Author

Raul Maia Falcão

Universidade Federal do Rio Grande do NorteORCID 0000-0003-3833-202XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Carlos Alexandre de Amorim Garcia· 1 shared Jorge Estefano Santana de SouzaiD· 1 shared Raquel Araújo Costa Uchôa· 1 shared Selma M. B. JerônimoiD· 1 shared Washington Candeia de AraújoiD· 1 shared

Activity by Year

2019-2019 · peak 1/yr

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5 top collaborators · 10 mutual co-author links

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1 shared paperGenomics

Carlos Alexandre de Amorim Garcia

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1 paper

Recent·Most cited

GenomicsbioRxivPreprintDec 17, 2019

Novel Variants in COL4A3 and COL4A4 are Causes of Alport Syndrome in Rio Grande do Norte, Brazil

Washington Candeia de Araújo, Raul Maia Falcão, Raquel Araújo Costa Uchôa…·Selma M. B. Jerônimo

The paper identifies novel deleterious variants in COL4A3 and COL4A4 in two unrelated Brazilian families with Alport Syndrome, linked to inbreeding through runs of homozygosity.

DOI 10.1101/2019.12.17.878918

humanwhole-exome sequencing

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