Dominic Rochefort, Ph.D. - Publications

Affiliations: 
Chemistry Université de Montréal, Montréal, Canada 

82 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
2018 Trinh ND, Lepage D, Aymé-Perrot D, Badia A, Dolle M, Rochefort D. An artificial lithium protective layer enables the use of acetonitrile-based electrolytes in lithium-metal batteries. Angewandte Chemie (International Ed. in English). PMID 29493905 DOI: 10.1002/anie.201801737  0.32
2015 Lone A, Anany H, Hakeem M, Aguis L, Avdjian AC, Bouget M, Atashi A, Brovko L, Rochefort D, Griffiths MW. Development of prototypes of bioactive packaging materials based on immobilized bacteriophages for control of growth of bacterial pathogens in foods. International Journal of Food Microbiology. 217: 49-58. PMID 26490649 DOI: 10.1016/j.ijfoodmicro.2015.10.011  1
2015 Jouan L, Ouled Amar Bencheikh B, Daoud H, Dionne-Laporte A, Dobrzeniecka S, Spiegelman D, Rochefort D, Hince P, Szuto A, Lassonde M, Barbelanne M, Tsang WY, Dion PA, Théoret H, Rouleau GA. Exome sequencing identifies recessive CDK5RAP2 variants in patients with isolated agenesis of corpus callosum. European Journal of Human Genetics : Ejhg. PMID 26197979 DOI: 10.1038/ejhg.2015.156  0.4
2015 Kaneb HM, Folkmann AW, Belzil VV, Jao LE, Leblond CS, Girard SL, Daoud H, Noreau A, Rochefort D, Hince P, Szuto A, Levert A, Vidal S, André-Guimont C, Camu W, et al. Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosis. Human Molecular Genetics. 24: 1363-73. PMID 25343993 DOI: 10.1093/hmg/ddu545  0.4
2015 Khakani SE, Forgie JC, Macneil DD, Rochefort D. Redox shuttles for lithium-ion batteries at concentrations up to 1 M using an electroactive ionic liquid based on 2,5-di-tert-butyl-1,4-dimethoxybenzene Journal of the Electrochemical Society. 162: A1432-A1438. DOI: 10.1149/2.0131508jes  1
2015 Meng X, Quenneville F, Venne F, Di Mauro E, Işlk D, Barbosa M, Drolet Y, Natile MM, Rochefort D, Soavi F, Santato C. Electrolyte-Gated WO3 Transistors: Electrochemistry, Structure, and Device Performance Journal of Physical Chemistry C. 119: 21732-21738. DOI: 10.1021/acs.jpcc.5b06777  1
2015 Gélinas B, Rochefort D. Synthesis and characterization of an electroactive ionic liquid based on the ferrocenylsulfonyl(trifluoromethylsulfonyl)imide anion Electrochimica Acta. 162: 36-44. DOI: 10.1016/j.electacta.2014.11.154  1
2014 Daoud H, Postuma RB, Bourassa CV, Rochefort D, Gauthier MT, Montplaisir J, Gagnon JF, Arnulf I, Dauvilliers Y, Charley CM, Inoue Y, Sasai T, Högl B, Desautels A, Frauscher B, et al. C9orf72 repeat expansions in rapid eye movement sleep behaviour disorder. The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques. 41: 759-62. PMID 25377888 DOI: 10.1017/cjn.2014.39  0.4
2014 Geand?linas B, Forgie JC, Rochefort D. Conductivity and electrochemistry of ferrocenyl-imidazolium redox ionic liquids with different alkyl chain lengths Journal of the Electrochemical Society. 161: H161-H165. DOI: 10.1149/2.017404jes  1
2014 Nguyen NL, Rochefort D. Electrochemistry of ruthenium dioxide composite electrodes in diethylmethylammonium-triflate protic ionic liquid and its mixtures with acetonitrile Electrochimica Acta. 147: 96-103. DOI: 10.1016/j.electacta.2014.08.143  1
