| Year |
Citation |
Score |
| 2020 |
Buffet A, Calsina B, Flores S, Giraud S, Lenglet M, Romanet P, Deflorenne E, Aller J, Bourdeau I, Bressac-de Paillerets B, Calatayud M, Dehais C, De Mones Del Pujol E, Elenkova A, Herman P, ... ... Richard S, et al. Germline mutations in the new E1' cryptic exon of the gene in patients with tumours of von Hippel-Lindau disease spectrum or with paraganglioma. Journal of Medical Genetics. PMID 31996412 DOI: 10.1136/Jmedgenet-2019-106519 |
0.304 |
|
| 2019 |
Hwang JW, Desterke C, Féraud O, Richard S, Ferlicot S, Verkarre V, Patard JJ, Loisel-Duwattez J, Foudi A, Griscelli F, Bennaceur-Griscelli A, Turhan AG. iPSC-Derived Embryoid Bodies as Models of c--Mutated Hereditary Papillary Renal Cell Carcinoma. International Journal of Molecular Sciences. 20. PMID 31575031 DOI: 10.3390/Ijms20194867 |
0.346 |
|
| 2019 |
Qiao X, Kim DI, Jun H, Ma Y, Knights AJ, Park MJ, Zhu K, Lipinski JH, Liao J, Li Y, Richard S, Weinman SA, Wu J. Protein arginine methyltransferase 1 interacts with PGC1α and modulates thermogenic fat activation. Endocrinology. PMID 31555811 DOI: 10.1210/En.2019-00504 |
0.302 |
|
| 2019 |
Guccione E, Richard S. The regulation, functions and clinical relevance of arginine methylation. Nature Reviews. Molecular Cell Biology. PMID 31350521 DOI: 10.1038/S41580-019-0155-X |
0.307 |
|
| 2019 |
Coppin L, Plouvier P, Crépin M, Jourdain AS, Yahya EA, Richard S, Paillerets BB, Cardot-Bauters C, Lejeune S, Leclerc J, Pigny P. Optimization of next-generation sequencing technologies for von Hippel Lindau (VHL) mosaic mutation detection and development of confirmation methods. The Journal of Molecular Diagnostics : Jmd. PMID 30731206 DOI: 10.1016/J.Jmoldx.2019.01.005 |
0.31 |
|
| 2019 |
Hwang JW, Desterke C, Feraud O, Richard S, Ferlicot S, Verkarre V, Patard JJ, Loisel-Duwattez J, Foudi A, Griscelli F, Griscelli AB, Turhan AG. Abstract 3688: iPSC-derived cancer organoids recapitulate genomic and phenotypic alterations of c-Met-mutated hereditary kidney cancer Cancer Research. 79: 3688-3688. DOI: 10.1158/1538-7445.Am2019-3688 |
0.347 |
|
| 2018 |
Chan LH, Zhou L, Ng KY, Wong TL, Lee TK, Sharma R, Loong JH, Ching YP, Yuan YF, Xie D, Lo CM, Man K, Artegiani B, Clevers H, Yan HH, ... ... Richard S, et al. PRMT6 Regulates RAS/RAF Binding and MEK/ERK-Mediated Cancer Stemness Activities in Hepatocellular Carcinoma through CRAF Methylation. Cell Reports. 25: 690-701.e8. PMID 30332648 DOI: 10.1016/J.Celrep.2018.09.053 |
0.302 |
|
| 2018 |
Gattolliat CH, Couvé S, Meurice G, Oréar C, Droin N, Chiquet M, Ferlicot S, Verkarre V, Vasiliu V, Molinié V, Méjean A, Dessen P, Giraud S, Bressac-De-Paillerets B, Gardie B, ... ... Richard S, et al. Integrative analysis of dysregulated microRNAs and mRNAs in multiple recurrent synchronized renal tumors from patients with von Hippel-Lindau disease. International Journal of Oncology. PMID 30066860 DOI: 10.3892/Ijo.2018.4490 |
0.318 |
|
| 2018 |
Gou Y, Li J, Jackson-Weaver O, Wu J, Zhang T, Gupta R, Cho I, Ho TV, Chen Y, Li M, Richard S, Wang J, Chai Y, Xu J. Protein Arginine Methyltransferase PRMT1 Is Essential for Palatogenesis. Journal of Dental Research. 22034518785164. PMID 29986157 DOI: 10.1177/0022034518785164 |
0.337 |
|
| 2018 |
Lenglet M, Robriquet F, Schwarz K, Camps C, Couturier A, Hoogewijs D, Buffet A, Knight SJ, Gad S, Couvé S, Chesnel F, Pacault M, Lindenbaum P, Job S, Dumont S, ... ... Richard S, et al. New lessons from an old gene: complex splicing and a novel cryptic exon in VHL gene cause erythrocytosis and VHL disease. Blood. PMID 29891534 DOI: 10.1182/Blood-2018-03-838235 |
0.352 |
|
| 2018 |
Vadnais C, Chen R, Fraszczak J, Yu Z, Boulais J, Pinder J, Frank D, Khandanpour C, Hébert J, Dellaire G, Côté JF, Richard S, Orthwein A, Drobetsky E, Möröy T. GFI1 facilitates efficient DNA repair by regulating PRMT1 dependent methylation of MRE11 and 53BP1. Nature Communications. 9: 1418. PMID 29651020 DOI: 10.1038/S41467-018-03817-5 |
0.318 |
|
| 2018 |
