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Marcel Pinheiro Caraciolo

Observed names: Caraciolo, Marcel Pinheiro, MARCEL PINHEIRO CARACIOLO, MP Caraciolo, Marcel Caraciolo, Marcel P. Caraciolo
ORCID: 0000-0002-0463-767X
Observed ORCID: 0000-0002-0463-767X
OpenAlex ID: A5055734370
The Brazilian Rare Genomes Project: Validation of Whole Genome Sequencing for Rare Diseases Diagnosis
2022 · Antonio Victor Campos Coelho, Bruna Mascaro Cordeiro de Azevedo, et al. · Frontiers in Molecular Biosciences · 41
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The genetics of hereditary cancer risk syndromes in Brazil: a comprehensive analysis of 1682 patients
2022 · Jarbas Maciel de Oliveira, Nuria Bengala Zurro, et al. · European Journal of Human Genetics · 21
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The hospital Israelita Albert Einstein standards for constitutional sequence variants classification: version 2023
2023 · Caio Robledo D’Angioli Costa Quaio, José Ricardo Magliocco Ceroni, et al. · Human Genomics · 11
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Genomic study of nonsyndromic hearing loss in unaffected individuals: Frequency of pathogenic and likely pathogenic variants in a Brazilian cohort of 2,097 genomes
2022 · Caio Robledo D’ Angioli Costa Quaio, Antonio Victor Campos Coelho, et al. · Frontiers in Genetics · 11
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Varstation: a complete and efficient tool to support NGS data analysis
2019 · ACO Faria, MP Caraciolo, et al. · bioRxiv (Cold Spring Harbor Laboratory) · 10
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Assessing the Risk Stratification of Breast Cancer Polygenic Risk Scores in a Brazilian Cohort
2024 · Rodrigo A.S. Barreiro, Tatiana F. de Almeida, et al. · Journal of Molecular Diagnostics · 5
Crab: A Recommendation Engine Framework for Python
2011 · Marcel Caraciolo, Bruno Melo, et al. · Proceedings of the Python in Science Conferences · 3
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Whole Genome Sequencing for the Diagnosis of Rare Disorders
2025 · Antonio Victor Campos Coelho, Rafael Sales de Albuquerque, et al. · medRxiv · 1
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Towards effective course-based recommendations for public tenders
2013 · Frederico Durao, Marcel Pinheiro Caraciolo, et al. · International Journal of Knowledge and Web Intelligence · 1
Genome sequencing for the diagnosis of rare disorders: The Brazilian Rare Genomes Project
2026 · Antonio Victor Campos Coelho, Rafael Sales de Albuquerque, et al. · Human Genetics and Genomics Advances
Enabling large-scale next-generation sequencing data analysis based on a high performance cloud computing architecture
2023 · Wilder Barbosa Galvão, George de Vasconcelos Carvalho Neto, et al. · Even3 Publicações eBooks
Additional file 1 of The hospital Israelita Albert Einstein standards for constitutional sequence variants classification: version 2023
2023 · Quaio, Caio Robledo D’Angioli Costa, Ceroni, José Ricardo Magliocco, et al. · Figshare
Assessing the risk stratification of breast cancer polygenic risk scores in two Brazilian samples
2022 · R.A.S Barreiro, TF Almeida, et al. · medRxiv
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Frequency of Pathogenic, "risk Factor" and Uncertain Significance Variants in 378 Brazilian Patients With Suspected Autoinflammatory Syndromes
2019 · NURIA BENGALA ZURRO, LAÍS RODRIGUES MOURA, et al.
Works count: 15
Citation count: 104
H-index: 5
I10-index: 5
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