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

Contribution of dominant and recessive model effects to the genetic architecture of Idiopathic Pulmonary Fibrosis

显性和隐性模型效应对特发性肺纤维化遗传结构的贡献

Hernandez-Beeftink, Tamara; Donoghue, Lauren J; Izquierdo, Abril; Moss, Samuel T; Chin, Daniel; Guillen-Guio, Beatriz; Bhatti, Konain Fatima; Biddie, Simon; Shrine, Nick; Packer, Richard; Adegunsoye, Ayodeji; Booth, Helen L; Fahy, William A; Fingerlin, Tasha E; Hall, Ian P; Hart, Simon P; Hill, Mike R; Hirani, Nik; Kaminski, Naftali; Lopez-Jimenez, Elena; Lorenzo-Salazar, Jose Miguel; Ma, Shwu-Fan; McAnulty, Robin J; McCarthy, Mark I; Stockwell, Amy D; Maher, Toby M; Millar, Ann B; Molyneaux, Philip L; Molina-Molina, Maria; Navaratnam, Vidya; Neighbors, Margaret; Oldham, Justin M; Parfrey, Helen; Saini, Gauri; Sayers, Ian; Sheng, X Rebecca; Strek, Mary E; Stewart, Iain; Tobin, Martin D; Whyte, Moira Kb; Zhang, Yingze; Martinez, Fernando J; Yaspan, Brian L; Reynolds, Carl J; Schwartz, David A; Flores, Carlos; Noth, Imre; John, Alison E; Jenkins, R Gisli; Allen, Richard J; Leavy, Olivia C; Wain, Louise V

Rare variants and survival of patients with idiopathic pulmonary fibrosis: analysis of a multicentre, observational cohort study with independent validation

罕见变异与特发性肺纤维化患者生存率:一项多中心观察性队列研究的分析及独立验证

Alonso-González, Aitana; Jáspez, David; Lorenzo-Salazar, José M; Ma, Shwu-Fan; Strickland, Emma; Mychaleckyj, Josyf; Kim, John S; Huang, Yong; Adegunsoye, Ayodeji; Oldham, Justin M; Stewart, Iain; Molyneaux, Philip L; Maher, Toby M; Wain, Louise V; Allen, Richard J; Gisli Jenkins, R; Kropski, Jonathan A; Yaspan, Brian; Blackwell, Timothy S; Zhang, David; Garcia, Christine Kim; Martinez, Fernando J; Noth, Imre; Flores, Carlos

HTRA1/lncRNA HTRA1-AS1 dominates in age-related macular degeneration reticular pseudodrusen genetic risk with no complement involvement

HTRA1/lncRNA HTRA1-AS1 在年龄相关性黄斑变性网状假性玻璃膜疣的遗传风险中占主导地位,且不涉及补体系统。

Farashi, Samaneh; Abbott, Carla J; Ansell, Brendan R E; Wu, Zhichao; Altay, Lebriz; Arnon, Ella; Arnould, Louis; Bagdasarova, Yelena; Balaskas, Konstantinos; Chen, Fred K; Chew, Emily; Chowers, Itay; Clarke, Steven; Cukras, Catherine; Delcourt, Cécile; Delyfer, Marie-Noëlle; den Hollander, Anneke I; Fauser, Sascha; Finger, Robert P; Gabrielle, Pierre-Henry; Han, Jiru; Hodgson, Lauren A B; Hogg, Ruth; Holz, Frank G; Hoyng, Carel; Kumar, Himeesh; Lad, Eleonora M; Lee, Aaron; Luhmann, Ulrich F O; Mauschitz, Matthias M; McKnight, Amy J; McLenachan, Samuel; Mishra, Aniket; Moghul, Ismail; Orozco, Luz D; Sampson, Danuta M; Scott, Liam W; Sitnilska, Vasilena; Song, Scott; Stockwell, Amy; Swaroop, Anand; Terheyden, Jan H; Tiosano, Liran; Tufail, Adnan; Yaspan, Brian L; Pébay, Alice; Fletcher, Erica L; Guymer, Robyn H; Bahlo, Melanie

Genome-wide association study of susceptibility to acute respiratory distress syndrome

全基因组关联研究探讨急性呼吸窘迫综合征的易感性

Guillen-Guio, Beatriz; Suarez-Pajes, Eva; Tosco-Herrera, Eva; Hernandez-Beeftink, Tamara; Lorenzo-Salazar, Jose Miguel; Chang, Diana; González-Montelongo, Rafaela; Rubio-Rodríguez, Luis A; Leavy, Olivia C; Allen, Richard J; Corrales, Almudena; Cruz, Raquel; Bardají-Carrillo, Miguel; Carracedo, Angel; Tamayo, Eduardo; Kerchberger, V Eric; Ware, Lorraine B; Yaspan, Brian L; Scholz, Markus; Scherag, André; Villar, Jesús; Wain, Louise V; Flores, Carlos

Integration of biobank-scale genetics and plasma proteomics reveals evidence for causal processes in asthma risk and heterogeneity

生物样本库规模的遗传学和血浆蛋白质组学的整合揭示了哮喘风险和异质性中因果过程的证据

Donoghue, Lauren J; Benner, Christian; Chang, Diana; Irudayanathan, Flaviyan Jerome; Pendergrass, Rion K; Yaspan, Brian L; Mahajan, Anubha; McCarthy, Mark I

