|
| Entrez Id: |
9213 |
| Gene Symbol: |
XPR1 |
XPR1
|
0.300 |
Biomarker
|
disease |
CTD_human |
Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export.
|
25938945 |
2015 |
|
| Entrez Id: |
5159 |
| Gene Symbol: |
PDGFRB |
PDGFRB
|
0.300 |
Biomarker
|
disease |
CTD_human |
Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export.
|
25938945 |
2015 |
|
| Entrez Id: |
6575 |
| Gene Symbol: |
SLC20A2 |
SLC20A2
|
0.300 |
Biomarker
|
disease |
CTD_human |
Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export.
|
25938945 |
2015 |
|
| Entrez Id: |
5155 |
| Gene Symbol: |
PDGFB |
PDGFB
|
0.300 |
Biomarker
|
disease |
CTD_human |
Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export.
|
25938945 |
2015 |
|
| Entrez Id: |
10367 |
| Gene Symbol: |
MICU1 |
MICU1
|
0.300 |
Biomarker
|
disease |
CTD_human |
Loss-of-function mutations in MICU1 cause a brain and muscle disorder linked to primary alterations in mitochondrial calcium signaling.
|
24336167 |
2014 |
|
| Entrez Id: |
8622 |
| Gene Symbol: |
PDE8B |
PDE8B
|
0.300 |
Biomarker
|
disease |
CTD_human |
Autosomal-dominant striatal degeneration is caused by a mutation in the phosphodiesterase 8B gene.
|
20085714 |
2010 |
|
| Entrez Id: |
1813 |
| Gene Symbol: |
DRD2 |
DRD2
|
0.300 |
Biomarker
|
disease |
CTD_human |
A common variant in DRD3 gene is associated with risperidone-induced extrapyramidal symptoms.
|
19506579 |
2009 |
|
| Entrez Id: |
1813 |
| Gene Symbol: |
DRD2 |
DRD2
|
0.300 |
Biomarker
|
disease |
CTD_human |
Sensitivity of older patients to antipsychotic motor side effects: a PET study examining potential mechanisms.
|
19225277 |
2009 |
|
| Entrez Id: |
80704 |
| Gene Symbol: |
SLC19A3 |
SLC19A3
|
0.300 |
Biomarker
|
disease |
CTD_human |
Mutations in a thiamine-transporter gene and Wernicke's-like encephalopathy.
|
19387023 |
2009 |
|
| Entrez Id: |
1814 |
| Gene Symbol: |
DRD3 |
DRD3
|
0.300 |
Biomarker
|
disease |
CTD_human |
A common variant in DRD3 gene is associated with risperidone-induced extrapyramidal symptoms.
|
19506579 |
2009 |
|
| Entrez Id: |
3356 |
| Gene Symbol: |
HTR2A |
HTR2A
|
0.300 |
Biomarker
|
disease |
CTD_human |
Aripiprazole-induced parkinsonism and its association with dopamine and serotonin receptor polymorphisms.
|
18480698 |
2008 |
|
| Entrez Id: |
1813 |
| Gene Symbol: |
DRD2 |
DRD2
|
0.300 |
Biomarker
|
disease |
CTD_human |
Aripiprazole-induced parkinsonism and its association with dopamine and serotonin receptor polymorphisms.
|
18480698 |
2008 |
|
| Entrez Id: |
1565 |
| Gene Symbol: |
CYP2D6 |
CYP2D6
|
0.300 |
Biomarker
|
disease |
CTD_human |
Delirium resolving upon switching from risperidone to quetiapine: implication of CYP2D6 genotype.
|
16000684 |
2005 |
|
| Entrez Id: |
1813 |
| Gene Symbol: |
DRD2 |
DRD2
|
0.300 |
Biomarker
|
disease |
CTD_human |
Prediction and assessment of extrapyramidal side effects induced by risperidone based on dopamine D(2) receptor occupancy.
|
12211096 |
2002 |
|
| Entrez Id: |
1813 |
| Gene Symbol: |
DRD2 |
DRD2
|
0.300 |
Biomarker
|
disease |
CTD_human |
D2 receptor occupancy under recommended and high doses of olanzapine: an iodine-123-iodobenzamide SPECT study.
|
11198054 |
2000 |
|
| Entrez Id: |
5617 |
| Gene Symbol: |
PRL |
PRL
|
0.300 |
Biomarker
|
disease |
CTD_human |
Clinical state, plasma levels of haloperidol and prolactin: a correlation study in chronic schizophrenia.
|
7214106 |
1980 |