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

Grace Yoon

University of Calgary

ORCID: 0000-0002-3450-3293

Also affiliated with University of Toronto, Hospital for Sick Children, SickKids Foundation, Pediatrics and Genetics

NeuroscienceBiochemistry, 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 100%percentile
0Author DataRank

Indexed papers

0in pilot corpus
datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 12 papers. Top paper: “Loss of aryl hydrocarbon receptor potentiates FoxM1 signaling to enhance self‐renewal of colonic stem and progenitor cells”.

Loss of aryl hydrocarbon receptor potentiates FoxM1 signaling to enhance self‐renewal of colonic stem and progenitor cells

The EMBO Journal(2020)10.15252/embj.2019104319
N/A
1.3DataRank · unranked
43 citations

Laurie A. Davidson, Yang‐Yi Fan, Jennifer S. Goldsby, Grace Yoon, Un‐Ho Jin +11 more

Heterozygous Variants in KDM4B Lead to Global Developmental Delay and Neuroanatomical Defects

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.11.001
N/A
0DataRank · unranked
30 citations

Antonio Vitobello, Stephan C. Collins, Valerie E. Vancollie, Christopher J. Lelliott, Lance H. Rodan +25 more

International retrospective natural history study of LMNA-related congenital muscular dystrophy

Brain Communications(2021)10.1093/braincomms/fcab075
N/A
0DataRank · unranked
35 citations

Pomi Yun, Ivana Dabaj, Gina Norato, Sandra Donkervoort, Hui Xiong +39 more

International retrospective natural history study of LMNA-related congenital muscular dystrophy Short Title: LMNA-CMD natural history

HAL (Le Centre pour la Communication Scientifique Directe)(2021)10.1093/braincomms/fcab075/6220465
N/A
0DataRank · unranked
0 citations

Pomi Yun, Adele D’Amico, Muntoni Francesco, C. Bönnemann, Ivana Dabaj +40 more

The clinical and molecular spectrum of ZFYVE26-associated hereditary spastic paraplegia: SPG15

Brain(2022)10.1093/brain/awac391
N/A
0DataRank · unranked
24 citations

Melanie Kellner, Catherine Jordan, Helena Rosengarten, Alisa Mo, Bo Zhang +29 more

Plasma Neurofilament Light Chain Is Elevated in Adaptor Protein Complex 4‐Related Hereditary Spastic Paraplegia

Movement Disorders(2023)10.1002/mds.29524
N/A
0DataRank · unranked
11 citations

Afshin Saffari, M. L. ZIEGLER, Catherine Jordan, Amy Tam, So Young Kim +12 more

Child Neurology: Progressive Cerebellar Atrophy and Retinal Dystrophy

Neurology(2023)10.1212/wnl.0000000000207649
N/A
0DataRank · unranked
1 citations

Ashutosh Pandey, Sundararajan Venkatesh, Roberto D. Noland, Gabriel Swanson, Debkumar Pain +4 more

Bi-allelic pathogenic variants in TRMT1 disrupt tRNA modification and induce a neurodevelopmental disorder

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.03.015
N/A
0DataRank · unranked
7 citations

Cailyn P Leo, Chenghong Deng, Sheng‐Jia Lin, Reza Maroofian, Reneé C. Lin +95 more

The recurrent deep intronic pseudoexon-inducing variant COL6A1 c.930+189C>T results in a consistently severe phenotype of COL6-related dystrophy: Towards clinical trial readiness for splice-modulating therapy

medRxiv(2024)10.1101/2024.03.29.24304673
N/A
0DataRank · unranked
2 citations

Véronique Bolduc, Fady Guirguis, Sandra Donkervoort, Ying Hu, Rotem Orbach +64 more

Biallelic pathogenic variants in TRMT1 disrupt tRNA modification and induce a syndromic neurodevelopmental disorder

medRxiv(2024)10.1101/2024.07.18.24310581
N/A
0DataRank · unranked
1 citations

Cailyn P Leo, Chenghong Deng, Kejia Zhang, Sheng‐Jia Lin, Reza Maroofian +75 more

De Novo variants in EEF2 cause a neurodevelopmental disorder with benign external hydrocephalus

Human Molecular Genetics(2020)10.1093/hmg/ddaa270
N/A
0DataRank · unranked
23 citations

Alexandra N. Olson, Grace Yoon, Graeme Nimmo, Christopher M. Gómez, Michèl A.A.P. Willemsen +7 more

Count of Neonatal Morbidities Predicts Outcomes at Age 10 and 15 Years in Infants Born Extremely Preterm

The Journal of Pediatrics(2025)10.1016/j.jpeds.2025.114709
N/A
0DataRank · unranked
3 citations

Joe Yi, T. Michael O’Shea, Elizabeth T. Jensen, Robert M. Joseph, Jeffrey Shenberger +94 more