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TMEM132D, a new candidate for anxiety phenotypes: evidence from human and mouse studies
Origins and functional impact of copy number variation in the human genome
The Wellcome Trust Case Control Consortium, Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls
RUNX2 polymorphisms associated with OPLL and OLF in the Han population
Regulatory polymorphism in transcription factor KLF5 at the MEF2 element alters the response to angiotensin II and is associated with human hypertension
Fast diagnostic test for the identification of an increased genetic predisposition to colon cancer (exemplified on a DNA test for recurrent mutations of the gene MMR)
Polymorphisms in the SERPINA1 (Alpha-1-Antitrypsin) gene are associated with severe chronic rhinosinusitis unresponsive to medical therapy
Paraoxonase-1 gene haplotypes are associated with metabolic disturbances, atherosclerosis, and immunologic outcome in HIV-infected patients
Association between single-nucleotide polymorphism in Mal/TIRAP and Interleukin-10 genes and susceptibility to invasive Haemophilus influenzea serotype b infection in immunized children
Folate pathway enzyme gene polymorphisms and the efficacy and toxicity of methotrexate in psoriatic arthritis