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: 174







List of co-cited articles
1029 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Mutations in SBDS are associated with Shwachman-Diamond syndrome.
Graeme R B Boocock, Jodi A Morrison, Maja Popovic, Nicole Richards, Lynda Ellis, Peter R Durie, Johanna M Rommens. Nat Genet 2003
458
54

The Shwachman-Bodian-Diamond syndrome protein mediates translational activation of ribosomes in yeast.
Tobias F Menne, Beatriz Goyenechea, Nuria Sánchez-Puig, Chi C Wong, Louise M Tonkin, Philip J Ancliff, Renée L Brost, Michael Costanzo, Charles Boone, Alan J Warren. Nat Genet 2007
222
45

Mechanism of eIF6 release from the nascent 60S ribosomal subunit.
Félix Weis, Emmanuel Giudice, Mark Churcher, Li Jin, Christine Hilcenko, Chi C Wong, David Traynor, Robert R Kay, Alan J Warren. Nat Struct Mol Biol 2015
100
40

Defective ribosome assembly in Shwachman-Diamond syndrome.
Chi C Wong, David Traynor, Nicolas Basse, Robert R Kay, Alan J Warren. Blood 2011
98
28

Defining the pathway of cytoplasmic maturation of the 60S ribosomal subunit.
Kai-Yin Lo, Zhihua Li, Cyril Bussiere, Stefan Bresson, Edward M Marcotte, Arlen W Johnson. Mol Cell 2010
132
23

DNAJC21 Mutations Link a Cancer-Prone Bone Marrow Failure Syndrome to Corruption in 60S Ribosome Subunit Maturation.
Hemanth Tummala, Amanda J Walne, Mike Williams, Nicholas Bockett, Laura Collopy, Shirleny Cardoso, Alicia Ellison, Rob Wynn, Thierry Leblanc, Jude Fitzgibbon,[...]. Am J Hum Genet 2016
40
55

Draft consensus guidelines for diagnosis and treatment of Shwachman-Diamond syndrome.
Yigal Dror, Jean Donadieu, Jutta Koglmeier, John Dodge, Sanna Toiviainen-Salo, Outi Makitie, Elizabeth Kerr, Cornelia Zeidler, Akiko Shimamura, Neil Shah,[...]. Ann N Y Acad Sci 2011
104
21

The nucle(ol)ar Tif6p and Efl1p are required for a late cytoplasmic step of ribosome synthesis.
B Senger, D L Lafontaine, J S Graindorge, O Gadal, A Camasses, A Sanni, J M Garnier, M Breitenbach, E Hurt, F Fasiolo. Mol Cell 2001
126
20

Ribosomopathies: human disorders of ribosome dysfunction.
Anupama Narla, Benjamin L Ebert. Blood 2010
479
20

Mitotic spindle destabilization and genomic instability in Shwachman-Diamond syndrome.
Karyn M Austin, Mohan L Gupta, Scott A Coats, Asmin Tulpule, Gustavo Mostoslavsky, Alejandro B Balazs, Richard C Mulligan, George Daley, David Pellman, Akiko Shimamura. J Clin Invest 2008
85
23

Mutations in EFL1, an SBDS partner, are associated with infantile pancytopenia, exocrine pancreatic insufficiency and skeletal anomalies in aShwachman-Diamond like syndrome.
Polina Stepensky, Montserrat Chacón-Flores, Katherine H Kim, Omar Abuzaitoun, Arnulfo Bautista-Santos, Natalia Simanovsky, Dritan Siliqi, Davide Altamura, Alfonso Méndez-Godoy, Abril Gijsbers,[...]. J Med Genet 2017
53
37

Impaired ribosomal subunit association in Shwachman-Diamond syndrome.
Nicholas Burwick, Scott A Coats, Tomoka Nakamura, Akiko Shimamura. Blood 2012
49
38

Release of eIF6 (p27BBP) from the 60S subunit allows 80S ribosome assembly.
Marcello Ceci, Cristina Gaviraghi, Chiara Gorrini, Leonardo A Sala, Nina Offenhäuser, Pier Carlo Marchisio, Stefano Biffo. Nature 2003
294
18

Crystal structure of the eukaryotic 60S ribosomal subunit in complex with initiation factor 6.
Sebastian Klinge, Felix Voigts-Hoffmann, Marc Leibundgut, Sofia Arpagaus, Nenad Ban. Science 2011
239
18

Mechanism of eIF6-mediated inhibition of ribosomal subunit joining.
Marco Gartmann, Michael Blau, Jean-Paul Armache, Thorsten Mielke, Maya Topf, Roland Beckmann. J Biol Chem 2010
77
20

