A citation-based method for searching scientific literature

Andrew J Finch, Christine Hilcenko, Nicolas Basse, Lesley F Drynan, Beatriz Goyenechea, Tobias F Menne, Africa González Fernández, Paul Simpson, Clive S D'Santos, Mark J Arends, Jean Donadieu, Christine Bellanné-Chantelot, Michael Costanzo, Charles Boone, Andrew N McKenzie, Stefan M V Freund, Alan J Warren. Genes Dev 2011
Times Cited: 175







List of co-cited articles
1027 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Synchronizing nuclear import of ribosomal proteins with ribosome assembly.
Dieter Kressler, Gert Bange, Yutaka Ogawa, Goran Stjepanovic, Bettina Bradatsch, Dagmar Pratte, Stefan Amlacher, Daniela Strauß, Yoshihiro Yoneda, Jun Katahira,[...]. Science 2012
68
8

Mutual protection of ribosomal proteins L5 and L11 from degradation is essential for p53 activation upon ribosomal biogenesis stress.
Sladana Bursać, Maja Cokarić Brdovčak, Martin Pfannkuchen, Ines Orsolić, Lior Golomb, Yan Zhu, Chen Katz, Lilyn Daftuar, Kristina Grabušić, Iva Vukelić,[...]. Proc Natl Acad Sci U S A 2012
126
6

Ribosomal mutations cause p53-mediated dark skin and pleiotropic effects.
Kelly A McGowan, Jun Z Li, Christopher Y Park, Veronica Beaudry, Holly K Tabor, Amit J Sabnis, Weibin Zhang, Helmut Fuchs, Martin Hrabé de Angelis, Richard M Myers,[...]. Nat Genet 2008
260
6

Mutation of a gene essential for ribosome biogenesis, EMG1, causes Bowen-Conradi syndrome.
Joy Armistead, Sunita Khatkar, Britta Meyer, Brian L Mark, Nehal Patel, Gail Coghlan, Ryan E Lamont, Shuangbo Liu, Jill Wiechert, Peter A Cattini,[...]. Am J Hum Genet 2009
74
8

Architecture of the 90S Pre-ribosome: A Structural View on the Birth of the Eukaryotic Ribosome.
Markus Kornprobst, Martin Turk, Nikola Kellner, Jingdong Cheng, Dirk Flemming, Isabelle Koš-Braun, Martin Koš, Matthias Thoms, Otto Berninghausen, Roland Beckmann,[...]. Cell 2016
114
6

Diverse roles of assembly factors revealed by structures of late nuclear pre-60S ribosomes.
Shan Wu, Beril Tutuncuoglu, Kaige Yan, Hailey Brown, Yixiao Zhang, Dan Tan, Michael Gamalinda, Yi Yuan, Zhifei Li, Jelena Jakovljevic,[...]. Nature 2016
111
6

Haploinsufficiency for ribosomal protein genes causes selective activation of p53 in human erythroid progenitor cells.
Shilpee Dutt, Anupama Narla, Katherine Lin, Ann Mullally, Nirmalee Abayasekara, Christine Megerdichian, Frederick H Wilson, Treeve Currie, Arati Khanna-Gupta, Nancy Berliner,[...]. Blood 2011
268
6

Exome sequencing identifies GATA1 mutations resulting in Diamond-Blackfan anemia.
Vijay G Sankaran, Roxanne Ghazvinian, Ron Do, Prathapan Thiru, Jo-Anne Vergilio, Alan H Beggs, Colin A Sieff, Stuart H Orkin, David G Nathan, Eric S Lander,[...]. J Clin Invest 2012
211
6

Diagnosing and treating Diamond Blackfan anaemia: results of an international clinical consensus conference.
Adrianna Vlachos, Sarah Ball, Niklas Dahl, Blanche P Alter, Sujit Sheth, Ugo Ramenghi, Joerg Meerpohl, Stefan Karlsson, Johnson M Liu, Thierry Leblanc,[...]. Br J Haematol 2008
254
6


Ribosomal protein S14 negatively regulates c-Myc activity.
Xiang Zhou, Qian Hao, Jun-Ming Liao, Peng Liao, Hua Lu. J Biol Chem 2013
43
13

p53 and ribosome biogenesis stress: the essentials.
Lior Golomb, Sinisa Volarevic, Moshe Oren. FEBS Lett 2014
129
6

Whole-exome sequencing in relapsing chronic lymphocytic leukemia: clinical impact of recurrent RPS15 mutations.
Viktor Ljungström, Diego Cortese, Emma Young, Tatjana Pandzic, Larry Mansouri, Karla Plevova, Stavroula Ntoufa, Panagiotis Baliakas, Ruth Clifford, Lesley-Ann Sutton,[...]. Blood 2016
94
6

