Weiyi Mu

1.2k total citations
28 papers, 346 citations indexed

About

Weiyi Mu is a scholar working on Genetics, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Weiyi Mu has authored 28 papers receiving a total of 346 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 12 papers in Molecular Biology and 7 papers in Cellular and Molecular Neuroscience. Recurrent topics in Weiyi Mu's work include Genomics and Rare Diseases (7 papers), Genetic Neurodegenerative Diseases (7 papers) and Mitochondrial Function and Pathology (5 papers). Weiyi Mu is often cited by papers focused on Genomics and Rare Diseases (7 papers), Genetic Neurodegenerative Diseases (7 papers) and Mitochondrial Function and Pathology (5 papers). Weiyi Mu collaborates with scholars based in United States, Brazil and Vietnam. Weiyi Mu's co-authors include Joann Bodurtha, Amanda L. Bergner, Jennifer Malinowski, Louise Bier, David Gloss, Annapurna Poduri, Beth Rosen Sheidley, Mélanie Viltard, Kai M. Schmidt‐Ott and Xia Chen and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and Epilepsia.

In The Last Decade

Weiyi Mu

23 papers receiving 342 citations

Peers

Weiyi Mu
Rebecca McClellan United States
Srinivasan Muthuswamy India
Tadashi Shiohama Japan
Kotaro Yuge Japan
Riccardo De Marco Italy
M. A. Mori Spain
Aude Charollais France
Mary O’Driscoll United Kingdom
Chloe Stutterd Australia
Marie Hully France
Rebecca McClellan United States
Weiyi Mu
Citations per year, relative to Weiyi Mu Weiyi Mu (= 1×) peers Rebecca McClellan

Countries citing papers authored by Weiyi Mu

Since Specialization
Citations

This map shows the geographic impact of Weiyi Mu'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 Weiyi Mu with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Weiyi Mu more than expected).

Fields of papers citing papers by Weiyi Mu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Weiyi Mu. 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 Weiyi Mu. The network helps show where Weiyi Mu may publish in the future.

Co-authorship network of co-authors of Weiyi Mu

This figure shows the co-authorship network connecting the top 25 collaborators of Weiyi Mu. A scholar is included among the top collaborators of Weiyi Mu 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 Weiyi Mu. Weiyi Mu 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.
Mu, Weiyi, et al.. (2026). Clinicopathologic Correlates: Progressive Downbeat Nystagmus in Spinocerebellar Ataxia Type 27B. Journal of Neuro-Ophthalmology. 46(1). 113–116.
2.
Jenny, Kim, Kristiana Salmon, Ashley Crook, et al.. (2025). The Importance of Offering Genetic Counseling and Testing to All Persons Diagnosed With Frontotemporal Degeneration Spectrum Disorders. Neurology. 105(3). e213814–e213814.
3.
Srinivasan, Sharan R., et al.. (2025). Practice Recommendations for Genetic Testing of Ataxias. Annals of Clinical and Translational Neurology. 12(12). 2398–2409. 1 indexed citations
4.
Gold, Daniel R., et al.. (2025). Causes of Diplopia, Strabismus Patterns, and Ocular Motor Features in Patients With Spinocerebellar Ataxia Type 27B. Journal of Neuro-Ophthalmology. 46(1). 73–80.
5.
Gold, Daniel R., et al.. (2025). Ocular Motor and Vestibular Profile in Spinocerebellar Ataxia Type 27B: Toward a Practical Bedside Diagnostic Framework. The Cerebellum. 24(5). 149–149. 1 indexed citations
6.
Gold, Daniel R., Jennifer L. Millar, Michael C. Schubert, et al.. (2025). Video head impulse test differentiates RFC1-CANVAS, FGF14-SCA27B, and idiopathic late-onset cerebellar ataxias. Journal of Neurology. 272(10). 679–679.
7.
Owczarzak, Jill, Weiyi Mu, Katheryn A Q Cousins, et al.. (2023). The lived experience of reconstructing identity in response to genetic risk of frontotemporal degeneration and amyotrophic lateral sclerosis. Journal of Genetic Counseling. 33(3). 515–527. 8 indexed citations
8.
Harrison, N. A., Maria A. Schmidt, Halima Amjad, et al.. (2023). A case of familial frontotemporal dementia caused by a progranulin gene mutation. Clinical Parkinsonism & Related Disorders. 9. 100213–100213. 1 indexed citations
9.
Mu, Weiyi, Elisabeth McCarty Wood, Brianna Morgan, et al.. (2022). Evaluation of an educational conference for persons affected by hereditary frontotemporal degeneration and amyotrophic lateral sclerosis. SHILAP Revista de lepidopterología. 2. 100108–100108. 2 indexed citations
10.
11.
Mu, Weiyi, et al.. (2022). The Genetic Testing Experience of Individuals with Parkinson's Disease. Movement Disorders Clinical Practice. 10(2). 248–257. 2 indexed citations
12.
Sheidley, Beth Rosen, Jennifer Malinowski, Amanda L. Bergner, et al.. (2021). Genetic testing for the epilepsies: A systematic review. Epilepsia. 63(2). 375–387. 67 indexed citations
13.
Lambe, Jeffrey, et al.. (2020). Relapsing–remitting clinical course expands the phenotype of Aicardi–Goutières syndrome. Annals of Clinical and Translational Neurology. 7(2). 254–258. 2 indexed citations
14.
Mu, Weiyi, et al.. (2019). A structured genetics rotation for pediatric residents: an important educational opportunity. Genetics in Medicine. 22(4). 793–796. 11 indexed citations
15.
Mu, Weiyi, Nicoline Schiess, Jennifer Orthmann‐Murphy, & Ayman W. El‐Hattab. (2019). The utility of whole exome sequencing in diagnosing neurological disorders in adults from a highly consanguineous population. Journal of Neurogenetics. 33(1). 21–26. 8 indexed citations
16.
Mu, Weiyi, et al.. (2019). Intracranial calcifications and dystonia associated with a novel deletion of chromosome 8p11.2 encompassing SLC20A2 and THAP1. BMJ Case Reports. 12(5). e228782–e228782. 9 indexed citations
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Fleming, Leah, Monica E. Lemmon, Weiyi Mu, et al.. (2015). Genotype–phenotype correlation of congenital anomalies in multiple congenital anomalies hypotonia seizures syndrome (MCAHS1)/PIGN‐related epilepsy. American Journal of Medical Genetics Part A. 170(1). 77–86. 34 indexed citations
20.
Diehl, Adam, Weiyi Mu, Denise Batista, & Meral Gunay‐Aygun. (2015). An atypical 0.73 MB microduplication of 22q11.21 and a novel SALL4 missense mutation associated with thumb agenesis and radioulnar synostosis. American Journal of Medical Genetics Part A. 167(7). 1644–1649. 8 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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