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Research 121–150 of 808
- A comprehensive genome-wide analysis for signatures of selection in goat (genus Capra) revealed new candidate genes for environmental adaptation and productive traits
- A Comprehensive Review of GWASs of Human Hair Traits
- Whole-genome resequencing to investigate the genetic diversity and the molecular basis underlying key economic traits in indigenous sheep breeds adapted to hypoxic environments
- Hirsutism Beyond PCOS: Genome-wide Evidence for Genetic Factors
- Causal effects of glutamine and lipid-related metabolites on alopecia areata: A 2-sample Mendelian randomization study
- The Biology and Genomics of Human Hair Follicles: A Focus on Androgenetic Alopecia
- Genetics and Epigenetics of Polycystic Ovary Syndrome
- Topical Finasteride: A Comprehensive Review of Androgenetic Alopecia Management for Men and Women
- Rare and Underappreciated Causes of Polycystic Ovarian Syndrome
- Deciphering the molecular drivers for cashmere/pashmina fiber production in goats: a comprehensive review
- Sequence Variation in Caprine KRTAP6-2 Affects Cashmere Fiber Diameter
- Evaluating HWE and Association in Genome Wide Association Studies: A Unified Procedure
- Candidate SNP markers of reproductive potential are predicted by a significant change in the affinity of TATA-binding protein for human gene promoters
- Genome-wide Target Enrichment-aided Chip Design: a 66 K SNP Chip for Cashmere Goat
- Genome-based analysis of the genetic pattern of black sheep in Qira sheep
- Two-Stage Machine Learning-Based GWAS for Wool Traits in Central Anatolian Merino Sheep
- Leveraging Single Nucleotide Polymorphism Profiling for Precision Skin Care: How SNPs Shape Individual Responses in Cosmetic Dermatology
- Who Am I? Eyebrow Follicles Minimize Donor-Derived DNA for Germline Testing After Hematopoietic Stem Cell Transplantation
- Hyperandrogenism in Women: Polycystic Ovary Syndrome
- Compilation of a comprehensive gene panel for systematic assessment of genes that govern an individual’s drug responses
- Cells to Surgery Quiz: April 2020
- A Clinical Genetics-Driven Dual Diagnosis of Prader–Willi Syndrome Due to Mosaic Maternal UPD(15) and NOTCH3-Related CADASIL
- The first broad replication study of SNPs and a pilot genome‐wide association study for androgenetic alopecia in Asian populations
- Landmark native breed of the Orenburg goats: progress in its breeding and genetics and future prospects
- SNP Markers: Analysis of Genetic Diversity and Identification of Genomic Regions in Pantaneiro Sheep and Texel Sheep Under Natural Selection
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Precision-Based Management of Chronic Hair Fall: A Genomic-Guided Trichology Approach - A Case Analysis from Qatar
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Sequence and structure based assessment of non-synonymous SNPs in hypertrichosis universalis