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Steven Marks

Showing results (11-20 of 18) with videos related to

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The Journal of Biological Chemistry|October 23, 2003
Mice expressing only covalent dimeric heparin binding-deficient lipoprotein lipase: muscles inefficiently secrete dimeric enzymeE Peer Lutz, Yuko Kako, Hiroaki Yagyu, et al.
Neuron|June 11, 2011
Rare de novo and transmitted copy-number variation in autistic spectrum disordersDan Levy, Michael Ronemus, Boris Yamrom, et al.
Biorxiv : the Preprint Server for Biology|February 19, 2024
The Genotype and Phenotypes in Families (GPF) platform manages the large and complex data at SFARILiubomir Chorbadjiev, Murat Cokol, Zohar Weinstein, et al.
Communications Biology|September 2, 2021
Rates of contributory de novo mutation in high and low-risk autism familiesSeungtai Yoon, Adriana Munoz, Boris Yamrom, et al.
Genome Research|September 16, 2025
Analyzing the large and complex SFARI autism cohort data using the Genotypes and Phenotypes in Families (GPF) platformLiubomir Chorbadjiev, Murat Cokol, Zohar Weinstein, et al.
Journal of Occupational and Environmental Medicine|August 10, 2020
Recommendations From the 2019 Symposium on Including Functional Status Measurement in Standard Patient CareKathryn L Mueller, Thomas Warner Hudson, Daniel Bruns, et al.
Neuron|May 1, 2012
De novo gene disruptions in children on the autistic spectrumIvan Iossifov, Michael Ronemus, Dan Levy, et al.
Nature|November 4, 2014
The contribution of de novo coding mutations to autism spectrum disorderIvan Iossifov, Brian J O'Roak, Stephan J Sanders, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
The Journal of Biological Chemistry|October 23, 2003
Mice expressing only covalent dimeric heparin binding-deficient lipoprotein lipase: muscles inefficiently secrete dimeric enzymeE Peer Lutz, Yuko Kako, Hiroaki Yagyu, et al.
Neuron|June 11, 2011
Rare de novo and transmitted copy-number variation in autistic spectrum disordersDan Levy, Michael Ronemus, Boris Yamrom, et al.
Biorxiv : the Preprint Server for Biology|February 19, 2024
The Genotype and Phenotypes in Families (GPF) platform manages the large and complex data at SFARILiubomir Chorbadjiev, Murat Cokol, Zohar Weinstein, et al.
Communications Biology|September 2, 2021
Rates of contributory de novo mutation in high and low-risk autism familiesSeungtai Yoon, Adriana Munoz, Boris Yamrom, et al.
Genome Research|September 16, 2025
Analyzing the large and complex SFARI autism cohort data using the Genotypes and Phenotypes in Families (GPF) platformLiubomir Chorbadjiev, Murat Cokol, Zohar Weinstein, et al.
Journal of Occupational and Environmental Medicine|August 10, 2020
Recommendations From the 2019 Symposium on Including Functional Status Measurement in Standard Patient CareKathryn L Mueller, Thomas Warner Hudson, Daniel Bruns, et al.
Neuron|May 1, 2012
De novo gene disruptions in children on the autistic spectrumIvan Iossifov, Michael Ronemus, Dan Levy, et al.
Nature|November 4, 2014
The contribution of de novo coding mutations to autism spectrum disorderIvan Iossifov, Brian J O'Roak, Stephan J Sanders, et al.
Pageof 2