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

Climate Change Challenges Grey Wolf Resilience: Insights From Dental Microwear

气候变化挑战灰狼的适应能力:来自牙齿微磨损的启示

Burtt, Amanda A; Adams, Neil F; Nowak, Sabina; Mysłajek, Robert W; Figura, Michal; Purnell, Mark A; Lamb, Angela L; Schreve, Danielle C

Medical Radiation Exposures in Canada: 2017

加拿大医疗辐射暴露情况:2017 年

Burtt, Julie J; Anandarajah, Seshan; Morrison, Andra; Wilkins, Ruth C

A resource of "bottom-line" variant associations for 1,281 complex traits by integrating data across published genome-wide association studies

通过整合已发表的全基因组关联研究数据,我们获得了1281个复杂性状的“最终”变异关联资源。

Nguyen, Trang; Büyükgöl, Furkan; Smadbeck, Patrick; Massung, Jeffrey; Costanzo, Maria C; Ruiz, Monica; Dornbos, Peter; Yoshiji, Satoshi; Koesterer, Ryan; Nguyen, Thanh Long; Jang, Dongkeun; Hoang, Quy; Ji, Yue; McMahon, Aoife; Sengupta, Sebanti; Yin, Xianyong; Ryan, Brady; Welch, Ryan P; Treur, Jorien; Bezzina, Connie R; Abecasis, Goncalo; Boehnke, Michael; Burtt, Noël P; Flannick, Jason

Carbonate formation and fluctuating habitability on Mars

火星上的碳酸盐形成和宜居性波动

Kite, Edwin S; Tutolo, Benjamin M; Turner, Madison L; Franz, Heather B; Burtt, David G; Bristow, Thomas F; Fischer, Woodward W; Milliken, Ralph E; Fraeman, Abigail A; Zhou, Daniel Y

Realizing the promise of genome-wide association studies for effector gene prediction

实现全基因组关联研究在效应基因预测方面的潜力

Costanzo, Maria C; Harris, Laura W; Ji, Yue; McMahon, Aoife; Burtt, Noël P; Flannick, Jason

Accelerating Medicines Partnership in Type 2 Diabetes and Common Metabolic Diseases: Collaborating to Maximize the Value of Genetic and Genomic Data

加速药物研发伙伴关系在 2 型糖尿病和常见代谢疾病领域的应用:携手合作,最大限度地发挥遗传和基因组数据的价值

Costanzo, Maria C; Akolkar, Beena; Claussnitzer, Melina; Florez, Jose C; Gloyn, Anna L; Grant, Struan F A; Kaestner, Klaus H; Manning, Alisa K; Mohlke, Karen L; Parker, Stephen C J; Titchenell, Paul M; Udler, Miriam S; Jones, Melissa A; Kamphaus, Tania N; Fischer, Rachel A; McCarthy, Mark I; Miller, Melissa R; Boehnke, Michael; Flannick, Jason; Burtt, Noël P

Erratum: The Neurodegenerative Disease Knowledge Portal: Propelling Discovery Through the Sharing of Neurodegenerative Disease Genomic Resources

更正:神经退行性疾病知识门户:通过共享神经退行性疾病基因组资源推动发现

Dilliott, Allison A; Costanzo, Maria C; Bandres-Ciga, Sara; Blauwendraat, Cornelis; Casey, Bradford; Hoang, Quy; Iwaki, Hirotaka; Jang, Dongkeun; Kim, Jonggeol Jeffrey; Leonard, Hampton L; Levine, Kristin S; Makarious, Mary; Nguyen, Trang T; Rouleau, Guy A; Singleton, Andrew B; Smadbeck, Patrick; Solle, J; Vitale, Dan; Nalls, Mike; Flannick, Jason; Burtt, Noël P; Farhan, Sali M K

The Neurodegenerative Disease Knowledge Portal: Propelling Discovery Through the Sharing of Neurodegenerative Disease Genomic Resources

神经退行性疾病知识门户:通过共享神经退行性疾病基因组资源推动发现

Dilliott, Allison A; Costanzo, Maria C; Bandres-Ciga, Sara; Blauwendraat, Cornelis; Casey, Bradford; Hoang, Quy; Iwaki, Hirotaka; Jang, Dongkeun; Kim, Jonggeol Jeffrey; Leonard, Hampton L; Levine, Kristin S; Makarious, Mary; Nguyen, Trang T; Rouleau, Guy A; Singleton, Andrew B; Smadbeck, Patrick; Solle, J; Vitale, Dan; Nalls, Mike; Flannick, Jason; Burtt, Noël P; Farhan, Sali M K

GWASHub: An Automated Cloud-Based Platform for Genome-Wide Association Study Meta-Analysis

GWASHub:用于全基因组关联研究荟萃分析的自动化云平台

Sunderland, Nicholas; Hite, Drew; Smadbeck, Patrick; Hoang, Quy; Jang, Dong-Keun; Tragante, Vinicius; Jiang, Jiayue-Clara; Shah, Sonia; Paternoster, Lavinia; Burtt, Noel P; Flannick, Jason; Lumbers, R Thomas

Selecting variant masks to improve power and replicability of gene-level burden tests

选择变异掩码以提高基因水平负担测试的效力和可重复性

Nguyen, Trang; Koesterer, Ryan; Jurgens, Sean J; Dornbos, Peter; Yoshiji, Satoshi; Llamas, Alex; Jang, Dongkeun; Smadbeck, Patrick; Moriondo, Annie; Hoang, Quy; Ruebenacker, Oliver; Ellinor, Patrick; Burtt, Noël; Flannick, Jason