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Research 271–300 of 1000+
- Six Novel Susceptibility Loci for Early-Onset Androgenetic Alopecia and Their Unexpected Association with Common Diseases
- Androgenetic Alopecia: Identification of Four Genetic Risk Loci and Evidence for the Contribution of WNT Signaling to Its Etiology
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Genome-wide Scan and Fine-Mapping Linkage Study of Androgenetic Alopecia Reveals a Locus on Chromosome 3q26
- Susceptibility variants on chromosome 7p21.1 suggest HDAC9 as a new candidate gene for male-pattern baldness
- Differential Expression between Human Dermal Papilla Cells from Balding and Non-Balding Scalps Reveals New Candidate Genes for Androgenetic Alopecia
- Hunting the genes in male‐pattern alopecia: how important are they, how close are we and what will they tell us?
- Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Investigation of the male pattern baldness major genetic susceptibility loci AR/EDA2R and 20p11 in female pattern hair loss
- Prediction of male-pattern baldness from genotypes
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Synaptic processes and immune-related pathways implicated in Tourette syndrome
- Genomewide analysis of copy number variants in alopecia areata in a Central European cohort reveals association with <i>MCHR2</i>
- Fine mapping of the human <i>AR/EDA2R</i> locus in androgenetic alopecia
- Evidence for a polygenic contribution to androgenetic alopecia
- Investigation of six novel susceptibility loci for male androgenetic alopecia in women with female pattern hair loss
- Investigation of four novel male androgenetic alopecia susceptibility loci: no association with female pattern hair loss
- Selected variants of the steroid-5-alpha-reductase isoforms SRD5A1 and SRD5A2 and the sex steroid hormone receptors ESR1, ESR2 and PGR: No association with female pattern hair loss identified
- Hormonal regulation in male androgenetic alopecia—Sex hormones and beyond: Evidence from recent genetic studies
- Investigation of variants of the aromatase gene (CYP19A1) in female pattern hair loss
- The hairless gene in androgenetic alopecia: results of a systematic mutation screening and a family-based association approach
- Marie Unna hereditary hypotrichosis: Identification of a U2HR mutation in the family from the original 1925 report
- Variant 1859G→A (Arg620Gln) of the “Hairless” Gene: Absence of Association with Papular Atrichia or Androgenetic Alopecia
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- Male-pattern baldness and incident coronary heart disease and risk factors in the Heinz Nixdorf Recall Study
- Exploring the overlap between alopecia areata and major depressive disorder: Epidemiological and genetic perspectives
- Selected variants of the melanocortin 4 receptor gene (MC4R) do not confer susceptibility to female pattern hair loss
- Insights into Male Androgenetic Alopecia: Differential Gene Expression Profiling of Plucked Hair Follicles and Integration with Genetic Data
- No genetic support for a contribution of prostaglandins to the aetiology of androgenetic alopecia