Chumei Li

4.1k total citations
36 papers, 1.7k citations indexed

About

Chumei Li is a scholar working on Genetics, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Chumei Li has authored 36 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 14 papers in Molecular Biology and 7 papers in Cellular and Molecular Neuroscience. Recurrent topics in Chumei Li's work include Genomic variations and chromosomal abnormalities (8 papers), Prenatal Screening and Diagnostics (5 papers) and Nerve injury and regeneration (5 papers). Chumei Li is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Prenatal Screening and Diagnostics (5 papers) and Nerve injury and regeneration (5 papers). Chumei Li collaborates with scholars based in Canada, United States and United Kingdom. Chumei Li's co-authors include John Roder, Bruce D. Trapp, Thomas O. Crawford, Virginia M.‐Y. Lee, Xinghua Yin, John W. Griffin, Xiaoqin Wang, Lorenz Meinel, Esther Wenk and David L. Kaplan and has published in prestigious journals such as Nature, Journal of Neuroscience and Advanced Functional Materials.

In The Last Decade

Chumei Li

34 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Chumei Li Canada 16 659 638 401 297 236 36 1.7k
Francesca E. Mackenzie United Kingdom 12 630 1.0× 650 1.0× 199 0.5× 206 0.7× 132 0.6× 14 1.5k
Ilaria Napoli United Kingdom 16 1.1k 1.7× 1.3k 2.0× 492 1.2× 504 1.7× 220 0.9× 19 2.6k
Sheng Yi China 31 1.2k 1.9× 912 1.4× 304 0.8× 265 0.9× 260 1.1× 95 2.6k
Rick I. Cohen United States 19 993 1.5× 407 0.6× 329 0.8× 227 0.8× 88 0.4× 32 1.6k
Ysander von Boxberg France 22 602 0.9× 813 1.3× 320 0.8× 122 0.4× 76 0.3× 36 1.5k
Tammy L. McGuire United States 25 922 1.4× 429 0.7× 543 1.4× 277 0.9× 82 0.3× 39 2.0k
William T. Hendriks Netherlands 16 614 0.9× 613 1.0× 226 0.6× 171 0.6× 49 0.2× 20 1.2k
Ana María Gonzalez United Kingdom 16 457 0.7× 442 0.7× 200 0.5× 99 0.3× 99 0.4× 34 1.2k
Vibhu Sahni United States 14 763 1.2× 555 0.9× 452 1.1× 85 0.3× 548 2.3× 16 1.7k
Serhiy Forostyak Czechia 18 498 0.8× 586 0.9× 193 0.5× 62 0.2× 167 0.7× 25 1.5k

