Author

Quintino Giorgio D’Alessandris

Università Cattolica del Sacro CuoreORCID 0000-0002-2953-9291Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Cell Biology· 1 Genomics· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Research Focus:differential expression· 2 Organism:human· 2 Research Focus:cell type annotation· 1 Research Focus:drug response / drug discovery· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Assay:Hi-C· 1 Assay:organoid / primary culture· 1

Frequent Co-Authors

Jay GopalakrishnaniD· 2 shared Lucia Ricci‐VitianiiD· 2 shared Omkar Suhas VinchureiD· 2 shared Roberto Pallini M. DiD· 2 shared Adi Danieli‐MackayiD· 1 shared Ali Mirsaidi· 1 shared Alysson Renato MuotriiD· 1 shared Anand RamaniiD· 1 shared

Activity by Year

2023-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 37 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 papersCell Biology

Jay GopalakrishnanORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Cell BiologyNature CommunicationsPeer-reviewedDec 19, 2024

Reliability of high-quantity human brain organoids for modeling microcephaly, glioma invasion, and drug screening

Anand Ramani, Giovanni Pasquini, Niklas J. Gerkau…·Jay Gopalakrishnan

This study develops a high-throughput method to generate reliable human brain organoids for modeling microcephaly, glioma invasion, and drug screening.

59 citationstop 2%

humanorganoid / primary culture

𝕏 PostBluesky

GenomicsbioRxivPreprintApr 20, 2023

Extreme structural heterogeneity rewires glioblastoma chromosomes to sustain patient-specific transcriptional programs

Ting Xie, Adi Danieli‐Mackay, Mariachiara Buccarelli…·Argyris Papantonis

The paper maps structural variants and neoloops in glioblastoma stem cells to show how they sustain tumor-specific transcriptional programs and identify patient-specific vulnerabilities.

2 citations

humanHi-C

𝕏 PostBluesky