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Showing results (351-360 of 388) with videos related to

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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.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 12, 2013
Implementing genomic medicine in the clinic: the future is hereTeri A Manolio, Rex L Chisholm, Brad Ozenberger, 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|July 28, 2014
The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained populationEllen Hanson, Raphael Bernier, Ken Porche, et al.
Nature Medicine|September 25, 2019
A framework for the investigation of rare genetic disorders in neuropsychiatryStephan J Sanders, Mustafa Sahin, Joseph Hostyk, et al.
American Journal of Human Genetics|August 14, 2018
A Model for Genome-First Care: Returning Secondary Genomic Findings to Participants and Their Healthcare Providers in a Large Research CohortMarci L B Schwartz, Cara Zayac McCormick, Amanda L Lazzeri, 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.
American Journal of Human Genetics|May 5, 2018
Profiling and Leveraging Relatedness in a Precision Medicine Cohort of 92,455 ExomesJeffrey Staples, Evan K Maxwell, Nehal Gosalia, et al.
The New England Journal of Medicine|March 3, 2016
Inactivating Variants in ANGPTL4 and Risk of Coronary Artery DiseaseFrederick E Dewey, Viktoria Gusarova, Colm O'Dushlaine, et al.
Autism Research : Official Journal of the International Society for Autism Research|May 14, 2014
Modest impact on risk for autism spectrum disorder of rare copy number variants at 15q11.2, specifically breakpoints 1 to 2Pauline Chaste, Stephan J Sanders, Kommu N Mohan, et al.
Pageof 39

Showing results (351-360 of 388) with videos related to

Sort By:
Pageof 39
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.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 12, 2013
Implementing genomic medicine in the clinic: the future is hereTeri A Manolio, Rex L Chisholm, Brad Ozenberger, 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|July 28, 2014
The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained populationEllen Hanson, Raphael Bernier, Ken Porche, et al.
Nature Medicine|September 25, 2019
A framework for the investigation of rare genetic disorders in neuropsychiatryStephan J Sanders, Mustafa Sahin, Joseph Hostyk, et al.
American Journal of Human Genetics|August 14, 2018
A Model for Genome-First Care: Returning Secondary Genomic Findings to Participants and Their Healthcare Providers in a Large Research CohortMarci L B Schwartz, Cara Zayac McCormick, Amanda L Lazzeri, 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.
American Journal of Human Genetics|May 5, 2018
Profiling and Leveraging Relatedness in a Precision Medicine Cohort of 92,455 ExomesJeffrey Staples, Evan K Maxwell, Nehal Gosalia, et al.
The New England Journal of Medicine|March 3, 2016
Inactivating Variants in ANGPTL4 and Risk of Coronary Artery DiseaseFrederick E Dewey, Viktoria Gusarova, Colm O'Dushlaine, et al.
Autism Research : Official Journal of the International Society for Autism Research|May 14, 2014
Modest impact on risk for autism spectrum disorder of rare copy number variants at 15q11.2, specifically breakpoints 1 to 2Pauline Chaste, Stephan J Sanders, Kommu N Mohan, et al.
Pageof 39