Robert J Bryson-Richardson

Scopus Author ID ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 25

Top Venues

Human molecular genetics

International journal of molecular sciences

Metabolites

Nature communications

MRC Human Genetics Unit (PHD)

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

Education History

MRC Human Genetics Unit

United Kingdom

PHD

Publications

Sandra Donkervoort, Martijn van de Locht, Dario Ronchi, Janine Reunert, Catriona A Mclean, Maha Saad Zaki, Rotem Orbach, Josine M de Winter, Stefan Conijn, Daan Hoomoedt, Osorio Lopes Abath Neto, Francesca Magri, Angela N Viaene, A Reghan Foley, Svetlana Gorokhova, Veronique Bolduc, Ying Hu, Nicole Acquaye, Laura Napoli, Julien H Park, Kalyan Immadisetty, Lee B Miles, Mona Essawi, Salar McModie, Leonardo F Ferreira, Simona Zanotti, Sarah B Neuhaus, Livija Medne, Nagham ElBagoury, Kory R Johnson, Yong Zhang, Nigel G Laing, Mark R Davis, Robert J Bryson-Richardson, Darren T Hwee, James J Hartman, Fady I Malik, Peter Michael Kekenes-Huskey, Giacomo Pietro Comi, Wessam E Sharaf-Eldin, Thorsten Marquardt, Gianina Ravenscroft, Carsten G Bonnemann, Coen A C Ottenheijm
Pathogenic TNNI1 variants disrupt sarcomere contractility resulting in hypo- and hypercontractile muscle disease. Science translational medicine 16 (741) (2024)
Emily A McKaige, Clara Lee, Vanessa Calcinotto, Saveen Giri, Simon Crawford, Meagan J McGrath, Georg Ramm, Robert J Bryson-Richardson
Mitochondrial abnormalities contribute to muscle weakness in a Dnajb6 deficient zebrafish model. Human molecular genetics 33 (14) (2024)
Emily A McKaige, Clara Lee, Vanessa Calcinotto, Saveen Giri, Simon Crawford, Meagan J McGrath, Georg Ramm, Robert J Bryson-Richardson
Mitochondrial abnormalities contribute to muscle weakness in a Dnajb6 deficient zebrafish model. Human molecular genetics 33 (14) (2024)
Sandra Donkervoort, Martijn van de Locht, Dario Ronchi, Janine Reunert, Catriona A Mclean, Maha Saad Zaki, Rotem Orbach, Josine M de Winter, Stefan Conijn, Daan Hoomoedt, Osorio Lopes Abath Neto, Francesca Magri, Angela N Viaene, A Reghan Foley, Svetlana Gorokhova, Veronique Bolduc, Ying Hu, Nicole Acquaye, Laura Napoli, Julien H Park, Kalyan Immadisetty, Lee B Miles, Mona Essawi, Salar McModie, Leonardo F Ferreira, Simona Zanotti, Sarah B Neuhaus, Livija Medne, Nagham ElBagoury, Kory R Johnson, Yong Zhang, Nigel G Laing, Mark R Davis, Robert J Bryson-Richardson, Darren T Hwee, James J Hartman, Fady I Malik, Peter Michael Kekenes-Huskey, Giacomo Pietro Comi, Wessam E Sharaf-Eldin, Thorsten Marquardt, Gianina Ravenscroft, Carsten G Bonnemann, Coen A C Ottenheijm
Pathogenic TNNI1 variants disrupt sarcomere contractility resulting in hypo- and hypercontractile muscle disease. Science translational medicine 16 (741) (2024)
Emily A McKaige, Clara Lee, Vanessa Calcinotto, Saveen Giri, Simon Crawford, Meagan J McGrath, Georg Ramm, Robert J Bryson-Richardson
Mitochondrial abnormalities contribute to muscle weakness in a Dnajb6 deficient zebrafish model. Human molecular genetics 33 (14) (2024)
Emily A McKaige, Clara Lee, Vanessa Calcinotto, Saveen Giri, Simon Crawford, Meagan J McGrath, Georg Ramm, Robert J Bryson-Richardson
