Dup15q 2015
Recent articles
Brain-wave patterns distinguish dup15q syndrome
Children with an extra copy of the 15q11-13 chromosomal region, the second most common genetic abnormality in people with autism, have unusually strong brain waves called beta oscillations. The preliminary findings, presented Friday at the Dup15q Alliance Scientific Meeting in Orlando, Florida, suggest that beta oscillations could distinguish children with dup15q syndrome from those with other forms of autism.
Brain-wave patterns distinguish dup15q syndrome
Children with an extra copy of the 15q11-13 chromosomal region, the second most common genetic abnormality in people with autism, have unusually strong brain waves called beta oscillations. The preliminary findings, presented Friday at the Dup15q Alliance Scientific Meeting in Orlando, Florida, suggest that beta oscillations could distinguish children with dup15q syndrome from those with other forms of autism.
Dispatches from the 2015 Dup15q Alliance Scientific Meeting
These short reports from our reporter, Nicholette Zeliadt, give you the inside scoop on developments at the 2015 Dup15q Alliance Scientific Meeting.
Dispatches from the 2015 Dup15q Alliance Scientific Meeting
These short reports from our reporter, Nicholette Zeliadt, give you the inside scoop on developments at the 2015 Dup15q Alliance Scientific Meeting.
Explore more from The Transmitter
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To understand decision-making, we need to truly challenge lab animals
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‘Overdue’ debate unfurls over neuroimaging method
After a January paper questioned the validity of an approach called lesion network mapping, its users are pressure testing their results.
‘Overdue’ debate unfurls over neuroimaging method
After a January paper questioned the validity of an approach called lesion network mapping, its users are pressure testing their results.
Nearly 400 compounds affect behaviors tied to autism-linked genes in zebrafish
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Nearly 400 compounds affect behaviors tied to autism-linked genes in zebrafish
Estropipate, paclitaxel and levocarnitine altered behaviors tied to SCN2A and DYRK1A variants specifically, a new open-source platform revealed.