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Research 511–540 of 1000+
- Gain‐of‐function variants in the <i>ODC1</i> gene cause a syndromic neurodevelopmental disorder associated with macrocephaly, alopecia, dysmorphic features, and neuroimaging abnormalities
- Thyroid antibodies in Hashimoto’s thyroiditis patients are positively associated with inflammation and multiple symptoms
- Sexual Dysfunction Related to Drugs: a Critical Review. Part V: α-Blocker and 5-ARI Drugs
- COVID-19 infection leading to acute pustular dermatoses
- Exploring the overlap between alopecia areata and major depressive disorder: Epidemiological and genetic perspectives
- The Polish version of Skindex-29: psychometric properties of an instrument to measure quality of life in dermatology
- Big head? Bald head! Skull expansion: alternative model for the primary mechanism of AGA
- Intrinsic factors in the pathogenesis of hidradenitis suppurativa: Genetics, hormones, and the microbiome
- Retinoids Putting the “A” in Alopecia
- The genetic evolution of skin squamous cell carcinoma: tumor suppressor identity matters
- Genetic Variants and Protective Immunity against SARS-CoV-2
- Mimicking Hair Disorders by Genetic Manipulation of Organ-Cultured Human Hair Follicles
- Advances in Hair Diseases
- Atopic dermatitis and risk of autoimmune diseases: a systematic review and meta-analysis
- Genetic and other epidemiological risk factors of infants and children with hypospadias: a case control study
- SNP variation in male pattern hair loss in Russians with different dihydrotestosterone levels
- Etiopathogenesis of Alopecia Areata
- Genetic Upregulation of Activated Protein C Mitigates Delayed Effects of Acute Radiation Exposure in the Mouse Plasma
- Alopecias
- Hirsutism Beyond PCOS: Genome-wide Evidence for Genetic Factors
- Genetic Variation in CYP2B6, UGT1A4 and Sulfotransferases Is Associated with Disease-Free Survival in South African Breast Cancer Patients Treated with Tamoxifen
- The impact of stigma on people with albinism in Africa: a narrative review
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Ichthyosis in Unani Medicine: A Comprehensive Review of Disorders of Cornification and their Modern Dermatological Correlates
- Genetics of infertility and “assisted fertilization” in the Bible: The case of Abraham and his family
- Uncovering the genetic architecture and evolutionary roots of androgenetic alopecia in African men
- Genetic Variants and Lifestyle Factors in Androgenetic Alopecia Patients: A Case–Control Study of Single Nucleotide Polymorphisms and Their Contribution to Baldness Risk
- Genetic Differences between Male and Female Pattern Hair Loss in a Korean Population
- Genetic Association Between Polycystic Ovary Syndrome and the <i>APOA5</i> rs662799 and <i>PLIN1</i> rs894160 Metabolic Variants in the Western Saudi Population: A Case-Control Study
- Pediatric Features of Genetic Predisposition to Polycystic Ovary Syndrome