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

Fostering Data Sharing

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Gyða Björnsdóttir

Gyða Björnsdóttir

deCODE Genetics (Iceland)

ORCID: 0000-0002-8100-0306

Biochemistry, Genetics and Molecular BiologyMedicine

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 10 papers. Top paper: “Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals”.

Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals

Nature Genetics(2022)10.1038/s41588-022-01016-z

N/A

8.1DataRank · unranked

699 citations

Yeda Wu, Nancy Wang, Hariharan Jayashankar, Michael Bennett, Seyed Moeen Nehzati +94 more

Genetic diversity fuels gene discovery for tobacco and alcohol use

Nature(2022)10.1038/s41586-022-05477-4

N/A

5.9DataRank · unranked

513 citations

Xingyan Wang, Fang Chen, Seon-Kyeong Jang, Mengzhen Liu, Chen Wang +95 more

Model-based assessment of replicability for genome-wide association meta-analysis

Nature Communications(2021)10.1038/s41467-021-21226-z

N/A

1.5DataRank · unranked

40 citations

Yu Jiang, Mengzhen Liu, J. Dylan Weissenkampen, Scott A. Eckert, Lina Yang +125 more

Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use

Nature Genetics(2019)10.1038/s41588-018-0307-5

N/A

1.1DataRank · unranked

2128 citations

Mengzhen Liu, HUNT All-In Psychiatry, Yu Jiang, Robbee Wedow, Yue Li +120 more

Loss-of-function variants in ITSN1 confer high risk of Parkinson’s disease

npj Parkinson s Disease(2024)10.1038/s41531-024-00752-9

N/A

0.385DataRank · unranked

12 citations

Vinicius Tragante, Garðar Sveinbjörnsson, Hannes Helgason, Árni Sturluson, Anna Bjornsdottir +18 more

Diagnosing migraine from genome-wide genotype data: a machine learning analysis

Brain(2025)10.1093/brain/awaf172

N/A

0.269DataRank · unranked

5 citations

Tjaša Kumelj, Bendik S Winsvold, Marte‐Helene Bjørk, Parashkev Nachev, Manjit Matharu +70 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

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

Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles

Nature Genetics(2022)10.1038/s41588-021-00990-0

N/A

0DataRank · unranked

399 citations

Bendik Slagsvold Winsvold, Sanni Ruotsalainen, Gyða Björnsdóttir, Aster V. E. Harder, Lisette J. A. Kogelman +68 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

0DataRank · unranked

56 citations

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