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

Methods for Prioritizing Causal Genes in Molecular Studies of Human Disease: The State of the Art

人类疾病分子研究中致病基因优先排序方法:最新进展

Patasova, Karina; Sedaghati-Khayat, Bahar; Knevel, Rachel; Cordell, Heather J; Pratt, Arthur G

Shared genetic susceptibility between idiopathic inflammatory myopathies and common B cell lymphoma subtypes found primarily in the human leucocyte antigen region

特发性炎症性肌病与常见B细胞淋巴瘤亚型之间存在共同的遗传易感性,主要位于人类白细胞抗原区域。

Che, Weng Ian; Öberg Sysojev, Anton; Zhu, Catherine; Patasova, Karina; Smedby, Karin E; Lundberg, Ingrid E; Westerlind, Helga; Holmqvist, Marie

Menopausal hormone therapy and the risk of systemic lupus erythematosus and systemic sclerosis: a population-based nested case-control study

更年期激素治疗与系统性红斑狼疮和系统性硬化症风险:一项基于人群的嵌套病例对照研究

Patasova, Karina; Dehara, Marina; Mantel, Ängla; Bixo, Marie; Arkema, Elizabeth V; Holmqvist, Marie

Increased risk of acute myocardial infarction in Swedish patients with systemic sclerosis: a population-based study

瑞典系统性硬化症患者急性心肌梗死风险增加:一项基于人群的研究

Bairkdar, Majd; Patasova, Karina; Andell, Pontus; Holmqvist, Marie

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

Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk

多种族全基因组关联分析提高了影响肺功能和慢性阻塞性肺疾病风险的基因和通路的分辨率。

Shrine, Nick; Izquierdo, Abril G; Chen, Jing; Packer, Richard; Hall, Robert J; Guyatt, Anna L; Batini, Chiara; Thompson, Rebecca J; Pavuluri, Chandan; Malik, Vidhi; Hobbs, Brian D; Moll, Matthew; Kim, Wonji; Tal-Singer, Ruth; Bakke, Per; Fawcett, Katherine A; John, Catherine; Coley, Kayesha; Piga, Noemi Nicole; Pozarickij, Alfred; Lin, Kuang; Millwood, Iona Y; Chen, Zhengming; Li, Liming; Wijnant, Sara R A; Lahousse, Lies; Brusselle, Guy; Uitterlinden, Andre G; Manichaikul, Ani; Oelsner, Elizabeth C; Rich, Stephen S; Barr, R Graham; Kerr, Shona M; Vitart, Veronique; Brown, Michael R; Wielscher, Matthias; Imboden, Medea; Jeong, Ayoung; Bartz, Traci M; Gharib, Sina A; Flexeder, Claudia; Karrasch, Stefan; Gieger, Christian; Peters, Annette; Stubbe, Beate; Hu, Xiaowei; Ortega, Victor E; Meyers, Deborah A; Bleecker, Eugene R; Gabriel, Stacey B; Gupta, Namrata; Smith, Albert Vernon; Luan, Jian'an; Zhao, Jing-Hua; Hansen, Ailin F; Langhammer, Arnulf; Willer, Cristen; Bhatta, Laxmi; Porteous, David; Smith, Blair H; Campbell, Archie; Sofer, Tamar; Lee, Jiwon; Daviglus, Martha L; Yu, Bing; Lim, Elise; Xu, Hanfei; O'Connor, George T; Thareja, Gaurav; Albagha, Omar M E; Suhre, Karsten; Granell, Raquel; Faquih, Tariq O; Hiemstra, Pieter S; Slats, Annelies M; Mullin, Benjamin H; Hui, Jennie; James, Alan; Beilby, John; Patasova, Karina; Hysi, Pirro; Koskela, Jukka T; Wyss, Annah B; Jin, Jianping; Sikdar, Sinjini; Lee, Mikyeong; May-Wilson, Sebastian; Pirastu, Nicola; Kentistou, Katherine A; Joshi, Peter K; Timmers, Paul R H J; Williams, Alexander T; Free, Robert C; Wang, Xueyang; Morrison, John L; Gilliland, Frank D; Chen, Zhanghua; Wang, Carol A; Foong, Rachel E; Harris, Sarah E; Taylor, Adele; Redmond, Paul; Cook, James P; Mahajan, Anubha; Lind, Lars; Palviainen, Teemu; Lehtimäki, Terho; Raitakari, Olli T; Kaprio, Jaakko; Rantanen, Taina; Pietiläinen, Kirsi H; Cox, Simon R; Pennell, Craig E; Hall, Graham L; Gauderman, W James; Brightling, Chris; Wilson, James F; Vasankari, Tuula; Laitinen, Tarja; Salomaa, Veikko; Mook-Kanamori, Dennis O; Timpson, Nicholas J; Zeggini, Eleftheria; Dupuis, Josée; Hayward, Caroline; Brumpton, Ben; Langenberg, Claudia; Weiss, Stefan; Homuth, Georg; Schmidt, Carsten Oliver; Probst-Hensch, Nicole; Jarvelin, Marjo-Riitta; Morrison, Alanna C; Polasek, Ozren; Rudan, Igor; Lee, Joo-Hyeon; Sayers, Ian; Rawlins, Emma L; Dudbridge, Frank; Silverman, Edwin K; Strachan, David P; Walters, Robin G; Morris, Andrew P; London, Stephanie J; Cho, Michael H; Wain, Louise V; Hall, Ian P; Tobin, Martin D

