Kim C. Worley

Biochemistry, Genetics and Molecular BiologyAgricultural and Biological Sciences

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

59.3Author DataRank

Indexed papers

8in 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 8 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.

Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project

Nature(2007)10.1038/nature05874

Top 1%

12.9DataRank

Top 1%5277 citations

J Stamatoyannopoulos, Simon G. Gregory, T Gingeras, Eoghan Harrington, Zhiping Weng +286 more

Papers

Driven by 38 papers — median percentile 98. Top paper: “Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project”.

Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project

Nature(2007)10.1038/nature05874

Top 1%

12.9DataRank

Top 1%5277 citations

J Stamatoyannopoulos, Simon G. Gregory, T Gingeras, Eoghan Harrington, Zhiping Weng +286 more

Initial sequencing and comparative analysis of the mouse genome

Nature(2002)10.1038/nature01262

Top 1%

12.6DataRank

Top 1%7282 citations

Robert H. Waterston, Kerstin Lindblad‐Toh, Julien Lagarde, Josep F. Abril, PANKAJ AGARWAL +189 more

The Sequence of the Human Genome

Science(2001)10.1126/science.1058040

Top 1%

11.2DataRank

Top 1%13680 citations

Mark D. Adams, Eugene W. Myers, Peter W. Li, Richard J. Mural, Granger G. Sutton +340 more

A framework for human microbiome research

Nature(2012)10.1038/nature11209

Top 2%

8.4DataRank

Top 2%2766 citations

Barbara A. Methé, William Nelson, Mihai Pop, Heather H. Creasy, Michelle Giglio +236 more

A high-resolution map of human evolutionary constraint using 29 mammals

Nature(2011)10.1038/nature10530

Top 2%

7.6DataRank

Top 2%1227 citations

Genome Institute at Washington University, Manuel Garber, Or Zuk, Alireza Heravi-Moussavi, Wouter Meuleman +49 more

Comparative validation of the D. melanogaster modENCODE transcriptome annotation

Genome Research(2014)10.1101/gr.159384.113

Top 5%

4.6DataRank

Top 5%192 citations

David Sturgill, Jiaxin Qu, Huaiyang Jiang, Soo Park, Nathan Boley +67 more

Primate phylogenomics uncovers multiple rapid radiations and ancient interspecific introgression

PLoS Biology(2020)10.1371/journal.pbio.3000954

N/A

2.9DataRank · unranked

120 citations

Bui Quang Minh, Robert Lanfear, Daniel Hughes, Shwetha C. Murali, R. Alan Harris +9 more

An improved ovine reference genome assembly to facilitate in-depth functional annotation of the sheep genome

GigaScience(2022)10.1093/gigascience/giab096

Top 11%

1.8DataRank

Top 11%92 citations

Derek M. Bickhart, Kim C. Worley, Shwetha C. Murali, Mazdak Salavati, Emily L. Clark +6 more

Structure, function and diversity of the healthy human microbiome

Nature(2012)10.1038/nature11234

N/A

1.4DataRank · unranked

10088 citations

Curtis Huttenhower, Dirk Gevers, Rob Knight, Sahar Abubucker, Jonathan H. Badger +235 more

Pilon: An Integrated Tool for Comprehensive Microbial Variant Detection and Genome Assembly Improvement

PLoS ONE(2014)10.1371/journal.pone.0112963

N/A

1.4DataRank · unranked

10052 citations

Thomas Abeel, Terrance Shea, Margaret Priest, Amr Abouelliel, Sharadha Sakthikumar +7 more

Author Correction: Comparative and demographic analysis of orang-utan genomes

Nature(2022)10.1038/s41586-022-04799-7

Top 67%

0.174DataRank

Top 67%2 citations

LaDeana W. Hillier, Wesley C. Warren, Kim C. Worley, Lynne V. Nazareth, Donna M. Muzny +95 more

Diagnostic utility of DNA methylation analysis in genetically unsolved pediatric epilepsies and CHD2 episignature refinement

Nature Communications(2024)10.1038/s41467-024-50159-6

N/A

0DataRank · unranked

24 citations

Cassandra Rastin, Soham Sengupta, Helen E. Pennington, Sophie Russ-Hall, Amy Schneider +50 more

Loss of the endoplasmic reticulum protein Tmem208 affects cell polarity, development, and viability

