Francesca Forzano

Guy's and St Thomas' NHS Foundation Trust

Biochemistry, Genetics and Molecular BiologyMedicine

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 6 papers. Top paper: “Profiling PI3K-AKT-MTOR variants in focal brain malformations reveals new insights for diagnostic care”.

Profiling PI3K-AKT-MTOR variants in focal brain malformations reveals new insights for diagnostic care

Brain(2021)10.1093/brain/awab376

N/A

0DataRank · unranked

55 citations

Matthew Berkseth, Rylee Shear, Lorenzo Gonzalez, Andrew E. Timms, Josef Šulc +19 more

Effects of eight neuropsychiatric copy number variants on human brain structure

Translational Psychiatry(2021)10.1038/s41398-021-01490-9

N/A

0DataRank · unranked

47 citations

Kuldeep Kumar, Clara Moreau, Sandra Martin‐Brevet, Guillaume Huguet, Catherine Schramm +95 more

De novo variants in the PSMC3 proteasome AAA-ATPase subunit gene cause neurodevelopmental disorders associated with type I interferonopathies

medRxiv(2021)10.1101/2021.12.07.21266342

N/A

0DataRank · unranked

3 citations

Sébastien Küry, Victoria Most, Cory Rosenfelt, Marie‐Pier Scott‐Boyer, Geeske M. van Woerden +67 more

PSMC3 proteasome subunit variants are associated with neurodevelopmental delay and type I interferon production

Science Translational Medicine(2023)10.1126/scitranslmed.abo3189

N/A

0DataRank · unranked

36 citations

Sébastien Küry, Victoria Most, Cory Rosenfelt, Marie‐Pier Scott‐Boyer, Geeske M. van Woerden +69 more

Modelling population genetic screening in rare neurodegenerative diseases

medRxiv(2023)10.1101/2023.07.03.23292187

N/A

0DataRank · unranked

1 citations

Alfredo Iacoangeli, Mina Ryten, Francesca Forzano, Neil Pearce, Ammar Al‐Chalabi +1 more

Modelling Population Genetic Screening in Rare Neurodegenerative Diseases

Biomedicines(2025)10.3390/biomedicines13051018

N/A

0DataRank · unranked

1 citations

Alfredo Iacoangeli, Mina Ryten, Francesca Forzano, Neil Pearce, Ammar Al‐Chalabi +1 more