Muller M, Guillaud-Bataille M, Salleron J, Genestie C, Deveaux S, Slama A, de Paillerets BB, Richard S, Benusiglio PR, Ferlicot S. Pattern multiplicity and fumarate hydratase (FH)/S-(2-succino)-cysteine (2SC) staining but not eosinophilic nucleoli with perinucleolar halos differentiate hereditary leiomyomatosis and renal cell carcinoma-associated renal cell carcinomas from kidney tumors without FH gene alteration. Modern Pathology : An Official Journal of the United States and Canadian Academy of Pathology, Inc. PMID 29410489 DOI: 10.1038/S41379-018-0017-7 |
0.324 |
|
| 2017 |
Darbelli L, Choquet K, Richard S, Kleinman CL. Transcriptome profiling of mouse brains with qkI-deficient oligodendrocytes reveals major alternative splicing defects including self-splicing. Scientific Reports. 7: 7554. PMID 28790308 DOI: 10.1038/S41598-017-06211-1 |
0.353 |
|
| 2016 |
Li N, Richard S. Sam68 functions as a transcriptional coactivator of the p53 tumor suppressor. Nucleic Acids Research. PMID 27365047 DOI: 10.1093/Nar/Gkw582 |
0.321 |
|
| 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 |
0.339 |
|
| 2016 |
Darbelli L, Richard S. Emerging functions of the Quaking RNA-binding proteins and link to human diseases. Wiley Interdisciplinary Reviews. Rna. 7: 399-412. PMID 26991871 DOI: 10.1002/Wrna.1344 |
0.343 |
|
| 2015 |
Messai Y, Gad S, Noman MZ, Le Teuff G, Couve S, Janji B, Kammerer SF, Rioux-Leclerc N, Hasmim M, Ferlicot S, Baud V, Mejean A, Mole DR, Richard S, Eggermont AM, et al. Renal Cell Carcinoma Programmed Death-ligand 1, a New Direct Target of Hypoxia-inducible Factor-2 Alpha, is Regulated by von Hippel-Lindau Gene Mutation Status. European Urology. PMID 26707870 DOI: 10.1016/J.Eururo.2015.11.029 |
0.336 |
|
| 2015 |
Benusiglio PR, Couvé S, Gilbert-Dussardier B, Deveaux S, Le Jeune H, Da Costa M, Fromont G, Memeteau F, Yacoub M, Coupier I, Leroux D, Méjean A, Escudier B, Giraud S, Gimenez-Roqueplo AP, ... ... Richard S, et al. A germline mutation in PBRM1 predisposes to renal cell carcinoma. Journal of Medical Genetics. 52: 426-30. PMID 25911086 DOI: 10.1136/Jmedgenet-2014-102912 |
0.35 |
|
| 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 |
0.351 |
|
| 2014 |
Gardie B, Percy MJ, Hoogewijs D, Chowdhury R, Bento C, Arsenault PR, Richard S, Almeida H, Ewing J, Lambert F, McMullin MF, Schofield CJ, Lee FS. The role of PHD2 mutations in the pathogenesis of erythrocytosis. Hypoxia (Auckland, N.Z.). 2: 71-90. PMID 27774468 DOI: 10.2147/Hp.S54455 |
0.353 |
|
| 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 |
0.366 |
|
| 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 |
0.321 |
|
| 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 |
0.324 |
|
| 2014 |
Gardie B, Couvé S, Ladroue C, Laine E, Mahtouk K, Guégan J, Gad S, Le Jeune H, Lecomte B, Pagès J, Benusiglio P, Bressac-de Paillerets B, Feunteun J, Dessen P, Hermouet S, ... ... Richard S, et al. A Comprehensive Study of the VHL-R200W Chuvash Polycythemia Mutation Reveals a Gradual Dysregulation of the Hypoxia Pathway in Oncogenesis Blood. 124: 4020-4020. DOI: 10.1182/Blood.V124.21.4020.4020 |
0.359 |
|
| 2013 |
Bueno MTD, Richard S. SUMOylation negatively modulates target gene occupancy of the KDM5B, a histone lysine demethylase Epigenetics. 8: 1162-1175. PMID 23970103 DOI: 10.4161/Epi.26112 |
0.327 |
|
| 2013 |
van der Veer EP, de Bruin RG, Kraaijeveld AO, de Vries MR, Bot I, Pera T, Segers FM, Trompet S, van Gils JM, Roeten MK, Beckers CM, van Santbrink PJ, Janssen A, van Solingen C, Swildens J, ... ... Richard S, et al. Quaking, an RNA-binding protein, is a critical regulator of vascular smooth muscle cell phenotype. Circulation Research. 113: 1065-75. PMID 23963726 DOI: 10.1161/Circresaha.113.301302 |
0.339 |
|
| 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 |
0.322 |
|
| 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 |
0.344 |
|
| 2013 |
Richard S, Gardie B, Couvé S, Gad S. Von Hippel-Lindau: how a rare disease illuminates cancer biology. Seminars in Cancer Biology. 23: 26-37. PMID 22659535 DOI: 10.1016/J.Semcancer.2012.05.005 |
0.355 |
|
| 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 |
0.301 |
|
| 2012 |
Neault M, Mallette FA, Vogel G, Michaud-Levesque J, Richard S. Ablation of PRMT6 reveals a role as a negative transcriptional regulator of the p53 tumor suppressor. Nucleic Acids Research. 40: 9513-21. PMID 22904064 DOI: 10.1093/Nar/Gks764 |
0.315 |
|
| 2012 |
