Sharon E. Plon

Also affiliated with Baylor School, Texas Children's Hospital, Children's Cancer Center, Baylor Genetics

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 3%percentile

1.6Author DataRank

Indexed papers

5in 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 5 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.

The Clinical Genome Resource (ClinGen): Advancing genomic knowledge through global curation

Genetics in Medicine(2024)10.1016/j.gim.2024.101228

Top 17%

1.2DataRank

Top 17%59 citations

Danielle R. Azzariti, Larry Babb, Jonathan S. Berg, Leslie G. Biesecker, Zo Bly +28 more

Papers

Driven by 46 papers — median percentile 22. Top paper: “A brief history of human disease genetics”.

A brief history of human disease genetics

Nature(2020)10.1038/s41586-019-1879-7

N/A

9.2DataRank · unranked

738 citations

Judy H. Cho, Rory Collins, Nancy J. Cox, Emmanouil T. Dermitzakis, Matthew E. Hurles +13 more

ClinGen Variant Curation Interface: a variant classification platform for the application of evidence criteria from ACMG/AMP guidelines

Genome Medicine(2022)10.1186/s13073-021-01004-8

N/A

2.6DataRank · unranked

85 citations

Matt W. Wright, Rao Madhavrao, Steven M. Harrison, Jennifer L Goldstein, Xi Luo +30 more

The Clinical Genome Resource (ClinGen): Advancing genomic knowledge through global curation

Genetics in Medicine(2024)10.1016/j.gim.2024.101228

Top 17%

1.2DataRank

Top 17%59 citations

Danielle R. Azzariti, Larry Babb, Jonathan S. Berg, Leslie G. Biesecker, Zo Bly +28 more

Gene-specific ACMG/AMP classification criteria for germline APC variants: Recommendations from the ClinGen InSiGHT Hereditary Colorectal Cancer/Polyposis Variant Curation Expert Panel

Genetics in Medicine(2023)10.1016/j.gim.2023.100992

N/A

1.0DataRank · unranked

33 citations

Xiaoyu Yin, Marcy E. Richardson, Marta Pineda, Andreas Laner, Deborah Ritter +27 more

Optimising clinical care through CDH1-specific germline variant curation: improvement of clinical assertions and updated curation guidelines

Journal of Medical Genetics(2022)10.1136/jmg-2022-108807

N/A

0.745DataRank · unranked

24 citations

Jamie L. Maciaszek, Bryony A. Thompson, Huei San Leong, Katherine Dixon, Sónia Sousa +19 more

Germline Cancer Predisposition Variants in Pediatric Rhabdomyosarcoma: A Report From the Children’s Oncology Group

JNCI Journal of the National Cancer Institute(2020)10.1093/jnci/djaa204

N/A

0.705DataRank · unranked

109 citations

Saumya D. Sisoudiya, Bailey A. Martin‐Giacalone, Michael M. Khayat, Shannon Dugan‐Perez, Deborah A. Marquez-Do +16 more

The genomic landscape of familial glioma

Science Advances(2023)10.1126/sciadv.ade2675

N/A

0.596DataRank · unranked

52 citations

Georgina Armstrong, Brittney Lozzi, Prashanth Vijayaraghavan, Sharon E. Plon, Terence C. Wong +85 more

Phenotypic Differences in Juvenile Polyposis Syndrome With or Without a Disease-causing SMAD4/BMPR1A Variant

Cancer Prevention Research(2020)10.1158/1940-6207.capr-20-0348

N/A

0.581DataRank · unranked

47 citations

Jessica Ebrahimzadeh, Kristin Zelley, Lubna Begum, Lee M. Bass, Randall E. Brand +18 more

Generating Clinical-Grade Gene–Disease Validity Classifications Through the ClinGen Data Platforms

Annual Review of Biomedical Data Science(2024)10.1146/annurev-biodatasci-102423-112456

N/A

0.502DataRank · unranked

16 citations

Courtney L Thaxton, Tristan H Nelson, Marina T. DiStefano, Juliann M. Savatt, Matthew Brush +25 more

Implementation of a dyadic nomenclature for monogenic diseases

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.07.019

N/A

0.477DataRank · unranked

23 citations

Leslie G. Biesecker, Marina T. DiStefano, Melissa A Haendel, Ada Hamosh, Emma Owens +4 more

Adult-Onset Cancer Predisposition Syndromes in Children and Adolescents—To Test or not to Test?

