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

Dan Doherty

Seattle Children's Hospital

ORCID: 0000-0001-9377-028X

Also affiliated with University of Washington, Brotman Baty Institute

Biochemistry, Genetics and Molecular BiologyMedicineNeuroscience

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 1%percentile
12.4Author DataRank

Indexed papers

4in 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 4 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.

A human cell atlas of fetal gene expression

Science(2020)10.1126/science.aba7721
Top 3%
6.2DataRank
Top 3%842 citations

Diana R. O’Day, Hannah A. Pliner, Paul D. Kingsley, Mei Deng, Riza M. Daza +12 more

Papers

Driven by 24 papers — median percentile 97. Top paper: “A human cell atlas of fetal gene expression”.

A human cell atlas of fetal gene expression

Science(2020)10.1126/science.aba7721
Top 3%
6.2DataRank
Top 3%842 citations

Diana R. O’Day, Hannah A. Pliner, Paul D. Kingsley, Mei Deng, Riza M. Daza +12 more

A human cell atlas of fetal chromatin accessibility

Science(2020)10.1126/science.aba7612
Top 3%
5.8DataRank
Top 3%466 citations

Andrew J. Hill, Riza M. Daza, Junyue Cao, Diana R. O’Day, Hannah A. Pliner +12 more

An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes

Nature Cell Biology(2015)10.1038/ncb3201
N/A
0.831DataRank · unranked
253 citations

Gabrielle Wheway, Miriam Schmidts, Dorus A. Mans, Katarzyna Szymanska, Thanh-Minh T. Nguyen +71 more

The Brain Gene Registry: a data snapshot

Journal of Neurodevelopmental Disorders(2024)10.1186/s11689-024-09530-3
Top 48%
0.373DataRank
Top 48%11 citations

Levi Kaster, Catherine Sancimino, Siddharth Srivastava, Sophie Molholm, Aditi Gupta +58 more

Loss of CBY1 results in a ciliopathy characterized by features of Joubert syndrome

Human Mutation(2020)10.1002/humu.24127
N/A
0DataRank · unranked
21 citations

Lokuliyange D. S. Senaratne, Elisabeth Ott, Asbjørn Holmgren, Dulika Sumathipala, Selma Mujezinović Larsen +25 more

Bi-allelic Loss-of-Function Variants in NUP188 Cause a Recognizable Syndrome Characterized by Neurologic, Ocular, and Cardiac Abnormalities

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.03.009
N/A
0DataRank · unranked
30 citations

Jennifer L. Cohen, Sarah E. Sheppard, Pavithran Guttipatti, Tsz Y. Lo, Natalie Weed +14 more

Targeted long-read sequencing resolves complex structural variants and identifies missing disease-causing variants

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.11.03.365395
N/A
0DataRank · unranked
10 citations

Arvis Sulovari, Tianyun Wang, Hailey Loucks, Kendra Hoekzema, Katherine M. Munson +32 more

Spatial and single-cell transcriptional landscape of human cerebellar development

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.06.30.174391
N/A
0DataRank · unranked
8 citations

Zach Thomson, Parthiv Haldipur, Mei Deng, Andrew E. Timms, Matthew Hirano +16 more

Cas12a-Capture: a novel, low-cost, and scalable method for targeted sequencing

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.11.18.388876
N/A
0DataRank · unranked
0 citations

Andrew Nishida, Brendan L. O’Connell, Caitlin V. Miller, Sally Grindstaff, Casey Thornton +4 more

Targeted long-read sequencing identifies missing disease-causing variation

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.06.006
N/A
0DataRank · unranked
242 citations

Arvis Sulovari, Tianyun Wang, Hailey Loucks, Kendra Hoekzema, Katherine M. Munson +45 more

The Joubert–Meckel–Nephronophthisis Spectrum of Ciliopathies

Annual Review of Genomics and Human Genetics(2022)10.1146/annurev-genom-121321-093528
N/A
0DataRank · unranked
63 citations

Arianna Gómez, Dan Doherty, Julie C. Van De Weghe

Discovering a new part of the phenotypic spectrum of Coffin-Siris syndrome in a fetal cohort

Genetics in Medicine(2022)10.1016/j.gim.2022.04.010
N/A
0DataRank · unranked
21 citations

