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Research 31–60 of 1000+
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Twins with psychiatric features and a nonsense HRAS variant affecting transcript processing
- Gene variants associated with acne vulgaris presentation and severity: a systematic review and meta-analysis
- An autosomal recessive nonsense variant in the EGFR gene induces perinatal lethality in “Blonde d'Aquitaine” calves
- Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- Novel genes and variants associated with longevity in Bulgarian centenarians revealed by whole exome sequencing DNA pools: a pilot study
- Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss
- Novel Androgen Receptor Gene Variant Containing a Premature Termination Codon in a Patient with Androgen Insensitivity Syndrome
- Exomic Sequencing of Immune-Related Genes Reveals Novel Candidate Variants Associated with Alopecia Universalis
- Resequencing and Signatures of Selective Scans Point to Candidate Genetic Variants for Hair Length Traits in Long-Haired and Normal-Haired Tianzhu White Yak
- Vitamin D deficiency in non-scarring and scarring alopecias: a systematic review and meta-analysis
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- Intra-host SARS-CoV-2 single-nucleotide variants emerged during the early stage of COVID-19 pandemic forecast population fixing mutations
- Human Hair as a Testing Substrate in the Era of Precision Medicine: Potential Role of ‘Omics-Based Approaches
- A Systematic Scoping Review and Conceptual Analysis of New-Onset Fibromyalgia Manifestations After Non-Hospitalized COVID-19: Empirics, Definitions, Methodologies, Pathophysiology, Mapping of Literature, and Knowledge Gaps
- Cutaneous lupus erythematosus
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Optimal processing for proteomic genotyping of single human hairs
- Advantages of Incomplete Digestion in Human Hair Shaft Proteomics, a Focus on Cuticular Keratins
- Poster Presentations at the 28th Joint Meeting of the International Society of Dermatopathology, March 5–6, 2025, Orlando, Florida, USA
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Two mutations at KRT74 and EDAR synergistically drive the fine-wool production in Chinese sheep
- The Genetic Architecture of Alopecia Areata
- Polycystic ovary syndrome and insulin-resistant hyperinsulinemia
- Clinical-exome sequencing unveils the genetic landscape of polycystic ovarian syndrome (PCOS) focusing on lean and obese phenotypes: implications for cost-effective diagnosis and personalized treatment
- Predicting Human Appearance from DNA for Forensic Investigations
- Cost-effectively dissecting the genetic architecture of complex wool traits in rabbits by low-coverage sequencing
- HSD3B1 gene polymorphism and female pattern hair loss in women with polycystic ovary syndrome
- Pediatric Psychocutaneous Disorders