J.E. Lai-Cheong - Concepedia

Author

J.E. Lai-Cheong

King's College London

Also Known As

J E Lai-Cheong, J Lai‐Cheong, J. E. Lai-Cheong, J.E. Lai-Cheong, JE Lai‐Cheong, Joey E. LAI‐CHEONG

Publications

869

Citations

H-Index

Concepts

All Affiliations

King's College London University Hospital Lewisham

About

J.E. Lai-Cheong is an author at King's College London specializing in medicine, pathology, and dermatology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	232
2	Molecular Genetics	2	2	35
3	Public Health	1	1	14
4	Cell Biology	1	1	91
5	Molecular Medicine	1	1	15

J.E. Lai-Cheong

Publications

427

Citations

H-Index

Page 1

	Year	Citations
Colocalization of Kindlin-1, Kindlin-2, and Migfilin at Keratinocyte Focal Adhesion and Relevance to the Pathophysiology of Kindler Syndrome J.E. Lai-Cheong, Siegfried Ussar, Ken Arita, Journal of Investigative Dermatology Cell AdhesionPathologyKindler SyndromeCytoskeletonDermatology	2008	91
Cutaneous manifestations of tuberculosis J.E. Lai-Cheong, A.D. Agulló Pérez, Vivian Tang, Clinical and Experimental Dermatology Pulmonary TuberculosisPulmonary PathologyM. TuberculosisMedicineTuberculosis Prevention	2007	77
Recurrent heterozygous missense mutation, p.Gly573Ser, in the TRPV3 gene in an Indian boy with sporadic Olmsted syndrome J.E. Lai-Cheong, Gomathy Sethuraman, M Ramam, British Journal of Dermatology	2012	74
Novel truncating mutations in <i>PKP1</i> and <i>DSP</i> cause similar skin phenotypes in two Brazilian families Akio Tanaka, J.E. Lai-Cheong, Maria Ester Massara Café, British Journal of Dermatology	2009	44
Mutations in AEC syndrome skin reveal a role for p63 in basement membrane adhesion, skin barrier integrity and hair follicle biology S.E. Clements, Tanasit Techanukul, J.E. Lai-Cheong, British Journal of Dermatology	2012	43
Autosomal dominant junctional epidermolysis bullosa Noor Almaani, L. Liu, Patricia J.C. Dopping-Hepenstal, British Journal of Dermatology	2008	34
MBTPS2 mutation in a British pedigree with keratosis follicularis spinulosa decalvans Kenneth Fong, E. Wedgeworth, J.E. Lai-Cheong, Clinical and Experimental Dermatology Ifap SyndromeMendelian DisorderBritish PedigreeGenetic DisorderGenetics	2012	21
Infantile systemic hyalinosis associated with a putative splice-site mutation in the ANTXR2 gene Kenneth Fong, Akella Radha Rama Devi, J.E. Lai-Cheong, Clinical and Experimental Dermatology Developmental AnomalyMolecular Diagnostic TechniquesDevelopmental BiologyInfantile Systemic HyalinosisGenetic Disorder	2012	15
New homozygous <i>SPINK5</i> mutation, p.Gln333X, in a Turkish pedigree with Netherton syndrome Kenneth Fong, S. Akdeniz, Hilmi İsi, Clinical and Experimental Dermatology Developmental BiologySpink5 GeneCongenital IchthyosisGenetic DisorderMendelian Disorder	2010	14
Bullous acute haemorrhagic oedema of skin in infancy J.E. Lai-Cheong, P. Banerjee, Virginia Hill, Clinical and Experimental Dermatology HistopathologyVeterinary ScienceClinical DermatologyDermatologyDermatopathology	2007	14

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