In an international collaboration, researchers have determined that psychiatric disorders may have important molecular similarities that are not reflected in current diagnostic categories.
A novel study reveals that the placenta could play an imperative role in schizophrenia and possibly other neurodevelopmental disorders.
Researchers have uncovered three new genes that are linked to the possibility of developing Alzheimer’s disease; potentially unlocking new treatment possibilities for patients.
A research team has identified a gene that, upon elimination, could potentially spur regeneration of axons in nerve cells severed by spinal cord injury.
Clinical trial announcements, orphan-drug designation and more: check out our round-up of the biggest news from the neuroscience and neurology industries this week.
For the first time, researchers have discovered that non-gene mutations could cause rare developmental disorders of the CNS.
Researchers have identified genes in the human genome that could modify the severity of amyotrophic lateral sclerosis and frontotemporal dementia.
Sara Mole (UCL) discusses her work on Batten disease, as well as the universal challenges encountered when researching and treating rare neurological diseases.
In these interviews, we speak to four early career researchers whose respective research findings were highlighted by the Society as ones to watch in the coming years.
This review from Biomarkers in Medicine examines the usefulness of telomere length as biomarkers for neurological conditions such as Alzheimer’s, Parkinson’s and autism.
