Year |
Citation |
Score |
2022 |
Hettige NC, Peng H, Wu H, Zhang X, Yerko V, Zhang Y, Jefri M, Soubannier V, Maussion G, Alsuwaidi S, Ni A, Rocha C, Krishnan J, McCarty V, Antonyan L, et al. FOXG1 dose tunes cell proliferation dynamics in human forebrain progenitor cells. Stem Cell Reports. PMID 35148845 DOI: 10.1016/j.stemcr.2022.01.010 |
0.541 |
|
2021 |
Vaillancourt K, Chen GG, Fiori L, Maussion G, Yerko V, Théroux JF, Ernst C, Labonté B, Calipari E, Nestler EJ, Nagy C, Mechawar N, Mash DC, Turecki G. Methylation of the tyrosine hydroxylase gene is dysregulated by cocaine dependence in the human striatum. Iscience. 24: 103169. PMID 34693223 DOI: 10.1016/j.isci.2021.103169 |
0.698 |
|
2020 |
Soubannier V, Maussion G, Chaineau M, Sigutova V, Rouleau G, Durcan TM, Stifani S. Characterization of human iPSC-derived astrocytes with potential for disease modeling and drug discovery. Neuroscience Letters. 135028. PMID 32380146 DOI: 10.1016/J.Neulet.2020.135028 |
0.437 |
|
2020 |
Jefri M, Bell S, Peng H, Hettige N, Maussion G, Soubannier V, Wu H, Silveira H, Theroux JF, Moquin L, Zhang X, Aouabed Z, Krishnan J, O'Leary LA, Antonyan L, et al. Stimulation of L-type calcium channels increases tyrosine hydroxylase and dopamine in ventral midbrain cells induced from somatic cells. Stem Cells Translational Medicine. PMID 32154672 DOI: 10.1002/Sctm.18-0180 |
0.477 |
|
2020 |
Labonté B, Abdallah K, Maussion G, Yerko V, Yang J, Bittar T, Quessy F, Golden SA, Navarro L, Checknita D, Gigek C, Lopez JP, Neve RL, Russo SJ, Tremblay RE, et al. Regulation of impulsive and aggressive behaviours by a novel lncRNA. Molecular Psychiatry. PMID 31907380 DOI: 10.1038/S41380-019-0637-4 |
0.766 |
|
2019 |
Maussion G, Demirova I, Gorwood P, Ramoz N. Induced Pluripotent Stem Cells; New Tools for Investigating Molecular Mechanisms in Anorexia Nervosa. Frontiers in Nutrition. 6: 118. PMID 31457016 DOI: 10.3389/Fnut.2019.00118 |
0.352 |
|
2019 |
Maussion G, Rocha C, Bernard G, Beitel LK, Durcan TM. Patient-Derived Stem Cells, Another Model, or the Missing Link Toward Novel Therapies for Autism Spectrum Disorders? Frontiers in Pediatrics. 7: 225. PMID 31245336 DOI: 10.3389/Fped.2019.00225 |
0.325 |
|
2018 |
Bell S, Maussion G, Jefri M, Peng H, Theroux JF, Silveira H, Soubannier V, Wu H, Hu P, Galat E, Torres-Platas SG, Boudreau-Pinsonneault C, O'Leary LA, Galat V, Turecki G, et al. Disruption of GRIN2B Impairs Differentiation in Human Neurons. Stem Cell Reports. PMID 29937144 DOI: 10.1016/J.Stemcr.2018.05.018 |
0.592 |
|
2018 |
Maussion G, Moalic JM, Simonneau M, Gorwood P, Ramoz N. Increased expression of BDNF mRNA in the frontal cortex of autistic patients. Behavioural Brain Research. PMID 29935919 DOI: 10.1016/J.Bbr.2018.06.023 |
0.352 |
|
2017 |
Lutz PE, Gross JA, Dhir SK, Maussion G, Yang J, Bramoulle A, Meaney MJ, Turecki G. Epigenetic Regulation of the Kappa Opioid Receptor by Child Abuse. Biological Psychiatry. PMID 28886759 DOI: 10.1016/J.Biopsych.2017.07.012 |
0.691 |
|
2017 |
