Brian S. Clark

3.9k total citations · 2 hit papers
35 papers, 2.2k citations indexed

About

Brian S. Clark is a scholar working on Molecular Biology, Cell Biology and Cancer Research. According to data from OpenAlex, Brian S. Clark has authored 35 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 9 papers in Cell Biology and 5 papers in Cancer Research. Recurrent topics in Brian S. Clark's work include Retinal Development and Disorders (15 papers), RNA Research and Splicing (7 papers) and Single-cell and spatial transcriptomics (6 papers). Brian S. Clark is often cited by papers focused on Retinal Development and Disorders (15 papers), RNA Research and Splicing (7 papers) and Single-cell and spatial transcriptomics (6 papers). Brian S. Clark collaborates with scholars based in United States, United Kingdom and British Virgin Islands. Brian S. Clark's co-authors include Seth Blackshaw, Jhumku D. Kohtz, Brian A. Link, Fion Shiau, Loyal A. Goff, Elana J. Fertig, Genevieve Stein-O’Brien, Thomas D. Sherman, Clayton P. Santiago and Joel B. Miesfeld and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and Neuron.

In The Last Decade

Brian S. Clark

34 papers receiving 2.2k citations

Hit Papers

The Evf-2 noncoding RNA is transcribed from the Dlx-5/6 u... 2006 2026 2012 2019 2006 2019 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Brian S. Clark United States 23 1.8k 716 382 190 149 35 2.2k
Pilar Esteve Spain 23 1.8k 1.0× 155 0.2× 260 0.7× 394 2.1× 279 1.9× 30 2.2k
Dieter Engelkamp Germany 17 2.6k 1.4× 260 0.4× 365 1.0× 521 2.7× 346 2.3× 20 3.0k
Andrew J. Waskiewicz Canada 24 2.3k 1.3× 178 0.2× 498 1.3× 197 1.0× 480 3.2× 48 2.9k
Dorothea Schulte Germany 24 1.5k 0.8× 142 0.2× 262 0.7× 331 1.7× 220 1.5× 53 1.7k
Per‐Henrik Edqvist Sweden 22 684 0.4× 282 0.4× 188 0.5× 112 0.6× 62 0.4× 43 1.3k
Jesús Torres‐Vázquez United States 20 1.1k 0.6× 162 0.2× 566 1.5× 356 1.9× 101 0.7× 26 1.5k
Monika S. Kowalczyk United States 15 2.1k 1.1× 561 0.8× 123 0.3× 206 1.1× 163 1.1× 17 3.1k
Kevin Huang United States 17 1.4k 0.8× 279 0.4× 58 0.2× 141 0.7× 228 1.5× 19 1.8k
Maria Cristina Gagliani Italy 18 1.5k 0.8× 183 0.3× 529 1.4× 409 2.2× 75 0.5× 40 2.1k
Begoña Díaz United States 23 919 0.5× 305 0.4× 633 1.7× 103 0.5× 77 0.5× 44 1.8k

Countries citing papers authored by Brian S. Clark

Since Specialization
Citations

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

Fields of papers citing papers by Brian S. Clark

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Brian S. Clark. 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 Brian S. Clark. The network helps show where Brian S. Clark may publish in the future.

