Author

Joey E. Lai‐Cheong

Observed names: J Lai-Cheong, J.E. Lai-Cheong, Joey E Lai-Cheong, Joey E. Lai-Cheong, Joey Lai-Cheong, Joey Lai‐Cheong, Joey E. Lai-Cheong, Lai-Cheong, J. E., Lai-Cheong, JE, Lai-Cheong, Joey, Lai-Cheong,Joey

Observed institutions: University of London, Guy's Hospital, St Thomas' Hospital, Queen Mary University of London, King's College London, Guy's and St Thomas' NHS Foundation Trust, Wexham Park Hospital, Frimley Park Hospital, Royal Liverpool and Broadgreen University Hospital NHS Trust, Frimley Health NHS Foundation Trust, King Edward VII Hospital, Broadgreen Hospital, King's College Hospital

OpenAlex ID: A5114254746

Structure and function of skin, hair and nails

2013 · Joey E. Lai-Cheong, John A. McGrath · Medicine · 183

Oncostatin M Receptor-β Mutations Underlie Familial Primary Localized Cutaneous Amyloidosis

2008 · Ken Arita, Andrew P. South, et al. · The American Journal of Human Genetics · 148

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Genetic Diseases of Junctions

2007 · Joey E. Lai-Cheong, Ken Arita, et al. · Journal of Investigative Dermatology · 146

Kindlin-1 controls Wnt and TGF-β availability to regulate cutaneous stem cell proliferation

2014 · Emanuel Rognoni, Moritz Widmaier, et al. · Nature Medicine · 140

A Homozygous Nonsense Mutation within the Dystonin Gene Coding for the Coiled-Coil Domain of the Epithelial Isoform of BPAG1 Underlies a New Subtype of Autosomal Recessive Epidermolysis Bullosa Simplex

2010 · Richard W. Groves, Lu Liu, et al. · Journal of Investigative Dermatology · 140

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Revertant mosaicism in skin: natural gene therapy

2010 · Joey E. Lai-Cheong, John A. McGrath, et al. · Trends in Molecular Medicine · 119

Structure and function of skin, hair and nails

2017 · Joey E. Lai-Cheong, John A. McGrath · Medicine · 87

Kindler Syndrome

2009 · Joey E. Lai-Cheong, John A. McGrath · Dermatologic Clinics · 79

Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome

2012 · Akio Tanaka, Sarah Weinel, et al. · The American Journal of Human Genetics · 78

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Structure and function of skin, hair and nails

2009 · Joey E. Lai-Cheong, John A. McGrath · Medicine · 76

HB-EGF Induces COL7A1 Expression in Keratinocytes and Fibroblasts: Possible Mechanism Underlying Allogeneic Fibroblast Therapy in Recessive Dystrophic Epidermolysis Bullosa

2011 · Nikoletta Nagy, Noor Almaani, et al. · Journal of Investigative Dermatology · 69

Novel IL31RA gene mutation and ancestral OSMR mutant allele in familial primary cutaneous amyloidosis

2009 · Ming-Wei Lin, Ding-Dar Lee, et al. · European Journal of Human Genetics · 68

Cutaneous Manifestations of Internal Malignancy

2006 · C Elise Kleyn, Joey E Lai-Cheong, et al. · American Journal of Clinical Dermatology · 60

Autosomal Recessive Epidermolysis Bullosa Simplex Due to Loss of BPAG1-e Expression

2011 · Lu Liu, Patricia J. Dopping-Hepenstal, et al. · Journal of Investigative Dermatology · 59

Revertant Mosaicism in Recessive Dystrophic Epidermolysis Bullosa

2010 · Noor Almaani, Nikoletta Nagy, et al. · Journal of Investigative Dermatology · 59

Structure and function of skin, hair and nails

2021 · Joey E. Lai-Cheong, John A. McGrath · Medicine · 58

Somatic Mitochondrial DNA Deletions Accumulate to High Levels in Aging Human Extraocular Muscles

2010 · Patrick Yu-Wai-Man, Joey Lai-Cheong, et al. · Investigative Ophthalmology & Visual Science · 54

Loss-of-Function FERMT1 Mutations in Kindler Syndrome Implicate a Role for Fermitin Family Homolog-1 in Integrin Activation

2009 · Joey E. Lai-Cheong, Maddy Parsons, et al. · American Journal Of Pathology · 46

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New Glycine Substitution Mutations in Type VII Collagen Underlying Epidermolysis Bullosa Pruriginosa but the Phenotype is not Explained by a Common Polymorphism in the Matrix Metalloproteinase-1 Gene Promoter

2009 · N Almaani, L Liu, et al. · Acta Dermato Venereologica · 46

The molecular skin pathology of familial primary localized cutaneous amyloidosis

2010 · Akio Tanaka, Joey E. Lai‐Cheong, et al. · Experimental Dermatology · 42

Five New Homozygous Mutations in the KIND1 Gene in Kindler Syndrome

2007 · Joey E. Lai-Cheong, Lu Liu, et al. · Journal of Investigative Dermatology · 36

Revertant Mosaicism in Kindler Syndrome

2011 · Joey E. Lai-Cheong, Celia Moss, et al. · Journal of Investigative Dermatology · 32

Focal dermal hypoplasia resulting from a new nonsense mutation, p.E300X, in the PORCN gene

2007 · Suzanne E. Clements, Vesarat Wessagowit, et al. · Journal of Dermatological Science · 32

cis-Urocanic Acid Enhances Prostaglandin E2 Release and Apoptotic Cell Death via Reactive Oxygen Species in Human Keratinocytes

2011 · Kazuyo Kaneko, Susan L. Walker, et al. · Journal of Investigative Dermatology · 27

Schöpf-Schulz-Passarge syndrome resulting from a homozygous nonsense mutation, p.Cys107X, in WNT10A

2011 · Gabriela Petrof, Kenneth Fong, et al. · Australasian Journal of Dermatology · 24

Works count: 56

Citation count: 2,048

H-index: 24

I10-index: 31