Bruce R. Korf

MedicineBiochemistry, 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 3%percentile

1.1Author 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.

Comparison of family health history in surveys vs electronic health record data mapped to the observational medical outcomes partnership data model in the All of Us Research Program

Journal of the American Medical Informatics Association(2020)10.1093/jamia/ocaa315

Top 18%

1.1DataRank

Top 18%19 citations

Alese E. Halvorson, Cassie Springer, Xiaoke Feng, Lina Sulieman, Roxana Loperena-Cortes +10 more

Papers

Driven by 23 papers — median percentile 82. Top paper: “Returning integrated genomic risk and clinical recommendations: The eMERGE study”.

Returning integrated genomic risk and clinical recommendations: The eMERGE study

Genetics in Medicine(2023)10.1016/j.gim.2023.100006

N/A

2.6DataRank · unranked

121 citations

Aimee Allworth, Harris T. Bland, Pedro J. Caraballo, Rex L. Chisholm, Ellen Wright Clayton +95 more

Cabozantinib for neurofibromatosis type 1–related plexiform neurofibromas: a phase 2 trial

Nature Medicine(2021)10.1038/s41591-020-01193-6

N/A

2.0DataRank · unranked

96 citations

Chie‐Schin Shih, Steven D. Rhodes, Amy E. Armstrong, Pamela L. Wolters, Eva Dombi +25 more

Comparison of family health history in surveys vs electronic health record data mapped to the observational medical outcomes partnership data model in the All of Us Research Program

Journal of the American Medical Informatics Association(2020)10.1093/jamia/ocaa315

Top 18%

1.1DataRank

Top 18%19 citations

Alese E. Halvorson, Cassie Springer, Xiaoke Feng, Lina Sulieman, Roxana Loperena-Cortes +10 more

The All of Us Research Program: Data quality, utility, and diversity

Patterns(2022)10.1016/j.patter.2022.100570

N/A

0.874DataRank · unranked

339 citations

Lina Sulieman, David J. Schlueter, Alese E. Halvorson, Jun Qian, Francis Ratsimbazafy +81 more

Updated diagnostic criteria and nomenclature for neurofibromatosis type 2 and schwannomatosis: An international consensus recommendation

Genetics in Medicine(2022)10.1016/j.gim.2022.05.007

N/A

0.846DataRank · unranked

281 citations

Ludwine Messiaen, Eric Legius, Patrice Pancza, Robert A. Avery, Jaishri O. Blakeley +79 more

Genetic regulation of OAS1 nonsense-mediated decay underlies association with COVID-19 hospitalization in patients of European and African ancestries

Nature Genetics(2022)10.1038/s41588-022-01113-z

N/A

0.742DataRank · unranked

140 citations

Megan L. Stanifer, Oscar Flórez-Vargas, Olusegun O. Onabajo, Brenen W. Papenberg, Muhammad Atif Zahoor +65 more

The All of Us Research Program: data quality, utility, and diversity

medRxiv(2020)10.1101/2020.05.29.20116905

N/A

0.416DataRank · unranked

15 citations

Lina Sulieman, David J. Schlueter, Alese E. Halvorson, Jun Qian, Francis Ratsimbazafy +42 more

Genetic regulation of OAS1 nonsense-mediated decay underlies association with risk of severe COVID-19

medRxiv(2021)10.1101/2021.07.09.21260221

N/A

0.396DataRank · unranked

13 citations

Megan L. Stanifer, Oscar Flórez-Vargas, Olusegun O. Onabajo, Muhammad Atif Zahoor, Brenen W. Papenberg +49 more

Guidance on use of race, ethnicity, and geographic origin as proxies for genetic ancestry groups in biomedical publications

Human Genetics and Genomics Advances(2024)10.1016/j.xhgg.2024.100282

N/A

0.261DataRank · unranked

4 citations

Robert D. Steiner, Anne Slavotinek, Tiago Faial, Michael J. Bamshad, Jehannine Austin +4 more

Does genetic testing offer utility as a supplement to traditional family health history intake for inherited disease risk?

