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source DB	source ID	text	size	updated at	# proj.	updated_at
PubMed	20363506	Genome-wide association study of normal tension glaucoma: common variants in SRBD1 and ELOVL5 contribute to disease susceptibility. PURPOSE: Factors contributing to the development of normal tension g	1.64 KB	2025-10-02	9	-
PubMed	24767015	MiRNA-206 and BDNF genes interacted in bipolar I disorder. BACKGROUND: Several lines of evidence have suggested that has-mir-206 (miRNA-206) may regulate brain-derived neurotrophic factor (BDNF) prote	1.63 KB	2025-10-02	8	-
PubMed	25420549	Genetic variants of GSK3B are associated with biomarkers for Alzheimer's disease and cognitive function. BACKGROUND: Glycogen synthase kinase 3 beta (GSK3B) is the major kinase phosphorylating tau pro	1.8 KB	2025-10-02	9	-
PubMed	19332048	Polymorphisms of MMP-2 gene are associated with systolic heart failure prognosis. BACKGROUND: MMP-2 is a proteolytic enzyme involved in myocardial remodeling that occurs in congestive heart failure (H	1.55 KB	2025-10-02	7	-
PubMed	20034444	Susceptibility for ischemic stroke in four constitution medicine is associated with polymorphisms of FCGR2A and IL1RN genes. OBJECTIVES: To determine the association between Four Constitutional classi	1.38 KB	2025-10-02	7	-
PubMed	20140301	VEGFA polymorphisms and cardiovascular anomalies in 22q11 microdeletion syndrome: a case-control and family-based study. Microdeletion 22q11 in humans causes velocardiofacial and DiGeorge syndromes. M	1.48 KB	2025-10-02	6	-
PubMed	21951294	A single nucleotide polymorphism rs9468925 of MHC region is associated with clinical features of generalized vitiligo in Chinese Han population. BACKGROUND: Vitiligo has been found to be associated wi	1.73 KB	2025-10-02	9	-
PubMed	25475391	Common genetic variants (rs4779584 and rs10318) at 15q13.3 contributes to colorectal adenoma and colorectal cancer susceptibility: evidence based on 22 studies. Several genome-wide association studies	1.79 KB	2025-10-02	8	-
PubMed	20030635	The TRAF1/C5 locus confers risk for familial and severe alopecia areata. BACKGROUND: Alopecia areata (AA) is a common hair loss disorder with a complex mode of inheritance. Autoimmune mechanisms are p	1.74 KB	2025-10-02	9	-
PubMed	21705081	Multidrug resistance gene expression and ABCB1 SNPs in plasma cell myeloma. Multi-drug resistance (MDR) leads to impaired treatment efficacy in all forms of malignancy. The main forms of MDR are thoug	1.13 KB	2025-10-02	9	-