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- Genetic and hormonal influence on SARS-CoV-2-infection susceptibility
- Improving human forensics through advances in genetics, genomics and molecular biology
- Androgenetic alopecia: Identification of four genetic risk loci and evidence for the contribution of WNT signaling to its etiology
- Role of polymorphism of the androgen receptor gene andnon-random x chromosome inactivation in the pathogenesisof androgenic alopecia
- The Who’s, What’s, and “Y”s: Y Sex Chromosome Loss and Methylation for Analysis in Male Aging and Mortality and Forensic Science Applications
- [Association of eight single nucleotide polymorphisms of chromosomes 20 and X with androgenetic alopecia among ethnic Han Chinese from Yunnan].
- Polymorphism of CAG and GGN repeats of androgen receptor gene in women with polycystic ovary syndrome
- Role of polymorphism of the androgen receptor gene and non-random X chromosome inactivation in the genesis of androgenic alopecia in women of childbearing potential
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- Prediction of male-pattern baldness from genotypes
- Human KAP Genes, Only the Half of it? Extensive Size Polymorphisms in Hair Keratin-Associated Protein Genes
- Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
- The Complexity of the Ovine and Caprine Keratin-Associated Protein Genes
- Evolution and genetic architecture of sex-limited polymorphism in cuckoos
- Sex-limited chromosomes and non-reproductive traits
- Dissection of genetic variation and evidence for pleiotropy in male pattern baldness
- Genome-wide association study in alopecia areata implicates both innate and adaptive immunity
- Resequencing and Signatures of Selective Scans Point to Candidate Genetic Variants for Hair Length Traits in Long-Haired and Normal-Haired Tianzhu White Yak
- Polygenic control of the wavy coat of the NCT mouse: involvement of an intracisternal A particle insertional mutation of the protease, serine 53 (Prss53) gene, and a modifier gene
- Fetal alpha 5-reductase Val89Leu mutation is associated with late miscarriage
- Genetic and other epidemiological risk factors of infants and children with hypospadias: a case control study
- Genetic prediction of male pattern baldness based on large independent datasets
- Utilising SNP Association Analysis as a Prospective Approach for Personalising Androgenetic Alopecia Treatment
- 17927 A pilot study of intrascalp platelet-rich plasma injections for hair loss in Nigerian patients
- Genetics of Diabetes in Childhood
- Wool Keratin-Associated Protein Genes in Sheep—A Review
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Association of AR rs6152G/A gene polymorphism with susceptibility to polycystic ovary syndrome in Chinese women
- CAG polymorphism in the androgen receptor gene in women may be associated with nodulocystic acne
- CAG Repeat Testing of Androgen Receptor Polymorphism: Is This Necessary for the Best Clinical Management of Hypogonadism?