Nicholas Marsh‐Armstrong

4.6k total citations · 1 hit paper
40 papers, 3.3k citations indexed

About

Nicholas Marsh‐Armstrong is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Ophthalmology. According to data from OpenAlex, Nicholas Marsh‐Armstrong has authored 40 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 15 papers in Cellular and Molecular Neuroscience and 12 papers in Ophthalmology. Recurrent topics in Nicholas Marsh‐Armstrong's work include Retinal Development and Disorders (16 papers), Glaucoma and retinal disorders (10 papers) and Retinal Diseases and Treatments (7 papers). Nicholas Marsh‐Armstrong is often cited by papers focused on Retinal Development and Disorders (16 papers), Glaucoma and retinal disorders (10 papers) and Retinal Diseases and Treatments (7 papers). Nicholas Marsh‐Armstrong collaborates with scholars based in United States, United Kingdom and Canada. Nicholas Marsh‐Armstrong's co-authors include Donald D. Brown, Haochu Huang, Ericka Oglesby, Ileana Soto, Monica L. Vetter, Denise M. Inman, Michael R. Steele, Chung-ha O. Davis, David J. Calkins and Brian P. Buckingham and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Neuron.

In The Last Decade

Nicholas Marsh‐Armstrong

39 papers receiving 3.3k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Transcellular degradation of axonal mitochondria

2014 513 citations Chung-ha O. Davis, Keun-Young Kim et al. Proceedings of the National Academy of Sciences profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Nicholas Marsh‐Armstrong United States	26	2.0k	1.1k	728	608	339	40	3.3k
Marta Agudo‐Barriuso Spain	42	3.2k 1.6×	2.4k 2.2×	1.1k 1.6×	643 1.1×	204 0.6×	124	4.6k
Martin L. Katz United States	38	2.7k 1.4×	1.2k 1.1×	569 0.8×	685 1.1×	313 0.9×	151	4.7k
Concepción Lillo United States	30	2.9k 1.5×	485 0.5×	972 1.3×	588 1.0×	548 1.6×	72	4.5k
Andy J. Fischer United States	46	4.2k 2.1×	1.4k 1.3×	1.5k 2.0×	886 1.5×	137 0.4×	105	5.5k
Donald G. Puro United States	41	2.3k 1.2×	824 0.8×	1.6k 2.2×	816 1.3×	168 0.5×	87	4.0k
Abigail S. Hackam United States	34	3.1k 1.6×	479 0.4×	2.3k 3.1×	199 0.3×	626 1.8×	76	4.2k
Ning Tian China	29	1.7k 0.9×	398 0.4×	1.4k 2.0×	260 0.4×	358 1.1×	100	2.9k
Francisco M. Nadal‐Nicolás Spain	31	2.1k 1.1×	1.7k 1.6×	733 1.0×	411 0.7×	161 0.5×	65	3.0k
Steven Nusinowitz United States	38	4.1k 2.1×	2.2k 2.1×	1.3k 1.8×	286 0.5×	84 0.2×	99	5.2k
Tudor C. Badea United States	30	2.4k 1.2×	434 0.4×	1.6k 2.2×	406 0.7×	73 0.2×	76	4.0k

Countries citing papers authored by Nicholas Marsh‐Armstrong

Since Specialization

Citations

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

Fields of papers citing papers by Nicholas Marsh‐Armstrong

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Nicholas Marsh‐Armstrong. 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 Nicholas Marsh‐Armstrong. The network helps show where Nicholas Marsh‐Armstrong may publish in the future.

Co-authorship network of co-authors of Nicholas Marsh‐Armstrong

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

All Works

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20 of 20 papers shown

Davis, Chung-ha O., Aaron M. Muscarella, Viraj Deshpande, et al.. (2025). Glaucoma-associated Optineurin mutations increase transcellular degradation of mitochondria in a vertebrate optic nerve. eLife. 14.

Zhang, Pengfei, Yanhong Ma, Guozhen Wang, et al.. (2023). Evaluating the performance of OCT in assessing static and potential dynamic properties of the retinal ganglion cells and nerve fiber bundles in the living mouse eye. Biomedical Optics Express. 14(12). 6422–6422. 2 indexed citations

Marsh‐Armstrong, Nicholas, et al.. (2023). Dual leucine zipper kinase is necessary for retinal ganglion cell axonal regeneration in Xenopus laevis. PNAS Nexus. 2(5). pgad109–pgad109. 3 indexed citations

Liu, Yin, et al.. (2021). The basic science of optic nerve regeneration. Annals of Translational Medicine. 9(15). 1276–1276. 23 indexed citations

