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

Katherine E. Bonini

Mount Sinai Health System

ORCID: 0000-0001-7721-8137

Also affiliated with Genomic Health (United States), Icahn School of Medicine at Mount Sinai

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 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 →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Using the linear references from the pangenome to discover missing autism variants

Nature Communications(2026)10.1038/s41467-026-68378-4

Top 65%

0.208DataRank

Top 65%3 citations

Jiadong Lin, Michelle D. Noyes, Young-Jun Kwon, Isaac Wong, Nidhi Koundinya +252 more

Papers

Driven by 13 papers — median percentile 35. Top paper: “Molecular diagnostic yield of genome sequencing versus targeted gene panel testing in racially and ethnically diverse pediatric patients”.

Molecular diagnostic yield of genome sequencing versus targeted gene panel testing in racially and ethnically diverse pediatric patients

medRxiv(2023)10.1101/2023.03.18.23286992

N/A

0.312DataRank · unranked

7 citations

Priya Marathe, Nicole Kelly, Katherine E. Bonini, Monisha Sebastin, Jacqueline A. Odgis +22 more

Using the linear references from the pangenome to discover missing autism variants

Nature Communications(2026)10.1038/s41467-026-68378-4

Top 65%

0.208DataRank

Top 65%3 citations

Jiadong Lin, Michelle D. Noyes, Young-Jun Kwon, Isaac Wong, Nidhi Koundinya +252 more

Molecular diagnostic yield of genome sequencing versus targeted gene panel testing in racially and ethnically diverse pediatric patients

Genetics in Medicine(2023)10.1016/j.gim.2023.100880

N/A

0DataRank · unranked

42 citations

Priya N. Marathe, Nicole R. Kelly, Katherine E. Bonini, Monisha Sebastin, Jacqueline A. Odgis +22 more

Identification of copy number variants with genome sequencing: Clinical experiences from the NYCKidSeq program

Clinical Genetics(2023)10.1111/cge.14365

N/A

0DataRank · unranked

6 citations

Amanda Thomas‐Wilson, Priya N. Marathe, Monisha Sebastin, Jacqueline A. Odgis, Miranda Di Biase +24 more

The NYCKidSeq randomized controlled trial: Impact of GUÍA digitally enhanced genetic results disclosure in diverse families

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.10.016

N/A

0DataRank · unranked

6 citations

Nicole Kelly, Jacqueline A. Odgis, Katie M. Gallagher, Monisha Sebastin, Katherine E. Bonini +18 more

Information-seeking preferences in diverse patients receiving a genetic testing result in the Clinical Sequencing Evidence-Generating Research (CSER) study

Genetics in Medicine(2023)10.1016/j.gim.2023.100899

N/A

0DataRank · unranked

0 citations

Hannah Prasad, Simon Outram, Sarah Scollon, Shannon Rego, Tiffany Yip +10 more

The NYCKidSeq randomized controlled trial: Impact of GUÍA digitally enhanced genetic counseling in racially and ethnically diverse families

medRxiv(2023)10.1101/2023.07.05.23292193

N/A

0DataRank · unranked

0 citations

Nicole Kelly, Jacqueline A. Odgis, Katie M. Gallagher, Monisha Sebastin, Katherine E. Bonini +18 more

Physician services and costs after disclosure of diagnostic sequencing results in the NYCKidSeq program

Genetics in Medicine(2023)10.1016/j.gim.2023.101011

N/A

0DataRank · unranked

0 citations

Nicole Kelly, Ashley Fisher, Samuel F. Hohmann, Monisha Sebastin, Miranda Di Biase +14 more

Employing effective recruitment and retention strategies to engage a diverse pediatric population in genomics research

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.10.015

N/A

0DataRank · unranked

4 citations

Katherine E. Bonini, Laura Scarimbolo, Nicole Kelly, Beverly J. Insel, Sabrina A. Suckiel +36 more

Evaluating parental personal utility of pediatric genetic and genomic testing in a diverse, multilingual population

Human Genetics and Genomics Advances(2024)10.1016/j.xhgg.2024.100321

N/A

0DataRank · unranked

1 citations

Sabrina A. Suckiel, Katherine E. Bonini, Nicole Kelly, Laura Scarimbolo, Beverly J. Insel +22 more

When families bridge the research-clinical divide: An exploration of values regarding cascade screening in genomic research

Genetics in Medicine Open(2025)10.1016/j.gimo.2025.103440

N/A

0DataRank · unranked

1 citations

Lauren Desrosiers, Ann Katherine M. Foreman, Nuriye Sahin‐Hodoglugil, Mary A. Majumder, Candice R. Finnila +9 more

Patient and providers’ perspectives on using the GUÍA digital tool to enhance genomic results disclosure

Genetics in Medicine Open(2025)10.1016/j.gimo.2025.103451

N/A

0DataRank · unranked

1 citations

Sabrina A. Suckiel, Laura Golfinopoulos, Nicole R. Kelly, Katherine E. Bonini, Priya N. Marathe +15 more

Detection of mosaic variants using genome sequencing in a large pediatric cohort

American Journal of Medical Genetics Part A(2022)10.1002/ajmg.a.63062

N/A

0DataRank · unranked

14 citations

Katie M. Gallagher, Atteeq U. Rehman, Priya Marathe, Katherine E. Bonini, Monisha Sebastin +21 more