Eddie M.K. Chung

5.3k citations

20 papers · 1.9k indexed · h-index 16

Molecular Biology top 10%
Genetics top 2%
Pulmonary and Respiratory Medicine top 5%
Surgery
Nutrition and Dietetics top 5%

Co-authors: R. Mark Gardiner Hannah M. Mitchison Richard J. Thompson Sandra Strautnieks France Ziereisen Bülend Yüksel Jean‐Pierre Fryns Lionel Van Maldergem
Topics: Intestinal Malrotation and Obstruction Disorders (6 papers)Genetic and Kidney Cyst Diseases (6 papers)Cystic Fibrosis Research Advances (5 papers)
Cited by: Genetics Nephrology Pulmonary and Respiratory Medicine
Journals: Proceedings of the National Academy of Sciences Nature Genetics The American Journal of Human Genetics
Partner nations: United Kingdom United States India

In The Last Decade

Eddie M.K. Chung

20 papers receiving 1.8k citations

Peers

Countries citing papers authored by Eddie M.K. Chung

Since Specialization

Citations

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

Fields of papers citing papers by Eddie M.K. Chung

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eddie M.K. Chung

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	C11orf70 Mutations Disrupting the Intraflagellar Transport-Dependent Assembly of Multiple Axonemal Dyneins Cause Primary Ciliary Dyskinesia 2018 ·The American Journal of Human Genetics ·Mahmoud R. Fassad,Amelia Shoemark,Pierrick Le Borgne,France Koll,Mitali Patel,Mellisa Dixon,Jane Hayward,(unknown),Emily Frost,Lucy Jenkins,Thomas Cullup,Eddie M.K. Chung,Michel Lemullois,Anne Aubusson‐Fleury,Claire Hogg,David R. Mitchell,Anne‐Marie Tassin,Hannah M. Mitchison	48
2	Primary ciliary dyskinesia with normal ultrastructure: three-dimensional tomography detects absence of DNAH11 2018 ·European Respiratory Journal ·Amelia Shoemark,Thomas Burgoyne,(unknown),Mellisa Dixon,Mitali Patel,Andrew Rogers,Alexandros Onoufriadis,Juliet Scully,(unknown),Thomas Cullup,Michael R. Loebinger,Robert Wilson,Eddie M.K. Chung,Andrew Bush,Hannah M. Mitchison,Claire Hogg	29
3	A novel missense mutation in the transcription factor FOXF1 cosegregating with infantile hypertrophic pyloric stenosis in the extended pedigree linked to IHPS5 on chromosome 16q24 2016 ·Pediatric Research ·Kate V. Everett,Paris Ataliotis,Barry A. Chioza,Charles Shaw‐Smith,Eddie M.K. Chung	9
4	Confirmation of two novel loci for infantile hypertrophic pyloric stenosis on chromosomes 3 and 5 2013 ·Journal of Human Genetics ·Kate V. Everett,Eddie M.K. Chung	8
5	Combined exome and whole-genome sequencing identifies mutations in ARMC4 as a cause of primary ciliary dyskinesia with defects in the outer dynein arm 2013 ·Journal of Medical Genetics ·Alexandros Onoufriadis,Amelia Shoemark,Mustafa M. Munye,Chela James,Miriam Schmidts,Mitali Patel,Elisabeth Rosser,Chiara Bacchelli,Philip L. Beales,Peter Scambler,Stephen L. Hart,(unknown),John J. Sloper,Sarah Hull,Claire Hogg,Richard D. Emes,Gerard Pals,Anthony T. Moore,Eddie M.K. Chung,Hannah M. Mitchison,(unknown)	63
6	Mutations in axonemal dynein assembly factor DNAAF3 cause primary ciliary dyskinesia 2012 ·Nature Genetics ·Hannah M. Mitchison,Miriam Schmidts,Niki T. Loges,Judy Freshour,Athina Dritsoula,Robert A. Hirst,Christopher O’Callaghan,Hannah Blau,Maha Al Dabbagh,Heike Olbrich,Philip L. Beales,Toshiki Yagi,Huda Mussaffi,Eddie M.K. Chung,Heymut Omran,David R. Mitchell	190
7	Splice-Site Mutations in the Axonemal Outer Dynein Arm Docking Complex Gene CCDC114 Cause Primary Ciliary Dyskinesia 2012 ·The American Journal of Human Genetics ·Alexandros Onoufriadis,Tamara Paff,Dinu Antony,Amelia Shoemark,Dimitra Micha,(unknown),Miriam Schmidts,Stavroula Petridi,(unknown),Eric G. Haarman,Johannes M. A. Daniels,Richard D. Emes,Robert Wilson,Claire Hogg,Peter Scambler,Eddie M.K. Chung,Gerard Pals,Hannah M. Mitchison	137
8	Genome-wide linkage analysis in families with infantile hypertrophic pyloric stenosis indicates novel susceptibility loci 2011 ·Journal of Human Genetics ·Anna Svenningsson,Cilla Söderhäll,(unknown),Fredrik Lundberg,Holger Luthman,Eddie M.K. Chung,Mark Gardiner,Ingrid Kockum,Agneta Nordenskjöld	10
9	Infantile hypertrophic pyloric stenosis: evaluation of three positional candidate genes, TRPC1, TRPC5 and TRPC6, by association analysis and re-sequencing 2009 ·Human Genetics ·Kate V. Everett,Barry A. Chioza,(unknown),Ashley Reece,R. Mark Gardiner,Eddie M.K. Chung	20