Speisky D, Duces A, Bièche I, Rebours V, Hammel P, Sauvanet A, Richard S, Bedossa P, Vidaud M, Murat A, Niccoli P, Scoazec JY, Ruszniewski P, Couvelard A. Molecular profiling of pancreatic neuroendocrine tumors in sporadic and Von Hippel-Lindau patients. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research. 18: 2838-49. PMID 22461457 DOI: 10.1158/1078-0432.Ccr-11-2759 |
0.309 |
|
| 2012 |
Huot MÉ, Vogel G, Zabarauskas A, Ngo CT, Coulombe-Huntington J, Majewski J, Richard S. The Sam68 STAR RNA-binding protein regulates mTOR alternative splicing during adipogenesis. Molecular Cell. 46: 187-99. PMID 22424772 DOI: 10.1016/J.Molcel.2012.02.007 |
0.317 |
|
| 2012 |
Tradewell ML, Yu Z, Tibshirani M, Boulanger MC, Durham HD, Richard S. Arginine methylation by PRMT1 regulates nuclear-cytoplasmic localization and toxicity of FUS/TLS harbouring ALS-linked mutations. Human Molecular Genetics. 21: 136-49. PMID 21965298 DOI: 10.1093/Hmg/Ddr448 |
0.318 |
|
| 2012 |
Ladroue C, Hoogewijs D, Gad S, Carcenac R, Storti F, Barrois M, Gimenez-Roqueplo AP, Leporrier M, Casadevall N, Hermine O, Kiladjian JJ, Baruchel A, Fakhoury F, Bressac-de Paillerets B, Feunteun J, ... ... Richard S, et al. Distinct deregulation of the hypoxia inducible factor by PHD2 mutants identified in germline DNA of patients with polycythemia. Haematologica. 97: 9-14. PMID 21933857 DOI: 10.3324/Haematol.2011.044644 |
0.355 |
|
| 2012 |
Ooi A, Whitten D, Yang XJ, Zhou M, Richard S, Teh BT, Furge KA. Abstract 1134: Fumarate activates NRF2 in tissues with fumarate hydratase mutation Cancer Research. 72: 1134-1134. DOI: 10.1158/1538-7445.Am2012-1134 |
0.331 |
|
| 2012 |
Varela I, Tarpey P, Raine K, Huang D, Ong CK, Stephens P, Davies H, Jones D, Lin M, Teague J, Bignell G, Butler A, Cho J, Dalgliesh GL, Galappaththige D, ... ... Richard S, et al. Erratum: Corrigendum: Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinoma Nature. 484: 130-130. DOI: 10.1038/Nature11027 |
0.305 |
|
| 2011 |
Huang J, Vogel G, Yu Z, Almazan G, Richard S. Type II arginine methyltransferase PRMT5 regulates gene expression of inhibitors of differentiation/DNA binding Id2 and Id4 during glial cell differentiation. The Journal of Biological Chemistry. 286: 44424-32. PMID 22041901 DOI: 10.1074/Jbc.M111.277046 |
0.321 |
|
| 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 |
0.357 |
|
| 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 |
0.36 |
|
| 2011 |
Joly D, Méjean A, Corréas JM, Timsit MO, Verkarre V, Deveaux S, Landais P, Grünfeld JP, Richard S. Progress in nephron sparing therapy for renal cell carcinoma and von Hippel-Lindau disease. The Journal of Urology. 185: 2056-60. PMID 21496837 DOI: 10.1016/J.Juro.2011.02.007 |
0.302 |
|
| 2011 |
Gavino C, Richard S. Patched1 haploinsufficiency impairs ependymal cilia function of the quaking viable mice, leading to fatal hydrocephalus Molecular and Cellular Neuroscience. 47: 100-107. PMID 21447392 DOI: 10.1016/J.Mcn.2011.03.004 |
0.306 |
|
| 2011 |
Gardie B, Remenieras A, Kattygnarath D, Bombled J, Lefèvre S, Perrier-Trudova V, Rustin P, Barrois M, Slama A, Avril MF, Bessis D, Caron O, Caux F, Collignon P, Coupier I, ... ... Richard S, et al. Novel FH mutations in families with hereditary leiomyomatosis and renal cell cancer (HLRCC) and patients with isolated type 2 papillary renal cell carcinoma. Journal of Medical Genetics. 48: 226-34. PMID 21398687 DOI: 10.1136/Jmg.2010.085068 |
0.342 |
|
| 2011 |
Maher ER, Neumann HP, Richard S. von Hippel-Lindau disease: a clinical and scientific review. European Journal of Human Genetics : Ejhg. 19: 617-23. PMID 21386872 DOI: 10.1038/Ejhg.2010.175 |
0.316 |
|
| 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 |
0.345 |
|
| 2011 |
Ooi A, Hm BW, Wong J, Perrier-Trudova V, Petillo D, Roossien D, Zhang Z, Tan M, Zhou M, Yang X, Richard S, Teh BT, Furge KA. Abstract 3820: Deregulation of KEAP1-NRF axis in phenotypically type 2 papillary renal cell carcinoma Cancer Research. 71: 3820-3820. DOI: 10.1158/1538-7445.Am2011-3820 |
0.348 |
|
| 2011 |
Varela I, Tarpey P, Raine K, Huang D, Ong CK, Stephens P, Davies H, Jones D, Lin M, Teague J, Bignell G, Butler A, Cho J, Dalgliesh GL, Galappaththige D, ... ... Richard S, et al. Abstract 2805: Exome sequencing identifies frequent mutation of the SWI/SNF complex genePBRM1in renal carcinoma Cancer Research. 71: 2805-2805. DOI: 10.1158/1538-7445.Am2011-2805 |
