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Joanne Morgan

Showing results (11-20 of 21) with videos related to

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The Journal of Molecular Diagnostics : JMD|January 14, 2012
Next-generation sequencing for simultaneous determination of human papillomavirus load, subtype, and associated genomic copy number changes in tumorsCaroline Conway, Rebecca Chalkley, Alec High, et al.
Genomics|November 5, 2011
A computational index derived from whole-genome copy number analysis is a novel tool for prognosis in early stage lung squamous cell carcinomaOrnella Belvedere, Stefano Berri, Rebecca Chalkley, et al.
Pilot and Feasibility Studies|July 7, 2018
Walk with Me: a protocol for a pilot RCT of a peer-led walking programme to increase physical activity in inactive older adultsMark A Tully, Conor Cunningham, Margaret E Cupples, et al.
Human Mutation|April 5, 2013
Simple and efficient identification of rare recessive pathologically important sequence variants from next generation exome sequence dataIan M Carr, Joanne Morgan, Christopher Watson, et al.
The New England Journal of Medicine|July 20, 2007
Complement C3 variant and the risk of age-related macular degenerationJohn R W Yates, Tiina Sepp, Baljinder K Matharu, et al.
Nucleic Acids Research|June 8, 2010
Using next-generation sequencing for high resolution multiplex analysis of copy number variation from nanogram quantities of DNA from formalin-fixed paraffin-embedded specimensHenry M Wood, Ornella Belvedere, Caroline Conway, et al.
Hepatology (Baltimore, Md.)|June 3, 2024
A randomized multicenter trial of a chronic disease management intervention for decompensated cirrhosis. The A ustra l ian L iver F a i lur e (ALFIE) trialAlan J Wigg, Sumudu Narayana, Richard J Woodman, et al.
Biological Psychiatry|November 14, 2018
Targeted Sequencing of 10,198 Samples Confirms Abnormalities in Neuronal Activity and Implicates Voltage-Gated Sodium Channels in Schizophrenia PathogenesisElliott Rees, Noa Carrera, Joanne Morgan, et al.
NAR Genomics and Bioinformatics|December 8, 2022
Repeat Detector: versatile sizing of expanded tandem repeats and identification of interrupted alleles from targeted DNA sequencingAlysha S Taylor, Dinis Barros, Nastassia Gobet, et al.
Nature Neuroscience|January 15, 2020
De novo mutations identified by exome sequencing implicate rare missense variants in SLC6A1 in schizophreniaElliott Rees, Jun Han, Joanne Morgan, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
The Journal of Molecular Diagnostics : JMD|January 14, 2012
Next-generation sequencing for simultaneous determination of human papillomavirus load, subtype, and associated genomic copy number changes in tumorsCaroline Conway, Rebecca Chalkley, Alec High, et al.
Genomics|November 5, 2011
A computational index derived from whole-genome copy number analysis is a novel tool for prognosis in early stage lung squamous cell carcinomaOrnella Belvedere, Stefano Berri, Rebecca Chalkley, et al.
Pilot and Feasibility Studies|July 7, 2018
Walk with Me: a protocol for a pilot RCT of a peer-led walking programme to increase physical activity in inactive older adultsMark A Tully, Conor Cunningham, Margaret E Cupples, et al.
Human Mutation|April 5, 2013
Simple and efficient identification of rare recessive pathologically important sequence variants from next generation exome sequence dataIan M Carr, Joanne Morgan, Christopher Watson, et al.
The New England Journal of Medicine|July 20, 2007
Complement C3 variant and the risk of age-related macular degenerationJohn R W Yates, Tiina Sepp, Baljinder K Matharu, et al.
Nucleic Acids Research|June 8, 2010
Using next-generation sequencing for high resolution multiplex analysis of copy number variation from nanogram quantities of DNA from formalin-fixed paraffin-embedded specimensHenry M Wood, Ornella Belvedere, Caroline Conway, et al.
Hepatology (Baltimore, Md.)|June 3, 2024
A randomized multicenter trial of a chronic disease management intervention for decompensated cirrhosis. The A ustra l ian L iver F a i lur e (ALFIE) trialAlan J Wigg, Sumudu Narayana, Richard J Woodman, et al.
Biological Psychiatry|November 14, 2018
Targeted Sequencing of 10,198 Samples Confirms Abnormalities in Neuronal Activity and Implicates Voltage-Gated Sodium Channels in Schizophrenia PathogenesisElliott Rees, Noa Carrera, Joanne Morgan, et al.
NAR Genomics and Bioinformatics|December 8, 2022
Repeat Detector: versatile sizing of expanded tandem repeats and identification of interrupted alleles from targeted DNA sequencingAlysha S Taylor, Dinis Barros, Nastassia Gobet, et al.
Nature Neuroscience|January 15, 2020
De novo mutations identified by exome sequencing implicate rare missense variants in SLC6A1 in schizophreniaElliott Rees, Jun Han, Joanne Morgan, et al.
Pageof 3