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Journal of Neurodevelopmental Disorders
|
March 7, 2026
Crossing the finish line towards a disease-modifying treatment for Angelman syndrome
Matthew C Judson, Luis Pereira de Almeida, Rebecca D Burdine, et al.
Biorxiv : the Preprint Server for Biology
|
April 10, 2026
Molecular dynamics of Brodmann Area 22 in development and autism
Varun Suresh, Emilie M Wigdor, Yuhan Hao, et al.
Cell
|
January 22, 2019
Predicting Splicing from Primary Sequence with Deep Learning
Kishore Jaganathan, Sofia Kyriazopoulou Panagiotopoulou, Jeremy F McRae, et al.
Nature Genetics
|
July 21, 2014
Most genetic risk for autism resides with common variation
Trent Gaugler, Lambertus Klei, Stephan J Sanders, et al.
Genome Medicine
|
August 21, 2025
Evaluation of familial phenotype deviation to measure the impact of de novo mutations in autism
Soo-Whee Kim, Hyeji Lee, Da Yea Song, et al.
AI Magazine
|
September 12, 2022
A biomedical open knowledge network harnesses the power of AI to understand deep human biology
Sergio E Baranzini, Katy Börner, John Morris, et al.
Nature Aging
|
February 22, 2024
Leveraging electronic health records and knowledge networks for Alzheimer's disease prediction and sex-specific biological insights
Alice S Tang, Katherine P Rankin, Gabriel Cerono, et al.
HGG Advances
|
July 20, 2025
Genotypic, functional, and phenotypic characterization in CTNNB1 neurodevelopmental syndrome
Nina Žakelj, David Gosar, Špela Miroševič, et al.
Molecular Autism
|
March 8, 2014
DAWN: a framework to identify autism genes and subnetworks using gene expression and genetics
Li Liu, Jing Lei, Stephan J Sanders, et al.
Molecular Psychiatry
|
October 5, 2023
Astrocytic β-catenin signaling via TCF7L2 regulates synapse development and social behavior
Lukasz Mateusz Szewczyk, Marcin Andrzej Lipiec, Ewa Liszewska, et al.
Page
of 16
Search research articles
Search
Showing results (71-80 of 154) with videos related to
Sort By:
Page
of 16
Journal of Neurodevelopmental Disorders
|
March 7, 2026
Crossing the finish line towards a disease-modifying treatment for Angelman syndrome
Matthew C Judson, Luis Pereira de Almeida, Rebecca D Burdine, et al.
Biorxiv : the Preprint Server for Biology
|
April 10, 2026
Molecular dynamics of Brodmann Area 22 in development and autism
Varun Suresh, Emilie M Wigdor, Yuhan Hao, et al.
Cell
|
January 22, 2019
Predicting Splicing from Primary Sequence with Deep Learning
Kishore Jaganathan, Sofia Kyriazopoulou Panagiotopoulou, Jeremy F McRae, et al.
Nature Genetics
|
July 21, 2014
Most genetic risk for autism resides with common variation
Trent Gaugler, Lambertus Klei, Stephan J Sanders, et al.
Genome Medicine
|
August 21, 2025
Evaluation of familial phenotype deviation to measure the impact of de novo mutations in autism
Soo-Whee Kim, Hyeji Lee, Da Yea Song, et al.
AI Magazine
|
September 12, 2022
A biomedical open knowledge network harnesses the power of AI to understand deep human biology
Sergio E Baranzini, Katy Börner, John Morris, et al.
Nature Aging
|
February 22, 2024
Leveraging electronic health records and knowledge networks for Alzheimer's disease prediction and sex-specific biological insights
Alice S Tang, Katherine P Rankin, Gabriel Cerono, et al.
HGG Advances
|
July 20, 2025
Genotypic, functional, and phenotypic characterization in CTNNB1 neurodevelopmental syndrome
Nina Žakelj, David Gosar, Špela Miroševič, et al.
Molecular Autism
|
March 8, 2014
DAWN: a framework to identify autism genes and subnetworks using gene expression and genetics
Li Liu, Jing Lei, Stephan J Sanders, et al.
Molecular Psychiatry
|
October 5, 2023
Astrocytic β-catenin signaling via TCF7L2 regulates synapse development and social behavior
Lukasz Mateusz Szewczyk, Marcin Andrzej Lipiec, Ewa Liszewska, et al.
Page
of 16