0.348 |
|
| 2010 |
Wang Y, Lacroix G, Haines J, Doukhanine E, Almazan G, Richard S. The QKI-6 RNA binding protein localizes with the MBP mRNAs in stress granules of glial cells. Plos One. 5. PMID 20862255 DOI: 10.1371/Journal.Pone.0012824 |
0.336 |
|
| 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 |
0.304 |
|
| 2010 |
Doukhanine E, Gavino C, Haines JD, Almazan G, Richard S. The QKI-6 RNA binding protein regulates actin-interacting protein-1 mRNA stability during oligodendrocyte differentiation. Molecular Biology of the Cell. 21: 3029-40. PMID 20631256 DOI: 10.1091/Mbc.E10-04-0305 |
0.341 |
|
| 2010 |
Marque M, Gardie B, Paillerets BBd, Rustin P, Guillot B, Richard S, Bessis D. Novel FH mutation in a patient with cutaneous leiomyomatosis associated with cutis verticis gyrata, eruptive collagenoma and Charcot-Marie-Tooth disease. British Journal of Dermatology. 163: 1337-1339. PMID 20560959 DOI: 10.1111/J.1365-2133.2010.09912.X |
0.354 |
|
| 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 |
0.311 |
|
| 2010 |
Vahteristo P, Koski TA, Näätsaari L, Kiuru M, Karhu A, Herva R, Sallinen SL, Vierimaa O, Björck E, Richard S, Gardie B, Bessis D, Van Glabeke E, Blanco I, Houlston R, et al. No evidence for a genetic modifier for renal cell cancer risk in HLRCC syndrome. Familial Cancer. 9: 245-51. PMID 20091131 DOI: 10.1007/S10689-009-9312-2 |
0.344 |
|
| 2010 |
Lim DH, Rehal PK, Nahorski MS, Macdonald F, Claessens T, Van Geel M, Gijezen L, Gille JJ, Giraud S, Richard S, van Steensel M, Menko FH, Maher ER. A new locus-specific database (LSDB) for mutations in the folliculin (FLCN) gene. Human Mutation. 31: E1043-51. PMID 19802896 DOI: 10.1002/Humu.21130 |
0.333 |
|
| 2010 |
Gardie B, Ladroue C, Carcenac R, Gad S, Barrois M, Bombled J, Hermine O, Leporrier M, Baruchel A, Jean-Claude K, Giraud S, Mazure N, Pouyssegur J, Richard S. Abstract 5011: Potential tumor suppressor role of PHD2 : functional study of mutations identified in germline DNA of patients with congenital polycythemia with or without paraganglioma Cancer Research. 70: 5011-5011. DOI: 10.1158/1538-7445.Am10-5011 |
0.384 |
|
| 2010 |
Lim DH, Rehal PK, Nahorski MS, Macdonald F, Claessens T, Geel MV, Gijezen L, Gille JJ, Giraud S, Richard S, Steensel MV, Menko F, Maher E. Abstract 1848: Folliculin (FLCN) sequence variants involved in Birt-Hogg-Dube syndrome Cancer Research. 70: 1848-1848. DOI: 10.1158/1538-7445.Am10-1848 |
0.334 |
|
| 2010 |
Koski TA, Vahteristo P, Näätsaari L, Kiuru M, Karhu A, Herva R, Sallinen S, Vierimaa O, Björck E, Richard S, Gardie B, Bessis D, Glabeke EV, Blanco I, Houlston R, et al. Abstract 1844: No evidence for genetic factor increasing renal cell cancer risk in Hereditary Leiomyomatosis and Renal Cell Cancer syndrome Cancer Research. 70: 1844-1844. DOI: 10.1158/1538-7445.Am10-1844 |
0.361 |
|
| 2009 |
Menko FH, van Steensel MA, Giraud S, Friis-Hansen L, Richard S, Ungari S, Nordenskjöld M, Hansen TV, Solly J, Maher ER. Birt-Hogg-Dubé syndrome: diagnosis and management. The Lancet. Oncology. 10: 1199-206. PMID 19959076 DOI: 10.1016/S1470-2045(09)70188-3 |
0.318 |
|
| 2009 |
Nicholson TB, Chen T, Richard S. The physiological and pathophysiological role of PRMT1-mediated protein arginine methylation. Pharmacological Research. 60: 466-74. PMID 19643181 DOI: 10.1016/J.Phrs.2009.07.006 |
0.33 |
|
| 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 |
0.337 |
|
| 2009 |
Michaud-Levesque J, Richard S. Thrombospondin-1 is a transcriptional repression target of PRMT6 Journal of Biological Chemistry. 284: 21338-21346. PMID 19509293 DOI: 10.1074/Jbc.M109.005322 |
0.353 |
|
| 2009 |
Galarneau A, Richard S. The STAR RNA binding proteins GLD-1, QKI, SAM68 and SLM-2 bind bipartite RNA motifs. Bmc Molecular Biology. 10: 47. PMID 19457263 DOI: 10.1186/1471-2199-10-47 |
0.325 |
|
| 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 |
0.311 |
|
| 2009 |
