International collaborative is formed to fund research to identify genes associated with autism spectrum disorders
An international collaborative of governmental
and private organizations is committing more than 21 million US
dollars for research to identify genes associated with autism spectrum
disorders. The effort is headed by the National Institutes of Health
(USA).
The coalition recently issued a Request for
Applications, "Identifying Autism Susceptibility Genes,"
which has an application receipt date of April 15, 2005. Applications
will undergo peer review during July 2005. The coalition will award
funding for research projects in the fall of 2005 and expects to
fund two to three organizations to participate in the 5-year project.
"The National Institute of Mental Health (NIMH) appreciates
the challenge of leading this impressive team," said Thomas
R. Insel, M., director of the NIMH. "This remarkable partnership
shows what can be accomplished when public/private efforts join
forces. This international approach can advance the autism field
by leaps and bounds."
With 3 to 6 new cases per 1,000 children, autism is more common
than several other disabling but better-understood diseases of childhood,
such as type 1 diabetes and cystic fibrosis. Although heredity,
in the form of multiple genes, appears to be a major determinant
of whether a particular individual develops autism, experts believe
that environmental influences also play a significant role.
Researchers have already reported progress on the genetics underlying
autism. There are reports of several chromosomal regions associated
with the disorder, but few specific genes have been identified.
The new program is intended to advance knowledge of the relation
between genetics and autism by examining existing data for genes
and gene variants that confer susceptibility to autism. The program
also requires researchers to assess the functional significance
of autism-associated genetic variants. This research may provide
a means to subdivide autism spectrum disorders into identifiable,
distinct disorders, with different molecular mechanisms.
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