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Research 511–540 of 764
- Global Landscapes of Human Phenotypic Variation in Inherited Traits
- Association Between Retinoid X Receptor Gene Variants and Dyslipidemia Risk in an Iranian Population
- A genome‐wide association study identified a genetic variant associated with hair thinning in Japanese women
- Baldness and the androgen receptor: the AR polyglycine repeat polymorphism does not confer susceptibility to androgenetic alopecia
- Genetic variations associated with response to dutasteride in the treatment of male subjects with androgenetic alopecia
- Compilation of a comprehensive gene panel for systematic assessment of genes that govern an individual’s drug responses
- Lipin 1 Gene Polymorphisms in Polycystic Ovary Syndrome
- Multi-ancestry tandem repeat association study of hair colour using exome-wide sequencing
- Cells to Surgery Quiz: April 2020
- Pilot study: genetic distribution of AR, FGF5, SULT1A1 and CYP3A5 polymorphisms in male Mexican population with androgenetic alopecia.
- Sex dependent influence of a functional polymorphism in steroid 5‐α‐reductase type 2 (<i>SRD5A2</i>) on post‐traumatic stress symptoms
- Genetic association of complement component 2 polymorphism with systemic lupus erythematosus
- Genome-based analysis of the genetic pattern of black sheep in Qira sheep
- A genetically informed brain atlas for enhancing brain imaging genomics
- Single nucleotide polymorphisms associated with elevated alanine aminotransferase in patients receiving asunaprevir plus daclatasvir combination therapy for chronic hepatitis C
- Genetic Polymorphisms of Immunity Regulatory Genes and Alopecia Areata Susceptibility in Jordanian Patients
- A Clinical Genetics-Driven Dual Diagnosis of Prader–Willi Syndrome Due to Mosaic Maternal UPD(15) and NOTCH3-Related CADASIL
- 8368 Functional Evaluation Of Novel CYP21A2 Variants: Expanding The Genetic Basis Of Non-classic CAH
- Natural Killer Group 2 Type D (NKG2D) Gene Polymorphism in Systemic Lupus Erythematosus-Suez Canal Region - Egypt
- A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in females
- Evaluation of the predictive capacity of DNA variants associated with straight hair in Europeans
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Candidate Gene Analysis Of Alopecia Areata In Jordanian Population Of Arab Descent: A Case–Control Study
- Association between <i>EGF</i> and <i>EGFR</i> Gene Polymorphisms and Susceptibility to Alopecia Areata in the Korean Population
- The first broad replication study of SNPs and a pilot genome‐wide association study for androgenetic alopecia in Asian populations
- Exploring imputation performance of phenotype-associated SNPs for forensic prediction models
- Polymorphisms in Genes Involved in Steroidogenesis in the Development of Severe Acne
- Association between epidermal growth factor and epidermal growth factor receptor gene polymorphisms and susceptibility to alopecia areata in Korean population
- 5α-Reductase type 2 gene variant associations with prostate cancer risk, circulating hormone levels and androgenetic alopecia
- GABRA2 Alleles Moderate the Subjective Effects of Alcohol, Which are Attenuated by Finasteride