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source DB	source ID	text	size	updated at	# proj.	updated_at
PubMed	20103646	Definition of a functional single nucleotide polymorphism in the cell migration inhibitory gene MIIP that affects the risk of breast cancer. The migration and invasion inhibitory protein MIIP is an in	1.37 KB	2025-10-02	8	-
PubMed	15820225	Bipolar disorder and polymorphisms in the dysbindin gene (DTNBP1). BACKGROUND: Several studies support the dysbindin (dystrobrevin binding protein 1) gene (DTNBP1) as a susceptibility gene for schizop	1.47 KB	2025-10-02	6	-
PubMed	15820319	Possible association of the MAG locus with schizophrenia in a Chinese Han cohort of family trios. Neurotransmitter-based hypotheses have so far led to only moderate success in predicting new pathogene	1.48 KB	2025-10-02	6	-
PubMed	15820616	IL-6 gene variation is not associated with increased serum levels of IL-6, muscle, weakness, or frailty in older women. Elevated levels of the inflammatory cytokine IL-6 are associated with the develo	1.43 KB	2025-10-02	3	-
PubMed	21826085	DPP6 as a candidate gene for neuroleptic-induced tardive dyskinesia. We implemented a two-step approach to detect potential predictor gene variants for neuroleptic-induced tardive dyskinesia (TD) in s	1.32 KB	2025-10-02	8	-
PubMed	22798246	The influence of the genetic and non-genetic factors on bone mineral density and osteoporotic fractures in Chinese women. To investigate the effects of genetic and non-genetic factors on bone mineral	1.39 KB	2025-10-02	6	-
PubMed	22862926	Incretin and pancreatic hormone secretion in Caucasian non-diabetic carriers of the TCF7L2 rs7903146 risk T allele. We characterised 62 non-diabetic, middle-aged, Caucasians with and without the T ris	1.23 KB	2025-10-02	5	-
PubMed	23000450	-116A and K BCHE gene variants associated with obesity and hypertriglyceridemia in adolescents from Southern Brazil. Butyrylcholinesterase (BChE) has been associated to body mass index (BMI), weight,	1.72 KB	2025-10-02	8	-
PubMed	23267857	CYP2C19*17 gain-of-function polymorphism is associated with peptic ulcer disease. Single-nucleotide polymorphisms (SNPs) in the CYP2C gene cluster have been extensively investigated as predisposing fa	1.15 KB	2025-10-02	10	-
PubMed	23471504	Interindividual variability of carboxymethylenebutenolidase homolog, a novel olmesartan medoxomil hydrolase, in the human liver and intestine. Olmesartan medoxomil (OM) is a prodrug-type angiotensin I	1.7 KB	2025-10-02	5	-