Cecilia Kim

12.2k total citations
38 papers, 1.4k citations indexed

About

Cecilia Kim is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Cecilia Kim has authored 38 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 9 papers in Molecular Biology and 6 papers in Surgery. Recurrent topics in Cecilia Kim's work include Genetic Associations and Epidemiology (6 papers), Asthma and respiratory diseases (6 papers) and Mitochondrial Function and Pathology (4 papers). Cecilia Kim is often cited by papers focused on Genetic Associations and Epidemiology (6 papers), Asthma and respiratory diseases (6 papers) and Mitochondrial Function and Pathology (4 papers). Cecilia Kim collaborates with scholars based in United States, Canada and United Kingdom. Cecilia Kim's co-authors include Håkon Håkonarson, Joseph Glessner, Jonathan P. Bradfield, Cuiping Hou, Michael Grunstein, Kai Wang, Zhi Wei, Edward C. Frackelton, Patrick Sleiman and Struan F.A. Grant and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and The Journal of Immunology.

In The Last Decade

Cecilia Kim

37 papers receiving 1.4k citations

Peers

Cecilia Kim
Donglei Hu United States
Rajeev Gupta United Kingdom
Mark M. Iles United Kingdom
A. P. Weetman United Kingdom
Jonathan P. Bradfield United States
Cecilia Kim
Citations per year, relative to Cecilia Kim Cecilia Kim (= 1×) peers Florence Busato

Countries citing papers authored by Cecilia Kim

Since Specialization
Citations

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

Fields of papers citing papers by Cecilia Kim

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cecilia Kim

This figure shows the co-authorship network connecting the top 25 collaborators of Cecilia Kim. A scholar is included among the top collaborators of Cecilia Kim 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 Cecilia Kim. Cecilia Kim 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.
Kim, Cecilia, Sunghee Bang, Nicole C. Howard, et al.. (2024). Vaginal lactobacilli produce anti-inflammatory β-carboline compounds. Cell Host & Microbe. 32(11). 1897–1909.e7. 11 indexed citations
2.
Kim, Cecilia, et al.. (2019). Examining Radiation Treatment Appointment Times at a Canadian Cancer Centre: A Timing Study. Journal of medical imaging and radiation sciences. 50(4). 536–542. 5 indexed citations
3.
Mahanna, Elizabeth, Todd A. Miano, John Augoustides, et al.. (2018). Does the melatonin receptor 1B gene polymorphism have a role in postoperative delirium?. PLoS ONE. 13(11). e0207941–e0207941. 11 indexed citations
4.
Garde, Ajay & Cecilia Kim. (2017). Form-Based Codes for Zoning Reform to Promote Sustainable Development: Insights From Cities in Southern California. Journal of the American Planning Association. 83(4). 346–364. 16 indexed citations
5.
Cui, Shuang, Steven F. EauClaire, Cecilia Kim, et al.. (2016). Methylation Microarray Studies Highlight PDGFA Expression as a Factor in Biliary Atresia. PLoS ONE. 11(3). e0151521–e0151521. 22 indexed citations
6.
Bhoj, Elizabeth, Dong Li, Margaret Harr, et al.. (2015). Expanding the SPECC1L mutation phenotypic spectrum to include Teebi hypertelorism syndrome. American Journal of Medical Genetics Part A. 167(11). 2497–2502. 17 indexed citations
7.
Chang, Xiao, Joseph Glessner, Adrienne Tin, et al.. (2015). Genome-wide association study reveals two loci for serum magnesium concentrations in European-American children. Scientific Reports. 5(1). 18792–18792. 2 indexed citations
8.
Li, Jin, Joseph M. McDonough, Zhi Wei, et al.. (2013). Gene Network Analysis in a Pediatric Cohort Identifies Novel Lung Function Genes. PLoS ONE. 8(9). e72899–e72899. 17 indexed citations
9.
Wei, Zhi, Wei Wang, Jonathan P. Bradfield, et al.. (2013). Large Sample Size, Wide Variant Spectrum, and Advanced Machine-Learning Technique Boost Risk Prediction for Inflammatory Bowel Disease. The American Journal of Human Genetics. 92(6). 1008–1012. 138 indexed citations
10.
Sleiman, Patrick, Dai Wang, Joseph Glessner, et al.. (2013). GWAS meta analysis identifies TSNARE1 as a novel Schizophrenia / Bipolar susceptibility locus. Scientific Reports. 3(1). 3075–3075. 36 indexed citations
11.
Shi, Lingling, Xu Zhang, Ryan Golhar, et al.. (2013). Whole-genome sequencing in an autism multiplex family. Molecular Autism. 4(1). 8–8. 54 indexed citations
12.
Wang, Kai, Cecilia Kim, Jonathan P. Bradfield, et al.. (2013). Whole-genome DNA/RNA sequencing identifies truncating mutations in RBCK1 in a novel Mendelian disease with neuromuscular and cardiac involvement. Genome Medicine. 5(7). 67–67. 62 indexed citations
13.
Li, Jin, Joseph Glessner, Haitao Zhang, et al.. (2012). GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children. Human Molecular Genetics. 22(7). 1457–1464. 58 indexed citations
14.
Attiyeh, Edward F., Sharon J. Diskin, Marc A. Attiyeh, et al.. (2009). Genomic copy number determination in cancer cells from single nucleotide polymorphism microarrays based on quantitative genotyping corrected for aneuploidy. Genome Research. 19(2). 276–283. 66 indexed citations
15.
Dubinsky, Marla C., Ling Mei, Tanvi Dhere, et al.. (2009). Genome wide association (GWA) predictors of anti-TNFα therapeutic responsiveness in pediatric inflammatory bowel disease. Inflammatory Bowel Diseases. 16(8). 1357–1366. 107 indexed citations
16.
Bisgaard, Hans, Klaus Bønnelykke, Patrick Sleiman, et al.. (2008). Chromosome 17q21 Gene Variants Are Associated with Asthma and Exacerbations but Not Atopy in Early Childhood. American Journal of Respiratory and Critical Care Medicine. 179(3). 179–185. 158 indexed citations
17.
Sindhi, Rakesh, Brandon W. Higgs, Daniel E. Weeks, et al.. (2008). Genetic Variants in Major Histocompatibility Complex-Linked Genes Associate With Pediatric Liver Transplant Rejection. Gastroenterology. 135(3). 830–839.e10. 21 indexed citations
18.
Håkonarson, Håkon, Russell S. Whelan, Cecilia Kim, et al.. (2002). T lymphocyte-mediated changes in airway smooth muscle responsiveness are attributed to induced autocrine release and actions of IL-5 and IL-1β. Journal of Allergy and Clinical Immunology. 110(4). 624–633. 13 indexed citations
19.
Håkonarson, Håkon, Cecilia Kim, Russell S. Whelan, Donald Campbell, & Michael Grunstein. (2001). Bi-Directional Activation Between Human Airway Smooth Muscle Cells and T Lymphocytes: Role in Induction of Altered Airway Responsiveness. The Journal of Immunology. 166(1). 293–303. 47 indexed citations
20.
Håkonarson, Håkon, et al.. (1999). Altered expression and action of the low-affinity IgE receptor FcϵRII (CD23) in asthmatic airway smooth muscle. Journal of Allergy and Clinical Immunology. 104(3). 575–584. 55 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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