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- PLCD1 and Pilar Cysts
- Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
- Polycystic ovary syndrome
- Organization and Expression of Hair Follicle Genes.
- Mammalian keratin associated proteins (KRTAPs) subgenomes: disentangling hair diversity and adaptation to terrestrial and aquatic environments
- Identification of reptilian genes encoding hair keratin-like proteins suggests a new scenario for the evolutionary origin of hair
- Dermatologic Disorders
- The possible implication of the S250C variant of the autoimmune regulator protein in a patient with autoimmunity and immunodeficiency: in silico analysis suggests a molecular pathogenic mechanism for the variant
- Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families
- Identification and sequence analysis of the keratin-associated protein 24‐1 (KAP24-1) gene homologue in sheep
- Genomic and transcriptomic landscape to decipher the genetic basis of hyperpigmentation in Lanping black-boned sheep (Ovis aries)
- Convergent Evolution of Cysteine-Rich Keratins in Hard Skin Appendages of Terrestrial Vertebrates
- The Genetics of Acne
- Characterization of hairless (Hr) and FGF5genes provides insights into the molecular basis of hair loss in cetaceans
- What does acne genetics teach us about disease pathogenesis?
- Clinical-exome sequencing unveils the genetic landscape of polycystic ovarian syndrome (PCOS) focusing on lean and obese phenotypes: implications for cost-effective diagnosis and personalized treatment
- Past, Present and Future Perspectives of Forensic Genetics
- The genetics of alopecia areata: New approaches, new findings, new treatments
- Current Genetics in Hair Diseases
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Atrichia congenita with papular lesions: A rare cause of pediatric alopecia
- One of These Things Is Not Like the Others: The Idea of Precedence in Health Technology Assessment and Coverage Decisions
- Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: a case report and review of the literature
- Congenital hair loss disorders: Rare, but not too rare
- Genetic Variants Associated with Hyperandrogenemia in PCOS Pathophysiology
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- Genetic hair and nail disorders
- Animal fibre: connecting science and production
- Recent advances in the genetics of alopecia areata
- Mini Review on Polycystic Ovary Syndrome (PCOS)