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Molecular Psychiatry
|
February 23, 2018
Altered TAOK2 activity causes autism-related neurodevelopmental and cognitive abnormalities through RhoA signaling
Melanie Richter, Nadeem Murtaza, Robin Scharrenberg, et al.
Nature Communications
|
October 30, 2022
Genome-wide rare variant score associates with morphological subtypes of autism spectrum disorder
Ada J S Chan, Worrawat Engchuan, Miriam S Reuter, et al.
Nature Medicine
|
May 15, 2020
High systemic and tumor-associated IL-8 correlates with reduced clinical benefit of PD-L1 blockade
Kobe C Yuen, Li-Fen Liu, Vinita Gupta, et al.
Nature
|
December 14, 2022
Recurrent repeat expansions in human cancer genomes
Graham S Erwin, Gamze Gürsoy, Rashid Al-Abri, et al.
Scientific Reports
|
July 2, 2016
Indexing Effects of Copy Number Variation on Genes Involved in Developmental Delay
Mohammed Uddin, Giovanna Pellecchia, Bhooma Thiruvahindrapuram, et al.
Nature Reviews. Genetics
|
April 23, 2020
A framework for an evidence-based gene list relevant to autism spectrum disorder
Christian P Schaaf, Catalina Betancur, Ryan K C Yuen, et al.
Nature Medicine
|
January 27, 2015
Whole-genome sequencing of quartet families with autism spectrum disorder
Ryan K C Yuen, Bhooma Thiruvahindrapuram, Daniele Merico, et al.
Human Molecular Genetics
|
May 8, 2023
Gene copy number variation and pediatric mental health/neurodevelopment in a general population
Mehdi Zarrei, Christie L Burton, Worrawat Engchuan, et al.
Ebiomedicine
|
February 28, 2024
Genome-wide enhancer-associated tandem repeats are expanded in cardiomyopathy
Aleksandra Mitina, Mahreen Khan, Robert Lesurf, 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 37
Search research articles
Search
Showing results (341-350 of 369) with videos related to
Sort By:
Page
of 37
Molecular Psychiatry
|
February 23, 2018
Altered TAOK2 activity causes autism-related neurodevelopmental and cognitive abnormalities through RhoA signaling
Melanie Richter, Nadeem Murtaza, Robin Scharrenberg, et al.
Nature Communications
|
October 30, 2022
Genome-wide rare variant score associates with morphological subtypes of autism spectrum disorder
Ada J S Chan, Worrawat Engchuan, Miriam S Reuter, et al.
Nature Medicine
|
May 15, 2020
High systemic and tumor-associated IL-8 correlates with reduced clinical benefit of PD-L1 blockade
Kobe C Yuen, Li-Fen Liu, Vinita Gupta, et al.
Nature
|
December 14, 2022
Recurrent repeat expansions in human cancer genomes
Graham S Erwin, Gamze Gürsoy, Rashid Al-Abri, et al.
Scientific Reports
|
July 2, 2016
Indexing Effects of Copy Number Variation on Genes Involved in Developmental Delay
Mohammed Uddin, Giovanna Pellecchia, Bhooma Thiruvahindrapuram, et al.
Nature Reviews. Genetics
|
April 23, 2020
A framework for an evidence-based gene list relevant to autism spectrum disorder
Christian P Schaaf, Catalina Betancur, Ryan K C Yuen, et al.
Nature Medicine
|
January 27, 2015
Whole-genome sequencing of quartet families with autism spectrum disorder
Ryan K C Yuen, Bhooma Thiruvahindrapuram, Daniele Merico, et al.
Human Molecular Genetics
|
May 8, 2023
Gene copy number variation and pediatric mental health/neurodevelopment in a general population
Mehdi Zarrei, Christie L Burton, Worrawat Engchuan, et al.
Ebiomedicine
|
February 28, 2024
Genome-wide enhancer-associated tandem repeats are expanded in cardiomyopathy
Aleksandra Mitina, Mahreen Khan, Robert Lesurf, 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 37