Maussion G, Cruceanu C, Rosenfeld JA, Bell SC, Jollant F, Szatkiewicz J, Collins RL, Hanscom C, Kolobova I, de Champfleur NM, Blumenthal I, Chiang C, Ota V, Hultman C, O'Dushlaine C, et al. Cover Image, Volume 173A, Number 2, February 2017. American Journal of Medical Genetics. Part A. 173: i. PMID 28102589 DOI: 10.1002/ajmg.a.37896 |
0.696 |
|
2017 |
Chen GG, Gross JA, Lutz PE, Vaillancourt K, Maussion G, Bramoulle A, Théroux JF, Gardini ES, Ehlert U, Bourret G, Masurel A, Lepage P, Mechawar N, Turecki G, Ernst C. Medium throughput bisulfite sequencing for accurate detection of 5-methylcytosine and 5-hydroxymethylcytosine. Bmc Genomics. 18: 96. PMID 28100169 DOI: 10.1186/S12864-017-3489-9 |
0.717 |
|
2017 |
Kelaï S, Ramoz N, Moalic JM, Noble F, Mechawar N, Imbeaud S, Turecki G, Simonneau M, Gorwood P, Maussion G. Netrin G1: its downregulation in the nucleus accumbens of cocaine-conditioned mice and genetic association in human cocaine dependence. Addiction Biology. PMID 28074533 DOI: 10.1111/Adb.12485 |
0.487 |
|
2016 |
Bell S, Peng H, Crapper L, Kolobova I, Maussion G, Vasuta C, Yerko V, Wong TP, Ernst C. A Rapid Pipeline to Model Rare Neurodevelopmental Disorders with Simultaneous CRISPR/Cas9 Gene Editing. Stem Cells Translational Medicine. PMID 28170165 DOI: 10.1002/Sctm.16-0158 |
0.516 |
|
2016 |
Maussion G, Cruceanu C, Rosenfeld JA, Bell SC, Jollant F, Szatkiewicz J, Collins RL, Hanscom C, Kolobova I, de Champfleur NM, Blumenthal I, Chiang C, Ota V, Hultman C, O'Dushlaine C, et al. Implication of LRRC4C and DPP6 in neurodevelopmental disorders. American Journal of Medical Genetics. Part A. PMID 27759917 DOI: 10.1002/Ajmg.A.38021 |
0.741 |
|
2016 |
Merner N, Forgeot d'Arc B, Bell SC, Maussion G, Peng H, Gauthier J, Crapper L, Hamdan FF, Michaud JL, Mottron L, Rouleau GA, Ernst C. A de novo frameshift mutation in chromodomain helicase DNA-binding domain 8 (CHD8): A case report and literature review. American Journal of Medical Genetics. Part A. PMID 26789910 DOI: 10.1002/Ajmg.A.37566 |
0.573 |
|
2016 |
Labonté B, Maussion G, Yerko, Yang J, Golden S, Suderman M, Navarro L, Checknita D, Gigek C, Lopez J, Neve R, Russo S, Côté G, Meaney M, Mechawar N, et al. Speaker 4: Gustavo Turecki, Canada The International Journal of Neuropsychopharmacology. 19: 11-12. DOI: 10.1093/Ijnp/Pyw042.028 |
0.627 |
|
2015 |
Maussion G, Diallo AB, Gigek CO, Chen ES, Crapper L, Théroux JF, Chen GG, Vasuta C, Ernst C. Investigation of genes important in neurodevelopment disorders in adult human brain. Human Genetics. PMID 26194112 DOI: 10.1007/S00439-015-1584-Z |
0.542 |
|
2015 |
Gigek CO, Chen ES, Ota VK, Maussion G, Peng H, Vaillancourt K, Diallo AB, Lopez JP, Crapper L, Vasuta C, Chen GG, Ernst C. A molecular model for neurodevelopmental disorders. Translational Psychiatry. 5: e565. PMID 25966365 DOI: 10.1038/Tp.2015.56 |
0.774 |
|
2015 |
Checknita D, Maussion G, Labonté B, Comai S, Tremblay RE, Vitaro F, Turecki N, Bertazzo A, Gobbi G, Côté G, Turecki G. Monoamine oxidase A gene promoter methylation and transcriptional downregulation in an offender population with antisocial personality disorder. The British Journal of Psychiatry : the Journal of Mental Science. 206: 216-22. PMID 25497297 DOI: 10.1192/Bjp.Bp.114.144964 |