The Shwachman-Bodian-Diamond syndrome gene encodes an RNA-binding protein that localizes to the pseudopod of Dictyostelium amoebae during chemotaxis.
Deborah Wessels, Thyagarajan Srikantha, Song Yi, Spencer Kuhl, L Aravind, David R Soll. J Cell Sci 2006
39
15


Somatic mutations and clonal hematopoiesis in congenital neutropenia.
Jun Xia, Christopher A Miller, Jack Baty, Amrita Ramesh, Matthew R M Jotte, Robert S Fulton, Tiphanie P Vogel, Megan A Cooper, Kelly J Walkovich, Vahagn Makaryan,[...]. Blood 2018
52
11

Congenital neutropenia in the era of genomics: classification, diagnosis, and natural history.
Jean Donadieu, Blandine Beaupain, Odile Fenneteau, Christine Bellanné-Chantelot. Br J Haematol 2017
56
10

Ribosome Levels Selectively Regulate Translation and Lineage Commitment in Human Hematopoiesis.
Rajiv K Khajuria, Mathias Munschauer, Jacob C Ulirsch, Claudia Fiorini, Leif S Ludwig, Sean K McFarland, Nour J Abdulhay, Harrison Specht, Hasmik Keshishian, D R Mani,[...]. Cell 2018
135
6

60S pre-ribosome formation viewed from assembly in the nucleolus until export to the cytoplasm.
Tracy A Nissan, Jochen Bassler, Elisabeth Petfalski, David Tollervey, Ed Hurt. EMBO J 2002
279
5

Suppression of Myc oncogenic activity by ribosomal protein haploinsufficiency.
Maria Barna, Aya Pusic, Ornella Zollo, Maria Costa, Nadya Kondrashov, Eduardo Rego, Pulivarthi H Rao, Davide Ruggero. Nature 2008
279
5

Translational control in cancer.
Deborah Silvera, Silvia C Formenti, Robert J Schneider. Nat Rev Cancer 2010
551
5

Characterization of the nuclear export adaptor protein Nmd3 in association with the 60S ribosomal subunit.
Jayati Sengupta, Cyril Bussiere, Jesper Pallesen, Matthew West, Arlen W Johnson, Joachim Frank. J Cell Biol 2010
50
10

Inhibition of RNA polymerase I as a therapeutic strategy to promote cancer-specific activation of p53.
Megan J Bywater, Gretchen Poortinga, Elaine Sanij, Nadine Hein, Abigail Peck, Carleen Cullinane, Meaghan Wall, Leonie Cluse, Denis Drygin, Kenna Anderes,[...]. Cancer Cell 2012
340
5

Proofreading of pre-40S ribosome maturation by a translation initiation factor and 60S subunits.
Simon Lebaron, Claudia Schneider, Robert W van Nues, Agata Swiatkowska, Dietrich Walsh, Bettina Böttcher, Sander Granneman, Nicholas J Watkins, David Tollervey. Nat Struct Mol Biol 2012
122
5

Structures of the human and Drosophila 80S ribosome.
Andreas M Anger, Jean-Paul Armache, Otto Berninghausen, Michael Habeck, Marion Subklewe, Daniel N Wilson, Roland Beckmann. Nature 2013
313
5

Functional dichotomy of ribosomal proteins during the synthesis of mammalian 40S ribosomal subunits.
Marie-Françoise O'Donohue, Valérie Choesmel, Marlène Faubladier, Gwennaële Fichant, Pierre-Emmanuel Gleizes. J Cell Biol 2010
130
5

Pre-ribosomes on the road from the nucleolus to the cytoplasm.
Herbert Tschochner, Ed Hurt. Trends Cell Biol 2003
375
5

Coordinated nuclear export of 60S ribosomal subunits and NMD3 in vertebrates.
Christopher R Trotta, Elsebet Lund, Lawrence Kahan, Arlen W Johnson, James E Dahlberg. EMBO J 2003
98
5

Both endonucleolytic and exonucleolytic cleavage mediate ITS1 removal during human ribosomal RNA processing.
Katherine E Sloan, Sandy Mattijssen, Simon Lebaron, David Tollervey, Ger J M Pruijn, Nicholas J Watkins. J Cell Biol 2013
89
5

SBDS-deficiency results in specific hypersensitivity to Fas stimulation and accumulation of Fas at the plasma membrane.
Ken-Ichiro Watanabe, Chhaya Ambekar, Hanming Wang, Amanda Ciccolini, Aaron D Schimmer, Yigal Dror. Apoptosis 2009
18
27

