Associated Papers
Forensic DNA Phenotyping: Genes and Genetic Variants for Eye Color Prediction.
Brancato D et al.
Genes, 2023
Genetic associations of protein-coding variants in human disease.
Sun BB et al.
Nature, 2022
Genomic diversity and post-admixture adaptation in the Uyghurs.
Pan Y et al.
National Science Review, 2022
35350227 (PubMed )
Supplement: nwab124_supplemental_file.pdf
Prioritising positively selected variants in whole-genome sequencing data using FineMAV.
Wahyudi F et al.
Bmc Bioinformatics, 2021
34922440 (PubMed )
Supplement: 12859_2021_4506_MOESM2_ESM.xlsx › SSIP
Analysis of Skin Pigmentation and Genetic Ancestry in Three Subpopulations from Pakistan: Punjabi, Pashtun, and Baloch.
Shan MA et al.
Genes, 2021
Skin pigmentation polymorphisms associated with increased risk of melanoma in a case-control sample from southern Brazil.
Reis LB et al.
Bmc Cancer, 2020
Germline and somatic albinism variants in amelanotic/hypomelanotic melanoma: Increased carriage of TYR and OCA2 variants.
Rayner JE et al.
Plos One, 2020
32966289 (PubMed )
Supplement: pone.0238529.s003.docx
Introducing the first whole genomes of nationals from the United Arab Emirates.
AlSafar HS et al.
Scientific Reports, 2019
31604968 (PubMed )
Supplement: 41598_2019_50876_MOESM1_ESM.xlsx › UAE_S001
How well do we understand the basis of classic selective sweeps in humans?
Szpak M et al.
Febs Letters, 2019
A GWAS in Latin Americans highlights the convergent evolution of lighter skin pigmentation in Eurasia.
Adhikari K et al.
Nature Communications, 2019
Four-dimensional, dynamic mosaicism is a hallmark of normal human skin that permits mapping of the organization and patterning of human epidermis during terminal differentiation.
Wang Y et al.
Plos One, 2018
An Unexpectedly Complex Architecture for Skin Pigmentation in Africans.
Martin AR et al.
Cell, 2017
Whole genome sequencing of one complex pedigree illustrates challenges with genomic medicine.
Fang H et al.
Bmc Medical Genomics, 2017
28228131 (PubMed )
Supplement: 12920_2017_246_MOESM2_ESM.pdf
SLC24A5 and ASIP as phenotypic predictors in Brazilian population for forensic purposes.
Lima FA et al.
Legal Medicine (tokyo, Japan), 2015
Association of genetic variants with self-assessed color categories in Brazilians.
Durso DF et al.
Plos One, 2014
Exome sequencing identifies SLC24A5 as a candidate gene for nonsyndromic oculocutaneous albinism.
Wei AH et al.
The Journal of Investigative Dermatology, 2013
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