Stephane Richard - Publications

Affiliations: 
McGill University, Montreal, QC, Canada 
Area:
Cell Biology

38 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
2016 Nielsen SM, Rhodes L, Blanco I, Chung WK, Eng C, Maher ER, Richard S, Giles RH. Von Hippel-Lindau Disease: Genetics and Role of Genetic Counseling in a Multiple Neoplasia Syndrome. Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology. PMID 27114602 DOI: 10.1200/JCO.2015.65.6140  0.64
2016 Blanc RS, Vogel G, Chen T, Crist C, Richard S. PRMT7 Preserves Satellite Cell Regenerative Capacity. Cell Reports. PMID 26854227 DOI: 10.1016/j.celrep.2016.01.022  0.64
2015 Thandapani P, Song J, Gandin V, Cai Y, Rouleau SG, Garant JM, Boisvert FM, Yu Z, Perreault JP, Topisirovic I, Richard S. Aven recognition of RNA G-quadruplexes regulates translation of the mixed lineage leukemia protooncogenes. Elife. 4. PMID 26267306 DOI: 10.7554/eLife.06234  0.64
2015 Gurunathan G, Yu Z, Coulombe Y, Masson JY, Richard S. Arginine methylation of hnRNPUL1 regulates interaction with NBS1 and recruitment to sites of DNA damage. Scientific Reports. 5: 10475. PMID 26020839 DOI: 10.1038/srep10475  0.64
2015 Bausch B, Wellner U, Peyre M, Boedeker CC, Hes FJ, Anglani M, de Campos JM, Kanno H, Maher ER, Krauss T, Sansó G, Barontini M, Letizia C, Hader C, Schiavi F, ... ... Richard S, et al. Characterization of endolymphatic sac tumors and von Hippel-Lindau disease in the International Endolymphatic Sac Tumor Registry. Head & Neck. PMID 25867206 DOI: 10.1002/hed.24067  0.64
2015 Song J, Richard S. Sam68 Regulates S6K1 Alternative Splicing during Adipogenesis. Molecular and Cellular Biology. 35: 1926-39. PMID 25776557 DOI: 10.1128/MCB.01488-14  0.64
2014 Couvé S, Ladroue C, Laine E, Mahtouk K, Guégan J, Gad S, Le Jeune H, Le Gentil M, Nuel G, Kim WY, Lecomte B, Pagès JC, Collin C, Lasne F, Benusiglio PR, ... ... Richard S, et al. Genetic evidence of a precisely tuned dysregulation in the hypoxia signaling pathway during oncogenesis. Cancer Research. 74: 6554-64. PMID 25371412 DOI: 10.1158/0008-5472.CAN-14-1161  0.64
2014 Menko FH, Maher ER, Schmidt LS, Middelton LA, Aittomäki K, Tomlinson I, Richard S, Linehan WM. Hereditary leiomyomatosis and renal cell cancer (HLRCC): renal cancer risk, surveillance and treatment. Familial Cancer. 13: 637-44. PMID 25012257 DOI: 10.1007/s10689-014-9735-2  0.64
2014 Lafleur VN, Richard S, Richard DE. Transcriptional repression of hypoxia-inducible factor-1 (HIF-1) by the protein arginine methyltransferase PRMT1. Molecular Biology of the Cell. 25: 925-35. PMID 24451260 DOI: 10.1091/mbc.E13-07-0423  0.64
2014 Bento C, Percy MJ, Gardie B, Maia TM, van Wijk R, Perrotta S, Della Ragione F, Almeida H, Rossi C, Girodon F, Aström M, Neumann D, Schnittger S, Landin B, Minkov M, ... ... Richard S, et al. Genetic basis of congenital erythrocytosis: mutation update and online databases. Human Mutation. 35: 15-26. PMID 24115288 DOI: 10.1002/humu.22448  0.64
2013 Thandapani P, O'Connor TR, Bailey TL, Richard S. Defining the RGG/RG motif. Molecular Cell. 50: 613-23. PMID 23746349 DOI: 10.1016/j.molcel.2013.05.021  0.64
2013 Auclair Y, Richard S. The role of arginine methylation in the DNA damage response Dna Repair. 12: 459-465. PMID 23684798 DOI: 10.1016/j.dnarep.2013.04.006  0.64
2013 Popova T, Hebert L, Jacquemin V, Gad S, Caux-Moncoutier V, Dubois-d'Enghien C, Richaudeau B, Renaudin X, Sellers J, Nicolas A, Sastre-Garau X, Desjardins L, Gyapay G, Raynal V, Sinilnikova OM, ... ... Richard S, et al. Germline BAP1 mutations predispose to renal cell carcinomas. American Journal of Human Genetics. 92: 974-80. PMID 23684012 DOI: 10.1016/j.ajhg.2013.04.012  0.64