10	Linkage of monogenic infantile hypertrophic pyloric stenosis to chromosome 16q24 2008 ·European Journal of Human Genetics ·Kate V. Everett,Francesca Capon,(unknown),Barry A. Chioza,Ashley Reece,Mervyn Jaswon,Agostino Pierro,Prem Puri,R. Mark Gardiner,Eddie M.K. Chung	19
11	Competency domains in an undergraduate Objective Structured Clinical Examination: their impact on compensatory standard setting 2008 ·Medical Education ·Ashley Reece,Eddie M.K. Chung,R. Mark Gardiner,(unknown)	10
12	Genome-wide High-Density SNP-Based Linkage Analysis of Infantile Hypertrophic Pyloric Stenosis Identifies Loci on Chromosomes 11q14-q22 and Xq23 2008 ·The American Journal of Human Genetics ·Kate V. Everett,Barry A. Chioza,(unknown),Ashley Reece,Francesca Capon,Keith A. Parker,(unknown),Paul McKeigue,Sally G. Mitton,Agostino Pierro,Prem Puri,Hannah M. Mitchison,Eddie M.K. Chung,R. Mark Gardiner	36
13	Linkage of Monogenic Infantile Hypertrophic Pyloric Stenosis to Chromosome 16p12-p13 and Evidence for Genetic Heterogeneity 2006 ·The American Journal of Human Genetics ·Francesca Capon,Ashley Reece,Rathi Ravindrarajah,Eddie M.K. Chung	24
14	Primary ciliary dyskinesia (Siewert's / Kartagener's Syndrome): Respiratory symptoms and psycho-social impact 2003 ·BMC Pulmonary Medicine ·I. C. McManus,Hannah M. Mitchison,Eddie M.K. Chung,(unknown),(unknown)	49
15	Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left–right asymmetry 2002 ·Nature Genetics ·Heike Olbrich,Karsten Häffner,Andreas Kispert,(unknown),(unknown),(unknown),Richard Reinhardt,Steffen Hennig,Hans Lehrach,N. Konietzko,Maimoona A. Zariwala,Peadar G. Noone,Michael R. Knowles,Hannah M. Mitchison,Maggie Meeks,Eddie M.K. Chung,Friedhelm Hildebrandt,Ralf Sudbrak,Heymut Omran	373
16	Mutations in the DNAH11 (axonemal heavy chain dynein type 11) gene cause one form of situs inversus totalis and most likely primary ciliary dyskinesia 2002 ·Proceedings of the National Academy of Sciences ·Lucia Bartoloni,Jean‐Louis Blouin,Yanzhen Pan,Corinne Gehrig,Amit K. Maiti,Nathalie Scamuffa,Colette Rossier,Mark Jorissen,M Armengot,Maggie Meeks,Hannah M. Mitchison,Eddie M.K. Chung,C.D. DeLozier-Blanchet,William J. Craigen,Stylianos E. Antonarakis	233
17	Axonemal Beta Heavy Chain Dynein DNAH9: cDNA Sequence, Genomic Structure, and Investigation of Its Role in Primary Ciliary Dyskinesia 2001 ·Genomics ·Lucia Bartoloni,Jean‐Louis Blouin,Amit K. Maiti,Amanda Sainsbury,Colette Rossier,Corinne Gehrig,Jin‐Xiong She,Michele P. Marron,Eric S. Lander,Maggie Meeks,Eddie M.K. Chung,Miquel Armengot‐Carbó,Mark Jorissen,Hamish S. Scott,C.D. DeLozier-Blanchet,R M Gardiner,Stylianos E. Antonarakis	39
18	Mutations in the gene encoding the human matrix Gla protein cause Keutel syndrome 1999 ·Nature Genetics ·Patricia B. Munroe,Rana Olguntürk,Jean‐Pierre Fryns,Lionel Van Maldergem,France Ziereisen,Bülend Yüksel,R. Mark Gardiner,Eddie M.K. Chung	314
19	Localisation of Pseudohypoaldosteronism Genes to Chromosome 16p12.2–13.11 and 12p13.1-Pter by Homozygosity Mapping 1996 ·Human Molecular Genetics ·Sandra Strautnieks,Richard J. Thompson,Aaron Hanukoglu,Michael J. Dillon,Israel Hanukoglu,Ursula Kuhnle,Jonathan R. Seckl,R. Mark Gardiner,Eddie M.K. Chung	57
20	A novel spice–site mutation in the γ subunit of the epithelial sodium channel gene in three pseudohypoaldosteronism type 1 families 1996 ·Nature Genetics ·Sandra Strautnieks,Richard J. Thompson,R. Mark Gardiner,Eddie M.K. Chung	185

About Eddie M.K. Chung

Eddie M.K. Chung is a scholar working on Family Practice, Gastroenterology and Genetics, having authored 20 papers that have together received 1.9k indexed citations. Recurring topics across this work include Intestinal Malrotation and Obstruction Disorders (6 papers), Genetic and Kidney Cyst Diseases (6 papers) and Cystic Fibrosis Research Advances (5 papers). The work is most often cited by research in Genetics (867 citations), Nephrology (151 citations) and Pulmonary and Respiratory Medicine (648 citations). Eddie M.K. Chung has collaborated with scholars based in United Kingdom, United States and India. Frequent co-authors include R. Mark Gardiner, Hannah M. Mitchison, Richard J. Thompson, Sandra Strautnieks, France Ziereisen, Bülend Yüksel, Jean‐Pierre Fryns, Lionel Van Maldergem, Patricia B. Munroe and Rana Olguntürk. Their work appears in journals such as Proceedings of the National Academy of Sciences, Nature Genetics and The American Journal of Human Genetics.

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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