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Simon Papillon-Cavanagh

Bristol-Myers Squibb
H指数:19
被引数:3,885

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荣誉奖项

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H3K27M induces defective chromatin spread of PRC2-mediated repressive H3K27me2/me3 and is essential for glioma tumorigenesis
NATURE COMMUNICATIONS
IF15.7
2019-03-19245
OAAI
Harutyunyan, Ashot S.; Krug, Brian; Chen, Haifen; Papillon-Cavanagh, Simon; Zeinieh, Michele; De Jay, Nicolas; Deshmukh, Shriya; Chen, Carol C. L.; Belle, Jad; Mikael, Leonie G.; Marchione, Dylan M.; Li, Rui; Nikbakht, Hamid; Hu, Bo; Cagnone, Gael; Cheung, Warren A.; Mohammadnia, Abdulshakour; Bechet, Denise; Faury, Damien; McConechy, Melissa K.; Pathania, Manav; Jain, Siddhant U.; Ellezam, Benjamin; Weil, Alexander G.; Montpetit, Alexandre; Salomoni, Paolo; Pastinen, Tomi; Lu, Chao; Lewis, Peter W.; Garcia, Benjamin A.; Kleinman, Claudia L.; Jabado, Nada; Majewski, Jacek
Spatial heterogeneity in medulloblastoma
NATURE GENETICS
IF31.8
2017-04-10112
OAAI
Morrissy, A. Sorana; Cavalli, Florence M. G.; Remke, Marc; Ramaswamy, Vijay; Shih, David J. H.; Holgado, Borja L.; Farooq, Hamza; Donovan, Laura K.; Garzia, Livia; Agnihotri, Sameer; Kiehna, Erin N.; Mercier, Eloi; Mayoh, Chelsea; Papillon-Cavanagh, Simon; Nikbakht, Hamid; Gayden, Tenzin; Torchia, Jonathon; Picard, Daniel; Merino, Diana M.; Vladoiu, Maria; Luu, Betty; Wu, Xiaochong; Daniels, Craig; Horswell, Stuart; Thompson, Yuan Yao; Hovestadt, Volker; Northcott, Paul A.; Jones, David T. W.; Peacock, John; Wang, Xin; Mack, Stephen C.; Reimand, Juri; Albrecht, Steffen; Fontebasso, Adam M.; Thiessen, Nina; Li, Yisu; Schein, Jacqueline E.; Lee, Darlene; Carlsen, Rebecca; Mayo, Michael; Tse, Kane; Tam, Angela; Dhalla, Noreen; Ally, Adrian; Chuah, Eric; Cheng, Young; Plettner, Patrick; Li, Haiyan I.; Corbett, Richard D.; Wong, Tina; Long, William; Loukides, James; Buczkowicz, Pawel; Hawkins, Cynthia E.; Tabori, Uri; Rood, Brian R.; Myseros, John S.; Packer, Roger J.; Korshunov, Andrey; Lichter, Peter; Kool, Marcel; Pfister, Stefan M.; Schueller, Ulrich; Dirks, Peter; Huang, Annie; Bouffet, Eric; Rutka, James T.; Bader, Gary D.; Swanton, Charles; Ma, Yusanne; Moore, Richard A.; Mungall, Andrew J.; Majewski, Jacek; Jones, Steven J. M.; Das, Sunit; Malkin, David; Jabado, Nada; Marra, Marco A.; Taylor, Michael D.
Impaired H3K36 methylation defines a subset of head and neck squamous cell carcinomas
NATURE GENETICS
IF31.8
2017-01-09219
OAAI
Papillon-Cavanagh, Simon; Lu, Chao; Gayden, Tenzin; Mikael, Leonie G.; Bechet, Denise; Karamboulas, Christina; Ailles, Laurie; Karamchandani, Jason; Marchione, Dylan M.; Garcia, Benjamin A.; Weinreb, Ilan; Goldstein, David; Lewis, Peter W.; Dancu, Octavia Maria; Dhaliwal, Sandeep; Stecho, William; Howlett, Christopher J.; Mymryk, Joe S.; Barrett, John W.; Nichols, Anthony C.; Allis, C. David; Majewski, Jacek; Jabado, Nada
Spatial and temporal homogeneity of driver mutations in diffuse intrinsic pontine glioma
NATURE COMMUNICATIONS
IF15.7
2016-04-06207
OAAI
Nikbakht, Hamid; Panditharatna, Eshini; Mikael, Leonie G.; Li, Rui; Gayden, Tenzin; Osmond, Matthew; Ho, Cheng-Ying; Kambhampati, Madhuri; Hwang, Eugene I.; Faury, Damien; Siu, Alan; Papillon-Cavanagh, Simon; Bechet, Denise; Ligon, Keith L.; Ellezam, Benjamin; Ingram, Wendy J.; Stinson, Caedyn; Moore, Andrew S.; Warren, Katherine E.; Karamchandani, Jason; Packer, Roger J.; Jabado, Nada; Majewski, Jacek; Nazarian, Javad
Mutation in The Nuclear-Encoded Mitochondrial Isoleucyl-tRNA Synthetase IARS2 in Patients with Cataracts, Growth Hormone Deficiency with Short Stature, Partial Sensorineural Deafness, and Peripheral Neuropathy or with Leigh Syndrome (vol 35, pg 1285, 2014)
HUMAN MUTATION
IF3.7
2015-02-041
