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

Miranda Galey

University of Washington

ORCID: 0000-0002-4721-7499
Biochemistry, 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 4%percentile
0.700Author DataRank

Indexed papers

3in 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 3 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.

Genome Report: chromosome-scale genome assembly of the African spiny mouse (Acomys cahirinus)

G3 Genes Genomes Genetics(2023)10.1093/g3journal/jkad177
Top 44%
0.421DataRank
Top 44%7 citations

Vahid Nikoonejad Fard, Bernard Kim, Sarah Collins, Miranda Galey, Branden R. Nelson +14 more

Papers

Driven by 19 papers — median percentile 50. Top paper: “Beyond the exome: What’s next in diagnostic testing for Mendelian conditions”.

Beyond the exome: What’s next in diagnostic testing for Mendelian conditions

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.06.009
N/A
2.2DataRank · unranked
123 citations

Chloe Reuter, Shruti Marwaha, Medhat Mahmoud, Michael Duyzend, Hayk Barseghyan +91 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

Genome Report: chromosome-scale genome assembly of the African spiny mouse (Acomys cahirinus)

G3 Genes Genomes Genetics(2023)10.1093/g3journal/jkad177
Top 44%
0.421DataRank
Top 44%7 citations

Vahid Nikoonejad Fard, Bernard Kim, Sarah Collins, Miranda Galey, Branden R. Nelson +14 more

GENOME REPORT: Chromosome-scale genome assembly of the African spiny mouse ( Acomys cahirinus )

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.04.03.535372
Top 57%
0.279DataRank
Top 57%4 citations

Vahid Nikoonejad Fard, Bernard Kim, Sarah Collins, Miranda Galey, Branden R. Nelson +14 more

Heterozygous Inversion Breakpoints Suppress Meiotic Crossovers by Altering Recombination Repair Outcomes

10.1101/2022.11.09.515852
N/A
0.165DataRank · unranked
2 citations

Erica Berent, Savannah Hadjipanteli, Miranda Galey, Danny E. Miller, Nicole Crown +1 more

Heterozygous inversion breakpoints suppress meiotic crossovers by altering recombination repair outcomes

PLoS Genetics(2023)10.1371/journal.pgen.1010702
N/A
0DataRank · unranked
15 citations

Erica Berent, Savana Hadjipanteli, Miranda Galey, Nigel Muhammad-Lahbabi, Danny E. Miller +2 more

CLN2 disease resulting from a novel homozygous deep intronic splice variant in TPP1 discovered using long-read sequencing

Molecular Genetics and Metabolism(2023)10.1016/j.ymgme.2023.107713
N/A
0DataRank · unranked
2 citations

Jill Borsuk, John Pappas, Miranda Galey, Anna Scott, Joseph M. Devaney +3 more

Targeted long-read sequencing identifies missing pathogenic variants in unsolved Werner syndrome cases

Journal of Medical Genetics(2022)10.1136/jmedgenet-2022-108485
N/A
0DataRank · unranked
26 citations

Lin Lee, Miranda Galey, Renuka Kandhaya‐Pillai, Marc Tischkowitz, Deepak Amalnath +11 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

Probabilistic models of biological enzymatic polymerization

PLoS ONE(2021)10.1371/journal.pone.0244858
N/A
0DataRank · unranked
4 citations

Miranda Galey, Clara M. Smoniewski, Sara L. Zimmer, Marshall Hampton

Considerations for reporting variants in novel candidate genes identified during clinical genomic testing

Genetics in Medicine(2024)10.1016/j.gim.2024.101199
N/A
0DataRank · unranked
14 citations

Seth Berger, Samantha Baxter, Erica D. Smith, Changrui Xiao, Daniel G. Calame +89 more

A distant global control region is essential for normal expression of anterior HOXA genes during mouse and human craniofacial development

Nature Communications(2024)10.1038/s41467-023-44506-2
N/A
0DataRank · unranked
16 citations

Eva D’haene, Machteld Baetens, Tara N. Yankee, Emma Wentworth Winchester, Nicole Glidden +13 more

Combined approaches, including long-read sequencing, address the diagnostic challenge of HYDIN in primary ciliary dyskinesia

European Journal of Human Genetics(2024)10.1038/s41431-024-01599-7
N/A
0DataRank · unranked
13 citations

Miranda Galey, Lizi Briggs, Matthew Edwards, Claire Hogg, Shibu John +18 more

Concordance of whole-genome long-read sequencing with standard clinical testing for Prader-Willi and Angelman syndromes

medRxiv(2024)10.1101/2024.04.02.24305233
N/A
0DataRank · unranked
1 citations

Miranda Galey, Anita E. Beck, Madelyn A. Gillentine, Jaya Narayanan, Nikhita Damaraju +4 more

CFAP47 is a novel causative gene implicated in X-linked polycystic kidney disease

medRxiv(2024)10.1101/2024.04.05.24304760
N/A
0DataRank · unranked
0 citations

Takuya Fujimaru, Chunyu Liu, Karynne Patterson, Kouhei Yamamoto, Takefumi Suzuki +18 more

Deep Intronic SVA_E Insertion Identified as the Most Common Pathogenic Variant Associated With Canavan Disease

Neurology Genetics(2025)10.1212/nxg.0000000000200291
N/A
0DataRank · unranked
3 citations

Katrina M. Bell, Ramakrishnan Rajagopalan, M. De Silva, Aída Lemes, Cristina Zoco Zabala +24 more

Long-Read Sequencing is Required for Precision Diagnosis of Incontinentia Pigmenti

Research Square(2025)10.21203/rs.3.rs-5811417/v1
N/A
0DataRank · unranked
0 citations

Robin D. Clark, Abdallah F. Elias, Casie A. Genetti, Jill A. Madden, Dana Simpson +21 more

Long‐read DNA sequencing resolves a rare case of alloimmune hemolysis mimicking autoimmune hemolysis

Transfusion(2025)10.1111/trf.18403
N/A
0DataRank · unranked
0 citations

Thomas Ma, Livia Hegerova, Theresa Nester, Nina Sen, Lay See Er +14 more

Targeted Long-Read Sequencing Identifies a Retrotransposon Insertion as a Cause of Altered GNAS Exon A/B Methylation in a Family With Autosomal Dominant Pseudohypoparathyroidism Type 1b (PHP1B)

Journal of Bone and Mineral Research(2020)10.1002/jbmr.4647
N/A
0DataRank · unranked
29 citations

Patrick Hanna, Miranda Galey, Monica Reyes, Agnès Linglart, Evan E. Eichler +2 more