Siew-Lan Ang

4.0k total citations
22 papers, 3.2k citations indexed

About

Siew-Lan Ang is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Developmental Neuroscience. According to data from OpenAlex, Siew-Lan Ang has authored 22 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 7 papers in Cellular and Molecular Neuroscience and 6 papers in Developmental Neuroscience. Recurrent topics in Siew-Lan Ang's work include Developmental Biology and Gene Regulation (15 papers), Pluripotent Stem Cells Research (7 papers) and Congenital heart defects research (7 papers). Siew-Lan Ang is often cited by papers focused on Developmental Biology and Gene Regulation (15 papers), Pluripotent Stem Cells Research (7 papers) and Congenital heart defects research (7 papers). Siew-Lan Ang collaborates with scholars based in France, United Kingdom and United States. Siew-Lan Ang's co-authors include Janet Rossant, Ou Jin, François Guillemot, Muriel Rhinn, Qiufu Ma, Simona Casarosa, Carol Fode, David J. Anderson, Hiroshi Sasaki and Nathalie Daigle and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Siew-Lan Ang

22 papers receiving 3.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Siew-Lan Ang France 22 2.7k 996 723 644 275 22 3.2k
Gonzalo Álvarez‐Bolado Germany 29 2.2k 0.8× 759 0.8× 561 0.8× 500 0.8× 337 1.2× 69 3.2k
Brian G. Condie United States 30 2.4k 0.9× 632 0.6× 404 0.6× 618 1.0× 299 1.1× 46 3.3k
Elisa Martı́ Spain 36 3.7k 1.4× 914 0.9× 785 1.1× 743 1.2× 579 2.1× 66 4.5k
Horst H. Simon Germany 23 2.3k 0.9× 1.4k 1.4× 518 0.7× 370 0.6× 363 1.3× 30 3.6k
Jonas Muhr Sweden 26 2.9k 1.1× 556 0.6× 947 1.3× 716 1.1× 377 1.4× 33 3.5k
Mineko Kengaku Japan 30 2.1k 0.8× 820 0.8× 411 0.6× 408 0.6× 587 2.1× 58 2.9k
G. Giacomo Consalez Italy 35 2.0k 0.7× 723 0.7× 454 0.6× 667 1.0× 371 1.3× 93 3.3k
Penny Rashbass United Kingdom 16 2.4k 0.9× 414 0.4× 629 0.9× 520 0.8× 495 1.8× 22 2.8k
Till Marquardt Germany 23 2.7k 1.0× 1.1k 1.1× 441 0.6× 492 0.8× 672 2.4× 29 3.4k
Thomas Theil United Kingdom 28 2.1k 0.8× 665 0.7× 498 0.7× 627 1.0× 383 1.4× 55 2.7k

Countries citing papers authored by Siew-Lan Ang

Since Specialization
Citations

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

Fields of papers citing papers by Siew-Lan Ang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Siew-Lan Ang. 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 Siew-Lan Ang. The network helps show where Siew-Lan Ang may publish in the future.

