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- Computational Drug Discovery in Chemotherapy-induced Alopecia via Text Mining and Biomedical Databases
- Table 1_Association between SQSTM1 dysregulation and risk in alopecia areata: a Mendelian randomization study.docx
- Integrated edge information and pathway topology for drug-disease associations
- Understanding the Molecular Landscape of Alopecia Areata: Key Genes, Regulatory Networks, and Therapeutic Targets
- Sequence and structure based assessment of non-synonymous SNPs in hypertrichosis universalis
- Neuropsychiatric Adverse Events of Montelukast: An Analysis of Real-World Datasets and drug−gene Interaction Network
- 555 Dermal single-cell atlas: a novel tool to explore fibroblast heterogeneity
- <i>De Novo</i>Transcriptome Assembly and Differential Gene Expression Profiling of Three<i>Capra hircus</i>Skin Types during Anagen of the Hair Growth Cycle
- MendelVar: gene prioritization at GWAS loci using phenotypic enrichment of Mendelian disease genes
- <i>signatureSearch</i>: environment for gene expression signature searching and functional interpretation
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- The keratin proteins and genes of wool and hair.
- Network-Based Drug Repositioning: Approaches, Resources, and Research Directions
- ELL Facilitates RNA Polymerase II–Mediated Transcription of Human Epidermal Proliferation Genes
- An Integrated Transcriptome Atlas of Embryonic Hair Follicle Progenitors, Their Niche, and the Developing Skin
- Olfactory receptor OR2AT4 regulates human hair growth
- 551 Combining Laser Capture Microdissection and RNAseq Analysis to Generate a Human Anagen Hair Follicle Transcriptome Atlas
- 731 Generation of a laser capture microdissection and RNAseq-based human anagen hair follicle transcriptome atlas
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- A new mutation resulting in the truncation of the TRAF6-interacting domain of XEDAR: a possible novel cause of hypohidrotic ectodermal dysplasia: Figure 1
- Pachyonychia congenita: Sporadic onset with mutation analysis
- Exploring the clinical implications of novel SRD5A2 variants in 46,XY disorders of sex development
- 8368 Functional Evaluation Of Novel CYP21A2 Variants: Expanding The Genetic Basis Of Non-classic CAH
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3
- Bioinformatics analysis of genes associated with the patchy-type alopecia areata: CD2 may be a new therapeutic target
- A curated catalog of canine and equine keratin genes
- Genetics of Wool and Cashmere Fibre: Progress, Challenges, and Future Research
- Analysis of the human diseasome using phenotype similarity between common, genetic and infectious diseases
- Effects of Collagen Peptides on Gene Expression Related to Hair Cycle Activation in the Skin