A p53-dependent mechanism underlies macrocytic anemia in a mouse model of human 5q- syndrome.
Jillian L Barlow, Lesley F Drynan, Duncan R Hewett, Luke R Holmes, Silvia Lorenzo-Abalde, Alison L Lane, Helen E Jolin, Richard Pannell, Angela J Middleton, See Heng Wong,[...]. Nat Med 2010
248
5


Targeted proteomics reveals compositional dynamics of 60S pre-ribosomes after nuclear export.
Martin Altvater, Yiming Chang, Andre Melnik, Laura Occhipinti, Sabina Schütz, Ute Rothenbusch, Paola Picotti, Vikram Govind Panse. Mol Syst Biol 2012
37
13

Features and development of Coot.
P Emsley, B Lohkamp, W G Scott, K Cowtan. Acta Crystallogr D Biol Crystallogr 2010
5

Lentiviral-mediated RNAi inhibition of Sbds in murine hematopoietic progenitors impairs their hematopoietic potential.
Amy S Rawls, Alyssa D Gregory, Jill R Woloszynek, Fulu Liu, Daniel C Link. Blood 2007
35
14

The ribosome-related protein, SBDS, is critical for normal erythropoiesis.
Saswati Sen, Hanming Wang, Chi Lan Nghiem, Kim Zhou, Janice Yau, Chetankumar S Tailor, Meredith S Irwin, Yigal Dror. Blood 2011
21
23

The nucleolus under stress.
Séverine Boulon, Belinda J Westman, Saskia Hutten, François-Michel Boisvert, Angus I Lamond. Mol Cell 2010
599
5

Hematologic abnormalities in Shwachman Diamond syndrome: lack of genotype-phenotype relationship.
Taco W Kuijpers, Mariel Alders, Anton T J Tool, Clemens Mellink, Dirk Roos, Raoul C M Hennekam. Blood 2005
60
8

Shwachman syndrome: exocrine pancreatic dysfunction and variable phenotypic expression.
D R Mack, G G Forstner, M Wilschanski, M H Freedman, P R Durie. Gastroenterology 1996
116
5

Mitochondrial function is impaired in yeast and human cellular models of Shwachman Diamond syndrome.
Adrianna L Henson, Joseph B Moore, Pascale Alard, Max M Wattenberg, Johnson M Liu, Steven R Ellis. Biochem Biophys Res Commun 2013
12
41


The Treacher Collins syndrome (TCOF1) gene product is involved in ribosomal DNA gene transcription by interacting with upstream binding factor.
Benigno C Valdez, Dale Henning, Rolando B So, Jill Dixon, Michael J Dixon. Proc Natl Acad Sci U S A 2004
180
5

A missense mutation (R565W) in cirhin (FLJ14728) in North American Indian childhood cirrhosis.
Pierre Chagnon, Jacques Michaud, Grant Mitchell, Jocelyne Mercier, Jean-François Marion, Eric Drouin, Andrée Rasquin-Weber, Thomas J Hudson, Andrea Richter. Am J Hum Genet 2002
58
8

eIF6 coordinates insulin sensitivity and lipid metabolism by coupling translation to transcription.
Daniela Brina, Annarita Miluzio, Sara Ricciardi, Kim Clarke, Peter K Davidsen, Gabriella Viero, Toma Tebaldi, Nina Offenhäuser, Jan Rozman, Birgit Rathkolb,[...]. Nat Commun 2015
47
10

An integrated genomics approach identifies drivers of proliferation in luminal-subtype human breast cancer.
Michael L Gatza, Grace O Silva, Joel S Parker, Cheng Fan, Charles M Perou. Nat Genet 2014
137
5

A RanGTP-independent mechanism allows ribosomal protein nuclear import for ribosome assembly.
Sabina Schütz, Ute Fischer, Martin Altvater, Purnima Nerurkar, Cohue Peña, Michaela Gerber, Yiming Chang, Stefanie Caesar, Olga T Schubert, Gabriel Schlenstedt,[...]. Elife 2014
38
13

The Dedicated Chaperone Acl4 Escorts Ribosomal Protein Rpl4 to Its Nuclear Pre-60S Assembly Site.
Benjamin Pillet, Juan J García-Gómez, Patrick Pausch, Laurent Falquet, Gert Bange, Jesús de la Cruz, Dieter Kressler. PLoS Genet 2015
36
13

'View From A Bridge': A New Perspective on Eukaryotic rRNA Base Modification.
Sunny Sharma, Denis L J Lafontaine. Trends Biochem Sci 2015
123
5

Dietary L-leucine improves the anemia in a mouse model for Diamond-Blackfan anemia.
Pekka Jaako, Shubhranshu Debnath, Karin Olsson, David Bryder, Johan Flygare, Stefan Karlsson. Blood 2012
58
8



Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.