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- News in brief
- Genetic Variants at 20p11 Confer Risk to Androgenetic Alopecia in the Chinese Han Population
- Disease causing homozygous variants in the human hairless gene
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer’s disease
- Mapping of cis-acting expression quantitative trait loci in human scalp hair follicles
- Roles of <i>jumonji</i> and <i>jumonji</i> family genes in chromatin regulation and development
- Genetic prediction of male pattern baldness
- Dissection of genetic variation and evidence for pleiotropy in male pattern baldness
- Hairless is a nuclear receptor corepressor essential for skin function
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Mettl3-catalyzed m <sup>6</sup> A regulates histone modifier and modification expression in self-renewing somatic tissue
- The pioneer factor SOX9 competes for epigenetic factors to switch stem cell fates
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Defining the identity of mouse embryonic dermal fibroblasts
- Age-Related Changes in Hair Shaft Protein Profiling and Genetically Variant Peptides
- Immunological aspects and gender bias during respiratory viral infections including novel Coronavirus disease‐19 (COVID‐19): A scoping review
- HR Gene Variants Identified in Mexican Patients with Alopecia Areata
- Hair Follicle-Related MicroRNA-34a Serum Expression and rs2666433A/G Variant in Patients with Alopecia: A Cross-Sectional Analysis
- Production of a 135-residue long N-truncated human keratinocyte growth factor 1 in Escherichia coli
- GWASs Identify Genetic Loci Associated with Human Scalp Hair Whorl Direction
- Identification of an Intronic Regulatory Element Necessary for Tissue-Specific Expression of <i>Foxn1</i> in Thymic Epithelial Cells
- Second International Symposium—Epigenetic Regulation of Skin Regeneration and Aging: From Chromatin Biology towards the Understanding of Epigenetic Basis of Skin Diseases
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- Genetic Polymorphisms of Immunity Regulatory Genes and Alopecia Areata Susceptibility in Jordanian Patients
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Hunting the genes in male‐pattern alopecia: how important are they, how close are we and what will they tell us?
- GRHL3 binding and enhancers rearrange as epidermal keratinocytes transition between functional states
- The genetics of autism and steroid-related traits in prenatal and postnatal life
- BJD Editor's Choice