Brynjar Ö. Jensson

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 2 papers. Top paper: “Loss-of-function variants in ITSN1 confer high risk of Parkinson’s disease”.

Loss-of-function variants in ITSN1 confer high risk of Parkinson’s disease

npj Parkinson s Disease(2024)10.1038/s41531-024-00752-9

N/A

0DataRank · unranked

12 citations

Vinicius Tragante, Garðar Sveinbjörnsson, Hannes Helgason, Árni Sturluson, Anna Bjornsdottir +18 more

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

0DataRank · unranked

44 citations

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