Riitta Sallinen

Also affiliated with Science for Life Laboratory, Karolinska Institutet, Institute for Molecular Medicine Finland

MedicineNeuroscienceBiochemistry, Genetics and Molecular BiologyHealth ProfessionsArts and Humanities

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 1 paper. Top paper: “Confirmation of the Type 2 Myotonic Dystrophy (CCTG)n Expansion Mutation in Patients with Proximal Myotonic Myopathy/Proximal Myotonic Dystrophy of Different European Origins: A Single Shared Haplotype Indicates an Ancestral Founder Effect”.

Confirmation of the Type 2 Myotonic Dystrophy (CCTG)n Expansion Mutation in Patients with Proximal Myotonic Myopathy/Proximal Myotonic Dystrophy of Different European Origins: A Single Shared Haplotype Indicates an Ancestral Founder Effect

UNC Libraries(2020)10.17615/gzep-km85

N/A

0DataRank · unranked

9 citations

Bjarne Udd, Richard T. Moxley, Fred A. Wright, B. Eymard, Armand Bottani +18 more