Grace Yoon

5.0k total citations
97 papers, 2.1k citations indexed

About

Grace Yoon is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Grace Yoon has authored 97 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 67 papers in Molecular Biology, 41 papers in Cellular and Molecular Neuroscience and 24 papers in Genetics. Recurrent topics in Grace Yoon's work include Mitochondrial Function and Pathology (32 papers), Genetic Neurodegenerative Diseases (29 papers) and Neurological diseases and metabolism (12 papers). Grace Yoon is often cited by papers focused on Mitochondrial Function and Pathology (32 papers), Genetic Neurodegenerative Diseases (29 papers) and Neurological diseases and metabolism (12 papers). Grace Yoon collaborates with scholars based in Canada, United States and United Kingdom. Grace Yoon's co-authors include Susan Blasér, Louis J. Ptáček, Ying‐Hui Fu, Keith W. Caldecott, Laura McAdam, Rudaina Banihani, Katherine A. Rauen, Sharon Smile, Annie Dupuis and Almundher Al‐Maawali and has published in prestigious journals such as Nature, Nature Communications and The EMBO Journal.

In The Last Decade

Grace Yoon

92 papers receiving 2.0k 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 25 1.4k 632 364 228 212 97 2.1k
Kazuhiro Haginoya Japan 28 1.2k 0.9× 352 0.6× 417 1.1× 179 0.8× 230 1.1× 159 2.7k
Hirofumi Komaki Japan 28 1.7k 1.3× 363 0.6× 276 0.8× 286 1.3× 223 1.1× 180 2.5k
Sabrina W. Yum United States 25 880 0.6× 543 0.9× 138 0.4× 107 0.5× 297 1.4× 63 1.8k
Ki Joong Kim South Korea 28 892 0.6× 396 0.6× 407 1.1× 87 0.4× 490 2.3× 199 3.0k
Manuela Corti United States 19 995 0.7× 242 0.4× 693 1.9× 138 0.6× 159 0.8× 48 1.8k
Gunnar Buyse Belgium 28 2.2k 1.6× 643 1.0× 359 1.0× 578 2.5× 149 0.7× 89 3.2k
Byung Chan Lim South Korea 23 750 0.5× 244 0.4× 436 1.2× 109 0.5× 244 1.2× 165 1.8k
Maja von der Hagen Germany 22 651 0.5× 249 0.4× 215 0.6× 154 0.7× 417 2.0× 80 1.5k
Salmo Raskin Brazil 28 1.5k 1.0× 1.1k 1.7× 578 1.6× 63 0.3× 670 3.2× 147 2.8k
Paolo Balestri Italy 30 944 0.7× 383 0.6× 835 2.3× 85 0.4× 268 1.3× 109 2.8k

