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Association between genetic variations in tumor necrosis factor receptor genes and survival of patients with T-cell lymphoma
Polymorphism discovery and allele frequency estimation using high-throughput DNA sequencing of target-enriched pooled DNA samples
Fragile X Mental Retardation 1 (FMR1) Intron 1 Methylation in Blood Predicts Verbal Cognitive Impairment in Female Carriers of Expanded FMR1 Alleles: Evidence from a Pilot Study
Genome wide expression profiling of two accession of G. herbaceum L. in response to drought
Chromosome 1p13 genetic variants antagonize the risk of myocardial infarction associated with high ApoB serum levels
Race-ethnic differences in the association of genetic loci with HbA1c levels and mortality in U.S. adults: the third National Health and Nutrition Examination
No Association of nineteen COX-2 gene variants to preclinical markers of atherosclerosis The Cardiovascular Risk in Young Finns Study
BRCA2 Variants and cardiovascular disease in a multi-ethnic study
Investigating the relationship between UMODL1 gene polymorphisms and high myopia: a case- control study in Chinese
Single nucleotide polymorphisms in thymic stromal lymphopoietin gene are not associated with allergic rhinitis susceptibility in Chinese subjects