A citation-based method for searching scientific literature

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, Alan J Warren, James S Wainscoat, Jacqueline Boultwood, Andrew N J McKenzie. Nat Med 2010
Times Cited: 249







List of co-cited articles
1290 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
636
56

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
271
41

Ribosomopathies: human disorders of ribosome dysfunction.
Anupama Narla, Benjamin L Ebert. Blood 2010
491
28

Identification of miR-145 and miR-146a as mediators of the 5q- syndrome phenotype.
Daniel T Starczynowski, Florian Kuchenbauer, Bob Argiropoulos, Sandy Sung, Ryan Morin, Andrew Muranyi, Martin Hirst, Donna Hogge, Marco Marra, Richard A Wells,[...]. Nat Med 2010
454
23

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
261
23

TP53 mutations in low-risk myelodysplastic syndromes with del(5q) predict disease progression.
Martin Jädersten, Leonie Saft, Alexander Smith, Austin Kulasekararaj, Sabine Pomplun, Gudrun Göhring, Anette Hedlund, Robert Hast, Brigitte Schlegelberger, Anna Porwit,[...]. J Clin Oncol 2011
316
22

Prevention of the neurocristopathy Treacher Collins syndrome through inhibition of p53 function.
Natalie C Jones, Megan L Lynn, Karin Gaudenz, Daisuke Sakai, Kazushi Aoto, Jean-Phillipe Rey, Earl F Glynn, Lacey Ellington, Chunying Du, Jill Dixon,[...]. Nat Med 2008
283
21

Lenalidomide in the myelodysplastic syndrome with chromosome 5q deletion.
Alan List, Gordon Dewald, John Bennett, Aristotle Giagounidis, Azra Raza, Eric Feldman, Bayard Powell, Peter Greenberg, Deborah Thomas, Richard Stone,[...]. N Engl J Med 2006
916
21

Clinical effect of point mutations in myelodysplastic syndromes.
Rafael Bejar, Kristen Stevenson, Omar Abdel-Wahab, Naomi Galili, Björn Nilsson, Guillermo Garcia-Manero, Hagop Kantarjian, Azra Raza, Ross L Levine, Donna Neuberg,[...]. N Engl J Med 2011
19

Lenalidomide promotes p53 degradation by inhibiting MDM2 auto-ubiquitination in myelodysplastic syndrome with chromosome 5q deletion.
S Wei, X Chen, K McGraw, L Zhang, R Komrokji, J Clark, G Caceres, D Billingsley, L Sokol, J Lancet,[...]. Oncogene 2013
66
27

Narrowing and genomic annotation of the commonly deleted region of the 5q- syndrome.
Jacqueline Boultwood, Carrie Fidler, Amanda J Strickson, Fiona Watkins, Susana Gama, Lyndal Kearney, Sabrina Tosi, Arek Kasprzyk, Jan-Fang Cheng, Rina J Jaju,[...]. Blood 2002
186
18

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
165
18

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
601
17

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
230
17

Role of casein kinase 1A1 in the biology and targeted therapy of del(5q) MDS.
Rebekka K Schneider, Vera Ademà, Dirk Heckl, Marcus Järås, Mar Mallo, Allegra M Lord, Lisa P Chu, Marie E McConkey, Rafael Kramann, Ann Mullally,[...]. Cancer Cell 2014
115
17

Revised international prognostic scoring system for myelodysplastic syndromes.
Peter L Greenberg, Heinz Tuechler, Julie Schanz, Guillermo Sanz, Guillermo Garcia-Manero, Francesc Solé, John M Bennett, David Bowen, Pierre Fenaux, Francois Dreyfus,[...]. Blood 2012
16

Clinical and biological implications of driver mutations in myelodysplastic syndromes.
Elli Papaemmanuil, Moritz Gerstung, Luca Malcovati, Sudhir Tauro, Gunes Gundem, Peter Van Loo, Chris J Yoon, Peter Ellis, David C Wedge, Andrea Pellagatti,[...]. Blood 2013
16

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
91
16

Signaling to p53: ribosomal proteins find their way.
Yanping Zhang, Hua Lu. Cancer Cell 2009
396
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
149
14

TP53 suppression promotes erythropoiesis in del(5q) MDS, suggesting a targeted therapeutic strategy in lenalidomide-resistant patients.
Gisela Caceres, Kathy McGraw, Bon Ham Yip, Andrea Pellagatti, Joseph Johnson, Ling Zhang, Kenian Liu, Lan Min Zhang, William J Fulp, Ji-Hyun Lee,[...]. Proc Natl Acad Sci U S A 2013
44
31

Myelodysplastic syndromes are propagated by rare and distinct human cancer stem cells in vivo.
Petter S Woll, Una Kjällquist, Onima Chowdhury, Helen Doolittle, David C Wedge, Supat Thongjuea, Rikard Erlandsson, Mtakai Ngara, Kristina Anderson, Qiaolin Deng,[...]. Cancer Cell 2014
188
14

Landscape of genetic lesions in 944 patients with myelodysplastic syndromes.
T Haferlach, Y Nagata, V Grossmann, Y Okuno, U Bacher, G Nagae, S Schnittger, M Sanada, A Kon, T Alpermann,[...]. Leukemia 2014
880
14

A randomized phase 3 study of lenalidomide versus placebo in RBC transfusion-dependent patients with Low-/Intermediate-1-risk myelodysplastic syndromes with del5q.
Pierre Fenaux, Aristoteles Giagounidis, Dominik Selleslag, Odile Beyne-Rauzy, Ghulam Mufti, Moshe Mittelman, Petra Muus, Peter Te Boekhorst, Guillermo Sanz, Consuelo Del Cañizo,[...]. Blood 2011
315
14

