Author

Pauline Lanting

University Medical Center GroningenORCID 0000-0002-7288-4445Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 3 Bioinformatics· 1

Signature Assays, Organisms & Methods

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Organism:human· 4 Approach:statistical model· 3 Assay:GWAS summary statistics· 2 Approach:benchmark study· 1 Research Focus:benchmarking· 1 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Research Focus:GWAS / association mapping· 1

Frequent Co-Authors

Lude FrankeiD· 4 shared Patrick DeeleniD· 3 shared Cisca WijmengaiD· 2 shared Esteban A. Lopera-MayaiD· 2 shared Lifelines Cohort Study· 2 shared Robert WarmerdamiD· 2 shared Adelita V. RanchoriD· 1 shared Adriaan van der GraafiD· 1 shared

Activity by Year

2020-2021 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 31 mutual co-author links

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4 shared papersGenetic & Genomic Medicine

Lude FrankeORCID

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4 papers

Recent·Most cited

BioinformaticsBioinformaticsPeer-reviewedNov 15, 2021

Idefix: identifying accidental sample mix-ups in biobanks using polygenic scores

Robert Warmerdam, Pauline Lanting, Lifelines Cohort Study…·Lude Franke

Idefix identifies sample mix-ups in biobanks using polygenic scores, achieving an AUC of 0.90 compared to 0.75 with sex alone.

6 citations

humanGWAS summary statistics

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Genetic & Genomic MedicinePLoS ONEPeer-reviewedAug 11, 2021

Using symptom-based case predictions to identify host genetic factors that contribute to COVID-19 susceptibility

Irene V. van Blokland, Pauline Lanting, Anil P. S. Ori…·Lude Franke

The paper uses symptom-based case predictions to conduct a GWAS on COVID-19, finding new genetic susceptibility insights and suggesting different genetic architectures for severity and susceptibility.

12 citations

humanGWAS summary statistics

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Genetic & Genomic MedicineJournal of Personalized MedicinePeer-reviewedDec 21, 2020

Practical barriers and facilitators experienced by patients, pharmacists and physicians to the implementation of pharmacogenomic screening in Dutch outpatient hospital care - an explorative pilot study

Pauline Lanting, Evelien Drenth, Ludolf G. Boven…·Rolf H. Sijmons

This study identifies barriers and facilitators to implementing pharmacogenomic screening in Dutch outpatient care through stakeholder perspectives.

35 citations

humanbenchmark study

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Genetic & Genomic MedicineFrontiers in GeneticsPeer-reviewedJun 8, 2020

Lack of association between genetic variants at ACE2 and TMPRSS2 genes involved in SARS-CoV-2 infection and human quantitative phenotypes

Esteban A. Lopera-Maya, Adriaan van der Graaf, Pauline Lanting…·Serena Sanna

This study investigates genetic variants in ACE2 and TMPRSS2 genes for associations with quantitative phenotypes and medication use in a population cohort, finding suggestive links with hypertension and inflammation-related drugs.

68 citationstop 1%

humanbulk RNA-seq

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