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

Aimee L. Davidson

QIMR Berghofer Medical Research Institute

ORCID: 0000-0001-5034-5996

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 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 7 papers. Top paper: “Whole-genome sequencing reveals clinically relevant insights into the aetiology of familial breast cancers”.

Whole-genome sequencing reveals clinically relevant insights into the aetiology of familial breast cancers

Annals of Oncology(2019)10.1093/annonc/mdz132

N/A

2.6DataRank · unranked

103 citations

J. Johnson, F. Newell, Ann‐Marie Patch, H. Thorne, S.H. Kazakoff +27 more

Co-observation of germline pathogenic variants in breast cancer predisposition genes: Results from analysis of the BRIDGES sequencing dataset

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.07.004

N/A

0.330DataRank · unranked

8 citations

Kyriaki Michailidou, Michael T. Parsons, Cristina Fortuño, Manjeet K. Bolla, Qin Wang +95 more

Regional-specific calibration enables application of bioinformatic evidence for clinical classification of 5’ cis-regulatory variants in Mendelian disease

medRxiv(2023)10.1101/2023.12.21.23300413

N/A

0DataRank · unranked

0 citations

Maddison E. McKenzie, Aimee L. Davidson, Amanda B. Spurdle, Rehan M. Villani

SpliceAI-10k calculator for the prediction of pseudoexonization, intron retention, and exon deletion

Bioinformatics(2023)10.1093/bioinformatics/btad179

N/A

0DataRank · unranked

26 citations

Aimee L. Davidson, Miguel de la Hoya, Michael T. Parsons, Dylan M. Glubb, Olga Kondrashova +2 more

The SeqSplice multiplexed minigene splicing assay for characterization and quantitation of variant-induced BRCA1 and BRCA2 splice isoforms

Genome Research(2025)10.1101/gr.279557.124

N/A

0DataRank · unranked

0 citations

Michael T. Parsons, Gemma Moir-Meyer, Troy Dumenil, Gemma Montalban, Erica Lin +7 more

Regional-specific calibration enables application of computational evidence for clinical classification of 5′ cis-regulatory variants in Mendelian disease

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.05.002

N/A

0DataRank · unranked

7 citations

Maddison E. McKenzie, Aimee L. Davidson, Amanda B. Spurdle, Rehan M. Villani

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