| Year |
Citation |
Score |
| 2024 |
Audet S, Triassi V, Gelinas M, Legault-Cadieux N, Ferraro V, Duquette A, Tetreault M. Integration of multi-omics technologies for molecular diagnosis in ataxia patients. Frontiers in Genetics. 14: 1304711. PMID 38239855 DOI: 10.3389/fgene.2023.1304711 |
0.658 |
|
| 2023 |
Nguyen E, Tétreault M, Toffa DH, Cossette P, Samarut É, Nguyen DK. Novel NALCN variant linked to temporal lobe epilepsy. American Journal of Medical Genetics. Part A. PMID 37046053 DOI: 10.1002/ajmg.a.63209 |
0.325 |
|
| 2022 |
Pellerin D, Danzi MC, Wilke C, Renaud M, Fazal S, Dicaire MJ, Scriba CK, Ashton C, Yanick C, Beijer D, Rebelo A, Rocca C, Jaunmuktane Z, Sonnen JA, Larivière R, et al. Deep Intronic GAA Repeat Expansion in Late-Onset Cerebellar Ataxia. The New England Journal of Medicine. PMID 36516086 DOI: 10.1056/NEJMoa2207406 |
0.666 |
|
| 2022 |
Mezreani J, Audet S, Martin F, Charbonneau J, Triassi V, Bareke E, Laplante A, Karamchandani J, Massie R, Chalk CH, O'Ferrall E, Tétreault M. Novel homozygous nonsense mutation of MLIP and compensatory alternative splicing. Npj Genomic Medicine. 7: 36. PMID 35672413 DOI: 10.1038/s41525-022-00307-y |
0.374 |
|
| 2021 |
Labrecque M, Touma L, Bhérer C, Duquette A, Tétreault M. Estimated prevalence of Niemann-Pick type C disease in Quebec. Scientific Reports. 11: 22621. PMID 34799641 DOI: 10.1038/s41598-021-01966-0 |
0.611 |
|
| 2021 |
Touma L, Labrecque M, Tetreault M, Duquette A. Identification and Classification of Rare Variants in NPC1 and NPC2 in Quebec. Scientific Reports. 11: 10344. PMID 33990640 DOI: 10.1038/s41598-021-89630-5 |
0.642 |
|
| 2020 |
Gauquelin L, Hartley T, Tarnopolsky M, Dyment DA, Brais B, Geraghty MT, Tétreault M, Ahmed S, Rojas S, Choquet K, Majewski J, Bernier F, Innes AM, Rouleau G, Suchowersky O, et al. Channelopathies Are a Frequent Cause of Genetic Ataxias Associated with Cerebellar Atrophy. Movement Disorders Clinical Practice. 7: 940-949. PMID 33163565 DOI: 10.1002/Mdc3.13086 |
0.633 |
|
| 2020 |
Nicolau S, Choquet K, Bareke E, Shao YH, Brais B, O'Ferrall EK, Tétreault M, Karamchandani J. A molecular diagnosis of LGMDR1 established by RNA sequencing. The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques. 1-11. PMID 32646536 DOI: 10.1017/Cjn.2020.141 |
0.512 |
|
| 2019 |
Mahjoub A, Cihlarova Z, Tétreault M, MacNeil L, Sondheimer N, Caldecott KW, Hanzlikova H, Yoon G. Homozygous pathogenic variant in associated with nonprogressive cerebellar ataxia. Neurology. Genetics. 5: e359. PMID 31742228 DOI: 10.1212/Nxg.0000000000000359 |
0.373 |
|
| 2018 |
Fitzsimons PE, Alston CL, Bonnen PE, Hughes J, Crushell E, Geraghty MT, Tetreault M, O'Reilly P, Twomey E, Sheikh Y, Walsh R, Waterham HR, Ferdinandusse S, Wanders RJA, Taylor RW, et al. Clinical, biochemical, and genetic features of four patients with short-chain enoyl-CoA hydratase (ECHS1) deficiency. American Journal of Medical Genetics. Part A. PMID 29575569 DOI: 10.1002/Ajmg.A.38658 |
0.446 |
|
| 2017 |
Gauquelin L, Tétreault M, Thiffault I, Farrow E, Miller N, Yoo B, Bareke E, Yoon G, Suchowersky O, Dupré N, Tarnopolsky M, Brais B, Wolf NI, Majewski J, Rouleau GA, et al. POLR3A variants in hereditary spastic paraplegia and ataxia. Brain : a Journal of Neurology. PMID 29228109 DOI: 10.1093/Brain/Awx290 |
0.67 |
|
| 2017 |
Bourque DK, Hartley T, Nikkel SM, Pohl D, Tétreault M, Kernohan KD, Dyment DA. A de novo mutation in RPL10 causes a rare X-linked ribosomopathy characterized by syndromic intellectual disability and epilepsy: A new case and review of the literature. European Journal of Medical Genetics. PMID 29066376 DOI: 10.1016/J.Ejmg.2017.10.011 |
0.531 |
|
| 2017 |
Tarnopolsky MA, Brady L, Tetreault M. TRMT5 mutations are associated with features of complex hereditary spastic paraparesis. Neurology. PMID 29021354 DOI: 10.1212/Wnl.0000000000004657 |
0.332 |
|
| 2017 |
Alcantara D, Elmslie F, Tetreault M, Bareke E, Hartley T, Majewski J, Boycott K, Innes AM, Dyment DA, O'Driscoll M. SHORT syndrome due to a novel de novo mutation in PRKCE (Protein Kinase Cɛ) impairing TORC2-dependent AKT activation. Human Molecular Genetics. 26: 3713-3721. PMID 28934384 DOI: 10.1093/Hmg/Ddx256 |
0.459 |
|
| 2017 |
Perrier S, Gauquelin L, Tétreault M, Tran L, Webb N, Srour M, Mitchell JJ, Brunel-Guitton C, Majewski J, Long V, Keller S, Gambello MJ, Simons C, Vanderver A, et al. Recessive Mutations in NDUFA2 Cause Mitochondrial Leukoencephalopathy. Clinical Genetics. PMID 28857146 DOI: 10.1111/Cge.13126 |
0.502 |
|
| 2017 |
