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PubMed 16192625 APOC3/A5 haplotypes, lipid levels, and risk of myocardial infarction in the Central Valley of Costa Rica. Genetic variation in the APOC3 and APOA5 genes has been associated with plasma triglyceride co 1.45 KB 2015-11-19 4 3
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PubMed 22898872 Slow development of ALS-like spinal cord pathology in mutant valosin-containing protein gene knock-in mice. Pathological features of amyotrophic lateral sclerosis (ALS) include, in addition to selecti 1.59 KB 2015-11-26 5 6
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PubMed 20414141 Family-based association study for bipolar affective disorder. In this study we aimed to evaluate 21 candidate loci for bipolar affective disorder (BPAD) identified earlier in a large genome-wide asso 954 Bytes 2025-10-02 6 3
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PubMed 19760522 Translin-associated factor X gene (TSNAX) may be associated with female major depressive disorder in the Japanese population. Several investigations have reported that the translin-associated factor X 1.8 KB 2025-10-02 7 3
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PubMed 20479154 Selective molecular potassium channel blockade prevents atrial fibrillation. BACKGROUND: Safety and efficacy limit currently available atrial fibrillation (AF) therapies. We hypothesized that atrial g 1.6 KB 2016-01-02 5 3
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PubMed 18639335 Polymorphisms and haplotypes in the multidrug resistance 1 gene (MDR1/ABCB1) and risk of multiple myeloma. MDR1(ABCB1) gene encodes for P-glycoprotein (P-gp, MDR1, ABCB1), an ATP-binding cassette supe 842 Bytes 2018-10-10 2 3
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PubMed 17922155 Effects of prolonged dark adaptation in patients with retinitis pigmentosa of Bothnia type: an electrophysiological study. Bothnia dystrophy (BD) is a variant of recessive retinitis punctata albescens 1.7 KB 2019-09-23 8 3
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PubMed 21497535 Association of interleukin-4 receptor gene polymorphisms with rheumatoid arthritis in Egyptian female patients. OBJECTIVES: The imbalance between proinflammatory and anti-inflammatory cytokines is a f 1.25 KB 2025-10-02 10 14
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PubMed 21403649 Association of polymorphisms in the TLR4 gene with the risk of developing neutropenia in children with leukemia. Infections are a major cause of morbidity and mortality in children with acute lymphobl 1.45 KB 2025-10-02 8 27
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PubMed 26936456 The impact of common polymorphisms in CETP and ABCA1 genes with the risk of coronary artery disease in Saudi Arabians. BACKGROUND: Coronary artery disease (CAD) is a leading cause of morbidity and mor 1.58 KB 2017-09-04 4 17
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