2014 Moumene M, Tabet-Aoul A, Gougis M, Rochefort D, Mohamedi M. Laser pulse deposited nanosized ceria for direct electron transfer of glucose oxidase International Journal of Electrochemical Science. 9: 176-184.  1
2013 Zhang Y, Rochefort D. Fast and effective paper based sensor for self-diagnosis of bacterial vaginosis. Analytica Chimica Acta. 800: 87-94. PMID 24120172 DOI: 10.1016/j.aca.2013.09.032  1
2013 Abu-Baker A, Laganiere J, Gaudet R, Rochefort D, Brais B, Neri C, Dion PA, Rouleau GA. Lithium chloride attenuates cell death in oculopharyngeal muscular dystrophy by perturbing Wnt/β-catenin pathway. Cell Death & Disease. 4: e821. PMID 24091664 DOI: 10.1038/cddis.2013.342  0.4
2013 Forgie JC, El Khakani S, MacNeil DD, Rochefort D. Electrochemical characterisation of a lithium-ion battery electrolyte based on mixtures of carbonates with a ferrocene-functionalised imidazolium electroactive ionic liquid. Physical Chemistry Chemical Physics : Pccp. 15: 7713-21. PMID 23595224 DOI: 10.1039/c3cp50560j  1
2013 Lesage S, Le Ber I, Condroyer C, Broussolle E, Gabelle A, Thobois S, Pasquier F, Mondon K, Dion PA, Rochefort D, Rouleau GA, Dürr A, Brice A. C9orf72 repeat expansions are a rare genetic cause of parkinsonism. Brain : a Journal of Neurology. 136: 385-91. PMID 23413259 DOI: 10.1093/brain/aws357  0.4
2013 Daoud H, Noreau A, Rochefort D, Paquin-Lanthier G, Gauthier MT, Provencher P, Pourcher E, Dupré N, Chouinard S, Jodoin N, Soland V, Fon EA, Dion PA, Rouleau GA. Investigation of C9orf72 repeat expansions in Parkinson's disease. Neurobiology of Aging. 34: 1710.e7-9. PMID 23273600 DOI: 10.1016/j.neurobiolaging.2012.11.025  0.4
2013 Piton A, Jouan L, Rochefort D, Dobrzeniecka S, Lachapelle K, Dion PA, Gauthier J, Rouleau GA. Analysis of the effects of rare variants on splicing identifies alterations in GABAA receptor genes in autism spectrum disorder individuals. European Journal of Human Genetics : Ejhg. 21: 749-56. PMID 23169495 DOI: 10.1038/ejhg.2012.243  0.4
2013 Berryer MH, Hamdan FF, Klitten LL, Møller RS, Carmant L, Schwartzentruber J, Patry L, Dobrzeniecka S, Rochefort D, Neugnot-Cerioli M, Lacaille JC, Niu Z, Eng CM, Yang Y, Palardy S, et al. Mutations in SYNGAP1 cause intellectual disability, autism, and a specific form of epilepsy by inducing haploinsufficiency. Human Mutation. 34: 385-94. PMID 23161826 DOI: 10.1002/humu.22248  0.4
2013 Forgie JC, Rochefort D. Electroactive imidazolium salts based on 1,4-dimethoxybenzene redox groups: Synthesis and electrochemical characterisation Rsc Advances. 3: 12035-12038. DOI: 10.1039/c3ra41345d  1
2013 Castro Ruiz CA, Bélanger D, Rochefort D. Electrochemical and spectroelectrochemical evidence of redox transitions involving protons in thin MnO2 electrodes in protic ionic liquids Journal of Physical Chemistry C. 117: 20397-20405. DOI: 10.1021/jp405047g  1
2013 Shul G, Ruiz CAC, Rochefort D, Brooksby PA, Bélanger D. Electrochemical functionalization of glassy carbon electrode by reduction of diazonium cations in protic ionic liquid Electrochimica Acta. 106: 378-385. DOI: 10.1016/j.electacta.2013.05.082  1
2013 Tremblay J, Nguyen NL, Rochefort D. Hydrogen absorption by a palladium electrode from a protic ionic liquid at temperatures exceeding 100 °C Electrochemistry Communications. 34: 102-104. DOI: 10.1016/j.elecom.2013.05.024  1
