Carl Fratter

Publication Activity (10 Years)

Years Active: 2019-2022
Publications (10 Years): 9

Top Topics

Circulating Tumor

Mitochondrial Dna

Cross Sectional

Top Venues

European journal of human genetics : EJHG

Nature communications

Genetics in medicine : official journal of the American College of Medical Genetics

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

Publications

Eleni Mavraki, Robyn Labrum, Kate Sergeant, Charlotte L Alston, Cathy Woodward, Conrad Smith, Charlotte V Y Knowles, Yogen Patel, Philip Hodsdon, Jack P Baines, Emma L Blakely, James M Polke, Robert W Taylor, Carl Fratter
Genetic testing for mitochondrial disease: the United Kingdom best practice guidelines. European journal of human genetics : EJHG 31 (2) (2022)
Eleni Mavraki, Robyn Labrum, Kate Sergeant, Charlotte L Alston, Cathy Woodward, Conrad Smith, Charlotte V Y Knowles, Yogen Patel, Philip Hodsdon, Jack P Baines, Emma L Blakely, James M Polke, Robert W Taylor, Carl Fratter
Genetic testing for mitochondrial disease: the United Kingdom best practice guidelines. European journal of human genetics : EJHG (2022)
Eleni Mavraki, Robyn Labrum, Kate Sergeant, Charlotte L Alston, Cathy Woodward, Conrad Smith, Charlotte V Y Knowles, Yogen Patel, Philip Hodsdon, Jack P Baines, Emma L Blakely, James M Polke, Robert W Taylor, Carl Fratter
Genetic testing for mitochondrial disease: the United Kingdom best practice guidelines. European journal of human genetics : EJHG 31 (2) (2022)
Eleni Mavraki, Robyn Labrum, Kate Sergeant, Charlotte L Alston, Cathy Woodward, Conrad Smith, Charlotte V Y Knowles, Yogen Patel, Philip Hodsdon, Jack P Baines, Emma L Blakely, James M Polke, Robert W Taylor, Carl Fratter
Genetic testing for mitochondrial disease: the United Kingdom best practice guidelines. European journal of human genetics : EJHG 31 (2) (2022)
Eleni Mavraki, Robyn Labrum, Kate Sergeant, Charlotte L Alston, Cathy Woodward, Conrad Smith, Charlotte V Y Knowles, Yogen Patel, Philip Hodsdon, Jack P Baines, Emma L Blakely, James M Polke, Robert W Taylor, Carl Fratter
Genetic testing for mitochondrial disease: the United Kingdom best practice guidelines. European journal of human genetics : EJHG (2022)
Wei Wei, Alistair T Pagnamenta, Nicholas Gleadall, Alba Sanchis-Juan, Jonathan Stephens, John Broxholme, Salih Tuna, Christopher A Odhams, null null, null null, Carl Fratter, Ernest Turro, Mark J Caulfield, Jenny C Taylor, Shamima Rahman, Patrick F Chinnery
Author Correction: Nuclear-mitochondrial DNA segments resemble paternally inherited mitochondrial DNA in humans. Nature communications 11 (1) (2020)
Wei Wei, Alistair T Pagnamenta, Nicholas Gleadall, Alba Sanchis-Juan, Jonathan Stephens, John Broxholme, Salih Tuna, Christopher A Odhams, null null, null null, Carl Fratter, Ernest Turro, Mark J Caulfield, Jenny C Taylor, Shamima Rahman, Patrick F Chinnery
Nuclear-mitochondrial DNA segments resemble paternally inherited mitochondrial DNA in humans. Nature communications 11 (1) (2020)
Carl Fratter, Raymond Dalgleish, Stephanie K Allen, Rosário Santos, Stephen Abbs, Sylvie Tuffery-Giraud, Alessandra Ferlini
EMQN best practice guidelines for genetic testing in dystrophinopathies. European journal of human genetics : EJHG 28 (9) (2020)
Nandaki Keshavan, Jose Abdenur, Glenn Anderson, Zahra Assouline, Giulia Barcia, Lamia Bouhikbar, Anupam Chakrapani, Maureen Cleary, Marta C Cohen, François Feillet, Carl Fratter, Natalie S Hauser, Tom Jacques, Amanda Lam, Helen McCullagh, Rahul Phadke, Agnès Rötig, Mark Sharrard, Mariella T Simon, Conrad Smith, Ewen W Sommerville, Robert W Taylor, Wyatt W Yue, Shamima Rahman
The natural history of infantile mitochondrial DNA depletion syndrome due to RRM2B deficiency. Genetics in medicine : official journal of the American College of Medical Genetics 22 (1) (2019)