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Comprehensive analysis of complement factor H and LOC387715/ARMS2/HTRA1 variants with respect to phenotype in advanced age-related macular degeneration
STK39 polymorphisms and blood pressure: an association study in British Caucasians and assessment of cis-acting influences on gene expression
Single nucleotide polymorphisms of complement component 5 and periodontitis
A rare haplotype of the vitamin D receptor gene is protective against diabetic nephropathy
An association study of common variation at the MAPT locus with late-onset Alzheimer’s disease.
A systemativ association mapping on chromosome 6q in bipolar affective disorder â€“ evidence for the melanin-concentrating-hormone-receptor-2 gene as a risk factor for bipolar-affective disorder
Sequence variants on chromosome 9p21.3 confer risk for atherosclerotic stroke.
Association on ERAP1, but not IL23R, with ankylosing spondylitis in a Han Chinese population
Applications of MALDI-TOF MS to large-scale human mtDNA population-based studies.
Characterization of single-nucleotide polymorphisms relevant to inflammatory bowel disease in commonly used gastrointestinal cell lines.