Jane E. Johnson

17.8k total citations · 3 hit papers
141 papers, 12.8k citations indexed

About

Jane E. Johnson is a scholar working on Molecular Biology, Developmental Neuroscience and Cellular and Molecular Neuroscience. According to data from OpenAlex, Jane E. Johnson has authored 141 papers receiving a total of 12.8k indexed citations (citations by other indexed papers that have themselves been cited), including 95 papers in Molecular Biology, 32 papers in Developmental Neuroscience and 17 papers in Cellular and Molecular Neuroscience. Recurrent topics in Jane E. Johnson's work include Developmental Biology and Gene Regulation (39 papers), Neurogenesis and neuroplasticity mechanisms (32 papers) and Pluripotent Stem Cells Research (20 papers). Jane E. Johnson is often cited by papers focused on Developmental Biology and Gene Regulation (39 papers), Neurogenesis and neuroplasticity mechanisms (32 papers) and Pluripotent Stem Cells Research (20 papers). Jane E. Johnson collaborates with scholars based in United States, United Kingdom and Japan. Jane E. Johnson's co-authors include Amy W. Helms, David J. Anderson, François Guillemot, Susan J. Birren, Stephen D. Hauschka, Huda Y. Zoghbi, Neil Segil, Tetsuichiro Saito, Alexandra L. Joyner and James Battiste and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Jane E. Johnson

138 papers receiving 12.6k citations

Hit Papers

Mammalian achaete-scute homolog 1 is required for the ear... 1993 2026 2004 2015 1993 2019 1997 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jane E. Johnson United States 55 8.4k 3.2k 2.6k 1.8k 1.5k 141 12.8k
Gerry Weinmaster United States 59 10.6k 1.3× 2.1k 0.6× 1.9k 0.7× 1.0k 0.6× 1.7k 1.2× 86 14.4k
Isabel Fariñas Spain 49 6.2k 0.7× 3.2k 1.0× 5.5k 2.1× 622 0.3× 1.2k 0.8× 110 13.3k
Larysa Pevny United States 39 8.6k 1.0× 1.9k 0.6× 1.3k 0.5× 822 0.4× 2.2k 1.5× 60 11.9k
Samuel Weiss Canada 49 8.4k 1.0× 8.8k 2.7× 5.8k 2.2× 1.6k 0.9× 892 0.6× 105 17.0k
Michael Wegner Germany 78 12.5k 1.5× 4.4k 1.4× 3.1k 1.2× 1.2k 0.7× 4.5k 3.0× 265 19.9k
Katsuhiko Mikoshiba Japan 65 9.0k 1.1× 1.2k 0.4× 2.5k 1.0× 422 0.2× 1.6k 1.1× 205 12.6k
Takeshi Yagi Japan 58 9.2k 1.1× 1.9k 0.6× 6.9k 2.7× 858 0.5× 1.6k 1.0× 190 14.9k
Albee Messing United States 65 8.8k 1.0× 2.2k 0.7× 4.8k 1.9× 813 0.4× 1.7k 1.2× 174 14.5k
Patrick Charnay France 63 8.7k 1.0× 2.0k 0.6× 4.7k 1.8× 760 0.4× 2.1k 1.4× 159 15.1k
Shinichi Aizawa Japan 71 13.0k 1.5× 1.2k 0.4× 3.6k 1.4× 1.9k 1.0× 2.6k 1.8× 193 19.5k

Countries citing papers authored by Jane E. Johnson

Since Specialization
Citations

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

Fields of papers citing papers by Jane E. Johnson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jane E. Johnson. 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 Jane E. Johnson. The network helps show where Jane E. Johnson may publish in the future.

