Brendan Kenna

Also affiliated with University Medical Center Utrecht

MedicineNeuroscience

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: “Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson’s disease”.

Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson’s disease

Nature Genetics(2024)10.1038/s41588-024-01787-7

N/A

0.641DataRank · unranked

71 citations

Dongbing Lai, Pamela Keagle, Desiree M. Baron, Brendan Kenna, Maarten Kooyman +17 more

Structural variation analysis of 6,500 whole genome sequences in amyotrophic lateral sclerosis

npj Genomic Medicine(2022)10.1038/s41525-021-00267-9

N/A

0.571DataRank · unranked

44 citations

Alfredo Iacoangeli, Joke J.F.A. van Vugt, Harry Bowles, Matthieu Moisse, Ramona A.J. Zwamborn +42 more