BaseSpace
Correlation
Engine-Public
Sign In
Register
Correlation Engine 2.0
Home
My Data
Bookmarks
Collaborations
Inbox
Import Your Data
QuickView
FAQ
What is QuickView?
What can my QuickView results tell me?
What are the sources for the General Info tab in QuickView?
More QuickView FAQs
Back to top
QuickView
Curated
Studies
Body
Atlas
Disease
Atlas
Pharmaco
Atlas
Knockdown
Atlas
Genetic
Markers
Pathway
Enrichment
Literature
Clinical
Trials
0
Meta-
Analysis
QuickView
Search sequence regions
(e.g.
Retina
,
DNA fingerprint
,
Valproic acid
,
rs2300478
,
CXCL2
,
Apoptosis
,
Influenza
)
Organisms
Chromosomes
Start
Stop
Homo Sapiens
Mus Musculus
Rattus Norvegicus
C. Elegans
D. Melanogaster
Saccharomyces Cerevisiae
QuickView
Go back to main search
Bookmark
Forward
QuickView
for
hyperprolactinemia
(phenotype)
Summary
General Info
Genetic Markers
Most Correlated Genes
Most Correlated SNPs
No genes found
No SNPs found
Explore Genetic Markers Results
Pathway Enrichment
Most Correlated Biogroups
No biogroups found
Explore Pathway Enrichment Results
Curated Studies
Most Correlated Studies
No studies found
Explore Curated Studies Results
Literature
Most Relevant Literature
The utility of rested prolactin sampling in the evaluation of hyperprolactinaemia.
Diagnosis of hyperprolactinemia in women: A Position Statement from the Brazilian Federation of Gyne…
Mild hyperprolactinemia in a couple: What impact on fertility?
Acute retinal pigment epitheliitis during treatment of hyperprolactinaemia.
Hyperprolactinemia-induced acute ischemic stroke.
Explore Literature Results
Clinical Trials
Most Relevant Clinical Trials
Risperidone-Induced Hyperprolactinemia Treated With Bromocriptine
Nurse's Role in the Management of Hyperprolactinemia
Hyperprolactinemia and Adrenal Steroidogenesis
Treatment of Hyperprolactinemia With the Non-ergoline Dopamine Agonist Ropinirole
Changes in Hyperprolactinemia Secondary to Antipsychotics After Switching to Quetiapine
Explore Clinical Trials Results
search
→
result
search
→
result
See more about this page
See complete FAQ