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

Genome-wide association meta-analyses over one million individuals identify 54 loci associated with urinary incontinence and its subtypes

对超过一百万人的全基因组关联荟萃分析确定了54个与尿失禁及其亚型相关的基因位点。

Moreno, Elisa; Arora, Nikhil; Bertucci-Richter, Emily; Eghtedarian, Reyhane; Andries, Aristomo; Thomas, Laurent F; Horn, Julie; Stafne, Signe N; Pathak, Sweta; FinnGen; Patil, Snehal; Gulla, Dagny; Ollila, Hanna M; Evans, David M; Ippolito, Giulia M; Zhou, Wei; Coward, Eivind; Hveem, Kristian; Surakka, Ida; Moksnes, Marta R; Wolford, Brooke N; Brumpton, Ben M

Leveraging a Genetic Proxy to Investigate the Effects of Lifelong Cardiac Sodium Channel Blockade

利用基因指标研究终身心脏钠通道阻滞的影响

Wanner, Julian S; Krafft, Maren; Niiranen, Teemu; Zimmerman, Dominic S; FinnGen; Ellinor, Patrick T; Nadkarni, Girish; Jurgens, Sean J; Rämö, Joel; Heyne, Henrike O

The association of a polygenic lifespan score with the risk of common age-related diseases and mortality

多基因寿命评分与常见年龄相关疾病风险和死亡率之间的关联

Tynkkynen, Niko Paavo; Koivunen, Kaisa; Herranen, Päivi; Joensuu, Laura; Törmäkangas, Timo; Sillanpää, Elina; FinnGen

High incidence and geographic distribution of cleft palate in Finland are associated with the IRF6 gene

芬兰腭裂的高发病率和地理分布与 IRF6 基因有关

Fedik Rahimov #, Pekka Nieminen #, Priyanka Kumari #, Emma Juuri, Tiit Nikopensius, Kitt Paraiso, Jakob German, Antti Karvanen, Mart Kals, Abdelrahman G Elnahas, Juha Karjalainen, Mitja Kurki, Aarno Palotie; FinnGen; Estonian Biobank Research Team; Arja Heliövaara, Tõnu Esko, Sakari Jukarainen, Prii

Deep learning of left atrial structure and function provides link to atrial fibrillation risk

左心房结构和功能的深度学习与心房颤动风险相关

James P Pirruccello, Paolo Di Achille, Seung Hoan Choi, Joel T Rämö, Shaan Khurshid, Mahan Nekoui, Sean J Jurgens, Victor Nauffal, Shinwan Kany; FinnGen; Kenney Ng, Samuel F Friedman, Puneet Batra, Kathryn L Lunetta, Aarno Palotie, Anthony A Philippakis, Jennifer E Ho, Steven A Lubitz, Patrick T Ell

SCGB1D2 inhibits growth of Borrelia burgdorferi and affects susceptibility to Lyme disease

SCGB1D2 抑制伯氏疏螺旋体的生长并影响莱姆病的易感性

Satu Strausz, Erik Abner #, Grace Blacker #, Sarah Galloway #, Paige Hansen #, Qingying Feng, Brandon T Lee, Samuel E Jones, Hele Haapaniemi, Sten Raak, George Ronald Nahass, Erin Sanders; FinnGen; Estonian Genome Centre; Estonian Biobank Research Team; Pilleriin Soodla, Urmo Võsa, Tõnu Esko, Nasa S

Genetic and functional analysis of Raynaud's syndrome implicates loci in vasculature and immunity

雷诺氏综合征的遗传和功能分析表明血管和免疫位点相关

Anniina Tervi, Markus Ramste, Erik Abner, Paul Cheng, Jacqueline M Lane, Matthew Maher, Jesse Valliere, Vilma Lammi, Satu Strausz, Juha Riikonen, Trieu Nguyen, Gabriella E Martyn, Maya U Sheth, Fan Xia, Mauro Lago Docampo, Wenduo Gu; FinnGen, Estonian Biobank research team; Tõnu Esko, Richa Saxena, 

Detection of a major Lynch Syndrome-causing MLH1 founder variant in a large-scale genotyped cohort

在大规模基因分型队列中检测到导致林奇综合征的主要MLH1创始变异

Sipilä, Lauri J; Aavikko, Mervi; Ravantti, Janne; Martin, Samantha; Kuopio, Teijo; Lahtinen, Laura; FinnGen; Peltomäki, Päivi; Mecklin, Jukka-Pekka; Aaltonen, Lauri A; Seppälä, Toni T

Central role of glycosylation processes in human genetic susceptibility to SARS-CoV-2 infections with Omicron variants

糖基化过程在人类对携带 Omicron 变异株的 SARS-CoV-2 感染的遗传易感性中起着核心作用

Geller, Frank; Wu, Xiaoping; Lammi, Vilma; Abner, Erik; Valliere, Jesse Tyler; Nastou, Katerina; Rasmussen, Morten; Andersson, Niklas Worm; Quinn, Liam; Aagaard, Bitten; Banasik, Karina; Bliddal, Sofie; Boding, Lasse; Brunak, Søren; Brøns, Nanna; Bybjerg-Grauholm, Jonas; Christoffersen, Lea Arregui Nordahl; Didriksen, Maria; Dinh, Khoa Manh; Erikstrup, Christian; Feldt-Rasmussen, Ulla; Grønbæk, Kirsten; Kaspersen, Kathrine Agergård; Mikkelsen, Christina; Nielsen, Claus Henrik; Nielsen, Henriette Svarre; Nielsen, Susanne Dam; Nissen, Janna; Sequeros, Celia Burgos; Tommerup, Niels; Ullum, Henrik; FinnGen; Spiliopoulos, Lampros; Bager, Peter; Hviid, Anders; Sørensen, Erik; Pedersen, Ole Birger; Lane, Jacqueline M; Lassaunière, Ria; Ollila, Hanna M; Ostrowski, Sisse Rye; Feenstra, Bjarke

Genome-Wide Polygenic Score for Muscle Strength Predicts Risk for Common Diseases and Lifespan: A Prospective Cohort Study

全基因组多基因肌肉力量评分预测常见疾病风险和寿命:一项前瞻性队列研究

Herranen, Päivi; Koivunen, Kaisa; Palviainen, Teemu; Kujala, Urho M; Ripatti, Samuli; Kaprio, Jaakko; Sillanpää, Elina; FinnGen