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- Richard J L Anney, Lambertus Klei, +163 authors Joachim F. Hallmayer
- Human molecular genetics
- 2010
Although autism spectrum disorders (ASDs) have a substantial genetic basis, most of the known genetic risk has been traced to rare variants, principally copy number variants (CNVs). To identify… (More)
- Daisuke Sato, Anath Christopher Lionel, +28 authors Stephen W. Scherer
- American journal of human genetics
- 2012
Recent studies have highlighted the involvement of rare (<1% frequency) copy-number variations and point mutations in the genetic etiology of autism spectrum disorder (ASD); these variants… (More)
- Claire S. Leblond, Caroline Nava, +57 authors Thomas Bourgeron
- PLoS genetics
- 2014
SHANK genes code for scaffold proteins located at the post-synaptic density of glutamatergic synapses. In neurons, SHANK2 and SHANK3 have a positive effect on the induction and maturation of… (More)
- Daisuke Sato, Yuanfang Xie, James N. Weiss, Zhilin Qu, Alan Garfinkel, Allen R. Sanderson
- Medical & Biological Engineering & Computing
- 2009
In this technical note we show the promise of using graphic processing units (GPUs) to accelerate simulations of electrical wave propagation in cardiac tissue, one of the more demanding computational… (More)
- Abdul Noor, Annabel Whibley, +53 authors John B Vincent
- Science translational medicine
- 2010
Autism is a common neurodevelopmental disorder with a complex mode of inheritance. It is one of the most highly heritable of the complex disorders, although the underlying genetic factors remain… (More)
While a photograph is a visual artifact, studies reveal that a number of people with visual impairments are also interested in being able to share their memories and experiences with their sighted… (More)
- Susumu Harada, Daisuke Sato, Hironobu Takagi, Chieko Asakawa
- INTERACT
- 2013
Smartphones and tablet devices have been rapidly proliferating, and multi-touch interaction, powerful processors and rich array of sensors make these devices an attractive service platform for older… (More)
There are billions of people who face problems in accessing webpages, including people with disabilities, elderly people, and illiterate people in developing countries. The needs for accessible… (More)
- Andrea K. Vaags, Anath Christopher Lionel, +24 authors Stephen W. Scherer
- American journal of human genetics
- 2012
The three members of the human neurexin gene family, neurexin 1 (NRXN1), neurexin 2 (NRXN2), and neurexin 3 (NRXN3), encode neuronal adhesion proteins that have important roles in synapse development… (More)
- Hironobu Takagi, Susumu Harada, Daisuke Sato, Chieko Asakawa
- INTERACT
- 2013
Crowd accessibility services for people with disabilities, driven by crowd-sourcing methods, are gaining traction as a viable means of realizing innovative services by leveraging both human and… (More)