'Racial' differences in genetic effects for complex diseases.
about
Fulfilling the promise of personalized medicine? Systematic review and field synopsis of pharmacogenetic studiesCommon variation in EMSY and risk of breast and ovarian cancer: a case-control study using HapMap tagging SNPs.An integrated approach of comparative genomics and heritability analysis of pig and human on obesity trait: evidence for candidate genes on human chromosome 2Local literature bias in genetic epidemiology: an empirical evaluation of the Chinese literatureEthnic background and genetic variation in the evaluation of cancer risk: a systematic reviewMeta-analysis of haplotype-association studies: comparison of methods and empirical evaluation of the literatureReplication of putative candidate-gene associations with rheumatoid arthritis in >4,000 samples from North America and Sweden: association of susceptibility with PTPN22, CTLA4, and PADI4Tests for the replication of an association between Egfr and natural variation in Drosophila melanogaster wing morphology.Associations among race/ethnicity, ApoC-III genotypes, and lipids in HIV-1-infected individuals on antiretroviral therapy.Genetic Misdiagnoses and the Potential for Health DisparitiesThe contribution of genomic research to explaining racial disparities in cardiovascular disease: a systematic reviewSystematic meta-analyses and field synopsis of genetic association studies in colorectal cancerRegulatory Polymorphisms in the Interleukin‐18 Promoter Are Associated with Hepatitis C Virus ClearanceHuman leukocyte antigen class II associations with hepatitis C virus clearance and virus‐specific CD4 T cell response among Caucasians and African AmericansTilting at quixotic trait loci (QTL): an evolutionary perspective on genetic causationEstimating the contribution of genetic variants to difference in incidence of disease between population groupsMeta-Analysis-Based Preliminary Exploration of the Connection between ATDILI and Schizophrenia by GSTM1/T1 Gene PolymorphismsCommon variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma riskCommon variation at 3p22.1 and 7p15.3 influences multiple myeloma riskCommon variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk.Transferability and fine-mapping of glucose and insulin quantitative trait loci across populations: CARe, the Candidate Gene Association Resource.Emerging concepts in biomarker discovery; the US-Japan Workshop on Immunological Molecular Markers in OncologyIn search of causal variants: refining disease association signals using cross-population contrasts.Genome-wide scan for signatures of human population differentiation and their relationship with natural selection, functional pathways and diseasesDo health and forensic DNA databases increase racial disparities?Concordance of functional in vitro data and epidemiological associations in complex disease genetics.Genetics of ischaemic stroke among persons of non-European descent: a meta-analysis of eight genes involving approximately 32,500 individuals.Patterns of population differentiation of candidate genes for cardiovascular disease.A comprehensive analysis of common genetic variation in prolactin (PRL) and PRL receptor (PRLR) genes in relation to plasma prolactin levels and breast cancer risk: the multiethnic cohort.Worldwide population differentiation at disease-associated SNPs.STrengthening the REporting of Genetic Association Studies (STREGA): an extension of the STROBE statement.Failure to replicate a genetic association may provide important clues about genetic architectureDisparities in allele frequencies and population differentiation for 101 disease-associated single nucleotide polymorphisms between Puerto Ricans and non-Hispanic whites.Leveraging genetic variability across populations for the identification of causal variants.Genetic variation in the 3'-untranslated region of PAK1 influences schizophrenia susceptibilityGenetic effects influencing risk for major depressive disorder in China and Europe.Leprosy and the adaptation of human toll-like receptor 1.Ancestry-shift refinement mapping of the C6orf97-ESR1 breast cancer susceptibility locus.The serotonin transporter promoter polymorphism is associated with cortisol response to psychosocial stress.Genetic variants associated with complex human diseases show wide variation across multiple populations.
P2860
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P2860
'Racial' differences in genetic effects for complex diseases.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年学术文章
@wuu
2004年学术文章
@zh
2004年学术文章
@zh-cn
2004年学术文章
@zh-hans
2004年学术文章
@zh-my
2004年学术文章
@zh-sg
2004年學術文章
@yue
2004年學術文章
@zh-hant
name
'Racial' differences in genetic effects for complex diseases.
@en
'Racial' differences in genetic effects for complex diseases.
@nl
type
label
'Racial' differences in genetic effects for complex diseases.
@en
'Racial' differences in genetic effects for complex diseases.
@nl
prefLabel
'Racial' differences in genetic effects for complex diseases.
@en
'Racial' differences in genetic effects for complex diseases.
@nl
P2860
P356
P1433
P1476
'Racial' differences in genetic effects for complex diseases.
@en
P2093
Evangelia E Ntzani
Thomas A Trikalinos
P2860
P2888
P304
P356
10.1038/NG1474
P407
P577
2004-11-14T00:00:00Z