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

Brett Trost

University of Toronto

ORCID: 0000-0003-4863-7273

Also affiliated with Great Ormond Street Hospital, Hospital for Sick Children, Institute of Computing Technology, SickKids Foundation, University College London

NeuroscienceBiochemistry, Genetics and Molecular Biology

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 6%percentile
0.208Author 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.

Genomic architecture of Autism Spectrum Disorder from comprehensive whole-genome sequence annotation

medRxiv(2022)10.1101/2022.05.05.22274031
Top 65%
0.208DataRank
Top 65%3 citations

Bhooma Thiruvahindrapuram, Ada J. S. Chan, Worrawat Engchuan, Edward J. Higginbotham, Jennifer Howe +95 more

Papers

Driven by 8 papers — median percentile 35. Top paper: “Chromosome X-wide common variant association study in autism spectrum disorder”.

Chromosome X-wide common variant association study in autism spectrum disorder

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.11.008
N/A
0.533DataRank · unranked
34 citations

D. Chen, Worrawat Engchuan, Thiago Peixoto Leal, Bhooma Thiruvahindrapuram, Brett Trost +15 more

Genomic architecture of Autism Spectrum Disorder from comprehensive whole-genome sequence annotation

medRxiv(2022)10.1101/2022.05.05.22274031
Top 65%
0.208DataRank
Top 65%3 citations

Bhooma Thiruvahindrapuram, Ada J. S. Chan, Worrawat Engchuan, Edward J. Higginbotham, Jennifer Howe +95 more

Chromosome X-Wide Common Variant Association Study (XWAS) in Autism Spectrum Disorder

medRxiv(2024)10.1101/2024.07.18.24310640
N/A
0.208DataRank · unranked
3 citations

D. Chen, Worrawat Engchuan, Thiago Peixoto Leal, Bhooma Thiruvahindrapuram, Brett Trost +15 more

Genetic variants in DDX53 contribute to autism spectrum disorder associated with the Xp22.11 locus

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.11.003
N/A
0DataRank · unranked
10 citations

Clarrisa A. Bradley, Jennifer Howe, Brett Trost, Nelson Bautista Salazar, Carole Shum +29 more

Genomic architecture of autism from comprehensive whole-genome sequence annotation

Cell(2022)10.1016/j.cell.2022.10.009
N/A
0DataRank · unranked
280 citations

Bhooma Thiruvahindrapuram, Ada J. S. Chan, Worrawat Engchuan, Edward J. Higginbotham, Jennifer Howe +95 more

Psychiatric Genetics in Clinical Practice: Essential Knowledge for Mental Health Professionals

American Journal of Psychiatry(2025)10.1176/appi.ajp.20240295
N/A
0DataRank · unranked
5 citations

M.A. Alnor, Mauricio Castaño, Lynn E. DeLisi, Dorothy E. Grice, Falk W. Lohoff +14 more

The Phenotypic variability of 16p11.2 distal BP2–BP3 deletion in a transgenerational family and in neurodevelopmentally ascertained samples

Journal of Medical Genetics(2023)10.1136/jmg-2022-108818
N/A
0DataRank · unranked
4 citations

Lia D’Abate, Dimitri J. Stavropoulos, Jennifer Howe, Irene Drmic, Ny Hoang +6 more

Genetic variants in DDX53 contribute to Autism Spectrum Disorder associated with the Xp22.11 locus

medRxiv(2023)10.1101/2023.12.21.23300383
N/A
0DataRank · unranked
4 citations

Clarrisa A. Bradley, Jennifer Howe, Brett Trost, Nelson Bautista Salazar, Carole Shum +22 more