Hartley T, Wagner JD, Warman-Chardon J, Tétreault M, Brady L, Baker S, Tarnopolsky M, Bourque PR, Parboosingh JS, Smith C, McInnes B, Innes AM, Bernier F, Curry CJ, Yoon G, et al. Whole-exome sequencing is a valuable diagnostic tool for inherited peripheral neuropathies: outcomes from a cohort of 50 families. Clinical Genetics. PMID 28708278 DOI: 10.1111/Cge.13101 |
0.473 |
|
| 2017 |
Ylikallio E, Woldegebriel R, Tumiati M, Isohanni P, Ryan MM, Stark Z, Walsh M, Sawyer SL, Bell KM, Oshlack A, Lockhart PJ, Shcherbii M, Estrada-Cuzcano A, Atkinson D, Hartley T, ... Tetreault M, et al. MCM3AP in recessive Charcot-Marie-Tooth neuropathy and mild intellectual disability. Brain : a Journal of Neurology. PMID 28633435 DOI: 10.1093/Brain/Awx138 |
0.444 |
|
| 2017 |
Johnstone DL, Nguyen TT, Murakami Y, Kernohan KD, Tétreault M, Goldsmith C, Doja A, Wagner JD, Huang L, Hartley T, St-Denis A, le Deist F, Majewski J, Bulman DE, et al. Compound heterozygous mutations in the gene PIGP are associated with early infantile epileptic encephalopathy. Human Molecular Genetics. PMID 28334793 DOI: 10.1093/Hmg/Ddx077 |
0.461 |
|
| 2017 |
Kernohan KD, Dyment DA, Pupavac M, Cramer Z, McBride A, Bernard G, Straub I, Tetreault M, Hartley T, Huang L, Sell E, Majewski J, Rosenblatt DS, Shoubridge E, Mhanni A, et al. Matchmaking facilitates the diagnosis of an autosomal-recessive mitochondrial disease caused by biallelic mutation of the tRNA isopentenyltransferase (TRIT1) gene. Human Mutation. PMID 28185376 DOI: 10.1002/Humu.23196 |
0.512 |
|
| 2017 |
Balci TB, Hartley T, Xi Y, Dyment DA, Beaulieu CL, Bernier FP, Dupuis L, Horvath G, Mendoza-Londono R, Prasad C, Richer J, Yang XR, Armour CM, Bareke E, Fernandez BA, et al. Debunking Occam's razor: Diagnosing multiple genetic diseases in families by whole exome sequencing. Clinical Genetics. PMID 28170084 DOI: 10.1111/Cge.12987 |
0.458 |
|
| 2017 |
La Piana R, Weraarpachai W, Ospina LH, Tetreault M, Majewski J, Bruce Pike G, Decarie JC, Tampieri D, Brais B, Shoubridge EA. Identification and functional characterization of a novel MTFMT mutation associated with selective vulnerability of the visual pathway and a mild neurological phenotype. Neurogenetics. PMID 28058511 DOI: 10.1007/S10048-016-0506-0 |
0.627 |
|
| 2016 |
Hoch NC, Hanzlikova H, Rulten SL, Tétreault M, Komulainen E, Ju L, Hornyak P, Zeng Z, Gittens W, Rey SA, Staras K, Mancini GM, McKinnon PJ, Wang ZQ, Wagner JD, et al. XRCC1 mutation is associated with PARP1 hyperactivation and cerebellar ataxia. Nature. PMID 28002403 DOI: 10.1038/Nature20790 |
0.443 |
|
| 2016 |
Ulrick N, Goldstein A, Simons C, Taft RJ, Helman G, Pizzino A, Bloom M, Vogt J, Pysden K, Diodato D, Martinelli D, Monavari A, Buhas D, van Karnebeek CD, Dorboz I, et al. RMND1-Related Leukoencephalopathy With Temporal Lobe Cysts and Hearing Loss-Another Mendelian Mimicker of Congenital Cytomegalovirus Infection. Pediatric Neurology. PMID 27843092 DOI: 10.1016/J.Pediatrneurol.2016.09.003 |
0.382 |
|
| 2016 |
Vasli N, Harris E, Karamchandani J, Bareke E, Majewski J, Romero NB, Stojkovic T, Barresi R, Tasfaout H, Charlton R, Malfatti E, Bohm J, Marini-Bettolo C, Choquet K, Dicaire MJ, et al. Recessive mutations in the kinase ZAK cause a congenital myopathy with fibre type disproportion. Brain : a Journal of Neurology. PMID 27816943 DOI: 10.1093/Brain/Aww257 |
0.668 |
|
| 2016 |
Hamilton A, Tétreault M, Dyment DA, Zou R, Kernohan K, Geraghty MT, Hartley T, Boycott KM. Concordance between whole-exome sequencing and clinical Sanger sequencing: implications for patient care. Molecular Genetics & Genomic Medicine. 4: 504-12. PMID 27652278 DOI: 10.1002/Mgg3.223 |
0.381 |
|
| 2016 |
Shao YH, Choquet K, La Piana R, Tétreault M, Dicaire MJ, Boycott KM, Majewski J, Brais B. Mutations in GALC cause late-onset Krabbe disease with predominant cerebellar ataxia. Neurogenetics. PMID 26915362 DOI: 10.1007/S10048-016-0476-2 |
0.638 |
|
| 2016 |
Ejaz R, Qin W, Huang L, Blaser S, Tetreault M, Hartley T, Boycott KM, Carter MT. Lateral meningocele (Lehman) syndrome: A child with a novel NOTCH3 mutation. American Journal of Medical Genetics. Part A. PMID 26754023 DOI: 10.1002/Ajmg.A.37541 |
0.481 |
|
| 2016 |
Stray-Pedersen A, Cobben J, Prescott T, Lee S, Cang C, Aranda K, Ahmed S, Alders M, Gerstner T, Aslaksen K, Tétreault M, Qin W, Hartley T, Jhangiani S, Muzny D, et al. Biallelic mutations in UNC80 cause severe hypotonia, muscle weakness, growth retardation, and intellectual disability Neuromuscular Disorders. 26. DOI: 10.1016/J.Nmd.2016.06.403 |
0.412 |
|
| 2016 |
Brais B, Conte T, Dicaire M, Tetreault M, O'Ferrall E, Ravenscroft G, Laing N, Lamont P, Taivasssalo T, Hepple R, Mathieu J. A missense mutation in the putative sarcoplasmic reticulum transmembrane protein DCST2 causes dominant strongman syndrome Neuromuscular Disorders. 26: S95. DOI: 10.1016/J.Nmd.2016.06.038 |
