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E

Erik Abner

University of Tartu
H指数:21
被引数:1,466

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荣誉奖项

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The genetic architecture of fibromyalgia across 2.5 million individuals

纤维肌痛的遗传结构：一项涉及250万个体的研究

Nature Medicine
IF50
2026-07-280
OA
Isabel Kerrebijn; Gyda Bjornsdottir; Keon Arbabi; Lea Urpa; Hele Haapaniemi; Gudmar Thorleifsson; Lilja Stefansdottir; Stephan Frangakis; Jesse Valliere; Lovemore Kunorozva; Erik Abner; Caleb Ji; Markus Kangur; Bitten Aagaard; Henning Bliddal; Søren Brunak; Mie T. Bruun; Maria Didriksen; Christian Erikstrup; Sarah Finer; Arni J. Geirsson; Daniel F. Gudbjartsson; Thomas F. Hansen; David van Heel; Ingileif Jonsdottir; Stacey Knight; Kirk U. Knowlton; Christina Mikkelsen; Lincoln D. Nadauld; Thorunn A. Olafsdottir; Sisse R. Ostrowski; Ole B. V. Pedersen; Saedis Saevarsdottir; Astros T. Skuladottir; Erik Sørensen; Hreinn Stefansson; Patrick Sulem; Olafur A. Sveinsson; Gudny E. Thorlacius; Unnur Thorsteinsdottir; Henrik Ullum; Arnor Vikingsson; Thomas M. Werge; Richa Saxena; Kari Stefansson; Chad M. Brummett; Bente Glintborg; Daniel J. Clauw; Thorgeir E. Thorgeirsson; Frances M. K. Williams; Nasa Sinnott-Armstrong; Hanna M. Ollila; Michael Wainberg
Genetic analysis of circulating metabolic traits in 619,372 individuals

619,372名个体循环代谢特征的遗传分析

Nature
IF48.5
2026-05-200
OA
Ralf Tambets; Mihkel Jesse; Jaanika Kronberg; Adriaan van der Graaf; Erik Abner; Urmo Võsa; Ida Rahu; Nele Taba; Anastassia Kolde; Dzvenymyra Yarish; Sariyya Abdullayeva; Anastasiia Alekseienko; Andres Veidenberg; Krista Fischer; Zoltán Kutalik; Tõnu Esko; Kaur Alasoo; Priit Palta
Author Correction: HLA allele-calling using multi-ancestry whole-exome sequencing from the UK Biobank identifies 129 novel associations in 11 autoimmune diseases

作者更正：使用来自英国生物银行的多祖先全外显子组测序进行HLA等位基因分型，在11种自身免疫性疾病中确定了129个新的关联。

Communications Biology
IF5.1
2026-04-020
OAAI
Guillaume Butler-Laporte; Joseph Farjoun; Tomoko Nakanishi; Tianyuan Lu; Erik Abner; Yiheng Chen; Michael Hultström; Andres Metspalu; Lili Milani; Reedik Mägi; Mari Nelis; Georgi Hudjashov; Satoshi Yoshiji; Yann Ilboudo; Kevin Y. H. Liang; Chen-Yang Su; Julian D. S. Willett; Tõnu Esko; Sirui Zhou; Vincenzo Forgetta; Daniel Taliun; J. Brent Richards
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Omicron变体的SARS-CoV-2感染的遗传易感性中的核心作用

Nature Genetics
IF29
2026-01-220
OAAI
Frank Geller; Xiaoping Wu; Vilma Lammi; Erik Abner; Jesse Tyler Valliere; Katerina Nastou; Angus Burns; Morten Rasmussen; Niklas Worm Andersson; Liam Quinn; Bitten Aagaard; Karina Banasik; Sofie Bliddal; Lasse Boding; Søren Brunak; Nanna Brøns; Jonas Bybjerg-Grauholm; Lea Arregui Nordahl Christoffersen; Maria Didriksen; Khoa Manh Dinh; Christian Erikstrup; Ulla Feldt-Rasmussen; Kirsten Grønbæk; Kathrine Agergård Kaspersen; Christina Mikkelsen; Claus Henrik Nielsen; Henriette Svarre Nielsen; Susanne Dam Nielsen; Janna Nissen; Celia Burgos Sequeros; Niels Tommerup; Henrik Ullum; Lampros Spiliopoulos; Peter Bager; Anders Hviid; Erik Sørensen; Ole Birger Pedersen; Jacqueline M. Lane; Ria Lassaunière; Hanna M. Ollila; Sisse Rye Ostrowski; Bjarke Feenstra
Genomic and transcriptomic analyses of aortic stenosis enhance therapeutic target discovery and disease prediction

