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Showing results (801-810 of 915) with videos related to

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Molecular Psychiatry|November 2, 2011
Genome-wide association analysis of copy number variation in recurrent depressive disorderJ J H Rucker, G Breen, D Pinto, et al.
Journal of Medical Genetics|April 14, 2016
Microduplications at the pseudoautosomal SHOX locus in autism spectrum disorders and related neurodevelopmental conditionsMaria Tropeano, Deirdre Howley, Matthew J Gazzellone, et al.
Nature Reviews. Genetics|April 23, 2020
A framework for an evidence-based gene list relevant to autism spectrum disorderChristian P Schaaf, Catalina Betancur, Ryan K C Yuen, et al.
American Journal of Human Genetics|May 14, 2026
A next-generation episignature for Kabuki syndrome enables fine mapping of the impact of KMT2D variants to inform precision medicineMengqi Wang, Shaimaa Helal, Arteen Torabi-Marashi, et al.
Nature Medicine|January 27, 2015
Whole-genome sequencing of quartet families with autism spectrum disorderRyan K C Yuen, Bhooma Thiruvahindrapuram, Daniele Merico, et al.
NPJ Genomic Medicine|July 11, 2017
The clinical impact of copy number variants in inherited bone marrow failure syndromesNicolas Waespe, Santhosh Dhanraj, Manju Wahala, et al.
Human Molecular Genetics|May 8, 2023
Gene copy number variation and pediatric mental health/neurodevelopment in a general populationMehdi Zarrei, Christie L Burton, Worrawat Engchuan, et al.
Frontiers in Molecular Neuroscience|April 23, 2024
Allelic heterogeneity and abnormal vesicle recycling in <i>PLAA</i>-related neurodevelopmental disordersMichele Iacomino, Nadia Houerbi, Sara Fortuna, et al.
Scientific Reports|July 2, 2016
Indexing Effects of Copy Number Variation on Genes Involved in Developmental DelayMohammed Uddin, Giovanna Pellecchia, Bhooma Thiruvahindrapuram, et al.
Cell Genomics|December 12, 2024
Effects of gene dosage on cognitive ability: A function-based association study across brain and non-brain processesGuillaume Huguet, Thomas Renne, Cécile Poulain, et al.
Pageof 92

Showing results (801-810 of 915) with videos related to

Sort By:
Pageof 92
Molecular Psychiatry|November 2, 2011
Genome-wide association analysis of copy number variation in recurrent depressive disorderJ J H Rucker, G Breen, D Pinto, et al.
Journal of Medical Genetics|April 14, 2016
Microduplications at the pseudoautosomal SHOX locus in autism spectrum disorders and related neurodevelopmental conditionsMaria Tropeano, Deirdre Howley, Matthew J Gazzellone, et al.
Nature Reviews. Genetics|April 23, 2020
A framework for an evidence-based gene list relevant to autism spectrum disorderChristian P Schaaf, Catalina Betancur, Ryan K C Yuen, et al.
American Journal of Human Genetics|May 14, 2026
A next-generation episignature for Kabuki syndrome enables fine mapping of the impact of KMT2D variants to inform precision medicineMengqi Wang, Shaimaa Helal, Arteen Torabi-Marashi, et al.
Nature Medicine|January 27, 2015
Whole-genome sequencing of quartet families with autism spectrum disorderRyan K C Yuen, Bhooma Thiruvahindrapuram, Daniele Merico, et al.
NPJ Genomic Medicine|July 11, 2017
The clinical impact of copy number variants in inherited bone marrow failure syndromesNicolas Waespe, Santhosh Dhanraj, Manju Wahala, et al.
Human Molecular Genetics|May 8, 2023
Gene copy number variation and pediatric mental health/neurodevelopment in a general populationMehdi Zarrei, Christie L Burton, Worrawat Engchuan, et al.
Frontiers in Molecular Neuroscience|April 23, 2024
Allelic heterogeneity and abnormal vesicle recycling in <i>PLAA</i>-related neurodevelopmental disordersMichele Iacomino, Nadia Houerbi, Sara Fortuna, et al.
Scientific Reports|July 2, 2016
Indexing Effects of Copy Number Variation on Genes Involved in Developmental DelayMohammed Uddin, Giovanna Pellecchia, Bhooma Thiruvahindrapuram, et al.
Cell Genomics|December 12, 2024
Effects of gene dosage on cognitive ability: A function-based association study across brain and non-brain processesGuillaume Huguet, Thomas Renne, Cécile Poulain, et al.
Pageof 92