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- Haplotype analysis of<i>VEGF</i>gene polymorphisms in polycystic ovary syndrome
- The Associations of Androgen-Related Genes CYP21A2 and CYP19A1 with Severe Acne Vulgaris in Patients from Southwest China
- Association of estrogen receptor gene variants (ESR1 and ESR2) with polycystic ovary syndrome in Tunisia
- Pitfalls of mapping a large Turkish consanguineous family with vertical monilethrix inheritance.
- Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot
- Spatiotemporal Expression and Haplotypes Identification of KRT84 Gene and Their Association with Wool Traits in Gansu Alpine Fine-Wool Sheep
- Genetic Analysis of Male Pattern Baldness and the 5α-Reductase Genes
- Alopecia Areata is associated with MICA and an extended HLA haplotype
- Correlation and regression analysis of the <i>KRT27</i> and <i>ELOVL4</i> genes in cashmere fineness and other production performances in Liaoning cashmere goats
- Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases
- 0040 Machine learning algorithms as tools for identifying predictive autoantibody biomarkers in pemphigus vulgaris
- Polymorphisms in the promoter regions of the CXCL1 and CXCL2 genes contribute to increased risk of alopecia areata in the Korean population
- Genome-Wide Association Study of Fiber Diameter in Alpacas
- 304 Sephardic Ancestry in Recessive Dystrophic Epidermolysis Bullosa Individuals Carrying the Prevalent c.6527insC Mutation
- Genetics of Wool and Cashmere Fibre: Progress, Challenges, and Future Research
- Variant 1859G→A (Arg620Gln) of the “Hairless” Gene: Absence of Association with Papular Atrichia or Androgenetic Alopecia
- Polymorphisms and association of FAT1 gene with wool quality traits in Chinese Merino sheep
- <i>IGF2BP2</i> and <i>IGFBP3</i> Genotypes, Haplotypes, and Genetic Models Studies in Polycystic Ovary Syndrome
- A Tale of Two Haplotypes: The EDA2R/AR Intergenic Region is the Most Divergent Genomic Segment between Africans and East Asians in the Human Genome
- Progress on genome-wide association studies and selection signature analysis for agronomic traits in Chinese sheep and goats: review
- Alopecia areata susceptibility variant identified by MHC risk haplotype sequencing reproduces symptomatic patched hair loss in mice
- Kin‐cohort analysis of <i>LRRK2</i>‐G2019S penetrance in Parkinson's disease
- Skin transcriptomic and selection signature analyses identify ASIP as a key gene in cattle coat color determination
- Analysis of Vitamin D Receptor (VDR) Gene Polymorphisms in Alopecia Areata
- ALOPECIA AREATA-A CLINICAL ANALYSIS
- Facial skin aging: an integrative analysis of genetics, epigenetics, and lifestyle factors
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer’s disease
- Atopic dermatitis and risk of autoimmune diseases: a systematic review and meta-analysis
- Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family