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P324Circadian genes in the regulation of lipids in coronary artery disease
Association study in Romanians confirms IL23A gene haplotype block rs2066808/rs11171806 as conferring risk to psoriatic arthritis
The Evidence for Association of ATP2B2 Polymorphisms with Autism in Chinese Han Population
A Non-Synonymous Coding Variant (L616F) in the TLR5 Gene Is Potentially Associated with Crohn’s Disease and Influences Responses to Bacterial Flagellin
Childhood maltreatment is associated with distinct genomic and epigenetic profiles in posttraumatic stress disorder
Association between PCSK9 and LDLR gene polymorphisms with coronary heart disease: Case-control study and meta-analysis
Methionine sulfoxide reductase A rs10903323 G/A polymorphism is associated with increased risk of coronary artery disease in a Chinese population
Discovery of novel non-synonymous SNP variants in 988 candidate genes from 6 centenarians by target capture and next-generation sequencing
Effect modification by Transferrin C2 polymorphism on lead exposure, hemoglobin levels, and IQ:
PAC1 receptor (ADCYAP1R1) genotype is associated with PTSD’s emotional numbing symptoms in Chinese earthquakesurvivors