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Author Details

John A McGrath
1990
577
68
PMIDPaper TitleJournal TitlePublished Year
36978220A review of genotrichoses and hair pathology associated with inherited skin diseases.2023
37655918Gluten-sensitive enteropathy in recessive dystrophic epidermolysis bullosa.2023
37559055Itch in recessive dystrophic epidermolysis bullosa: findings of PEBLES, a prospective register study.2023
37690594Genome-wide meta-analysis implicates variation affecting mast cell biology in urticaria.2023
37212630KLK11 ichthyosis: large truncal hyperkeratotic pigmented plaques underscore a distinct autosomal dominant disorder of cornification.2023
37150587Spatial transcriptomics in human skin research.2023
37337559Innovations in the Treatment of Dystrophic Epidermolysis Bullosa (DEB): Current Landscape and Prospects.2023
37211199Shared Genetic Risk Variants in Both Male and Female Frontal Fibrosing Alopecia.J Invest Dermatol2023
36774976Loss of RhoE Function in Dermatofibroma Promotes Disorganized Dermal Fibroblast Extracellular Matrix and Increased Integrin Activation.2023
36763865Treatment of multifactorial anaemia in adults with severe epidermolysis bullosa using intravenous ferric carboxymaltose: a single institution, observational, retrospective study.2023
36763859Two phase III trials of baricitinib for alopecia areata: a critically appraised research paper.2023
36757922Atrichia with papular lesions in a 1-year-old girl resulting from a new homozygous nonsense pathogenic variant in the hairless gene.2023
37001733Physical urticaria: Clinical features, pathogenesis, diagnostic work-up, and management.2023
36868990ABCB5 mesenchymal stromal cells facilitate complete and durable wound closure in recessive dystrophic epidermolysis bullosa.2023
36864587Familial hypotrichosis simplex of the scalp associated with a novel heterozygous nonsense variant in CDSN.2023
36796725Systematic review of the clinical characteristics and natural history of solar urticaria.J Am Acad Dermatol2023
36689522Biallelic TUFT1 variants cause woolly hair, superficial skin fragility and desmosomal defects.Br J Dermatol2023
36929380A novel heterozygous missense variant in ribosomal protein L21 associated with familial hypotrichosis simplex.Clin Exp Dermatol2023
36730518Actinic lichen planopilaris: a new variant of lichen planopilaris triggered by ultraviolet radiation.2023
36598763Comorbidities of Keloid and Hypertrophic Scars Among Participants in UK Biobank.JAMA Dermatol2023
37517864Corrigendum to ABCB5+ mesenchymal stromal cells facilitate complete and durable wound closure in recessive dystrophic epidermolysis bullosa [Cytotherapy 25 (2023) 782-788/1562].2023
34806203Localized autosomal recessive epidermolysis bullosa simplex arising from a novel homozygous frameshift mutation in DST (BPAG1).Clinical and Experimental Dermatology2022
35909063Plasma metabolomic profiling reflects the malnourished and chronic inflammatory state in recessive dystrophic epidermolysis bullosa.2022
35584643Restoring type VII collagen in skin.Med2022
35763388Vitamin C concentrations in patients with epidermolysis bullosa.British Journal of Dermatology2022
35491651Autosomal dominant epidermolysis bullosa simplex exacerbated by hyperkeratotic scabies.2022
35779741Collagen VII maintains proteostasis in dermal fibroblasts by scaffolding TANGO1 cargo.Matrix Biology2022
36578049Mutational analysis of epidermolysis bullosa in Taiwan by whole-exome sequencing complemented by RNA sequencing: a series of 77 patients.2022
34310949Transcriptomic Analysis of Blaschko-Linear Psoriasis Reveals Shared and Distinct Features with Psoriasis Vulgaris.2022
34927719The epidemiology of epidermolysis bullosa in England and Wales: data from the national epidermolysis bullosa database.Br J Dermatol2022
34862606The potential of gene therapy for recessive dystrophic epidermolysis bullosa.British Journal of Dermatology2022
35267209Incontinentia pigmenti in a male infant and a proposed diagnostic algorithm.Clinical and Experimental Dermatology2022
34726314Pathogenesis of solar urticaria: Classic perspectives and emerging concepts.Exp Dermatol2022
34665888Plasma metabolomic and lipidomic profiling highlights metabolic changes in keloid-prone individuals.Experimental Dermatology2022
35191062WNT10A variant and severe scoliosis?2022
35023595Transcriptomic response of peripheral blood mononuclear cells to secukinumab in an 8-year-old boy with juvenile generalized pustular psoriasis.Journal of the European Academy of Dermatology and Venereology2022
35131257The Past and Future of Rare Skin Disease Research and Therapy.2022
34596894Unravelling the genetic basis of contact allergy.Contact Dermatitis2022
34999892Mutations in the ribosome biogenesis factor gene LTV1 are linked to LIPHAK syndrome, a novel poikiloderma-like disorder.Hum Mol Genet2022
34480347Clinical characteristics of male frontal fibrosing alopecia: a single-centre case series from London, UK.British Journal of Dermatology2022
35104371A clinician's guide to omics resources in dermatology.Clinical and Experimental Dermatology2022
34694680Transcriptomic profiling of recessive dystrophic epidermolysis bullosa wounded skin highlights drug repurposing opportunities to improve wound healing.Exp Dermatol2022
35196402Single-cell transcriptomics in human skin research: available technologies, technical considerations and disease applications.Experimental Dermatology2022
34756815Corrigendum to "Metabolic perturbations in fibrosis disease" [Int. J. Biochem. Cell Biol. 139 (2021) 106073].International Journal of Biochemistry and Cell Biology2021
34292508Investigational Treatments for Epidermolysis Bullosa.2021
34284275Induced pluripotent stem cell (iPSC) line MLi-004A derived from a patient with recessive dystrophic epidermolysis bullosa (RDEB).Stem Cell Research2021
34231856Complexity of Transcriptional and Translational Interference of Laminin-332 Subunits in Junctional Epidermolysis Bullosa with LAMB3 Mutations.Acta Dermato-Venereologica2021
34230977Cutaneous Squamous Cell Carcinoma in Epidermolysis Bullosa: a 28-year Retrospective Study.Acta Dermato-Venereologica2021
33961311A truncating variant in SERPINA3, skin pustules and adult-onset immunodeficiency.2021
33797104Synergistic multiple early therapy (SMET) for inflammatory diseases with pathogenic autoinflammatory feedback circuits.British Journal of Dermatology2021
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