Author

Monicke O. Lima

Universidade de São PauloORCID 0000-0003-0747-2345Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:gene regulatory network inference· 1 Organism:human· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Carolina CappiiD· 1 shared Emily OlfsoniD· 1 shared Guilherme V. PolanczykiD· 1 shared Gwyneth C. ZaiiD· 1 shared James L. KennedyiD· 1 shared Justin M. ParentiD· 1 shared Lawrence Anthony Vitulano· 1 shared Luís C. FarhatiD· 1 shared

Activity by Year

2023-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Carolina CappiORCID

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1 paper

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintMay 19, 2023

Ultra-rare de novo damaging coding variants are enriched in attention-deficit/hyperactivity disorder and identify risk genes

Emily Olfson, Luís C. Farhat, Wenzhong Liu…·Thomas V. Fernandez

This paper identifies ultra-rare de novo damaging variants in ADHD cases and finds KDM5B as a high-confidence risk gene, along with enriched biological pathways.

2 citations

humanwhole-exome sequencing

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