Countries citing papers authored by Chumei Li

Since Specialization
Citations

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

Fields of papers citing papers by Chumei Li

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Chumei Li

This figure shows the co-authorship network connecting the top 25 collaborators of Chumei Li. A scholar is included among the top collaborators of Chumei Li 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 Chumei Li. Chumei Li 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.
Brady, Lauren, et al.. (2022). Further characterization of the 9q31 microdeletion phenotype; delineation of a common region of overlap containing ZNF462. Molecular Genetics & Genomic Medicine. 11(3). e2116–e2116. 5 indexed citations
2.
Li, Chumei & Anne Slavotinek. (2019). FREM1 Autosomal Recessive Disorders. Europe PMC (PubMed Central). 1 indexed citations
3.
4.
Ng, Bobby G., Kati J. Buckingham, Kimiyo Raymond, et al.. (2013). Mosaicism of the UDP-Galactose Transporter SLC35A2 Causes a Congenital Disorder of Glycosylation. The American Journal of Human Genetics. 92(4). 632–636. 95 indexed citations
5.
Mullegama, Sureni V., Christian R. Marshall, Anath C. Lionel, et al.. (2011). Severe intellectual disability and autistic features associated with microduplication 2q23.1. European Journal of Human Genetics. 20(4). 398–403. 27 indexed citations
6.
Goh, Elaine, et al.. (2010). The Roberts syndrome/SC phocomelia spectrum—A case report of an adult with review of the literature. American Journal of Medical Genetics Part A. 152A(2). 472–478. 29 indexed citations
7.
Nagamani, Sandesh C. Sreenath, Ayelet Erez, Joseph Shen, et al.. (2009). Clinical spectrum associated with recurrent genomic rearrangements in chromosome 17q12. European Journal of Human Genetics. 18(3). 278–284. 103 indexed citations
8.
Li, Chumei. (2009). A new syndrome of ankyloglossia and ulnar ray defects in a Newfoundland kindred. Clinical Dysmorphology. 18(3). 158–159. 1 indexed citations
9.
Li, Chumei & Sarah D. McDonald. (2008). Increased Nuchal Translucency and Other Ultrasound Findings in a Case of Simpson-Golabi-Behmel Syndrome. Fetal Diagnosis and Therapy. 25(2). 211–215. 18 indexed citations
10.
Li, Chumei, Elena Di Pierro, Valentina Brancaleoni, Maria Domenica Cappellini, & David P. Steensma. (2008). A novel large deletion and three polymorphisms in the FECH gene associated with erythropoietic protoporphyria. Clinical Chemistry and Laboratory Medicine (CCLM). 47(1). 44–6. 5 indexed citations
11.
Li, Chumei, John R. Mernagh, & Jacqueline M. Bourgeois. (2008). Novel craniofacial and extracraniofacial findings in a case of Treacher Collins syndrome with a pathogenic mutation and a missense variant in the TCOF1 gene. Clinical Dysmorphology. 18(1). 63–66. 7 indexed citations
12.
Li, Chumei, Sandra L. Marles, Cheryl R. Greenberg, et al.. (2007). Manitoba oculotrichoanal (MOTA) syndrome: Report of eight new cases. American Journal of Medical Genetics Part A. 143A(8). 853–857. 16 indexed citations
13.
Wang, Changguang, Jianbin Hu, Paul S. Bernstein, et al.. (2007). Intravitreal Injection of Triamcinolone Acetonide for Macular Edema Due to Retinitis Pigmentosa and Other Retinal Diseases. Advances in experimental medicine and biology. 572. 309–314. 8 indexed citations
14.
Langlois, Sylvie, R. Douglas Wilson, Victoria M. Allen, et al.. (2006). Carrier Screening for Genetic Disorders in Individuals of Ashkenazi Jewish Descent. Journal of Obstetrics and Gynaecology Canada. 28(4). 324–332. 14 indexed citations
15.
Yin, Xinghua, Thomas O. Crawford, John W. Griffin, et al.. (1998). Myelin-Associated Glycoprotein Is a Myelin Signal that Modulates the Caliber of Myelinated Axons. Journal of Neuroscience. 18(6). 1953–1962. 381 indexed citations
16.
Messing, Albee, Shing Yan Chiu, S. Rock Levinson, et al.. (1997). Sodium channel distribution in axons of hypomyelinated and MAG null mutant mice. Journal of Neuroscience Research. 50(2). 321–336. 43 indexed citations
17.
Messing, Albee, Shing Yan Chiu, S. Rock Levinson, et al.. (1997). Sodium channel distribution in axons of hypomyelinated and MAG null mutant mice. Journal of Neuroscience Research. 50(2). 321–336. 3 indexed citations
18.
Ng, Wai Pui, et al.. (1996). Myelin from MAG- deficient mice is a strong inhibitor of neurite outgrowth. Neuroreport. 7(4). 861–864. 12 indexed citations
19.
Li, Maria, Annemarie Shibata, Chumei Li, et al.. (1996). Myelin-associated glycoprotein inhibits neurite/axon growth and causes growth cone collapse. Journal of Neuroscience Research. 46(4). 404–414. 155 indexed citations
20.
Li, Chumei, Michael B. Tropak, Robert Gerlai, et al.. (1994). Myelination in the absence of myelin-associated glycoprotein. Nature. 369(6483). 747–750. 295 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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