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Human Genetics
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October 3, 2018
Replication of a rare risk haplotype on 1p36.33 for autism spectrum disorder
N H Chapman, R A Bernier, S J Webb, et al.
American Journal of Human Genetics
|
December 2, 2019
Sex-Based Analysis of De Novo Variants in Neurodevelopmental Disorders
Tychele N Turner, Amy B Wilfert, Trygve E Bakken, et al.
Current Biology : CB
|
August 21, 2018
Sex Differences in Visual Motion Processing
Scott O Murray, Michael-Paul Schallmo, Tamar Kolodny, et al.
Journal of Neurodevelopmental Disorders
|
June 1, 2017
Exploring the heterogeneity of neural social indices for genetically distinct etiologies of autism
Caitlin M Hudac, Holly A F Stessman, Trent D DesChamps, et al.
Alzheimer'S & Dementia (Amsterdam, Netherlands)
|
April 7, 2022
The neuroinflammatory marker sTNFR2 relates to worse cognition and tau in women across the Alzheimer's disease spectrum
Rachel A Bernier, Sarah J Banks, Matthew S Panizzon, et al.
Nature Communications
|
September 19, 2014
De novo TBR1 mutations in sporadic autism disrupt protein functions
Pelagia Deriziotis, Brian J O'Roak, Sarah A Graham, et al.
Autism Research : Official Journal of the International Society for Autism Research
|
July 27, 2023
Characterizing the autism spectrum phenotype in DYRK1A-related syndrome
Evangeline C Kurtz-Nelson, Hannah M Rea, Aiva C Petriceks, et al.
Clinical Case Reports
|
January 30, 2018
Longitudinal report of child with de novo 16p11.2 triplication
Arianne S Wallace, Caitlin M Hudac, Kyle J Steinman, et al.
Autism : the International Journal of Research and Practice
|
March 15, 2021
The gap between IQ and adaptive functioning in autism spectrum disorder: Disentangling diagnostic and sex differences
Goldie A McQuaid, Kevin A Pelphrey, Susan Y Bookheimer, et al.
Nucleic Acids Research
|
December 2, 2016
denovo-db: a compendium of human de novo variants
Tychele N Turner, Qian Yi, Niklas Krumm, et al.
Page
of 17
Search research articles
Search
Showing results (91-100 of 169) with videos related to
Sort By:
Page
of 17
Human Genetics
|
October 3, 2018
Replication of a rare risk haplotype on 1p36.33 for autism spectrum disorder
N H Chapman, R A Bernier, S J Webb, et al.
American Journal of Human Genetics
|
December 2, 2019
Sex-Based Analysis of De Novo Variants in Neurodevelopmental Disorders
Tychele N Turner, Amy B Wilfert, Trygve E Bakken, et al.
Current Biology : CB
|
August 21, 2018
Sex Differences in Visual Motion Processing
Scott O Murray, Michael-Paul Schallmo, Tamar Kolodny, et al.
Journal of Neurodevelopmental Disorders
|
June 1, 2017
Exploring the heterogeneity of neural social indices for genetically distinct etiologies of autism
Caitlin M Hudac, Holly A F Stessman, Trent D DesChamps, et al.
Alzheimer'S & Dementia (Amsterdam, Netherlands)
|
April 7, 2022
The neuroinflammatory marker sTNFR2 relates to worse cognition and tau in women across the Alzheimer's disease spectrum
Rachel A Bernier, Sarah J Banks, Matthew S Panizzon, et al.
Nature Communications
|
September 19, 2014
De novo TBR1 mutations in sporadic autism disrupt protein functions
Pelagia Deriziotis, Brian J O'Roak, Sarah A Graham, et al.
Autism Research : Official Journal of the International Society for Autism Research
|
July 27, 2023
Characterizing the autism spectrum phenotype in DYRK1A-related syndrome
Evangeline C Kurtz-Nelson, Hannah M Rea, Aiva C Petriceks, et al.
Clinical Case Reports
|
January 30, 2018
Longitudinal report of child with de novo 16p11.2 triplication
Arianne S Wallace, Caitlin M Hudac, Kyle J Steinman, et al.
Autism : the International Journal of Research and Practice
|
March 15, 2021
The gap between IQ and adaptive functioning in autism spectrum disorder: Disentangling diagnostic and sex differences
Goldie A McQuaid, Kevin A Pelphrey, Susan Y Bookheimer, et al.
Nucleic Acids Research
|
December 2, 2016
denovo-db: a compendium of human de novo variants
Tychele N Turner, Qian Yi, Niklas Krumm, et al.
Page
of 17