Beijing Institute of Genomics Chinese Academy of Sciences
49 papers found
Novel quantitative pigmentation phenotyping enhances genetic association, epistasis, and prediction of human eye colour.
Pigmentation-Independent Susceptibility Loci for Actinic Keratosis Highlighted by Compound Heterozygosity Analysis
MHC Class II Risk Alleles and Amino Acid Residues in Idiopathic Membranous Nephropathy.
Human age estimation from blood using mRNA, DNA methylation, DNA rearrangement, and telomere length
The MC1R Gene and Youthful Looks
CollapsABEL: an R library for detecting compound heterozygote alleles in genome-wide association studies
Evaluation of mRNA markers for estimating blood deposition time: Towards alibi testing from human forensic stains with rhythmic biomarkers
An Automatic 3D Facial Landmarking Algorithm Using 2D Gabor Wavelets
Association of Melanocortin-1 Receptor Variants with Pigmentary Traits in Humans: A Pooled Analysis from the M-Skip Project
MC1R gene variants and non-melanoma skin cancer: a pooled-analysis from the M-SKIP project
Genetics of skin color variation in Europeans: genome-wide association studies with functional follow-up
IRF4, MC1R and TYR genes are risk factors for actinic keratosis independent of skin color
A genome-wide association study identifies the skin color genes IRF4, MC1R, ASIP, and BNC2 influencing facial pigmented spots
Validation of image analysis techniques to measure skin aging features from facial photographs
Intrinsic and Extrinsic Risk Factors for Sagging Eyelids
GAGA: A New Algorithm for Genomic Inference of Geographic Ancestry Reveals Fine Level Population Substructure in Europeans
PHOX2B polyalanine repeat length is associated with sudden infant death syndrome and unclassified sudden infant death in the Dutch population
Developmental validation of the HIrisPlex system: DNA-based eye and hair colour prediction for forensic and anthropological usage
Common DNA variants predict tall stature in Europeans
Of sex and IrisPlex eye colour prediction: A reply to Martinez-Cadenas et al.
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