David Coelho

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 8

Top Venues

Cells

Nature communications

International journal of molecular sciences

Journal of human genetics

University Children's Hospital Zurich

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

Affiliation History

University Children's Hospital Zurich Jan 01 2011 - Mar 31 2013

Switzerland

Postdoctoral Fellow :: Metabolic Unit

UKBB Universitäts-Kinderspital Jan 01 2003 - Oct 31 2010

Switzerland

Postdoctoral Fellow :: Metabolic Unit

Publications

Ziad Hassan, David Coelho, Carine Bossenmeyer-Pourié, Karim Matmat, Carole Arnold, Aurélie Savladori, Jean-Marc Alberto, Rémy Umoret, Jean-Louis Guéant, Grégory Pourié
Cognitive Impairment Is Associated with AMPAR Glutamatergic Dysfunction in a Mouse Model of Neuronal Methionine Synthase Deficiency. Cells 12 (9) (2023)
Ziad Hassan, David Coelho, Carine Bossenmeyer-Pourié, Karim Matmat, Carole Arnold, Aurélie Savladori, Jean-Marc Alberto, Rémy Umoret, Jean-Louis Guéant, Grégory Pourié
Cognitive Impairment Is Associated with AMPAR Glutamatergic Dysfunction in a Mouse Model of Neuronal Methionine Synthase Deficiency. Cells 12 (9) (2023)
Ziad Hassan, David Coelho, Carine Bossenmeyer-Pourié, Karim Matmat, Carole Arnold, Aurélie Savladori, Jean-Marc Alberto, Rémy Umoret, Jean-Louis Guéant, Grégory Pourié
Cognitive Impairment Is Associated with AMPAR Glutamatergic Dysfunction in a Mouse Model of Neuronal Methionine Synthase Deficiency. Cells 12 (9) (2023)
Viola J Kosgei, David Coelho, Rosa-Maria Guéant-Rodriguez, Jean-Louis Guéant
Sirt1-PPARS Cross-Talk in Complex Metabolic Diseases and Inherited Disorders of the One Carbon Metabolism. Cells 9 (8) (2020)
Arnaud Wiedemann, Céline Chery, David Coelho, Justine Flayac, Naïg Gueguen, Valérie Desquiret-Dumas, François Feillet, Christian Lavigne, Jean-Philippe Neau, Brian Fowler, Matthias R Baumgartner, Pascal Reynier, Jean-Louis Guéant, Abderrahim Oussalah
Mutations in MTHFR and POLG impaired activity of the mitochondrial respiratory chain in 46-year-old twins with spastic paraparesis. Journal of human genetics 65 (2) (2019)
Ziad Hassan, David Coelho, Tunay Kokten, Jean-Marc Alberto, Rémy Umoret, Jean-Luc Daval, Jean-Louis Guéant, Carine Bossenmeyer-Pourié, Grégory Pourié
Brain Susceptibility to Methyl Donor Deficiency: From Fetal Programming to Aging Outcome in Rats. International journal of molecular sciences 20 (22) (2019)
Jean-Louis Guéant, Céline Chéry, Abderrahim Oussalah, Javad Nadaf, David Coelho, Thomas Josse, Justine Flayac, Aurélie Robert, Isabelle Koscinski, Isabelle Gastin, Pierre Filhine-Tresarrieu, Mihaela Pupavac, Alison Brebner, David Watkins, Tomi Pastinen, Alexandre Montpetit, Fadi Hariri, David Tregouët, Benjamin A Raby, Wendy K Chung, Pierre-Emmanuel Morange, D Sean Froese, Matthias R Baumgartner, Jean-François Benoist, Can Ficicioglu, Virginie Marchand, Yuri Motorin, Chrystèle Bonnemains, François Feillet, Jacek Majewski, David S Rosenblatt
Publisher Correction: A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients. Nature communications 9 (1) (2018)
Jean-Louis Guéant, Céline Chéry, Abderrahim Oussalah, Javad Nadaf, David Coelho, Thomas Josse, Justine Flayac, Aurélie Robert, Isabelle Koscinski, Isabelle Gastin, Pierre Filhine-Tresarrieu, Mihaela Pupavac, Alison Brebner, David Watkins, Tomi Pastinen, Alexandre Montpetit, Fadi Hariri, David Tregouët, Benjamin A Raby, Wendy K Chung, Pierre-Emmanuel Morange, D Sean Froese, Matthias R Baumgartner, Jean-François Benoist, Can Ficicioglu, Virginie Marchand, Yuri Motorin, Chrystèle Bonnemains, François Feillet, Jacek Majewski, David S Rosenblatt
APRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients. Nature communications 9 (1) (2018)

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Publication Activity (10 Years)

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David Coelho