ICHG 2011

Recent articles

Spectrum from The Transmitter.

Growth factor improves autism symptoms in mice

Mice lacking a copy of SHANK3, a gene associated with autism and intellectual disability, show marked improvements in brain signaling after being treated with insulin-like growth factor 1, according to unpublished findings presented Saturday at the International Congress of Human Genetics in Montreal, Canada.

By Deborah Rudacille
19 October 2011 | 5 min read
Spectrum from The Transmitter.

Researchers debut mice with links to Williams syndrome

Mouse pups with a duplication of GTF2I, a gene linked to Williams syndrome and autism, show extreme separation anxiety when separated from their mothers, according to unpublished findings presented Thursday at the International Congress of Human Genetics in Montreal, Canada.

By Deborah Rudacille
17 October 2011 | 5 min read
Spectrum from The Transmitter.

Fast-evolving gene is key player in brain development

A gene that changed rapidly after the human genome diverged from that of Neanderthals plays a critical role in brain development, according to unpublished results presented Thursday at the International Congress of Human Genetics in Montreal, Canada.

By Deborah Rudacille
14 October 2011 | 4 min read

Explore more from The Transmitter

Avis Cohen.

Remembering Avis H. Cohen, who bridged disciplines to decode lamprey locomotion

The founding director of the University of Maryland’s Neuroscience and Cognitive Science program brought neuroscience, math and engineering together.

By Sarah Thau
26 June 2026 | 8 min read
Photo collage featuring a portrait of Tempest McDonald.

When autistic kids grow up, Chapter 4: How did things unfold?

Tempest McDonald sues Vanderbilt University Medical Center through the Equal Employment Opportunity Commission. Her published NIH paper finds allies.

By Brady Huggett
25 June 2026 | 27 min listen
Researchers looking at KEMRI biobank vials.

NeuroDev study maps previously unseen genetic variation in Africa

The project is helping to fill critical gaps in the genetic underpinnings of autism and other neurodevelopmental conditions.

By Brianna Abbott
25 June 2026 | 5 min read