0.63 |
|
| 2015 |
Stray-Pedersen A, Cobben JM, Prescott TE, Lee S, Cang C, Aranda K, Ahmed S, Alders M, Gerstner T, Aslaksen K, Tétreault M, Qin W, Hartley T, Jhangiani SN, Muzny DM, et al. Biallelic Mutations in UNC80 Cause Persistent Hypotonia, Encephalopathy, Growth Retardation, and Severe Intellectual Disability. American Journal of Human Genetics. PMID 26708751 DOI: 10.1016/J.Ajhg.2015.11.004 |
0.42 |
|
| 2015 |
Choquet K, Zurita-Rendón O, La Piana R, Yang S, Dicaire MJ, Boycott KM, Majewski J, Shoubridge EA, Brais B, Tétreault M. Autosomal recessive cerebellar ataxia caused by a homozygous mutation in PMPCA. Brain : a Journal of Neurology. PMID 26657514 DOI: 10.1093/brain/awv362 |
0.624 |
|
| 2015 |
Boycott KM, Beaulieu CL, Kernohan KD, Gebril OH, Mhanni A, Chudley AE, Redl D, Qin W, Hampson S, Küry S, Tetreault M, Puffenberger EG, Scott JN, Bezieau S, Reis A, et al. Autosomal-Recessive Intellectual Disability with Cerebellar Atrophy Syndrome Caused by Mutation of the Manganese and Zinc Transporter Gene SLC39A8. American Journal of Human Genetics. 97: 886-93. PMID 26637978 DOI: 10.1016/J.Ajhg.2015.11.002 |
0.423 |
|
| 2015 |
Choquet K, Tétreault M, Yang S, La Piana R, Dicaire MJ, Vanstone MR, Mathieu J, Bouchard JP, Rioux MF, Rouleau GA, Boycott KM, Majewski J, Brais B. SPG7 mutations explain a significant proportion of French Canadian spastic ataxia cases. European Journal of Human Genetics : Ejhg. PMID 26626314 DOI: 10.1038/Ejhg.2015.240 |
0.73 |
|
| 2015 |
Vanstone JR, Smith AM, McBride S, Naas T, Holcik M, Antoun G, Harper ME, Michaud J, Sell E, Chakraborty P, Tetreault M, Majewski J, Baird S, Boycott KM, et al. DNM1L-related mitochondrial fission defect presenting as refractory epilepsy. European Journal of Human Genetics : Ejhg. PMID 26604000 DOI: 10.1038/Ejhg.2015.243 |
0.333 |
|
| 2015 |
Faden M, AlZahrani F, Mendoza-Londono R, Dupuis L, Hartley T, Kannu P, Raiman JA, Howard A, Qin W, Tetreault M, Xi JQ, Al-Thamer I, Maas RL, Boycott K, et al. Identification of a Recognizable Progressive Skeletal Dysplasia Caused by RSPRY1 Mutations. American Journal of Human Genetics. 97: 608-15. PMID 26365341 DOI: 10.1016/J.Ajhg.2015.08.007 |
0.53 |
|
| 2015 |
Kernohan KD, Tétreault M, Liwak-Muir U, Geraghty MT, Qin W, Venkateswaran S, Davila J, Holcik M, Majewski J, Richer J, Boycott KM. Homozygous mutation in the eukaryotic translation initiation factor 2alpha phosphatase gene, PPP1R15B, is associated with severe microcephaly, short stature and intellectual disability. Human Molecular Genetics. 24: 6293-300. PMID 26307080 DOI: 10.1093/Hmg/Ddv337 |
0.435 |
|
| 2015 |
Wagner JD, Huang L, Tetreault M, Majewski J, Boycott KM, Bulman DE, Dyment DA, McMillan HJ. Autosomal recessive axonal polyneuropathy in a sibling pair due to a novel homozygous mutation in IGHMBP2. Neuromuscular Disorders : Nmd. 25: 794-9. PMID 26298607 DOI: 10.1016/J.Nmd.2015.07.017 |
0.555 |
|
| 2015 |
Imai A, Nakaya A, Fahiminiya S, Tétreault M, Majewski J, Sakata Y, Takashima S, Lathrop M, Ott J. Beyond Homozygosity Mapping: Family-Control analysis based on Hamming distance for prioritizing variants in exome sequencing. Scientific Reports. 5: 12028. PMID 26143870 DOI: 10.1038/Srep12028 |
0.415 |
|
| 2015 |
Tetreault M, Fahiminiya S, Antonicka H, Mitchell GA, Geraghty MT, Lines M, Boycott KM, Shoubridge EA, Mitchell JJ, Michaud JL, Majewski J. Whole-exome sequencing identifies novel ECHS1 mutations in Leigh syndrome. Human Genetics. 134: 981-91. PMID 26099313 DOI: 10.1007/S00439-015-1577-Y |
0.505 |
|
| 2015 |
Sawyer SL, Cheuk-Him Ng A, Innes AM, Wagner JD, Dyment DA, Tetreault M, Majewski J, Boycott KM, Screaton RA, Nicholson G. Homozygous mutations in MFN2 cause multiple symmetric lipomatosis associated with neuropathy. Human Molecular Genetics. PMID 26085578 DOI: 10.1093/Hmg/Ddv229 |
0.531 |
|
| 2015 |
Mendoza-Londono R, Fahiminiya S, Majewski J, Tétreault M, Nadaf J, Kannu P, Sochett E, Howard A, Stimec J, Dupuis L, Roschger P, Klaushofer K, Palomo T, Ouellet J, et al. Recessive osteogenesis imperfecta caused by missense mutations in SPARC. American Journal of Human Genetics. 96: 979-85. PMID 26027498 DOI: 10.1016/J.Ajhg.2015.04.021 |
0.378 |
|
| 2015 |
Tetreault M, Bareke E, Nadaf J, Alirezaie N, Majewski J. Whole-exome sequencing as a diagnostic tool: current challenges and future opportunities. Expert Review of Molecular Diagnostics. 15: 749-60. PMID 25959410 DOI: 10.1586/14737159.2015.1039516 |
0.366 |
|
| 2015 |