Clinical Cancer Research(2024)10.1158/1078-0432.ccr-23-3683

N/A

0.477DataRank · unranked

23 citations

Philip J. Lupo, Kristin Zelley, Jaclyn Schienda, Kim E. Nichols, Douglas R. Stewart +6 more

Male Sex and the Risk of Childhood Cancer: The Mediating Effect of Birth Defects

JNCI Cancer Spectrum(2020)10.1093/jncics/pkaa052

N/A

0.442DataRank · unranked

18 citations

Jeremy M. Schraw, Tania A. Desrosiers, Wendy N. Nembhard, Peter H. Langlois, Mark A. Canfield +4 more

Assessment of the evidence yield for the calibrated PP3/BP4 computational recommendations

Genetics in Medicine(2024)10.1016/j.gim.2024.101213

N/A

0.434DataRank · unranked

17 citations

Vikas Pejaver, Timothy Bergquist, Leslie G. Biesecker, Alicia B. Byrne, Emily A.W. Nadeau +21 more

Mondo: integrating disease terminology across communities

Genetics(2025)10.1093/genetics/iyaf215

N/A

0.425DataRank · unranked

16 citations

Sabrina Toro, Nicolas A Matentzoglu, Joseph E Flack, Kathleen R. Mullen, Harshad Hegde +95 more

Combined bioinformatic and splicing analysis of likely benign intronic and synonymous variants reveals evidence for pathogenicity

Genetics in Medicine Open(2024)10.1016/j.gimo.2024.101850

Top 56%

0.292DataRank

Top 56%4 citations

Stephanie A. Felker, Surya P. Rednam, Kelly Vallance, D. Williams Parsons, Angshumoy Roy +3 more

Defining and Reducing Variant Classification Disparities

medRxiv(2024)10.1101/2024.04.11.24305690

N/A

0.165DataRank · unranked

2 citations

Shawn Fayer, Sriram Pendyala, Mason Post, Divya Kalra, Karynne Patterson +13 more

Design and implementation of an action plan for justice, equity, diversity, and inclusion within the Clinical Genome Resource

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2024.12.009

N/A

0.165DataRank · unranked

2 citations

Deborah Ritter, Danielle R. Azzariti, Jonathan S. Berg, Joanna E. Bulkley, Mildred K. Cho +12 more

Co-occurrence of congenital anomalies and childhood brain tumors in 22 million live births

Neuro-Oncology(2025)10.1093/neuonc/noaf087

Top 78%

0.104DataRank

Top 78%1 citations

Jeremy M. Schraw, Charles Shumate, Tania A. Desrosiers, Wendy N. Nembhard, Mahsa M. Yazdy +12 more

Combined Bioinformatic and Splicing Analysis of Likely Benign Intronic and Synonymous Variants Reveals Evidence for Pathogenicity

medRxiv(2023)10.1101/2023.10.30.23297632

Top 100%

0DataRank

Top 100%0 citations

Stephanie A. Felker, Surya P. Rednam, Kelly Vallance, D. Williams Parsons, Angshumoy Roy +3 more

Update on Recommendations for Cancer Screening and Surveillance in Children with Genomic Instability Disorders

Clinical Cancer Research(2024)10.1158/1078-0432.ccr-24-1098

N/A

0DataRank · unranked

23 citations

Roland P. Kuiper, Kim E. Nichols, Christopher C. Porter, Harry Lesmana, Julia Meade +13 more

Pediatric Cancer Screening in Hereditary Gastrointestinal Cancer Risk Syndromes: An Update from the AACR Childhood Cancer Predisposition Working Group

Clinical Cancer Research(2024)10.1158/1078-0432.ccr-24-0953

N/A

0DataRank · unranked

18 citations

Kerri Becktell, Kami Wolfe Schneider, Roland P. Kuiper, Harry Lesmana, Julia Meade +14 more

Large-scale application of ClinGen-InSiGHT APC-specific ACMG/AMP variant classification criteria leads to substantial reduction in VUS

