Grace Yoon

1.5k total citations
22 papers, 503 citations indexed

About

Grace Yoon is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Grace Yoon has authored 22 papers receiving a total of 503 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 6 papers in Genetics and 3 papers in Genetics. Recurrent topics in Grace Yoon's work include Genomics and Rare Diseases (3 papers), Neurological diseases and metabolism (3 papers) and RNA regulation and disease (3 papers). Grace Yoon is often cited by papers focused on Genomics and Rare Diseases (3 papers), Neurological diseases and metabolism (3 papers) and RNA regulation and disease (3 papers). Grace Yoon collaborates with scholars based in Canada, United States and United Kingdom. Grace Yoon's co-authors include Gregory Costain, Aya Uchida, Waleed Rahmani, Anowara Islam, Fábio Rossi, Nicole L. Rosin, Sepideh Abbasi, Prajay Shah, T. Michael Underhill and Jeff Biernaskie and has published in prestigious journals such as Nature Communications, Brain and Neurology.

In The Last Decade

Grace Yoon

20 papers receiving 498 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Grace Yoon Canada 9 197 114 77 67 46 22 503
Daniel Jaffurs United States 10 259 1.3× 169 1.5× 25 0.3× 53 0.8× 62 1.3× 16 820
Maryline Favier France 10 341 1.7× 75 0.7× 26 0.3× 26 0.4× 31 0.7× 14 509
Masahito Yoshihara Japan 13 595 3.0× 122 1.1× 21 0.3× 50 0.7× 28 0.6× 36 991
Laura M. Pérez Spain 18 278 1.4× 122 1.1× 69 0.9× 230 3.4× 136 3.0× 34 1.0k
Chunbo Yang China 17 595 3.0× 75 0.7× 16 0.2× 52 0.8× 33 0.7× 46 915
E Torchiana Italy 8 281 1.4× 53 0.5× 40 0.5× 83 1.2× 46 1.0× 9 467
J.E. Castillo Guerra Spain 4 313 1.6× 29 0.3× 87 1.1× 94 1.4× 38 0.8× 4 444
Marco Casasco Italy 13 159 0.8× 79 0.7× 21 0.3× 48 0.7× 10 0.2× 44 503
Michael P. O’Quinn United States 11 419 2.1× 30 0.3× 152 2.0× 32 0.5× 154 3.3× 16 688
Emilia Manole Romania 12 580 2.9× 52 0.5× 35 0.5× 107 1.6× 95 2.1× 35 909

Countries citing papers authored by Grace Yoon

Since Specialization
Citations

This map shows the geographic impact of Grace Yoon's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Grace Yoon with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Grace Yoon more than expected).

Fields of papers citing papers by Grace Yoon

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Grace Yoon. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Grace Yoon. The network helps show where Grace Yoon may publish in the future.