Tétreault M, Gonzalez M, Dicaire MJ, Allard P, Gehring K, Leblanc D, Leclerc N, Schondorf R, Mathieu J, Zuchner S, Brais B. Adult-onset painful axonal polyneuropathy caused by a dominant NAGLU mutation. Brain : a Journal of Neurology. 138: 1477-83. PMID 25818867 DOI: 10.1093/Brain/Awv074 |
0.653 |
|
| 2015 |
Xi Y, Honeywell C, Zhang D, Schwartzentruber J, Beaulieu CL, Tetreault M, Hartley T, Marton J, Vidal SM, Majewski J, Aravind L, Gollob M, Boycott KM, Gow RM. Whole exome sequencing identifies the TNNI3K gene as a cause of familial conduction system disease and congenital junctional ectopic tachycardia. International Journal of Cardiology. 185: 114-6. PMID 25791106 DOI: 10.1016/J.Ijcard.2015.03.130 |
0.338 |
|
| 2015 |
Dyment DA, Tétreault M, Beaulieu CL, Hartley T, Ferreira P, Chardon JW, Marcadier J, Sawyer SL, Mosca SJ, Innes AM, Parboosingh JS, Bulman DE, Schwartzentruber J, Majewski J, Tarnopolsky M, et al. Whole-exome sequencing broadens the phenotypic spectrum of rare pediatric epilepsy: a retrospective study. Clinical Genetics. 88: 34-40. PMID 25046240 DOI: 10.1111/Cge.12464 |
0.489 |
|
| 2014 |
Conte T, Tetreault M, Dicaire M, Provost S, Al-Bustani N, Beland B, Dube M, Bolduc V, Srour M, O’Ferrall E, Bouchard J, Ravenscroft G, Laing N, Lamont P, Mathieu J, et al. G.P.197 Neuromuscular Disorders. 24: 875-876. DOI: 10.1016/J.Nmd.2014.06.273 |
0.598 |
|
| 2013 |
Thiffault I, Dicaire MJ, Tetreault M, Huang KN, Demers-Lamarche J, Bernard G, Duquette A, Larivière R, Gehring K, Montpetit A, McPherson PS, Richter A, Montermini L, Mercier J, Mitchell GA, et al. Diversity of ARSACS mutations in French-Canadians. The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques. 40: 61-6. PMID 23250129 DOI: 10.1017/S0317167100012968 |
0.748 |
|
| 2012 |
Tetreault M, Choquet K, Orcesi S, Tonduti D, Ballotin U, Teichmann M, Fribourg S, Schiffmann R, Brais B, Vanderver A, Bernard G. Recessive Mutations in POLR3B Encoding the Second Largest Subunit of Pol III Cause a Rare Hypomyelinating Leukodystrophy (P05.136) Neurology. 78. DOI: 10.1212/Wnl.78.1_Meetingabstracts.P05.136 |
0.657 |
|
| 2012 |
Al-Bustani N, Tétreault M, Provost S, Bolduc V, Srour M, O’Ferrall E, Dubé M, Bouchard J, Ravenscroft G, Laing N, Bignell D, Lamont P, Mathieu J, Brais B. G.P.126 “Strongman syndrome”: A new autosomal dominant herculean painful myopathy Neuromuscular Disorders. 22: 904. DOI: 10.1016/J.Nmd.2012.06.332 |
0.622 |
|
| 2010 |
Bernard G, Thiffault I, Tetreault M, Putorti ML, Bouchard I, Sylvain M, Melançon S, Laframboise R, Langevin P, Bouchard JP, Vanasse M, Vanderver A, Sébire G, Brais B. Tremor-ataxia with central hypomyelination (TACH) leukodystrophy maps to chromosome 10q22.3-10q23.31. Neurogenetics. 11: 457-64. PMID 20640464 DOI: 10.1007/S10048-010-0251-8 |
0.583 |
|
| 2008 |
Gosselin I, Thiffault I, Tétreault M, Chau V, Dicaire MJ, Loisel L, Emond M, Senderek J, Mathieu J, Dupré N, Vanasse M, Puymirat J, Brais B. Founder SH3TC2 mutations are responsible for a CMT4C French-Canadians cluster. Neuromuscular Disorders : Nmd. 18: 483-92. PMID 18511281 DOI: 10.1016/J.Nmd.2008.04.001 |
0.664 |
|
| 2006 |
Thiffault I, Rioux MF, Tetreault M, Jarry J, Loiselle L, Poirier J, Gros-Louis F, Mathieu J, Vanasse M, Rouleau GA, Bouchard JP, Lesage J, Brais B. A new autosomal recessive spastic ataxia associated with frequent white matter changes maps to 2q33-34. Brain : a Journal of Neurology. 129: 2332-40. PMID 16672289 DOI: 10.1093/Brain/Awl110 |
0.67 |
|
| 2006 |
Bolduc V, Jarry J, Rioux MF, Robitaille Y, Khoury V, Thiffault I, Tétreault M, Loisel L, Bouchard JP, Brais B. P.O.4 A novel autosomal recessive limb-girdle muscular dystrophy with quadriceps atrophy maps to 11p13-p12 Neuromuscular Disorders. 16: 684. DOI: 10.1016/J.Nmd.2006.05.136 |
0.502 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2012 |
Yang Y, Tarapore RS, Jarmel MH, Tetreault MP, Katz JP. p53 mutation alters the effect of the esophageal tumor suppressor KLF5 on keratinocyte proliferation. Cell Cycle (Georgetown, Tex.). 11: 4033-9. PMID 22990386 DOI: 10.4161/cc.22265 |
0.248 |
|
| 2021 |
Fournier S, Dauvilliers Y, Warby SC, Labrecque M, Zadra A, Boucetta S, El Gewely M, Kaddioui H, Lopez R, Montplaisir JY, Bareke E, Tétreault M, Desautels A. Does the adenosine deaminase (ADA) gene confer risk of sleepwalking? Journal of Sleep Research. e13537. PMID 34913218 DOI: 10.1111/jsr.13537 |
0.243 |
|
| 2018 |
Tétreault M, Deshaies JE, Semmler S, Sidibé H, Shkreta L, Volkening K, Soreq H, Strong MJ, Chabot B, Vande Velde C. Reply: TDP-43 mutations increase HNRNP A1-7B through gain of splicing function. Brain : a Journal of Neurology. PMID 30364932 DOI: 10.1093/Brain/Awy261 |
0.231 |
|
| 2021 |