Co-authorship network of co-authors of Jane E. Johnson

This figure shows the co-authorship network connecting the top 25 collaborators of Jane E. Johnson. A scholar is included among the top collaborators of Jane E. Johnson 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 Jane E. Johnson. Jane E. Johnson 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.
Nakada, Yuji, et al.. (2025). ASCL1 protein domains with distinct functions in neuronal differentiation and subtype specification. Developmental Biology. 523. 32–42.
2.
Savage, Trisha K., Su Deng, Ping Mu, et al.. (2023). Abstract PR004: Exploring the role of ASCL1 in neuroendocrine prostate cancer. Cancer Research. 83(11_Supplement). PR004–PR004. 1 indexed citations
3.
Kollipara, Rahul K., Karine Pozo, Shreoshi Pal Choudhuri, et al.. (2022). Inhibition of Karyopherin β1-Mediated Nuclear Import Disrupts Oncogenic Lineage-Defining Transcription Factor Activity in Small Cell Lung Cancer. Cancer Research. 82(17). 3058–3073. 9 indexed citations
4.
Zhu, Mingrui, Yi Huang, Luc Girard, et al.. (2021). Evasion of Innate Immunity Contributes to Small Cell Lung Cancer Progression and Metastasis. Cancer Research. 81(7). 1813–1826. 56 indexed citations
5.
Pozo, Karine, et al.. (2021). ASCL1, NKX2-1, and PROX1 co-regulate subtype-specific genes in small-cell lung cancer. iScience. 24(9). 102953–102953. 31 indexed citations
6.
Casey, Bradford, Rahul K. Kollipara, Karine Pozo, & Jane E. Johnson. (2018). Intrinsic DNA binding properties demonstrated for lineage-specifying basic helix-loop-helix transcription factors. Genome Research. 28(4). 484–496. 30 indexed citations
7.
Borromeo, Mark D., Trisha K. Savage, Rahul K. Kollipara, et al.. (2016). ASCL1 and NEUROD1 Reveal Heterogeneity in Pulmonary Neuroendocrine Tumors and Regulate Distinct Genetic Programs. Cell Reports. 16(5). 1259–1272. 318 indexed citations
8.
Niu, Wenze, Tong Zang, Derek K. Smith, et al.. (2015). SOX2 Reprograms Resident Astrocytes into Neural Progenitors in the Adult Brain. Stem Cell Reports. 4(5). 780–794. 161 indexed citations
9.
Kim, Euiseok J., et al.. (2011). Ascl1 (Mash1) Defines Cells with Long-Term Neurogenic Potential in Subgranular and Subventricular Zones in Adult Mouse Brain. PLoS ONE. 6(3). e18472–e18472. 192 indexed citations
10.
Savage, Trisha K., et al.. (2010). Neurogenin 1 (Neurog1) expression in the ventral neural tube is mediated by a distinct enhancer and preferentially marks ventral interneuron lineages. Developmental Biology. 340(2). 283–292. 34 indexed citations
11.
Kim, Euiseok J., et al.. (2010). Spatiotemporal fate map of neurogenin1 (Neurog1) lineages in the mouse central nervous system. The Journal of Comparative Neurology. 519(7). 1355–1370. 52 indexed citations
12.
Miyoshi, Goichi, Jens Hjerling‐Leffler, Theofanis Karayannis, et al.. (2010). Genetic Fate Mapping Reveals That the Caudal Ganglionic Eminence Produces a Large and Diverse Population of Superficial Cortical Interneurons. Journal of Neuroscience. 30(5). 1582–1594. 421 indexed citations
13.
Raft, Steven, Edmund J. Koundakjian, Chathurani S. Jayasena, et al.. (2007). Cross-regulation ofNgn1andMath1coordinates the production of neurons and sensory hair cells during inner ear development. Development. 134(24). 4405–4415. 165 indexed citations
14.
Kessler, Jessica D., Tracy‐Ann Read, Constanze Kaiser, et al.. (2005). Isolation of neural stem cells from the postnatal cerebellum. Nature Neuroscience. 8(6). 723–729. 366 indexed citations
15.
Parras, Carlos, Rossella Galli, Olivier Britz, et al.. (2004). Mash1 specifies neurons and oligodendrocytes in the postnatal brain. The EMBO Journal. 23(22). 4495–4505. 301 indexed citations
16.
Doetzlhofer, Angelika, Patricia M. White, Jane E. Johnson, Neil Segil, & Andrew K. Groves. (2004). In vitro growth and differentiation of mammalian sensory hair cell progenitors: a requirement for EGF and periotic mesenchyme. Developmental Biology. 272(2). 432–447. 79 indexed citations
17.
Ebert, Philip J., John R. Timmer, Yuji Nakada, et al.. (2003). Zic1 represses Math1 expression via interactions with the Math1 enhancer and modulation of Math1 autoregulation. Development. 130(9). 1949–1959. 79 indexed citations
18.
Chen, Ping, Jane E. Johnson, Huda Y. Zoghbi, & Neil Segil. (2002). The role of Math1 in inner ear development: Uncoupling the establishment of the sensory primordium from hair cell fate determination. Development. 129(10). 2495–2505. 429 indexed citations
19.
Meredith, Andrea L. & Jane E. Johnson. (2000). Negative Autoregulation of Mash1 Expression in CNS Development. Developmental Biology. 222(2). 336–346. 36 indexed citations
20.
Boone, William R., et al.. (1996). Sources of variation in measurements of carbon dioxide levels inside incubators. Journal of Assisted Reproduction and Genetics. 13(7). 606–608. 1 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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