主动脉狭窄的基因组和转录组学分析可增强治疗靶点的发现和疾病预测

Nature Genetics
IF29
2025-12-190
OAAI
Aeron M. Small; Ta-Yu Yang; Shinsuke Itoh; Sébastien Thériault; Line Dufresne; Ryo Kurosawa; Issei Komuro; Koichi Matsuda; Ha My T. Vy; Eric H. Farber-Eger; Lauren Lee Shaffer; Kristin M. Boulier; Kristin M. Corey; Megan E. Ramaker; Fabien Laporte; Jean-Jacques Schott; Solena Le Scouarnec; Sasha A. Singh; Abhijeet R. Sonawane; Harry A. Smith; Nicholas Rafaels; Jonas Ghouse; Anna A. Raja; Sisse R. Ostrowski; Erik Sørensen; Christina Mikkelsen; Ole B. Pedersen; Christian Erikstrup; Henrik Ullum; Gardar Sveinbjornsson; Daniel F. Gudbjartsson; Erik Abner; Jiwoo Lee; Andrea Ganna; Ulrike Nowak-Göttl; Sarah Finer; Johannes Schumacher; Carlo Maj; Baravan Al-Kassou; Georg Nickenig; Teresa Trenkwalder; Martina Dreβen; Markus Krane; Markus M. Nöthen; Marta R. Moksnes; Ben M. Brumpton; Stacey Knight; Kirk U. Knowlton; Lincoln Nadauld; Radek Debiec; Muntaser D. Musameh; Peter S. Braund; Christopher P. Nelson; Tomasz Czuba; Olle Melander; Margaret Sunitha Selvaraj; Satoshi Koyama; Rohan Bhukar; Yunfeng Ruan; Johan Ljungberg; Scott M. Damrauer; Michael G. Levin; Andre Franke; Klaus Berger; Christian T. Ruff; Giorgio E. M. Melloni; Frederick K. Kamanu; Kaoru Ito; Ron Do; Ruth J. F. Loos; Heribert Schunkert; Quinn S. Wells; Svati H. Shah; Thierry Le Tourneau; David Messika-Zeitoun; Christopher Gignoux; Henning Bundgaard; Susanna C. Larsson; Karl Michaëlsson; Hilma Holm; Anna Helgadottir; Tonu Esko; David A. van Heel; Patrick Mathieu; Nilesh J. Samani; J. Gustav Smith; Stefan Söderberg; Daniel J. Rader; Nicholas A. Marston; Marc S. Sabatine; Bogdan Pasaniuc; Kelly Cho; Peter W. F. Wilson; Christopher J. O’Donnell; Kari Stefansson; Yohan Bossé; Elena Aikawa; James C. Engert; Gina M. Peloso; Pradeep Natarajan; George Thanassoulis
Large-scale GWAS of strabismus identifies risk loci and provides support for a link with maternal smoking

大规模斜视全基因组关联研究（GWAS）确定了风险位点，并为与母亲吸烟的关联提供了支持。

Nature Communications
IF15.7
2025-08-230
OAAI
Weixiong He; Peter J. van der Most; Jue-Sheng Ong; Liang-Dar Hwang; Yeda Wu; Morten S. Magnø; Jelle Vehof; Kristi Krebs; Laura Mauring; Katrin Õunap; Erik Abner; Nicholas G. Martin; Denis Plotnikov; Chen Jiang; Ronald B. Melles; Puya Gharahkhani; Harold Snieder; Teele Palumaa; Kuldar Kaljurand; Jeremy A. Guggenheim; David A. Mackey; Elizabeth C. Engle; Hélène Choquet; Stuart MacGregor
Genome-Wide Association Study of Varenicline-Aided Smoking Cessation
NICOTINE & TOBACCO RESEARCH
IF3
2025-01-100
OAAI
Coley, Kayesha; Wang, Qingning; Packer, Richard; John, Catherine; Abner, Erik; Reis, Kadri; Estonian Biobank Research Team, Khaled F.; Bedair, Khaled F.; Srinivasan, Sundararajan; Paciga, Sara; Hyde, Craig; Free, Robert C.; Reeve, Nicola F.; Shepherd, David J.; Esko, Tonu; Palmer, Colin; Pearson, Ewan; Malarstig, Anders; Tobin, Martin D.; Batini, Chiara
Genome wide association study meta-analysis of 19,487 individuals with mitral valve prolapse identifies 52 novel genomic regions and highlights pro-fibrosis genes

19,487例二尖瓣脱垂患者的全基因组关联研究荟萃分析鉴定出52个新基因组区域，并突出了促纤维化基因

CIRCULATION
IF38.6
2024-11-120
PRE
Small, Aeron; Berrandou, Takiy-Eddine; Georges, Adrien; Morningstar, Jordan; Huff, Matthew; Yang, Ta-Yu; Lee, Jiwoo; Abner, Erik; Bundgaard, Henning; Wells, Quinn; Wilson, Peter; Cho, Kelly; Rader, Daniel; Ganna, Andrea; Helgadottir, Anna; Holm, Hilma; Stefansson, Kari; Gudbjartsson, Daniel; Vy, Ha My; Rosenberg, Michael; Milan, David; Borger, Michael; Dieterlen, Maja-Theresa; Kontorovich, Amy; Engert, Jamie; Thanassoulis, George; Farber-Eger, Eric; Gignoux, Christopher; Ellinor, Patrick; Peloso, Gina; Norris, Russell; Yu, Mengyao; Bouatia-Naji, Nabila; Natarajan, Pradeep
Genetic and functional analysis of Raynaud's syndrome implicates loci in vasculature and immunity