Chasseloup F, Bourdeau I, Tabarin A, Regazzo D, Dumontet C, Ladurelle N, Tosca L, Amazit L, Proust A, Scharfmann R, Mignot T, Fiore F, Tsagarakis S, Vassiliadi D, Maiter D, et al. Loss of KDM1A in GIP-dependent primary bilateral macronodular adrenal hyperplasia with Cushing's syndrome: a multicentre, retrospective, cohort study. The Lancet. Diabetes & Endocrinology. 9: 813-824. PMID 34655521 DOI: 10.1016/S2213-8587(21)00236-9 |
0.219 |
|
| 2001 |
Tetreault M, Rongey SH, Feher G, Okamura MY. Interaction between cytochrome c2 and the photosynthetic reaction center from Rhodobacter sphaeroides: effects of charge-modifying mutations on binding and electron transfer. Biochemistry. 40: 8452-62. PMID 11456482 DOI: 10.1021/bi010222p |
0.162 |
|
| 2022 |
Li J, Toffa DH, Lefèbvre M, Tétreault M, Cossette P, Samarut É, Nguyen DK. Usage of Genetic Panels in an Adult Epilepsy Clinic. The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques. 1-21. PMID 35478072 DOI: 10.1017/cjn.2022.49 |
0.161 |
|
| 2015 |
Bourdin B, Shakeri B, Tétreault MP, Sauvé R, Lesage S, Parent L. Functional characterization of CaVα2δ mutations associated with sudden cardiac death. The Journal of Biological Chemistry. 290: 2854-69. PMID 25527503 DOI: 10.1074/Jbc.M114.597930 |
0.153 |
|
| 2005 |
Pralong E, Pollo C, Coubes P, Bloch J, Roulet E, Tétreault MH, Debatisse D, Villemure JG. Electrophysiological characteristics of limbic and motor globus pallidus internus (GPI) neurons in two cases of Lesch-Nyhan syndrome. Neurophysiologie Clinique = Clinical Neurophysiology. 35: 168-73. PMID 16530134 DOI: 10.1016/j.neucli.2005.12.004 |
0.124 |
|
| 2021 |
Sidibé H, Khalfallah Y, Xiao S, Gómez NB, Fakim H, Tank EMH, Tomasso GD, Bareke E, Aulas A, McKeever PM, Melamed Z, Destroimaisons L, Deshaies JE, Zinman L, Parker JA, et al. TDP-43 stabilizes G3BP1 mRNA: relevance to amyotrophic lateral sclerosis/frontotemporal dementia. Brain : a Journal of Neurology. PMID 34115105 DOI: 10.1093/brain/awab217 |
0.111 |
|
| 2022 |
Labarre A, Guitard E, Tossing G, Forest A, Bareke E, Labrecque M, Tétreault M, Ruiz M, Alex Parker J. Fatty acids derived from the probiotic Lacticaseibacillus rhamnosus HA-114 suppress age-dependent neurodegeneration. Communications Biology. 5: 1340. PMID 36477191 DOI: 10.1038/s42003-022-04295-8 |
0.1 |
|
| 2015 |
Nair A, Gan J, Bush-Joseph C, Verma N, Tetreault MW, Saha K, Margulis A, Fogg L, Scanzello CR. Synovial chemokine expression and relationship with knee symptoms in patients with meniscal tears. Osteoarthritis and Cartilage / Oars, Osteoarthritis Research Society. 23: 1158-64. PMID 25724256 DOI: 10.1016/J.Joca.2015.02.016 |
0.097 |
|
| 2007 |
Pralong E, Pollo C, Debatisse D, Tétreault M, Villemure J. Modulation of pallidum activity by DBS in Lesch-Nyhan syndrome Clinical Neurophysiology. 118: e4. DOI: 10.1016/j.clinph.2006.06.732 |
0.093 |
|
| 2010 |
Tetreault MP, Yang Y, Travis J, Yu QC, Klein-Szanto A, Tobias JW, Katz JP. Esophageal squamous cell dysplasia and delayed differentiation with deletion of krüppel-like factor 4 in murine esophagus. Gastroenterology. 139: 171-81.e9. PMID 20347813 DOI: 10.1053/j.gastro.2010.03.048 |
0.085 |
|
| 2012 |
Chen AF, Chivukula S, Jacobs LJ, Tetreault MW, Lee JY. What is the prevalence of MRSA colonization in elective spine cases? Clinical Orthopaedics and Related Research. 470: 2684-9. PMID 22441994 DOI: 10.1007/s11999-012-2316-5 |
0.082 |
|
| 2015 |
Long A, Giroux V, Whelan KA, Hamilton KE, Tétreault MP, Tanaka K, Lee JS, Klein-Szanto AJ, Nakagawa H, Rustgi AK. WNT10A promotes an invasive and self-renewing phenotype in esophageal squamous cell carcinoma. Carcinogenesis. 36: 598-606. PMID 25795715 DOI: 10.1093/Carcin/Bgv025 |
0.081 |
|
| 2023 |
Andriamboavonjy L, MacDonald A, Hamilton LK, Labrecque M, Boivin MN, Karamchandani J, Stratton JA, Tetreault M. Comparative analysis of methods to reduce activation signature gene expression in PBMCs. Scientific Reports. 13: 23086. PMID 38155174 DOI: 10.1038/s41598-023-49611-2 |
0.08 |
|
| 2012 |
Cooper HJ, Della Valle CJ, Berger RA, Tetreault M, Paprosky WG, Sporer SM, Jacobs JJ. Corrosion at the head-neck taper as a cause for adverse local tissue reactions after total hip arthroplasty. The Journal of Bone and Joint Surgery. American Volume. 94: 1655-61. PMID 23289127 DOI: 10.2106/Jbjs.K.01352 |
0.08 |
|
| 2022 |
Hamilton LK, Moquin-Beaudry G, Mangahas CL, Pratesi F, Aubin M, Aumont A, Joppé SE, Légiot A, Vachon A, Plourde M, Mounier C, Tétreault M, Fernandes KJL. Stearoyl-CoA Desaturase inhibition reverses immune, synaptic and cognitive impairments in an Alzheimer's disease mouse model. Nature Communications. 13: 2061. PMID 35443751 DOI: 10.1038/s41467-022-29506-y |
