E. Chung

571 total citations
9 papers, 267 citations indexed

About

E. Chung is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, E. Chung has authored 9 papers receiving a total of 267 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Surgery. Recurrent topics in E. Chung's work include Genetics and Neurodevelopmental Disorders (2 papers), ATP Synthase and ATPases Research (2 papers) and Ion Transport and Channel Regulation (2 papers). E. Chung is often cited by papers focused on Genetics and Neurodevelopmental Disorders (2 papers), ATP Synthase and ATPases Research (2 papers) and Ion Transport and Channel Regulation (2 papers). E. Chung collaborates with scholars based in United Kingdom, Switzerland and Australia. E. Chung's co-authors include David Curtis, R M Gardiner, Hannah M. Mitchison, I. C. McManus, Mark I. Rees, Weiming Xu, K L Parker, Rebecca C.J. Twells, Guanjie Chen and Anders Sundqvist and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Proceedings of the Royal Society B Biological Sciences and Journal of Medical Genetics.

In The Last Decade

E. Chung

9 papers receiving 255 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
E. Chung United Kingdom	8	103	98	57	51	46	9	267
Rik Hendrickx Belgium	7	130 1.3×	123 1.3×	32 0.6×	66 1.3×	19 0.4×	17	329
Radoslava Vazharova Bulgaria	7	103 1.0×	106 1.1×	21 0.4×	46 0.9×	21 0.5×	26	235
Teresa Francavilla Italy	7	59 0.6×	38 0.4×	53 0.9×	58 1.1×	26 0.6×	10	249
Tung‐Ming Chang Taiwan	11	49 0.5×	89 0.9×	20 0.4×	47 0.9×	23 0.5×	33	313
Rosa Mostardini Italy	11	138 1.3×	96 1.0×	17 0.3×	117 2.3×	13 0.3×	22	349
V. Sgrò Italy	9	150 1.5×	61 0.6×	20 0.4×	170 3.3×	64 1.4×	15	337
Mutluay Arslan Türkiye	10	78 0.8×	106 1.1×	26 0.5×	40 0.8×	13 0.3×	29	245
Carina Cutmore Australia	5	47 0.5×	87 0.9×	26 0.5×	121 2.4×	22 0.5×	6	255
Michael Quach United States	10	90 0.9×	59 0.6×	16 0.3×	95 1.9×	167 3.6×	19	327
Abdelrahim A. Sadek Egypt	8	73 0.7×	54 0.6×	11 0.2×	48 0.9×	67 1.5×	33	228

Countries citing papers authored by E. Chung

Since Specialization

Citations

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

Fields of papers citing papers by E. Chung

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of E. Chung

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

All Works

Sort: Min cites: Since: Top N: Style:

9 of 9 papers shown

Paff, Tamara, Alexandros Onoufriadis, Daniel C. Anthony, et al.. (2013). Mutation in the CCDC114 gene causes Primary Ciliary Dyskinesia with normal fertility in the isolated Volendam population. Tijdschrift voor kindergeneeskunde. 81(S1). 92–92. 3 indexed citations

McManus, I. C., et al.. (2004). Handedness and situs inversus in primary ciliary dyskinesia. Proceedings of the Royal Society B Biological Sciences. 271(1557). 2579–2582. 58 indexed citations

Maiti, Amit K., Lucia Bartoloni, Hannah M. Mitchison, et al.. (2000). No deleterious mutations in the FOXJ1 (alias HFH-4) gene in patients with Primary Ciliary Dyskinesia (PCD). Cytogenetic and Genome Research. 90(1-2). 119–122. 27 indexed citations

Chung, E., David Curtis, Guanjie Chen, et al.. (1996). Genetic evidence for the neuronal nitric oxide synthase gene (NOS1) as a susceptibility locus for infantile pyloric stenosis.. PubMed. 58(2). 363–70. 68 indexed citations

Chung, E.. (1995). Exclusion of the locus for autosomal recessive pseudohypoaldosteronism type 1 from the mineralocorticoid receptor gene region on human chromosome 4q by linkage analysis. The Journal of Clinical Endocrinology & Metabolism. 80(11). 3341–3345. 11 indexed citations

Chung, E., Aaron Hanukoglu, Mark I. Rees, et al.. (1995). Exclusion of the locus for autosomal recessive pseudohypoaldosteronism type 1 from the mineralocorticoid receptor gene region on human chromosome 4q by linkage analysis.. The Journal of Clinical Endocrinology & Metabolism. 80(11). 3341–3345. 11 indexed citations

Rees, Mark I., David Curtis, K L Parker, et al.. (1994). Linkage Analysis of Idiopathic Generalised Epilepsy in Families of Probands with Juvenile Myoclonic Epilepsy and Marker Loci in the Region of EPM 1 on Chromosome 21 q: Unverricht-Lundborg Disease and JME are not Allelic Variants. Neuropediatrics. 25(1). 20–25. 8 indexed citations

Chung, E., Ronald G. Coffey, Keith A. Parker, et al.. (1993). Linkage analysis of infantile pyloric stenosis and markers from chromosome 9q11-q33: no evidence for a major gene in this candidate region.. Journal of Medical Genetics. 30(5). 393–395. 9 indexed citations

Whitehouse, William, Mark I. Rees, David Curtis, et al.. (1993). Linkage analysis of idiopathic generalized epilepsy (IGE) and marker loci on chromosome 6p in families of patients with juvenile myoclonic epilepsy: no evidence for an epilepsy locus in the HLA region.. PubMed. 53(3). 652–62. 72 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.

Explore authors with similar magnitude of impact