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Daisuke Sato

Showing results (531-540 of 538) with videos related to

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American Journal of Human Genetics|April 17, 2012
SHANK1 Deletions in Males with Autism Spectrum DisorderDaisuke Sato, Anath C Lionel, Claire S Leblond, et al.
Human Molecular Genetics|February 9, 2013
Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizuresAnath C Lionel, Andrea K Vaags, Daisuke Sato, et al.
Plos Genetics|September 5, 2014
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairmentsClaire S Leblond, Caroline Nava, Anne Polge, et al.
Science Translational Medicine|September 17, 2010
Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disabilityAbdul Noor, Annabel Whibley, Christian R Marshall, et al.
Journal of Medical Genetics|December 18, 2013
A genome-wide copy number association study of osteoporotic fractures points to the 6p25.1 locusLing Oei, Yi-Hsiang Hsu, Unnur Styrkarsdottir, et al.
Nature Genetics|January 10, 2017
SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndromeNatalie D Shaw, Harrison Brand, Zachary A Kupchinsky, et al.
Human Molecular Genetics|July 29, 2010
A genome-wide scan for common alleles affecting risk for autismRichard Anney, Lambertus Klei, Dalila Pinto, et al.
Nature|June 10, 2010
Functional impact of global rare copy number variation in autism spectrum disordersDalila Pinto, Alistair T Pagnamenta, Lambertus Klei, et al.
Pageof 54

Showing results (531-540 of 538) with videos related to

Sort By:
Pageof 54
You have reached the last page of results.This site can display upto 538 results.
American Journal of Human Genetics|April 17, 2012
SHANK1 Deletions in Males with Autism Spectrum DisorderDaisuke Sato, Anath C Lionel, Claire S Leblond, et al.
Human Molecular Genetics|February 9, 2013
Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizuresAnath C Lionel, Andrea K Vaags, Daisuke Sato, et al.
Plos Genetics|September 5, 2014
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairmentsClaire S Leblond, Caroline Nava, Anne Polge, et al.
Science Translational Medicine|September 17, 2010
Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disabilityAbdul Noor, Annabel Whibley, Christian R Marshall, et al.
Journal of Medical Genetics|December 18, 2013
A genome-wide copy number association study of osteoporotic fractures points to the 6p25.1 locusLing Oei, Yi-Hsiang Hsu, Unnur Styrkarsdottir, et al.
Nature Genetics|January 10, 2017
SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndromeNatalie D Shaw, Harrison Brand, Zachary A Kupchinsky, et al.
Human Molecular Genetics|July 29, 2010
A genome-wide scan for common alleles affecting risk for autismRichard Anney, Lambertus Klei, Dalila Pinto, et al.
Nature|June 10, 2010
Functional impact of global rare copy number variation in autism spectrum disordersDalila Pinto, Alistair T Pagnamenta, Lambertus Klei, et al.
Pageof 54