Author Correction: Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk

作者更正:多祖先全基因组关联分析提高了影响肺功能和慢性阻塞性肺疾病风险的基因和通路的分辨率。

Shrine, Nick; Izquierdo, Abril G; Chen, Jing; Packer, Richard; Hall, Robert J; Guyatt, Anna L; Batini, Chiara; Thompson, Rebecca J; Pavuluri, Chandan; Malik, Vidhi; Hobbs, Brian D; Moll, Matthew; Kim, Wonji; Tal-Singer, Ruth; Bakke, Per; Fawcett, Katherine A; John, Catherine; Coley, Kayesha; Piga, Noemi Nicole; Pozarickij, Alfred; Lin, Kuang; Millwood, Iona Y; Chen, Zhengming; Li, Liming; Wijnant, Sara R A; Lahousse, Lies; Brusselle, Guy; Uitterlinden, Andre G; Manichaikul, Ani; Oelsner, Elizabeth C; Rich, Stephen S; Barr, R Graham; Kerr, Shona M; Vitart, Veronique; Brown, Michael R; Wielscher, Matthias; Imboden, Medea; Jeong, Ayoung; Bartz, Traci M; Gharib, Sina A; Flexeder, Claudia; Karrasch, Stefan; Gieger, Christian; Peters, Annette; Stubbe, Beate; Hu, Xiaowei; Ortega, Victor E; Meyers, Deborah A; Bleecker, Eugene R; Gabriel, Stacey B; Gupta, Namrata; Smith, Albert Vernon; Luan, Jian'an; Zhao, Jing-Hua; Hansen, Ailin F; Langhammer, Arnulf; Willer, Cristen; Bhatta, Laxmi; Porteous, David; Smith, Blair H; Campbell, Archie; Sofer, Tamar; Lee, Jiwon; Daviglus, Martha L; Yu, Bing; Lim, Elise; Xu, Hanfei; O'Connor, George T; Thareja, Gaurav; Albagha, Omar M E; Suhre, Karsten; Granell, Raquel; Faquih, Tariq O; Hiemstra, Pieter S; Slats, Annelies M; Mullin, Benjamin H; Hui, Jennie; James, Alan; Beilby, John; Patasova, Karina; Hysi, Pirro; Koskela, Jukka T; Wyss, Annah B; Jin, Jianping; Sikdar, Sinjini; Lee, Mikyeong; May-Wilson, Sebastian; Pirastu, Nicola; Kentistou, Katherine A; Joshi, Peter K; Timmers, Paul R H J; Williams, Alexander T; Free, Robert C; Wang, Xueyang; Morrison, John L; Gilliland, Frank D; Chen, Zhanghua; Wang, Carol A; Foong, Rachel E; Harris, Sarah E; Taylor, Adele; Redmond, Paul; Cook, James P; Mahajan, Anubha; Lind, Lars; Palviainen, Teemu; Lehtimäki, Terho; Raitakari, Olli T; Kaprio, Jaakko; Rantanen, Taina; Pietiläinen, Kirsi H; Cox, Simon R; Pennell, Craig E; Hall, Graham L; Gauderman, W James; Brightling, Chris; Wilson, James F; Vasankari, Tuula; Laitinen, Tarja; Salomaa, Veikko; Mook-Kanamori, Dennis O; Timpson, Nicholas J; Zeggini, Eleftheria; Dupuis, Josée; Hayward, Caroline; Brumpton, Ben; Langenberg, Claudia; Weiss, Stefan; Homuth, Georg; Schmidt, Carsten Oliver; Probst-Hensch, Nicole; Jarvelin, Marjo-Riitta; Morrison, Alanna C; Polasek, Ozren; Rudan, Igor; Lee, Joo-Hyeon; Sayers, Ian; Rawlins, Emma L; Dudbridge, Frank; Silverman, Edwin K; Strachan, David P; Walters, Robin G; Morris, Andrew P; London, Stephanie J; Cho, Michael H; Wain, Louise V; Hall, Ian P; Tobin, Martin D

Genetic Influences in Cancer-Associated Myositis

癌症相关肌炎的遗传影响

Patasova, Karina; Lundberg, Ingrid E; Holmqvist, Marie

Rare variant analyses across multiethnic cohorts identify novel genes for refractive error

对多民族人群的罕见变异分析发现了与屈光不正相关的新基因。

Musolf, Anthony M; Haarman, Annechien E G; Luben, Robert N; Ong, Jue-Sheng; Patasova, Karina; Trapero, Rolando Hernandez; Marsh, Joseph; Jain, Ishika; Jain, Riya; Wang, Paul Zhiping; Lewis, Deyana D; Tedja, Milly S; Iglesias, Adriana I; Li, Hengtong; Cowan, Cameron S; Biino, Ginevra; Klein, Alison P; Duggal, Priya; Mackey, David A; Hayward, Caroline; Haller, Toomas; Metspalu, Andres; Wedenoja, Juho; Pärssinen, Olavi; Cheng, Ching-Yu; Saw, Seang-Mei; Stambolian, Dwight; Hysi, Pirro G; Khawaja, Anthony P; Vitart, Veronique; Hammond, Christopher J; van Duijn, Cornelia M; Verhoeven, Virginie J M; Klaver, Caroline C W; Bailey-Wilson, Joan E

A genome-wide analysis of 340 318 participants identifies four novel loci associated with the age of first spectacle wear

一项对 340,318 名参与者进行的全基因组分析,发现了四个与首次佩戴眼镜年龄相关的新基因位点。

Patasova, Karina; Khawaja, Anthony P; Wojciechowski, Robert; Mahroo, Omar A; Falchi, Mario; Rahi, Jugnoo S; Hammond, Chris J; Hysi, Pirro G