Paronetto MP, Messina V, Bianchi E, Barchi M, Vogel G, Moretti C, Palombi F, Stefanini M, Geremia R, Richard S, Sette C. Sam68 regulates translation of target mRNAs in male germ cells, necessary for mouse spermatogenesis. The Journal of Cell Biology. 185: 235-49. PMID 19380878 DOI: 10.1083/Jcb.200811138 |
0.326 |
|
| 2009 |
Yu Z, Chen T, Hébert J, Li E, Richard S. A mouse PRMT1 null allele defines an essential role for arginine methylation in genome maintenance and cell proliferation. Molecular and Cellular Biology. 29: 2982-96. PMID 19289494 DOI: 10.1128/Mcb.00042-09 |
0.324 |
|
| 2009 |
Périgny M, Hammel P, Corcos O, Larochelle O, Giraud S, Richard S, Sauvanet A, Belghiti J, Ruszniewski P, Bedossa P, Couvelard A. Pancreatic endocrine microadenomatosis in patients with von Hippel-Lindau disease: characterization by VHL/HIF pathway proteins expression. The American Journal of Surgical Pathology. 33: 739-48. PMID 19238077 DOI: 10.1097/Pas.0B013E3181967992 |
0.337 |
|
| 2009 |
Alexandre I, Billemont B, Meric JB, Richard S, Rixe O. Axitinib induces paradoxical erythropoietin synthesis in metastatic renal cell carcinoma. Journal of Clinical Oncology. 27: 472-473. PMID 19075253 DOI: 10.1200/Jco.2008.20.1087 |
0.313 |
|
| 2008 |
Ladroue C, Carcenac R, Leporrier M, Gad S, Le Hello C, Galateau-Salle F, Feunteun J, Pouysségur J, Richard S, Gardie B. PHD2 mutation and congenital erythrocytosis with paraganglioma. The New England Journal of Medicine. 359: 2685-92. PMID 19092153 DOI: 10.1056/Nejmoa0806277 |
0.367 |
|
| 2008 |
Woodward ER, Ricketts C, Killick P, Gad S, Morris MR, Kavalier F, Hodgson SV, Giraud S, Bressac-de Paillerets B, Chapman C, Escudier B, Latif F, Richard S, Maher ER. Familial non-VHL clear cell (conventional) renal cell carcinoma: clinical features, segregation analysis, and mutation analysis of FLCN. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research. 14: 5925-30. PMID 18794106 DOI: 10.1158/1078-0432.Ccr-08-0608 |
0.331 |
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| 2008 |
Zhang ZF, Matsuda D, Khoo SK, Buzzitta K, Block E, Petillo D, Richard S, Anema J, Furge KA, Teh BT. A comparison study reveals important features of agreement and disagreement between summarized DNA and RNA data obtained from renal cell carcinoma. Mutation Research. 657: 77-83. PMID 18790077 DOI: 10.1016/J.Mrgentox.2008.08.009 |
0.327 |
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| 2008 |
Frew IJ, Minola A, Georgiev S, Hitz M, Moch H, Richard S, Vortmeyer AO, Krek W. Combined VHLH and PTEN mutation causes genital tract cystadenoma and squamous metaplasia. Molecular and Cellular Biology. 28: 4536-48. PMID 18474617 DOI: 10.1128/Mcb.02132-07 |
0.332 |
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| 2008 |
Yadav N, Cheng D, Richard S, Morel M, Iyer VR, Aldaz CM, Bedford MT. CARM1 promotes adipocyte differentiation by coactivating PPARgamma. Embo Reports. 9: 193-8. PMID 18188184 DOI: 10.1038/Sj.Embor.7401151 |
0.312 |
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| 2008 |
Iberg AN, Espejo A, Cheng D, Kim D, Michaud-Levesque J, Richard S, Bedford MT. Arginine methylation of the histone H3 tail impedes effector binding. The Journal of Biological Chemistry. 283: 3006-10. PMID 18077460 DOI: 10.1074/Jbc.C700192200 |
0.303 |
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| 2008 |
Lukong KE, Richard S. Breast tumor kinase BRK requires kinesin-2 subunit KAP3A in modulation of cell migration. Cellular Signalling. 20: 432-42. PMID 18077133 DOI: 10.1016/J.Cellsig.2007.11.003 |
0.31 |
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| 2008 |
Chénard CA, Richard S. New implications for the QUAKING RNA binding protein in human disease Journal of Neuroscience Research. 86: 233-242. PMID 17787018 DOI: 10.1002/Jnr.21485 |
0.314 |
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| 2008 |
Rad FH, Ulusakarya A, Gad S, Sibony M, Juin F, Richard S, Machover D, Uzan G. Novel somatic mutations of the VHL gene in an erythropoietin‐producing renal carcinoma associated with secondary polycythemia and elevated circulating endothelial progenitor cells American Journal of Hematology. 83: 155-158. PMID 17696210 DOI: 10.1002/Ajh.21019 |
0.362 |
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| 2007 |
