Area of research
Immunology · Dermatology
Research interest
Research interests include Skin and Cellular Biology Research, Psoriasis: Treatment and Pathogenesis, Dermatology and Skin Diseases, and Acne and Rosacea Treatments and Effects.
GWAS meta-analysis of psoriasis identifies new susceptibility alleles impacting disease mechanisms and therapeutic targets
Genetic basis of early onset and progression of type 2 diabetes in South Asians
Exploring the Link Between Genetic Predictors of Cardiovascular Disease and Psoriasis
Genetic architecture of routinely acquired blood tests in a British South Asian cohort
Mutation detection in saliva from oral cancer patients
A genome-wide meta-analysis of palmoplantar pustulosis implicates TH2 responses and cigarette smoking in disease pathogenesis
Systematic review of deep learning image analyses for the diagnosis and monitoring of skin disease
Genome-wide association meta-analysis identifies 29 new acne susceptibility loci
Comparative Genetic Analysis of Psoriatic Arthritis and Psoriasis for the Discovery of Genetic Risk Factors and Risk Prediction Modeling
Pathogenic variants in SLF2 and SMC5 cause segmented chromosomes and mosaic variegated hyperploidy
Exome Sequencing Highlights a Potential Role for Concealed Cardiomyopathies in Youthful Sudden Cardiac Death
Patients with triple-negative, <i>JAK2</i>V617F- and <i>CALR</i>-mutated essential thrombocythemia share a unique gene expression signature
Phenotypic and genetic spectrum of epilepsy with myoclonic atonic seizures
Mitochondria function associated genes contribute to Parkinson’s Disease risk and later age at onset
Genome-wide association study in frontal fibrosing alopecia identifies four susceptibility loci including HLA-B*07:02
Genotype–phenotype correlation in a large English cohort of patients with autosomal recessive ichthyosis
Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia
De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
The ADAMTS13–VWF axis is dysregulated in chronic thromboembolic pulmonary hypertension
Frequency of pathogenic germline variants in BRCA1, BRCA2, PALB2, CHEK2 and TP53 in ductal carcinoma in situ diagnosed in women under the age of 50 years
Frequency of Pathogenic Germline Variants in <i>CDH1, BRCA2, CHEK2, PALB2, BRCA1</i>, and <i>TP53</i> in Sporadic Lobular Breast Cancer
HLA-C*06:02 genotype is a predictive biomarker of biologic treatment response in psoriasis
Report from the fifth international consensus meeting to harmonize core outcome measures for atopic eczema/dermatitis clinical trials (HOME initiative)
Cardiac Genetic Predisposition in Sudden Infant Death Syndrome
Dysfunction of NaV1.4, a skeletal muscle voltage-gated sodium channel, in sudden infant death syndrome: a case-control study
Genome-wide meta-analysis implicates mediators of hair follicle development and morphogenesis in risk for severe acne
Mutation in GNE is associated with severe congenital thrombocytopenia
Importance of Variant Interpretation in Whole-Exome Molecular Autopsy
Exome Sequencing and Rare Variant Analysis Reveals Multiple Filaggrin Mutations in Bangladeshi Families with Atopic Eczema and Additional Risk Genes