A citation-based method for searching scientific literature

Adam Amsterdam, Kirsten C Sadler, Kevin Lai, Sarah Farrington, Roderick T Bronson, Jacqueline A Lees, Nancy Hopkins. PLoS Biol 2004
Times Cited: 326







List of co-cited articles
1066 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
277
25

Ribosomopathies: human disorders of ribosome dysfunction.
Anupama Narla, Benjamin L Ebert. Blood 2010
515
24

tp53 mutant zebrafish develop malignant peripheral nerve sheath tumors.
Stéphane Berghmans, Ryan D Murphey, Erno Wienholds, Donna Neuberg, Jeffery L Kutok, Christopher D M Fletcher, John P Morris, Ting Xi Liu, Stefan Schulte-Merker, John P Kanki,[...]. Proc Natl Acad Sci U S A 2005
447
24

Loss of p53 synthesis in zebrafish tumors with ribosomal protein gene mutations.
Alyson W MacInnes, Adam Amsterdam, Charles A Whittaker, Nancy Hopkins, Jacqueline A Lees. Proc Natl Acad Sci U S A 2008
106
21

Ribosome-mediated specificity in Hox mRNA translation and vertebrate tissue patterning.
Nadya Kondrashov, Aya Pusic, Craig R Stumpf, Kunihiko Shimizu, Andrew C Hsieh, Junko Ishijima, Toshihiko Shiroishi, Maria Barna. Cell 2011
362
19

Incidence of neoplasia in Diamond Blackfan anemia: a report from the Diamond Blackfan Anemia Registry.
Adrianna Vlachos, Philip S Rosenberg, Eva Atsidaftos, Blanche P Alter, Jeffrey M Lipton. Blood 2012
187
18

Inactivation of ribosomal protein L22 promotes transformation by induction of the stemness factor, Lin28B.
Shuyun Rao, Sang-Yun Lee, Alejandro Gutierrez, Jacqueline Perrigoue, Roshan J Thapa, Zhigang Tu, John R Jeffers, Michele Rhodes, Stephen Anderson, Tamas Oravecz,[...]. Blood 2012
103
18

Ribosomal protein L5 and L11 mutations are associated with cleft palate and abnormal thumbs in Diamond-Blackfan anemia patients.
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,[...]. Am J Hum Genet 2008
295
17

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
279
16

Identification of RPS14 as a 5q- syndrome gene by RNA interference screen.
Benjamin L Ebert, Jennifer Pretz, Jocelyn Bosco, Cindy Y Chang, Pablo Tamayo, Naomi Galili, Azra Raza, David E Root, Eyal Attar, Steven R Ellis,[...]. Nature 2008
652
15


The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemia.
N Draptchinskaia, P Gustavsson, B Andersson, M Pettersson, T N Willig, I Dianzani, S Ball, G Tchernia, J Klar, H Matsson,[...]. Nat Genet 1999
615
15

Many ribosomal protein mutations are associated with growth impairment and tumor predisposition in zebrafish.
Kevin Lai, Adam Amsterdam, Sarah Farrington, Roderick T Bronson, Nancy Hopkins, Jacqueline A Lees. Dev Dyn 2009
68
22

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
273
14

How common are extraribosomal functions of ribosomal proteins?
Jonathan R Warner, Kerri B McIntosh. Mol Cell 2009
472
14

An ARF-independent c-MYC-activated tumor suppression pathway mediated by ribosomal protein-Mdm2 Interaction.
Everardo Macias, Aiwen Jin, Chad Deisenroth, Krishna Bhat, Hua Mao, Mikael S Lindström, Yanping Zhang. Cancer Cell 2010
154
13

BRAF mutations are sufficient to promote nevi formation and cooperate with p53 in the genesis of melanoma.
E Elizabeth Patton, Hans R Widlund, Jeffery L Kutok, Kamden R Kopani, James F Amatruda, Ryan D Murphey, Stephane Berghmans, Elizabeth A Mayhall, David Traver, Christopher D M Fletcher,[...]. Curr Biol 2005
447
13

Bypass of the pre-60S ribosomal quality control as a pathway to oncogenesis.
Sergey O Sulima, Stephanie Patchett, Vivek M Advani, Kim De Keersmaecker, Arlen W Johnson, Jonathan D Dinman. Proc Natl Acad Sci U S A 2014
56
23


