A citation-based method for searching scientific literature

Hanna T Gazda, Mee Rie Sheen, Adrianna Vlachos, Valerie Choesmel, Marie-Françoise O'Donohue, Hal Schneider, Natasha Darras, Catherine Hasman, Colin A Sieff, Peter E Newburger, Sarah E Ball, Edyta Niewiadomska, Michal Matysiak, Jan M Zaucha, Bertil Glader, Charlotte Niemeyer, Joerg J Meerpohl, Eva Atsidaftos, Jeffrey M Lipton, Pierre-Emmanuel Gleizes, Alan H Beggs. Am J Hum Genet 2008
Times Cited: 281



Nenad Ban, Roland Beckmann, Jamie H D Cate, Jonathan D Dinman, François Dragon, Steven R Ellis, Denis L J Lafontaine, Lasse Lindahl, Anders Liljas, Jeffrey M Lipton, Michael A McAlear, Peter B Moore, Harry F Noller, Joaquin Ortega, Vikram Govind Panse, V Ramakrishnan, Christian M T Spahn, Thomas A Steitz, Marek Tchorzewski, David Tollervey, Alan J Warren, James R Williamson, Daniel Wilson, Ada Yonath, Marat Yusupov. Curr Opin Struct Biol 2014
Times Cited: 312




List of shared articles



Times cited

The Use of B-Cell Polysome Profiling to Validate Novel RPL5 (uL18) and RPL26 (uL24) Variants in Diamond-Blackfan Anemia.
Alexander Ludlow, Nicholas George, Megan Glassford, Katie Udenberg, Mark C Hannibal, Carla Schwalm, Katie Scott, Thomas L Rothstein, Sharon A Singh. J Pediatr Hematol Oncol 2021
0

Biallelic splicing variants in the nucleolar 60S assembly factor RBM28 cause the ribosomopathy ANE syndrome.
Carson J Bryant, Cláudia F Lorea, Hiram Larangeira de Almeida, Letícia Weinert, Leonardo Vedolin, Filippo Pinto E Vairo, Susan J Baserga. Proc Natl Acad Sci U S A 2021
1

Hallmarks of ribosomopathies.
Kim R Kampen, Sergey O Sulima, Stijn Vereecke, Kim De Keersmaecker. Nucleic Acids Res 2020
27

Ribosomal protein gene RPL9 variants can differentially impair ribosome function and cellular metabolism.
Marco Lezzerini, Marianna Penzo, Marie-Françoise O'Donohue, Carolina Marques Dos Santos Vieira, Manon Saby, Hyung L Elfrink, Illja J Diets, Anne-Marie Hesse, Yohann Couté, Marc Gastou,[...]. Nucleic Acids Res 2020
7

Sequence variation, common tissue expression patterns and learning models: a genome-wide survey of vertebrate ribosomal proteins.
Konstantinos A Kyritsis, Christos A Ouzounis, Lefteris Angelis, Ioannis S Vizirianakis. NAR Genom Bioinform 2020
0

Rare ribosomopathies: insights into mechanisms of cancer.
Anna Aspesi, Steven R Ellis. Nat Rev Cancer 2019
35

Maternal Ribosomes Are Sufficient for Tissue Diversification during Embryonic Development in C. elegans.
Elif Sarinay Cenik, Xuefeng Meng, Ngang Heok Tang, Richard Nelson Hall, Joshua A Arribere, Can Cenik, Yishi Jin, Andrew Fire. Dev Cell 2019
10


The GAIT translational control system.
Abul Arif, Peng Yao, Fulvia Terenzi, Jie Jia, Partho Sarothi Ray, Paul L Fox. Wiley Interdiscip Rev RNA 2018
21

Recurring mutations in RPL15 are linked to hydrops fetalis and treatment independence in Diamond-Blackfan anemia.
Marcin W Wlodarski, Lydie Da Costa, Marie-Françoise O'Donohue, Marc Gastou, Narjesse Karboul, Nathalie Montel-Lehry, Ina Hainmann, Dominika Danda, Amina Szvetnik, Victor Pastor,[...]. Haematologica 2018
5


Novel and known ribosomal causes of Diamond-Blackfan anaemia identified through comprehensive genomic characterisation.
Lisa Mirabello, Payal P Khincha, Steven R Ellis, Neelam Giri, Seth Brodie, Settara C Chandrasekharappa, Frank X Donovan, Weiyin Zhou, Belynda D Hicks, Joseph F Boland,[...]. J Med Genet 2017
55

How Ribosomes Translate Cancer.
Sergey O Sulima, Isabel J F Hofman, Kim De Keersmaecker, Jonathan D Dinman. Cancer Discov 2017
74