Yazdanyar, Amirfarbod, et al.. (2021). Analysis of the retinal capillary plexus layers in a murine model with diabetic retinopathy: effect of intravitreal injection of human CD34+ bone marrow stem cells. Annals of Translational Medicine. 9(15). 1273–1273. 8 indexed citations

Yazdanyar, Amirfarbod, Pengfei Zhang, Zeljka Smit‐McBride, et al.. (2019). Effects of intravitreal injection of human CD34+ bone marrow stem cells in a murine model of diabetic retinopathy. Experimental Eye Research. 190. 107865–107865. 23 indexed citations

Zhou, Yi, Allison Bond, Yunhua Zhu, et al.. (2018). Autocrine Mfge8 Signaling Prevents Developmental Exhaustion of the Adult Neural Stem Cell Pool. Cell stem cell. 23(3). 444–452.e4. 77 indexed citations

Jang, Geeng-Fu, Lei Zhang, Juan Reynaud, et al.. (2018). Alterations in Optic Nerve Head (ONH) Endoplasmic Reticulum (ER) Stress Response Proteins in Non-Human Primate (NHP) Early Experimental Glaucoma (EG).. Investigative Ophthalmology & Visual Science. 59(9). 3514–3514. 2 indexed citations

Xu, Leyan, Jiwon Ryu, Judy V. Nguyen, et al.. (2015). Evidence for accelerated tauopathy in the retina of transgenic P301S tau mice exposed to repetitive mild traumatic brain injury. Experimental Neurology. 273. 168–176. 28 indexed citations

10.

Davis, Chung-ha O., Keun-Young Kim, Eric A. Bushong, et al.. (2014). Transcellular degradation of axonal mitochondria. Proceedings of the National Academy of Sciences. 111(26). 9633–9638. 513 indexed citations breakdown →

11.

Peters, Owen M., Steven J. Millership, Tatyana A. Shelkovnikova, et al.. (2012). Selective pattern of motor system damage in gamma-synuclein transgenic mice mirrors the respective pathology in amyotrophic lateral sclerosis. Neurobiology of Disease. 48(1). 124–131. 29 indexed citations

12.

Lee, Ryan, Elizabeth Mills, Neil Schwartz, et al.. (2010). Neurodevelopmental effects of chronic exposure to elevated levels of pro-inflammatory cytokines in a developing visual system. Neural Development. 5(1). 2–2. 51 indexed citations

13.

Soto, Ileana, et al.. (2010). Glaucomatous optic nerve injury involves early astrocyte reactivity and late oligodendrocyte loss. Glia. 58(7). 780–789. 115 indexed citations

14.

Suli, Arminda, Yi Pan, Nicholas Marsh‐Armstrong, et al.. (2008). Temporal regulation of Ath5 gene expression during eye development. Developmental Biology. 326(2). 471–481. 26 indexed citations

15.

Buckingham, Brian P., Denise M. Inman, Wendi S. Lambert, et al.. (2008). Progressive Ganglion Cell Degeneration Precedes Neuronal Loss in a Mouse Model of Glaucoma. Journal of Neuroscience. 28(11). 2735–2744. 352 indexed citations

16.

Soto, Ileana, Ericka Oglesby, Brian P. Buckingham, et al.. (2008). Retinal Ganglion Cells Downregulate Gene Expression and Lose Their Axons within the Optic Nerve Head in a Mouse Glaucoma Model. Journal of Neuroscience. 28(2). 548–561. 232 indexed citations

17.

Luo, Wenqin, Nicholas Marsh‐Armstrong, Amir Rattner, & Jeremy Nathans. (2004). An Outer Segment Localization Signal at the C Terminus of the Photoreceptor-Specific Retinol Dehydrogenase. Journal of Neuroscience. 24(11). 2623–2632. 49 indexed citations

18.

Kefalov, Vladimir J., Yingbin Fu, Nicholas Marsh‐Armstrong, & King‐Wai Yau. (2003). Role of visual pigment properties in rod and cone phototransduction. Nature. 425(6957). 526–531. 107 indexed citations

19.

Marsh‐Armstrong, Nicholas, et al.. (1999). Asymmetric Growth and Development of the Xenopus laevis Retina during Metamorphosis Is Controlled by Type III Deiodinase. Neuron. 24(4). 871–878. 130 indexed citations

20.

Marsh‐Armstrong, Nicholas, Peter McCaffery, George A. Hyatt, et al.. (1995). Retinoic acid in the anteroposterior patterning of the zebrafish trunk. Development Genes and Evolution. 205(3-4). 103–113. 22 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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