2013 Moumene M, Rochefort D, Mohamedi M. Electrochemical functionalization as a promising avenue for glucose oxidase immobilization at carbon nanotubes: Enhanced direct electron transfer process International Journal of Electrochemical Science. 8: 2009-2022.  1
2012 Zhang Y, Rochefort D. Characterisation and applications of microcapsules obtained by interfacial polycondensation. Journal of Microencapsulation. 29: 636-49. PMID 22494033 DOI: 10.3109/02652048.2012.676092  1
2012 Shekarabi M, Moldrich RX, Rasheed S, Salin-Cantegrel A, Laganière J, Rochefort D, Hince P, Huot K, Gaudet R, Kurniawan N, Sotocinal SG, Ritchie J, Dion PA, Mogil JS, Richards LJ, et al. Loss of neuronal potassium/chloride cotransporter 3 (KCC3) is responsible for the degenerative phenotype in a conditional mouse model of hereditary motor and sensory neuropathy associated with agenesis of the corpus callosum. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 32: 3865-76. PMID 22423107 DOI: 10.1523/JNEUROSCI.3679-11.2012  0.4
2012 Stochmanski SJ, Therrien M, Laganière J, Rochefort D, Laurent S, Karemera L, Gaudet R, Vyboh K, Van Meyel DJ, Di Cristo G, Dion PA, Gaspar C, Rouleau GA. Expanded ATXN3 frameshifting events are toxic in Drosophila and mammalian neuron models. Human Molecular Genetics. 21: 2211-8. PMID 22337953 DOI: 10.1093/hmg/dds036  0.4
2012 Noujeim N, Samsam S, Eberlin L, Sanon SH, Rochefort D, Schmitzer AR. Mesomorphic and ion conducting properties of dialkyl(1,4-phenylene) diimidazolium salts Soft Matter. 8: 10914-10920. DOI: 10.1039/c2sm26213d  1
2011 Rivière JB, Ramalingam S, Lavastre V, Shekarabi M, Holbert S, Lafontaine J, Srour M, Merner N, Rochefort D, Hince P, Gaudet R, Mes-Masson AM, Baets J, Houlden H, Brais B, et al. KIF1A, an axonal transporter of synaptic vesicles, is mutated in hereditary sensory and autonomic neuropathy type 2. American Journal of Human Genetics. 89: 219-30. PMID 21820098 DOI: 10.1016/j.ajhg.2011.06.013  0.4
2011 Salin-Cantegrel A, Rivière JB, Shekarabi M, Rasheed S, Dacal S, Laganière J, Gaudet R, Rochefort D, Lesca G, Gaspar C, Dion PA, Lapointe JY, Rouleau GA. Transit defect of potassium-chloride Co-transporter 3 is a major pathogenic mechanism in hereditary motor and sensory neuropathy with agenesis of the corpus callosum. The Journal of Biological Chemistry. 286: 28456-65. PMID 21628467 DOI: 10.1074/jbc.M111.226894  0.4
2011 Savolainen A, Zhang Y, Rochefort D, Holopainen U, Erho T, Virtanen J, Smolander M. Printing of polymer microcapsules for enzyme immobilization on paper substrate. Biomacromolecules. 12: 2008-15. PMID 21568314 DOI: 10.1021/bm2003434  1
2011 Zhang Y, Rochefort D. Activity, conformation and thermal stability of laccase and glucose oxidase in poly(ethyleneimine) microcapsules for immobilization in paper Process Biochemistry. 46: 993-1000. DOI: 10.1016/j.procbio.2011.01.006  1
2011 Guerrero MP, Bertrand F, Rochefort D. Activity, stability and inhibition of a bioactive paper prepared by large-scale coating of laccase microcapsules Chemical Engineering Science. 66: 5313-5320. DOI: 10.1016/j.ces.2011.07.026  1
2011 Saidani F, Rochefort D, Mohamedi M. Synthesis, Characterization of Nanostructured Rhodium Films and their Electrochemical Behavior towards Carbon Monoxide Oxidation Electrocatalysis. 2: 114-122. DOI: 10.1007/s12678-011-0045-2  1