雷诺综合征的遗传和功能分析与血管和免疫相关的基因座有关

CELL GENOMICS
IF9
2024-09-010
OAAI
Tervi, Anniina; Ramste, Markus; Abner, Erik; Cheng, Paul; Lane, Jacqueline M.; Maher, Matthew; Valliere, Jesse; Lammi, Vilma; Strausz, Satu; Riikonen, Juha; Nguyen, Trieu; Martyn, Gabriella E.; Sheth, Maya U.; Xia, Fan; Docampo, Mauro Lago; Gu, Wenduo; Esko, Tonu; Saxena, Richa; Pirinen, Matti; Palotie, Aarno; Ripatti, Samuli; Sinnott-Armstrong, Nasa; Daly, Mark; Engreitz, Jesse M.; Rabinovitch, Marlene; Heckman, Caroline A.; Quertermous, Thomas; Jones, Samuel E.; Ollila, Hanna M.
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

NATURE COMMUNICATIONS
IF15.7
2024-03-194
OAAI
Strausz, Satu; Abner, Erik; Blacker, Grace; Galloway, Sarah; Hansen, Paige; Feng, Qingying; Lee, Brandon T.; Jones, Samuel E.; Haapaniemi, Hele; Raak, Sten; Nahass, George Ronald; Sanders, Erin; Soodla, Pilleriin; Vosa, Urmo; Esko, Tonu; Sinnott-Armstrong, Nasa; Weissman, Irving L.; Daly, Mark; Aivelo, Tuomas; Tal, Michal Caspi; Ollila, Hanna M.
Integrative genomic analyses identify candidate causal genes for calcific aortic valve stenosis involving tissue-specific regulation

综合基因组分析确定涉及组织特异性调节的钙化性主动脉瓣狭窄的候选致病基因

NATURE COMMUNICATIONS
IF15.7
2024-03-185
OAAI
Theriault, Sebastien; Li, Zhonglin; Abner, Erik; Luan, Jian'an; Manikpurage, Hasanga D.; Houessou, Ursula; Zamani, Pardis; Briend, Mewen; Estonian Biobank Res Team; Boudreau, Dominique K.; Gaudreault, Nathalie; Frenette, Lily; Argaud, Deborah; Dahmene, Manel; Dagenais, Francois; Clavel, Marie-Annick; Pibarot, Philippe; Arsenault, Benoit J.; Boekholdt, S. Matthijs; Wareham, Nicholas J.; Esko, Tonu; Mathieu, Patrick; Bosse, Yohan
Genome-wide association study of thyroid-stimulating hormone highlights new genes, pathways and associations with thyroid disease

促甲状腺激素的全基因组关联研究突出了新的基因，途径以及与甲状腺疾病的关联

NATURE COMMUNICATIONS
IF15.7
2023-10-235
OAAI
Williams, Alexander T.; Chen, Jing; Coley, Kayesha; Batini, Chiara; Izquierdo, Abril; Packer, Richard; Abner, Erik; Kanoni, Stavroula; Shepherd, David J.; Free, Robert C.; Hollox, Edward J.; Brunskill, Nigel J.; Ntalla, Ioanna; Reeve, Nicola; Brightling, Christopher E.; Venn, Laura; Adams, Emma; Bee, Catherine; Wallace, Susan E.; Pareek, Manish; Hansell, Anna L.; Esko, Tonu; Stow, Daniel; Jacobs, Benjamin M.; van Heel, David A.; Rao, Balasubramanya S.; Hennah, William; Rao, Balasubramanya S.; Dudbridge, Frank; Wain, Louise V.; Shrine, Nick; Tobin, Martin D.; John, Catherine

研究方向

暂未获取到该数据
T
Tōnu Esko
H 指数:165论文数:827被引数:15.8万
H
Hanna M. Ollila
H 指数:41论文数:259被引数:1.1万
S
Sébastien Thériault
H 指数:33论文数:206被引数:6,894
H
Hasanga D. Manikpurage
H 指数:14论文数:51被引数:864
P
Patrick Mathieu
H 指数:73论文数:518被引数:1.9万
B
Benoît J. Arsenault
H 指数:55论文数:339被引数:1.5万
N
Nele Taba
H 指数:16论文数:50被引数:984
P
Patricia L. Mitchell
H 指数:25论文数:116被引数:2,491
É
Éloi Gagnon
H 指数:14论文数:65被引数:844
S
Satu Strausz
H 指数:15论文数:62被引数:926