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

Mie Topholm Bruun

Odense University Hospital

ORCID: 0000-0002-8819-5388
MedicineImmunology and Microbiology

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 3%percentile
1.4Author 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 →

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.

Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis

Nature Genetics(2024)10.1038/s41588-024-01720-y
Top 15%
1.4DataRank
Top 15%63 citations

Garðar Sveinbjörnsson, Marijana Vujković, Anne-Sofie Seidelin, Helene Gellert‐Kristensen, Gustav Ahlberg +47 more

Papers

Driven by 16 papers — median percentile 85. Top paper: “Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis”.

Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis

Nature Genetics(2024)10.1038/s41588-024-01720-y
Top 15%
1.4DataRank
Top 15%63 citations

Garðar Sveinbjörnsson, Marijana Vujković, Anne-Sofie Seidelin, Helene Gellert‐Kristensen, Gustav Ahlberg +47 more

Genome-wide association study of febrile seizures implicates fever response and neuronal excitability genes

Brain(2021)10.1093/brain/awab260
N/A
0.626DataRank · unranked
64 citations

João Fadista, Jonas Bybjerg‐Grauholm, Vivek Appadurai, Michael S. Hildebrand, Thomas Folkmann Hansen +34 more

Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction

Nature Genetics(2024)10.1038/s41588-024-01763-1
N/A
0.609DataRank · unranked
57 citations

Chen Zhao, Steven Bell, Maria Didriksen, Muhammad Sulaman Nawaz, Nathalie Schandra +65 more

Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without aura

Nature Genetics(2023)10.1038/s41588-023-01538-0
N/A
0.606DataRank · unranked
56 citations

Mona Ameri Chalmer, Lilja Stefánsdóttir, Ástrós Skúladóttir, Guðmundur Einarsson, Margrét B. Andrésdóttir +88 more

Genome-wide analyses identify 25 infertility loci and relationships with reproductive traits across the allele frequency spectrum

Nature Genetics(2025)10.1038/s41588-025-02156-8
N/A
0.464DataRank · unranked
21 citations

Laura B. L. Wittemans, Duncan S. Palmer, Nikolas Baya, Teresa Ferreira, Barney Hill +57 more

Genome-wide meta-analysis identifies nine loci associated with higher risk of hepatocellular carcinoma development

JHEP Reports(2025)10.1016/j.jhepr.2025.101485
N/A
0.410DataRank · unranked
11 citations

Helene Gellert‐Kristensen, Colm J. O’Rourke, Anne-Sofie Seidelin, Gudmar Thorleifsson, Garðar Sveinbjörnsson +43 more

Genome-wide association study of borderline personality disorder identifies 11 loci and highlights shared risk with mental and somatic disorders

medRxiv(2024)10.1101/2024.11.12.24316957
N/A
0.241DataRank · unranked
4 citations

Swapnil Awasthi, Alisha S. M. Hall, Alice Braun, Maria Niarchou, Eirini Marouli +95 more

Genome-wide association study of febrile seizures identifies seven new loci implicating fever response and neuronal excitability genes

medRxiv(2020)10.1101/2020.11.18.20233916
N/A
0.208DataRank · unranked
3 citations

João Fadista, Jonas Bybjerg‐Grauholm, Vivek Appadurai, Michael S. Hildebrand, Thomas Folkmann Hansen +34 more

Genome-wide analyses identify 21 infertility loci and over 400 reproductive hormone loci across the allele frequency spectrum

medRxiv(2024)10.1101/2024.03.19.24304530
N/A
0DataRank · unranked
15 citations

Laura B. L. Wittemans, Duncan S. Palmer, Nikolas Baya, Teresa Ferreira, Barney Hill +46 more

Biallelic variants in POPDC2 cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathy

medRxiv(2024)10.1101/2024.07.04.24309755
N/A
0DataRank · unranked
0 citations

Alexa M.C. Vermeer, Pieter G. Postema, Rafik Tadros, Forrest Z. Bowling, Hildur M. Aegisdottir +65 more

Genome-wide association meta-analysis identifies five loci associated with postpartum hemorrhage

Nature Genetics(2024)10.1038/s41588-024-01839-y
N/A
0DataRank · unranked
10 citations

Valgerður Steinthórsdóttir, Lilja Stefánsdóttir, Palle Duun Rohde, Xiaoping Wu, Frank Geller +37 more

A meta-analysis uncovers the first sequence variant conferring risk of Bell’s palsy

Scientific Reports(2021)10.1038/s41598-021-82736-w
N/A
0DataRank · unranked
15 citations

Gyða Björnsdóttir, Guðmar Þorleifsson, G. Bragi Walters, Muhammad Sulaman Nawaz, Kristjan H. S. Moore +28 more

The 2024 international survey of platelet products and practice

Transfusion and Apheresis Science(2025)10.1016/j.transci.2025.104086
N/A
0DataRank · unranked
6 citations

Willy A. Flegel, Pieter F. van der Meer, Alain M. Ngoma, Kenneth E. Nollet, Nabajyoti Choudhury +56 more

Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathy

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.04.016
N/A
0DataRank · unranked
2 citations

Alexa M.C. Vermeer, Pieter G. Postema, Rafik Tadros, Forrest Z. Bowling, Hildur M. Aegisdottir +66 more

Genome-wide study of somatic symptom and related disorders identifies novel genomic loci and map genetic architecture

medRxiv(2025)10.1101/2025.07.16.25331639
N/A
0DataRank · unranked
1 citations

Piotr Jahołkowski, Alexey Shadrin, Elise Koch, Laura Birgit Luitva, Dorte Helenius Mikkelsen +27 more

The genetic architecture of fibromyalgia across 2.5 million individuals

medRxiv(2025)10.1101/2025.09.18.25335914
N/A
0DataRank · unranked
1 citations

Gyða Björnsdóttir, Keon Arbabi, Lea Urpa, Hele Haapaniemi, Gudmar Thorleifsson +46 more