2011 Tabet-Aoul A, Saidani F, Rochefort D, Mohamedi M. Pulsed laser synthesis of SnO 2-Pt nano-thin films onto carbon nanotubes and their electrocatalytic activity towards ethanol oxidation International Journal of Electrochemical Science. 6: 6385-6397.  1
2010 Hamdan FF, Daoud H, Rochefort D, Piton A, Gauthier J, Langlois M, Foomani G, Dobrzeniecka S, Krebs MO, Joober R, Lafrenière RG, Lacaille JC, Mottron L, Drapeau P, Beauchamp MH, et al. De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment. American Journal of Human Genetics. 87: 671-8. PMID 20950788 DOI: 10.1016/j.ajhg.2010.09.017  0.4
2010 Zhang Y, Rochefort D. Comparison of emulsion and vibration nozzle methods for microencapsulation of laccase and glucose oxidase by interfacial reticulation of poly(ethyleneimine). Journal of Microencapsulation. 27: 703-13. PMID 20716009 DOI: 10.3109/02652048.2010.509518  1
2010 Srour M, Rivière JB, Pham JM, Dubé MP, Girard S, Morin S, Dion PA, Asselin G, Rochefort D, Hince P, Diab S, Sharafaddinzadeh N, Chouinard S, Théoret H, Charron F, et al. Mutations in DCC cause congenital mirror movements. Science (New York, N.Y.). 328: 592. PMID 20431009 DOI: 10.1126/science.1186463  0.4
2010 Gauthier J, Champagne N, Lafrenière RG, Xiong L, Spiegelman D, Brustein E, Lapointe M, Peng H, Côté M, Noreau A, Hamdan FF, Addington AM, Rapoport JL, Delisi LE, Krebs MO, et al. De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia. Proceedings of the National Academy of Sciences of the United States of America. 107: 7863-8. PMID 20385823 DOI: 10.1073/pnas.0906232107  0.4
2010 Kabashi E, Lin L, Tradewell ML, Dion PA, Bercier V, Bourgouin P, Rochefort D, Bel Hadj S, Durham HD, Vande Velde C, Rouleau GA, Drapeau P. Gain and loss of function of ALS-related mutations of TARDBP (TDP-43) cause motor deficits in vivo. Human Molecular Genetics. 19: 671-83. PMID 19959528 DOI: 10.1093/hmg/ddp534  0.4
2010 Mohamedi M, Saidani F, Rochefort D. Carbon monoxide oxidation on nanostructured Pt thin films synthesized by pulsed laser deposition: Insights into the morphology effects Laser Chemistry. 2010. DOI: 10.1155/2010/143684  1
2010 Mayrand-Provencher L, Lin S, Lazzerini D, Rochefort D. Pyridinium-based protic ionic liquids as electrolytes for RuO2 electrochemical capacitors Journal of Power Sources. 195: 5114-5121. DOI: 10.1016/j.jpowsour.2010.02.073  1
2009 Roman-Gusetu G, Waldron KC, Rochefort D. Development of an enzymatic microreactor based on microencapsulated laccase with off-line capillary electrophoresis for measurement of oxidation reactions. Journal of Chromatography. A. 1216: 8270-6. PMID 19767010 DOI: 10.1016/j.chroma.2009.08.069  1
2009 Mayrand-Provencher L, Rochefort D. Influence of the conductivity and viscosity of protic ionic liquids electrolytes on the e of RuO2 electrodes Journal of Physical Chemistry C. 113: 1632-1639. DOI: 10.1021/jp8084149  1
2009 Mayrand-Provencher L, Rochefort D. Origin and effect of impurities in protic ionic liquids based on 2-methylpyridine and trifluoroacetic acid for applications in electrochemistry Electrochimica Acta. 54: 7422-7428. DOI: 10.1016/j.electacta.2009.07.075  1
2009 Kouisni L, Rochefort D. Confocal microscopy study of polymer microcapsules for enzyme immobilisation in paper substrates Journal of Applied Polymer Science. 111: 1-10. DOI: 10.1002/app.28997  1