Proceedings of the National Academy of Sciences(2024)10.1073/pnas.2322582121

N/A

0DataRank · unranked

6 citations

Oguz Kanca, Rishi V. Shridharan, Paul C. Marcogliese, Benjamin Steger, Marie Morimoto +92 more

Dominant missense variants in SREBF2 are associated with complex dermatological, neurological, and skeletal abnormalities

Genetics in Medicine(2024)10.1016/j.gim.2024.101174

N/A

0DataRank · unranked

4 citations

Kristhen N Atala, Yiming Zheng, Debdeep Dutta, Dorothy K. Grange, Wen‐Wen Lin +95 more

A comparative study of structural variant calling in WGS from Alzheimer’s disease families

Life Science Alliance(2024)10.26508/lsa.202302181

N/A

0DataRank · unranked

6 citations

John J. Farrell, Li Charlie Xia, Beth A. Dombroski, Gautami Das, Jessica Way +14 more

Development and evaluation of a training curriculum to engage researchers on accessing and analyzing the All of Us data

Journal of the American Medical Informatics Association(2024)10.1093/jamia/ocae240

N/A

0DataRank · unranked

3 citations

Jasmine N Baker, Shamika Ketkar, Ashley M. Butler, LaTerrica Williams, Latanya Hammonds-Odie +5 more

Experiences in providing a community educational resource for the All of Us Researcher Workbench

Journal of the American Medical Informatics Association(2024)10.1093/jamia/ocae226

N/A

0DataRank · unranked

2 citations

Jinyoung Byun, Jun Wang, Stephen Richards, Pamela N. Luna, LaTerrica Williams +11 more

Exploring the complexity of systemic sclerosis etiology by trio whole genome sequencing

Human Molecular Genetics(2024)10.1093/hmg/ddae105

N/A

0DataRank · unranked

1 citations

Shamika Ketkar, Taotao Tan, Elizabeth G. Atkinson, Lindsay C. Burrage, Kim C. Worley +6 more

Heterozygous variants in PLCG1 affect hearing, vision, cardiac, and immune function

eLife(2024)10.7554/elife.95887

N/A

0DataRank · unranked

2 citations

Yiming Zheng, Mingxi Deng, Shenzhao Lu, Xueyang Pan, Xi Luo +25 more

Heterozygous variants in PLCG1 affect hearing, vision, cardiac, and immune function

medRxiv(2024)10.1101/2024.01.08.23300523

N/A

0DataRank · unranked

0 citations

Yiming Zheng, Mingxi Deng, Shenzhao Lu, Xueyang Pan, Xi Luo +25 more

Dominant negative ATP5F1A variants disrupt oxidative phosphorylation causing neurological disorders

EMBO Molecular Medicine(2025)10.1038/s44321-025-00290-8

N/A

0DataRank · unranked

8 citations

Marisa W. Friederich, Daniella H. Hock, Jessie R. Zhang, Liana Valin, Jill A. Rosenfeld +35 more

The utility of ultra-deep RNA sequencing in Mendelian disorder diagnostics

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.09.013

N/A

0DataRank · unranked

3 citations

Jefferson C. Sinson, Shenglan Li, Jill A. Rosenfeld, Gladys Zapata, Kristina Macakova +15 more

A guide to developing harmonized research workflows in a team science context

Experimental Neurology(2025)10.1016/j.expneurol.2025.115333

N/A

0DataRank · unranked

2 citations

Joost Wagenaar, Bella Mehta, Ilias Ziogas, Lyndie Swanson, Kim C. Worley +7 more

The Utility of Ultra-Deep RNA sequencing in Mendelian Disorder Diagnostics

medRxiv(2025)10.1101/2025.01.28.25321295

N/A

0DataRank · unranked

1 citations

Jefferson Sinson, Shenglan Li, Jill A. Rosenfeld, Gladys Zapata, Kristina Macakova +16 more

The SHR/Akr Y chromosome reveals repeated turnover of the rat pseudoautosomal region

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.05.28.656580

N/A

0DataRank · unranked

1 citations

Helen Skaletsky, Jennifer F. Hughes, Laura G. Brown, Tatyana Pyntikova, Ting-Jan Cho +15 more

Dominant negative ATP5F1A variants disrupt oxidative phosphorylation causing neurological disorders

medRxiv(2025)10.1101/2025.07.08.25330848

N/A

0DataRank · unranked

1 citations

Marisa W. Friederich, Daniella H. Hock, Jessie R. Zhang, Liana Valin, Jill A. Rosenfeld +35 more