0.713 |
|
2014 |
Chen ES, Gigek CO, Rosenfeld JA, Diallo AB, Maussion G, Chen GG, Vaillancourt K, Lopez JP, Crapper L, Poujol R, Shaffer LG, Bourque G, Ernst C. Molecular convergence of neurodevelopmental disorders. American Journal of Human Genetics. 95: 490-508. PMID 25307298 DOI: 10.1016/J.Ajhg.2014.09.013 |
0.757 |
|
2014 |
Lopez JP, Lim R, Cruceanu C, Crapper L, Fasano C, Labonte B, Maussion G, Yang JP, Yerko V, Vigneault E, El Mestikawy S, Mechawar N, Pavlidis P, Turecki G. miR-1202 is a primate-specific and brain-enriched microRNA involved in major depression and antidepressant treatment. Nature Medicine. 20: 764-8. PMID 24908571 DOI: 10.1038/Nm.3582 |
0.739 |
|
2014 |
Maussion G, Yang J, Suderman M, Diallo A, Nagy C, Arnovitz M, Mechawar N, Turecki G. Functional DNA methylation in a transcript specific 3'UTR region of TrkB associates with suicide. Epigenetics : Official Journal of the Dna Methylation Society. 9: 1061-70. PMID 24802768 DOI: 10.4161/Epi.29068 |
0.686 |
|
2013 |
Labonté B, Suderman M, Maussion G, Lopez JP, Navarro-Sánchez L, Yerko V, Mechawar N, Szyf M, Meaney MJ, Turecki G. Genome-wide methylation changes in the brains of suicide completers. The American Journal of Psychiatry. 170: 511-20. PMID 23511308 DOI: 10.1176/Appi.Ajp.2012.12050627 |
0.778 |
|
2012 |
Talkowski ME, Maussion G, Crapper L, Rosenfeld JA, Blumenthal I, Hanscom C, Chiang C, Lindgren A, Pereira S, Ruderfer D, Diallo AB, Lopez JP, Turecki G, Chen ES, Gigek C, et al. Disruption of a large intergenic noncoding RNA in subjects with neurodevelopmental disabilities. American Journal of Human Genetics. 91: 1128-34. PMID 23217328 DOI: 10.1016/J.Ajhg.2012.10.016 |
0.707 |
|
2012 |
Perlis RH, Ruderfer D, Maussion G, Chambert K, Gallagher P, Turecki G, Ernst C. Bipolar disorder and a history of suicide attempts with a duplication in 5HTR1A. The American Journal of Psychiatry. 169: 1213-4. PMID 23128927 DOI: 10.1176/Appi.Ajp.2012.12050592 |
0.576 |
|
2012 |
Maussion G, Yang J, Yerko V, Barker P, Mechawar N, Ernst C, Turecki G. Regulation of a truncated form of tropomyosin-related kinase B (TrkB) by Hsa-miR-185* in frontal cortex of suicide completers. Plos One. 7: e39301. PMID 22802923 DOI: 10.1371/Journal.Pone.0039301 |
0.57 |
|
2012 |
Labonté B, Suderman M, Maussion G, Navaro L, Yerko V, Mahar I, Bureau A, Mechawar N, Szyf M, Meaney MJ, Turecki G. Genome-wide epigenetic regulation by early-life trauma. Archives of General Psychiatry. 69: 722-31. PMID 22752237 DOI: 10.1001/Archgenpsychiatry.2011.2287 |
0.732 |
|
2011 |
Torres-Platas SG, Hercher C, Davoli MA, Maussion G, Labonté B, Turecki G, Mechawar N. Astrocytic hypertrophy in anterior cingulate white matter of depressed suicides. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. 36: 2650-8. PMID 21814185 DOI: 10.1038/Npp.2011.154 |
0.458 |
|
2010 |
