Nick D L Owens (Nick Owens)

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 12

Top Topics

Intellectual Disability

Genome Wide Identification

Top Venues

European journal of human genetics : EJHG

Nature genetics

Nature communications

This page only lists publications with an associated author ORCID identifier.

Publications

Thomas W Laver, Matthew N Wakeling, Richard C Caswell, Benjamin Bunce, Daphne Yau, Jonna M E Männistö, Jayne A L Houghton, Jasmin J Hopkins, Michael N Weedon, Vrinda Saraff, Melanie Kershaw, Engela M Honey, Nuala Murphy, Dinesh Giri, Stuart Nath, Ana Tangari Saredo, Indraneel Banerjee, Khalid Hussain, Nick D L Owens, Sarah E. Flanagan
Chromosome 20p11.2 deletions cause congenital hyperinsulinism via the loss of FOXA2 or its regulatory elements. European journal of human genetics : EJHG 32 (7) (2024)
Thomas W Laver, Matthew N Wakeling, Richard C Caswell, Benjamin Bunce, Daphne Yau, Jonna M E Männistö, Jayne A L Houghton, Jasmin J Hopkins, Michael N Weedon, Vrinda Saraff, Melanie Kershaw, Engela M Honey, Nuala Murphy, Dinesh Giri, Stuart Nath, Ana Tangari Saredo, Indraneel Banerjee, Khalid Hussain, Nick D L Owens, Sarah E. Flanagan
Chromosome 20p11.2 deletions cause congenital hyperinsulinism via the loss of FOXA2 or its regulatory elements. European journal of human genetics : EJHG (2024)
Thomas W Laver, Matthew N Wakeling, Richard C Caswell, Benjamin Bunce, Daphne Yau, Jonna M E Männistö, Jayne A L Houghton, Jasmin J Hopkins, Michael N Weedon, Vrinda Saraff, Melanie Kershaw, Engela M Honey, Nuala Murphy, Dinesh Giri, Stuart Nath, Ana Tangari Saredo, Indraneel Banerjee, Khalid Hussain, Nick D L Owens, Sarah E. Flanagan
Chromosome 20p11.2 deletions cause congenital hyperinsulinism via the loss of FOXA2 or its regulatory elements. European journal of human genetics : EJHG 32 (7) (2024)
Thomas W Laver, Matthew N Wakeling, Richard C Caswell, Benjamin Bunce, Daphne Yau, Jonna M E Männistö, Jayne A L Houghton, Jasmin J Hopkins, Michael N Weedon, Vrinda Saraff, Melanie Kershaw, Engela M Honey, Nuala Murphy, Dinesh Giri, Stuart Nath, Ana Tangari Saredo, Indraneel Banerjee, Khalid Hussain, Nick D L Owens, Sarah E. Flanagan
Chromosome 20p11.2 deletions cause congenital hyperinsulinism via the loss of FOXA2 or its regulatory elements. European journal of human genetics : EJHG 32 (7) (2024)
Thomas W Laver, Matthew N Wakeling, Richard C Caswell, Benjamin Bunce, Daphne Yau, Jonna M E Männistö, Jayne A L Houghton, Jasmin J Hopkins, Michael N Weedon, Vrinda Saraff, Melanie Kershaw, Engela M Honey, Nuala Murphy, Dinesh Giri, Stuart Nath, Ana Tangari Saredo, Indraneel Banerjee, Khalid Hussain, Nick D L Owens, Sarah E. Flanagan
Chromosome 20p11.2 deletions cause congenital hyperinsulinism via the loss of FOXA2 or its regulatory elements. European journal of human genetics : EJHG 32 (7) (2024)
Stasa Stankovic, Saleh Shekari, Qin Qin Huang, Eugene J Gardner, Erna V Ivarsdottir, Nick D L Owens, Nasim Mavaddat, Ajuna Azad, Gareth Hawkes, Katherine A Kentistou, Robin N Beaumont, Felix R Day, Yajie Zhao, Hakon Jonsson, Thorunn Rafnar, Vinicius Tragante, Gardar Sveinbjornsson, Asmundur Oddsson, Unnur Styrkarsdottir, Julius Gudmundsson, Simon N Stacey, Daniel F Gudbjartsson, null null, Kitale Kennedy, Andrew R Wood, Michael N Weedon, Ken K Ong, Caroline Fiona Wright, Eva R Hoffmann, Patrick Sulem, Matthew E Hurles, Katherine S Ruth, Hilary C Martin, Kari Stefansson, John R B Perry, Anna Murray
Genetic links between ovarian ageing, cancer risk and de novo mutation rates. Nature (2024)
Elisa De Franco, Nick D L Owens, Hossam Montaser, Matthew N Wakeling, Jonna Saarimäki-Vire, Athina Triantou, Hazem Ibrahim, Diego Balboa, Richard C Caswell, Rachel E Jennings, Jouni A Kvist, Matthew B Johnson, Sachin Muralidharan, Sian Ellard, Caroline Fiona Wright, Sateesh Maddirevula, Fowzan Sami Alkuraya, null null, Neil A Hanley, Sarah E. Flanagan, Timo Otonkoski, Andrew T Hattersley, Michael Imbeault
Primate-specific ZNF808 is essential for pancreatic development in humans. Nature genetics (2023)
Emily Sempou, Valentyna Kostiuk, Jie Zhu, M Cecilia Guerra, Leonid Tyan, Woong Hwang, Elena Camacho-Aguilar, Michael J Caplan, David Zenisek, Aryeh Warmflash, Nick D L Owens, Mustafa K Khokha
Author Correction: Membrane potential drives the exit from pluripotency and cell fate commitment via calcium and mTOR. Nature communications 14 (1) (2023)
Emily Sempou, Valentyna Kostiuk, Jie Zhu, M Cecilia Guerra, Leonid Tyan, Woong Hwang, Elena Camacho-Aguilar, Michael J Caplan, David Zenisek, Aryeh Warmflash, Nick D L Owens, Mustafa K Khokha
Membrane potential drives the exit from pluripotency and cell fate commitment via calcium and mTOR. Nature communications 13 (1) (2022)
Matthew N Wakeling, Nick D L Owens, Jessica R Hopkinson, Matthew B Johnson, Jayne A L Houghton, Antonia Dastamani, Christine S Flaxman, Rebecca C Wyatt, Thomas I Hewat, Jasmin J Hopkins, Thomas W Laver, Rachel van Heugten, Michael N Weedon, Elisa De Franco, Kashyap A Patel, Sian Ellard, Noel G Morgan, Edmund Cheesman, Indraneel Banerjee, Andrew T Hattersley, Mark J Dunne, null null, Sarah J Richardson, Sarah E. Flanagan
Non-coding variants disrupting a tissue-specific regulatory element in HK1 cause congenital hyperinsulinism. Nature genetics 54 (11) (2022)
Nicola Festuccia, Nick D L Owens, Almira Chervova, Agnès Dubois, Pablo Navarro
The combined action of Esrrb and Nr5a2 is essential for murine naïve pluripotency. Development (Cambridge, England) 148 (17) (2021)
Nick D L Owens, Thaleia Papadopoulou, Nicola Festuccia, Alexandra Tachtsidi, Inma Gonzalez, Agnes Dubois, Sandrine Vandormael-Pournin, Elphège P Nora, Benoit G Bruneau, Michel Cohen-Tannoudji, Pablo Navarro
CTCF confers local nucleosome resiliency after DNA replication and during mitosis. eLife 8 (2019)