2008 Salin-Cantegrel A, Shekarabi M, Holbert S, Dion P, Rochefort D, Laganière J, Dacal S, Hince P, Karemera L, Gaspar C, Lapointe JY, Rouleau GA. HMSN/ACC truncation mutations disrupt brain-type creatine kinase-dependant activation of K+/Cl- co-transporter 3. Human Molecular Genetics. 17: 2703-11. PMID 18566107 DOI: 10.1093/hmg/ddn172  0.4
2008 Shekarabi M, Girard N, Rivière JB, Dion P, Houle M, Toulouse A, Lafrenière RG, Vercauteren F, Hince P, Laganiere J, Rochefort D, Faivre L, Samuels M, Rouleau GA. Mutations in the nervous system--specific HSN2 exon of WNK1 cause hereditary sensory neuropathy type II. The Journal of Clinical Investigation. 118: 2496-505. PMID 18521183 DOI: 10.1172/JCI34088  0.4
2008 Hébert M, Rochefort D. Investigation of microencapsulated laccase as enzyme immobilization template for application in biofuel Ecs Transactions. 16: 85-97. DOI: 10.1149/1.2981108  1
2008 Rochefort D, Kouisni L, Gendron K. Physical immobilization of laccase on an electrode by means of poly(ethyleneimine) microcapsules Journal of Electroanalytical Chemistry. 617: 53-63. DOI: 10.1016/j.jelechem.2008.01.027  1
2008 Hébert M, Rochefort D. Electrode passivation by reaction products of the electrochemical and enzymatic oxidation of p-phenylenediamine Electrochimica Acta. 53: 5272-5279. DOI: 10.1016/j.electacta.2008.02.031  1
2007 Messaed C, Dion PA, Abu-Baker A, Rochefort D, Laganiere J, Brais B, Rouleau GA. Soluble expanded PABPN1 promotes cell death in oculopharyngeal muscular dystrophy. Neurobiology of Disease. 26: 546-57. PMID 17418585 DOI: 10.1016/j.nbd.2007.02.004  0.4
2007 Jin J, Prochaska M, Rochefort D, Kim DK, Zhuang L, DiSalvo FJ, van Dover RB, Abruña HD. A high-throughput search for direct methanol fuel cell anode electrocatalysts of type PtxBiyPbz Applied Surface Science. 254: 653-661. DOI: 10.1016/j.apsusc.2007.06.077  1
2006 Prochaska M, Jin J, Rochefort D, Zhuang L, Disalvo FJ, Abrun?a HD, Van Dover RB. High throughput screening of electrocatalysts for fuel cell applications Review of Scientific Instruments. 77. DOI: 10.1063/1.2202919  1
2006 Blasini DR, Rochefort D, Fachini E, Alden LR, DiSalvo FJ, Cabrera CR, Abruña HD. Surface composition of ordered intermetallic compounds PtBi and PtPb Surface Science. 600: 2670-2680. DOI: 10.1016/j.susc.2006.04.014  1
2006 Rochefort D, Pont AL. Pseudocapacitive behaviour of RuO2 in a proton exchange ionic liquid Electrochemistry Communications. 8: 1539-1543. DOI: 10.1016/j.elecom.2006.06.032  1
2005 Duan QL, Nikpoor B, Dube MP, Molinaro G, Meijer IA, Dion P, Rochefort D, Saint-Onge J, Flury L, Brown NJ, Gainer JV, Rouleau JL, Agostoni A, Cugno M, Simon P, et al. A variant in XPNPEP2 is associated with angioedema induced by angiotensin I-converting enzyme inhibitors. American Journal of Human Genetics. 77: 617-26. PMID 16175507 DOI: 10.1086/496899  0.4
2005 Dion P, Shanmugam V, Gaspar C, Messaed C, Meijer I, Toulouse A, Laganiere J, Roussel J, Rochefort D, Laganiere S, Allen C, Karpati G, Bouchard JP, Brais B, Rouleau GA. Transgenic expression of an expanded (GCG)13 repeat PABPN1 leads to weakness and coordination defects in mice. Neurobiology of Disease. 18: 528-36. PMID 15755680 DOI: 10.1016/j.nbd.2004.09.021  0.4