Co-authorship network of co-authors of Grace Yoon

This figure shows the co-authorship network connecting the top 25 collaborators of Grace Yoon. A scholar is included among the top collaborators of Grace Yoon based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Grace Yoon. Grace Yoon is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Yoon, Grace, et al.. (2025). Identification of CXCL8, IL1A, and IL1B as Hub Genes of Therapeutic Resistance in Glioblastoma Multiforme via Bioinformatics Analysis. Cancer Genomics & Proteomics. 22(5). 791–808. 1 indexed citations
2.
Blaser, Susan, et al.. (2025). Child Neurology: Severe GMPPB -Related Congenital Muscular Dystrophy With Rapidly Progressive Encephalopathy Leading to Infantile Death. Neurology. 104(3). e210300–e210300. 1 indexed citations
3.
Nguyen, Tan, Grace Yoon, Martine Tétreault, et al.. (2025). Biallelic SIDT2 loss-of-function in a child with cerebellar ataxia and lysosomal dysfunction mimics impairment of SIDT2 in mice. Journal of Medical Genetics. 62(9). 592–599. 1 indexed citations
4.
Khan, Debjit, Iyappan Ramachandiran, K.I. Vasu, et al.. (2024). Homozygous EPRS1 missense variant causing hypomyelinating leukodystrophy-15 alters variant-distal mRNA m6A site accessibility. Nature Communications. 15(1). 4284–4284. 2 indexed citations
5.
Amburgey, Kimberly, Kyoko E. Yuki, Lianna Kyriakopoulou, et al.. (2024). A novel deep intronic variant in LAMA2 identified by RNA sequencing. Neuromuscular Disorders. 39. 19–23.
6.
Mroczek, Magdalena, Cheryl Longman, Maria Elena Farrugia, et al.. (2022). FXR1-related congenital myopathy: expansion of the clinical and genetic spectrum. Journal of Medical Genetics. 59(11). 1069–1074. 3 indexed citations
7.
Ding, Yu‐Shin, Jiacheng Wang, Vinay Kumar, et al.. (2022). Evidence For Cannabidiol Modulation of Serotonergic Transmission in a Model of Osteoarthritis via in vivo PET Imaging and Behavioral Assessment. International Journal of Innovative Research in Medical Science. 7(6). 254–271. 2 indexed citations
8.
Ngo, Kathie J., John Provias, Steven K. Baker, et al.. (2021). De novo pathogenic variant in SETX causes a rapidly progressive neurodegenerative disorder of early childhood-onset with severe axonal polyneuropathy. Acta Neuropathologica Communications. 9(1). 194–194. 5 indexed citations
9.
Davidson, Laurie A., Martha E. Hensel, Grace Yoon, et al.. (2021). Loss of Aryl Hydrocarbon Receptor Promotes Colon Tumorigenesis in ApcS580/+; KrasG12D/+ Mice. Molecular Cancer Research. 19(5). 771–783. 32 indexed citations
10.
Abbasi, Sepideh, Sarthak Sinha, Elodie Labit, et al.. (2021). Distinct Regulatory Programs Control the Latent Regenerative Potential of Dermal Fibroblasts during Wound Healing. Cell stem cell. 28(3). 581–583. 22 indexed citations
11.
Yoon, Grace, Laurie A. Davidson, Jennifer S. Goldsby, et al.. (2021). Exfoliated epithelial cell transcriptome reflects both small and large intestinal cell signatures in piglets. American Journal of Physiology-Gastrointestinal and Liver Physiology. 321(1). G41–G51. 6 indexed citations
12.
Abbasi, Sepideh, Sarthak Sinha, Elodie Labit, et al.. (2020). Distinct Regulatory Programs Control the Latent Regenerative Potential of Dermal Fibroblasts during Wound Healing. Cell stem cell. 27(3). 396–412.e6. 143 indexed citations
13.
Chong, Michael, Grace Yoon, Delia Susan‐Resiga, et al.. (2019). Hypolipidaemia among patients with PMM2-CDG is associated with low circulating PCSK9 levels: a case report followed by observational and experimental studies. Journal of Medical Genetics. 57(1). 11–17. 8 indexed citations
14.
Costain, Gregory, Rebekah Jobling, Susan Walker, et al.. (2018). Periodic reanalysis of whole-genome sequencing data enhances the diagnostic advantage over standard clinical genetic testing. European Journal of Human Genetics. 26(5). 740–744. 65 indexed citations
15.
Krishnan, Pradeep, et al.. (2017). Andermann Syndrome in a Pakistani Family Caused by a Novel Mutation in SLC12A6. Journal of Pediatric Neurology. 15(2). 90–94. 2 indexed citations
16.
Chénier, Sébastien, Grace Yoon, Bob Argiropoulos, et al.. (2014). CHD2 haploinsufficiency is associated with developmental delay, intellectual disability, epilepsy and neurobehavioural problems. Journal of Neurodevelopmental Disorders. 6(1). 9–9. 63 indexed citations
17.
Yoon, Grace, et al.. (2010). Cap myopathy caused by a mutation of the skeletal alpha-actin gene ACTA1. Neuromuscular Disorders. 20(4). 238–240. 40 indexed citations
18.
Westmacott, Robyn, et al.. (2010). Childhood-Onset CADASIL: Clinical, Imaging, and Neurocognitive Features. Journal of Child Neurology. 25(5). 623–627. 20 indexed citations
19.
Jegatheesan, Priya, Grace Yoon, Emil T. Lin, et al.. (2008). Increased Indomethacin Dosing for Persistent Patent Ductus Arteriosus in Preterm Infants: A Multicenter, Randomized, Controlled Trial. The Journal of Pediatrics. 153(2). 183–189. 39 indexed citations
20.
Frain, Laura, et al.. (1998). Usefulness of Serial Algorithms of Illness Severity as a Proxy for Impending Death in the NICU: Not Much ♦ 157. Pediatric Research. 43. 29–29. 1 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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