Loe-Mie Y, Lepagnol-Bestel AM, Maussion G, Doron-Faigenboim A, Imbeaud S, Delacroix H, Aggerbeck L, Pupko T, Gorwood P, Simonneau M, Moalic JM. SMARCA2 and other genome-wide supported schizophrenia-associated genes: regulation by REST/NRSF, network organization and primate-specific evolution. Human Molecular Genetics. 19: 2841-57. PMID 20457675 DOI: 10.1093/Hmg/Ddq184 |
0.388 |
|
2009 |
Lepagnol-Bestel AM, Zvara A, Maussion G, Quignon F, Ngimbous B, Ramoz N, Imbeaud S, Loe-Mie Y, Benihoud K, Agier N, Salin PA, Cardona A, Khung-Savatovsky S, Kallunki P, Delabar JM, et al. DYRK1A interacts with the REST/NRSF-SWI/SNF chromatin remodelling complex to deregulate gene clusters involved in the neuronal phenotypic traits of Down syndrome. Human Molecular Genetics. 18: 1405-14. PMID 19218269 DOI: 10.1093/Hmg/Ddp047 |
0.354 |
|
2008 |
Maussion G, Carayol J, Lepagnol-Bestel AM, Tores F, Loe-Mie Y, Milbreta U, Rousseau F, Fontaine K, Renaud J, Moalic JM, Philippi A, Chedotal A, Gorwood P, Ramoz N, Hager J, et al. Convergent evidence identifying MAP/microtubule affinity-regulating kinase 1 (MARK1) as a susceptibility gene for autism. Human Molecular Genetics. 17: 2541-51. PMID 18492799 DOI: 10.1093/Hmg/Ddn154 |
0.32 |
|
2008 |
Kelai S, Maussion G, Noble F, Boni C, Ramoz N, Moalic JM, Peuchmaur M, Gorwood P, Simonneau M. Nrxn3 upregulation in the globus pallidus of mice developing cocaine addiction. Neuroreport. 19: 751-5. PMID 18418251 DOI: 10.1097/Wnr.0B013E3282Fda231 |
0.343 |
|
2007 |
Lepagnol-Bestel AM, Maussion G, Ramoz N, Moalic JM, Gorwood P, Simonneau M. Nrsf silencing induces molecular and subcellular changes linked to neuronal plasticity. Neuroreport. 18: 441-6. PMID 17496800 DOI: 10.1097/Wnr.0B013E328011Dc81 |
0.356 |
|
Low-probability matches (unlikely to be authored by this person) |
2019 |
Maussion G, Clarke J, Gorwood P, Ramoz N. Level of DNA methylation in BDNF gene is significantly decreased in anorexia nervosa European Neuropsychopharmacology. 29: S275-S276. DOI: 10.1016/j.euroneuro.2018.11.436 |
0.275 |
|
2010 |
Moalic JM, Le Strat Y, Lepagnol-Bestel AM, Ramoz N, Loe-Mie Y, Maussion G, Gorwood P, Simonneau M. Primate-accelerated evolutionary genes: novel routes to drug discovery in psychiatric disorders. Current Medicinal Chemistry. 17: 1300-16. PMID 20166940 DOI: 10.2174/092986710790936338 |
0.257 |
|
2023 |
Maussion G, Rocha C, Abdian N, Yang D, Turk J, Carrillo Valenzuela D, Pimentel L, You Z, Morquette B, Nicouleau M, Deneault E, Higgins S, Chen CX, Reintsch WE, Ho S, et al. Transcriptional Dysregulation and Impaired Neuronal Activity in Knock-Out and Fragile X Patients' iPSC-Derived Models. International Journal of Molecular Sciences. 24. PMID 37834379 DOI: 10.3390/ijms241914926 |
0.249 |
|
2008 |
Lepagnol-Bestel AM, Maussion G, Boda B, Cardona A, Iwayama Y, Delezoide AL, Moalic JM, Muller D, Dean B, Yoshikawa T, Gorwood P, Buxbaum JD, Ramoz N, Simonneau M. SLC25A12 expression is associated with neurite outgrowth and is upregulated in the prefrontal cortex of autistic subjects. Molecular Psychiatry. 13: 385-97. PMID 18180767 DOI: 10.1038/sj.mp.4002120 |
