Deborah Ritter

Also affiliated with Texas Children's Hospital

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 1%percentile

7.1Author DataRank

Indexed papers

4in 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 4 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.

A harmonized meta-knowledgebase of clinical interpretations of somatic genomic variants in cancer

Nature Genetics(2020)10.1038/s41588-020-0603-8

Top 4%

4.9DataRank

Top 4%178 citations

Brian Walsh, Georgia Mayfield, David Tamborero, Dmitriy Sonkin, Kilannin Krysiak +34 more

Papers

Driven by 17 papers — median percentile 82. Top paper: “A harmonized meta-knowledgebase of clinical interpretations of somatic genomic variants in cancer”.

A harmonized meta-knowledgebase of clinical interpretations of somatic genomic variants in cancer

Nature Genetics(2020)10.1038/s41588-020-0603-8

Top 4%

4.9DataRank

Top 4%178 citations

Brian Walsh, Georgia Mayfield, David Tamborero, Dmitriy Sonkin, Kilannin Krysiak +34 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

CIViCdb 2022: evolution of an open-access cancer variant interpretation knowledgebase

Nucleic Acids Research(2022)10.1093/nar/gkac979

Top 19%

1.0DataRank

Top 19%46 citations

Arpad Danos, Jason Saliba, Joshua F. McMichael, Adam Coffman, Susanna Kiwala +60 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

Interpreting the functional impact of genetic variants: The need for context qualifiers

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.11.007

N/A

0.208DataRank · unranked

3 citations

Hélène Cavé, Alessandro De Luca, Marina T. DiStefano, Rachel Karchin, Ana Clara Lugones +8 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

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

0.165DataRank · unranked

2 citations

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

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

Specifications of the ACMG/AMP Variant Classification Guidelines for Germline DICER1 Variant Curation

Human Mutation(2023)10.1155/2023/9537832

N/A

0DataRank · unranked

15 citations

Megan N. Frone, Hannah C. Cox, Stephanie B. Crowley, Susan Hiraki, Noriko N. Yokoyama +20 more

Macrocephaly and developmental delay caused by missense variants in RAB5C

Human Molecular Genetics(2023)10.1093/hmg/ddad130

N/A

0DataRank · unranked

4 citations

Weimin Yuan, Federico Tessadori, Wilmer R. Rodriguez-Polanco, Jeremy J. Grubbs, Bo Zhang +94 more

Evolution of the open-access CIViC knowledgebase is driven by the needs of the cancer variant interpretation community

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.06.13.448171

Top 100%

0DataRank

Top 100%0 citations

Arpad Danos, Susanna Kiwala, Joshua F. McMichael, Adam Coffman, Erica K. Barnell +47 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

Bioinformatics Bootcamp: A model for training clinical researchers

Medical Research Archives(2020)10.18103/mra.v8i5.2108

N/A

0DataRank · unranked

1 citations

Jennifer Drummond, Deborah Ritter, Kirt Martin, Lori Banks, Dewayne Whittington +1 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

Standardized evidence-based approach for assessment of oncogenic and clinical significance of NTRK fusions

Cancer Genetics(2022)10.1016/j.cancergen.2022.03.001

N/A

0DataRank · unranked

10 citations

Alanna J. Church, Shruti Rao, Arpad Danos, Larissa V. Furtado, Theodore W. Laetsch +11 more

Deborah Ritter

Indexed papers

Top data-sharing exemplar

Papers