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Author

Enaldo Vieira de Melo

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Universidade Federal de SergipeORCID 0000-0002-9314-4331Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 1Approach:statistical model· 1

Frequent Co-Authors

Ana Beatriz Leite AragãoiD· 1 sharedAntônio Carlos Sobral SousaiD· 1 sharedAntónio P. de AlmeidaiD· 1 sharedBárbara Letícia Lima dos SantosiD· 1 sharedBeatriz Carolina de Araujo PereiraiD· 1 sharedCaio Fraga Barreto de Matos FerreiraiD· 1 sharedEmerson de Santana SantosiD· 1 sharedGabriel da Costa KuhniD· 1 shared

Activity by Year

2025-2025 · peak 1/yr
012025: 1 paper (click to filter)12025

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links
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MeloAna Beatriz Leite Aragão · 1 shared paperAragão · 1Antônio Carlos Sobral Sousa · 1 shared paperSousa · 1António P. de Almeida · 1 shared paperAlmeida · 1Bárbara Letícia Lima dos Santos · 1 shared paperSantos · 1Beatriz Carolina de Araujo Pereira · 1 shared paperPereira · 1Caio Fraga Barreto de Matos Ferreira · 1 shared paperFerreira · 1Emerson de Santana Santos · 1 shared paperSantos · 1Gabriel da Costa Kuhn · 1 shared paperKuhn · 1Irlaneide da Silva Tavares · 1 shared paperTavares · 1João Victor Andrade Pimentel · 1 shared paperPimentel · 1
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1 shared paperGenetic & Genomic Medicine
Ana Beatriz Leite AragãoORCID

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1 paper

Recent·Most cited

Genetic, Clinical, and Sociodemographic Profile in Individuals with Diagnosis or Family History of Hypertrophic Cardiomyopathy: Insights from a Prospective Cohort

Emerson de Santana Santos, Gabriel da Costa Kuhn, António P. de Almeida, João Victor Andrade Pimentel, Newton Vital Figueiredo Neto, Larissa Rebeca da Silva Tavares, Bárbara Letícia Lima dos Santos, Ana Beatriz Leite Aragão, Beatriz Carolina de Araujo Pereira, Caio Fraga Barreto de Matos Ferreira, Willian Moreira Leão e Silva, Enaldo Vieira de Melo, Irlaneide da Silva Tavares, Antônio Carlos Sobral Sousa, Joselina Luzia Menezes Oliveira

This study examines genetic, clinical, and sociodemographic profiles of individuals with HCM or family history of SCD, finding higher genetic variant rates in HCM-diagnosed individuals and those with family history of SCD.

Genes · Sep 17, 2025Peer-reviewedGenetic & Genomic Medicine