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PubPharm (309)
1
Genomic and phenomic insights from an atlas of genetic effects on DNA methylation
enthalten in:
bioRxiv.org
| 2024
von
Min, J.
|
Hemani, G.
|
Hannon, E.
| +152
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2
Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors
enthalten in:
bioRxiv.org
| 2024
von
Thibord, F.
|
Klarin, D.
|
Brody, J.
| +84
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3
Genome-wide association study of a semicontinuous trait: Illustration of the impact of the modeling strategy through the study of Neutrophil Extracellular Traps levels
enthalten in:
bioRxiv.org
| 2024
von
Munsch, G.
|
Proust, C.
|
Labrouche-Colomer, S.
| +13
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4
Novel uAUG creating variants in the 5’UTR of ENG causing Hereditary Hemorrhagic Telangiectasia
enthalten in:
bioRxiv.org
| 2024
von
Soukarieh, O.
|
Tillet, E.
|
Proust, C.
| +6
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5
Causal relationships between risk of venous thromboembolism and 18 cancers: a bidirectional Mendelian randomisation analysis
enthalten in:
bioRxiv.org
| 2024
von
Cornish, N.
|
Haycock, P.
|
Brenner, H.
| +16
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6
Next Generation Sequencing strategies in venous thromboembolism : in whom and for what purpose ?
enthalten in:
Journal of thrombosis and haemostasis : JTH
| 2024
von
Trégouët, D.
|
Pierre-Emmanuel, M.
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7
Impaired balance between neutrophil extracellular trap formation and degradation by DNases in COVID-19 disease
enthalten in:
Journal of translational medicine
| 2024
von
Garcia, G.
|
Labrouche-Colomer, S.
|
Duvignaud, A.
| +11
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8
Impaired balance between neutrophil extracellular trap formation and degradation by DNases in COVID-19 disease
enthalten in:
Journal of translational medicine
| 2024
von
Garcia, G.
|
Labrouche-Colomer, S.
|
Duvignaud, A.
| +11
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9
DNA-pools targeted-sequencing as a robust cost-effective method to detect rare variants : Application to dilated cardiomyopathy genetic diagnosis
enthalten in:
Clinical genetics
| 2024
von
Perret, C.
|
Proust, C.
|
Esslinger, U.
| +9
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10
A genome wide search for non-additive allele effects identifies PSKH2 as involved in the variability of Factor V activity.
enthalten in:
bioRxiv.org
| 2024
von
Gendre, B.
|
Martinez-Perez, A.
|
Kleber, M.
| +15
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9
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9
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8
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8
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genetics
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