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.09.002

N/A

0DataRank · unranked

15 citations

Marcy E. Richardson, Andreas Laner, Xuemei Shi, Elisabet Ognedal, Valeria Vasta +27 more

Update on Recommendations for Surveillance for Children with Predisposition to Hematopoietic Malignancy

Clinical Cancer Research(2024)10.1158/1078-0432.ccr-24-0685

N/A

0DataRank · unranked

20 citations

Marcin W. Włodarski, Sun Young Kim, Alison A. Bertuch, Gaëlle Bougeard, Vivian Y. Chang +15 more

Germline Genetic Testing and Survival Outcomes Among Children With Rhabdomyosarcoma

JAMA Network Open(2024)10.1001/jamanetworkopen.2024.4170

N/A

0DataRank · unranked

13 citations

He Li, Michael E. Scheurer, Dana L. Casey, Shannon Dugan‐Perez, Deborah A. Marquez-Do +19 more

An evaluation of genetic predisposition to congenital anomalies and pediatric cancer supports KAT6B as a novel neuroblastoma susceptibility gene

Genetics in Medicine Open(2024)10.1016/j.gimo.2024.101901

N/A

0DataRank · unranked

3 citations

Xi Yao, Saumya D. Sisoudiya, Pamela Mishra, He Li, Jeremy M. Schraw +16 more

Germline Genetic Testing and Survival Outcomes Among Children With Rhabdomyosarcoma

UNC Libraries(2024)10.17615/m7sp-3e70

N/A

0DataRank · unranked

0 citations

Shannon Dugan‐Perez, Michael E. Scheurer, Sharon E. Plon, Brian D. Crompton, Philip J. Lupo +19 more

Calibration of additional computational tools expands ClinGen recommendation options for variant classification with PP3/BP4 criteria

Genetics in Medicine(2025)10.1016/j.gim.2025.101402

N/A

0DataRank · unranked

45 citations

Sarah L. Stenton, Emily A.W. Nadeau, Alicia B. Byrne, Marc S. Greenblatt, Steven M. Harrison +20 more

A quantitative, Bayesian-informed approach to gene-specific variant classification: Updated Expert Panel recommendations improve classification of TP53 germline variants for Li-Fraumeni syndrome

Genome Medicine(2025)10.1186/s13073-025-01536-3

N/A

0DataRank · unranked

5 citations

Megan N. Frone, Jessica L. Mester, Miguel de la Hoya, Phuong L. Mai, Tina Pesaran +32 more

Associations between birth defects and childhood and adolescent germ cell tumors according to sex, histologic subtype, and site

Cancer(2023)10.1002/cncr.34906

N/A

0DataRank · unranked

8 citations

Pagna Sok, Tania A. Desrosiers, Amanda E. Janitz, Peter H. Langlois, Mark A. Canfield +5 more

Specifications of the ACMG/AMP variant interpretation guidelines for germline TP53 variants

Human Mutation(2020)10.1002/humu.24152

N/A

0DataRank · unranked

166 citations

Kristy Lee, Magali Olivier, Tina Pesaran, Phuong L. Mai, Kelvin C. de Andrade +19 more

Specifications of the ACMG/AMP variant interpretation guidelines for germline TP53 variants

medRxiv(2020)10.1101/2020.04.25.20078931

N/A

0DataRank · unranked

5 citations

Kristy Lee, Magali Olivier, Tina Pesaran, Phuong L. Mai, Kelvin C. de Andrade +18 more

Identifying gene disruptions in novel balanced de novo constitutional translocations in childhood cancer patients by whole-genome sequencing

UNC Libraries(2020)10.17615/y8x1-pz12

N/A

0DataRank · unranked

0 citations

Patrick A. Thompson, Sharon E. Plon, David A. Wheeler, Richard A. Gibbs, Chester Brown

A survey of informatics approaches to whole-exome and whole-genome clinical reporting in the electronic health record

UNC Libraries(2020)10.17615/4zec-ff92

N/A

0DataRank · unranked

0 citations

Matthew S. Lebo, Samuel Aronson, Laura M. Amendola, Levi A. Garraway, Gail P. Jarvik +10 more

ClinGen Pathogenicity Calculator: a configurable system for assessing pathogenicity of genetic variants

