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

Tanner Koomar

University of Iowa

ORCID: 0000-0003-0777-8678
NeuroscienceBiochemistry, Genetics and Molecular BiologyPsychology

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 1%percentile
4.6Author DataRank

Indexed papers

2in 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 2 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.

Estimating the Prevalence and Genetic Risk Mechanisms of ARFID in a Large Autism Cohort

Frontiers in Psychiatry(2021)10.3389/fpsyt.2021.668297
Top 7%
3.0DataRank
Top 7%93 citations

Taylor Thomas, Natalie Pottschmidt, Michael Lutter, Jacob J. Michaelson, Tanner Koomar

Papers

Driven by 12 papers — median percentile 90. Top paper: “Estimating the Prevalence and Genetic Risk Mechanisms of ARFID in a Large Autism Cohort”.

Estimating the Prevalence and Genetic Risk Mechanisms of ARFID in a Large Autism Cohort

Frontiers in Psychiatry(2021)10.3389/fpsyt.2021.668297
Top 7%
3.0DataRank
Top 7%93 citations

Taylor Thomas, Natalie Pottschmidt, Michael Lutter, Jacob J. Michaelson, Tanner Koomar

Integrated gene analyses of de novo variants from 46,612 trios with autism and developmental disorders

Proceedings of the National Academy of Sciences(2022)10.1073/pnas.2203491119
Top 14%
1.5DataRank
Top 14%73 citations

Chang N. Kim, Trygve E. Bakken, Madelyn A. Gillentine, Barbara Henning, Yafei Mao +94 more

Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people

Proceedings of the National Academy of Sciences(2022)10.1073/pnas.2202764119
N/A
0.738DataRank · unranked
136 citations

Nazanin Mirza‐Schreiber, Eveline L. de Zeeuw, Carol A. Wang, Dongnhu T. Truong, Andrea G. Allegrini +90 more

Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities

Translational Psychiatry(2022)10.1038/s41398-022-02250-z
N/A
0.406DataRank · unranked
14 citations

Karen Wigg, Else Eising, Yu Feng, Kirsten Blokland, Margaret Wilkinson +85 more

Genome-wide association analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.11.04.466897
N/A
0.406DataRank · unranked
14 citations

Nazanin Mirza‐Schreiber, Eveline L. de Zeeuw, Carol A. Wang, Dongnhu T. Truong, Andrea G. Allegrini +85 more

Clinical autism subscales have common genetic liabilities that are heritable, pleiotropic, and generalizable to the general population

medRxiv(2021)10.1101/2021.08.30.21262845
N/A
0.312DataRank · unranked
7 citations

Tanner Koomar, Lucas G. Casten, Ashton J. Tener, Ethan Bahl, Jacob J. Michaelson +1 more

Genomic dissection of sleep archetypes in a large autism cohort

medRxiv(2025)10.1101/2025.04.04.25325272
N/A
0DataRank · unranked
1 citations

Natalie Pottschmidt, Tanner Koomar, Taylor Thomas, Jacob J. Michaelson, Leo Brueggeman

Genetic and morphological estimates of androgen exposure predict social deficits in multiple neurodevelopmental disorder cohorts

medRxiv(2020)10.1101/2020.08.03.20155671
N/A
0DataRank · unranked
0 citations

Yongchao Huang, Kévin Vervier, Dabney Hofamman, Mary Cafferata, Seima Al‐Momani +13 more

Genetic and morphological estimates of androgen exposure predict social deficits in multiple neurodevelopmental disorder cohorts

Molecular Autism(2021)10.1186/s13229-021-00450-w
N/A
0DataRank · unranked
12 citations

Yongchao Huang, Kévin Vervier, Dabney Hofammann, Mary Cafferata, Seima Al‐Momani +13 more

Clinical autism subscales have common genetic liabilities that are heritable, pleiotropic, and generalizable to the general population

Translational Psychiatry(2022)10.1038/s41398-022-01982-2
N/A
0DataRank · unranked
24 citations

Tanner Koomar, Lucas G. Casten, Ashton J. Tener, Ethan Bahl, Jacob J. Michaelson +1 more

Increasing power in language genetics with Lingo: a web-based digital phenotyping platform

medRxiv(2024)10.1101/2024.03.29.24305034
N/A
0DataRank · unranked
1 citations

Tanner Koomar, Muhammad Elsadany, Ying Hsu, Emily Kelly, Gabriella Snyder +6 more

Forecasting risk gene discovery in autism with machine learning and genome-scale data

Scientific Reports(2020)10.1038/s41598-020-61288-5
N/A
0DataRank · unranked
52 citations

Tanner Koomar, Jacob J. Michaelson, Leo Brueggeman