Integrity of the P-site is probed during maturation of the 60S ribosomal subunit.
Cyril Bussiere, Yaser Hashem, Sucheta Arora, Joachim Frank, Arlen W Johnson. J Cell Biol 2012
56
28

Biallelic mutations in DNAJC21 cause Shwachman-Diamond syndrome.
Santhosh Dhanraj, Anna Matveev, Hongbing Li, Supanun Lauhasurayotin, Lawrence Jardine, Michaela Cada, Bozana Zlateska, Chetankumar S Tailor, Joseph Zhou, Roberto Mendoza-Londono,[...]. Blood 2017
60
26


Shwachman-Bodian Diamond syndrome is a multi-functional protein implicated in cellular stress responses.
Heather L Ball, Bing Zhang, J Jacob Riches, Rikesh Gandhi, Jing Li, Johanna M Rommens, Jeremy S Myers. Hum Mol Genet 2009
39
38

Variable clinical presentation of Shwachman-Diamond syndrome: update from the North American Shwachman-Diamond Syndrome Registry.
Kasiani C Myers, Audrey Anna Bolyard, Barbara Otto, Trisha E Wong, Amanda T Jones, Richard E Harris, Stella M Davies, David C Dale, Akiko Shimamura. J Pediatr 2014
70
21

Mutations in signal recognition particle SRP54 cause syndromic neutropenia with Shwachman-Diamond-like features.
Raphael Carapito, Martina Konantz, Catherine Paillard, Zhichao Miao, Angélique Pichot, Magalie S Leduc, Yaping Yang, Katie L Bergstrom, Donald H Mahoney, Deborah L Shardy,[...]. J Clin Invest 2017
64
23

THE SYNDROME OF PANCREATIC INSUFFICIENCY AND BONE MARROW DYSFUNCTION.
H SHWACHMAN, L K DIAMOND, F A OSKI, K T KHAW. J Pediatr 1964
364
14

Ribosome biogenesis in the yeast Saccharomyces cerevisiae.
John L Woolford, Susan J Baserga. Genetics 2013
414
14

In Vivo Senescence in the Sbds-Deficient Murine Pancreas: Cell-Type Specific Consequences of Translation Insufficiency.
Marina E Tourlakis, Siyi Zhang, Heather L Ball, Rikesh Gandhi, Hongrui Liu, Jian Zhong, Julie S Yuan, Cynthia J Guidos, Peter R Durie, Johanna M Rommens. PLoS Genet 2015
22
63

Deficiency of the ribosome biogenesis gene Sbds in hematopoietic stem and progenitor cells causes neutropenia in mice by attenuating lineage progression in myelocytes.
Noemi A Zambetti, Eric M J Bindels, Paulina M H Van Strien, Marijke G Valkhof, Maria N Adisty, Remco M Hoogenboezem, Mathijs A Sanders, Johanna M Rommens, Ivo P Touw, Marc H G P Raaijmakers. Haematologica 2015
32
43

Structural and mutational analysis of the SBDS protein family. Insight into the leukemia-associated Shwachman-Diamond Syndrome.
Camille Shammas, Tobias F Menne, Christine Hilcenko, Stephen R Michell, Beatriz Goyenechea, Graeme R B Boocock, Peter R Durie, Johanna M Rommens, Alan J Warren. J Biol Chem 2005
84
15

Maturation of eukaryotic ribosomes: acquisition of functionality.
Vikram Govind Panse, Arlen W Johnson. Trends Biochem Sci 2010
140
13

Eukaryotic initiation factor 6 is rate-limiting in translation, growth and transformation.
Valentina Gandin, Annarita Miluzio, Anna Maria Barbieri, Anne Beugnet, Hiroaki Kiyokawa, Pier Carlo Marchisio, Stefano Biffo. Nature 2008
144
12

Loss of the mouse ortholog of the shwachman-diamond syndrome gene (Sbds) results in early embryonic lethality.
Siyi Zhang, Mingjun Shi, Chi-Chung Hui, Johanna M Rommens. Mol Cell Biol 2006
73
16

Classification of and risk factors for hematologic complications in a French national cohort of 102 patients with Shwachman-Diamond syndrome.
Jean Donadieu, Odile Fenneteau, Blandine Beaupain, Sandrine Beaufils, Florence Bellanger, Nizar Mahlaoui, Anne Lambilliotte, Nathalie Aladjidi, Yves Bertrand, Valérie Mialou,[...]. Haematologica 2012
66
18