2005 Rochefort D, Razafitrimo H, Guay D, Schulz R. Surface modification of co-evaporated thin films upon oxygen and air exposure Surface Science. 595: 73-86. DOI: 10.1016/j.susc.2005.08.001  1
2005 Rochefort D, Guay D. Modification to the composition of nanocrystalline RuO2 through reactive milling under O2 Journal of Alloys and Compounds. 400: 257-264. DOI: 10.1016/j.jallcom.2005.03.072  1
2004 Verlaan DJ, Laurent SB, Rochefort DL, Liquori CL, Marchuk DA, Siegel AM, Rouleau GA. CCM2 mutations account for 13% of cases in a large collection of kindreds with hereditary cavernous malformations. Annals of Neurology. 55: 757-8. PMID 15122722 DOI: 10.1002/ana.20112  0.4
2004 Desautels A, Turecki G, Xiong L, Rochefort D, Montplaisir J, Rouleau GA. Mutational analysis of neurotensin in familial restless legs syndrome. Movement Disorders : Official Journal of the Movement Disorder Society. 19: 90-4. PMID 14743366 DOI: 10.1002/mds.10617  0.4
2004 Rochefort D, Hamel C, Guay D. Effect of graphite on the electrochemical properties of ballmilled RuO 2 Journal of the Electrochemical Society. 151: A1141-A1146. DOI: 10.1149/1.1766308  1
2004 Barrière F, Ferry Y, Rochefort D, Leech D. Targetting redox polymers as mediators for laccase oxygen reduction in a membrane-less biofuel cell Electrochemistry Communications. 6: 237-241. DOI: 10.1016/j.elecom.2003.12.006  1
2004 Rochefort D, Leech D, Bourbonnais R. Electron transfer mediator systems for bleaching of paper pulp Green Chemistry. 6: 14-24.  1
2003 Hand CK, Devon RS, Gros-Louis F, Rochefort D, Khoris J, Meininger V, Bouchard JP, Camu W, Hayden MR, Rouleau GA. Mutation screening of the ALS2 gene in sporadic and familial amyotrophic lateral sclerosis. Archives of Neurology. 60: 1768-71. PMID 14676054 DOI: 10.1001/archneur.60.12.1768  0.4
2003 Toulouse A, Rochefort D, Roussel J, Joober R, Rouleau GA. Molecular cloning and characterization of human RAI1, a gene associated with schizophrenia. Genomics. 82: 162-71. PMID 12837267 DOI: 10.1016/S0888-7543(03)00101-0  0.4
2003 Szijan I, Rochefort D, Bruder C, Surace E, Machiavelli G, Dalamon V, Cotignola J, Ferreiro V, Campero A, Basso A, Dumanski JP, Rouleau GA. NF2 tumor suppressor gene: a comprehensive and efficient detection of somatic mutations by denaturing HPLC and microarray-CGH. Neuromolecular Medicine. 3: 41-52. PMID 12665675 DOI: 10.1385/NMM:3:1:41  0.4
2003 Cossette P, Loukas A, Lafrenière RG, Rochefort D, Harvey-Girard E, Ragsdale DS, Dunn RJ, Rouleau GA. Functional characterization of the D188V mutation in neuronal voltage-gated sodium channel causing generalized epilepsy with febrile seizures plus (GEFS). Epilepsy Research. 53: 107-17. PMID 12576172 DOI: 10.1016/S0920-1211(02)00259-0  0.4
2003 Rochefort D, Dabo P, Guay D, Sherwood PMA. XPS investigations of thermally prepared RuO2 electrodes in reductive conditions Electrochimica Acta. 48: 4245-4252. DOI: 10.1016/S0013-4686(03)00611-X  1
2002 Howard HC, Mount DB, Rochefort D, Byun N, Dupré N, Lu J, Fan X, Song L, Rivière JB, Prévost C, Horst J, Simonati A, Lemcke B, Welch R, England R, et al. The K-Cl cotransporter KCC3 is mutant in a severe peripheral neuropathy associated with agenesis of the corpus callosum. Nature Genetics. 32: 384-92. PMID 12368912 DOI: 10.1038/ng1002  0.4
