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Tag: Simons VIP

November 2013
News

Results of 16p11.2 study show promise for autism biomarker

by  /  12 November 2013

The level of activity of a cellular signaling pathway correlates with the degree of social and cognitive impairments in children with an autism-linked genetic abnormality, according to unpublished research presented Sunday at the 2013 Society for Neuroscience annual meeting in San Diego.

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October 2013
News / Profiles

Elliott Sherr: Coaching teams to tackle autism’s mysteries

by  /  10 October 2013

Elliott Sherr is unraveling the effects of genetics and brain structure in a handful of disparate disorders that each illuminates some aspect of autism.

2 Comments
May 2013
Opinion / Viewpoint

Developmental disorders should be viewed as continuum

by  /  6 May 2013

Intellectual disability, autism, epilepsy and schizophrenia should be considered part of a spectrum of developmental brain dysfunction, says David Ledbetter.

3 Comments
October 2012
Opinion / Viewpoint

A call for open-science approaches in autism research

by  /  16 October 2012

Sharing data and tools is universally efficient, but the study of autism in particular presents challenges that can benefit from an open-science framework, says Randy Buckner.

1 Comment
March 2012
News

More sensitive prenatal tests detect autism-linked variants

by  /  12 March 2012

Prenatal genetic tests that can detect copy number variations, including those linked to autism, could raise tough questions for doctors and parents.

1 Comment
July 2011
News / Profiles

Wendy Chung: Genetic sleuth is advocate for families

by  /  21 July 2011

Wendy Chung planned to spend her career in a research lab, identifying rare pathologies. But life had other plans for her.

9 Comments
February 2011
News

Families hint at diverse effects of chromosome 16p deletion

by  /  14 February 2011

Two new studies of families carrying glitches on a region of chromosome 16, which has been strongly associated with autism, reveal the wide range of effects caused by the variant and narrow the list of possible culprit genes.

4 Comments
December 2010
News

Clinical research: Chromosome deletion linked to autism features

by  /  13 December 2010

Individuals with a deletion in the 16p11.2 chromosomal region — which has been linked to autism in several studies — show features of autism spectrum disorders including language delay, according to a study published in October.

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