Co-authorship network of co-authors of Brian S. Clark

This figure shows the co-authorship network connecting the top 25 collaborators of Brian S. Clark. A scholar is included among the top collaborators of Brian S. Clark 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 Brian S. Clark. Brian S. Clark 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
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Noel, Nicole C. L., Chi‐Kuo Hu, Lut Arckens, et al.. (2024). Age‐related dysregulation of the retinal transcriptome in African turquoise killifish. Aging Cell. 23(8). e14192–e14192. 5 indexed citations
3.
Mattar, Pierre, et al.. (2021). A Casz1–NuRD complex regulates temporal identity transitions in neural progenitors. Scientific Reports. 11(1). 42–42. 21 indexed citations
4.
Clark, Brian S., Qing Shi, Fion Shiau, et al.. (2021). Atoh7-independent specification of retinal ganglion cell identity. Science Advances. 7(11). 37 indexed citations
5.
Shiau, Fion, Philip A. Ruzycki, & Brian S. Clark. (2021). A single-cell guide to retinal development: Cell fate decisions of multipotent retinal progenitors in scRNA-seq. Developmental Biology. 478. 41–58. 23 indexed citations
6.
Clark, Brian S., et al.. (2021). Dynamic Polarization of Rab11a Modulates Crb2a Localization and Impacts Signaling to Regulate Retinal Neurogenesis. Frontiers in Cell and Developmental Biology. 8. 608112–608112. 5 indexed citations
7.
Lyu, Pin, Thanh Hoang, Clayton P. Santiago, et al.. (2021). Gene regulatory networks controlling temporal patterning, neurogenesis, and cell-fate specification in mammalian retina. Cell Reports. 37(7). 109994–109994. 69 indexed citations
8.
Menuchin-Lasowski, Yotam, Andrea Conidi, Ahuvit David, et al.. (2020). Zeb2 regulates the balance between retinal interneurons and Müller glia by inhibition of BMP–Smad signaling. Developmental Biology. 468(1-2). 80–92. 4 indexed citations
9.
Ray, Thomas A., Kelly Cochran, Christopher Kozlowski, et al.. (2020). Comprehensive identification of mRNA isoforms reveals the diversity of neural cell-surface molecules with roles in retinal development and disease. Nature Communications. 11(1). 3328–3328. 74 indexed citations
10.
Ling, Jonathan P., Christopher Wilks, Patrick J. Leavey, et al.. (2020). ASCOT identifies key regulators of neuronal subtype-specific splicing. Nature Communications. 11(1). 137–137. 45 indexed citations
11.
Stein-O’Brien, Genevieve, Brian S. Clark, Thomas D. Sherman, et al.. (2019). Decomposing Cell Identity for Transfer Learning across Cellular Measurements, Platforms, Tissues, and Species. Cell Systems. 8(5). 395–411.e8. 81 indexed citations
12.
Himmelstein, Diana S., et al.. (2017). SHH E176/E177-Zn2+ conformation is required for signaling at endogenous sites. Developmental Biology. 424(2). 221–235. 8 indexed citations
13.
Melo, Jimmy de, Brian S. Clark, & Seth Blackshaw. (2016). Multiple intrinsic factors act in concert with Lhx2 to direct retinal gliogenesis. Scientific Reports. 6(1). 32757–32757. 28 indexed citations
14.
Miesfeld, Joel B., Gaia Gestri, Brian S. Clark, et al.. (2015). Yap and Taz regulate retinal pigment epithelial cell fate. Development. 142(17). 3021–32. 118 indexed citations
15.
Clark, Brian S. & Seth Blackshaw. (2014). Long non-coding RNA-dependent transcriptional regulation in neuronal development and disease. Frontiers in Genetics. 5. 164–164. 125 indexed citations
16.
Buckley, Clare E., Xiaoyun Ren, Laura Ward, et al.. (2012). Mirror‐symmetric microtubule assembly and cell interactions drive lumen formation in the zebrafish neural rod. The EMBO Journal. 32(1). 30–44. 50 indexed citations
17.
Clark, Brian S., et al.. (2012). Integrin α5/fibronectin1 and focal adhesion kinase are required for lens fiber morphogenesis in zebrafish. Molecular Biology of the Cell. 23(24). 4725–4738. 31 indexed citations
18.
Clark, Brian S., Mark Winter, Andrew R. Cohen, & Brian A. Link. (2011). Generation of Rab‐based transgenic lines for in vivo studies of endosome biology in zebrafish. Developmental Dynamics. 240(11). 2452–2465. 76 indexed citations
19.
Himmelstein, Diana S., et al.. (2010). Balanced Shh signaling is required for proper formation and maintenance of dorsal telencephalic midline structures. BMC Developmental Biology. 10(1). 118–118. 13 indexed citations
20.
Clark, Brian S., et al.. (2006). The Evf-2 noncoding RNA is transcribed from the Dlx-5/6 ultraconserved region and functions as a Dlx-2 transcriptional coactivator. Genes & Development. 20(11). 1470–1484. 569 indexed citations breakdown →

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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