CHB cohort

Aliases

Chinese, Han Chinese, Han Chinese from Beijing, Han Chinese in Beijing, Han Chinese in Beijing, China, HapMap CHB, unrelated individuals from Beijing, China

Related entities (17)

Mentioned in (23)

Papers in which this entity is mentioned.

• Multi-ancestry study of the genetics of problematic alcohol use in over 1 million individuals. (2023)
• Principal Component Analyses (PCA)-based findings in population genetic studies are highly biased and must be reevaluated. (2022)
• Rapid genotype imputation from sequence with reference panels. (2021)
• Genotypes of informative loci from 1000 Genomes data allude evolution and mixing of human populations. (2021)
• Eigenanalysis of SNP data with an identity by descent interpretation. (2016)
• Detecting Genomic Signatures of Natural Selection with Principal Component Analysis: Application to the 1000 Genomes Data. (2016)
• Dissecting ancestry genomic background in substance dependence genome-wide association studies. (2015)
• A global reference for human genetic variation. (2015)
• A global reference for human genetic variation. (2015)
• Genome-wide association study of nicotine dependence in American populations: identification of novel risk loci in both African-Americans and European-Americans. (2015)
• Genome-wide association study of cocaine dependence and related traits: FAM53B identified as a risk gene. (2014)
• Mosaic epigenetic dysregulation of ectodermal cells in autism spectrum disorder. (2014)
• An integrated map of genetic variation from 1,092 human genomes. (2012)
• The genetics of the opioid system and specific drug addictions. (2012)
• The neuronal transporter gene SLC6A15 confers risk to major depression. (2011)
• LocusZoom: regional visualization of genome-wide association scan results. (2010)
• LocusZoom: regional visualization of genome-wide association scan results. (2010)
• Genetic structure of Europeans: a view from the North-East. (2009)
• Ancestry informative marker sets for determining continental origin and admixture proportions in common populations in America. (2009)
• The CHRNA5-CHRNA3-CHRNB4 nicotinic receptor subunit gene cluster affects risk for nicotine dependence in African-Americans and in European-Americans. (2009)
• Marker selection for genetic case-control association studies. (2009)
• PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data. (2007)
• A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC. (2006)

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