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Research 22
- Evidence for two independent functional variants for androgenetic alopecia around the androgen receptor gene
- Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA
- Ancient Genomes Reveal the Evolutionary History and Origin of Cashmere-Producing Goats in China
- From bedside to bench: regulation of host factors in SARS-CoV-2 infection
- Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot
- ESGCT and FSGT Collaborative Congress Helsinki, Finland September 17–20, 2015 Abstracts
- Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness
- Dissection of genetic variation and evidence for pleiotropy in male pattern baldness
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- Prediction of male-pattern baldness from genotypes
- Melatonin promotes Cashmere goat (<i>Capra hircus</i>) secondary hair follicle growth: a view from integrated analysis of long non-coding and coding RNAs
- Identification of ultraviolet B radiation-induced microRNAs in normal human dermal papilla cells
- The androgen receptor gene polyglycine repeat polymorphism is associated with memory performance in healthy Chinese individuals
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- sc-eQTL unveil immunogenetic architecture of polycystic ovary syndrome
- Evolutionary Divergence of Fibroblast Growth Factors Across Species: Insight into Functional Diversification
- Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss
- Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness
- Forensic DNA Phenotyping
- Genetic Variants and Protective Immunity against SARS-CoV-2
- The Roles of EDA2R in Ageing and Disease
- Identification of A p300–SP1–BRD4 Transcriptional Axis as a Key Driver of AR Hyperactivation in Polycystic Ovarian Syndrome