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- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Prediction of male-pattern baldness from genotypes
- Genetic correlation analysis does not associate male pattern baldness with COVID-19
- Uncovering the genetic architecture and evolutionary roots of androgenetic alopecia in African men
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- Diagnostic approach to low‐renin hypertension
- Improving human forensics through advances in genetics, genomics and molecular biology
- Six SNPs and a TTG indel in sheep desmoglein 4 gene are in complete linkage disequilibrium
- Sequence and structure based assessment of non-synonymous SNPs in hypertrichosis universalis
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Biology and Genetics of Hair
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Finding bald spots on chromosome 20p11
- Multi-ancestry tandem repeat association study of hair colour using exome-wide sequencing
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- Evaluation of the predictive capacity of DNA variants associated with straight hair in Europeans
- A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in females
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- The inconsistent regulation of HOXC13 on different keratins and the regulation mechanism on HOXC13 in cashmere goat (Capra hircus)
- The genetics of alopecia areata
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- Genome-Wide Association Study of Alopecia Areata in Taiwan: The Conflict Between Individuals and Hair Follicles
- STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
- Studying the genetic predisposing factors in the pathogenesis of acne vulgaris
- The Role of rs6152 Allele and Non-Genetic Factors in Androgenetic Alopecia: A Pilot Study in the Indonesian Local Population
- Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability
- Uncovering the genetic architecture and evolutionary roots of androgenetic alopecia in African men
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome