Author

Philip F. Giampietro

University of Illinois ChicagoORCID 0000-0003-2874-8064Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:mouse· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Adam S. ArterberyiD· 1 shared Adam S.L. GraefeiD· 1 shared Ana Laura Arenas-Díaz· 1 shared Andrés HernándeziD· 1 shared Anita M BagleyiD· 1 shared Anne‐Sophie Jourdain· 1 shared Anxhela Gjyshi GustafsoniD· 1 shared Barbara R. PoberiD· 1 shared

Activity by Year

2023-2026 · peak 1/yr

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10 top collaborators · 20 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Adam S. ArterberyORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicineThe American Journal of Human GeneticsPeer-reviewedSep 1, 2026

A Phenotypic Paradigm for Cerebral Palsy Genetics

Adam S. Arterbery, Michael A. Gargano, Anita M Bagley…·Peter N. Robinson

The paper identifies pathogenic variants in 15.8% of CP patients and finds only 16 of 60 genes have significant CP association.

DOI 10.1016/j.ajhg.2026.08.007

humanstatistical model

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Genetic & Genomic MedicineThe American Journal of Human GeneticsPeer-reviewedSep 25, 2023

Missense variants affecting the actin-binding domains of PLS3 cause X-linked congenital diaphragmatic hernia and body wall defects

Florence Petit, Mauro Longoni, Julie M. Wells…·Frances A. High

The paper identifies missense variants in PLS3 causing X-linked congenital diaphragmatic hernia and body wall defects through genetic analysis and functional studies.

11 citations

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