Author

Fernanda Milanezi

DASA (Brazil)

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Research Focus:benchmarking· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Ana Cristina Victorino KrepischiiD· 2 shared Carla RosenbergiD· 2 shared Darine VillelaiD· 2 shared Michele Patricia MigliavaccaiD· 2 shared Patricia C. MazzonettoiD· 2 shared Rodrigo Guarischi‐SousaiD· 2 shared Silvia Souza da CostaiD· 2 shared Adriano Bonaldi· 1 shared

Activity by Year

2022-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 43 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Ana Cristina Victorino KrepischiORCID

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2 papers

Recent·Most cited

Low-pass whole genome sequencing is a reliable and cost-effective approach for copy number variant analysis in the clinical setting

Patricia C. Mazzonetto, Darine Villela, Silvia Souza da Costa, Ana Cristina Victorino Krepischi, Fernanda Milanezi, Michele Patricia Migliavacca, Paulo Marques Pierry, Adriano Bonaldi, Luiz Gustavo Dufner‐Almeida, Camila Alves Souza, José Eduardo Kroll, Marcelo G. Paula, Rodrigo Guarischi‐Sousa, Cristovam Scapulatempo‐Neto, Carla Rosenberg

This study validates low-pass whole genome sequencing as a reliable and cost-effective method for detecting copy number variants in clinical settings.

Annals of Human Genetics · Oct 9, 2023Peer-reviewedGenetic & Genomic Medicine

Chromosomal microarray analyses from 5,778 patients with neurodevelopmental disorders and congenital anomalies in Brazil

Ana Cristina Victorino Krepischi, Darine Villela, Silvia Souza da Costa, Patricia C. Mazzonetto, Juliana da Silveira Schauren, Michele Patricia Migliavacca, Fernanda Milanezi, Juliana Gomes dos Santos, Gustavo Guida, Rodrigo Guarischi‐Sousa, Gustavo Campana, Fernando Kok, David Schlesinger, João Paulo Kitajima, Francine Campagnari, , Carla Rosenberg

This study analyzes chromosomal microarray data from 5,778 Brazilian patients with neurodevelopmental disorders and congenital anomalies to assess genetic bases and evaluate cost-effectiveness of variant analysis.

Scientific Reports · Sep 7, 2022Peer-reviewedGenetic & Genomic Medicine