PREAI
Schwartzentruber, Jeremy; Buhas, Daniela; Majewski, Jacek; Sasarman, Florin; Papillon-Cavanagh, Simon; Thiffault, Isabelle; Sheldon, Katherine M.; Massicotte, Christine; Patry, Lysanne; Simon, Mariella; Zare, Amir S.; McKernan, Kevin J.; Michaud, Jacques; Boles, Richard G.; Deal, Cheri L.; Desilets, Valerie; Shoubridge, Eric A.; Samuels, Mark E.
Mutation in The Nuclear-Encoded Mitochondrial Isoleucyl-tRNA Synthetase IARS2 in Patients with Cataracts, Growth Hormone Deficiency with Short Stature, Partial Sensorineural Deafness, and Peripheral Neuropathy or with Leigh Syndrome
HUMAN MUTATION
IF3.7
2014-10-1878
PREAI
Schwartzentruber, Jeremy; Buhas, Daniela; Majewski, Jacek; Sasarman, Florin; Papillon-Cavanagh, Simon; Thiffaut, Isabelle; Sheldon, Katherine M.; Massicotte, Christine; Patry, Lysanne; Simon, Mariella; Zare, Amir S.; McKernan, Kevin J.; Michaud, Jacques; Boles, Richard G.; Deal, Cheri L.; Desilets, Valerie; Shoubridge, Eric A.; Samuels, Mark E.
Recurrent somatic mutations in ACVR1 in pediatric midline high-grade astrocytoma
NATURE GENETICS
IF31.8
2014-04-06389
OAAI
Fontebasso, Adam M.; Papillon-Cavanagh, Simon; Schwartzentruber, Jeremy; Nikbakht, Hamid; Gerges, Noha; Fisett, Pierre-Olivier; Bechet, Denise; Faury, Damien; De Jay, Nicolas; Ramkissoon, Lori A.; Corcoran, Aoife; Jones, David T. W.; Sturm, Dominik; Johann, Pascal; Tomita, Tadanori; Goldman, Stewart; Nagib, Mahmoud; Bendel, Anne; Goumnerova, Liliana; Bowers, Daniel C.; Leonard, Jeffrey R.; Rubin, Joshua B.; Alden, Tord; Browd, Samuel; Geyer, J. Russell; Leary, Sarah; Jallo, George; Cohen, Kenneth; Gupta, Nalin; Prados, Michael D.; Carret, Anne-Sophie; Ellezam, Benjamin; Crevier, Louis; Klekner, Almos; Bognar, Laszlo; Hauser, Peter; Garami, Miklos; Myseros, John; Dong, Zhifeng; Siege, Peter M.; Malkin, Hay Ley; Ligon, Azra H.; Albrecht, Steffen; Pfister, Stefan M.; Ligon, Keith L.; Majewski, Jacek; Jabado, Nada; Kieran, Mark W.
Fusion of TTYH1 with the C19MC microRNA cluster drives expression of a brain-specific DNMT3B isoform in the embryonal brain tumor ETMR
NATURE GENETICS
IF31.8
2013-12-08165
PREAI
Kleinman, Claudia L.; Gerges, Noha; Papillon-Cavanagh, Simon; Sin-Chan, Patrick; Pramatarova, Albena; Quang, Dong-Anh Khuong; Adoue, Veronique; Busche, Stephan; Caron, Maxime; Djambazian, Haig; Bemmo, Amandine; Fontebasso, Adam M.; Spence, Tara; Schwartzentruber, Jeremy; Albrecht, Steffen; Hauser, Peter; Garami, Miklos; Klekner, Almos; Bognar, Laszlo; Montes, Jose-Luis; Staffa, Alfredo; Montpetit, Alexandre; Berube, Pierre; Zakrzewska, Magdalena; Zakrzewski, Krzysztof; Liberski, Pawel P.; Dong, Zhifeng; Siegel, Peter M.; Duchaine, Thomas; Perotti, Christian; Fleming, Adam; Faury, Damien; Remke, Marc; Gallo, Marco; Dirks, Peter; Taylor, Michael D.; Sladek, Robert; Pastinen, Tomi; Chan, Jennifer A.; Huang, Annie; Majewski, Jacek; Jabado, Nada
Mutations in C5ORF42 Cause Joubert Syndrome in the French Canadian Population
AMERICAN JOURNAL OF HUMAN GENETICS
IF8.1
2012-04-01121
OAAI
Srour, Myriam; Schwartzentruber, Jeremy; Hamdan, Fadi F.; Ospina, Luis H.; Patry, Lysanne; Labuda, Damian; Massicotte, Christine; Dobrzeniecka, Sylvia; Capo-Chichi, Jose-Mario; Papillon-Cavanagh, Simon; Samuels, Mark E.; Boycott, Kym M.; Shevell, Michael I.; Laframboise, Rachel; Desilets, Valerie; Maranda, Bruno; Rouleau, Guy A.; Majewski, Jacek; Michaud, Jacques L.

研究方向

暂未获取到该数据
J
Jacek Majewski
H 指数:93论文数:461被引数:3.2万
N
Nada Jabado
H 指数:107论文数:801被引数:4.8万
T
Tenzin Gayden
H 指数:27论文数:82被引数:3,308
A
Alice M. Walsh
H 指数:17论文数:69被引数:2,021
H
Hamid Nikbakht
H 指数:17论文数:47被引数:4,172
J
Jeremy Schwartzentruber
H 指数:64论文数:178被引数:2.2万
D
Damien Faury
H 指数:30论文数:227被引数:1.1万
M
Mark E. Samuels
H 指数:31论文数:70被引数:3,868
L
Leonie G. Mikael
H 指数:25论文数:106被引数:3,336
D
Denise Béchet
H 指数:16论文数:72被引数:3,097