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Tomas Fitzgerald

Showing results (31-40 of 44) with videos related to

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European Journal of Human Genetics : EJHG|March 20, 2019
De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genesNirmal Vadgama, Alan Pittman, Michael Simpson, et al.
Biorxiv : the Preprint Server for Biology|June 26, 2025
Direct RNA nanopore sequencing reveals rapid RNA modification changes following glucose stimulation of human pancreatic beta-cell linesLogan Mulroney, Henry J Taylor, Angela Lee, et al.
Human Genetics|May 11, 2015
Copy number variation in the human Y chromosome in the UK populationWei Wei, Tomas W Fitzgerald, Tomas Fitzgerald, et al.
Nature Communications|December 11, 2021
RNA modifications detection by comparative Nanopore direct RNA sequencingAdrien Leger, Paulo P Amaral, Luca Pandolfini, et al.
Journal of Medical Genetics|February 1, 2011
High incidence of recurrent copy number variants in patients with isolated and syndromic Müllerian aplasiaSerena Nik-Zainal, Reiner Strick, Mekayla Storer, et al.
American Journal of Human Genetics|January 29, 2013
Genetic basis of Y-linked hearing impairmentQiuju Wang, Yali Xue, Yujun Zhang, et al.
Genome Biology|February 22, 2022
Genomic variations and epigenomic landscape of the Medaka Inbred Kiyosu-Karlsruhe (MIKK) panelAdrien Leger, Ian Brettell, Jack Monahan, et al.
Plos One|April 19, 2013
Massively parallel sequencing reveals the complex structure of an irradiated human chromosome on a mouse background in the Tc1 model of Down syndromeSusan M Gribble, Frances K Wiseman, Stephen Clayton, et al.
Genome Biology|February 22, 2022
The Medaka Inbred Kiyosu-Karlsruhe (MIKK) panelTomas Fitzgerald, Ian Brettell, Adrien Leger, et al.
Nature|October 9, 2009
Origins and functional impact of copy number variation in the human genomeDonald F Conrad, Dalila Pinto, Richard Redon, et al.
Pageof 5

Showing results (31-40 of 44) with videos related to

Sort By:
Pageof 5
European Journal of Human Genetics : EJHG|March 20, 2019
De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genesNirmal Vadgama, Alan Pittman, Michael Simpson, et al.
Biorxiv : the Preprint Server for Biology|June 26, 2025
Direct RNA nanopore sequencing reveals rapid RNA modification changes following glucose stimulation of human pancreatic beta-cell linesLogan Mulroney, Henry J Taylor, Angela Lee, et al.
Human Genetics|May 11, 2015
Copy number variation in the human Y chromosome in the UK populationWei Wei, Tomas W Fitzgerald, Tomas Fitzgerald, et al.
Nature Communications|December 11, 2021
RNA modifications detection by comparative Nanopore direct RNA sequencingAdrien Leger, Paulo P Amaral, Luca Pandolfini, et al.
Journal of Medical Genetics|February 1, 2011
High incidence of recurrent copy number variants in patients with isolated and syndromic Müllerian aplasiaSerena Nik-Zainal, Reiner Strick, Mekayla Storer, et al.
American Journal of Human Genetics|January 29, 2013
Genetic basis of Y-linked hearing impairmentQiuju Wang, Yali Xue, Yujun Zhang, et al.
Genome Biology|February 22, 2022
Genomic variations and epigenomic landscape of the Medaka Inbred Kiyosu-Karlsruhe (MIKK) panelAdrien Leger, Ian Brettell, Jack Monahan, et al.
Plos One|April 19, 2013
Massively parallel sequencing reveals the complex structure of an irradiated human chromosome on a mouse background in the Tc1 model of Down syndromeSusan M Gribble, Frances K Wiseman, Stephen Clayton, et al.
Genome Biology|February 22, 2022
The Medaka Inbred Kiyosu-Karlsruhe (MIKK) panelTomas Fitzgerald, Ian Brettell, Adrien Leger, et al.
Nature|October 9, 2009
Origins and functional impact of copy number variation in the human genomeDonald F Conrad, Dalila Pinto, Richard Redon, et al.
Pageof 5