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
292
12

Absence of nucleolar disruption after impairment of 40S ribosome biogenesis reveals an rpL11-translation-dependent mechanism of p53 induction.
Stefano Fumagalli, Alessandro Di Cara, Arti Neb-Gulati, Francois Natt, Sandy Schwemberger, Jonathan Hall, George F Babcock, Rosa Bernardi, Pier Paolo Pandolfi, George Thomas. Nat Cell Biol 2009
243
12

L-Leucine improves the anemia and developmental defects associated with Diamond-Blackfan anemia and del(5q) MDS by activating the mTOR pathway.
Elspeth M Payne, Maria Virgilio, Anupama Narla, Hong Sun, Michelle Levine, Barry H Paw, Nancy Berliner, A Thomas Look, Benjamin L Ebert, Arati Khanna-Gupta. Blood 2012
106
12

Does the ribosome translate cancer?
Davide Ruggero, Pier Paolo Pandolfi. Nat Rev Cancer 2003
726
12

Deficiency of ribosomal protein S19 during early embryogenesis leads to reduction of erythrocytes in a zebrafish model of Diamond-Blackfan anemia.
Tamayo Uechi, Yukari Nakajima, Anirban Chakraborty, Hidetsugu Torihara, Sayomi Higa, Naoya Kenmochi. Hum Mol Genet 2008
79
15


The 5S RNP couples p53 homeostasis to ribosome biogenesis and nucleolar stress.
Katherine E Sloan, Markus T Bohnsack, Nicholas J Watkins. Cell Rep 2013
175
12

Partial Loss of Rpl11 in Adult Mice Recapitulates Diamond-Blackfan Anemia and Promotes Lymphomagenesis.
Lucia Morgado-Palacin, Gianluca Varetti, Susana Llanos, Gonzalo Gómez-López, Dolores Martinez, Manuel Serrano. Cell Rep 2015
50
24

Deletion of ribosomal protein genes is a common vulnerability in human cancer, especially in concert with TP53 mutations.
Ram Ajore, David Raiser, Marie McConkey, Magnus Jöud, Bernd Boidol, Brenton Mar, Gordon Saksena, David M Weinstock, Scott Armstrong, Steven R Ellis,[...]. EMBO Mol Med 2017
60
20

Frameshift mutation in p53 regulator RPL26 is associated with multiple physical abnormalities and a specific pre-ribosomal RNA processing defect in diamond-blackfan anemia.
Hanna T Gazda, Milena Preti, Mee Rie Sheen, Marie-Françoise O'Donohue, Adrianna Vlachos, Stella M Davies, Antonis Kattamis, Leana Doherty, Michael Landowski, Christopher Buros,[...]. Hum Mutat 2012
107
11

Hematopoietic defects in rps29 mutant zebrafish depend upon p53 activation.
Alison M Taylor, Jessica M Humphries, Richard M White, Ryan D Murphey, Caroline E Burns, Leonard I Zon. Exp Hematol 2012
52
21

Targeted disruption of the ribosomal protein S19 gene is lethal prior to implantation.
Hans Matsson, Edward J Davey, Natalia Draptchinskaia, Isao Hamaguchi, Andreas Ooka, Per Levéen, Erik Forsberg, Stefan Karlsson, Niklas Dahl. Mol Cell Biol 2004
122
11

Signaling to p53: ribosomal proteins find their way.
Yanping Zhang, Hua Lu. Cancer Cell 2009
411
11


Ribosomal protein L11 mutation in zebrafish leads to haematopoietic and metabolic defects.
Nadia Danilova, Kathleen M Sakamoto, Shuo Lin. Br J Haematol 2011
70
15

Highly aneuploid zebrafish malignant peripheral nerve sheath tumors have genetic alterations similar to human cancers.
Guangjun Zhang, Sebastian Hoersch, Adam Amsterdam, Charles A Whittaker, Jacqueline A Lees, Nancy Hopkins. Proc Natl Acad Sci U S A 2010
29
37