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
346
13

Induction of p53 and up-regulation of the p53 pathway in the human 5q- syndrome.
Andrea Pellagatti, Teresa Marafioti, Jennifer C Paterson, Jillian L Barlow, Lesley F Drynan, Aristoteles Giagounidis, Stefano A Pileri, Mario Cazzola, Andrew N J McKenzie, James S Wainscoat,[...]. Blood 2010
53
24

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
341
13


New insights into the prognostic impact of the karyotype in MDS and correlation with subtypes: evidence from a core dataset of 2124 patients.
Detlef Haase, Ulrich Germing, Julie Schanz, Michael Pfeilstöcker, Thomas Nösslinger, Barbara Hildebrandt, Andrea Kundgen, Michael Lübbert, Regina Kunzmann, Aristoteles A N Giagounidis,[...]. Blood 2007
527
13

Frequent pathway mutations of splicing machinery in myelodysplasia.
Kenichi Yoshida, Masashi Sanada, Yuichi Shiraishi, Daniel Nowak, Yasunobu Nagata, Ryo Yamamoto, Yusuke Sato, Aiko Sato-Otsubo, Ayana Kon, Masao Nagasaki,[...]. Nature 2011
13

The 5S RNP couples p53 homeostasis to ribosome biogenesis and nucleolar stress.
Katherine E Sloan, Markus T Bohnsack, Nicholas J Watkins. Cell Rep 2013
165
13

Rps14 haploinsufficiency causes a block in erythroid differentiation mediated by S100A8 and S100A9.
Rebekka K Schneider, Monica Schenone, Monica Ventura Ferreira, Rafael Kramann, Cailin E Joyce, Christina Hartigan, Fabian Beier, Tim H Brümmendorf, Ulrich Germing, Uwe Platzbecker,[...]. Nat Med 2016
124
13

Ribosomal protein S14 unties the MDM2-p53 loop upon ribosomal stress.
X Zhou, Q Hao, J Liao, Q Zhang, H Lu. Oncogene 2013
112
12

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
285
12


Distinct haematological disorder with deletion of long arm of no. 5 chromosome.
H Van den Berghe, J J Cassiman, G David, J P Fryns, J L Michaux, G Sokal. Nature 1974
393
12

Lenalidomide induces ubiquitination and degradation of CK1α in del(5q) MDS.
Jan Krönke, Emma C Fink, Paul W Hollenbach, Kyle J MacBeth, Slater N Hurst, Namrata D Udeshi, Philip P Chamberlain, D R Mani, Hon Wah Man, Anita K Gandhi,[...]. Nature 2015
409
12

Haematopoietic stem cells require a highly regulated protein synthesis rate.
Robert A J Signer, Jeffrey A Magee, Adrian Salic, Sean J Morrison. Nature 2014
309
12

The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia.
Daniel A Arber, Attilio Orazi, Robert Hasserjian, Jürgen Thiele, Michael J Borowitz, Michelle M Le Beau, Clara D Bloomfield, Mario Cazzola, James W Vardiman. Blood 2016
12

The p53 tumor suppressor causes congenital malformations in Rpl24-deficient mice and promotes their survival.
Martina Barkić, Sladana Crnomarković, Kristina Grabusić, Ivana Bogetić, Linda Panić, Sanda Tamarut, Maja Cokarić, Ines Jerić, Sandra Vidak, Sinisa Volarević. Mol Cell Biol 2009
78
14

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
129
11

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
298
11

International scoring system for evaluating prognosis in myelodysplastic syndromes.
P Greenberg, C Cox, M M LeBeau, P Fenaux, P Morel, G Sanz, M Sanz, T Vallespi, T Hamblin, D Oscier,[...]. Blood 1997
11

A critical role for phosphatase haplodeficiency in the selective suppression of deletion 5q MDS by lenalidomide.
Sheng Wei, Xianghong Chen, Kathy Rocha, P K Epling-Burnette, Julie Y Djeu, Qing Liu, John Byrd, Lubomir Sokol, Nick Lawrence, Roberta Pireddu,[...]. Proc Natl Acad Sci U S A 2009
155
11

Gene expression profiling of CD34+ cells in patients with the 5q- syndrome.
Jacqueline Boultwood, Andrea Pellagatti, Helen Cattan, Charles H Lawrie, Aristoteles Giagounidis, Luca Malcovati, Matteo G Della Porta, Martin Jädersten, Sally Killick, Carrie Fidler,[...]. Br J Haematol 2007
117
11

TET2 mutations predict response to hypomethylating agents in myelodysplastic syndrome patients.
Rafael Bejar, Allegra Lord, Kristen Stevenson, Michal Bar-Natan, Albert Pérez-Ladaga, Jacques Zaneveld, Hui Wang, Bennett Caughey, Petar Stojanov, Gad Getz,[...]. Blood 2014
390
11

Somatic SF3B1 mutation in myelodysplasia with ring sideroblasts.
E Papaemmanuil, M Cazzola, J Boultwood, L Malcovati, P Vyas, D Bowen, A Pellagatti, J S Wainscoat, E Hellstrom-Lindberg, C Gambacorti-Passerini,[...]. N Engl J Med 2011
808
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
266
11

Ribosomal protein SA haploinsufficiency in humans with isolated congenital asplenia.
Alexandre Bolze, Nizar Mahlaoui, Minji Byun, Bridget Turner, Nikolaus Trede, Steven R Ellis, Avinash Abhyankar, Yuval Itan, Etienne Patin, Samuel Brebner,[...]. Science 2013
120
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.