Thomas Bourgeron
Thomas Bourgeron
Institut Pasteur - Université Paris Diderot - CNRS
Bestätigte E-Mail-Adresse bei pasteur.fr
Titel
Zitiert von
Zitiert von
Jahr
BLAST+: architecture and applications
C Camacho, G Coulouris, V Avagyan, N Ma, J Papadopoulos, K Bealer, ...
BMC bioinformatics 10 (1), 421, 2009
80802009
Functional impact of global rare copy number variation in autism spectrum disorders
D Pinto, AT Pagnamenta, L Klei, R Anney, D Merico, R Regan, J Conroy, ...
Nature 466 (7304), 368-372, 2010
18742010
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism
S Jamain, H Quach, C Betancur, M Råstam, C Colineaux, IC Gillberg, ...
Nature genetics 34 (1), 27-29, 2003
18222003
The Astropy project: Building an open-science project and status of the v2. 0 core package
AM Price-Whelan, BM Sipőcz, HM Günther, PL Lim, SM Crawford, ...
The Astronomical Journal 156 (3), 123, 2018
15742018
Description and performance of track and primary-vertex reconstruction with the CMS tracker
CMS collaboration
Journal of Instrumentation 9 (10), P10009, 2014
15622014
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders
CM Durand, C Betancur, TM Boeckers, J Bockmann, P Chaste, ...
Nature genetics 39 (1), 25-27, 2007
14672007
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
P Szatmari, AD Paterson, L Zwaigenbaum, W Roberts, J Brian, XQ Liu, ...
Nature genetics 39 (3), 319, 2007
14302007
Biochemical and molecular investigations in respiratory chain deficiencies
P Rustin, D Chretien, T Bourgeron, B Gerard, A Rötig, JM Saudubray, ...
Clinica chimica acta 228 (1), 35-51, 1994
12861994
Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency
T Bourgeron, P Rustin, D Chretien, M Birch-Machin, M Bourgeois, ...
Nature genetics 11 (2), 144-149, 1995
7831995
Convergence of genes and cellular pathways dysregulated in autism spectrum disorders
D Pinto, E Delaby, D Merico, M Barbosa, A Merikangas, L Klei, ...
The American Journal of Human Genetics 94 (5), 677-694, 2014
7012014
A synaptic trek to autism
T Bourgeron
Current opinion in neurobiology 19 (2), 231-234, 2009
6372009
Searching for ways out of the autism maze: genetic, epigenetic and environmental clues
AM Persico, T Bourgeron
Trends in neurosciences 29 (7), 349-358, 2006
6102006
A genome-wide scan for common alleles affecting risk for autism
R Anney, L Klei, D Pinto, R Regan, J Conroy, TR Magalhaes, C Correia, ...
Human molecular genetics 19 (20), 4072-4082, 2010
5802010
Genome-wide scan for autism susceptibility genes
A Philippe, M Martinez, M Guilloud-Bataille, C Gillberg, M Råstam, ...
Human molecular genetics 8 (5), 805-812, 1999
5291999
From the genetic architecture to synaptic plasticity in autism spectrum disorder
T Bourgeron
Nature Reviews Neuroscience 16 (9), 551-563, 2015
5242015
Reduced social interaction and ultrasonic communication in a mouse model of monogenic heritable autism
S Jamain, K Radyushkin, K Hammerschmidt, S Granon, S Boretius, ...
Proceedings of the National Academy of Sciences 105 (5), 1710-1715, 2008
5162008
Performance of the CMS muon detector and muon reconstruction with proton-proton collisions at√ s= 13 TeV
AM Sirunyan, A Tumasyan, W Adam, F Ambrogi, E Asilar, T Bergauer, ...
Journal of Instrumentation 13 (06), P06015-P06015, 2018
5012018
Autistic-like behaviours and hyperactivity in mice lacking ProSAP1/Shank2
MJ Schmeisser, E Ey, S Wegener, J Bockmann, AV Stempel, A Kuebler, ...
Nature 486 (7402), 256-260, 2012
4772012
Abnormal melatonin synthesis in autism spectrum disorders
J Melke, HG Botros, P Chaste, C Betancur, G Nygren, H Anckarsäter, ...
Molecular psychiatry 13 (1), 90-98, 2008
4522008
Performance of the CMS missing transverse momentum reconstruction in pp data at√ s= 8 TeV
CMS collaboration
Journal of Instrumentation 10 (02), P02006, 2015
4442015
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