David H. Ledbetter

Also affiliated with Florida A&M University - Florida State University College of Engineering

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 2%percentile

2.4Author DataRank

Indexed papers

3in 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 3 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.

Electronic health record analysis identifies kidney disease as the leading risk factor for hospitalization in confirmed COVID-19 patients

PLoS ONE(2020)10.1371/journal.pone.0242182

Top 9%

2.4DataRank

Top 9%43 citations

Jonathan Z. Luo, Alex R. Chang, Joseph B. Leader, Dustin N. Hartzel, Bryn S. Moore +7 more

Papers

Driven by 20 papers — median percentile 91. Top paper: “Localization of the X inactivation centre on the human X chromosome in Xq13”.

Localization of the X inactivation centre on the human X chromosome in Xq13

Nature(1991)10.1038/349082a0

N/A

15.0DataRank · unranked

382 citations

Ronald G. Lafreniere, Vicki E. Powers, Gianfranco Sebastio, Andrea Ballabio, Anjana L. Pettigrew +5 more

Electronic health record analysis identifies kidney disease as the leading risk factor for hospitalization in confirmed COVID-19 patients

PLoS ONE(2020)10.1371/journal.pone.0242182

Top 9%

2.4DataRank

Top 9%43 citations

Jonathan Z. Luo, Alex R. Chang, Joseph B. Leader, Dustin N. Hartzel, Bryn S. Moore +7 more

Feasibility of blood testing combined with PET-CT to screen for cancer and guide intervention

Science(2020)10.1126/science.abb9601

N/A

0.977DataRank · unranked

673 citations

Adam H. Buchanan, Isaac Kinde, Andrew Warren, Ashley Honushefsky, Ariella Cohain +35 more

Gene dosage is a mechanism for Charcot-Marie-Tooth disease type 1A

Nature Genetics(1992)10.1038/ng0492-29

N/A

0.852DataRank · unranked

291 citations

Carol A. Wise, Akira Kuwano, Liu Pentao, Julie T. Parke, Daniel G. Glaze +4 more

Frequency of truncating FLCN variants and Birt-Hogg-Dubé–associated phenotypes in a health care system population

Genetics in Medicine(2022)10.1016/j.gim.2022.05.006

N/A

0.529DataRank · unranked

33 citations

Hermela Shimelis, Andrés Moreno-De-Luca, Natasha T. Strande, Matthew T. Oetjens, David H. Ledbetter +4 more

Genomic Variation: Lessons Learned from Whole-Genome CNV Analysis

Current Genetic Medicine Reports(2014)10.1007/s40142-014-0048-4

N/A

0.477DataRank · unranked

23 citations

David H. Ledbetter, Christa Lese Martin, Erin Rooney Riggs

Recontacting registry participants with genetic updates through GenomeConnect, the ClinGen patient registry

Genetics in Medicine(2021)10.1038/s41436-021-01197-8

N/A

0.434DataRank · unranked

17 citations

Danielle R. Azzariti, David H. Ledbetter, Emily Palen, Heidi L. Rehm, Erin Rooney Riggs +2 more

A genome-first study of sex chromosome aneuploidies provides evidence of Y chromosome dosage effects on autism risk

Nature Communications(2024)10.1038/s41467-024-53211-7

N/A

0.416DataRank · unranked

15 citations

Brenda Finucane, Scott M. Myers, Lauren K. Walsh, John M. Seibert, Christa Lese Martin +3 more

ClinGen — The Clinical Genome Resource

UNC Libraries(2020)10.17615/js2g-yk58

N/A

0DataRank · unranked

0 citations

Erin M. Ramos, David H. Ledbetter, Carlos D. Bustamante, Stephen T. Sherry, Michael S. Watson +9 more

Diagnostic genetic testing for neurodevelopmental psychiatric disorders: closing the gap between recommendation and clinical implementation

Current Opinion in Genetics & Development(2021)10.1016/j.gde.2020.12.016

N/A

0DataRank · unranked

52 citations

David H. Ledbetter, Jacob Vorstman, Brenda Finucane

Contributors

Genomic and Personalized Medicine(2013)10.1016/b978-0-12-382227-7.00124-5

N/A

0DataRank · unranked

0 citations

Minhaz Uddin Ahmed, Sun Hee Ahn, R. Rand Allingham, Jude Alsarraj, Matthew L. Anderson +228 more

Response to Buxbaum et al.

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.09.012

N/A

0DataRank · unranked

3 citations

Thomas D. Challman, Christa Leese Martin, David H. Ledbetter, Scott M. Myers

Phenotypic shift in copy number variants: Evidence in 16p11.2 duplication syndrome

Genetics in Medicine(2022)10.1016/j.gim.2022.09.011

N/A

0DataRank · unranked

10 citations

Brenda Finucane, Andrés Moreno-De-Luca, Lauren K. Walsh, Christa Lese Martin, David H. Ledbetter +1 more

Frequency of FLCN Loss of Function Variants and Birt-Hogg-Dubé-Associated Phenotypes in a Healthcare System Population

medRxiv(2022)10.1101/2022.01.31.22269926

N/A

0DataRank · unranked

0 citations

Hermela Shimelis, Andrés Moreno-De-Luca, Natasha T. Strande, Matthew T. Oetjens, David H. Ledbetter +4 more

Systematic analysis of variants escaping nonsense-mediated decay uncovers candidate Mendelian diseases

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.11.007

N/A

0DataRank · unranked

37 citations

María J. Guillen Sacoto, Francisca Millan, Zhancheng Zhang, Stephen McGee, Matthew T. Oetjens +11 more

A novel application of spectrograms with machine learning can detect patient ventilator dyssynchrony

Biomedical Signal Processing and Control(2023)10.1016/j.bspc.2023.105251

N/A

0DataRank · unranked

14 citations

Benjamin Yoon, David H. Ledbetter, Melissa Aczon, Eugene Laksana, Alice X. Zhou +5 more

X and Y gene dosage effects are primary contributors to human sexual dimorphism: The case of height

Proceedings of the National Academy of Sciences(2025)10.1073/pnas.2503039122

N/A

0DataRank · unranked

4 citations

Brenda Finucane, Scott M. Myers, Christa L. Martin, David H. Ledbetter, Huntington F. Willard +2 more

Clinical outcomes of a genomic screening program for actionable genetic conditions

Genetics in Medicine(2020)10.1038/s41436-020-0876-4

N/A

0DataRank · unranked

154 citations

H. Lester Kirchner, M. Schwartz, Melissa Kelly, Tara Schmidlen, Laney K. Jones +15 more

Insufficient Evidence for “Autism-Specific” Genes

OSF Preprints (OSF Preprints)(2020)10.31219/osf.io/24gm3

N/A

0DataRank · unranked

3 citations

Thomas D. Challman, Raphael Bernier, Thomas Bourgeron, Wendy K. Chung, John N. Constantino +8 more

Insufficient Evidence for “Autism-Specific” Genes

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.04.004

N/A

0DataRank · unranked

169 citations

Thomas D. Challman, Raphael Bernier, Thomas Bourgeron, Wendy K. Chung, John N. Constantino +8 more

David H. Ledbetter

Indexed papers

Top data-sharing exemplar

Papers