Publications by authors named "Eddie Chung"

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pH Sensitive Erythrocyte-Derived Membrane for Acute Systemic Retention and Increased Infectivity of Coated Oncolytic Vaccinia Virus.
Kaelan T Samoranos, Alexandra L Krisiewicz, Bianca C Karpinecz, Philip A Glover, Trevor V Gale, Eddie Y Chung

Pharmaceutics· August 2022

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Clinical utility of NGS diagnosis and disease stratification in a multiethnic primary ciliary dyskinesia cohort.
Mahmoud R Fassad, Mitali P Patel, Amelia Shoemark, Thomas Cullup, Jane Hayward, Eddie M K Chung

J Med Genet· May 2020

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Risk factors for situs defects and congenital heart disease in primary ciliary dyskinesia.
Sunayna Best, Amelia Shoemark, Bruna Rubbo, Mitali P Patel, Mahmoud R Fassad, Eddie Mk Chung

Thorax· February 2019

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C11orf70 Mutations Disrupting the Intraflagellar Transport-Dependent Assembly of Multiple Axonemal Dyneins Cause Primary Ciliary Dyskinesia.
Mahmoud R Fassad, Amelia Shoemark, Pierrick le Borgne, France Koll, Mitali Patel, Eddie M K Chung

Am J Hum Genet· May 2018

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High prevalence of p.His154Pro mutation causing primary ciliary dyskinesia disrupts protein oligomerisation and is associated with normal diagnostic investigations.
Amelia Shoemark, Eduardo Moya, Robert A Hirst, Mitali P Patel, Evelyn A Robson, Eddie M K Chung

Thorax· February 2018

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Primary ciliary dyskinesia with normal ultrastructure: three-dimensional tomography detects absence of DNAH11.
Amelia Shoemark, Thomas Burgoyne, Robert Kwan, Mellisa Dixon, Mitali P Patel, Eddie M K Chung

Eur Respir J· February 2018

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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.
Kate V Everett, Paris Ataliotis, Barry A Chioza, Charles Shaw-Smith, Eddie M K Chung

Pediatr Res· April 2017

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X-linked primary ciliary dyskinesia due to mutations in the cytoplasmic axonemal dynein assembly factor PIH1D3.
Chiara Olcese, Mitali P Patel, Amelia Shoemark, Santeri Kiviluoto, Marie Legendre, Eddie M K Chung

Nat Commun· February 2017

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Activatable and Cell-Penetrable Multiplex FRET Nanosensor for Profiling MT1-MMP Activity in Single Cancer Cells.
Eddie Y Chung, Christopher J Ochs, Yi Wang, Lei Lei, Qin Qin

Nano Lett· August 2015

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CCDC151 mutations cause primary ciliary dyskinesia by disruption of the outer dynein arm docking complex formation.
Rim Hjeij, Alexandros Onoufriadis, Christopher M Watson, Christopher E Slagle, Nikolai T Klena, Eddie M K Chung

Am J Hum Genet· September 2014

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Targeted NGS gene panel identifies mutations in RSPH1 causing primary ciliary dyskinesia and a common mechanism for ciliary central pair agenesis due to radial spoke defects.
Alexandros Onoufriadis, Amelia Shoemark, Miriam Schmidts, Mitali Patel, Gina Jimenez, Eddie M K Chung

Hum Mol Genet· July 2014

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MCIDAS mutations result in a mucociliary clearance disorder with reduced generation of multiple motile cilia.
Mieke Boon, Julia Wallmeier, Lina Ma, Niki Tomas Loges, Martine Jaspers, Eddie M K Chung

Nat Commun· July 2014

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Combined exome and whole-genome sequencing identifies mutations in ARMC4 as a cause of primary ciliary dyskinesia with defects in the outer dynein arm.
Alexandros Onoufriadis, Amelia Shoemark, Mustafa M Munye, Chela T James, Miriam Schmidts, Eddie M K Chung

J Med Genet· January 2014

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Mutations in ZMYND10, a gene essential for proper axonemal assembly of inner and outer dynein arms in humans and flies, cause primary ciliary dyskinesia.
Daniel J Moore, Alexandros Onoufriadis, Amelia Shoemark, Michael A Simpson, Petra I zur Lage, Eddie M K Chung

Am J Hum Genet· August 2013

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Confirmation of two novel loci for infantile hypertrophic pyloric stenosis on chromosomes 3 and 5.
Kate V Everett, Eddie M K Chung

J Hum Genet· April 2013

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Mutations in CCDC39 and CCDC40 are the major cause of primary ciliary dyskinesia with axonemal disorganization and absent inner dynein arms.
Dinu Antony, Anita Becker-Heck, Maimoona A Zariwala, Miriam Schmidts, Alexandros Onoufriadis, Eddie M K Chung

Hum Mutat· March 2013

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Splice-site mutations in the axonemal outer dynein arm docking complex gene CCDC114 cause primary ciliary dyskinesia.
Alexandros Onoufriadis, Tamara Paff, Dinu Antony, Amelia Shoemark, Dimitra Micha, Eddie M K Chung

Am J Hum Genet· January 2013

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Recessive HYDIN mutations cause primary ciliary dyskinesia without randomization of left-right body asymmetry.
Heike Olbrich, Miriam Schmidts, Claudius Werner, Alexandros Onoufriadis, Niki T Loges, Eddie M K Chung

Am J Hum Genet· October 2012

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CCDC103 mutations cause primary ciliary dyskinesia by disrupting assembly of ciliary dynein arms.
Jennifer R Panizzi, Anita Becker-Heck, Victoria H Castleman, Dalal A Al-Mutairi, Yan Liu, Eddie M K Chung

Nat Genet· May 2012

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Hypersensitivity reactions to marijuana.
Ayla Tessmer, Noam Berlin, Gordon Sussman, Nathan Leader, Eddie Chu Chung

Ann Allergy Asthma Immunol· April 2012

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Mutations in axonemal dynein assembly factor DNAAF3 cause primary ciliary dyskinesia.
Hannah M Mitchison, Miriam Schmidts, Niki T Loges, Judy Freshour, Athina Dritsoula, Eddie M K Chung

Nat Genet· March 2012

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Genome-wide linkage analysis in families with infantile hypertrophic pyloric stenosis indicates novel susceptibility loci.
Anna Svenningsson, Cilla Söderhäll, Sofia Persson, Fredrik Lundberg, Holger Luthman, Eddie Chung

J Hum Genet· February 2012

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Infantile hypertrophic pyloric stenosis: evaluation of three positional candidate genes, TRPC1, TRPC5 and TRPC6, by association analysis and re-sequencing.
Kate V Everett, Barry A Chioza, Christina Georgoula, Ashley Reece, R Mark Gardiner, Eddie M K Chung

Hum Genet· December 2009

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Mutations in radial spoke head protein genes RSPH9 and RSPH4A cause primary ciliary dyskinesia with central-microtubular-pair abnormalities.
Victoria H Castleman, Leila Romio, Rahul Chodhari, Robert A Hirst, Sandra C P de Castro, Eddie M K Chung

Am J Hum Genet· February 2009

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Infantile hypertrophic pyloric stenosis: genes and environment.
Eddie Chung

Arch Dis Child· December 2008

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