Location: University of Michigan Autism & Communication
Disorders Center, Ann Arbor, MI
Principal Investigator: Dr. Catherine
Lord
Contact Information: Barbara Hanna, Study Manager, phone: (734)
936-8600, email: hannab@umich.edu
The Simons Simplex Collection
is following in the tradition set by AGRE in setting up a biobank
of phenotype and biological samples of families with one child
with ASD and at least one child with typical development to be
available to interested scientists around the world. Children with
ASD and their family members will receive a comprehensive assessment
and will become part of an autism initiative to be followed through
their centers as new advances emerge.
We are looking for families
interested in helping researchers understand the genetic causes
of ASD. Sponsored by the Simons Foundation, the University of Michigan
Autism and Communication Disorders Center (UMACC) is one of 13
clinical centers around the U.S. and Canada that are recruiting
families to participate. The Simons Foundation provides support
to researchers studying ASD. For additional information about the
Simons Foundation, see: www.simonsfoundation.org.
For this study,
we are recruiting families who have: One child aged four or older
with ASD or a suspected ASD diagnosis, One or more child(ren) age
four or older without ASD (preferred, but not required), and Both
biological parents also willing to participate.If your child has
not previously participated in a diagnostic assessment at UMACC,
he/she may be eligible for a free research assessment as part of
this study. We will provide your family with a brief written report
describing the results of the assessment.
Additionally, participation
in this study involves the completion of interviews, questionnaires,
and a blood draw. Blood will be donated to the Simons Simplex Collection.
The Simons Simplex Collection obtains, stores, and distributes
DNA to researchers who are studying the genetics of ASD. Through
performing genetic analyses, we hope to discover information that
will help us better understand and treat this disorder.
As compensation
for your time and travel, each participating family member will
receive a $25 gift certificate for completing the initial questionnaire
packet, and a $50 gift certificate upon completion of the entire
protocol (including the blood draw).
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