Family Practice(2023)10.1093/fampra/cmad017

N/A

0DataRank · unranked

2 citations

Crystal Lederhos Smith, Whitley V. Kelley, Kelly M. East, Lori A. Orlando, J. Nicholas Cochran +6 more

Author Correction: The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparities

Communications Biology(2024)10.1038/s42003-024-06408-x

N/A

0DataRank · unranked

0 citations

Karynne Patterson, Divya Kalra, Marsha M. Wheeler, Yi–Ju Chen, Sara E. Kalla +93 more

An optimized variant prioritization process for rare disease diagnostics: recommendations for Exomiser and Genomiser

Genome Medicine(2025)10.1186/s13073-025-01546-1

N/A

0DataRank · unranked

8 citations

Shruti Marwaha, Alistair Ward, Shilpa N. Kobren, Jennefer N. Carter, Undiagnosed Diseases Network +94 more

Psychosocial functioning and determinants of the health-related quality of life in children with neurofibromatosis type 1 and cognitive impairments

Journal of Neuro-Oncology(2025)10.1007/s11060-025-05024-x

N/A

0DataRank · unranked

2 citations

Pamela L. Wolters, Karin S. Walsh, Nicole J. Ullrich, Tena Rosser, James H. Tonsgard +11 more

A phase II study of continuous oral mTOR inhibitor everolimus for recurrent, radiographic-progressive neurofibromatosis type 1–associated pediatric low-grade glioma: a Neurofibromatosis Clinical Trials Consortium study

Neuro-Oncology(2020)10.1093/neuonc/noaa071

N/A

0DataRank · unranked

82 citations

Sanjay P. Prabhu, Alyssa Reddy, Michael J. Fisher, Roger J. Packer, Stewart Goldman +15 more

Genotype-first assessment of presentation and penetrance of neurofibromatosis type 1, autosomal dominant polycystic kidney disease, and Marfan syndrome within the All of Us research program cohort

Genetics in Medicine(2025)10.1016/j.gim.2025.101650

N/A

0DataRank · unranked

1 citations

Bruce R. Korf, Gregory S. Barsh, Stephanie A. Felker

Recruiting diversity where it exists: The Alabama Genomic Health Initiative

Journal of Genetic Counseling(2020)10.1002/jgc4.1258

N/A

0DataRank · unranked

18 citations

Ashley Cannon, Irene Moss, Mariko Nakano‐Okuno, Sharonda Hardy, Edrika L. Miskell +13 more

Pitfalls and challenges in genetic test interpretation: An exploration of genetic professionals experience with interpretation of results

Clinical Genetics(2021)10.1111/cge.13917

N/A

0DataRank · unranked

56 citations

Catherine Gooch, Alexander Katz, Jessica Wakelee, Anne Slavotinek, Bruce R. Korf +1 more

De novo coding variants in the AGO1 gene cause a neurodevelopmental disorder with intellectual disability

Journal of Medical Genetics(2021)10.1136/jmedgenet-2021-107751

N/A

0DataRank · unranked

30 citations

Margot A. Cousin, Nikita R. Dsouza, Thomas D. Challman, Karen E. Wain, Zöe Powis +67 more

Evaluation of population‐level pharmacogenetic actionability in Alabama

Clinical and Translational Science(2021)10.1111/cts.13097

N/A

0DataRank · unranked

7 citations

Kelly W. Williams, Devin Absher, Bruce R. Korf, Nita A. Limdi, Brittney H. Davis

Restoration of Normal NF1 Function with Antisense Morpholino Treatment of Recurrent Pathogenic Patient-Specific Variant c.1466A>G; p.Y489C

Journal of Personalized Medicine(2021)10.3390/jpm11121320

N/A

0DataRank · unranked

5 citations

Marc T. Moore, Hui Liu, Lukasz Ciszewski, Laura Lambert, Bruce R. Korf +4 more

Exon Skipping as a Therapeutic for Neurofibromatosis Type I

Research Square(2021)10.21203/rs.3.rs-751331/v1

N/A

0DataRank · unranked

1 citations

André Leier, Marc T. Moore, Michael Daniel, Hui Liu, Alexis Hyde +10 more

The seventh international RASopathies symposium: Pathways to a cure—expanding knowledge, enhancing research, and therapeutic discovery

American Journal of Medical Genetics Part A(2022)10.1002/ajmg.a.62716

N/A

0DataRank · unranked

16 citations

Amy E. Roberts, Lisa Schill, Lisa Schoyer, Beth Stronach, Grégor Andelfinger +37 more

Medical and psychosocial outcomes of state‐funded population genomic screening

Clinical Genetics(2023)10.1111/cge.14394

N/A

0DataRank · unranked

3 citations

Olivia J. L. McMillan, Whitley V. Kelley, Kelly M. East, Meagan E. Cochran, Edrika L. Miskell +7 more

Bruce R. Korf

Indexed papers

Top data-sharing exemplar

Papers