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/vufind/Search/Results?lookfor=%22Forgetta%2C+Vincenzo%22&type=Person&sort=year
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PubPharm (136)
1
Vitamin D and COVID-19 susceptibility and severity in the COVID-19 Host Genetics Initiative: A Mendelian randomization study
enthalten in:
bioRxiv.org
| 2024
von
Butler-Laporte, G.
|
Nakanishi, T.
|
Mooser, V.
| +13
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2
Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative
enthalten in:
bioRxiv.org
| 2024
von
Butler-Laporte, G.
|
Povysil, G.
|
Kosmicki, J.
| +152
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3
Proteome-wide Mendelian randomization implicates nephronectin as an actionable mediator of the effect of obesity on COVID-19 severity
enthalten in:
bioRxiv.org
| 2024
von
Yoshiji, S.
|
Butler-Laporte, G.
|
Lu, T.
| +28
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4
COL6A3-derived endotrophin mediates the effect of obesity on coronary artery disease: an integrative proteogenomics analysis
enthalten in:
bioRxiv.org
| 2023
von
Yoshiji, S.
|
Lu, T.
|
Butler-Laporte, G.
| +20
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5
Identifying Rare Genetic Determinants for Improved Polygenic Risk Prediction of Bone Mineral Density and Fracture Risk
enthalten in:
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
| 2023
von
Lu, T.
|
Forgetta, V.
|
Zhou, S.
| +2
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6
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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7
An Atlas of Human and Murine Genetic Influences on Osteoporosis
enthalten in:
bioRxiv.org
| 2023
von
Morris, J.
|
Kemp, J.
|
Youlten, S.
| +56
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8
Converging evidence from exome sequencing and common variants implicates target genes for osteoporosis
enthalten in:
Nature genetics
| 2023
von
Zhou, S.
|
Sosina, O.
|
Bovijn, J.
| +27
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9
Increasing serum iron levels and their role in the risk of infectious diseases : a Mendelian randomization approach
enthalten in:
International journal of epidemiology
| 2023
von
Butler-Laporte, G.
|
Farjoun, Y.
|
Chen, Y.
| +7
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10
Predicting ExWAS findings from GWAS data : a shorter path to causal genes
enthalten in:
Human genetics
| 2023
von
Liang, K.
|
Farjoun, Y.
|
Forgetta, V.
| +4
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