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.
Branson, Helen M., et al.. (2024). Imaging Findings and MRI Patterns in a Cohort of 18q Chromosomal Abnormalities. American Journal of Neuroradiology. 45(10). 1578–1585.
2.
Lynch, David R., S. H. Subramony, Kimberly Y. Lin, et al.. (2024). Characterization of Cardiac-Onset Initial Presentation in Friedreich Ataxia. Pediatric Cardiology. 46(2). 379–382. 2 indexed citations
3.
Saffari, Afshin, M. L. ZIEGLER, Catherine Jordan, et al.. (2023). Plasma Neurofilament Light Chain Is Elevated in Adaptor Protein Complex 4‐Related Hereditary Spastic Paraplegia. Movement Disorders. 38(9). 1742–1750. 6 indexed citations
4.
Cihlářová, Zuzana, Jan Kubovčiak, Margarita Sobol, et al.. (2022). BRAT1 links Integrator and defective RNA processing with neurodegeneration. Nature Communications. 13(1). 5026–5026. 15 indexed citations
5.
Estiar, Mehrdad A., Simon Veyron, Kheireddin Mufti, et al.. (2022). Genetic, structural and clinical analysis of spastic paraplegia 4. Parkinsonism & Related Disorders. 98. 62–69. 14 indexed citations
6.
Rummey, Christian, Louise A. Corben, Martin B. Delatycki, et al.. (2022). Natural History of Friedreich Ataxia. Neurology. 99(14). e1499–e1510. 33 indexed citations
7.
Yoon, Grace, Mehrdad A. Estiar, Simon Veyron, et al.. (2021). GCH1 mutations in hereditary spastic paraplegia. Clinical Genetics. 100(1). 51–58. 5 indexed citations
8.
Estiar, Mehrdad A., Eric Yu, Jay P. Ross, et al.. (2021). Evidence for Non‐Mendelian Inheritance in Spastic Paraplegia 7. Movement Disorders. 36(7). 1664–1675. 14 indexed citations
9.
Rummey, Christian, John M. Flynn, Louise A. Corben, et al.. (2021). Scoliosis in Friedreich's ataxia: longitudinal characterization in a large heterogeneous cohort. Annals of Clinical and Translational Neurology. 8(6). 1239–1250. 17 indexed citations
10.
Pinard, Maxime, Constance Smith‐Hicks, Trevor L. Hoffman, et al.. (2021). De novo variants in POLR3B cause ataxia, spasticity, and demyelinating neuropathy. The American Journal of Human Genetics. 108(1). 186–193. 16 indexed citations
11.
Davidson, Laurie A., Yang‐Yi Fan, Jennifer S. Goldsby, et al.. (2020). Loss of aryl hydrocarbon receptor potentiates FoxM1 signaling to enhance self‐renewal of colonic stem and progenitor cells. The EMBO Journal. 39(19). e104319–e104319. 33 indexed citations
12.
Sparks, Holly D., Nicole L. Rosin, Grace Yoon, et al.. (2019). Adult Human Dermal Progenitor Cell Transplantation Modulates the Functional Outcome of Split-Thickness Skin Xenografts. Stem Cell Reports. 13(6). 1068–1082. 11 indexed citations
13.
Cihlářová, Zuzana, Martine Tétreault, Lauren MacNeil, et al.. (2019). Homozygous pathogenic variant in BRAT1 associated with nonprogressive cerebellar ataxia. Neurology Genetics. 5(5). e359–e359. 11 indexed citations
14.
Léveillé, Etienne, Hernán Gonorazky, Marie‐France Rioux, et al.. (2018). Triple A syndrome presenting as complicated hereditary spastic paraplegia. Molecular Genetics & Genomic Medicine. 6(6). 1134–1139. 8 indexed citations
15.
Yoon, Grace & Keith W. Caldecott. (2018). Nonsyndromic cerebellar ataxias associated with disorders of DNA single-strand break repair. Handbook of clinical neurology. 155. 105–115. 29 indexed citations
16.
Wang, Ben X., Stephanie A. Grover, Pekka Kannus, et al.. (2017). Interferon-Stimulated Gene Expression as a Preferred Biomarker for Disease Activity in Aicardi–Goutières Syndrome. Journal of Interferon & Cytokine Research. 37(4). 147–152. 7 indexed citations
17.
Lemaire, Mathieu, Steven P. Miller, Christoph Licht, et al.. (2017). Neonatal stroke and haematuria: Questions. Pediatric Nephrology. 33(5). 805–806. 1 indexed citations
18.
Stray‐Pedersen, Asbjørg, Jan-Maarten Cobben, Trine Prescott, et al.. (2015). Biallelic Mutations in UNC80 Cause Persistent Hypotonia, Encephalopathy, Growth Retardation, and Severe Intellectual Disability. The American Journal of Human Genetics. 98(1). 202–209. 35 indexed citations
19.
Goh, Elaine, César P. Canales, Phillip Ruiz, et al.. (2012). Definition of a critical genetic interval related to kidney abnormalities in the Potocki–Lupski syndrome. American Journal of Medical Genetics Part A. 158A(7). 1579–1588. 7 indexed citations
20.
Yoon, Grace, et al.. (2007). Neurological complications of cardio‐facio‐cutaneous syndrome. Developmental Medicine & Child Neurology. 49(12). 894–899. 96 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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