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Research 61–90 of 1000+
- Use of genetics in the prediction of success in male pattern hair loss therapy and mechanistic studies
- Facial skin aging: an integrative analysis of genetics, epigenetics, and lifestyle factors
- Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
- No genetic support for a contribution of prostaglandins to the aetiology of androgenetic alopecia
- Potential genetic associations of acne scar phenotypes: IL1A in fibrotic scarring and CYB5R1 in atrophic scarring
- The genetic basis of dermatophytosis skin infection susceptibility
- Hormonal regulation in male androgenetic alopecia—Sex hormones and beyond: Evidence from recent genetic studies
- Cost-effectively dissecting the genetic architecture of complex wool traits in rabbits by low-coverage sequencing
- Genomic and transcriptomic landscape to decipher the genetic basis of hyperpigmentation in Lanping black-boned sheep (Ovis aries)
- The Polycystic Ovary Syndrome Evolutionary Paradox: a Genome-Wide Association Studies–Based, in silico, Evolutionary Explanation
- Genome-wide meta-analysis identifies novel loci conferring risk of acne vulgaris
- Testing the impact of trait prevalence priors in Bayesian-based genetic prediction modeling of human appearance traits
- Rare and common genetic determinants of metabolic individuality and their effects on human health
- Human Pigmentation: A Review of Molecular Mechanisms, Genetic Architecture, Evolution, Forensic DNA Phenotyping and Health Implications
- Central centrifugal cicatricial alopecia: possible familial aetiology in two African families from South Africa
- Management and Genetics of Alopecia Areata within the USA: A Cross-Sectional Study of All of Us
- Genetic Variation in CYP2B6, UGT1A4 and Sulfotransferases Is Associated with Disease-Free Survival in South African Breast Cancer Patients Treated with Tamoxifen
- The Genetic Landscape of Androgenetic Alopecia: Current Knowledge and Future Perspectives
- 304 Sephardic Ancestry in Recessive Dystrophic Epidermolysis Bullosa Individuals Carrying the Prevalent c.6527insC Mutation
- Androgenetic alopecia: Identification of four genetic risk loci and evidence for the contribution of WNT signaling to its etiology
- Androgen Signaling Regulates SARS-CoV-2 Receptor Levels and Is Associated with Severe COVID-19 Symptoms in Men
- Comparative genome analyses reveal the unique genetic composition and selection signals underlying the phenotypic characteristics of three Chinese domestic goat breeds
- The Rotterdam Study: 2018 update on objectives, design and main results
- The Rotterdam Study: 2016 objectives and design update
- What causes hidradenitis suppurativa ?—15 years after
- GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk
- Genetic predictors of testosterone and their associations with cardiovascular disease and risk factors: A Mendelian randomization investigation
- Sulphation catalysed by the human cytosolic sulphotransferases - chemical defence or molecular terrorism?
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- Genetic Variants Associated with Hyperandrogenemia in PCOS Pathophysiology