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/vufind/Search/Results?lookfor=%22Abner%2C+Erik%22&type=Person&sort=year
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PubPharm (40)
1
A multivariable Mendelian randomization analysis disentangling the causal relations between abdominal obesity, non-alcoholic fatty liver disease and cardiometabolic diseases
enthalten in:
bioRxiv.org
| 2024
von
Pelletier, W.
|
Gagnon, .
|
Gobeil, .
| +13
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2
SCGB1D2 inhibits growth of Borrelia burgdorferi and affects susceptibility to Lyme disease
enthalten in:
Nature communications
| 2024
von
Strausz, S.
|
Abner, E.
|
Blacker, G.
| +21
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3
Integrative genomic analyses identify candidate causal genes for calcific aortic valve stenosis involving tissue-specific regulation
enthalten in:
Nature communications
| 2024
von
Thériault, S.
|
Li, Z.
|
Abner, E.
| +20
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4
Myopia and hyperopia are associated with opposite chronotypes in a sample of 71,016 individuals
enthalten in:
bioRxiv.org
| 2024
von
Palumaa, T.
|
Taba, N.
|
Teder-Laving, M.
| +5
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5
Associations between common genetic variants and income provide insights about the socioeconomic health gradient
enthalten in:
bioRxiv.org
| 2024
von
Kweon, H.
|
Burik, C.
|
Ning, Y.
| +65
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6
Associations between common genetic variants and income provide insights about the socioeconomic health gradient
enthalten in:
ResearchSquare.com
| 2024
von
Koellinger, P.
|
Kweon, H.
|
Burik, C.
| +65
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7
Genetic assessment of efficacy and safety profiles of coagulation cascade proteins identifies Factors II and XI as actionable anticoagulant targets
enthalten in:
bioRxiv.org
| 2023
von
Gagnon, E.
|
Girard, A.
|
Bourgault, J.
| +8
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8
HLA allele-calling using multi-ancestry whole-exome sequencing from the UK Biobank identifies 129 novel associations in 11 autoimmune diseases
enthalten in:
Communications biology
| 2023
von
Butler-Laporte, G.
|
Farjoun, J.
|
Nakanishi, T.
| +20
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9
Genome-wide association study of thyroid-stimulating hormone highlights new genes, pathways and associations with thyroid disease
enthalten in:
Nature communications
| 2023
von
Williams, A.
|
Chen, J.
|
Coley, K.
| +31
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10
The α
2A
-adrenergic receptor (
ADRA2A
) modulates susceptibility to Raynaud’s syndrome
enthalten in:
bioRxiv.org
| 2023
von
Tervi, A.
|
Ramste, M.
|
Abner, E.
| +19
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EC 3.1.3.48
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HIV latency
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PTPN22 protein, human
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non-alcoholic fatty liver disease
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(+)-JQ1 compound
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103964-84-7
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23andMe
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50936-63-5
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Erscheinungszeitraum
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2020-
6
2010-2019
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40
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