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The American Journal of Psychiatry
|
March 3, 2022
Genes To Mental Health (G2MH): A Framework to Map the Combined Effects of Rare and Common Variants on Dimensions of Cognition and Psychopathology
Sébastien Jacquemont, Guillaume Huguet, Marieke Klein, et al.
Human Molecular Genetics
|
February 9, 2013
Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizures
Anath C Lionel, Andrea K Vaags, Daisuke Sato, et al.
American Journal of Human Genetics
|
February 7, 2008
Structural variation of chromosomes in autism spectrum disorder
Christian R Marshall, Abdul Noor, John B Vincent, et al.
Molecular Psychiatry
|
June 1, 2016
Chromosomal contacts connect loci associated with autism, BMI and head circumference phenotypes
M N Loviglio, M Leleu, K Männik, et al.
American Journal of Medical Genetics. Part A
|
October 21, 2016
Implication of LRRC4C and DPP6 in neurodevelopmental disorders
Gilles Maussion, Cristiana Cruceanu, Jill A Rosenfeld, et al.
Genome Medicine
|
October 7, 2023
Genomic architecture of autism spectrum disorder in Qatar: The BARAKA-Qatar Study
Mona Abdi, Elbay Aliyev, Brett Trost, et al.
NPJ Genomic Medicine
|
November 5, 2021
A recurrent SHANK3 frameshift variant in Autism Spectrum Disorder
Livia O Loureiro, Jennifer L Howe, Miriam S Reuter, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 20, 2016
Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression
Chelsea Lowther, Marsha Speevak, Christine M Armour, et al.
American Journal of Human Genetics
|
December 20, 2024
Genetic variants in DDX53 contribute to autism spectrum disorder associated with the Xp22.11 locus
Marcello Scala, Clarrisa A Bradley, Jennifer L Howe, et al.
JAMA
|
September 2, 2015
Molecular Diagnostic Yield of Chromosomal Microarray Analysis and Whole-Exome Sequencing in Children With Autism Spectrum Disorder
Kristiina Tammimies, Christian R Marshall, Susan Walker, et al.
Page
of 92
Search research articles
Search
Showing results (821-830 of 915) with videos related to
Sort By:
Page
of 92
The American Journal of Psychiatry
|
March 3, 2022
Genes To Mental Health (G2MH): A Framework to Map the Combined Effects of Rare and Common Variants on Dimensions of Cognition and Psychopathology
Sébastien Jacquemont, Guillaume Huguet, Marieke Klein, et al.
Human Molecular Genetics
|
February 9, 2013
Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizures
Anath C Lionel, Andrea K Vaags, Daisuke Sato, et al.
American Journal of Human Genetics
|
February 7, 2008
Structural variation of chromosomes in autism spectrum disorder
Christian R Marshall, Abdul Noor, John B Vincent, et al.
Molecular Psychiatry
|
June 1, 2016
Chromosomal contacts connect loci associated with autism, BMI and head circumference phenotypes
M N Loviglio, M Leleu, K Männik, et al.
American Journal of Medical Genetics. Part A
|
October 21, 2016
Implication of LRRC4C and DPP6 in neurodevelopmental disorders
Gilles Maussion, Cristiana Cruceanu, Jill A Rosenfeld, et al.
Genome Medicine
|
October 7, 2023
Genomic architecture of autism spectrum disorder in Qatar: The BARAKA-Qatar Study
Mona Abdi, Elbay Aliyev, Brett Trost, et al.
NPJ Genomic Medicine
|
November 5, 2021
A recurrent SHANK3 frameshift variant in Autism Spectrum Disorder
Livia O Loureiro, Jennifer L Howe, Miriam S Reuter, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 20, 2016
Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression
Chelsea Lowther, Marsha Speevak, Christine M Armour, et al.
American Journal of Human Genetics
|
December 20, 2024
Genetic variants in DDX53 contribute to autism spectrum disorder associated with the Xp22.11 locus
Marcello Scala, Clarrisa A Bradley, Jennifer L Howe, et al.
JAMA
|
September 2, 2015
Molecular Diagnostic Yield of Chromosomal Microarray Analysis and Whole-Exome Sequencing in Children With Autism Spectrum Disorder
Kristiina Tammimies, Christian R Marshall, Susan Walker, et al.
Page
of 92