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Menachem Fromer

Showing results (31-40 of 60) with videos related to

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Biological Psychiatry|November 27, 2019
Characterization of Single Gene Copy Number Variants in SchizophreniaJin P Szatkiewicz, Menachem Fromer, Randal J Nonneman, et al.
Plos One|August 12, 2021
A holistic approach for suppression of COVID-19 spread in workplaces and universitiesSarah F Poole, Jessica Gronsbell, Dale Winter, et al.
Genome Medicine|December 22, 2017
Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disordersHoang T Nguyen, Julien Bryois, April Kim, et al.
The New England Journal of Medicine|November 27, 2014
Clonal hematopoiesis and blood-cancer risk inferred from blood DNA sequenceGiulio Genovese, Anna K Kähler, Robert E Handsaker, et al.
Cell Reports|December 3, 2014
A role for noncoding variation in schizophreniaPanos Roussos, Amanda C Mitchell, Georgios Voloudakis, et al.
JMIR Mental Health|August 12, 2021
Toward a Mobile Platform for Real-world Digital Measurement of Depression: User-Centered Design, Data Quality, and Behavioral and Clinical ModelingStefanie Nickels, Matthew D Edwards, Sarah F Poole, et al.
Nature Neuroscience|January 15, 2020
Exome sequencing in schizophrenia-affected parent-offspring trios reveals risk conferred by protein-coding de novo mutationsDaniel P Howrigan, Samuel A Rose, Kaitlin E Samocha, et al.
Cell Reports|October 19, 2017
Arc Requires PSD95 for Assembly into Postsynaptic Complexes Involved with Neural Dysfunction and IntelligenceEsperanza Fernández, Mark O Collins, René A W Frank, et al.
Nature Biotechnology|April 12, 2016
Analysis of 589,306 genomes identifies individuals resilient to severe Mendelian childhood diseasesRong Chen, Lisong Shi, Jörg Hakenberg, et al.
Circulation Research|September 11, 2014
Increased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence dataJoseph T Glessner, Alexander G Bick, Kaoru Ito, et al.
Pageof 6

Showing results (31-40 of 60) with videos related to

Sort By:
Pageof 6
Biological Psychiatry|November 27, 2019
Characterization of Single Gene Copy Number Variants in SchizophreniaJin P Szatkiewicz, Menachem Fromer, Randal J Nonneman, et al.
Plos One|August 12, 2021
A holistic approach for suppression of COVID-19 spread in workplaces and universitiesSarah F Poole, Jessica Gronsbell, Dale Winter, et al.
Genome Medicine|December 22, 2017
Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disordersHoang T Nguyen, Julien Bryois, April Kim, et al.
The New England Journal of Medicine|November 27, 2014
Clonal hematopoiesis and blood-cancer risk inferred from blood DNA sequenceGiulio Genovese, Anna K Kähler, Robert E Handsaker, et al.
Cell Reports|December 3, 2014
A role for noncoding variation in schizophreniaPanos Roussos, Amanda C Mitchell, Georgios Voloudakis, et al.
JMIR Mental Health|August 12, 2021
Toward a Mobile Platform for Real-world Digital Measurement of Depression: User-Centered Design, Data Quality, and Behavioral and Clinical ModelingStefanie Nickels, Matthew D Edwards, Sarah F Poole, et al.
Nature Neuroscience|January 15, 2020
Exome sequencing in schizophrenia-affected parent-offspring trios reveals risk conferred by protein-coding de novo mutationsDaniel P Howrigan, Samuel A Rose, Kaitlin E Samocha, et al.
Cell Reports|October 19, 2017
Arc Requires PSD95 for Assembly into Postsynaptic Complexes Involved with Neural Dysfunction and IntelligenceEsperanza Fernández, Mark O Collins, René A W Frank, et al.
Nature Biotechnology|April 12, 2016
Analysis of 589,306 genomes identifies individuals resilient to severe Mendelian childhood diseasesRong Chen, Lisong Shi, Jörg Hakenberg, et al.
Circulation Research|September 11, 2014
Increased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence dataJoseph T Glessner, Alexander G Bick, Kaoru Ito, et al.
Pageof 6