2013 Frantzen C, van Asselt SJ, Kruizinga RC, Abadie C, Coupier I, Richard S, Alsmeier G, Graff JW, van Pampus MG, Giles RH, Links TP. Letter to the editor: Pregnancy and von Hippel-Lindau disease Journal of Neurosurgery. 118: 1380. PMID 23581592  0.64
2013 Dhar S, Vemulapalli V, Patananan AN, Huang GL, Di Lorenzo A, Richard S, Comb MJ, Guo A, Clarke SG, Bedford MT. Loss of the major Type I arginine methyltransferase PRMT1 causes substrate scavenging by other PRMTs. Scientific Reports. 3: 1311. PMID 23419748 DOI: 10.1038/srep01311  0.64
2012 Mallette FA, Richard S. JMJD2A Promotes Cellular Transformation by Blocking Cellular Senescence through Transcriptional Repression of the Tumor Suppressor CHD5 Cell Reports. 2: 1233-1243. PMID 23168260 DOI: 10.1016/j.celrep.2012.09.033  0.64
2012 Vogel G, Richard S. Emerging roles for Sam68 in adipogenesis and neuronal development Rna Biology. 9: 1129-1133. PMID 23018781 DOI: 10.4161/rna.21409  0.64
2012 Mallette FA, Richard S. K48-linked ubiquitination and protein degradation regulate 53BP1 recruitment at DNA damage sites Cell Research. 22: 1221-1223. PMID 22491476 DOI: 10.1038/cr.2012.58  0.64
2012 Mallette FA, Richard S. The fight of the Tudor domain "Royal family" for a broken DNA throne Cell Cycle. 11: 1483-1484. PMID 22487685 DOI: 10.4161/cc.20124  0.64
2012 Mallette FA, Mattiroli F, Cui G, Young LC, Hendzel MJ, Mer G, Sixma TK, Richard S. RNF8- and RNF168-dependent degradation of KDM4A/JMJD2A triggers 53BP1 recruitment to DNA damage sites. The Embo Journal. 31: 1865-78. PMID 22373579 DOI: 10.1038/emboj.2012.47  0.64
2012 Yu Z, Vogel G, Coulombe Y, Dubeau D, Spehalski E, Hébert J, Ferguson DO, Masson JY, Richard S. The MRE11 GAR motif regulates DNA double-strand break processing and ATR activation. Cell Research. 22: 305-20. PMID 21826105 DOI: 10.1038/cr.2011.128  0.64
2011 Iijima T, Wu K, Witte H, Hanno-Iijima Y, Glatter T, Richard S, Scheiffele P. SAM68 regulates neuronal activity-dependent alternative splicing of neurexin-1. Cell. 147: 1601-14. PMID 22196734 DOI: 10.1016/j.cell.2011.11.028  0.64
2011 Ooi A, Wong JC, Petillo D, Roossien D, Perrier-Trudova V, Whitten D, Min BW, Tan MH, Zhang Z, Yang XJ, Zhou M, Gardie B, Molinié V, Richard S, Tan PH, et al. An antioxidant response phenotype shared between hereditary and sporadic type 2 papillary renal cell carcinoma. Cancer Cell. 20: 511-23. PMID 22014576 DOI: 10.1016/j.ccr.2011.08.024  0.64
2011 Bertolotto C, Lesueur F, Giuliano S, Strub T, de Lichy M, Bille K, Dessen P, d'Hayer B, Mohamdi H, Remenieras A, Maubec E, de la Fouchardière A, Molinié V, Vabres P, Dalle S, ... ... Richard S, et al. A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma. Nature. 480: 94-8. PMID 22012259 DOI: 10.1038/nature10539  0.64
2011 Thalappilly S, Feng X, Pastyryeva S, Suzuki K, Muruve D, Larocque D, Richard S, Truss M, von Deimling A, Riabowol K, Tallen G. The p53 tumor suppressor is stabilized by inhibitor of growth 1 (ING1) by blocking polyubiquitination. Plos One. 6: e21065. PMID 21731648 DOI: 10.1371/journal.pone.0021065  0.64
2011 Paronetto MP, Messina V, Barchi M, Geremia R, Richard S, Sette C. Sam68 marks the transcriptionally active stages of spermatogenesis and modulates alternative splicing in male germ cells Nucleic Acids Research. 39: 4961-4974. PMID 21355037 DOI: 10.1093/nar/gkr085  0.64
2011 Varela I, Tarpey P, Raine K, Huang D, Ong CK, Stephens P, Davies H, Jones D, Lin ML, Teague J, Bignell G, Butler A, Cho J, Dalgliesh GL, Galappaththige D, ... ... Richard S, et al. Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinoma. Nature. 469: 539-42. PMID 21248752 DOI: 10.1038/nature09639  0.64
