Erik Abner - Present address: Molecular Biology Institute of Barcelona, Carrer Baldiri Reixac 15-21, 08028 Barcelona, Spain.

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论文共 38 篇作者统计合作学者相似作者

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Myopia and hyperopia are associated with opposite chronotypes in a sample of 71,016 individuals

Teele Palumaa,Nele Taba,Maris Teder-Laving, Kadi-Liis Kivi,Kadri Reis,Urmo Võsa, Estonian Biobank Research Team,Tõnu Esko,Erik Abner

medrxiv（2024）

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Integrative genomic analyses identify candidate causal genes for calcific aortic valve stenosis involving tissue-specific regulation

Sébastien Thériault,Zhonglin Li,Erik Abner, Jian’an Luan,Hasanga D. Manikpurage, Ursula Houessou, Pardis Zamani, Mewen Briend, Dominique K. Boudreau,Nathalie Gaudreault, Lily Frenette,Déborah Argaud,

Nature Communications（2024）

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Associations between common genetic variants and income provide insights about the socioeconomic health gradient

Hyeokmoon Kweon,Casper A.P. Burik, Yuchen Ning,Rafael Ahlskog,Charley Xia,Erik Abner,Yanchun Bao,Laxmi Bhatta,Tariq Faquih, Maud Feijter,Paul Fisher, Andrea Gelemanovic,

biorxiv（2024）

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

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,

Nature Communicationsno. 1 (2024): 1-11

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Mapping the aetiological foundations of the heart failure spectrum using human genetics

Albert Henry, Xiaodong Mo,Chris Finan,Mark D. Chaffin,Doug Speed, Hanane Issa,Spiros Denaxas,James S. Ware,Sean L. Zheng,Anders Malarstig,Jasmine Gratton, Isabelle Bond,

medRxiv (Cold Spring Harbor Laboratory) (2023)

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The α2A-adrenergic receptor (ADRA2A) modulates susceptibility to Raynaud’s syndrome

Anniina Tervi, Markus Ramste,Erik Abner,Paul Cheng,Jacqueline M. Lane,Matthew Maher, Vilma Lammi,Satu Strausz,Trieu Nguyen, Mauro Lago Docampo,Wenduo Gu, FinnGen, Estonian biobank research team,

medRxiv (Cold Spring Harbor Laboratory) (2023)

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HLA allele-calling using multi-ancestry whole-exome sequencing from the UK Biobank identifies 129 novel associations in 11 autoimmune diseases

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,

Communications biology（2023）

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Genome-wide association study of thyroid-stimulating hormone highlights new genes, pathways and associations with thyroid disease susceptibility and age-of-onset

Alexander T Williams,Jing Chen,Kayesha Coley,Chiara Batini,Abril Izquierdo,Richard Packer,Erik Abner,David J Shepherd,Robert C Free,Edward J Hollox,Nigel J Brunskill,Ioanna Ntalla,

Nature Communicationsno. 1 (2023): 1-14

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Genome-wide association analysis reveals insights into the molecular etiology underlying dilated cardiomyopathy

Sean L Zheng,Albert Henry,Douglas Cannie,Michael Lee, David Miller,Kathryn A McGurk,Isabelle Bond, Xiao Xu,Hanane Issa,Catherine Francis,Antonio De Marvao,Pantazis I Theotokis,

medRxiv (Cold Spring Harbor Laboratory) (2023)

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Genome-wide association study of obstructive sleep apnoea in the Million Veteran Program uncovers genetic heterogeneity by sex

Tamar Sofer,Nuzulul Kurniansyah,Michael Murray,Yuk-Lam Ho,Erik Abner,Tõnu Esko,Jennifer E Huffman,Kelly Cho,Peter W F Wilson,Daniel J Gottlieb

EBioMedicine（2023）

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