0.077 |
|
| 2014 |
Tetreault MW, Wetters NG, Moric M, Gross CE, Della Valle CJ. Is synovial C-reactive protein a useful marker for periprosthetic joint infection? Clinical Orthopaedics and Related Research. 472: 3997-4003. PMID 25070920 DOI: 10.1007/s11999-014-3828-y |
0.074 |
|
| 2009 |
Rangiah K, Tippornwong M, Sangar V, Austin D, Tétreault MP, Rustgi AK, Blair IA, Yu KH. Differential secreted proteome approach in murine model for candidate biomarker discovery in colon cancer. Journal of Proteome Research. 8: 5153-64. PMID 19769411 DOI: 10.1021/Pr900518V |
0.069 |
|
| 2015 |
Brown NM, Tetreault M, Cipriano CA, Della Valle CJ, Paprosky W, Sporer S. Modular tapered implants for severe femoral bone loss in THA: reliable osseointegration but frequent complications. Clinical Orthopaedics and Related Research. 473: 555-60. PMID 25053289 DOI: 10.1007/s11999-014-3811-7 |
0.063 |
|
| 2013 |
Tetreault MP, Yang Y, Katz JP. Krüppel-like factors in cancer. Nature Reviews. Cancer. 13: 701-13. PMID 24060862 DOI: 10.1038/nrc3582 |
0.061 |
|
| 2006 |
Tetreault ML, Horrigan DM, Kim JA, Zimmerman AL. Retinoids restore normal cyclic nucleotide sensitivity of mutant ion channels associated with cone dystrophy. Molecular Vision. 12: 1699-705. PMID 17213799 |
0.061 |
|
| 2013 |
Tetreault MW, Wetters NG, Aggarwal VK, Moric M, Segreti J, Huddleston JI, Parvizi J, Della Valle CJ. Should draining wounds and sinuses associated with hip and knee arthroplasties be cultured? The Journal of Arthroplasty. 28: 133-6. PMID 23906868 DOI: 10.1016/J.Arth.2013.04.057 |
0.059 |
|
| 2023 |
Hamilton LK, Moquin-Beaudry G, Mangahas CL, Pratesi F, Aubin M, Aumont A, Joppé SE, Légiot A, Vachon A, Plourde M, Mounier C, Tétreault M, Fernandes KJL. Author Correction: Stearoyl-CoA Desaturase inhibition reverses immune, synaptic and cognitive impairments in an Alzheimer's disease mouse model. Nature Communications. 14: 2674. PMID 37160868 DOI: 10.1038/s41467-023-38295-x |
0.058 |
|
| 2010 |
Basora N, Tétreault MP, Boucher MP, Herring E, Beaulieu JF. Polycystin-1 is a microtubule-driven desmosome-associated component in polarized epithelial cells. Experimental Cell Research. 316: 1454-64. PMID 20211617 DOI: 10.1016/j.yexcr.2010.02.033 |
0.057 |
|
| 2002 |
Tetreault M, Cusanovich M, Meyer T, Axelrod H, Okamura MY. Double mutant studies identify electrostatic interactions that are important for docking cytochrome c2 onto the bacterial reaction center Biochemistry. 41: 5807-5815. PMID 11980484 DOI: 10.1021/bi012053e |
0.054 |
|
| 2011 |
Yang Y, Nakagawa H, Tetreault MP, Billig J, Victor N, Goyal A, Sepulveda AR, Katz JP. Loss of transcription factor KLF5 in the context of p53 ablation drives invasive progression of human squamous cell cancer. Cancer Research. 71: 6475-84. PMID 21868761 DOI: 10.1158/0008-5472.CAN-11-1702 |
0.053 |
|
| 2013 |
Zmistowski B, Tetreault MW, Alijanipour P, Chen AF, Della Valle CJ, Parvizi J. Recurrent periprosthetic joint infection: persistent or new infection? The Journal of Arthroplasty. 28: 1486-9. PMID 23587491 DOI: 10.1016/J.Arth.2013.02.021 |
0.053 |
|
| 2004 |
Pralong E, Pollo C, Bloch J, Villemure JG, Daniel RT, Tétreault MH, Debatisse D. Recording of ventral posterior lateral thalamus neuron response to contact heat evoked potential in patient with neurogenic pain. Neuroscience Letters. 367: 332-5. PMID 15337260 DOI: 10.1016/j.neulet.2004.06.024 |
0.051 |
|
| 2005 |
Horrigan DM, Tetreault ML, Tsomaia N, Vasileiou C, Borhan B, Mierke DF, Crouch RK, Zimmerman AL. Defining the retinoid binding site in the rod cyclic nucleotide-gated channel. The Journal of General Physiology. 126: 453-60. PMID 16230468 DOI: 10.1085/Jgp.200509387 |
0.049 |
|
| 2014 |
Erickson BJ, Harris JD, Tetreault M, Bush-Joseph C, Cohen M, Romeo AA. Is Tommy John Surgery Performed More Frequently in Major League Baseball Pitchers From Warm Weather Areas? Orthopaedic Journal of Sports Medicine. 2: 2325967114553916. PMID 26535277 DOI: 10.1177/2325967114553916 |
0.047 |
|
| 2008 |
Tétreault MP, Chailler P, Beaulieu JF, Rivard N, Ménard D. Specific signaling cascades involved in cell spreading during healing of micro-wounded gastric epithelial monolayers. Journal of Cellular Biochemistry. 105: 1240-9. PMID 18802922 DOI: 10.1002/Jcb.21924 |
0.047 |
|
| 2021 |
Brunet-Ratnasingham E, Anand SP, Gantner P, Dyachenko A, Moquin-Beaudry G, Brassard N, Beaudoin-Bussières G, Pagliuzza A, Gasser R, Benlarbi M, Point F, Prévost J, Laumaea A, Niessl J, Nayrac M, et al. Integrated immunovirological profiling validates plasma SARS-CoV-2 RNA as an early predictor of COVID-19 mortality. Science Advances. 7: eabj5629. PMID 34826237 DOI: 10.1126/sciadv.abj5629 |