Charbotel B, Gad S, Caïola D, Béroud C, Fevotte J, Bergeret A, Ferlicot S, Richard S. Trichloroethylene exposure and somatic mutations of the VHL gene in patients with Renal Cell Carcinoma Journal of Occupational Medicine and Toxicology. 2: 13-13. PMID 17997830 DOI: 10.1186/1745-6673-2-13 |
0.326 |
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| 2007 |
Lukong KE, Richard S. Targeting the RNA-binding protein Sam68 as a treatment for cancer? Future Oncology (London, England). 3: 539-44. PMID 17927519 DOI: 10.2217/14796694.3.5.539 |
0.346 |
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| 2007 |
Xie B, Invernizzi CF, Richard S, Wainberg MA. Arginine methylation of the human immunodeficiency virus type 1 Tat protein by PRMT6 negatively affects Tat Interactions with both cyclin T1 and the Tat transactivation region. Journal of Virology. 81: 4226-34. PMID 17267505 DOI: 10.1128/Jvi.01888-06 |
0.304 |
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| 2007 |
Gad S, Lefèvre SH, Khoo SK, Giraud S, Vieillefond A, Vasiliu V, Ferlicot S, Molinié V, Denoux Y, Thiounn N, Chrétien Y, Méjean A, Zerbib M, Benoît G, Hervé JM, ... ... Richard S, et al. Mutations in BHD and TP53 genes, but not in HNF1beta gene, in a large series of sporadic chromophobe renal cell carcinoma. British Journal of Cancer. 96: 336-40. PMID 17133269 DOI: 10.1038/Sj.Bjc.6603492 |
0.341 |
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| 2006 |
Tremblay GA, Richard S. mRNAs associated with the Sam68 RNA binding protein. Rna Biology. 3: 90-3. PMID 17179751 DOI: 10.4161/Rna.3.2.3204 |
0.312 |
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| 2005 |
Larocque D, Richard S. QUAKING KH domain proteins as regulators of glial cell fate and myelination Rna Biology. 2: 37-40. PMID 17132940 DOI: 10.4161/Rna.2.2.1603 |
0.338 |
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| 2005 |
Richard S, Morel M, Cléroux P. Arginine methylation regulates IL-2 gene expression: a role for protein arginine methyltransferase 5 (PRMT5) Biochemical Journal. 388: 379-386. PMID 15654770 DOI: 10.1042/Bj20040373 |
0.32 |
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| 2005 |
Larocque D, Galarneau A, Liu HN, Scott M, Almazan G, Richard S. Protection of p27(Kip1) mRNA by quaking RNA binding proteins promotes oligodendrocyte differentiation. Nature Neuroscience. 8: 27-33. PMID 15568022 DOI: 10.1038/Nn1359 |
0.343 |
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| 2004 |
Haegebarth A, Heap D, Bie W, Derry JJ, Richard S, Tyner AL. The nuclear tyrosine kinase BRK/Sik phosphorylates and inhibits the RNA-binding activities of the Sam68-like mammalian proteins SLM-1 and SLM-2. The Journal of Biological Chemistry. 279: 54398-404. PMID 15471878 DOI: 10.1074/Jbc.M409579200 |
0.344 |
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| 2004 |
Gallou C, Chauveau D, Richard S, Joly D, Giraud S, Olschwang S, Martin N, Saquet C, Chrétien Y, Méjean A, Correas JM, Benoît G, Colombeau P, Grünfeld JP, Junien C, et al. Genotype-phenotype correlation in von Hippel-Lindau families with renal lesions. Human Mutation. 24: 215-24. PMID 15300849 DOI: 10.1002/Humu.20082 |
0.351 |
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| 2004 |
Rapley EA, Hockley S, Warren W, Johnson L, Huddart R, Crockford G, Forman D, Leahy MG, Oliver DT, Tucker K, Friedlander M, Phillips KA, Hogg D, Jewett MA, Lohynska R, ... ... Richard S, et al. Somatic mutations of KIT in familial testicular germ cell tumours. British Journal of Cancer. 90: 2397-401. PMID 15150569 DOI: 10.1038/Sj.Bjc.6601880 |
0.32 |
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| 2004 |
Kim J, Lee J, Yadav N, Wu Q, Carter C, Richard S, Richie E, Bedford MT. Loss of CARM1 results in hypomethylation of thymocyte cyclic AMP-regulated phosphoprotein and deregulated early T cell development. The Journal of Biological Chemistry. 279: 25339-44. PMID 15096520 DOI: 10.1074/Jbc.M402544200 |
0.322 |
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| 2004 |
Richard S, Graff J, Lindau J, Resche F. Von Hippel-Lindau disease. The Lancet. 363: 1231-1234. PMID 15081659 DOI: 10.1016/S0140-6736(04)15957-6 |
0.302 |
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| 2004 |
