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Daniel Moreno

Showing results (271-280 of 283) with videos related to

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Molecular Autism|October 17, 2012
Common genetic variants, acting additively, are a major source of risk for autismLambertus Klei, Stephan J Sanders, Michael T Murtha, et al.
NPJ Precision Oncology|April 1, 2022
A blood-based miRNA signature with prognostic value for overall survival in advanced stage non-small cell lung cancer treated with immunotherapyTimothy Rajakumar, Rastislav Horos, Julia Jehn, et al.
Autism Research : Official Journal of the International Society for Autism Research|May 14, 2014
Modest impact on risk for autism spectrum disorder of rare copy number variants at 15q11.2, specifically breakpoints 1 to 2Pauline Chaste, Stephan J Sanders, Kommu N Mohan, et al.
Data in Brief|June 9, 2025
Pan-European forest maps produced with a combination of earth observation data and national forest inventory plotsJukka Miettinen, Johannes Breidenbach, Patricia Adame, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 17, 2011
An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilitiesErin B Kaminsky, Vineith Kaul, Justin Paschall, et al.
Journal of Thoracic Oncology : Official Publication of the International Association for the Study of Lung Cancer|July 12, 2023
Early Detection of Lung Cancer Using Small RNAsTobias Sikosek, Rastislav Horos, Franziska Trudzinski, et al.
American Journal of Human Genetics|November 9, 2010
Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophreniaDaniel Moreno-De-Luca, , Jennifer G Mulle, et al.
Neuron|September 25, 2015
Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk LociStephan J Sanders, Xin He, A Jeremy Willsey, et al.
Neuron|June 11, 2011
Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autismStephan J Sanders, A Gulhan Ercan-Sencicek, Vanessa Hus, et al.
Nature Genetics|April 2, 2025
Psychiatric genetics in the diverse landscape of Latin American populationsEstela M Bruxel, Diego L Rovaris, Sintia I Belangero, et al.
Pageof 29

Showing results (271-280 of 283) with videos related to

Sort By:
Pageof 29
Molecular Autism|October 17, 2012
Common genetic variants, acting additively, are a major source of risk for autismLambertus Klei, Stephan J Sanders, Michael T Murtha, et al.
NPJ Precision Oncology|April 1, 2022
A blood-based miRNA signature with prognostic value for overall survival in advanced stage non-small cell lung cancer treated with immunotherapyTimothy Rajakumar, Rastislav Horos, Julia Jehn, et al.
Autism Research : Official Journal of the International Society for Autism Research|May 14, 2014
Modest impact on risk for autism spectrum disorder of rare copy number variants at 15q11.2, specifically breakpoints 1 to 2Pauline Chaste, Stephan J Sanders, Kommu N Mohan, et al.
Data in Brief|June 9, 2025
Pan-European forest maps produced with a combination of earth observation data and national forest inventory plotsJukka Miettinen, Johannes Breidenbach, Patricia Adame, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 17, 2011
An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilitiesErin B Kaminsky, Vineith Kaul, Justin Paschall, et al.
Journal of Thoracic Oncology : Official Publication of the International Association for the Study of Lung Cancer|July 12, 2023
Early Detection of Lung Cancer Using Small RNAsTobias Sikosek, Rastislav Horos, Franziska Trudzinski, et al.
American Journal of Human Genetics|November 9, 2010
Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophreniaDaniel Moreno-De-Luca, , Jennifer G Mulle, et al.
Neuron|September 25, 2015
Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk LociStephan J Sanders, Xin He, A Jeremy Willsey, et al.
Neuron|June 11, 2011
Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autismStephan J Sanders, A Gulhan Ercan-Sencicek, Vanessa Hus, et al.
Nature Genetics|April 2, 2025
Psychiatric genetics in the diverse landscape of Latin American populationsEstela M Bruxel, Diego L Rovaris, Sintia I Belangero, et al.
Pageof 29