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Research 30 of 347
- Dissection of genetic variation and evidence for pleiotropy in male pattern baldness
- Genetic correlation by pedigree analysis in patients diagnosed with PCOS as per Rotterdam’s criteria
- Ovarian Morphology Is a Marker of Heritable Biochemical Traits in Sisters with Polycystic Ovaries
- What does acne genetics teach us about disease pathogenesis?
- Investigation of the association of the MLPH gene with seasonal canine flank alopecia in Rhodesian Ridgeback dogs
- Genomic prediction and genome-wide association studies of morphological traits and distraction index in Korean Sapsaree dogs
- Genetic Basis of Male Pattern Baldness
- Genome-wide association study for cashmere traits in Inner Mongolia cashmere goat population reveals new candidate genes and haplotypes
- Genome-Wide Association Study for Udder Conformation Traits in Chinese Holstein Cattle
- Male-pattern hair loss: Comprehensive identification of the associated genes as a basis for understanding pathophysiology
- Hair coat characteristics in Friesian heifers in the Netherlands and Kenya : experimental data and a review of literature
- Use of genetics in the prediction of success in male pattern hair loss therapy and mechanistic studies
- 17927 A pilot study of intrascalp platelet-rich plasma injections for hair loss in Nigerian patients
- GABRA2 Alleles Moderate the Subjective Effects of Alcohol, Which are Attenuated by Finasteride
- Genetic Variants and Lifestyle Factors in Androgenetic Alopecia Patients: A Case–Control Study of Single Nucleotide Polymorphisms and Their Contribution to Baldness Risk
- Forensic DNA phenotyping: a review on SNP panels, genotyping techniques, and prediction models
- Genome-Wide Association Study of Fiber Diameter in Alpacas
- Uncovering the genetic architecture and evolutionary roots of androgenetic alopecia in African men
- The Genetics of Human Skin Disease
- Genetics of Wool and Cashmere Fibre: Progress, Challenges, and Future Research
- Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)
- Cost-effectively dissecting the genetic architecture of complex wool traits in rabbits by low-coverage sequencing
- High-throughput Sequencing to Identify Monogenic Etiologies in a Preselected Polycystic Ovary Syndrome Cohort
- Genetic Insights into Acne, Androgenetic Alopecia, and Alopecia Areata: Implications for Mechanisms and Precision Dermatology
- Meeting Report: 68th Montagna Symposium on the Biology of Skin “Decoding Complex Skin Diseases: Integrating Genetics, Genomics, and Disease Biology”
- Bifidobacterium Is Enriched in Gut Microbiome of Kashmiri Women with Polycystic Ovary Syndrome
- Next-generation Sequencing Identified a Novel EDA Mutation in a Chinese Pedigree of Hypohidrotic Ectodermal Dysplasia with Hyperplasia of the Sebaceous Glands
- Mutation analysis of type II hair keratin gene in a pedigree with monilethrix
- Novel variant in <i>WNT10A</i> caused short anagen hair syndrome in a Chinese pedigree
- Complete defect in PA-PLA1α secretion function leading to autosomal recessive woolly hair and hypotrichosis: insights from a novel compound heterozygous LIPH variant study in a Chinese pedigree