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Research 61–90 of 1000+
- Genetics and other factors in the aetiology of female pattern hair loss
- Genetic association of <i>HLA‐DQB1</i> and <i>HLA‐DRB1</i> polymorphisms with alopecia areata in the Italian population
- Genetics of Polycystic Ovary Syndrome
- Polygenic risk score predicting susceptibility and outcome of benign prostatic hyperplasia in the Han Chinese
- Study of Human Leukocyte Antigen ( HLA ) in 13 cases of familial frontal fibrosing alopecia: CYP 21A2 gene p.V281L mutation from congenital adrenal hyperplasia linked to HLA class I haplotype HLA ‐ A*33:01 ; B*14:02; C*08:02 as a genetic marker
- Identification of seven new prostate cancer susceptibility loci through a genome-wide association study
- Association between angiotensin‐converting enzyme gene insertion deletion polymorphism and androgenetic alopecia susceptibility among Egyptian patients: A preliminary case‐controlled study
- The L412F variant of Toll-like receptor 3 (TLR3) is associated with cutaneous candidiasis, increased susceptibility to cytomegalovirus, and autoimmunity
- BH26 First reported case of lichen planopilaris in siblings: evidence for a genetic link?
- Association of JAK 1 and JAK 2 gene polymorphism with alopecia areata risk: a case–control genetic study
- Generalized Vitiligo Associated Autoimmune Diseases in Japanese Patients Their Families
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- Genetic analysis of the role of androgen metabolism in the pathogenesis of prostate cancer
- Faculty Opinions recommendation of Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases.
- Third International Research Workshop on Alopecia Areata
- Association of Autoimmune Regulator Gene Rs2075876 Variant, but Not Gene Expression with Alopecia Areata in Males: A Case–control Study
- Candidate Gene Analysis Of Alopecia Areata In Jordanian Population Of Arab Descent: A Case–Control Study
- Pseudofolliculitis barbae; current treatment options
- Association of HSPA1B SNP rs6457452 with Alopecia Areata in the Korean Population
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- The Genetic Landscape of Androgenetic Alopecia: Current Knowledge and Future Perspectives
- Traditional and Integrative Approaches to the Treatment of Alopecia
- Diagnosis and treatment of alopecia areata
- Genome-wide Scan and Fine-Mapping Linkage Study of Androgenetic Alopecia Reveals a Locus on Chromosome 3q26
- Major Histocompatibility Complex Class I Chain-Related Gene A Polymorphisms and Extended Haplotypes Are Associated with Familial Alopecia Areata
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- New Horizons in the Genetics of Polycystic Ovary Syndrome: From Predisposition to Precision Medicine.
- Genetics of Vitiligo: A Review
- Utilizing functional genomics approaches to characterize risk genes in alopecia areata
- 1381 Molecular mechanisms of donor dominance in androgenetic alopecia