Jonathon LeFaive

Biochemistry, 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 1%percentile

8.4Author 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 →

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 16 papers — median percentile 59. 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

Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries

Nature Communications(2018)10.1038/s41467-018-04668-w

N/A

3.7DataRank · unranked

109 citations

Sanni Ruotsalainen, Robert E. Handsaker, Maris Alver, Jonathan M. Bloom, Timothy Poterba +442 more

Exploring various polygenic risk scores for skin cancer in the phenomes of the Michigan genomics initiative and the UK Biobank with a visual catalog: PRSWeb

PLOS Genetics(2019)10.1371/journal.pgen.1008202

N/A

1.7DataRank · unranked

35 citations

Lauren J. Beesley, Peter VandeHaar, Robert B. Peng, Maxwell Salvatore, Matthew Zawistowski +13 more

Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease

Nature Communications(2020)10.1038/s41467-020-20086-3

N/A

1.6DataRank · unranked

91 citations

Oren Rom, Ida Surakka, Sarah E. Graham, Wei Zhou, Tanmoy Roychowdhury +95 more

Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension

Hypertension(2022)10.1161/hypertensionaha.122.19324

Top 24%

0.842DataRank

Top 24%29 citations

Xiao Sun, Karen He, Michael R. Brown, Sarah A. Gagliano Taliun, Jacklyn N. Hellwege +95 more

Genome-wide association study of cardiac troponin I in the general population

Human Molecular Genetics(2021)10.1093/hmg/ddab124

N/A

0.732DataRank · unranked

20 citations

Helge Røsjø, Anne Richmond, Magnus Nakrem Lyngbakken, Sarah E. Graham, Ailin Falkmo Hansen +25 more

FixItFelix: improving genomic analysis by fixing reference errors

Genome biology(2023)10.1186/s13059-023-02863-7

N/A

0.500DataRank · unranked

27 citations

Jonathon LeFaive, Peter Orchard, Medhat Mahmoud, Luis F. Paulin, Jesse Farek +7 more

Robust, flexible, and scalable tests for Hardy–Weinberg equilibrium across diverse ancestries

Genetics(2021)10.1093/genetics/iyab044

N/A

0.489DataRank · unranked

25 citations

Thomas W. Blackwell, Jonathon LeFaive, Mariza de Andrade, John Barnard, Kathleen C. Barnes +42 more

False discovery rates for genome-wide association tests in biobanks with thousands of phenotypes

10.21203/rs.3.rs-873449/v1

N/A

0.330DataRank · unranked

8 citations

Anita Pandit, Jonathon LeFaive, Sarah Gagliano Taliun, Lars G. Fritsche, Peter VandeHaar +5 more

Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries

Nature Communications(2020)10.1038/s41467-020-15236-6

Top 57%

0.275DataRank

Top 57%2 citations

Sanni Ruotsalainen, Robert E. Handsaker, Maris Alver, Jonathan M. Bloom, Timothy Poterba +442 more

Robust, flexible, and scalable tests for Hardy-Weinberg Equilibrium across diverse ancestries

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.06.23.167759

N/A

0.269DataRank · unranked

5 citations

Thomas W. Blackwell, Jonathon LeFaive, Mariza de Andrade, John Barnard, Kathleen C. Barnes +42 more

Fixing reference errors efficiently improves sequencing results

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.07.18.500506

Top 65%

0.208DataRank

Top 65%3 citations

Jonathon LeFaive, Peter Orchard, Medhat Mahmoud, Luis F. Paulin, Jesse Farek +7 more

Tutorial: a statistical genetics guide to identifying HLA alleles driving complex disease

Nature Protocols(2023)10.1038/s41596-023-00853-4

N/A

0DataRank · unranked

44 citations

Saisriram Gurajala, Michelle Curtis, Yang Luo, Wanson Choi, Kazuyoshi Ishigaki +14 more

Using human genetics to understand the causes and consequences of circulating cardiac troponin I in the general population

medRxiv(2020)10.1101/2020.09.04.20187401

N/A

0DataRank · unranked

0 citations

Helge Røsjø, Anne Richmond, Magnus Nakrem Lyngbakken, Sarah E. Graham, Ailin Falkmo Hansen +22 more

cellSTAAR: incorporating single-cell-sequencing-based functional data to boost power in rare variant association testing of noncoding regions

Nature Methods(2025)10.1038/s41592-025-02919-5

N/A

0DataRank · unranked

0 citations

Yi Zhang, Xihao Li, Margaret Sunitha Selvaraj, Zilin Li, Hufeng Zhou +544 more

Sparse allele vectors and the savvy software suite

Bioinformatics(2021)10.1093/bioinformatics/btab378

N/A

0DataRank · unranked

15 citations

Albert V. Smith, Hyun Min Kang, Gonçalo R. Abecasis, Jonathon LeFaive

Jonathon LeFaive

Indexed papers

Top data-sharing exemplar

Papers