Effects of RAS on the genesis of embryonal rhabdomyosarcoma.
David M Langenau, Matthew D Keefe, Narie Y Storer, Jeffrey R Guyon, Jeffery L Kutok, Xiuning Le, Wolfram Goessling, Donna S Neuberg, Louis M Kunkel, Leonard I Zon. Genes Dev 2007
247
11

Ribosomal proteins: functions beyond the ribosome.
Xiang Zhou, Wen-Juan Liao, Jun-Ming Liao, Peng Liao, Hua Lu. J Mol Cell Biol 2015
324
11

Germline mutation of RPS20, encoding a ribosomal protein, causes predisposition to hereditary nonpolyposis colorectal carcinoma without DNA mismatch repair deficiency.
Taina T Nieminen, Marie-Françoise O'Donohue, Yunpeng Wu, Hannes Lohi, Stephen W Scherer, Andrew D Paterson, Pekka Ellonen, Wael M Abdel-Rahman, Satu Valo, Jukka-Pekka Mecklin,[...]. Gastroenterology 2014
110
11

MYC as a regulator of ribosome biogenesis and protein synthesis.
Jan van Riggelen, Alper Yetil, Dean W Felsher. Nat Rev Cancer 2010
540
10

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
254
10

Ribosomal deficiencies in Diamond-Blackfan anemia impair translation of transcripts essential for differentiation of murine and human erythroblasts.
Rastislav Horos, Hanna Ijspeert, Dagmar Pospisilova, Regine Sendtner, Charlotte Andrieu-Soler, Erdogan Taskesen, Andrzej Nieradka, Radek Cmejla, Michael Sendtner, Ivo P Touw,[...]. Blood 2012
113
10

Proliferation, but not growth, blocked by conditional deletion of 40S ribosomal protein S6.
S Volarevic, M J Stewart, B Ledermann, F Zilberman, L Terracciano, E Montini, M Grompe, S C Kozma, G Thomas. Science 2000
307
10

Mice with ribosomal protein S19 deficiency develop bone marrow failure and symptoms like patients with Diamond-Blackfan anemia.
Pekka Jaako, Johan Flygare, Karin Olsson, Ronan Quere, Mats Ehinger, Adrianna Henson, Steven Ellis, Axel Schambach, Christopher Baum, Johan Richter,[...]. Blood 2011
96
10

Ribosomal protein S24 gene is mutated in Diamond-Blackfan anemia.
Hanna T Gazda, Agnieszka Grabowska, Lilia B Merida-Long, Elzbieta Latawiec, Hal E Schneider, Jeffrey M Lipton, Adrianna Vlachos, Eva Atsidaftos, Sarah E Ball, Karen A Orfali,[...]. Am J Hum Genet 2006
209
10


Ribosomal protein L23 activates p53 by inhibiting MDM2 function in response to ribosomal perturbation but not to translation inhibition.
Mu-Shui Dai, Shelya X Zeng, Yetao Jin, Xiao-Xin Sun, Larry David, Hua Lu. Mol Cell Biol 2004
384
10

Ribosomal protein gene knockdown causes developmental defects in zebrafish.
Tamayo Uechi, Yukari Nakajima, Akihiro Nakao, Hidetsugu Torihara, Anirban Chakraborty, Kunio Inoue, Naoya Kenmochi. PLoS One 2006
71
14

Comparative oncogenomic analysis of copy number alterations in human and zebrafish tumors enables cancer driver discovery.
GuangJun Zhang, Sebastian Hoersch, Adam Amsterdam, Charles A Whittaker, Eline Beert, Julian M Catchen, Sarah Farrington, John H Postlethwait, Eric Legius, Nancy Hopkins,[...]. PLoS Genet 2013
25
40

Frequent mutations in the RPL22 gene and its clinical and functional implications.
Akiva P Novetsky, Israel Zighelboim, Dominic M Thompson, Matthew A Powell, David G Mutch, Paul J Goodfellow. Gynecol Oncol 2013
48
20

Altered translation of GATA1 in Diamond-Blackfan anemia.
Leif S Ludwig, Hanna T Gazda, Jennifer C Eng, Stephen W Eichhorn, Prathapan Thiru, Roxanne Ghazvinian, Tracy I George, Jason R Gotlib, Alan H Beggs, Colin A Sieff,[...]. Nat Med 2014
183
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.