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

The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions

子宫内膜异位症的遗传基础及其与其他疼痛和炎症性疾病的合并症

Rahmioglu, Nilufer; Mortlock, Sally; Ghiasi, Marzieh; Møller, Peter L; Stefansdottir, Lilja; Galarneau, Geneviève; Turman, Constance; Danning, Rebecca; Law, Matthew H; Sapkota, Yadav; Christofidou, Paraskevi; Skarp, Sini; Giri, Ayush; Banasik, Karina; Krassowski, Michal; Lepamets, Maarja; Marciniak, Błażej; Nõukas, Margit; Perro, Danielle; Sliz, Eeva; Sobalska-Kwapis, Marta; Thorleifsson, Gudmar; Topbas-Selcuki, Nura F; Vitonis, Allison; Westergaard, David; Arnadottir, Ragnheidur; Burgdorf, Kristoffer S; Campbell, Archie; Cheuk, Cecilia S K; Clementi, Caterina; Cook, James; De Vivo, Immaculata; DiVasta, Amy; Dorien, O; Donoghue, Jacqueline F; Edwards, Todd; Fontanillas, Pierre; Fung, Jenny N; Geirsson, Reynir T; Girling, Jane E; Harkki, Paivi; Harris, Holly R; Healey, Martin; Heikinheimo, Oskari; Holdsworth-Carson, Sarah; Hostettler, Isabel C; Houlden, Henry; Houshdaran, Sahar; Irwin, Juan C; Jarvelin, Marjo-Riitta; Kamatani, Yoichiro; Kennedy, Stephen H; Kepka, Ewa; Kettunen, Johannes; Kubo, Michiaki; Kulig, Bartosz; Kurra, Venla; Laivuori, Hannele; Laufer, Marc R; Lindgren, Cecilia M; MacGregor, Stuart; Mangino, Massimo; Martin, Nicholas G; Matalliotaki, Charoula; Matalliotakis, Michail; Murray, Alison D; Ndungu, Anne; Nezhat, Camran; Olsen, Catherine M; Opoku-Anane, Jessica; Padmanabhan, Sandosh; Paranjpe, Manish; Peters, Maire; Polak, Grzegorz; Porteous, David J; Rabban, Joseph; Rexrode, Kathyrn M; Romanowicz, Hanna; Saare, Merli; Saavalainen, Liisu; Schork, Andrew J; Sen, Sushmita; Shafrir, Amy L; Siewierska-Górska, Anna; Słomka, Marcin; Smith, Blair H; Smolarz, Beata; Szaflik, Tomasz; Szyłło, Krzysztof; Takahashi, Atsushi; Terry, Kathryn L; Tomassetti, Carla; Treloar, Susan A; Vanhie, Arne; Vincent, Katy; Vo, Kim C; Werring, David J; Zeggini, Eleftheria; Zervou, Maria I; Adachi, Sosuke; Buring, Julie E; Ridker, Paul M; D'Hooghe, Thomas; Goulielmos, George N; Hapangama, Dharani K; Hayward, Caroline; Horne, Andrew W; Low, Siew-Kee; Martikainen, Hannu; Chasman, Daniel I; Rogers, Peter A W; Saunders, Philippa T; Sirota, Marina; Spector, Tim; Strapagiel, Dominik; Tung, Joyce Y; Whiteman, David C; Giudice, Linda C; Velez-Edwards, Digna R; Uimari, Outi; Kraft, Peter; Salumets, Andres; Nyholt, Dale R; Mägi, Reedik; Stefansson, Kari; Becker, Christian M; Yurttas-Beim, Piraye; Steinthorsdottir, Valgerdur; Nyegaard, Mette; Missmer, Stacey A; Montgomery, Grant W; Morris, Andrew P; Zondervan, Krina T

A cross-disorder dosage sensitivity map of the human genome

人类基因组的跨疾病剂量敏感性图谱

Collins, Ryan L; Glessner, Joseph T; Porcu, Eleonora; Lepamets, Maarja; Brandon, Rhonda; Lauricella, Christopher; Han, Lide; Morley, Theodore; Niestroj, Lisa-Marie; Ulirsch, Jacob; Everett, Selin; Howrigan, Daniel P; Boone, Philip M; Fu, Jack; Karczewski, Konrad J; Kellaris, Georgios; Lowther, Chelsea; Lucente, Diane; Mohajeri, Kiana; Nõukas, Margit; Nuttle, Xander; Samocha, Kaitlin E; Trinh, Mi; Ullah, Farid; Võsa, Urmo; Hurles, Matthew E; Aradhya, Swaroop; Davis, Erica E; Finucane, Hilary; Gusella, James F; Janze, Aura; Katsanis, Nicholas; Matyakhina, Ludmila; Neale, Benjamin M; Sanders, David; Warren, Stephanie; Hodge, Jennelle C; Lal, Dennis; Ruderfer, Douglas M; Meck, Jeanne; Mägi, Reedik; Esko, Tõnu; Reymond, Alexandre; Kutalik, Zoltán; Hakonarson, Hakon; Sunyaev, Shamil; Brand, Harrison; Talkowski, Michael E

