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- Somatic Mutations in Normal Tissues: New Perspectives on Early Carcinogenesis
- An in vivo method for the detection of somatic mutations at the cellular level in mice
- Somatic mutations distinguish melanocyte subpopulations in human skin
- Mutation of the doublecortin gene in male patients with double cortex syndrome: Somatic mosaicism detected by hair root analysis
- Identification of Somatic <i>KRAS</i> Mutation in a Korean Baby with Nevus Sebaceus Syndrome
- Cutaneous Lymphadenoma Is a Distinct Trichoblastoma-like Lymphoepithelial Tumor With Diffuse Androgen Receptor Immunoreactivity, Notch1 Ligand in Reed-Sternberg–like Cells, and Common EGFR Somatic Mutations
- Systematic analysis of somatic mutations driving cancer: uncovering functional protein regions in disease development
- Identification of somatic and germline mosaicism for a keratin 5 mutation in epidermolysis bullosa simplex in a family of which the proband was previously regarded as a sporadic case
- Androgen Receptor Mutations and Polymorphisms in African American Prostate Cancer
- A Monoallelic Two-Hit Mechanism in PLCD1 Explains the Genetic Pathogenesis of Hereditary Trichilemmal Cyst Formation
- Clonal analysis of stem cells in differentiation and disease
- Montagna Symposium 2014—Skin Aging: Molecular Mechanisms and Tissue Consequences
- Challenges associated with the identification of germline variants on myeloid malignancy genomic profiling—a Singaporean experience
- Regeneration, Wound Healing and Cancer
- Hairless-knockout piglets generated using the clustered regularly interspaced short palindromic repeat/CRISPR-associated-9 exhibit abnormalities in the skin and thymus
- GWAS Identifies Three Susceptibility Loci for Trichilemmal Cysts
- A family of type I keratin genes and the homeobox-2 gene complex are closely linked to the rex locus on mouse chromosome 11
- Mitochondrial dysfunction as a cause of ageing
- CPC14 Blaschko-linear trichoepitheliomas: unveiling type 1 segmental mosaicism
- Ichthyosis with confetti: clinics, molecular genetics and management
- Exome analysis for Cronkhite-Canada syndrome: A case report
- Identification and characterization of Birt–Hogg–Dubé associated renal carcinoma
- Novel <i>RNF113A</i> Variant Underlying X‐Linked Trichothiodystrophy With Presumed Mosaicism in an Unaffected Mother
- Great Expectations: Induced pluripotent stem cell technologies in neurodevelopmental impairments
- Tracing the cellular origin of cancer
- Porokeratotic adnexal ostial nevus: a paradigm of cutaneous mosaicism
- Seborrheic keratosis
- Beyond Coincidence in Neurofibromatosis Type 1: Becker Nevus Adjacent to Plexiform Neurofibroma with Brachial Plexus Involvement and Integrated Mechanistic Illustration
- Congenital cataract and slowly progressing facial skin lesions in a 5‐year‐old boy
- Identificación de la variación molecular y genética subyacente a las enfermedades de la piel