Noah M. Walton

1.9k total citations
19 papers, 1.4k citations indexed

About

Noah M. Walton is a scholar working on Molecular Biology, Developmental Neuroscience and Genetics. According to data from OpenAlex, Noah M. Walton has authored 19 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 13 papers in Developmental Neuroscience and 4 papers in Genetics. Recurrent topics in Noah M. Walton's work include Neurogenesis and neuroplasticity mechanisms (13 papers), Pluripotent Stem Cells Research (5 papers) and Congenital heart defects research (3 papers). Noah M. Walton is often cited by papers focused on Neurogenesis and neuroplasticity mechanisms (13 papers), Pluripotent Stem Cells Research (5 papers) and Congenital heart defects research (3 papers). Noah M. Walton collaborates with scholars based in United States, Japan and China. Noah M. Walton's co-authors include Dennis A. Steindler, Björn Scheffler, Mitsuyuki Matsumoto, Benjamin M. Sutter, Gregory P. Marshall, Eric D. Laywell, Lindsay H. Levkoff, Katsunori Tajinda, Carrie Heusner and Tsuyoshi Miyakawa and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Neuroscience and PLoS ONE.

In The Last Decade

Noah M. Walton

19 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Noah M. Walton United States 14 605 561 419 307 180 19 1.4k
Naoko Kaneko Japan 26 924 1.5× 758 1.4× 734 1.8× 477 1.6× 162 0.9× 44 2.2k
Philip J. Horner United States 19 815 1.3× 828 1.5× 714 1.7× 419 1.4× 143 0.8× 27 2.0k
Emanuele Cacci Italy 20 780 1.3× 640 1.1× 523 1.2× 615 2.0× 113 0.6× 37 1.7k
Richard Fairless Germany 23 315 0.5× 518 0.9× 597 1.4× 231 0.8× 102 0.6× 39 1.4k
Sonja Rakić United Kingdom 24 793 1.3× 662 1.2× 802 1.9× 239 0.8× 223 1.2× 27 1.7k
Jean‐Claude Platel United States 21 671 1.1× 676 1.2× 596 1.4× 236 0.8× 168 0.9× 34 1.4k
Fabienne Agasse Portugal 24 506 0.8× 654 1.2× 696 1.7× 333 1.1× 63 0.3× 37 1.7k
Jennifer Orthmann‐Murphy United States 12 458 0.8× 506 0.9× 341 0.8× 434 1.4× 143 0.8× 23 1.1k
Gerald J. Sun United States 10 1.1k 1.7× 650 1.2× 659 1.6× 268 0.9× 181 1.0× 13 1.5k
Julius A. Steinbeck United States 13 392 0.6× 1.1k 1.9× 726 1.7× 249 0.8× 124 0.7× 15 1.8k

Countries citing papers authored by Noah M. Walton

Since Specialization
Citations

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

Fields of papers citing papers by Noah M. Walton

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Noah M. Walton. 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 Noah M. Walton. The network helps show where Noah M. Walton may publish in the future.