0.046 |
|
| 2009 |
Maher FA, Tetreault MK. Diversity and privilege Academe. 95: 17-20. |
0.045 |
|
| 2006 |
Maher FA, Tetreault MKT. Privilege and diversity in the academy Privilege and Diversity in the Academy. 1-232. DOI: 10.4324/9780203944561 |
0.042 |
|
| 2004 |
Pralong E, Villemure JG, Bloch J, Pollo C, Daniels RT, Ghika J, Vingerhoets F, Tetreault MH, Debatisse D. Quality index for the quantification of the information recorded along standard microelectrode tracks to the subthalamic nucleus in parkinsonian patients. Neurophysiologie Clinique = Clinical Neurophysiology. 34: 209-15. PMID 15639130 DOI: 10.1016/j.neucli.2004.08.001 |
0.036 |
|
| 2010 |
Khan S, Perry C, Tetreault ML, Henry D, Trimmer JS, Zimmerman AL, Matthews G. A novel cyclic nucleotide-gated ion channel enriched in synaptic terminals of isotocin neurons in zebrafish brain and pituitary. Neuroscience. 165: 79-89. PMID 19778592 DOI: 10.1016/j.neuroscience.2009.09.040 |
0.035 |
|
| 2004 |
McCabe SL, Pelosi DM, Tetreault M, Miri A, Nguitragool W, Kovithvathanaphong P, Mahajan R, Zimmerman AL. All-trans-retinal is a closed-state inhibitor of rod cyclic nucleotide-gated ion channels. The Journal of General Physiology. 123: 521-31. PMID 15078915 DOI: 10.1085/Jgp.200409011 |
0.035 |
|
| 2006 |
Tetreault ML, Henry D, Horrigan DM, Matthews G, Zimmerman AL. Characterization of a novel cyclic nucleotide-gated channel from zebrafish brain. Biochemical and Biophysical Research Communications. 348: 441-9. PMID 16887101 DOI: 10.1016/J.Bbrc.2006.07.074 |
0.035 |
|
| 2014 |
Tetreault MW, Wetters NG, Aggarwal V, Mont M, Parvizi J, Della Valle CJ. The Chitranjan Ranawat Award: Should prophylactic antibiotics be withheld before revision surgery to obtain appropriate cultures? Clinical Orthopaedics and Related Research. 472: 52-6. PMID 23633187 DOI: 10.1007/S11999-013-3016-5 |
0.034 |
|
| 2005 |
Tétreault MP, Chailler P, Rivard N, Ménard D. Differential growth factor induction and modulation of human gastric epithelial regeneration. Experimental Cell Research. 306: 285-97. PMID 15878352 DOI: 10.1016/J.Yexcr.2005.02.019 |
0.032 |
|
| 2014 |
Sundman EA, Cole BJ, Karas V, Della Valle C, Tetreault MW, Mohammed HO, Fortier LA. The anti-inflammatory and matrix restorative mechanisms of platelet-rich plasma in osteoarthritis. The American Journal of Sports Medicine. 42: 35-41. PMID 24192391 DOI: 10.1177/0363546513507766 |
0.031 |
|
| 2008 |
Tétreault MP, Chailler P, Beaulieu JF, Rivard N, Ménard D. Epidermal growth factor receptor-dependent PI3K-activation promotes restitution of wounded human gastric epithelial monolayers. Journal of Cellular Physiology. 214: 545-57. PMID 17708540 DOI: 10.1002/Jcp.21239 |
0.029 |
|
| 2013 |
Hansen E, Tetreault M, Zmistowski B, Della Valle CJ, Parvizi J, Haddad FS, Hozack WJ. Outcome of one-stage cementless exchange for acute postoperative periprosthetic hip infection. Clinical Orthopaedics and Related Research. 471: 3214-22. PMID 23775569 DOI: 10.1007/S11999-013-3079-3 |
0.029 |
|
| 2015 |
Tetreault MW, Della Valle CJ, Bohl DD, Lodha SJ, Biswas D, Wysocki RW. What Factors Influence the Success of Medial Gastrocnemius Flaps in the Treatment of Infected TKAs? Clinical Orthopaedics and Related Research. PMID 26573319 DOI: 10.1007/s11999-015-4624-z |
0.027 |
|
| 2010 |
Tetreault MP, Wang ML, Yang Y, Travis J, Yu QC, Klein-Szanto AJ, Katz JP. Klf4 overexpression activates epithelial cytokines and inflammation-mediated esophageal squamous cell cancer in mice. Gastroenterology. 139: 2124-2134.e9. PMID 20816834 DOI: 10.1053/j.gastro.2010.08.048 |
0.026 |
|
| 1993 |
Tetreault M, Marcos B, Lapointe J. Forcing function and time delay in qualitative simulation Applications of Artificial Intelligence in Engineering. 2: 109-120. |
0.026 |
|
| 2008 |
Yang Y, Tetreault MP, Yermolina YA, Goldstein BG, Katz JP. Krüppel-like factor 5 controls keratinocyte migration via the integrin-linked kinase. The Journal of Biological Chemistry. 283: 18812-20. PMID 18450752 DOI: 10.1074/jbc.M801384200 |
0.025 |
|
| 2014 |
Chen AF, Tetreault MW, Levicoff EA, Fedorka CJ, Rothenberg AC, Klatt BA. Increased incidence of patella baja after total knee arthroplasty revision for infection. American Journal of Orthopedics (Belle Mead, N.J.). 43: 562-6. PMID 25490011 |
0.024 |
|
| 1999 |
Messenger JR, Smith JC, Tetreault MJ, Vitasovic C, Zhou S, Scott P, Kozicki M. The use of dynamic BNR and two-dimensional clarifier modelling to investigate nitrogen removal at Eastern Treatment Plant, Melbourne, Australia Water Science and Technology. 39: 89-96. DOI: 10.1016/S0273-1223(99)00126-2 |
