🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Jesper Eisfeldt

Karolinska University Hospital

ORCID: 0000-0003-3716-4917

Also affiliated with Science for Life Laboratory, Karolinska Institutet

Biochemistry, Genetics and Molecular BiologyAgricultural and Biological Sciences

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

3in 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 3 indexed papers 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 →

Top data-sharing exemplar

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Comprehensive structural variation genome map of individuals carrying complex chromosomal rearrangements

PLOS Genetics(2019)10.1371/journal.pgen.1007858
Top 33%
0.590DataRank
Top 33%50 citations

Maria Pettersson, Francesco Vezzi, Josephine Wincent, Max Käller, Joel Gruselius +5 more

Papers

Driven by 8 papers — median percentile 67. Top paper: “Comprehensive structural variation genome map of individuals carrying complex chromosomal rearrangements”.

Comprehensive structural variation genome map of individuals carrying complex chromosomal rearrangements

PLOS Genetics(2019)10.1371/journal.pgen.1007858
Top 33%
0.590DataRank
Top 33%50 citations

Maria Pettersson, Francesco Vezzi, Josephine Wincent, Max Käller, Joel Gruselius +5 more

Replicative and non-replicative mechanisms in the formation of clustered CNVs are indicated by whole genome characterization

PLOS Genetics(2018)10.1371/journal.pgen.1007780
N/A
0.557DataRank · unranked
40 citations

Jesper Eisfeldt, Maria Pettersson, Johanna Lundin, Daniel Nilsson, Josephine Wincent +19 more

Chromatin interactions in differentiating keratinocytes reveal novel atopic dermatitis– and psoriasis-associated genes

Journal of Allergy and Clinical Immunology(2021)10.1016/j.jaci.2020.09.035
N/A
0.553DataRank · unranked
39 citations

Rapolas Spalinskas, Samina Asad, Kunal Das Mahapatra, Pontus Höjer, Anandashankar Anil +15 more

Structural variant allelic heterogeneity in MECP2 duplication syndrome provides insight into clinical severity and variability of disease expression

Genome Medicine(2024)10.1186/s13073-024-01411-7
N/A
0.474DataRank · unranked
17 citations

Jesse D. Bengtsson, Sameer S. Bajikar, Christopher M. Grochowski, Ming Yin Lun, Mira Gandhi +38 more

Leveraging the T2T assembly to resolve rare and pathogenic inversions in reference genome gaps

Genome Research(2024)10.1101/gr.279346.124
N/A
0.396DataRank · unranked
13 citations

Jesper Eisfeldt, Jesse D. Bengtsson, Ming Yin Lun, Christopher M. Grochowski, Medhat Mahmoud +17 more

Balanced chromosomal rearrangements offer insights into coding and noncoding genomic features associated with developmental disorders

medRxiv(2022)10.1101/2022.02.15.22270795
N/A
0.373DataRank · unranked
11 citations

Mana M. Mehrjouy, Ryan L. Collins, Mads Bak, Olga Dudchenko, Harrison Brand +95 more

Mind the gap: the relevance of the genome reference to resolve rare and pathogenic inversions

medRxiv(2024)10.1101/2024.04.22.24305780
N/A
0DataRank · unranked
1 citations

Jesper Eisfeldt, Jesse D. Bengtsson, Ming Yin Lun, Christopher M. Grochowski, Medhat Mahmoud +14 more

Cytogenetically visible inversions are formed by multiple molecular mechanisms

Human Mutation(2020)10.1002/humu.24106
N/A
0DataRank · unranked
27 citations

Christopher M. Grochowski, Josephine Wincent, Jesper Eisfeldt, Amy M. Breman, Sau Wai Cheung +11 more