Author

Lawrence Anthony Vitulano

Yale University

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· 1

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 Luís C. FarhatiD· 1 shared Monicke O. LimaiD· 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

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, Lawrence Anthony Vitulano, Gwyneth C. Zai, Monicke O. Lima, Justin M. Parent, Guilherme V. Polanczyk, Carolina Cappi, James L. Kennedy, 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.

medRxiv · May 19, 2023 · PreprintGenetic & Genomic Medicine