
Scientific publications
Publications
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2017
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Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance
- Ashley P. L. Marsh
- Delphine Héron
- Timothy J. Edwards
- Angélique Quartier
- Charles Galea
- Caroline Nava
- Agnès Rastetter
- Marie-Laure Moutard
- Vicki Anderson
- Pierre Bitoun
- Jens Bunt
- Anne Faudet
- Catherine Garel
- Greta Gillies
- Ilan Gobius
- Justine Guegan
- Solveig Heide
- Boris Keren
- Fabien Lesne
- Vesna Lukic
- ...
Nature Genetics ; Volume: 49 ; Page: 511-514
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Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU
- Christel Depienne
- Caroline Nava
- Boris Keren
- Solveig Heide
- Agnès Rastetter
- Sandrine Passemard
- Sandra Chantot-Bastaraud
- Marie-Laure Moutard
- Pankaj B. Agrawal
- Grace Vannoy
- Joan M. Stoler
- David J. Amor
- Thierry Billette De Villemeur
- Diane Doummar
- Caroline Alby
- Valérie Cormier-Daire
- Catherine Garel
- Pauline Marzin
- Sophie Scheidecker
- Anne de Saint-Martin
- ...
Human Genetics ; Volume: 136 ; Page: 463-479
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219th ENMC International Workshop Titinopathies International database of titin mutations and phenotypes, Heemskerk, The Netherlands, 29 April–1 May 2016
- Peter Hackman
- Bjarne Udd
- Carsten Bönnemann
- Ana Ferreiro
Neuromuscular Disorders ; Volume: 27 ; Page: 396-407
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Hox functional diversity: Novel insights from flexible motif folding and plastic protein interaction
- Miguel Ortiz-Lombardía
- Nicolas Foos
- Corinne Maurel-Zaffran
- Andrew Saurin
- Yacine Graba
BioEssays ; Volume: 39
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Fluorescent nanodiamond tracking reveals intraneuronal transport abnormalities induced by brain-disease-related genetic risk factors
- Simon Haziza
- Nitin Mohan
- Yann Loe-Mie
- Aude-Marie Lepagnol-Bestel
- Sophie Massou
- Marie-Pierre Adam
- Xuan Loc Le
- Julia Viard
- Christine Plancon
- Rachel Daudin
- Pascale Koebel
- Emilie Dorard
- Christiane Rose
- Feng-Jen Hsieh
- Chih-Che Wu
- Brigitte Potier
- Yann Hérault
- Carlo Sala
- Aiden Corvin
- Bernadette Allinquant
- ...
Nature Nanotechnology ; Volume: 12 ; Page: 322-328
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Intragenic FMR1 disease-causing variants: a significant mutational mechanism leading to Fragile-X syndrome
- Laurence Faivre
- Amélie Piton
- Helene Poquet
- Paul Kuentz
- Julien Thevenon
- Anne-Laure Mosca-Boidron
- Patrick Callier
- Frédéric Huet
- Benoit Trojak
- Daphne Lehalle
- Christel Thauvin-Robinet
European Journal of Human Genetics ; Volume: 25 ; Page: 423-431
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Experimental atopic dermatitis depends on IL-33R signaling via MyD88 in dendritic cells
- Changwei Li
- Isabelle Maillet
- Claire Mackowiak
- Camille Viala
- Franco Di Padova
- Mei Li
- Dieudonnée Togbe
- Valérie Quesniaux
- Yuping Lai
- Bernhard Ryffel
Cell Death and Disease ; Volume: 8 ; Page: e2735-e2735
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Subacute parkinsonism as a complication of Lyme disease.
- Guillaume Pisché
- Meriam Koob
- Thomas Wirth
- Véronique Quenardelle
- Ouhaïd Lagha-Boukbiza
- Mathilde Renaud
- Mathieu Anheim
- Christine Tranchant
Journal of Neurology ; Page: 1015-1019
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Low cancer prevalence in polyglutamine expansion diseases
- Morgane Sonia Thion
- Giulia Coarelli
- Alhassane Diallo
- Daisy Rinaldi
- Fabienne Calvas
- Ouahid Lagha Boukbiza
- Alina Tataru
- Perrine Charles
- Christine Tranchant
- Cecilia Marelli
- Claire Ewenczyk
- Maya Tchikviladzé
- Marie-Lorraine Monin
- Bertrand Carlander
- Mathieu Anheim
- Alexis Brice
- Fanny Mochel
- Sophie Tezenas Du Montcel
- Sandrine Humbert
- Alexandra Durr
Neurology ; Volume: 88 ; Page: 1114-1119
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