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

Sandra T. Cooper

The University of Sydney

ORCID: 0000-0002-7314-5097

Also affiliated with Children's Medical Research Institute, Children's Hospital at Westmead

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 6%percentile
0.252Author 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.

Expert panel curation of 31 genes in relation to limb girdle muscular dystrophy

Annals of Clinical and Translational Neurology(2024)10.1002/acn3.52127
Top 60%
0.252DataRank
Top 60%4 citations

Shannon McNulty, Courtney L Thaxton, Marwa Elnagheeb, Emma Owens, May Flowers +25 more

Papers

Driven by 17 papers — median percentile 40. Top paper: “Factors associated with smokefree rules in the homes of Black/African American women smokers residing in low-resource rural communities”.

Factors associated with smokefree rules in the homes of Black/African American women smokers residing in low-resource rural communities

Preventive Medicine(2022)10.1016/j.ypmed.2022.107340
N/A
0.279DataRank · unranked
5 citations

Sandilyn Bullock, Katherine Donald, Sandra T. Cooper, Wonda Miller, Anna Huff Davis +6 more

Expert panel curation of 31 genes in relation to limb girdle muscular dystrophy

Annals of Clinical and Translational Neurology(2024)10.1002/acn3.52127
Top 60%
0.252DataRank
Top 60%4 citations

Shannon McNulty, Courtney L Thaxton, Marwa Elnagheeb, Emma Owens, May Flowers +25 more

Evidence-based practices are effective in increasing smoke-free home rules among Black women who smoke

JNCI Monographs(2025)10.1093/jncimonographs/lgaf026
N/A
0.104DataRank · unranked
1 citations

Ashley H. Clawson, Jing Jin, Sandilyn Bullock, Katherine Donald, Sandra T. Cooper +8 more

Neonatal-lethal dilated cardiomyopathy due to a homozygous LMOD2 donor splice-site variant

European Journal of Human Genetics(2022)10.1038/s41431-022-01043-8
N/A
0DataRank · unranked
19 citations

Lisa Worgan, Jessika Iwanski, Christopher T. Pappas, Himanshu Joshi, Jared M. Churko +7 more

Prevalence, parameters, and pathogenic mechanisms for splice-altering acceptor variants that disrupt the AG exclusion zone

Human Genetics and Genomics Advances(2022)10.1016/j.xhgg.2022.100125
N/A
0DataRank · unranked
11 citations

Michaela Yuen, Himanshu Joshi, Ruebena Dawes, Katharine Zhang, Jessica K. Lu +8 more

SpliceVault predicts the precise nature of variant-associated mis-splicing

Nature Genetics(2023)10.1038/s41588-022-01293-8
N/A
0DataRank · unranked
94 citations

Adam Bournazos, Samantha J. Bryen, Shobhana Bommireddipalli, Rhett G. Marchant, Himanshu Joshi +2 more

Compound heterozygous splicing variants expand the genotypic spectrum of EMC1 ‐related disorders

Clinical Genetics(2023)10.1111/cge.14311
N/A
0DataRank · unranked
8 citations

Katharine Zhang, Gregory Dziaduch, Shobhana Bommireddipalli, Take Naseri, Muagututi‘a Sefuiva Reupena +8 more

Pathogenic deep intronic MTM1 variant activates a pseudo-exon encoding a nonsense codon resulting in severe X-linked myotubular myopathy

European Journal of Human Genetics(2020)10.1038/s41431-020-00715-7
N/A
0DataRank · unranked
14 citations

Emily C. Oates, Frances J. Evesson, Jessica K. Lu, Leigh B. Waddell, Himanshu Joshi +7 more

Genome Sequencing for Diagnosing Rare Diseases

New England Journal of Medicine(2024)10.1056/nejmoa2314761
N/A
0DataRank · unranked
189 citations

Gabrielle Lemire, Eva Berger, Maha S. Zaki, Mariel Wissmann, Wathone Win +84 more

Digenic inheritance involving a muscle-specific protein kinase and the giant titin protein causes a skeletal muscle myopathy

Nature Genetics(2024)10.1038/s41588-023-01651-0
N/A
0DataRank · unranked
33 citations

Dan Cox, Irina Zaharieva, Valeria Di Leo, J. Sarparanta, Per Harald Jonson +80 more

Genome and RNA sequencing boost neuromuscular diagnoses to 62% from 34% with exome sequencing alone

Annals of Clinical and Translational Neurology(2024)10.1002/acn3.52041
N/A
0DataRank · unranked
23 citations

Samantha J. Bryen, Melanie Bahlo, Anita Cairns, Katherine R. Chao, Alastair Corbett +25 more

Genome sequencing enables diagnosis and treatment of SLC5A6 neuropathy

European Journal of Human Genetics(2024)10.1038/s41431-024-01641-8
N/A
0DataRank · unranked
6 citations

Subrata Sabui, Hamid M. Said, Aram Niaz, Katta M. Girisha, Periyasamy Radhakrishnan +10 more

Expert Panel Curation of 31 Genes in Relation to Limb Girdle Muscular Dystrophy

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.05.03.592369
N/A
0DataRank · unranked
0 citations

Shannon McNulty, Courtney L Thaxton, Marwa Elnagheeb, Emma Owens, May Flowers +25 more

Caregiver restrictions on child access to tobacco in the home and home Smoking/Vaping bans among Black/African American women caregivers who smoke and live in Resource-limited, rural areas

Preventive Medicine Reports(2024)10.1016/j.pmedr.2024.102918
N/A
0DataRank · unranked
0 citations

Dina M. Jones, Jing Jin, Ruofei Du, Sandilyn Bullock, Katherine Donald +5 more

Unique Capabilities of Genome Sequencing for Rare Disease Diagnosis

medRxiv(2023)10.1101/2023.08.08.23293829
N/A
0DataRank · unranked
8 citations

Gabrielle Lemire, Maha S. Zaki, Mariel Wissman, Wathone Win, S. White +70 more

Empirical prediction of variant-associated cryptic-donors with 87% sensitivity and 95% specificity

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.07.18.452855
N/A
0DataRank · unranked
4 citations

Himanshu Joshi, Sandra T. Cooper, Ruebena Dawes

Empirical prediction of variant-activated cryptic splice donors using population-based RNA-Seq data

Nature Communications(2022)10.1038/s41467-022-29271-y
N/A
0DataRank · unranked
33 citations

Himanshu Joshi, Sandra T. Cooper, Ruebena Dawes