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Author Details
Full Name
Vincenzo Forgetta
Affiliation
5 Prime Sciences Inc.
ORCID
Career Start Year
2003
Papers
78
H Index
29
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36280454
Circulating Proteins Influencing Psychiatric Disease: A Mendelian Randomization Study.
Biol Psychiatry
2023
36280454
Circulating Proteins Influencing Psychiatric Disease: A Mendelian Randomization Study.
Biol Psychiatry
2023
37830501
Identifying Rare Genetic Determinants for Improved Polygenic Risk Prediction of Bone Mineral Density and Fracture Risk.
J Bone Miner Res
2023
37923823
HLA allele-calling using multi-ancestry whole-exome sequencing from the UK Biobank identifies 129 novel associations in 11 autoimmune diseases.
Commun Biol
2023
36773317
Increasing serum iron levels and their role in the risk of infectious diseases: a Mendelian randomization approach.
Int J Epidemiol
2023
36635386
Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases.
Nat Genet
2023
37069249
Circulating proteins to predict COVID-19 severity.
Sci Rep
2023
37009933
Predicting ExWAS findings from GWAS data: a shorter path to causal genes.
Hum Genet
2023
36805566
Proteome-wide Mendelian randomization implicates nephronectin as an actionable mediator of the effect of obesity on COVID-19 severity.
Nat Metab
2023
37830501
Identifying Rare Genetic Determinants for Improved Polygenic Risk Prediction of Bone Mineral Density and Fracture Risk.
J Bone Miner Res
2023
37923823
HLA allele-calling using multi-ancestry whole-exome sequencing from the UK Biobank identifies 129 novel associations in 11 autoimmune diseases.
Commun Biol
2023
37009933
Predicting ExWAS findings from GWAS data: a shorter path to causal genes.
Hum Genet
2023
37069249
Circulating proteins to predict COVID-19 severity.
Sci Rep
2023
36805566
Proteome-wide Mendelian randomization implicates nephronectin as an actionable mediator of the effect of obesity on COVID-19 severity.
Nat Metab
2023
36773317
Increasing serum iron levels and their role in the risk of infectious diseases: a Mendelian randomization approach.
Int J Epidemiol
2023
36635386
Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases.
Nat Genet
2023
34172473
Genetically increased circulating FUT3 level leads to reduced risk of idiopathic pulmonary fibrosis: a Mendelian randomisation study.
Eur Respir J
2022
36376796
Correction: The dynamic changes and sex differences of 147 immune-related proteins during acute COVID-19 in 580 individuals.
Clin Proteomics
2022
36250789
Genetic determinants of polygenic prediction accuracy within a population.
Genetics
2022
35460399
Polygenic risk score as a possible tool for identifying familial monogenic causes of complex diseases.
Genet Med
2022
35710731
Capturing additional genetic risk from family history for improved polygenic risk prediction.
Commun Biol
2022
35689460
Identifying Causes of Fracture Beyond Bone Mineral Density: Evidence From Human Genetics.
J Bone Miner Res
2022
36271419
Dehydration is associated with production of organic osmolytes and predicts physical long-term symptoms after COVID-19: a multicenter cohort study.
Crit Care
2022
36327219
Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative.
PLoS Genet
2022
34172473
Genetically increased circulating FUT3 level leads to reduced risk of idiopathic pulmonary fibrosis: a Mendelian randomisation study.
Eur Respir J
2022
35273064
Cohort profile: genomic data for 26 622 individuals from the Canadian Longitudinal Study on Aging (CLSA).
BMJ Open
2022
35147782
An effector index to predict target genes at GWAS loci.
Hum Genet
2022
34758976
Clinically Relevant Circulating Protein Biomarkers for Type 1 Diabetes: Evidence From a Two-Sample Mendelian Randomization Study.
Diabetes Care
2022
35710731
Capturing additional genetic risk from family history for improved polygenic risk prediction.
Commun Biol
2022
35460399
Polygenic risk score as a possible tool for identifying familial monogenic causes of complex diseases.
Genet Med
2022
35689460
Identifying Causes of Fracture Beyond Bone Mineral Density: Evidence From Human Genetics.
J Bone Miner Res
2022
36250789
Genetic determinants of polygenic prediction accuracy within a population.
Genetics
2022
36271419
Dehydration is associated with production of organic osmolytes and predicts physical long-term symptoms after COVID-19: a multicenter cohort study.
Crit Care
2022
36327219
Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative.
PLoS Genet
2022
36376796
Correction: The dynamic changes and sex differences of 147 immune-related proteins during acute COVID-19 in 580 individuals.
Clin Proteomics
2022
35147782
An effector index to predict target genes at GWAS loci.
Hum Genet
2022
35273064
Cohort profile: genomic data for 26 622 individuals from the Canadian Longitudinal Study on Aging (CLSA).
BMJ Open
2022
34758976
Clinically Relevant Circulating Protein Biomarkers for Type 1 Diabetes: Evidence From a Two-Sample Mendelian Randomization Study.
Diabetes Care
2022
33349849
The effect of angiotensin-converting enzyme levels on COVID-19 susceptibility and severity: a Mendelian randomization study.
Int J Epidemiol
2021
33914743
Correction: Vitamin D levels and risk of type 1 diabetes: A Mendelian randomization study.
PLoS Med
2021
33749377
Childhood obesity and multiple sclerosis: A Mendelian randomization study.
Mult Scler
2021
33633408
A Neanderthal OAS1 isoform protects individuals of European ancestry against COVID-19 susceptibility and severity.
Nat Med
2021
33536041
Improved prediction of fracture risk leveraging a genome-wide polygenic risk score.
Genome Med
2021
34061844
Vitamin D and COVID-19 susceptibility and severity in the COVID-19 Host Genetics Initiative: A Mendelian randomization study.
PLoS Med
2021
33630834
Vitamin D levels and risk of type 1 diabetes: A Mendelian randomization study.
PLoS Med
2021
33788949
A Polygenic Risk Score to Predict Future Adult Short Stature Among Children.
J Clin Endocrinol Metab
2021
34043590
Rare loss-of-function variants in type I IFN immunity genes are not associated with severe COVID-19.
J Clin Invest
2021
33440130
Polygenic Risk Score for Low-Density Lipoprotein Cholesterol Is Associated With Risk of Ischemic Heart Disease and Enriches for Individuals With Familial Hypercholesterolemia.
Circ Genom Precis Med
2021
33349849
The effect of angiotensin-converting enzyme levels on COVID-19 susceptibility and severity: a Mendelian randomization study.
Int J Epidemiol
2021
33110269
Individuals with common diseases but with a low polygenic risk score could be prioritized for rare variant screening.
Genet Med
2021
1 - 50 of 156
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University of Gothenburg
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Klaudia Walter
Wellcome Sanger Institute
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