2002 Rochefort D, Bourbonnais R, Leech D, Paice MG. Oxidation of lignin model compounds by organic and transition metal-based electron transfer mediators. Chemical Communications (Cambridge, England). 1182-3. PMID 12109072  1
2002 Rochefort D, Bourbonnais R, Leech D, Renaud S, Paice M. Electrochemical oxidation of transition metal-based mediators for pulp delignification Journal of the Electrochemical Society. 149: D15-D20. DOI: 10.1149/1.1427077  1
2001 Fortin A, Diez E, Rochefort D, Laroche L, Malo D, Rouleau GA, Gros P, Skamene E. Recombinant congenic strains derived from A/J and C57BL/6J: a tool for genetic dissection of complex traits. Genomics. 74: 21-35. PMID 11374899 DOI: 10.1006/geno.2001.6528  0.4
2001 Bourbonnais R, Rochefort D, Paice MG, Leech D. Development of stable redox complexes to mediate delignification of kraft pulp by laccase Acs Symposium Series. 785: 391-399.  1
2000 Shanmugam V, Dion P, Rochefort D, Laganière J, Brais B, Rouleau GA. PABP2 polyalanine tract expansion causes intranuclear inclusions in oculopharyngeal muscular dystrophy. Annals of Neurology. 48: 798-802. PMID 11079546 DOI: 10.1002/1531-8249(200011)48:5<798::AID-ANA16>3.0.CO;2-U  0.4
1998 Xie YG, Rochefort D, Brais B, Howard H, Han FY, Gou LP, Maciel P, The BT, Larsson C, Rouleau GA. Restriction map of a YAC and cosmid contig encompassing the oculopharyngeal muscular dystrophy candidate region on chromosome 14q11.2-q13. Genomics. 52: 201-4. PMID 9782086 DOI: 10.1006/geno.1998.5421  0.4
1998 Brais B, Bouchard JP, Xie YG, Rochefort DL, Chrétien N, Tomé FM, Lafrenière RG, Rommens JM, Uyama E, Nohira O, Blumen S, Korczyn AD, Heutink P, Mathieu J, Duranceau A, et al. Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy. Nature Genetics. 18: 164-7. PMID 9462747 DOI: 10.1038/ng0298-164  0.4
1997 Lafrenière RG, Kibar Z, Rochefort DL, Han FY, Fon EA, Dubé MP, Kang X, Baird S, Korneluk RG, Rommens JM, Rouleau GA. Genomic structure of the human GT334 (EHOC-1) gene mapping to 21q22.3. Gene. 198: 313-21. PMID 9370297 DOI: 10.1016/S0378-1119(97)00333-8  0.4
1997 Lafrenière RG, Rochefort DL, Chrétien N, Rommens JM, Cochius JI, Kälviäinen R, Nousiainen U, Patry G, Farrell K, Söderfeldt B, Federico A, Hale BR, Cossio OH, Sørensen T, Pouliot MA, et al. Unstable insertion in the 5' flanking region of the cystatin B gene is the most common mutation in progressive myoclonus epilepsy type 1, EPM1. Nature Genetics. 15: 298-302. PMID 9054946 DOI: 10.1038/ng0397-298  0.4
1996 Lafrenière RG, Rochefort DL, Kibar Z, Fon EA, Han F, Cochius J, Kang X, Baird S, Korneluk RG, Andermann E, Rommens JM, Rouleau GA. Isolation and characterization of GT335, a novel human gene conserved in Escherichia coli and mapping to 21q22.3. Genomics. 38: 264-72. PMID 8975701 DOI: 10.1006/geno.1996.0627  0.4
1996 Lafrenière RG, Rochefort DL, Chrétien N, Neville CE, Korneluk RG, Zuo L, Wei Y, Lichter J, Rouleau GA. Isolation and genomic structure of a human homolog of the yeast periodic tryptophan protein 2 (PWP2) gene mapping to 21q22.3. Genome Research. 6: 1216-26. PMID 8973917  0.4
1995 Tremblay P, Houde M, Arbour N, Rochefort D, Masure S, Mandeville R, Opdenakker G, Oth D. Differential effects of PKC inhibitors on gelatinase B and interleukin 6 production in the mouse macrophage. Cytokine. 7: 130-6. PMID 7540056 DOI: 10.1006/cyto.1995.1017  0.4
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