Mitochondrial abnormalities contribute to muscle weakness in a Dnajb6 deficient zebrafish model. Human molecular genetics (2024)
Sandra Donkervoort, Martijn van de Locht, Dario Ronchi, Janine Reunert, Catriona A Mclean, Maha Saad Zaki, Rotem Orbach, Josine M de Winter, Stefan Conijn, Daan Hoomoedt, Osorio Lopes Abath Neto, Francesca Magri, Angela N Viaene, A Reghan Foley, Svetlana Gorokhova, Veronique Bolduc, Ying Hu, Nicole Acquaye, Laura Napoli, Julien H Park, Kalyan Immadisetty, Lee B Miles, Mona Essawi, Salar McModie, Leonardo F Ferreira, Simona Zanotti, Sarah B Neuhaus, Livija Medne, Nagham ElBagoury, Kory R Johnson, Yong Zhang, Nigel G Laing, Mark R Davis, Robert J Bryson-Richardson, Darren T Hwee, James J Hartman, Fady I Malik, Peter Michael Kekenes-Huskey, Giacomo Pietro Comi, Wessam E Sharaf-Eldin, Thorsten Marquardt, Gianina Ravenscroft, Carsten G Bonnemann, Coen A C Ottenheijm
Pathogenic TNNI1 variants disrupt sarcomere contractility resulting in hypo- and hypercontractile muscle disease. Science translational medicine 16 (741) (2024)
Lee B Miles, Vanessa Calcinotto, Sara Oveissi, Rita J Serrano, Carmen Sonntag, Orlen Mulia, Clara Lee, Robert J Bryson-Richardson
CRIMP: a CRISPR/Cas9 insertional mutagenesis protocol and toolkit. Nature communications 15 (1) (2024)
Emily A McKaige, Clara Lee, Vanessa Calcinotto, Saveen Giri, Simon Crawford, Meagan J McGrath, Georg Ramm, Robert J Bryson-Richardson
Mitochondrial abnormalities contribute to muscle weakness in a Dnajb6 deficient zebrafish model. Human molecular genetics 33 (14) (2024)
Lee B Miles, Vanessa Calcinotto, Sara Oveissi, Rita J Serrano, Carmen Sonntag, Orlen Mulia, Clara Lee, Robert J Bryson-Richardson
CRIMP: a CRISPR/Cas9 insertional mutagenesis protocol and toolkit. Nature communications 15 (1) (2024)
Lee B Miles, Vanessa Calcinotto, Sara Oveissi, Rita J Serrano, Carmen Sonntag, Orlen Mulia, Clara Lee, Robert J Bryson-Richardson
CRIMP: a CRISPR/Cas9 insertional mutagenesis protocol and toolkit. Nature communications 15 (1) (2024)
Connie Fung, Brendan Wilding, Ralf Bernd Schittenhelm, Robert J Bryson-Richardson, Phillip I Bird
Expression of the Z Variant of α1-Antitrypsin Suppresses Hepatic Cholesterol Biosynthesis in Transgenic Zebrafish. International journal of molecular sciences 24 (3) (2023)
Connie Fung, Brendan Wilding, Ralf Bernd Schittenhelm, Robert J Bryson-Richardson, Phillip I Bird
Expression of the Z Variant of α1-Antitrypsin Suppresses Hepatic Cholesterol Biosynthesis in Transgenic Zebrafish. International journal of molecular sciences 24 (3) (2023)
Jessica R Terrill, Corinne Huchet, Caroline Le Guiner, Aude Lafoux, Dorian Caudal, Ankita Tulangekar, Robert J Bryson-Richardson, Tamar E Sztal, Miranda D Grounds, Peter G Arthur
Muscle Pathology in Dystrophic Rats and Zebrafish Is Unresponsive to Taurine Treatment, Compared to the mdx Mouse Model for Duchenne Muscular Dystrophy. Metabolites 13 (2) (2023)
Jessica R Terrill, Corinne Huchet, Caroline Le Guiner, Aude Lafoux, Dorian Caudal, Ankita Tulangekar, Robert J Bryson-Richardson, Tamar E Sztal, Miranda D Grounds, Peter G Arthur
Muscle Pathology in Dystrophic Rats and Zebrafish Is Unresponsive to Taurine Treatment, Compared to the mdx Mouse Model for Duchenne Muscular Dystrophy. Metabolites 13 (2) (2023)
