Bruce Nmezi

468 total citations
10 papers, 289 citations indexed

About

Bruce Nmezi is a scholar working on Molecular Biology, Cell Biology and Nutrition and Dietetics. According to data from OpenAlex, Bruce Nmezi has authored 10 papers receiving a total of 289 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 3 papers in Cell Biology and 2 papers in Nutrition and Dietetics. Recurrent topics in Bruce Nmezi's work include RNA Research and Splicing (7 papers), Nuclear Structure and Function (5 papers) and Genomics and Chromatin Dynamics (3 papers). Bruce Nmezi is often cited by papers focused on RNA Research and Splicing (7 papers), Nuclear Structure and Function (5 papers) and Genomics and Chromatin Dynamics (3 papers). Bruce Nmezi collaborates with scholars based in United States, Netherlands and China. Bruce Nmezi's co-authors include Quasar Saleem Padiath, Guillermo Rodríguez Bey, Yiping Tu, Rao Fu, Jianquan Xu, Mara Sullivan, Natalie Chen, Hongqiang Ma, Yang Liu and Kris Noel Dahl and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Neuroscience and Brain.

In The Last Decade

Bruce Nmezi

10 papers receiving 288 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Bruce Nmezi United States	7	237	77	36	27	26	10	289
Francesca W. van Tartwijk United Kingdom	7	173 0.7×	60 0.8×	23 0.6×	48 1.8×	13 0.5×	8	262
Guillermo Rodríguez Bey United States	7	211 0.9×	58 0.8×	28 0.8×	37 1.4×	12 0.5×	9	266
Debamitra Das United States	10	191 0.8×	41 0.5×	23 0.6×	26 1.0×	29 1.1×	13	253
Barbara Viljetić Croatia	9	219 0.9×	31 0.4×	42 1.2×	32 1.2×	31 1.2×	19	294
Marta Guerrero‐Valero Spain	8	238 1.0×	144 1.9×	37 1.0×	79 2.9×	17 0.7×	9	321
Hannah C. Webber United States	10	236 1.0×	71 0.9×	10 0.3×	26 1.0×	25 1.0×	14	381
Jiaqi Yao China	6	246 1.0×	26 0.3×	35 1.0×	51 1.9×	21 0.8×	15	326
Nicholas Tolman United States	8	129 0.5×	35 0.5×	22 0.6×	27 1.0×	31 1.2×	11	289
Jisoo S. Han United States	6	176 0.7×	162 2.1×	50 1.4×	34 1.3×	17 0.7×	7	266
Julia Guez-Haddad Israel	10	183 0.8×	98 1.3×	24 0.7×	78 2.9×	19 0.7×	11	331

Countries citing papers authored by Bruce Nmezi

Since Specialization

Citations

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

Fields of papers citing papers by Bruce Nmezi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bruce Nmezi

This figure shows the co-authorship network connecting the top 25 collaborators of Bruce Nmezi. A scholar is included among the top collaborators of Bruce Nmezi 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 Bruce Nmezi. Bruce Nmezi is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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10 of 10 papers shown

Vollmer, Laura L., Fang Liu, Bruce Nmezi, et al.. (2025). A high throughput, high content screen for non-toxic small molecules that reduce levels of the nuclear lamina protein, Lamin B1. Scientific Reports. 15(1). 7314–7314. 1 indexed citations

Bey, Guillermo Rodríguez, Bruce Nmezi, Fang Liu, et al.. (2022). Variants in the zinc transporterTMEM163cause a hypomyelinating leukodystrophy. Brain. 145(12). 4202–4209. 6 indexed citations

Liao, Jun, Keith A. Coffman, Joseph Locker, et al.. (2021). Deletion of conserved non‐coding sequences downstream from NKX2‐1: A novel disease‐causing mechanism for benign hereditary chorea. Molecular Genetics & Genomic Medicine. 9(4). e1647–e1647. 4 indexed citations

Nmezi, Bruce, Laura L. Vollmer, Tong Ying Shun, et al.. (2020). Development and Optimization of a High-Content Analysis Platform to Identify Suppressors of Lamin B1 Overexpression as a Therapeutic Strategy for Autosomal Dominant Leukodystrophy. SLAS DISCOVERY. 25(8). 939–949. 4 indexed citations

Nmezi, Bruce, Jianquan Xu, Rao Fu, et al.. (2019). Concentric organization of A- and B-type lamins predicts their distinct roles in the spatial organization and stability of the nuclear lamina. Proceedings of the National Academy of Sciences. 116(10). 4307–4315. 103 indexed citations

Nmezi, Bruce, Elisa Giorgio, Raili Raininko, et al.. (2019). Genomic deletions upstream of lamin B1 lead to atypical autosomal dominant leukodystrophy. Neurology Genetics. 5(1). e305–e305. 15 indexed citations

Curiel, Julian, Guillermo Rodríguez Bey, Asako Takanohashi, et al.. (2017). TUBB4A mutations result in specific neuronal and oligodendrocytic defects that closely match clinically distinct phenotypes. Human Molecular Genetics. 26(22). 4506–4518. 53 indexed citations

Nmezi, Bruce, et al.. (2015). CAPOS syndrome and hemiplegic migraine in a novel pedigree with the specific ATP1A3 mutation. Journal of the Neurological Sciences. 358(1-2). 453–456. 21 indexed citations

Rolyan, Harshvardhan, Yulia Y. Tyurina, Maria Hernandez, et al.. (2015). Defects of Lipid Synthesis Are Linked to the Age-Dependent Demyelination Caused by Lamin B1 Overexpression. Journal of Neuroscience. 35(34). 12002–12017. 52 indexed citations

10.

Mancini, Cecilia, Yiran Guo, Yulan Chen, et al.. (2014). Adult-onset autosomal recessive ataxia associated with neuronal ceroid lipofuscinosis type 5 gene (CLN5) mutations. Journal of Neurology. 262(1). 173–178. 30 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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