🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Bryony A. Thompson

The Royal Melbourne Hospital

ORCID: 0000-0001-8655-1839
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 100%percentile
0Author 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 →

Papers

Driven by 9 papers. Top paper: “Optimising clinical care through CDH1-specific germline variant curation: improvement of clinical assertions and updated curation guidelines”.

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

Evidence-based recommendations for gene-specific ACMG/AMP variant classification from the ClinGen ENIGMA BRCA1 and BRCA2 Variant Curation Expert Panel

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.07.013
N/A
0.689DataRank · unranked
98 citations

Miguel de la Hoya, Marcy E. Richardson, Emma Tudini, Michael Anderson, Windy Berkofsky-Fessler +38 more

Contribution of mRNA Splicing to Mismatch Repair Gene Sequence Variant Interpretation

Frontiers in Genetics(2020)10.3389/fgene.2020.00798
N/A
0.470DataRank · unranked
22 citations

Rhiannon Walters, Michael T. Parsons, Troy Dumenil, Mark Drost, Yvonne Tiersma +5 more

Comprehensive evaluation and efficient classification of BRCA1 RING domain missense substitutions

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.05.004
N/A
0.457DataRank · unranked
20 citations

Andrew Paquette, Kayoko Tao, Russell Bell, Julie L. Boyle, Judith Rosenthal +12 more

Genomic risk prediction for breast cancer in older women

medRxiv(2021)10.1101/2021.05.03.21256567
N/A
0DataRank · unranked
0 citations

Andrew Bakshi, Moeen Riaz, Suzanne G. Orchard, Jane Tiller, Franz–Josef Neumann +24 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

Genomic Risk Prediction for Breast Cancer in Older Women

Cancers(2021)10.3390/cancers13143533
N/A
0DataRank · unranked
10 citations

Andrew Bakshi, Moeen Riaz, Suzanne G. Orchard, Jane Tiller, Franz–Josef Neumann +24 more

Piloting an Interpretive External Quality Assurance Model for Genomic Testing for Childhood Syndromes and Intellectual Disability

Journal of Molecular Diagnostics(2025)10.1016/j.jmoldx.2025.11.006
N/A
0DataRank · unranked
0 citations

Sze Yee Chai, Alicia B. Byrne, Dimitar N. Azmanov, John Christodoulou, Matilda Haas +7 more

Genetic variants associated with inherited cardiovascular disorders among 13,131 asymptomatic older adults of European descent

npj Genomic Medicine(2021)10.1038/s41525-021-00211-x
N/A
0DataRank · unranked
20 citations

Robert Sebra, Moeen Riaz, Jodie Ingles, Jane Tiller, Bryony A. Thompson +9 more