Jessica R Terrill, Corinne Huchet, Caroline Le Guiner, Aude Lafoux, Dorian Caudal, Ankita Tulangekar, Robert J Bryson-Richardson, Tamar E Sztal, Miranda D Grounds, Peter G Arthur
Muscle Pathology in Dystrophic Rats and Zebrafish Is Unresponsive to Taurine Treatment, Compared to the mdx Mouse Model for Duchenne Muscular Dystrophy. Metabolites 13 (2) (2023)
Connie Fung, Brendan Wilding, Ralf Bernd Schittenhelm, Robert J Bryson-Richardson, Phillip I Bird
Expression of the Z Variant of α1-Antitrypsin Suppresses Hepatic Cholesterol Biosynthesis in Transgenic Zebrafish. International journal of molecular sciences 24 (3) (2023)
Jessica R Terrill, Corinne Huchet, Caroline Le Guiner, Aude Lafoux, Dorian Caudal, Ankita Tulangekar, Robert J Bryson-Richardson, Tamar E Sztal, Miranda D Grounds, Peter G Arthur
Muscle Pathology in Dystrophic Rats and Zebrafish Is Unresponsive to Taurine Treatment, Compared to the mdx Mouse Model for Duchenne Muscular Dystrophy. Metabolites 13 (2) (2023)
Connie Fung, Brendan Wilding, Ralf Bernd Schittenhelm, Robert J Bryson-Richardson, Phillip I Bird
Expression of the Z Variant of α1-Antitrypsin Suppresses Hepatic Cholesterol Biosynthesis in Transgenic Zebrafish. International journal of molecular sciences 24 (3) (2023)
Rita J Serrano, Viola Oorschot, Dashika Palipana, Vanessa Calcinotto, Carmen Sonntag, Georg Ramm, Robert J Bryson-Richardson
Genetic model of UBA5 deficiency highlights the involvement of both peripheral and central nervous systems and identifies widespread mitochondrial abnormalities. Brain communications 5 (6) (2023)
Rita J Serrano, Clara Lee, Alon M Douek, Jan Kaslin, Robert J Bryson-Richardson, Tamar E Sztal
Novel preclinical model for CDKL5 deficiency disorder. Disease models & mechanisms 15 (3) (2022)
Avnika A Ruparelia, Emily A McKaige, Caitlin Williams, Keith E Schulze, Margit Fuchs, Viola Oorschot, Emmanuelle Lacene, Mirella Meregalli, Clara Lee, Rita J Serrano, Emily C Baxter, Keyne Monro, Yvan Torrente, Georg Ramm, Tanya Stojkovic, Josée N Lavoie, Robert J Bryson-Richardson
Metformin rescues muscle function in BAG3 myofibrillar myopathy models. Autophagy 17 (9) (2020)
Callum Dark, Caitlin Williams, Mark A Bellgrove, Ziarih Hawi, Robert J Bryson-Richardson
Functional validation of CHMP7 as an ADHD risk gene. Translational psychiatry 10 (1) (2020)
Tamar E Sztal, Emily A McKaige, Caitlin Williams, Avnika A Ruparelia, Robert J Bryson-Richardson
Genetic compensation triggered by actin mutation prevents the muscle damage caused by loss of actin protein. PLoS genetics 14 (2) (2018)
Adriana M Messineo, Charlotte Gineste, Tamar E Sztal, Elyshia L McNamara, Christophe Vilmen, Augustin C Ogier, Dorothee Hahne, David Bendahan, Nigel G Laing, Robert J Bryson-Richardson, Julien Gondin, Kristen J Nowak
L-tyrosine supplementation does not ameliorate skeletal muscle dysfunction in zebrafish and mouse models of dominant skeletal muscle α-actin nemaline myopathy. Scientific reports 8 (1) (2018)

Robert J Bryson-Richardson.css-eqlu8i{font-size:small;padding-left:4px;}

Publication Activity (10 Years)

Top Topics

Top Venues

Robert J Bryson-Richardson