Michael A. Simpson

King's College London — United Kingdom

Biochemistry, Genetics and Molecular Biology · Life Sciences

76h-index38.8kcitations391works4.32yr avg
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Research Topics

Skin and Cellular Biology Research(30), Psoriasis: Treatment and Pathogenesis(22), Dermatology and Skin Diseases(19), Immunodeficiency and Autoimmune Disorders(18), Neurological diseases and metabolism(18)

Publications380 total

P18 Genome-wide meta-analysis identifies <i>ERAP1</i> in epistasis with MHC class I alleles in frontal fibrosing alopecia
British Journal of Dermatology·2026
O07 Solar urticaria is associated with novel rare missense variants in <i>ACACA</i>
British Journal of Dermatology·2026
The Skin Genetics Consortium
British Journal of Dermatology·2025Open Access
MSR177 Qualitative Analysis of Results From a Delphi Study to Formalize a Treatment Protocol for Children With Early Diagnosed Duchenne Muscular Disease (DMD) Using Giles®, an Artificial Intelligence Agent for Healthcare Research
Value in Health·2025
231 Genome-wide meta-analysis establishes the genetic basis of lichen sclerosus
Journal of Investigative Dermatology·2025
101 Comparative genetic analysis of atopic dermatitis and psoriasis and the potential therapeutic implications
Journal of Investigative Dermatology·2025
073 Identifying the severe psoriasis at-risk population: development of an integrated psoriasis severity risk stratification tool
Journal of Investigative Dermatology·2025Open Access
258 Genome-wide association meta-regression identifies stem cell lineage orchestration as a key driver of acne risk
Journal of Investigative Dermatology·2025
Unravelling the causal link between gut microbiota and acne risk using a genetic approach
Skin Health and Disease·2025Open Access
214 Longitudinal and Exploratory Genome-Wide Analysis in Alopecia AreaTA (LEGAATA): A Study of FinnGen Participants
Journal of Investigative Dermatology·2025Open Access
Investigating the interplay between prematurity and genetic variation in the context of rare developmental disorders
Genome Medicine·2025Open Access
Undiagnosed G6PD Deficiency in Black and Asian Individuals Is Prevalent and Contributes to Health Inequalities in Type 2 Diabetes Diagnosis and Complications
Diabetes Care·2025· 3 citedOpen Access
XBP1 expression in pancreatic islet cells is associated with poor glycaemic control especially in young non-obese onset diabetes across ancestries
Communications Medicine·2025Open Access
EE158 Assessing the Budget Impact and Time Savings of Introducing Nivolumab and Hyaluronidase SC to Patients Receiving Nivolumab IV Across Multiple Indications on a US Healthcare Plan
Value in Health·2025
Genome-wide association meta-regression identifies stem cell lineage orchestration as a key driver of acne risk
2025Open Access
O10 Acne polygenic risk score derived from genome-wide association metaregression enables prediction of severity
British Journal of Dermatology·2025· 1 citedOpen Access
Genetic exploration of the relationship between liability to psychiatric disorders and acne vulgaris
2025Open Access
Investigating the Genetic Basis of the Influence of Adiposity on Psoriasis: A Cross-Sectional Study in a Large United Kingdom Population–Based Biobank
Journal of Investigative Dermatology·2025· 4 citedOpen Access
Inherited deficiency of DIAPH1 identifies a DNA double strand break repair pathway regulated by γ-actin
Nature Communications·2025Open Access
Characterization of the clinical and photobiologic features of solar urticaria: a UK multicentre cross-sectional study
British Journal of Dermatology·2025Open Access
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Frequent Co-authors

Richard C. Trembath(16), Juliet N. Barker(11), Catherine Smith(9), Peter Mortimer(7), Andrew H. Crosby(7), Francesca Capon(6), Glen Brice(6), Sahar Mansour(6), Alexandros Onoufriadis(5), Andrew Pink(5), Pia Østergaard(5), Dimitra Dafou(5), Steve Jeffery(5), Venu Pullabhatla(4), A. David Burden(4), Fiona Connell(4), Wesley J. Woollard(4), Charu Deshpande(4), Pamela J. Shaw(3), Niovi Setta-Kaffetzi(3)