Johanna Palmio

Also affiliated with Tampere University

Biochemistry, Genetics and Molecular BiologyMedicineNeuroscience

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

1in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 1 indexed paper attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

Papers

Driven by 6 papers. Top paper: “Anoctamin-5 related muscle disease: clinical and genetic findings in a large European cohort”.

Anoctamin-5 related muscle disease: clinical and genetic findings in a large European cohort

Brain(2023)10.1093/brain/awad088

N/A

0.345DataRank · unranked

9 citations

Federica Montagnese, Sonja Holm-Yildiz, Nanna Scharff Poulsen, Tanya Stojkovic, Anthony Behin +28 more

Development of a standard of care for patients with valosin-containing protein associated multisystem proteinopathy

Orphanet Journal of Rare Diseases(2022)10.1186/s13023-022-02172-5

N/A

0DataRank · unranked

36 citations

Allison Peck, Lindsay N. Alfano, Kenneth I. Berger, M. James, Nupur Ghoshal +50 more

Provisional practice recommendation for the management of myopathy in VCP‐associated multisystem proteinopathy

Annals of Clinical and Translational Neurology(2023)10.1002/acn3.51760

N/A

0DataRank · unranked

9 citations

Allison Peck, Teresinha Evangelista, Gerald Pfeffer, Leo Wang, Jordi Díaz‐Manera +15 more

Heterozygous loss-of-function variants in SPTAN1 cause a novel early childhood onset distal myopathy with chronic neurogenic features

medRxiv(2024)10.1101/2024.09.23.24313872

N/A

0DataRank · unranked

3 citations

Liedewei Van de Vondel, Biljana Ermanoska, Alice Monticelli, Arnaud Isapof, Enzo Cohen +33 more

The recurrent deep intronic pseudoexon-inducing variant COL6A1 c.930+189C>T results in a consistently severe phenotype of COL6-related dystrophy: Towards clinical trial readiness for splice-modulating therapy

medRxiv(2024)10.1101/2024.03.29.24304673

N/A

0DataRank · unranked

2 citations

Véronique Bolduc, Fady Guirguis, Sandra Donkervoort, Ying Hu, Rotem Orbach +64 more

Heterozygous loss-of-function variants in SPTAN1 cause an early childhood onset distal myopathy

Genetics in Medicine(2025)10.1016/j.gim.2025.101399

N/A

0DataRank · unranked

5 citations

Liedewei Van de Vondel, Biljana Ermanoska, Alice Monticelli, Arnaud Isapof, Enzo Cohen +32 more