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

Lincoln Nadauld

Intermountain Healthcare

ORCID: 0000-0002-1935-4998

Also affiliated with University of Iceland

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 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 12 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

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 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

Germline variants of ATG7 in familial cholangiocarcinoma alter autophagy and p62

Scientific Reports(2022)10.1038/s41598-022-13569-4
N/A
0DataRank · unranked
13 citations

Jiamin Chen, Margrét H. Ögmundsdóttir, Carlos Ayala, Billy T. Lau, Richard Glenn C. Delacruz +12 more

The single-cell spatial landscape of stage III colorectal cancers

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.11.07.622577
N/A
0DataRank · unranked
1 citations

HoJoon Lee, Minh‐Phuong Tran, Richard Cruz, Anuja Sathe, Xiangqi Bai +11 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

The single-cell spatial landscape of stage III colorectal cancers

npj Precision Oncology(2025)10.1038/s41698-025-00853-5
N/A
0DataRank · unranked
10 citations

HoJoon Lee, Minh Tran, Richard Cruz, Anuja Sathe, Xiangqi Bai +11 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

Whole genome analysis identifies the association of TP53 genomic deletions with lower survival in Stage III colorectal cancer

Scientific Reports(2020)10.1038/s41598-020-61643-6
N/A
0DataRank · unranked
14 citations

Paul Van Hummelen, Matthew Kubit, HoJoon Lee, John Bell, Susan M. Grimes +9 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

Characterization of the consensus mucosal microbiome of colorectal cancer

NAR Cancer(2021)10.1093/narcan/zcab049
N/A
0DataRank · unranked
21 citations

Susan M. Grimes, Stephanie Greer, Matthew Kubit, HoJoon Lee, Lincoln Nadauld +2 more

Characterization of the consensus mucosal microbiome of colorectal cancer

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.06.02.446807
N/A
0DataRank · unranked
3 citations

Susan M. Grimes, Stephanie Greer, Matthew Kubit, HoJoon Lee, Lincoln Nadauld +2 more