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/vufind/Search/Results?lookfor=%22Porcu%2C+Eleonora%22&type=Person&sort=year
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PubPharm (165)
1
GWAS of Retinal Vessel Tortuosity Identifies 173 Novel Loci Revealing Genes and Pathways Associated with Vascular Pathomechanics and Cardiometabolic Diseases
enthalten in:
bioRxiv.org
| 2024
von
Tomasoni, M.
|
Beyeler, M.
|
Vela, S.
| +11
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2
Correction for participation bias in the UK Biobank reveals non-negligible impact on genetic associations and downstream analyses
enthalten in:
bioRxiv.org
| 2024
von
Schoeler, T.
|
Speed, D.
|
Porcu, E.
| +3
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3
DNA methylation may partly explain psychotropic drug-induced metabolic side effects : results from a prospective 1-month observational study
enthalten in:
Clinical epigenetics
| 2024
von
Dubath, C.
|
Porcu, E.
|
Delacrétaz, A.
| +8
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4
DNA methylation may partly explain psychotropic drug-induced metabolic side effects: results from a prospective 1-month observational study
enthalten in:
Clinical epigenetics
| 2024
von
Dubath, C.
|
Porcu, E.
|
Delacrétaz, A.
| +8
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5
Exploiting the mediating role of the metabolome to unravel transcript-to-phenotype associations
enthalten in:
bioRxiv.org
| 2023
von
Auwerx, C.
|
Sadler, M.
|
Reymond, A.
| +2
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6
Genome-wide Association Studies of Retinal Vessel Tortuosity Identify Numerous Novel Loci Revealing Genes and Pathways Associated With Ocular and Cardiometabolic Diseases
enthalten in:
Ophthalmology science
| 2023
von
Tomasoni, M.
|
Beyeler, M.
|
Vela, S.
| +11
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7
Participation bias in the UK Biobank distorts genetic associations and downstream analyses
enthalten in:
Nature human behaviour
| 2023
von
Schoeler, T.
|
Speed, D.
|
Porcu, E.
| +3
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8
Understanding the genetic complexity of puberty timing across the allele frequency spectrum
enthalten in:
bioRxiv.org
| 2023
von
Kentistou, K.
|
Kaisinger, L.
|
Stankovic, S.
| +217
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9
Understanding the genetic complexity of puberty timing across the allele frequency spectrum
enthalten in:
medRxiv : the preprint server for health sciences
| 2023
von
Kentistou, K.
|
Kaisinger, L.
|
Stankovic, S.
| +105
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10
Author Correction : Possible association of 16p11.2 copy number variation with altered lymphocyte and neutrophil counts
enthalten in:
NPJ genomic medicine
| 2023
von
Giannuzzi, G.
|
Chatron, N.
|
Mannik, K.
| +32
ErratumFor: NPJ Genom Med. 2022 Jun 17;7(1):38. - PMID 35715439
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