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

Douglas P. Loesch

AstraZeneca (United Kingdom)

ORCID: 0000-0001-5716-4557

Also affiliated with University of Maryland, Baltimore, AstraZeneca (Australia), AstraZeneca (Singapore)

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 1%percentile
8.9Author DataRank

Indexed papers

6in 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 6 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.

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

Nature(2021)10.1038/s41586-021-03205-y
Top 3%
7.0DataRank
Top 3%2322 citations

Daniel Harris, Michael D. Kessler, Jedidiah Carlson, Zachary A. Szpiech, Raúl Torres +95 more

Papers

Driven by 11 papers — median percentile 61. Top paper: “Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program”.

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

Nature(2021)10.1038/s41586-021-03205-y
Top 3%
7.0DataRank
Top 3%2322 citations

Daniel Harris, Michael D. Kessler, Jedidiah Carlson, Zachary A. Szpiech, Raúl Torres +95 more

De novo mutations across 1,465 diverse genomes reveal mutational insights and reductions in the Amish founder population

Proceedings of the National Academy of Sciences(2020)10.1073/pnas.1902766117
N/A
3.0DataRank · unranked
112 citations

Douglas P. Loesch, James A. Perry, Nancy L. Heard‐Costa, Daniel Taliun, Brian E. Cade +93 more

Genetics of Latin American Diversity Project: Insights into population genetics and association studies in admixed groups in the Americas

Cell Genomics(2024)10.1016/j.xgen.2024.100692
Top 31%
0.635DataRank
Top 31%30 citations

Douglas P. Loesch, Bing Guo, Roland Laboulaye, Diego Véliz-Otani, Jennifer N. French +70 more

Whole genome sequence association analysis of fasting glucose and fasting insulin levels in diverse cohorts from the NHLBI TOPMed program

Communications Biology(2022)10.1038/s42003-022-03702-4
Top 34%
0.582DataRank
Top 34%16 citations

Sheila M. Gaynor, Emily M. Russell, Kenneth E. Westerman, Laura M. Raffield, Timothy D. Majarian +88 more

Polygenic risk prediction and SNCA haplotype analysis in a Latino Parkinson's disease cohort

Parkinsonism & Related Disorders(2022)10.1016/j.parkreldis.2022.06.010
Top 44%
0.425DataRank
Top 44%12 citations

Andréa R. V. R. Horimoto, Elif Irem Sarihan, Miguel Inca‐Martinez, Emily Mason, Mario Cornejo‐Olivas +30 more

X-Chromosome Association Study in Latin American Cohorts Identifies New Loci in Parkinson Disease

medRxiv(2023)10.1101/2023.01.31.23285199
Top 66%
0.186DataRank
Top 66%2 citations

Jennifer N. French, Mateus H. Gouveia, Víctor Borda, Miguel Inca‐Martinez, Emily Mason +36 more

Polygenic risk prediction and SNCA haplotype analysis in a Latino Parkinson’s disease cohort

medRxiv(2021)10.1101/2021.11.09.21265082
N/A
0DataRank · unranked
0 citations

Andréa R. V. R. Horimoto, Elif Irem Sarihan, Miguel Inca‐Martinez, Emily Mason, Mario Cornejo‐Olivas +30 more

X‐Chromosome Association Study in Latin American Cohorts Identifies New Loci in Parkinson's Disease

Movement Disorders(2023)10.1002/mds.29508
N/A
0DataRank · unranked
20 citations

Shilpa C. Rao, Jennifer N. French, Mateus H. Gouveia, Víctor Borda, Sara Bandrés‐Ciga +43 more

Characterizing the genetic architecture of Parkinson’s disease in Latinos

medRxiv(2020)10.1101/2020.11.09.20227124
N/A
0DataRank · unranked
5 citations

Andréa R. V. R. Horimoto, Karl Heilbron, Elif Irem Sarihan, Miguel Inca‐Martinez, Emily Mason +32 more

Whole genome sequence association analysis of fasting glucose and fasting insulin levels in diverse cohorts from the NHLBI TOPMed program

UNC Libraries(2024)10.17615/75fz-j027
Top 100%
0DataRank
Top 100%0 citations

J.E. Curran, S.L.R. Kardia, Márcio Rodrigues de Almeida, J.B. Meigs, M.R. Irvin +88 more

Genetics of Latin American Diversity Project: Insights into population genetics and association studies in admixed groups in the Americas

Lume (Universidade Federal do Rio Grande do Sul)(2024)10.17615/anr2-h090
N/A
0DataRank · unranked
0 citations

Carla Luana Dinardo, Bing Guo, Ignácio F. Mata, Jill M. Johnsen, Robert C. Kaplan +73 more