Boulanger MC, Miranda TB, Clarke S, Di Fruscio M, Suter B, Lasko P, Richard S. Characterization of the Drosophila protein arginine methyltransferases DART1 and DART4. The Biochemical Journal. 379: 283-9. PMID 14705965 DOI: 10.1042/Bj20031176 |
0.334 |
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| 2003 |
Richard S. von Hippel-Lindau disease: Recent advances and therapeutic perspectives Expert Review of Anticancer Therapy. 3: 215-233. PMID 12722881 DOI: 10.1586/14737140.3.2.215 |
0.364 |
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| 2003 |
Di Fruscio M, Styhler S, Wikholm E, Boulanger MC, Lasko P, Richard S. Kep1 interacts genetically with dredd/caspase-8, and kep1 mutants alter the balance of dredd isoforms. Proceedings of the National Academy of Sciences of the United States of America. 100: 1814-9. PMID 12563030 DOI: 10.1073/Pnas.0236048100 |
0.318 |
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| 2002 |
Boisvert FM, Cote J, Boulanger MC, Cleroux P, Bachand F, Autexier C, Richard S. Symmetrical dimethylarginine methylation is required for the localization of SMN in Cajal bodies and pre-mRNA splicing. The Journal of Cell Biology. 159: 957-69. PMID 12486110 DOI: 10.1083/Jcb.200207028 |
0.31 |
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| 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 |
0.748 |
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| 2002 |
Bachand F, Boisvert FM, Côté J, Richard S, Autexier C. The product of the survival of motor neuron (SMN) gene is a human telomerase-associated protein. Molecular Biology of the Cell. 13: 3192-202. PMID 12221125 DOI: 10.1091/Mbc.E02-04-0216 |
0.317 |
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| 2002 |
Chauveau D, Burckle C, Béroud C, Correas J, Duclos J, Michel P, Richard S, Grünfeld J. Diagnosis of pheochromocytoma and laparoscopic adrenalectomy in two anephric patients with von hippel-lindau disease American Journal of Kidney Diseases. 39. PMID 11840397 DOI: 10.1053/Ajkd.2002.30571 |
0.302 |
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| 2001 |
Chen T, Côté J, Carvajal HV, Richard S. Identification of Sam68 arginine glycine-rich sequences capable of conferring nonspecific RNA binding to the GSG domain. Journal of Biological Chemistry. 276: 30803-30811. PMID 11395494 DOI: 10.1074/Jbc.M102247200 |
0.302 |
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| 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 |
0.743 |
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| 2000 |
Levy M, Richard S. Attitudes of von Hippel-Lindau disease patients towards presymptomatic genetic diagnosis in children and prenatal diagnosis Journal of Medical Genetics. 37: 476-478. PMID 10928862 DOI: 10.1136/Jmg.37.6.476 |
0.315 |
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| 2000 |
Derry JJ, Richard S, Valderrama Carvajal H, Ye X, Vasioukhin V, Cochrane AW, Chen T, Tyner AL. Sik (BRK) phosphorylates Sam68 in the nucleus and negatively regulates its RNA binding ability. Molecular and Cellular Biology. 20: 6114-26. PMID 10913193 DOI: 10.1128/Mcb.20.16.6114-6126.2000 |
0.311 |
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| 2000 |
Richard S, David P, Marsot-Dupuch K, Giraud S, Béroud C, Resche F. Central nervous system hemangioblastomas, endolymphatic sac tumors, and von Hippel-Lindau disease. Neurosurgical Review. 23: 1-22. PMID 10809480 DOI: 10.1007/S101430050024 |
0.33 |
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| 1999 |
Chen T, Boisvert FM, Bazett-Jones DP, Richard S. A role for the GSG domain in localizing Sam68 to novel nuclear structures in cancer cell lines Molecular Biology of the Cell. 10: 3015-3033. PMID 10473643 DOI: 10.1091/Mbc.10.9.3015 |
0.337 |
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| 1999 |
Gallou C, Joly D, Méjean A, Staroz F, Martin N, Tarlet G, Orfanelli MT, Bouvier R, Droz D, Chrétien Y, Maréchal JM, Richard S, Junien C, Béroud C. Mutations of the VHL gene in sporadic renal cell carcinoma: definition of a risk factor for VHL patients to develop an RCC. Human Mutation. 13: 464-75. PMID 10408776 DOI: 10.1002/(Sici)1098-1004(1999)13:6<464::Aid-Humu6>3.0.Co;2-A |
0.327 |
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| 1999 |