Co-authorship network of co-authors of Noah M. Walton

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

All Works

19 of 19 papers shown
1.
McDonnell, Scott R., et al.. (2024). Mezagitamab in systemic lupus erythematosus: clinical and mechanistic findings of CD38 inhibition in an autoimmune disease. Lupus Science & Medicine. 11(1). e001112–e001112. 10 indexed citations
2.
Matsumoto, Mitsuyuki, Noah M. Walton, Hiroshi Yamada, et al.. (2017). The impact of genetics on future drug discovery in schizophrenia. Expert Opinion on Drug Discovery. 12(7). 673–686. 8 indexed citations
3.
Kogan, Jeffrey H., Robert E. Featherstone, Rick Shin, et al.. (2015). Mouse Model of Chromosome 15q13.3 Microdeletion Syndrome Demonstrates Features Related to Autism Spectrum Disorder. Journal of Neuroscience. 35(49). 16282–16294. 42 indexed citations
4.
Hagihara, Hideo, Hirotaka Shoji, Keizo Takao, et al.. (2014). [Immaturity of brain as an endophenotype of neuropsychiatric disorders].. PubMed. 34(3). 67–79. 3 indexed citations
5.
Walton, Noah M., Anoek de Koning, Rick Shin, et al.. (2014). Gastrin-Releasing Peptide Contributes to the Regulation of Adult Hippocampal Neurogenesis and Neuronal Development. Stem Cells. 32(9). 2454–2466. 17 indexed citations
6.
Shin, Rick, Katsunori Kobayashi, Hideo Hagihara, et al.. (2013). The immature dentate gyrus represents a shared phenotype of mouse models of epilepsy and psychiatric disease. Bipolar Disorders. 15(4). 405–421. 55 indexed citations
7.
Koning, Anoek de, Noah M. Walton, Rick Shin, et al.. (2013). Derivation of neural stem cells from an animal model of psychiatric disease. Translational Psychiatry. 3(11). e323–e323. 4 indexed citations
8.
Hagihara, Hideo, Keizo Takao, Noah M. Walton, Mitsuyuki Matsumoto, & Tsuyoshi Miyakawa. (2013). Immature Dentate Gyrus: An Endophenotype of Neuropsychiatric Disorders. Neural Plasticity. 2013(1). 318596–318596. 98 indexed citations
9.
Walton, Noah M., Yuan Zhou, Jeffrey H. Kogan, et al.. (2012). Detection of an immature dentate gyrus feature in human schizophrenia/bipolar patients. Translational Psychiatry. 2(7). e135–e135. 111 indexed citations
10.
Chen, Qian, Jeffrey H. Kogan, Yuan Zhou, et al.. (2012). SREB2/GPR85, a schizophrenia risk factor, negatively regulates hippocampal adult neurogenesis and neurogenesis‐dependent learning and memory. European Journal of Neuroscience. 36(5). 2597–2608. 42 indexed citations
11.
Walton, Noah M., Rick Shin, Katsunori Tajinda, et al.. (2012). Adult Neurogenesis Transiently Generates Oxidative Stress. PLoS ONE. 7(4). e35264–e35264. 103 indexed citations
12.
Park, Donghyun, Andy Peng Xiang, Frank Fuxiang Mao, et al.. (2010). Nestin Is Required for the Proper Self-Renewal of Neural Stem Cells. Stem Cells. 28(12). 2162–2171. 269 indexed citations
13.
Park, Donghyun, Andy Peng Xiang, Li Zhang, et al.. (2009). The radial glia antibody RC2 recognizes a protein encoded by Nestin. Biochemical and Biophysical Research Communications. 382(3). 588–592. 23 indexed citations
14.
Lee, Jae‐Hyun, Noah M. Walton, Jedidiah Gaetz, et al.. (2008). Systematic identification of cis-silenced genes by trans complementation. Human Molecular Genetics. 18(5). 835–846. 13 indexed citations
15.
Walton, Noah M., Gregory E. Snyder, Donghyun Park, et al.. (2008). Gliotypic Neural Stem Cells Transiently Adopt Tumorigenic Properties During Normal Differentiation. Stem Cells. 27(2). 280–289. 20 indexed citations
16.
Laywell, Eric D., et al.. (2006). Fusion of neural stem cells in culture. Experimental Neurology. 198(1). 129–135. 37 indexed citations
17.
Walton, Noah M., Benjamin M. Sutter, Eric D. Laywell, et al.. (2006). Microglia instruct subventricular zone neurogenesis. Glia. 54(8). 815–825. 304 indexed citations
18.
Walton, Noah M., Benjamin M. Sutter, Huanxin Chen, et al.. (2006). Derivation and large-scale expansion of multipotent astroglial neural progenitors from adult human brain. Development. 133(18). 3671–3681. 81 indexed citations
19.
Scheffler, Björn, et al.. (2005). Phenotypic and functional characterization of adult brain neuropoiesis. Proceedings of the National Academy of Sciences. 102(26). 9353–9358. 111 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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