English
日本語
signup
login
Repository
Search
Annotators
Editors
Evaluators
NEWS
Documentation
>
top
>
projects
>
DisGeNET5_variant_disease
> docs
DisGeNET5_variant_disease
Documents
(31,966)
JSON
TSV
source DB
source ID
text
size
updated at
# proj.
# Ann.
updated_at
PubMed
19117022
The influence of genetic variations in HHEX gene on insulin metabolism in the German MESYBEPO cohort. BACKGROUND: In the present study, we aimed to validate the type 2 diabetes (T2DM) susceptibility a
1.86 KB
2025-10-02
6
14
-
PubMed
16315267
GSK3B polymorphisms alter transcription and splicing in Parkinson's disease. Parkinson's disease (PD) is a neurodegenerative disorder characterized by a combination of motor symptoms. We identified tw
1.52 KB
2025-10-02
6
5
-
PubMed
24911064
Association of FTO polymorphisms with obesity and metabolic parameters in Han Chinese adolescents. BACKGROUND: Previous studies have suggested that fat mass-and obesity-associated (FTO) gene is associ
2.08 KB
2016-01-17
5
3
-
PubMed
19046748
Variation in eicosanoid genes, non-fatal myocardial infarction and ischemic stroke. OBJECTIVES: Eicosanoids are lipid mediators that may play a role in atherosclerosis. We investigated the association
1.74 KB
2015-11-24
3
14
-
PubMed
21261977
Variants in KCNQ1 increase type II diabetes susceptibility in South Asians: a study of 3,310 subjects from India and the US. BACKGROUND: Polymorphisms in intron 15 of potassium voltage-gated channel,
2.03 KB
2015-11-25
4
5
-
PubMed
18771913
Associations between XPC polymorphisms and risk of cancers: A meta-analysis. Several polymorphisms (Lys(939)Gln, PAT+/- and Ala(499)Val) in the DNA nuclear excision repair gene xeroderma pigmentosum c
1.7 KB
2015-11-24
4
6
-
PubMed
17849003
Brain expressed microRNAs implicated in schizophrenia etiology. BACKGROUND: Protein encoding genes have long been the major targets for research in schizophrenia genetics. However, with the identifica
2.04 KB
2015-11-23
5
5
-
PubMed
22194935
Cardiac alpha-myosin (MYH6) is the predominant sarcomeric disease gene for familial atrial septal defects. Secundum-type atrial septal defects (ASDII) account for approximately 10% of all congenital h
1.69 KB
2015-11-26
6
39
-
PubMed
23122776
Neuropeptide Y polymorphism increases the risk for asthma in overweight subjects; protection from atherosclerosis in asthmatic subjects--the cardiovascular risk in young Finns study. AIMS: The role of
2.07 KB
2025-10-02
8
75
-
PubMed
26111027
DNMT3A moderates cognitive decline in subjects with mild cognitive impairment: replicated evidence from two mild cognitive impairment cohorts. Epigenetic dysregulation has been associated with cogniti
694 Bytes
2025-10-02
6
5
-
Page 11