Advancing our understanding of genetic risk factors and potential personalized strategies for pelvic organ prolapse

加深我们对盆腔器官脱垂遗传风险因素和潜在个性化治疗策略的理解

Pujol-Gualdo, Natàlia; Läll, Kristi; Lepamets, Maarja; Rossi, Henna-Riikka; Arffman, Riikka K; Piltonen, Terhi T; Mägi, Reedik; Laisk, Triin

The individual and global impact of copy-number variants on complex human traits

拷贝数变异对复杂人类性状的个体和全球影响

Auwerx, Chiara; Lepamets, Maarja; Sadler, Marie C; Patxot, Marion; Stojanov, Miloš; Baud, David; Mägi, Reedik; Porcu, Eleonora; Reymond, Alexandre; Kutalik, Zoltán

Omics-informed CNV calls reduce false-positive rates and improve power for CNV-trait associations

基于组学信息的CNV检测可降低假阳性率并提高CNV与性状关联分析的效力。

Lepamets, Maarja; Auwerx, Chiara; Nõukas, Margit; Claringbould, Annique; Porcu, Eleonora; Kals, Mart; Jürgenson, Tuuli; Morris, Andrew Paul; Võsa, Urmo; Bochud, Murielle; Stringhini, Silvia; Wijmenga, Cisca; Franke, Lude; Peterson, Hedi; Vilo, Jaak; Lepik, Kaido; Mägi, Reedik; Kutalik, Zoltán

Genome-wide association study identifies five risk loci for pernicious anemia

全基因组关联研究确定了恶性贫血的五个风险位点

Laisk, Triin; Lepamets, Maarja; Koel, Mariann; Abner, Erik; Mägi, Reedik

The genetic architecture of sporadic and multiple consecutive miscarriage

散发性和多次连续性流产的遗传结构

Laisk, Triin; Soares, Ana Luiza G; Ferreira, Teresa; Painter, Jodie N; Censin, Jenny C; Laber, Samantha; Bacelis, Jonas; Chen, Chia-Yen; Lepamets, Maarja; Lin, Kuang; Liu, Siyang; Millwood, Iona Y; Ramu, Avinash; Southcombe, Jennifer; Andersen, Marianne S; Yang, Ling; Becker, Christian M; Børglum, Anders D; Gordon, Scott D; Bybjerg-Grauholm, Jonas; Helgeland, Øyvind; Hougaard, David M; Jin, Xin; Johansson, Stefan; Juodakis, Julius; Kartsonaki, Christiana; Kukushkina, Viktorija; Lind, Penelope A; Metspalu, Andres; Montgomery, Grant W; Morris, Andrew P; Mors, Ole; Mortensen, Preben B; Njølstad, Pål R; Nordentoft, Merete; Nyholt, Dale R; Lippincott, Margaret; Seminara, Stephanie; Salumets, Andres; Snieder, Harold; Zondervan, Krina; Werge, Thomas; Chen, Zhengming; Conrad, Donald F; Jacobsson, Bo; Li, Liming; Martin, Nicholas G; Neale, Benjamin M; Nielsen, Rasmus; Walters, Robin G; Granne, Ingrid; Medland, Sarah E; Mägi, Reedik; Lawlor, Deborah A; Lindgren, Cecilia M

Genome-wide Study Identifies Association between HLA-B(∗)55:01 and Self-Reported Penicillin Allergy

全基因组研究发现HLA-B(∗)55:01与自我报告的青霉素过敏之间存在关联

Krebs, Kristi; Bovijn, Jonas; Zheng, Neil; Lepamets, Maarja; Censin, Jenny C; Jürgenson, Tuuli; Särg, Dage; Abner, Erik; Laisk, Triin; Luo, Yang; Skotte, Line; Geller, Frank; Feenstra, Bjarke; Wang, Wei; Auton, Adam; Raychaudhuri, Soumya; Esko, Tõnu; Metspalu, Andres; Laur, Sven; Roden, Dan M; Wei, Wei-Qi; Holmes, Michael V; Lindgren, Cecilia M; Phillips, Elizabeth J; Mägi, Reedik; Milani, Lili; Fadista, João

Rare mutations in the complement regulatory gene CSMD1 are associated with male and female infertility

补体调节基因 CSMD1 的罕见突变与男性和女性不育有关

Arthur S Lee, Jannette Rusch, Ana C Lima, Abul Usmani, Ni Huang, Maarja Lepamets, Katinka A Vigh-Conrad, Ronald E Worthington, Reedik Mägi, Xiaobo Wu, Kenneth I Aston, John P Atkinson, Douglas T Carrell, Rex A Hess, Moira K O'Bryan, Donald F Conrad

GenomeTester4: a toolkit for performing basic set operations - union, intersection and complement on k-mer lists

GenomeTester4:用于对 k-mer 列表执行基本集合运算(并集、交集和补集)的工具包

Kaplinski, Lauris; Lepamets, Maarja; Remm, Maido