Author

Giulia Pascolini

Azienda Ospedaliera San Camillo-ForlaniniORCID 0000-0002-2440-7441Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Developmental Biology· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Research Focus:differential expression· 2 Organism:human· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1 Assay:DNA methylation· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Antonio NovelliiD· 2 shared Emanuele AgoliniiD· 2 shared Paola GrammaticoiD· 2 shared Ada HamoshiD· 1 shared Agatino BattagliaiD· 1 shared Alan H. BeggsiD· 1 shared Alexander KolevzoniD· 1 shared Alice PoissoniD· 1 shared

Activity by Year

2020-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersGenetic & Genomic Medicine

Antonio NovelliORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Disruption of RFX family transcription factors causes autism, attention-deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior

Holly K. Harris, Tojo Nakayama, Jenny F. Lai, Boxun Zhao, Nikoleta Argyrou, Cynthia Sophia Gubbels, Aubrie Soucy, Casie A. Genetti, Victoria Suslovitch, Lance H. Rodan, George E. Tiller, Gaëtan Lesca, Karen Webster Gripp, Reza Asadollahi, Ada Hamosh, , Timothy W. Yu

The paper identifies RFX3, RFX4, and RFX7 mutations as causes of neurodevelopmental disorders including autism, ADHD, and intellectual disability, and links these genes to ASD risk genes through bioinformatic analysis.

Genetics in Medicine · Mar 3, 2021Peer-reviewedGenetic & Genomic Medicine

Episignatures stratifying ADNP syndrome show modest correlation with phenotype

Michael S. Breen, Paras Garg, Lara Tang, Danielle Mendonca, Tess Levy, Mafalda Barbosa, Anne B. Arnett, Evangeline C. Kurtz‐Nelson, Emanuele Agolini, Agatino Battaglia, Andreas G. Chiocchetti, Christine Margarete Freitag, Alicia García-Alcón, Paola Grammatico, Irva Hertz‐Picciotto, , Silvia De Rubeis

The paper identifies two methylation-based episignatures in ADNP syndrome but finds limited correlation with clinical phenotypes.

bioRxiv · Apr 1, 2020 · PreprintDevelopmental Biology