Stuart; Medland, Sarah E; Thorsteinsdóttir, Unnur; Stefánsson, Kári; Karaderi, Tugce; Egan, Kathleen M; Bocklage, Therese; McCrary, Hilary C; Riedlinger, Gregory; Salhia, Bodour; Shriver, Craig; Phan, Minh D; Farlow, Janice L; Edge, Stephen; Kaur, Varinder; Churchman, Michelle L; Rounbehler, Robert J; Brock, Pamela L; Ringel, Matthew D; Pividori, Milton; Schweppe, Rebecca; Raeburn, Christopher D; Walters, Robin G; Chen, Zhengming; Li, Liming; Matsuda, Koichi; Okada, Yukinori; Zöllner, Sebastian; Verma, Anurag; Preuss, Michael H; Kenny, Eimear; Hendricks, Audrey E; Fishbein, Lauren; Kraft, Peter; Daly, Mark J; Neale, Benjamin M; Martin, Alicia R; Cole, Joanne B; Haugen, Bryan R; Gignoux, Christopher R; Pozdeyev, Nikita

Risk for coronary artery disease among individuals with normal low-density lipoprotein cholesterol (LDL-C) levels

低密度脂蛋白胆固醇(LDL-C)水平正常人群患冠状动脉疾病的风险

Shi, Zhuqing; Mulford, Ashley J; Wei, Jun; Tran, Huy; Ashworth, Annabelle; Zheng, S Lilly; Helfand, Brian T; Duggan, David; Dunnenberger, Henry M; Hulick, Peter J; Davidson, David J; Qamar, Arman; Sanders, Alan R; Xu, Jianfeng

Female iPSC X-chromosome inactivation (XCI) erosion and its transcriptomic effects during CRISPR gene editing and neural differentiation

女性诱导多能干细胞X染色体失活(XCI)侵蚀及其在CRISPR基因编辑和神经分化过程中的转录组效应

Thapa, Christina; Oh, Emily K; Sirkin, David; Lahey, Jennifer; de León Guerrerro, Sol Díaz; McCarroll, Ada; Gowda, Prarthana; Zhang, Hanwen; Barishman, Alexandra; Peyton, Lilia; Zhang, Siwei; Pollak, Rebecca M; Hart, Ronald P; Pato, Carlos N; Kreimer, Anat; Mulle, Jennifer G; Sanders, Alan R; Pang, Zhiping; Duan, Jubao

PICALM Alzheimer's risk allele causes aberrant lipid droplets in microglia.

PICALM 阿尔茨海默病风险等位基因导致小胶质细胞中出现异常脂滴。

Kozlova Alena, Zhang Siwei, Sudwarts Ari, Zhang Hanwen, Smirnou Stanislau, Byeon Seul Kee, Thapa Christina, Sun Xiaotong, Stephenson Kimberley, Zhao Xiaojie, Jamison Brendan, Ponnusamy Moorthi, He Xin, Schneider Julie A, Pandey Akhilesh, Bennett David A, Pang Zhiping P, Sanders Alan R, Bellen Hugo J, Thinakaran Gopal, Duan Jubao

Alzheimer's disease protective allele of Clusterin modulates neuronal excitability through lipid-droplet-mediated neuron-glia communication.

阿尔茨海默病保护性簇蛋白等位基因通过脂滴介导的神经元-胶质细胞通讯调节神经元兴奋性

Zhao Xiaojie, Li Yan, Zhang Siwei, Sudwarts Ari, Zhang Hanwen, Kozlova Alena, Moulton Matthew J, Goodman Lindsey D, Pang Zhiping P, Sanders Alan R, Bellen Hugo J, Thinakaran Gopal, Duan Jubao

Polygenic Score Complements Family History and Lynch Syndrome Genes for Predicting Colorectal Cancer Risk

多基因评分可与家族史和林奇综合征基因共同预测结直肠癌风险。

Helfand, Talia Y; Wei, Jun; Mulford, Ashley J; Tran, Huy; Shi, Zhuqing; Wang, Chi-Hsiung; Rifkin, Andrew S; Ashworth, Annabelle; Zheng, S Lilly; Helfand, Brian T; Dunnenberger, Henry M; Duggan, David; Hulick, Peter J; DePersia, Allison; Sanders, Alan R; Xu, Jianfeng

Lipid trajectories improve risk models for Alzheimer's disease and mild cognitive impairment

脂质轨迹可改善阿尔茨海默病和轻度认知障碍的风险模型

Chase, Bruce A; Frigerio, Roberta; Yucus, Chad J; Patel, Smita; Maraganore, Demetrius; Sanders, Alan R; Duan, Jubao; Markopoulou, Katerina

Development and validation of a genetic probability for venous thromboembolism

静脉血栓栓塞遗传概率的建立与验证

Shi, Zhuqing; Mulford, Ashley J; Tran, Huy; Filipczak, Michal; Gao, Song; Xie, Stevie; Lobel, Jason; Wei, Jun; Rifkin, Andrew S; Ashworth, Annabelle; Zheng, Siqun Lilly; Wiske, Clay; Duggan, David; Helfand, Brian T; Qamar, Arman; Sanders, Alan R; Tafur, Alfonso J; Xu, Jianfeng

Estimating Cancer Penetrance in Carriers of BRCA2 Pathogenic Variants Using Cancer-Specific Polygenic Scores

利用癌症特异性多基因评分估计BRCA2致病变异携带者的癌症外显率

Prassas, Brendan; Shi, Zhuqing; Tran, Huy; Wei, Jun; Wang, Chi-Hsiung; Rifkin, Andrew S; Ashworth, Annabelle; Zheng, S Lilly; Mulford, Ashley J; Sanders, Alan R; Pesce, Catherine E; Helfand, Brian T; Dunnenberger, Henry M; Duggan, David; Hulick, Peter J; DePersia, Allison; Xu, Jianfeng

Validation of GenProb-T1D and its clinical utility for differentiating types of diabetes in a biobank from a US healthcare system

验证 GenProb-T1D 及其在美国医疗保健系统生物样本库中区分糖尿病类型的临床应用价值

Billings, Liana K; Shi, Zhuqing; Mulford, Ashley J; Wei, Jun; Tran, Huy; Ashworth, Annabelle; Zheng, S Lilly; Dunnenberger, Henry M; Hulick, Peter J; Sanders, Alan R; Xu, Jianfeng