Benoit Martin - Publications

Universite d'Orleans, Orléans, Centre-Val de Loire, France 

18 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2014 Powell KL, Tang H, Ng C, Guillemain I, Dieuset G, Dezsi G, Çarçak N, Onat F, Martin B, O'Brien TJ, Depaulis A, Jones NC. Seizure expression, behavior, and brain morphology differences in colonies of Genetic Absence Epilepsy Rats from Strasbourg. Epilepsia. 55: 1959-68. PMID 25377760 DOI: 10.1111/epi.12840  0.6
2014 Schubert J, Siekierska A, Langlois M, May P, Huneau C, Becker F, Muhle H, Suls A, Lemke JR, de Kovel CG, Thiele H, Konrad K, Kawalia A, Toliat MR, Sander T, ... ... Martin B, et al. Mutations in STX1B, encoding a presynaptic protein, cause fever-associated epilepsy syndromes. Nature Genetics. 46: 1327-32. PMID 25362483 DOI: 10.1038/Ng.3130  0.6
2014 Boillot M, Huneau C, Marsan E, Lehongre K, Navarro V, Ishida S, Dufresnois B, Ozkaynak E, Garrigue J, Miles R, Martin B, Leguern E, Anderson MP, Baulac S. Glutamatergic neuron-targeted loss of LGI1 epilepsy gene results in seizures. Brain : a Journal of Neurology. 137: 2984-96. PMID 25234641 DOI: 10.1093/Brain/Awu259  0.6
2013 Huneau C, Benquet P, Dieuset G, Biraben A, Martin B, Wendling F. Shape features of epileptic spikes are a marker of epileptogenesis in mice. Epilepsia. 54: 2219-27. PMID 24134559 DOI: 10.1111/epi.12406  0.6
2013 Gigout S, Louvel J, Rinaldi D, Martin B, Pumain R. Thalamocortical relationships and network synchronization in a new genetic model "in mirror" for absence epilepsy. Brain Research. 1525: 39-52. PMID 23743261 DOI: 10.1016/j.brainres.2013.05.044  0.6
2012 Lagarrigue M, Alexandrov T, Dieuset G, Perrin A, Lavigne R, Baulac S, Thiele H, Martin B, Pineau C. New analysis workflow for MALDI imaging mass spectrometry: application to the discovery and identification of potential markers of childhood absence epilepsy. Journal of Proteome Research. 11: 5453-63. PMID 22994238 DOI: 10.1021/pr3006974  0.6
2012 Demont-Guignard S, Benquet P, Gerber U, Biraben A, Martin B, Wendling F. Distinct hyperexcitability mechanisms underlie fast ripples and epileptic spikes. Annals of Neurology. 71: 342-52. PMID 22451202 DOI: 10.1002/Ana.22610  0.6
2012 Yacoubi ME, Popa D, Martin B, Zimmer L, Hamon M, Adrien J, Vaugeois JM. Genetic association between helpless trait and depression-related phenotypes: evidence from crossbreeding studies with H/Rouen and NH/Rouen mice. The International Journal of Neuropsychopharmacology / Official Scientific Journal of the Collegium Internationale Neuropsychopharmacologicum (Cinp). 15: 363-74. PMID 21557882 DOI: 10.1017/S1461145711000605  0.6
2011 Brault V, Martin B, Costet N, Bizot JC, Hérault Y. Characterization of PTZ-induced seizure susceptibility in a down syndrome mouse model that overexpresses CSTB. Plos One. 6: e27845. PMID 22140471 DOI: 10.1371/journal.pone.0027845  0.6
2011 Pietropaolo S, Guilleminot A, Martin B, D'Amato FR, Crusio WE. Genetic-background modulation of core and variable autistic-like symptoms in Fmr1 knock-out mice. Plos One. 6: e17073. PMID 21364941 DOI: 10.1371/Journal.Pone.0017073  0.6
2010 Huneau C, Demont-Guignard S, Benquet P, Martin B, Wendling F. Time-domain features of epileptic spikes as potential bio-markers of the epileptogenesis process. Conference Proceedings : ... Annual International Conference of the Ieee Engineering in Medicine and Biology Society. Ieee Engineering in Medicine and Biology Society. Annual Conference. 2010: 6007-10. PMID 21097111 DOI: 10.1109/IEMBS.2010.5627592  0.6
2010 Cloix JF, Tahi Z, Martin B, Hévor T. Selection of two lines of mice based on latency to onset of methionine sulfoximine seizures. Epilepsia. 51: 118-28. PMID 20015245 DOI: 10.1111/j.1528-1167.2009.02200.x  0.6
2007 Chaix Y, Ferraro TN, Lapouble E, Martin B. Chemoconvulsant-induced seizure susceptibility: toward a common genetic basis? Epilepsia. 48: 48-52. PMID 17910581 DOI: 10.1111/j.1528-1167.2007.01289.x  0.6
2007 Martin B, Lapouble E, Chaix Y. Involvement of the Gli3 (extra-toes) gene region in body weight in mice. Thescientificworldjournal. 7: 83-6. PMID 17334602 DOI: 10.1100/tsw.2007.40  0.6
2007 Blizard DA, Takahashi A, Galsworthy MJ, Martin B, Koide T. Test standardization in behavioural neuroscience: a response to Stanford. Journal of Psychopharmacology (Oxford, England). 21: 136-9. PMID 17329289 DOI: 10.1177/0269881107074513  0.6
1995 Clément Y, Martin B, Venault P, Chapouthier G. Involvement of regions of the 4th and 7th chromosomes in the open-field activity of mice Behavioural Brain Research. 70: 51-57. PMID 8519428 DOI: 10.1016/0166-4328(94)00177-H  0.6
1995 Martin B, Clement Y, Venault P, Chapouthier G. Mouse chromosomes 4 and 13 are involved in β-carboline-induced seizures Journal of Heredity. 86: 274-279. PMID 7657995 DOI: 10.1093/OXFORDJOURNALS.JHERED.A111581  0.6
1994 Martin B, Marchaland C, Chapouthier G, Motta R. Evidence for a multigenic system controlling methyl-β-carboline-3-carboxylate (β-CCM)-induced seizures Behavior Genetics. 24: 285-297. PMID 7945158 DOI: 10.1007/BF01067195  0.6
Show low-probability matches.