Marieke Joosten, Caroline Alby, Tania Attié‐Bitach, Kelly L. Gilmore, Christèle Dubourg +50 more

Systematic analysis of cilia characteristics and Hedgehog signaling in five immortal cell lines

PLoS ONE(2022)10.1371/journal.pone.0266433
N/A
0DataRank · unranked
17 citations

Angela K Christman, Julie C. Van De Weghe, Malaney Finn, Dan Doherty, Arianna Gómez

Single-cell census of human tooth development enables generation of human enamel

Developmental Cell(2023)10.1016/j.devcel.2023.07.013
N/A
0DataRank · unranked
73 citations

Sesha Hanson-Drury, Anjali P. Patni, Devon Duron Ehnes, Yan Ting Zhao, Zicong Li +19 more

Species-specific FMRP regulation of RACK1 is critical for prenatal cortical development

Neuron(2023)10.1016/j.neuron.2023.09.014
N/A
0DataRank · unranked
38 citations

Carissa L. Sirois, Yu Guo, Meng Li, Qiping Dong, Natasha M. Méndez-Albelo +20 more

Elevated levels of FMRP-target MAP1B impair human and mouse neuronal development and mouse social behaviors via autophagy pathway

Nature Communications(2023)10.1038/s41467-023-39337-0
N/A
0DataRank · unranked
37 citations

Minjie Shen, Qiping Dong, Natasha M. Méndez-Albelo, Sabrina X. Huang, Carissa L. Sirois +15 more

Multimodal analyses reveal genes driving electrophysiological maturation of neurons in the primate prefrontal cortex

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.06.02.543460
N/A
0DataRank · unranked
4 citations

Qiping Dong, Kalpana Hanthanan Arachchilage, Ryan D. Risgaard, Moosa Syed, Jie Sheng +12 more

SeqFirst: Building equity access to a precise genetic diagnosis in critically ill newborns

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.02.003
N/A
0DataRank · unranked
16 citations

Abbey Scott, Lukas Kruidenier, Megan Sikes, Alexandra Keefe, Kati J. Buckingham +28 more

Multimodal analyses reveal genes driving electrophysiological maturation of neurons in the primate prefrontal cortex

Neuron(2025)10.1016/j.neuron.2025.04.025
N/A
0DataRank · unranked
11 citations

Qiping Dong, Kalpana Hanthanan Arachchilage, Ryan D. Risgaard, Moosa Syed, Jie Sheng +16 more

Artificial intelligence-driven genotype–epigenotype–phenotype approaches to resolve challenges in syndrome diagnostics

EBioMedicine(2025)10.1016/j.ebiom.2025.105677
N/A
0DataRank · unranked
6 citations

Hannah Klinkhammer, Sanaa Choufani, Nikola Reko, Angela K Christman, Elise Pisan +36 more

Ontogeny Dictates Oncogenic Potential, Lineage Hierarchy, and Therapy Response in Pediatric Leukemia

Cancer Discovery(2025)10.1158/2159-8290.cd-25-0556
N/A
0DataRank · unranked
2 citations

Shayan Saniei, Nikita Poddar, Isabella G. Martinez, C. Chao, Subrina Persaud +45 more

A clinical and genotype-phenotype analysis of MACF1 variants

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.08.010
N/A
0DataRank · unranked
1 citations

Rachel Schot, Kimberly A. Aldinger, David B. Everman, Camerun Washington, Julie R. Jones +85 more

TMEM218 dysfunction causes ciliopathies, including Joubert and Meckel syndromes

Human Genetics and Genomics Advances(2020)10.1016/j.xhgg.2020.100016
N/A
0DataRank · unranked
14 citations

Jessica L. Giordano, Inge B. Mathijssen, Majid Mojarrad, Dorien Lugtenberg, Caitlin V. Miller +15 more

Dysfunction of the ciliary ARMC9/TOGARAM1 protein module causes Joubert syndrome

Journal of Clinical Investigation(2020)10.1172/jci131656
N/A
0DataRank · unranked
88 citations

Julie C. Van De Weghe, Tamara D. S. Rusterholz, Stef J.F. Letteboer, Arianna Gómez, Ranad Shaheen +23 more