Implementing a training resource for large-scale genomic data analysis in the All of Us Researcher Workbench

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.06.018

N/A

0DataRank · unranked

0 citations

Erik Stricker, Julie Coleman, Shamika Ketkar, Taotao Tan, Ashley M. Butler +7 more

Designing and implementing solution-oriented team science initiatives—a chronic pain example

Frontiers in Pain Research(2025)10.3389/fpain.2025.1669072

N/A

0DataRank · unranked

0 citations

Armen N. Akopian, Kyle D. Allen, Yenisel Cruz-Almeida, Christopher R. Donnelly, Brendan Lee +7 more

Unusual sequence characteristics of human chromosome 19 are conserved across 11 nonhuman primates

BMC Evolutionary Biology(2020)10.1186/s12862-020-1595-9

N/A

0DataRank · unranked

50 citations

Muthuswamy Raveendran, Kim C. Worley, Jeffrey Rogers, R. Alan Harris

Loss of the Polyketide Synthase StlB Results in Stalk Cell Overproduction in Polysphondylium violaceum

Genome Biology and Evolution(2020)10.1093/gbe/evaa079

N/A

0DataRank · unranked

17 citations

Yoshinori Kawabe, Koryu Kin, Richard A. Gibbs, Adam Kuspa, Donna M. Muzny +6 more

Sequence analysis in Bos taurus reveals pervasiveness of X–Y arms races in mammalian lineages

Genome Research(2020)10.1101/gr.269902.120

N/A

0DataRank · unranked

50 citations

Helen Skaletsky, Tatyana Pyntikova, Natalia Koutseva, Terje Raudsepp, Laura G. Brown +19 more

The genomic basis of evolutionary differentiation among honey bees

Genome Research(2021)10.1101/gr.272310.120

N/A

0DataRank · unranked

35 citations

Philipp Brand, Hung N. Nguyen, Jacob Herman, Francisco Câmara Ferreira, Daniel Ence +18 more

LMOD2‐related dilated cardiomyopathy presenting in late infancy

American Journal of Medical Genetics Part A(2022)10.1002/ajmg.a.62699

N/A

0DataRank · unranked

17 citations

Mahshid S. Azamian, Susan W. Denfield, William J. Dreyer, Joseph A. Spinner, Debra L. Kearney +5 more

Clinical exome sequencing uncovers a high frequency of Mendelian disorders in infants with stroke: A retrospective analysis

American Journal of Medical Genetics Part A(2022)10.1002/ajmg.a.62967

N/A

0DataRank · unranked

7 citations

Linyan Meng, Pengfei Liu, Christina Y. Miyake, Kim C. Worley, Weimin He +2 more

A comparative study of structural variant calling strategies using the Alzheimer’s Disease Sequencing Project’s whole genome family data

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.05.19.492472

N/A

0DataRank · unranked

1 citations

John J. Farrell, Li Charlie Xia, Beth A. Dombroski, Wan‐Ping Lee, Gautami Das +14 more

Dominant negative variants in IKZF2 cause ICHAD syndrome, a new disorder characterised by immunodysregulation, craniofacial anomalies, hearing impairment, athelia and developmental delay

Journal of Medical Genetics(2023)10.1136/jmg-2022-109127

N/A

0DataRank · unranked

12 citations

Maryam Vaseghi‐Shanjani, Jill A. Rosenfeld, Gui Xiang Yang, Henry Y. Lu, Mehul Sharma +23 more

Diagnostic Utility of Genome-wide DNA Methylation Analysis in Genetically Unsolved Developmental and Epileptic Encephalopathies and Refinement of a CHD2 Episignature

medRxiv(2023)10.1101/2023.10.11.23296741

N/A

0DataRank · unranked

1 citations

Cassandra Rastin, Soham Sengupta, Helen E. Pennington, Sophie Russ-Hall, Amy Schneider +48 more

The clinical utility and diagnostic implementation of human subject cell transdifferentiation followed by RNA sequencing

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.03.007

N/A

0DataRank · unranked

28 citations

Sen Zhao, Jefferson C. Sinson, Aleksandar Bajić, Jill A. Rosenfeld, Matthew B. Neeley +23 more

Kim C. Worley

Indexed papers

Top data-sharing exemplar

Papers