0.211 |
|
2021 |
Lepagnol-Bestel AM, Zvara A, Maussion G, Quignon F, Ngimbous B, Ramoz N, Imbeaud S, Loe-Mie Y, Benihoud K, Agier N, Salin PA, Cardona A, Khung-Savatovsky S, Kallunki P, Delabar JM, et al. Corrigendum to: DYRK1A interacts with the REST/NRSF-SWI/SNF chromatin remodelling complex to deregulate gene clusters involved in the neuronal phenotypic traits of Down syndrome. Human Molecular Genetics. PMID 34918050 DOI: 10.1093/hmg/ddab346 |
0.161 |
|
2007 |
Ramoz N, Bestel-Lepagnol A, Maussion G, Moalic J, Buxbaum J, Gorwood P, Simonneau M. Autism: a molecular plasticity disorder European Psychiatry. 22: S32. DOI: 10.1016/j.eurpsy.2007.01.127 |
0.15 |
|
2021 |
Maussion G, Thomas RA, Demirova I, Gu G, Cai E, Chen CX, Abdian N, Strauss TJP, Kelaï S, Nauleau-Javaudin A, Beitel LK, Ramoz N, Gorwood P, Durcan TM. Auto-qPCR; a python-based web app for automated and reproducible analysis of qPCR data. Scientific Reports. 11: 21293. PMID 34716395 DOI: 10.1038/s41598-021-99727-6 |
0.146 |
|
2021 |
Mohamed NV, Sirois J, Ramamurthy J, Mathur M, Lépine P, Deneault E, Maussion G, Nicouleau M, Chen CX, Abdian N, Soubannier V, Cai E, Nami H, Thomas RA, Wen D, et al. Midbrain organoids with an gene triplication model key features of synucleinopathy. Brain Communications. 3: fcab223. PMID 34632384 DOI: 10.1093/braincomms/fcab223 |
0.146 |
|
2023 |
Hooshmandi M, Sharma V, Thörn Perez C, Sood R, Krimbacher K, Wong C, Lister KC, Ureña Guzmán A, Bartley TD, Rocha C, Maussion G, Nadler E, Roque PM, Gantois I, Popic J, et al. Excitatory neuron-specific suppression of the integrated stress response contributes to autism-related phenotypes in fragile X syndrome. Neuron. PMID 37473758 DOI: 10.1016/j.neuron.2023.06.017 |
0.143 |
|
2021 |
Chen CX, Abdian N, Maussion G, Thomas RA, Demirova I, Cai E, Tabatabaei M, Beitel LK, Karamchandani J, Fon EA, Durcan TM. A Multistep Workflow to Evaluate Newly Generated iPSCs and Their Ability to Generate Different Cell Types. Methods and Protocols. 4. PMID 34287353 DOI: 10.3390/mps4030050 |
0.139 |
|
2005 |
Viemari JC, Maussion G, Bévengut M, Burnet H, Pequignot JM, Népote V, Pachnis V, Simonneau M, Hilaire G. Ret deficiency in mice impairs the development of A5 and A6 neurons and the functional maturation of the respiratory rhythm. The European Journal of Neuroscience. 22: 2403-12. PMID 16307583 DOI: 10.1111/J.1460-9568.2005.04441.X |
0.095 |
|
2010 |
Kelai S, Maussion G, Munoz N, Boni C, Ramoz N, Simonneau M, Gorwood P. P.1.017 Netrin G1 polymorphisms in cocaine and alcohol codependence vulnerability: from mice to men European Neuropsychopharmacology. 20: S16. DOI: 10.1016/S0924-977X(10)70020-1 |
0.089 |
|
2010 |
Kelai S, Maussion G, Munoz N, Boni C, Ramoz N, Simonneau M, Gorwood P. S.07.06 Netrin G1 polymorphisms in cocaine and alcohol codependence vulnerability: from mice to men European Neuropsychopharmacology. 20: S173. DOI: 10.1016/S0924-977X(10)70150-4 |
0.085 |
|
Hide low-probability matches. |