Thomas Bourgeron
Thomas Bourgeron
Institut Pasteur - Université Paris Diderot - CNRS
Verified email at pasteur.fr
Title
Cited by
Cited by
Year
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
17942010
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
17572003
Description and performance of track and primary-vertex reconstruction with the CMS tracker
CMS collaboration
Journal of Instrumentation 9 (10), P10009, 2014
14562014
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
14062007
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
13942007
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
12561994
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
10612018
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
7631995
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
6352014
A synaptic trek to autism
T Bourgeron
Current opinion in neurobiology 19 (2), 231-234, 2009
6042009
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
5992006
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
5542010
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
5391999
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
4922008
From the genetic architecture to synaptic plasticity in autism spectrum disorder
T Bourgeron
Nature Reviews Neuroscience 16 (9), 551-563, 2015
4542015
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
4332012
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
4222008
Fragile X syndrome and autism at the intersection of genetic and neural networks
MK Belmonte, T Bourgeron
Nature neuroscience 9 (10), 1221-1225, 2006
3622006
Patency rates of the arteriovenous fistula for hemodialysis: a systematic review and meta-analysis
AA Al-Jaishi, MJ Oliver, SM Thomas, CE Lok, JC Zhang, AX Garg, ...
American Journal of Kidney Diseases 63 (3), 464-478, 2014
3552014
The genetic landscapes of autism spectrum disorders
G Huguet, E Ey, T Bourgeron
Annual review of genomics and human genetics 14, 191-213, 2013
3482013
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Articles 1–20