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

Claire E. Shepherd

UNSW Sydney

ORCID: 0000-0002-0399-3218

Also affiliated with Parkinson's Foundation, Neuroscience Research Australia

Medicine

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
0.769Author 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 →

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.

Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)

npj Parkinson s Disease(2023)10.1038/s41531-023-00533-w
Top 26%
0.769DataRank
Top 26%39 citations

Madeleine Richer, Simona Jasaityte, Eleanor J. Stafford, Julie Joubert, Tarek Antar +95 more

Papers

Driven by 8 papers — median percentile 74. Top paper: “Multi-ancestry genome-wide association meta-analysis of Parkinson’s disease”.

Multi-ancestry genome-wide association meta-analysis of Parkinson’s disease

Nature Genetics(2023)10.1038/s41588-023-01584-8
N/A
0.839DataRank · unranked
268 citations

Dan Vitale, Diego Véliz Otani, Michelle Mulan Lian, Karl Heilbron, Stella Aslibekyan +95 more

Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)

npj Parkinson s Disease(2023)10.1038/s41531-023-00533-w
Top 26%
0.769DataRank
Top 26%39 citations

Madeleine Richer, Simona Jasaityte, Eleanor J. Stafford, Julie Joubert, Tarek Antar +95 more

Insights into ancestral diversity in Parkinson’s disease risk: a comparative assessment of polygenic risk scores

npj Parkinson s Disease(2025)10.1038/s41531-025-00967-4
N/A
0.269DataRank · unranked
5 citations

Spencer Grant, Mary B. Makarious, Inas Elsayed, Arinola O. Sanyaolu, Peter Wild Crea +95 more

Multi-region brain transcriptomic analysis of amyotrophic lateral sclerosis reveals widespread RNA alterations and substantial cerebellum involvement

Molecular Neurodegeneration(2025)10.1186/s13024-025-00820-5
N/A
0DataRank · unranked
12 citations

Andrew Smith, Claire E. Shepherd, Lyndal Henden, Thiri Zaw, Luke Carroll +5 more

CYLD is a causative gene for frontotemporal dementia – amyotrophic lateral sclerosis

Brain(2020)10.1093/brain/awaa039
N/A
0DataRank · unranked
87 citations

Marianne Hallupp, Hamideh Shahheydari, Audrey Ragagnin, Zac Chatterton, Francine Carew‐Jones +34 more

The LRRK2 p.L1795F variant causes Parkinson’s disease in the European population

npj Parkinson s Disease(2025)10.1038/s41531-025-00896-2
N/A
0DataRank · unranked
4 citations

Kristin Levine, Susan H. Fox, Connie Marras, Nazish Ahmed, Nicole Kuznetsov +95 more

Analysis of neurodegenerative disease-causing genes in dementia with Lewy bodies

Acta Neuropathologica Communications(2020)10.1186/s40478-020-0879-z
N/A
0DataRank · unranked
42 citations

Dena G. Hernandez, Owen A. Ross, Célia Kun‐Rodrigues, Lee Darwent, Claire E. Shepherd +47 more

Prion-like α-synuclein pathology in the brain of infants with Krabbe disease

Brain(2022)10.1093/brain/awac002
N/A
0DataRank · unranked
28 citations

Simona S. Ghanem, David J. Koss, Ilham Y. Abdi, Elizabeth Gibbons, Rita Guerreiro +71 more