Co-authorship network of co-authors of Siew-Lan Ang

This figure shows the co-authorship network connecting the top 25 collaborators of Siew-Lan Ang. A scholar is included among the top collaborators of Siew-Lan Ang 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 Siew-Lan Ang. Siew-Lan Ang 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.
Brisson, G. J., Hélène Doucet-Beaupré, Charleen Salesse, et al.. (2017). Transcriptional repression of Plxnc1 by Lmx1a and Lmx1b directs topographic dopaminergic circuit formation. Nature Communications. 8(1). 933–933. 23 indexed citations
2.
Pristerà, Alessandro, Wei Lin, Anna-Kristin Kaufmann, et al.. (2015). Transcription factors FOXA1 and FOXA2 maintain dopaminergic neuronal properties and control feeding behavior in adult mice. Proceedings of the National Academy of Sciences. 112(35). E4929–38. 57 indexed citations
3.
Yan, Carol H., Martin Lévesque, Suzanne Claxton, Randy L. Johnson, & Siew-Lan Ang. (2011). Lmx1a and Lmx1b Function Cooperatively to Regulate Proliferation, Specification, and Differentiation of Midbrain Dopaminergic Progenitors. Journal of Neuroscience. 31(35). 12413–12425. 110 indexed citations
4.
Ferri, Luca, Wei Lin, Yannis Emmanuel Mavromatakis, et al.. (2007). Foxa1andFoxa2regulate multiple phases of midbrain dopaminergic neuron development in a dosage-dependent manner. Development. 134(15). 2761–2769. 227 indexed citations
5.
Jacob, John, Luca Ferri, Fabrice Prin, et al.. (2007). Transcriptional repression coordinates the temporal switch from motor to serotonergic neurogenesis. Nature Neuroscience. 10(11). 1433–1439. 72 indexed citations
6.
Puelles, Eduardo, Dario Acampora, Francesca Tuorto, et al.. (2006). Otx2 Controls Identity and Fate of Glutamatergic Progenitors of the Thalamus by Repressing GABAergic Differentiation. Journal of Neuroscience. 26(22). 5955–5964. 51 indexed citations
7.
Kele, Julianna, Luca Ferri, Helena Mira, et al.. (2006). Neurogenin 2 is required for the development of ventral midbrain dopaminergic neurons. Development. 133(3). 495–505. 189 indexed citations
8.
Borgkvist, Anders, Eduardo Puelles, Manolo Carta, et al.. (2005). Altered dopaminergic innervation and amphetamine response in adult Otx2 conditional mutant mice. Molecular and Cellular Neuroscience. 31(2). 293–302. 29 indexed citations
9.
Vernay, Bertrand, Muriel Koch, Flora M. Vaccarino, et al.. (2005). Otx2 Regulates Subtype Specification and Neurogenesis in the Midbrain. Journal of Neuroscience. 25(19). 4856–4867. 118 indexed citations
10.
Jing, Naihe, et al.. (2005). Synergistic activity of Sef and Sprouty proteins in regulating the expression ofGbx2 in the mid-hindbrain region. genesis. 41(3). 110–115. 34 indexed citations
11.
Puelles, Eduardo, Alessandro Annino, Francesca Tuorto, et al.. (2004). Otx2 regulates the extent, identity and fate of neuronal progenitor domains in the ventral midbrain. Development. 131(9). 2037–2048. 178 indexed citations
12.
Puelles, Eduardo, Dario Acampora, Emmanuel Lacroix, et al.. (2003). Otx dose-dependent integrated control of antero-posterior and dorso-ventral patterning of midbrain. Nature Neuroscience. 6(5). 453–460. 115 indexed citations
13.
Hallonet, Marc, Klaus H. Kaestner, Luis Martín-Parras, et al.. (2002). Maintenance of the Specification of the Anterior Definitive Endoderm and Forebrain Depends on the Axial Mesendoderm: A Study Using HNF3β/Foxa2 Conditional Mutants. Developmental Biology. 243(1). 20–33. 50 indexed citations
14.
Perea-Gómez, Aitana, William Shawlot, Mustapha Oulad‐Abdelghani, et al.. (2002). Nodal Antagonists in the Anterior Visceral Endoderm Prevent the Formation of Multiple Primitive Streaks. Developmental Cell. 3(5). 745–756. 301 indexed citations
15.
Fode, Carol, Qiufu Ma, Simona Casarosa, et al.. (2000). A role for neural determination genes in specifying the dorsoventral identity of telencephalic neurons. Genes & Development. 14(1). 67–80. 499 indexed citations
16.
Klingensmith, John, Siew-Lan Ang, Daniel Bachiller, & Janet Rossant. (1999). Neural Induction and Patterning in the Mouse in the Absence of the Node and Its Derivatives. Developmental Biology. 216(2). 535–549. 82 indexed citations
17.
Perea-Gómez, Aitana, William Shawlot, Hiroshi Sasaki, Richard R. Behringer, & Siew-Lan Ang. (1999). HNF3β and Lim1 interact in the visceral endoderm to regulate primitive streak formation and anterior-posterior polarity in the mouse embryo. Development. 126(20). 4499–4511. 113 indexed citations
18.
Filosa, Stefania, Jaime A. Rivera‐Pérez, Anne Gansmüller, et al.. (1997). goosecoid and HNF-3β genetically interact to regulate neural tube patterning during mouse embryogenesis. Development. 124(14). 2843–2854. 109 indexed citations
19.
20.
Kaestner, Klaus H., A. Paula Monaghan, Heidrun Kern, et al.. (1995). The Mouse fkh-2 Gene. Journal of Biological Chemistry. 270(50). 30029–30035. 37 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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