Esther Lim

481 total citations
10 papers, 295 citations indexed

About

Esther Lim is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Esther Lim has authored 10 papers receiving a total of 295 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 3 papers in Genetics and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Esther Lim's work include Receptor Mechanisms and Signaling (3 papers), Muscle Physiology and Disorders (2 papers) and Epigenetics and DNA Methylation (2 papers). Esther Lim is often cited by papers focused on Receptor Mechanisms and Signaling (3 papers), Muscle Physiology and Disorders (2 papers) and Epigenetics and DNA Methylation (2 papers). Esther Lim collaborates with scholars based in Australia, United States and Singapore. Esther Lim's co-authors include Kevin D. G. Pfleger, Karin A. Eidne, Walter G. Thomas, Suzanna E.L. Temple, C. Almeida, Grant Waterer, Patricia Price, Kristin Ardlie, Nigel G. Laing and Karey Cheong and has published in prestigious journals such as Blood, Annals of Neurology and Molecular Pharmacology.

In The Last Decade

Esther Lim

9 papers receiving 294 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Esther Lim Australia 7 219 97 70 45 40 10 295
Katherina Hemmen Germany 11 122 0.6× 17 0.2× 15 0.2× 39 0.9× 13 0.3× 21 260
Madhav Mantri United States 7 307 1.4× 36 0.4× 21 0.3× 42 0.9× 9 0.2× 11 387
Chia‐Huei Chu Taiwan 9 252 1.2× 12 0.1× 34 0.5× 27 0.6× 13 0.3× 29 533
Christin Collins United States 8 210 1.0× 34 0.4× 56 0.8× 95 2.1× 24 0.6× 13 425
Tanvi Saxena United States 10 522 2.4× 32 0.3× 36 0.5× 18 0.4× 140 3.5× 14 665
Magda Zachara Switzerland 5 263 1.2× 73 0.8× 55 0.8× 86 1.9× 8 0.2× 5 538
Ellen L. van Agtmaal Netherlands 7 200 0.9× 39 0.4× 24 0.3× 50 1.1× 79 2.0× 7 317
Samuel Koller Switzerland 10 191 0.9× 19 0.2× 11 0.2× 19 0.4× 14 0.3× 26 266
Simone Pizzi Italy 11 185 0.8× 18 0.2× 45 0.6× 24 0.5× 53 1.3× 31 313
Joseph R. Smith-Arica United Kingdom 9 333 1.5× 16 0.2× 19 0.3× 20 0.4× 21 0.5× 13 433

Countries citing papers authored by Esther Lim

Since Specialization
Citations

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

Fields of papers citing papers by Esther Lim

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Esther Lim. 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 Esther Lim. The network helps show where Esther Lim may publish in the future.

Co-authorship network of co-authors of Esther Lim

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

All Works

10 of 10 papers shown
2.
Clarke, Nigel F., Hanna Kolski, Danielle E. Dye, et al.. (2008). Mutations in TPM3 are a common cause of congenital fiber type disproportion. Annals of Neurology. 63(3). 329–337. 102 indexed citations
3.
Nowak, Kristen L., Connie Jackaman, Esther Lim, et al.. (2007). T.O.3 Transgenic expression of cardiac actin rescues skeletal actin-null mice. Neuromuscular Disorders. 17(9-10). 899–899. 6 indexed citations
4.
Jackaman, Connie, Kristen L. Nowak, Gianina Ravenscroft, et al.. (2007). Novel application of flow cytometry: Determination of muscle fiber types and protein levels in whole murine skeletal muscles and heart. Cell Motility and the Cytoskeleton. 64(12). 914–925. 9 indexed citations
5.
Endersby, Raelene, Ian J. Majewski, Louise N Winteringham, et al.. (2007). Hls5 regulated erythroid differentiation by modulating GATA-1 activity. Blood. 111(4). 1946–1950. 4 indexed citations
6.
Pfleger, Kevin D. G., et al.. (2006). Extended bioluminescence resonance energy transfer (eBRET) for monitoring prolonged protein–protein interactions in live cells. Cellular Signalling. 18(10). 1664–1670. 85 indexed citations
7.
Pfleger, Kevin D. G., et al.. (2006). Orexin receptors: Distinct β-arrestin and internalization profiles for subtypes 1 and 2. Frontiers in Neuroendocrinology. 27(1). 83–83. 1 indexed citations
8.
Dinh, Diem, Hongwei Qian, Ruth M. Seeber, et al.. (2004). Helix I of β-Arrestin Is Involved in Postendocytic Trafficking but Is Not Required for Membrane Translocation, Receptor Binding, and Internalization. Molecular Pharmacology. 67(2). 375–382. 9 indexed citations
9.
Temple, Suzanna E.L., Esther Lim, Karey Cheong, et al.. (2003). Alleles carried at positions ?819 and ?592 of the IL10 promoter affect transcription following stimulation of peripheral blood cells with Streptococcus pneumoniae. Immunogenetics. 55(9). 629–632. 62 indexed citations
10.

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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