Schmidt L, Junker K, Nakaigawa N, Kinjerski T, Weirich G, Miller M, Lubensky I, Neumann HP, Brauch H, Decker J, Vocke C, Brown JA, Jenkins R, Richard S, Bergerheim U, et al. Novel mutations of the MET proto-oncogene in papillary renal carcinomas Oncogene. 18: 2343-2350. PMID 10327054 DOI: 10.1038/Sj.Onc.1202547 |
0.332 |
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| 1999 |
Fruscio MD, Chen T, Richard S. Characterization of Sam68-like mammalian proteins SLM-1 and SLM-2: SLM-1 is a Src substrate during mitosis Proceedings of the National Academy of Sciences of the United States of America. 96: 2710-2715. PMID 10077576 DOI: 10.1073/Pnas.96.6.2710 |
0.313 |
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| 1999 |
Aarts MM, Levy D, He B, Stregger S, Chen T, Richard S, Henderson JE. Parathyroid hormone-related protein interacts with RNA. The Journal of Biological Chemistry. 274: 4832-8. PMID 9988723 DOI: 10.1074/Jbc.274.8.4832 |
0.328 |
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| 1998 |
Olschwang S, Richard S, Boisson C, Giraud S, Laurent-Puig P, Resche F, Thomas G. Germline mutation profile of the VHL gene in von Hippel-Lindau disease and in sporadic hemangioblastoma Human Mutation. 12: 424-430. PMID 9829912 DOI: 10.1002/(Sici)1098-1004(1998)12:6<424::Aid-Humu9>3.0.Co;2-H |
0.348 |
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| 1998 |
Di Fruscio M, Chen T, Bonyadi S, Lasko P, Richard S. The identification of two Drosophila K homology domain proteins. Kep1 and SAM are members of the Sam68 family of GSG domain proteins. The Journal of Biological Chemistry. 273: 30122-30. PMID 9804767 DOI: 10.1074/Jbc.273.46.30122 |
0.316 |
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| 1998 |
Chen T, Richard S. Structure-function analysis of Qk1: A lethal point mutation in mouse quaking prevents homodimerization Molecular and Cellular Biology. 18: 4863-4871. PMID 9671495 DOI: 10.1128/Mcb.18.8.4863 |
0.33 |
|
| 1998 |
Saffman EE, Styhler S, Rother K, Li W, Richard S, Lasko P. Premature translation of oskar in oocytes lacking the RNA-binding protein bicaudal-C. Molecular and Cellular Biology. 18: 4855-62. PMID 9671494 DOI: 10.1128/Mcb.18.8.4855 |
0.322 |
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| 1998 |
Schmidt L, Duh F-, Chen F, Kishida T, Glenn G, Choyke P, Scherer SW, Zhuang Z, Lubensky I, Dean M, Allikmets R, Chidambaram A, Bergerheim UR, Feltis JT, Casadevall C, ... ... Richard S, et al. Germline and Somatic Mutations in the Tyrosine Kinase Domain of the MET Proto-Oncogene in Papillary Renal Carcinomas The Journal of Urology. 159: 619-619. DOI: 10.1016/S0022-5347(01)63909-0 |
0.304 |
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| 1997 |
Schmidt L, Duh FM, Chen F, Kishida T, Glenn G, Choyke P, Scherer SW, Zhuang Z, Lubensky I, Dean M, Allikmets R, Chidambaram A, Bergerheim UR, Feltis JT, Casadevall C, ... ... Richard S, et al. Germline and somatic mutations in the tyrosine kinase domain of the MET proto-oncogene in papillary renal carcinomas. Nature Genetics. 16: 68-73. PMID 9140397 DOI: 10.1038/Ng0597-68 |
0.344 |
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| 1996 |
Zbar B, Kishida T, Chen F, Schmidt L, Maher ER, Richards FM, Crossey PA, Webster AR, Affara NA, Ferguson-Smith MA, Brauch H, Glavac D, Neumann HP, Tisherman S, Mulvihill JJ, ... ... Richard S, et al. Germline mutations in the Von Hippel-Lindau disease (VHL) gene in families from North America, Europe, and Japan. Human Mutation. 8: 348-57. PMID 8956040 DOI: 10.1002/(Sici)1098-1004(1996)8:4<348::Aid-Humu8>3.0.Co;2-3 |
0.315 |
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| 1994 |
Richard S, Beigelman C, Duclos J, Fendler J, Plauchu H, Plouin P, Resche F, Schlumberger M, Vermesse B, Proye C. Pheochromocytoma as the first manifestation of von Hippel-Lindau disease. Surgery. 116: 1076-1081. DOI: 10.5555/Uri:Pii:0039606094903077 |
0.302 |
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| 1991 |
Richard S, Zingg HH. Identification of cis-acting regulatory elements in the human oxytocin gene promoter Molecular and Cellular Neuroscience. 2: 501-510. DOI: 10.1016/1044-7431(91)90017-I |
0.302 |
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