Author

Paula Rodrigues Andrade da Cunha Loureiro

ORCID 0000-0003-1849-0047Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Assay:DNA methylation· 1 Approach:experimental assay· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Approach:statistical model· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Éster Cerdeira SabinoiD· 2 shared Shannon KellyiD· 2 shared Adam S. ButterworthiD· 1 shared Adriana MendeziD· 1 shared Aitzkoa Lopez de Lapuente PortillaiD· 1 shared Allison E. Ashley‐KochiD· 1 shared Andrew LeeiD· 1 shared Angelika Hammerer‐LercheriD· 1 shared

Activity by Year

2019-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 38 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Éster Cerdeira SabinoORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicineNaturePeer-reviewedSep 30, 2026

Human genetics implicates a BACH2-NRF2 axis in fetal hemoglobin activation

C. Guo, Uma P. Arora, Xiaoheng Cheng…·Vijay G. Sankaran

This study identifies a BACH2-NRF2 axis regulating fetal hemoglobin activation through genetic and functional analyses in a large multi-ancestry cohort.

DOI 10.1038/s41586-026-11113-2

humanGWAS summary statistics

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Molecular BiologyPLoS ONEPeer-reviewedDec 12, 2019

Use of an automated pyrosequencing technique for confirmation of Sickle Cell Disease

CC Martino, Cecília Salete Alencar, Paula Rodrigues Andrade da Cunha Loureiro…·for the International Component of the NHLBI Recipient Epidemiology and Donor Evaluation Study (REDS-III)

The paper develops an automated pyrosequencing technique to confirm sickle cell disease and detect HBB gene mutations, showing high accuracy in identifying hemoglobin variants.

12 citations

humanDNA methylation

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