Cynthia Lim

828 total citations
9 papers, 231 citations indexed

About

Cynthia Lim is a scholar working on Genetics, Molecular Biology and Nephrology. According to data from OpenAlex, Cynthia Lim has authored 9 papers receiving a total of 231 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 3 papers in Molecular Biology and 2 papers in Nephrology. Recurrent topics in Cynthia Lim's work include Genomic variations and chromosomal abnormalities (4 papers), Pancreatic and Hepatic Oncology Research (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Cynthia Lim is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Pancreatic and Hepatic Oncology Research (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Cynthia Lim collaborates with scholars based in United States, Denmark and Brazil. Cynthia Lim's co-authors include Bassem A. Bejjani, Arthur S. Aylsworth, Lisa G. Shaffer, Aaron Theisen, Marie McDonald, Jay W. Ellison, Sulagna C. Saitta, Blake C. Ballif, Dana Kostiner and Tamim H. Shaikh and has published in prestigious journals such as Journal of Clinical Oncology, Cancer and The American Journal of Human Genetics.

In The Last Decade

Cynthia Lim

9 papers receiving 204 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Cynthia Lim United States	5	145	126	39	34	29	9	231
Emiel Baten Belgium	8	147 1.0×	133 1.1×	32 0.8×	30 0.9×	9 0.3×	8	234
Katalin Szakszon Hungary	10	103 0.7×	178 1.4×	16 0.4×	8 0.2×	27 0.9×	29	276
Xingbo Cheng China	7	148 1.0×	167 1.3×	58 1.5×	18 0.5×	6 0.2×	21	295
Stefano Petrocchi Italy	8	129 0.9×	84 0.7×	16 0.4×	19 0.6×	5 0.2×	15	236
Julie Kaylor United States	9	104 0.7×	103 0.8×	35 0.9×	9 0.3×	8 0.3×	11	206
Antoinet C.J. Gijsbers Netherlands	12	356 2.5×	212 1.7×	94 2.4×	67 2.0×	7 0.2×	15	426
Jeannette Hoogeboom Netherlands	9	201 1.4×	155 1.2×	34 0.9×	8 0.2×	7 0.2×	13	325
Lindsey Campbell United States	4	268 1.8×	130 1.0×	69 1.8×	74 2.2×	4 0.1×	5	316
Beth A. Torchia United States	7	281 1.9×	139 1.1×	177 4.5×	71 2.1×	7 0.2×	11	369
Emilie Ait‐Yahya France	7	151 1.0×	171 1.4×	42 1.1×	42 1.2×	6 0.2×	18	366

Countries citing papers authored by Cynthia Lim

Since Specialization

Citations

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

Fields of papers citing papers by Cynthia Lim

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cynthia Lim

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

All Works

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9 of 9 papers shown

Woo, Keng Thye, Choong Meng Chan, Marjorie Foo, et al.. (2021). Evolution of IgA nephropathy in Singapore over four decades and a comparison of two cohorts from the first and fourth decade. Clinical Nephrology. 95(5). 256–272. 1 indexed citations

Woo, Keng-Thye, Cynthia Lim, Jason Choo, et al.. (2019). Changes in primary glomerulonephritis in Singapore over four decades. Clinical Nephrology. 91(3). 155–161. 4 indexed citations

Peters, Mary Linton B., Beth Dudley, Virginia Speare, et al.. (2019). Family communication and patient distress after germline genetic testing in individuals with pancreatic ductal adenocarcinoma. Cancer. 125(14). 2488–2496. 9 indexed citations

Peters, Mary Linton B., Randall E. Brand, Erkut Borazanci, et al.. (2017). Germline genetic testing in unselected pancreatic ductal adenocarcinoma (PDAC) patients.. Journal of Clinical Oncology. 35(15_suppl). 1501–1501. 1 indexed citations

Carvalho, Claudia M.B., Shivakumar Vasanth, Marwan Shinawi, et al.. (2014). Dosage Changes of a Segment at 17p13.1 Lead to Intellectual Disability and Microcephaly as a Result of Complex Genetic Interaction of Multiple Genes. The American Journal of Human Genetics. 95(5). 565–578. 39 indexed citations

Brautbar, Ariel, Jing Wang, José E. Abdenur, et al.. (2008). The mitochondrial 13513G>A mutation is associated with Leigh disease phenotypes independent of complex I deficiency in muscle. Molecular Genetics and Metabolism. 94(4). 485–490. 35 indexed citations

Sawyer, Jeffrey R., Regina Lichti Binz, Charles M. Swanson, & Cynthia Lim. (2007). De novo proximal duplication of 1(q12q22) in a female infant with multiple congenital anomalies. American Journal of Medical Genetics Part A. 143A(4). 338–342. 15 indexed citations

Shaffer, Lisa G., Aaron Theisen, Bassem A. Bejjani, et al.. (2007). The discovery of microdeletion syndromes in the post-genomic era: review of the methodology and characterization of a new 1q41q42 microdeletion syndrome. Genetics in Medicine. 9(9). 607–616. 124 indexed citations

Lennon, Patrick A., M. Lance Cooper, Cynthia Lim, et al.. (2006). Array‐based comparative genomic hybridization facilitates identification of breakpoints of a novel der(1)t(1;18)(p36.3;q23)dn in a child presenting with mental retardation. American Journal of Medical Genetics Part A. 140A(11). 1156–1163. 3 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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