Publications scientifiques
Les chercheurs de l’IGBMC publient régulièrement leurs découvertes dans des revues scientifiques, reflet du dynamisme de notre institut.
Découvrez ici leurs dernières publications.
Publications
2020
Pré-publication, Document de travail
BIN1 genetic risk factor for Alzheimer is sufficient to induce early structural tract alterations in entorhinal cortex-dentate gyrus pathway and related hippocampal multi-scale impairments
- R Daudin
- D Marechal
- Q Wang
- Y Abe
- N Bourg
- M Sartori
- Y Loe-Mie
- J Lipecka
- C Guerrera
- A Mckenzie
- B Potier
- P Dutar
- J Viard
- A.M Lepagnol-Bestel
- A Winkeler
- V Hindié
- Mc Birling
- L Lindner
- C Chevalier
- G Pavlovic
- ...
Pré-publication, Document de travail
Spontaneous social communication in laboratory mice - placing ultrasonic vocalizations in their behavioral context
- Elodie Ey
- Fabrice de Chaumont
- Thomas Bourgeron
Article dans une revue
Delirium and encephalopathy in severe COVID-19: a cohort analysis of ICU patients
- Julie Helms
- Stephane Kremer
- Hamid Merdji
- Malika Schenck
- François Séverac
- Raphael Clere-Jehl
- Antoine Studer
- Mirjana Radosavljevic
- Christine Kummerlen
- Alexandra Monnier
- Clotilde Boulay
- Samira Fafi-Kremer
- Vincent Castelain
- Mickaël Ohana
- Mathieu Anheim
- Francis Schneider
- Ferhat Meziani
Critical Care ; Volume: 24
Pré-publication, Document de travail
A network-based data-mining approach to investigate indole-related microbiota-host co-metabolism
- Ana Luisa Neves
- Andrea Rodriguez-Martinez
- Rafael Ayala
- Joram Posma
- Mr Abellona U
- Julien Chilloux
- Jeremy Nicholson
- Marc-Emmanuel Dumas
- Lesley Hoyles
Article dans une revue
The Cockayne syndrome group A and B proteins are part of a ubiquitin–proteasome degradation complex regulating cell division
- Elena Paccosi
- Federico Costanzo
- Michele Costantino
- Alessio Balzerano
- Laura Monteonofrio
- Silvia Soddu
- Giorgio Prantera
- Stefano Brancorsini
- Jean-Marc Egly
- Luca Proietti-De-Santis
Proceedings of the National Academy of Sciences of the United States of America ; Volume: 117 ; Page: 30498-30508
Article dans une revue
TBPL2/TFIIA complex establishes the maternal transcriptome through oocyte-specific promoter usage
- Changwei Yu
- Nevena Cvetesic
- Vincent Hisler
- Kapil Gupta
- Tao Ye
- Emese Gazdag
- Luc Negroni
- Petra Hajkova
- Imre Berger
- Boris Lenhard
- Ferenc Müller
- Stéphane D Vincent
- László Tora
Nature Communications ; Volume: 11 ; Page: 6439
Article dans une revue
Autosomal Recessive Cerebellar Ataxias With Elevated Alpha‐Fetoprotein: Uncommon Diseases, Common Biomarker
- Mathilde Renaud
- Christine Tranchant
- Michel Koenig
- Mathieu Anheim
Movement Disorders ; Volume: 35 ; Page: 2139-2149
Article dans une revue
Mutations in the KIF21B kinesin gene cause neurodevelopmental disorders through imbalanced canonical motor activity
- Laure Asselin
- José Rivera Alvarez
- Solveig Heide
- Camille Bonnet
- Peggy Tilly
- Hélène Vitet
- Chantal Weber
- Carlos Bacino
- Kristin Baranaño
- Anna Chassevent
- Amy Dameron
- Laurence Faivre
- Neil Hanchard
- Sonal Mahida
- Kirsty Mcwalter
- Cyril Mignot
- Caroline Nava
- Agnès Rastetter
- Haley Streff
- Christel Thauvin-Robinet
- ...
Nature Communications ; Volume: 11
Article dans une revue
µgreen-db: a reference database for the 23S rRNA gene of eukaryotic plastids and cyanobacteria
- Christophe Djemiel
- Damien Plassard
- Sébastien Terrat
- Olivier Crouzet
- Joana Sauze
- Samuel Mondy
- Virginie Nowak
- Lisa Wingate
- Jérôme Ogée
- Pierre-Alain Maron
Scientific Reports ; Volume: 10 ; Page: 1-11
Article dans une revue
DISSEQ: Double-blind Next-Generation-Sequencing technologies (exome and gene panel) in the diagnosis of a cohort of 330 patients with an intellectual disability: concordance, discrepancies, and efficiencies.
- A. Bruel
- B. Gerard
- A. Piton
- F. Tran Mau-Them
- A. Sorlin
- A. Sorly
- D. Lacombe
- S. Manouvrier
- P. Edery
- Nicole Philip
- D. Genevieve
- A. Verloes
- S. Odent
- J. Thevenon
- A. Toutain
- D. Bonneau
- S. El Chehadeh
- M. Doco-Fenzy
- B. Isidor
- A. Goldenberg
- ...
European Journal of Human Genetics ; Volume: 28 ; Page: 333-334