The beta4 integrin interactor p27(BBP/eIF6) is an essential nuclear matrix protein involved in 60S ribosomal subunit assembly.
F Sanvito, S Piatti, A Villa, M Bossi, G Lucchini, P C Marchisio, S Biffo. J Cell Biol 1999
95
11

Defining the order in which Nmd3p and Rpl10p load onto nascent 60S ribosomal subunits.
Matthew West, John B Hedges, Anthony Chen, Arlen W Johnson. Mol Cell Biol 2005
99
11


Driving ribosome assembly.
Dieter Kressler, Ed Hurt, Jochen Bassler. Biochim Biophys Acta 2010
331
11



A new system for naming ribosomal proteins.
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,[...]. Curr Opin Struct Biol 2014
310
11

Exome sequencing identifies mutation in CNOT3 and ribosomal genes RPL5 and RPL10 in T-cell acute lymphoblastic leukemia.
Kim De Keersmaecker, Zeynep Kalender Atak, Ning Li, Carmen Vicente, Stephanie Patchett, Tiziana Girardi, Valentina Gianfelici, Ellen Geerdens, Emmanuelle Clappier, Michaël Porcu,[...]. Nat Genet 2013
260
11

A functional network involved in the recycling of nucleocytoplasmic pre-60S factors.
Alice Lebreton, Cosmin Saveanu, Laurence Decourty, Jean-Christophe Rain, Alain Jacquier, Micheline Fromont-Racine. J Cell Biol 2006
85
11

Eukaryotic initiation factor 6 mediates a continuum between 60S ribosome biogenesis and translation.
Annarita Miluzio, Anne Beugnet, Viviana Volta, Stefano Biffo. EMBO Rep 2009
61
16

Deletion of chromosome 20 in bone marrow of patients with Shwachman-Diamond syndrome, loss of the EIF6 gene and benign prognosis.
Barbara Pressato, Roberto Valli, Cristina Marletta, Lydia Mare, Giuseppe Montalbano, Francesco Lo Curto, Francesco Pasquali, Emanuela Maserati. Br J Haematol 2012
32
31

60S ribosome biogenesis requires rotation of the 5S ribonucleoprotein particle.
Christoph Leidig, Matthias Thoms, Iris Holdermann, Bettina Bradatsch, Otto Berninghausen, Gert Bange, Irmgard Sinning, Ed Hurt, Roland Beckmann. Nat Commun 2014
87
11

Skeletal phenotype in patients with Shwachman-Diamond syndrome and mutations in SBDS.
O Mäkitie, L Ellis, P R Durie, J A Morrison, E B Sochett, J M Rommens, W G Cole. Clin Genet 2004
78
12

Shwachman syndrome: phenotypic manifestations of sibling sets and isolated cases in a large patient cohort are similar.
H Ginzberg, J Shin, L Ellis, J Morrison, W Ip, Y Dror, M Freedman, L A Heitlinger, M A Belt, M Corey,[...]. J Pediatr 1999
147
10


Arx1 functions as an unorthodox nuclear export receptor for the 60S preribosomal subunit.
Bettina Bradatsch, Jun Katahira, Eva Kowalinski, Gert Bange, Wei Yao, Toshihiro Sekimoto, Viola Baumgärtel, Guido Boese, Jochen Bassler, Klemens Wild,[...]. Mol Cell 2007
91
10

Yvh1 is required for a late maturation step in the 60S biogenesis pathway.
Stefan Kemmler, Laura Occhipinti, Maria Veisu, Vikram Govind Panse. J Cell Biol 2009
79
12

The human Shwachman-Diamond syndrome protein, SBDS, associates with ribosomal RNA.
Karthik A Ganapathi, Karyn M Austin, Chung-Sheng Lee, Anusha Dias, Maggie M Malsch, Robin Reed, Akiko Shimamura. Blood 2007
98
10

Deficiency of Sbds in the mouse pancreas leads to features of Shwachman-Diamond syndrome, with loss of zymogen granules.
Marina E Tourlakis, Jian Zhong, Rikesh Gandhi, Siyi Zhang, Lingling Chen, Peter R Durie, Johanna M Rommens. Gastroenterology 2012
24
41

Mutations in genes encoding subunits of RNA polymerases I and III cause Treacher Collins syndrome.
Johannes G Dauwerse, Jill Dixon, Saskia Seland, Claudia A L Ruivenkamp, Arie van Haeringen, Lies H Hoefsloot, Dorien J M Peters, Agnes Clement-de Boers, Cornelia Daumer-Haas, Robert Maiwald,[...]. Nat Genet 2011
185
10


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.