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

Amy Schneider

The University of Melbourne

ORCID: 0000-0001-5260-7187

Also affiliated with Austin Health

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 4%percentile
0.907Author DataRank

Indexed papers

2in 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 2 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 →

Top data-sharing exemplar

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Predicting 180-day mortality for women with ovarian cancer using machine learning and patient-reported outcome data

Scientific Reports(2022)10.1038/s41598-022-22614-1
Top 25%
0.803DataRank
Top 25%18 citations

Charlotte C. Sun, Amy Schneider, Sheng-Chieh Lu, Karen H. Lu, Alexi A. Wright +2 more

Papers

Driven by 15 papers — median percentile 49. Top paper: “Predicting 180-day mortality for women with ovarian cancer using machine learning and patient-reported outcome data”.

Predicting 180-day mortality for women with ovarian cancer using machine learning and patient-reported outcome data

Scientific Reports(2022)10.1038/s41598-022-22614-1
Top 25%
0.803DataRank
Top 25%18 citations

Charlotte C. Sun, Amy Schneider, Sheng-Chieh Lu, Karen H. Lu, Alexi A. Wright +2 more

Germline variants in tumor suppressor FBXW7 lead to impaired ubiquitination and a neurodevelopmental syndrome

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.03.002
N/A
0.568DataRank · unranked
43 citations

Gregory Costain, Laura E.R. Blok, Michael Silk, Thanh Nguyen, Xiaomin Dong +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
0.489DataRank · unranked
25 citations

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

Pathogenic MAST3 Variants in the STK Domain Are Associated with Epilepsy

Annals of Neurology(2021)10.1002/ana.26147
N/A
0.442DataRank · unranked
18 citations

Kyle R. Christensen, Emily Bryant, Amy Schneider, Jennifer Rakotomamonjy, Alison M. Muir +32 more

Pathogenic MAST3 variants in the STK domain are associated with epilepsy

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.03.09.434675
N/A
0.165DataRank · unranked
2 citations

Kyle R. Christensen, Emily Bryant, Amy Schneider, Jennifer Rakotomamonjy, Alison M. Muir +25 more

Predicting 180-day mortality for women with ovarian cancer using machine learning and patient-reported outcome data.

Journal of Clinical Oncology(2021)10.1200/jco.2021.39.15_suppl.e13555
Top 78%
0.104DataRank
Top 78%1 citations

Charlotte C. Sun, Cai Xu, Amy Schneider, Sheng-Chieh Lu, Ishwaria M. Subbiah +3 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

Solving the Etiology of Developmental and Epileptic Encephalopathy with Spike–Wave Activation in Sleep (D/EE‐SWAS)

Annals of Neurology(2024)10.1002/ana.27041
N/A
0DataRank · unranked
18 citations

Karen Oliver, Brigid M. Regan, Amy Schneider, Candace T. Myers, Michele G. Mehaffey +22 more

NEXMIF encephalopathy: an X-linked disorder with male and female phenotypic patterns

Genetics in Medicine(2020)10.1038/s41436-020-00988-9
N/A
0DataRank · unranked
56 citations

Trine Bjørg Hammer, Elena Gardella, Danique R.M. Vlaskamp, Birgitte Bertelsen, Simone Mandelstam +80 more

Determination of quality of life-related health utilities for surgical complications in ovarian cancer

Gynecologic Oncology(2024)10.1016/j.ygyno.2024.01.041
N/A
0DataRank · unranked
2 citations

Charlotte C. Sun, Amy Schneider, Karen H. Lu, Sharon H. Giordano, Larissa A. Meyer +1 more

Germline and Mosaic Variants in PRKACA and PRKACB Cause a Multiple Congenital Malformation Syndrome

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.09.005
N/A
0DataRank · unranked
54 citations

Phillip C. Aoto, Erik M.F. Machal, Ana Rivera‐Barahona, Patricia Soto‐Bielicka, Daniela Bertinetti +37 more

Financial toxicity and patient-reported outcomes over time: A longitudinal study of women with recurrent ovarian cancer.

Journal of Clinical Oncology(2020)10.1200/jco.2020.38.15_suppl.6079
N/A
0DataRank · unranked
3 citations

Amy Schneider, Tsun Hsuan Chen, Xin Shelley Wang, Charlotte C. Sun, Larissa A. Meyer

The severe epilepsy syndromes of infancy: A population‐based study

Epilepsia(2021)10.1111/epi.16810
N/A
0DataRank · unranked
67 citations

Jeremy L. Freeman, Mark T. Mackay, Michael Fahey, John S. Archer, Samuel F. Berkovic +24 more

Development and Validation of a Prediction Model for Early Diagnosis of SCN1A -Related Epilepsies

Neurology(2022)10.1212/wnl.0000000000200028
N/A
0DataRank · unranked
73 citations

Eduardo Pérez‐Palma, Ismael Ghanty, Xinge Ji, Eva H. Brilstra, Berten Ceulemans +17 more

BRAT1–related disorders: phenotypic spectrum and phenotype-genotype correlations from 97 patients

European Journal of Human Genetics(2023)10.1038/s41431-023-01410-z
N/A
0DataRank · unranked
10 citations

Stéphanie Valence, Geoffroy Delplancq, Reza Maroofian, Andrea Accogli, Emanuele Agolini +85 more