UNC Libraries(2020)10.17615/0r6z-dk65

N/A

0DataRank · unranked

0 citations

Kevin Riehle, Heidi L. Rehm, Rajarshi Ghosh, Tristan H Nelson, Aaron B. Baker +16 more

Processes and preliminary outputs for identification of actionable genes as incidental findings in genomic sequence data in the Clinical Sequencing Exploratory Research Consortium

UNC Libraries(2020)10.17615/x7nz-xc34

N/A

0DataRank · unranked

0 citations

Levi A. Garraway, Elizabeth T. DeChene, Heidi L. Rehm, Matthew C. Dulik, James P. Evans +12 more

Evaluating the Clinical Validity of Gene-Disease Associations: An Evidence-Based Framework Developed by the Clinical Genome Resource

UNC Libraries(2020)10.17615/dtq0-px12

Top 100%

0DataRank

Top 100%0 citations

Ozge Ceyhan‐Birsoy, Bryce A. Seifert, Tam P. Sneddon, Natasha T. Strande, Erin M. Ramos +18 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

ClinGen Variant Curation Interface: A Variant Classification Platform for the Application of Evidence Criteria from ACMG/AMP Guidelines

medRxiv(2021)10.1101/2021.02.12.21251663

N/A

0DataRank · unranked

5 citations

Matt W. Wright, Rao Madhavrao, Steven M. Harrison, Jennifer L Goldstein, Xi Luo +30 more

ClinGen CDH1 specifications for the ACMG/AMP guidelines: improvement of germline variant clinical assertions and updated curation guidelines

medRxiv(2021)10.1101/2021.11.01.21265332

N/A

0DataRank · unranked

0 citations

Jamie L. Maciaszek, Bryony A. Thompson, Huei San Leong, Katherine Dixon, Sónia Sousa +19 more

Calibration of computational tools for missense variant pathogenicity classification and ClinGen recommendations for PP3/BP4 criteria

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.10.013

N/A

0DataRank · unranked

548 citations

Alicia B. Byrne, Bing Feng, Kymberleigh A. Pagel, Sean D. Mooney, Rachel Karchin +20 more

Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC)

Genetics in Medicine(2022)10.1016/j.gim.2022.01.001

N/A

0DataRank · unranked

245 citations

Malachi Griffith, Arpad Danos, Beth A. Pitel, Subha Madhavan, Xue‐Lu Liu +42 more

Evolution of germline TP53 variant classification in children with cancer

Cancer Genetics(2022)10.1016/j.cancergen.2022.02.011

N/A

0DataRank · unranked

9 citations

Sarah Scollon, Deborah Ritter, Sharon E. Plon, Eran Tallis

Using the ACMG/AMP framework to capture evidence related to predicted and observed impact on splicing: Recommendations from the ClinGen SVI Splicing Subgroup

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.06.002

N/A

0DataRank · unranked

315 citations

Miguel de la Hoya, George A. R. Wiggins, Amanda Lindy, Lisa M. Vincent, Michael T. Parsons +28 more

Germline pathogenic SMARCA4 variants in neuroblastoma

Journal of Medical Genetics(2023)10.1136/jmg-2022-108854

N/A

0DataRank · unranked

19 citations

Kim E. Nichols, Marjolijn C.J. Jongmans, Nienke van Engelen, Ronald R. de Krijger, Jennifer Herrera-Mullar +10 more

Frequency and spectrum of clinically significant molecular alterations detected by tumor gene panel testing for pediatric cancer patients in the Texas KidsCanSeq study.

Journal of Clinical Oncology(2023)10.1200/jco.2023.41.16_suppl.10018

N/A

0DataRank · unranked

0 citations

Jacquelyn Reuther, Samara L. Potter, Ross Mangum, Carrie Mohila, John Hicks +15 more

Male sex and the risk of childhood cancer: The mediating effect of birth defects

UNC Libraries(2023)10.17615/8dth-0h63

N/A

0DataRank · unranked

0 citations

Mark A. Canfield, T. Desrosiers, Erin L. Marcotte, Wendy N. Nembhard, R. E. Meyer +4 more

Sharon E. Plon

Indexed papers

Top data-sharing exemplar

Papers