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

Ásmundur Oddsson

deCODE Genetics (Iceland)

ORCID: 0000-0002-4606-5163

Also affiliated with Mahindra and Mahindra Limited (India)

Biochemistry, Genetics and Molecular BiologyNeuroscienceMedicine

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 4 papers. Top paper: “Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without aura”.

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 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

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

Data from Loss-of-Function Variants in the Tumor-Suppressor Gene PTPN14 Confer Increased Cancer Risk

(2023)10.1158/0008-5472.c.6512925.v1
N/A
0DataRank · unranked
0 citations

Simon Stacey, Garðar Sveinbjörnsson, Guðmar Þorleifsson, Kristján Norland, Bárður Sigurgeirsson +34 more