Dídac Casas‐Alba

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 4 papers. Top paper: “Mutations in the small nuclear RNA gene RNU2-2 cause a severe neurodevelopmental disorder with prominent epilepsy”.

Mutations in the small nuclear RNA gene RNU2-2 cause a severe neurodevelopmental disorder with prominent epilepsy

Nature Genetics(2025)10.1038/s41588-025-02159-5

N/A

0.571DataRank · unranked

44 citations

Koenraad De Wispelaere, Jonathan Lees, Marta Codina‐Solà, Brynjar Ö. Jensson, Emma Hales +47 more

Genomic and serologic characterization of enterovirus A71 brainstem encephalitis

Neurology Neuroimmunology & Neuroinflammation(2020)10.1212/nxi.0000000000000703

N/A

0.520DataRank · unranked

31 citations

Ryan Schubert, Dídac Casas‐Alba, Isobel A. Hawes, Prashanth Ramachandran, Akshaya Ramesh +15 more

Efficacy of baricitinib on chronic pericardial effusion in a patient with Aicardi–Goutières syndrome

Lara D. Veeken(2021)10.1093/rheumatology/keab860

N/A

0DataRank · unranked

9 citations

Alejandra Darling, Eva Caballero, Anna Mensa‐Vilaró, Joaquim Bartrons, Jordi Antón +4 more

Heterozygous MAP3K20 variants cause ectodermal dysplasia, craniosynostosis, sensorineural hearing loss, and limb anomalies

Human Genetics(2024)10.1007/s00439-024-02657-2

N/A

0DataRank · unranked

6 citations

Elizabeth A. Burke, Sukyeong Lee, Tanya N. Eble, Melanie O’Leary, Ikeoluwa Osei‐Owusu +18 more