Sex-specific genetic effects on susceptibility to idiopathic pulmonary fibrosis

性别特异性基因对特发性肺纤维化易感性的影响

Leavy, Olivia C; Goemans, Anne F; Hernandez-Beeftink, Tamara; Stockwell, Amy D; Allen, Richard J; Guillen-Guio, Beatriz; Adegunsoye, Ayodeji; Booth, Helen L; Fahy, William A; Fingerlin, Tasha E; Virk, Harvinder S; Hall, Ian P; Hart, Simon P; Hill, Mike R; Hirani, Nik; Kaminski, Naftali; Ma, Shwu-Fan; McAnulty, Robin J; Sheng, X Rebecca; Millar, Ann B; Molina-Molina, Maria; Navaratnam, Vidya; Neighbors, Margaret; Parfrey, Helen; Saini, Gauri; Sayers, Ian; Strek, Mary E; Tobin, Martin D; Whyte, Moira K B; Zhang, Yingze; Maher, Toby M; Molyneaux, Philip L; Oldham, Justin M; Yaspan, Brian L; Flores, Carlos; Martinez, Fernando; Reynolds, Carl J; Schwartz, David A; Noth, Imre; Jenkins, R Gisli; Wain, Louise V

Genome-wide association study of Idiopathic Pulmonary Fibrosis susceptibility using clinically-curated European-ancestry datasets

利用临床整理的欧洲血统数据集进行特发性肺纤维化易感性的全基因组关联研究

Chin, Daniel; Hernandez-Beeftink, Tamara; Donoghue, Lauren; Guillen-Uio, Beatriz; Leavy, Olivia C; Adegunsoye, Ayodeji; Booth, Helen L; Fahy, William A; Fingerlin, Tasha E; Gooptu, Bibek; Hall, Ian P; Hart, Simon P; Hill, Mike R; Hirani, Nik; Hubbard, Richard B; Johnson, Simon; Kaminski, Naftali; Lorenzo-Salazar, Jose Miguel; Ma, Shwu-Fan; McAnulty, Robin J; McCarthy, Mark; Stockwell, Amy D; Maher, Toby M; Millar, Ann B; Molyneaux, Philip L; Molina-Molina, Maria; Navaratnam, Vidya; Neighbors, Margaret; Oldham, Justin M; Parfrey, Helen; Saini, Gauri; Sayers, Ian; Rebecca Sheng, X; Stewart, Iain D; Strek, Mary E; Tobin, Martin D; Whyte, Moira Kb; Zarcone, Maria C; Zhang, Yingze; Martinez, Fernando; Yaspan, Brian L; Reynolds, Carl J; Schwartz, David A; Flores, Carlos; Noth, Imre; Gisli Jenkins, R; Allen, Richard J; Wain, Louise V

Genome-wide association analyses identify distinct genetic architectures for age-related macular degeneration across ancestries

全基因组关联分析揭示了不同种族人群中与年龄相关性黄斑变性相关的独特遗传结构

Gorman, Bryan R; Voloudakis, Georgios; Igo, Robert P Jr; Kinzy, Tyler; Halladay, Christopher W; Bigdeli, Tim B; Zeng, Biao; Venkatesh, Sanan; Cooke Bailey, Jessica N; Crawford, Dana C; Markianos, Kyriacos; Dong, Frederick; Schreiner, Patrick A; Zhang, Wen; Hadi, Tamer; Anger, Matthew D; Stockwell, Amy; Melles, Ronald B; Yin, Jie; Choquet, Hélène; Kaye, Rebecca; Patasova, Karina; Patel, Praveen J; Yaspan, Brian L; Jorgenson, Eric; Hysi, Pirro G; Lotery, Andrew J; Gaziano, J Michael; Tsao, Philip S; Fliesler, Steven J; Sullivan, Jack M; Greenberg, Paul B; Wu, Wen-Chih; Assimes, Themistocles L; Pyarajan, Saiju; Roussos, Panos; Peachey, Neal S; Iyengar, Sudha K

SLC16A8 is a causal contributor to age-related macular degeneration risk

SLC16A8是导致年龄相关性黄斑变性风险的致病因素。

Nouri, Navid; Gussler, Bailey Hannon; Stockwell, Amy; Truong, Tom; Kang, Gyeong Jin; Browder, Kristen C; Malato, Yann; Sene, Abdoulaye; Van Everen, Sherri; Wykoff, Charles C; Brown, David; Fu, Arthur; Palmer, James D; Lima de Carvalho, Jose Ronaldo; Ullah, Ehsan; Al Rawi, Ranya; Chew, Emily Y; Zein, Wadih M; Guan, Bin; McCarthy, Mark I; Hofmann, Jeffrey W; Chaney, Shawnta Y; Jasper, Heinrich; Yaspan, Brian L

Association study of human leukocyte antigen variants and idiopathic pulmonary fibrosis

人类白细胞抗原变异与特发性肺纤维化的关联研究

Guillen-Guio, Beatriz; Paynton, Megan L; Allen, Richard J; Chin, Daniel P W; Donoghue, Lauren J; Stockwell, Amy; Leavy, Olivia C; Hernandez-Beeftink, Tamara; Reynolds, Carl; Cullinan, Paul; Martinez, Fernando; Booth, Helen L; Fahy, William A; Hall, Ian P; Hart, Simon P; Hill, Mike R; Hirani, Nik; Hubbard, Richard B; McAnulty, Robin J; Millar, Ann B; Navaratnam, Vidya; Oballa, Eunice; Parfrey, Helen; Saini, Gauri; Sayers, Ian; Tobin, Martin D; Whyte, Moira K B; Adegunsoye, Ayodeji; Kaminski, Naftali; Ma, Shwu-Fan; Strek, Mary E; Zhang, Yingze; Fingerlin, Tasha E; Molina-Molina, Maria; Neighbors, Margaret; Sheng, X Rebecca; Oldham, Justin M; Maher, Toby M; Molyneaux, Philip L; Flores, Carlos; Noth, Imre; Schwartz, David A; Yaspan, Brian L; Jenkins, R Gisli; Wain, Louise V; Hollox, Edward J