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Matthew W State

Showing results (81-90 of 123) with videos related to

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Plos Genetics|January 27, 2015
No evidence for association of autism with rare heterozygous point mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Proteins or ContactinsJohn D Murdoch, Abha R Gupta, Stephan J Sanders, et al.
Science (New York, N.Y.)|September 8, 2012
Mutations in BCKD-kinase lead to a potentially treatable form of autism with epilepsyGaia Novarino, Paul El-Fishawy, Hulya Kayserili, et al.
Neuron|January 14, 2014
Histidine decarboxylase deficiency causes tourette syndrome: parallel findings in humans and miceLissandra Castellan Baldan, Kyle A Williams, Jean-Dominique Gallezot, et al.
Nature|March 26, 2015
Loss of δ-catenin function in severe autismTychele N Turner, Kamal Sharma, Edwin C Oh, et al.
Biological Psychiatry|June 11, 2013
Adjusting head circumference for covariates in autism: clinical correlates of a highly heritable continuous traitPauline Chaste, Lambertus Klei, Stephan J Sanders, et al.
Biological Psychiatry|December 24, 2014
A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?Pauline Chaste, Lambertus Klei, Stephan J Sanders, et al.
Biological Psychiatry|December 16, 2011
Rare copy number variants in tourette syndrome disrupt genes in histaminergic pathways and overlap with autismThomas V Fernandez, Stephan J Sanders, Ilana R Yurkiewicz, et al.
Circulation Research|September 11, 2014
Increased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence dataJoseph T Glessner, Alexander G Bick, Kaoru Ito, et al.
Molecular Autism|October 17, 2012
Common genetic variants, acting additively, are a major source of risk for autismLambertus Klei, Stephan J Sanders, Michael T Murtha, et al.
Science (New York, N.Y.)|October 15, 2005
Sequence variants in SLITRK1 are associated with Tourette's syndromeJesse F Abelson, Kenneth Y Kwan, Brian J O'Roak, et al.
Pageof 13

Showing results (81-90 of 123) with videos related to

Sort By:
Pageof 13
Plos Genetics|January 27, 2015
No evidence for association of autism with rare heterozygous point mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Proteins or ContactinsJohn D Murdoch, Abha R Gupta, Stephan J Sanders, et al.
Science (New York, N.Y.)|September 8, 2012
Mutations in BCKD-kinase lead to a potentially treatable form of autism with epilepsyGaia Novarino, Paul El-Fishawy, Hulya Kayserili, et al.
Neuron|January 14, 2014
Histidine decarboxylase deficiency causes tourette syndrome: parallel findings in humans and miceLissandra Castellan Baldan, Kyle A Williams, Jean-Dominique Gallezot, et al.
Nature|March 26, 2015
Loss of δ-catenin function in severe autismTychele N Turner, Kamal Sharma, Edwin C Oh, et al.
Biological Psychiatry|June 11, 2013
Adjusting head circumference for covariates in autism: clinical correlates of a highly heritable continuous traitPauline Chaste, Lambertus Klei, Stephan J Sanders, et al.
Biological Psychiatry|December 24, 2014
A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?Pauline Chaste, Lambertus Klei, Stephan J Sanders, et al.
Biological Psychiatry|December 16, 2011
Rare copy number variants in tourette syndrome disrupt genes in histaminergic pathways and overlap with autismThomas V Fernandez, Stephan J Sanders, Ilana R Yurkiewicz, et al.
Circulation Research|September 11, 2014
Increased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence dataJoseph T Glessner, Alexander G Bick, Kaoru Ito, et al.
Molecular Autism|October 17, 2012
Common genetic variants, acting additively, are a major source of risk for autismLambertus Klei, Stephan J Sanders, Michael T Murtha, et al.
Science (New York, N.Y.)|October 15, 2005
Sequence variants in SLITRK1 are associated with Tourette's syndromeJesse F Abelson, Kenneth Y Kwan, Brian J O'Roak, et al.
Pageof 13