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Stephen T Warren

Showing results (61-70 of 99) with videos related to

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American Journal of Human Genetics|February 24, 2009
Replication stress induces genome-wide copy number changes in human cells that resemble polymorphic and pathogenic variantsMartin F Arlt, Jennifer G Mulle, Valerie M Schaibley, et al.
Nature Neuroscience|January 3, 2004
Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathwayPeng Jin, Daniela C Zarnescu, Stephanie Ceman, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 11, 2011
Local RNA translation at the synapse and in diseaseLiqun Liu-Yesucevitz, Gary J Bassell, Aaron D Gitler, et al.
The European Journal of Neuroscience|December 28, 2019
Partial FMRP expression is sufficient to normalize neuronal hyperactivity in Fragile X neuronsJohn D Graef, Hao Wu, Carrie Ng, et al.
Human Molecular Genetics|October 9, 2012
Genome-wide DNA hydroxymethylation changes are associated with neurodevelopmental genes in the developing human cerebellumTao Wang, Qian Pan, Li Lin, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 17, 2017
Reply to Plüss et al.: The strength of PEMapper/PECaller lies in unbiased calling using large sample sizesH Richard Johnston, Pankaj Chopra, Thomas S Wingo, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 23, 2017
PEMapper and PECaller provide a simplified approach to whole-genome sequencingH Richard Johnston, Pankaj Chopra, Thomas S Wingo, et al.
Plos One|March 12, 2010
Array-based FMR1 sequencing and deletion analysis in patients with a fragile X syndrome-like phenotypeStephen C Collins, Brad Coffee, Paul J Benke, et al.
BMC Genomics|February 15, 2014
Array-based assay detects genome-wide 5-mC and 5-hmC in the brains of humans, non-human primates, and micePankaj Chopra, Ligia A Papale, Andrew T J White, et al.
Human Molecular Genetics|May 24, 2007
Genome-wide expression profiling of lymphoblastoid cell lines distinguishes different forms of autism and reveals shared pathwaysYuhei Nishimura, Christa L Martin, Araceli Vazquez-Lopez, et al.
Pageof 10

Showing results (61-70 of 99) with videos related to

Sort By:
Pageof 10
American Journal of Human Genetics|February 24, 2009
Replication stress induces genome-wide copy number changes in human cells that resemble polymorphic and pathogenic variantsMartin F Arlt, Jennifer G Mulle, Valerie M Schaibley, et al.
Nature Neuroscience|January 3, 2004
Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathwayPeng Jin, Daniela C Zarnescu, Stephanie Ceman, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 11, 2011
Local RNA translation at the synapse and in diseaseLiqun Liu-Yesucevitz, Gary J Bassell, Aaron D Gitler, et al.
The European Journal of Neuroscience|December 28, 2019
Partial FMRP expression is sufficient to normalize neuronal hyperactivity in Fragile X neuronsJohn D Graef, Hao Wu, Carrie Ng, et al.
Human Molecular Genetics|October 9, 2012
Genome-wide DNA hydroxymethylation changes are associated with neurodevelopmental genes in the developing human cerebellumTao Wang, Qian Pan, Li Lin, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 17, 2017
Reply to Plüss et al.: The strength of PEMapper/PECaller lies in unbiased calling using large sample sizesH Richard Johnston, Pankaj Chopra, Thomas S Wingo, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 23, 2017
PEMapper and PECaller provide a simplified approach to whole-genome sequencingH Richard Johnston, Pankaj Chopra, Thomas S Wingo, et al.
Plos One|March 12, 2010
Array-based FMR1 sequencing and deletion analysis in patients with a fragile X syndrome-like phenotypeStephen C Collins, Brad Coffee, Paul J Benke, et al.
BMC Genomics|February 15, 2014
Array-based assay detects genome-wide 5-mC and 5-hmC in the brains of humans, non-human primates, and micePankaj Chopra, Ligia A Papale, Andrew T J White, et al.
Human Molecular Genetics|May 24, 2007
Genome-wide expression profiling of lymphoblastoid cell lines distinguishes different forms of autism and reveals shared pathwaysYuhei Nishimura, Christa L Martin, Araceli Vazquez-Lopez, et al.
Pageof 10