Thea Giacomini

Also affiliated with Istituti di Ricovero e Cura a Carattere Scientifico, University of Genoa

MedicineBiochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 4 papers. Top paper: “Epilepsy Course and Developmental Trajectories in STXBP1 -DEE”.

Epilepsy Course and Developmental Trajectories in STXBP1 -DEE

Neurology Genetics(2022)10.1212/nxg.0000000000000676

N/A

0DataRank · unranked

49 citations

Julie Xian, Antonella Riva, Francesca Marchese, Bruria Ben Zeev, Loreto Ríos +53 more

Biallelic loss-of-function variants in CACHD1 cause a novel neurodevelopmental syndrome with facial dysmorphism and multisystem congenital abnormalities

Genetics in Medicine(2023)10.1016/j.gim.2023.101057

N/A

0DataRank · unranked

11 citations

Kamal Khan, Claire Bénéteau, Rachel Fox, Sandra von Hardenberg, Ayaz Khan +23 more

Patterns of subregional cerebellar atrophy across epilepsy syndromes: An ENIGMA-Epilepsy study

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.10.21.562994

N/A

0DataRank · unranked

4 citations

Andrew Perry, Lucy Vivash, Terence J. O’Brien, Marina K. M. Alvim, Donatello Arienzo +60 more

Patterns of subregional cerebellar atrophy across epilepsy syndromes: An ENIGMA‐Epilepsy study

Epilepsia(2024)10.1111/epi.17881

N/A

0DataRank · unranked

23 citations

Andrew Perry, Lucy Vivash, Terence J. O’Brien, Marina K. M. Alvim, Donatello Arienzo +59 more