2011 Peyre M, Gaillard S, van Effenterre R, Giraud S, Richard S. Conservative management of endolymphatic sac tumors in von Hippel-Lindau disease: case report. Acta Neurochirurgica. 153: 42-7; discussion 47. PMID 21103895 DOI: 10.1007/s00701-010-0873-5  0.64
2010 Klomp JA, Petillo D, Niemi NM, Dykema KJ, Chen J, Yang XJ, Sääf A, Zickert P, Aly M, Bergerheim U, Nordenskjöld M, Gad S, Giraud S, Denoux Y, Yonneau L, ... ... Richard S, et al. Birt-Hogg-Dubé renal tumors are genetically distinct from other renal neoplasias and are associated with up-regulation of mitochondrial gene expression. Bmc Medical Genomics. 3: 59. PMID 21162720 DOI: 10.1186/1755-8794-3-59  0.64
2010 Peyre M, David P, Van Effenterre R, François P, Thys M, Emery E, Redondo A, Decq P, Aghakhani N, Parker F, Tadié M, Lacroix C, Bhangoo R, Giraud S, Richard S, et al. Natural history of supratentorial hemangioblastomas in von Hippel-Lindau disease. Neurosurgery. 67: 577-87; discussion 5. PMID 20647972 DOI: 10.1227/01.NEU.0000374846.86409.A7  0.64
2010 Tan MH, Wong CF, Tan HL, Yang XJ, Ditlev J, Matsuda D, Khoo SK, Sugimura J, Fujioka T, Furge KA, Kort E, Giraud S, Ferlicot S, Vielh P, Amsellem-Ouazana D, ... ... Richard S, et al. Genomic expression and single-nucleotide polymorphism profiling discriminates chromophobe renal cell carcinoma and oncocytoma. Bmc Cancer. 10: 196. PMID 20462447 DOI: 10.1186/1471-2407-10-196  0.64
2010 Codreanu CM, Duet M, Hautefort C, Wassef M, Guichard JP, Giraud S, Richard S, Roqueplo AP, Tran Ba Huy P. Endolymphatic sac tumors in von Hippel-Lindau disease: report of three cases. Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology. 31: 660-4. PMID 20351605 DOI: 10.1097/MAO.0b013e3181d8d863  0.64
2010 Mai PL, Friedlander M, Tucker K, Phillips KA, Hogg D, Jewett MA, Lohynska R, Daugaard G, Richard S, Bonaïti-Pellié C, Heidenreich A, Albers P, Bodrogi I, Geczi L, Olah E, et al. The International Testicular Cancer Linkage Consortium: a clinicopathologic descriptive analysis of 461 familial malignant testicular germ cell tumor kindred. Urologic Oncology. 28: 492-9. PMID 19162511 DOI: 10.1016/j.urolonc.2008.10.004  0.64
2009 Larocque D, Fragoso G, Huang J, Mushynski WE, Loignon M, Richard S, Almazan G. The QKI-6 and QKI-7 RNA binding proteins block proliferation and promote Schwann cell myelination. Plos One. 4: e5867. PMID 19517016 DOI: 10.1371/journal.pone.0005867  0.64
2009 Lukong KE, Huot ME, Richard S. BRK phosphorylates PSF promoting its cytoplasmic localization and cell cycle arrest. Cellular Signalling. 21: 1415-22. PMID 19439179 DOI: 10.1016/j.cellsig.2009.04.008  0.64
2009 Hornemann T, Penno A, Richard S, Nicholson G, van Dijk FS, Rotthier A, Timmerman V, von Eckardstein A. A systematic comparison of all mutations in hereditary sensory neuropathy type I (HSAN I) reveals that the G387A mutation is not disease associated. Neurogenetics. 10: 135-43. PMID 19132419 DOI: 10.1007/s10048-008-0168-7  0.64
2002 Larocque D, Pilotte J, Chen T, Cloutier F, Massie B, Pedraza L, Couture R, Lasko P, Almazan G, Richard S. Nuclear retention of MBP mRNAs in the quaking viable mice. Neuron. 36: 815-29. PMID 12467586 DOI: 10.1016/S0896-6273(02)01055-3  0.64
2001 Pilotte J, Larocque D, Richard S. Nuclear translocation controlled by alternatively spliced isoforms inactivates the QUAKING apoptotic inducer Genes and Development. 15: 845-858. PMID 11297509 DOI: 10.1101/gad.860301  0.64
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