0.02 |
|
| 1986 |
Tetreault MJ, Benedict AH, Kaempfer C, Barth EF. Biological phosphorus removal: A technology evaluation Journal of the Water Pollution Control Federation. 58: 823-837. |
0.018 |
|
| 2014 |
Tetreault MW, Shukla SK, Yi PH, Sporer SM, Della Valle CJ. Are short fully coated stems adequate for "simple" femoral revisions? Clinical Orthopaedics and Related Research. 472: 577-83. PMID 23846608 DOI: 10.1007/s11999-013-3167-4 |
0.018 |
|
| 1985 |
Tétreault M. [Not Available]. Historical Papers / the Canadian Historical Association = Communications Historiques / La SociéTé Historique Du Canada. Canadian Historical Association. Meeting. 29-44. PMID 11617099 |
0.015 |
|
| 1983 |
Tétreault M. [Not Available]. Revue D'Histoire De L'AméRique FrançAise. 36: 507-26. PMID 11632928 |
0.015 |
|
| 1997 |
Maher FA, Tetreault MKT. Learning in the Dark: How Assumptions of Whiteness Shape Classroom Knowledge Harvard Educational Review. 67: 321-349. |
0.015 |
|
| 2015 |
Tétreault MP. Esophageal Cancer: Insights From Mouse Models. Cancer Growth and Metastasis. 8: 37-46. PMID 26380556 DOI: 10.4137/CGM.S21218 |
0.014 |
|
| 2012 |
Tetreault MP, Alrabaa R, McGeehan M, Katz JP. Krüppel-like factor 5 protects against murine colitis and activates JAK-STAT signaling in vivo. Plos One. 7: e38338. PMID 22675454 DOI: 10.1371/journal.pone.0038338 |
0.014 |
|
| 2015 |
Huddleston JI, Tetreault MW, Yu M, Bedair H, Hansen VJ, Choi HR, Goodman SB, Sporer SM, della Valle CJ. Is There a Benefit to Modularity in ‘Simpler’ Femoral Revisions? Clinical Orthopaedics and Related Research. DOI: 10.1007/s11999-015-4474-8 |
0.014 |
|
| 2015 |
Huddleston JI, Tetreault MW, Yu M, Bedair H, Hansen VJ, Choi HR, Goodman SB, Sporer SM, Della Valle CJ. Is There a Benefit to Modularity in 'Simpler' Femoral Revisions? Clinical Orthopaedics and Related Research. PMID 26245164 DOI: 10.1007/s11999-015-4474-8 |
0.012 |
|
| 1992 |
Parker DS, Merrill MS, Tetreault MJ. Wastewater treatment process theory and practice: The emerging convergence Water Science and Technology. 25: 301-315. |
0.011 |
|
| 2012 |
Tetreault MP, Katz JP. Transgenic Animal Models of Gastrointestinal Function Physiology of the Gastrointestinal Tract. 1: 97-113. DOI: 10.1016/B978-0-12-382026-6.00005-1 |
0.011 |
|
| 2015 |
Wilde P, Tetreault M, Franco SB. Talking back: Writing assistants renegotiate the public memory of writing centers Pedagogies of Public Memory: Teaching Writing and Rhetoric At Museums, Archives, and Memorials. 105-116. DOI: 10.4324/9781315696676 |
0.01 |
|
| 2011 |
Maher FA, Tetreault MKT. Long-term transformations: Excavating privilege and diversity in the academy Gender and Education. 23: 281-297. DOI: 10.1080/09540253.2010.491790 |
0.01 |
|
| 2011 |
Tetreault M, Hogan R, Stanton F, Rom E. RINSC thermal column cooling system upgrade Transactions of the American Nuclear Society. 105: 75-76. |
0.01 |
|
| 2009 |
Tetreault MA. La longue durée and energy security in the gulf British Journal of Middle Eastern Studies. 36: 375-393. DOI: 10.1080/13530190903338920 |
0.01 |
|
| 1999 |
Tetreault MA. Sex and violence: Social reactions to economic restructuring in Kuwait International Feminist Journal of Politics. 1: 237-255. DOI: 10.1080/146167499359907 |
0.01 |
|
| 1996 |
Young RR, Tetreault MA. Brief field experiences: An instructional tool for undergraduate political science classes Ps - Political Science and Politics. 29: 695-700. |
0.01 |
|
| 1996 |
Tetreault MA. Gulf winds: Inclement political weather in the Arabian peninsula Current History. 95: 23-27. |
0.01 |
|
| 1995 |
Tetreault MA, Al-Mughni H. Gender, citizenship and nationalism in kuwait British Journal of Middle Eastern Studies. 22: 64-80. DOI: 10.1080/13530199508705612 |
0.01 |
|
| 1993 |
Maher FA, Tetreault MKT. Doing feminist ethnography: Lessons from feminist classrooms International Journal of Qualitative Studies in Education. 6: 19-32. DOI: 10.1080/0951839930060103 |
0.01 |
|
| 1993 |
Tetreault MA. Independence, sovereignty, and vested glory: oil and politics in the second Gulf War Orient. 34: 87-103. |
0.01 |
|
| 1988 |
Fahim A, Tetreault M, Necsulescu DS. Robot trajectory optimisation with dynamic constraints The International Journal of Advanced Manufacturing Technology. 3: 71-76. DOI: 10.1007/BF02601502 |
0.01 |
|
| 1988 |
Tetreault MA. Energy policy and the Reagan administration Forum For Applied Research & Public Policy. 3: 70-79. |
0.01 |
|
| 1987 |
Tetreault MJ, Diemer DM. Control of anaerobic digester foaming Journal of the Water Pollution Control Federation. 59: 987-988. |
0.01 |
|
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