A citation-based method for searching scientific literature

Kevin Oakley, Yufen Han, Bandana A Vishwakarma, Su Chu, Ravi Bhatia, Kristbjorn O Gudmundsson, Jonathan Keller, Xiongfong Chen, Vasyl Vasko, Nancy A Jenkins, Neal G Copeland, Yang Du. Blood 2012
Times Cited: 49







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



Times Cited
  Times     Co-cited
Similarity


Recurrent SETBP1 mutations in atypical chronic myeloid leukemia.
Rocco Piazza, Simona Valletta, Nils Winkelmann, Sara Redaelli, Roberta Spinelli, Alessandra Pirola, Laura Antolini, Luca Mologni, Carla Donadoni, Elli Papaemmanuil,[...]. Nat Genet 2013
240
69

SETBP1 overexpression is a novel leukemogenic mechanism that predicts adverse outcome in elderly patients with acute myeloid leukemia.
Ion Cristóbal, Francisco J Blanco, Laura Garcia-Orti, Nerea Marcotegui, Carmen Vicente, José Rifon, Francisco J Novo, Eva Bandres, María J Calasanz, Carmelo Bernabeu,[...]. Blood 2010
107
55

Somatic SETBP1 mutations in myeloid malignancies.
Hideki Makishima, Kenichi Yoshida, Nhu Nguyen, Bartlomiej Przychodzen, Masashi Sanada, Yusuke Okuno, Kwok Peng Ng, Kristbjorn O Gudmundsson, Bandana A Vishwakarma, Andres Jerez,[...]. Nat Genet 2013
170
46

De novo mutations of SETBP1 cause Schinzel-Giedion syndrome.
Alexander Hoischen, Bregje W M van Bon, Christian Gilissen, Peer Arts, Bart van Lier, Marloes Steehouwer, Petra de Vries, Rick de Reuver, Nienke Wieskamp, Geert Mortier,[...]. Nat Genet 2010
320
40

Exome sequencing identifies secondary mutations of SETBP1 and JAK3 in juvenile myelomonocytic leukemia.
Hirotoshi Sakaguchi, Yusuke Okuno, Hideki Muramatsu, Kenichi Yoshida, Yuichi Shiraishi, Mariko Takahashi, Ayana Kon, Masashi Sanada, Kenichi Chiba, Hiroko Tanaka,[...]. Nat Genet 2013
148
38

SETBP1 mutations in 658 patients with myelodysplastic syndromes, chronic myelomonocytic leukemia and secondary acute myeloid leukemias.
F Damm, R Itzykson, O Kosmider, N Droin, A Renneville, V Chesnais, V Gelsi-Boyer, S de Botton, N Vey, C Preudhomme,[...]. Leukemia 2013
86
30

Identification and characterization of SEB, a novel protein that binds to the acute undifferentiated leukemia-associated protein SET.
M Minakuchi, N Kakazu, M J Gorrin-Rivas, T Abe, T D Copeland, K Ueda, Y Adachi. Eur J Biochem 2001
58
24

SETBP1 mutation analysis in 944 patients with MDS and AML.
F Thol, K J Suchanek, C Koenecke, M Stadler, U Platzbecker, C Thiede, T Schroeder, G Kobbe, S Kade, P Löffeld,[...]. Leukemia 2013
53
24

CSF3R T618I is a highly prevalent and specific mutation in chronic neutrophilic leukemia.
A Pardanani, T L Lasho, R R Laborde, M Elliott, C A Hanson, R A Knudson, R P Ketterling, J E Maxson, J W Tyner, A Tefferi. Leukemia 2013
157
22

Runx1 repression by histone deacetylation is critical for Setbp1-induced mouse myeloid leukemia development.
B A Vishwakarma, N Nguyen, H Makishima, N Hosono, K O Gudmundsson, V Negi, K Oakley, Y Han, B Przychodzen, J P Maciejewski,[...]. Leukemia 2016
19
57

SETBP1 mutations in 415 patients with primary myelofibrosis or chronic myelomonocytic leukemia: independent prognostic impact in CMML.
R R Laborde, M M Patnaik, T L Lasho, C M Finke, C A Hanson, R A Knudson, R P Ketterling, A Pardanani, A Tefferi. Leukemia 2013
68
20


SETBP1 mutations drive leukemic transformation in ASXL1-mutated MDS.
D Inoue, J Kitaura, H Matsui, H-A Hou, W-C Chou, A Nagamachi, K C Kawabata, K Togami, R Nagase, S Horikawa,[...]. Leukemia 2015
47
21

Myb expression is critical for myeloid leukemia development induced by Setbp1 activation.
Nhu Nguyen, Bandana A Vishwakarma, Kevin Oakley, Yufen Han, Bartlomiej Przychodzen, Jaroslaw P Maciejewski, Yang Du. Oncotarget 2016
14
71

Oncogenic CSF3R mutations in chronic neutrophilic leukemia and atypical CML.
Julia E Maxson, Jason Gotlib, Daniel A Pollyea, Angela G Fleischman, Anupriya Agarwal, Christopher A Eide, Daniel Bottomly, Beth Wilmot, Shannon K McWeeney, Cristina E Tognon,[...]. N Engl J Med 2013
315
18

SETBP1 mutations occur in 9% of MDS/MPN and in 4% of MPN cases and are strongly associated with atypical CML, monosomy 7, isochromosome i(17)(q10), ASXL1 and CBL mutations.
M Meggendorfer, U Bacher, T Alpermann, C Haferlach, W Kern, C Gambacorti-Passerini, T Haferlach, S Schnittger. Leukemia 2013
111
18

Fusion of NUP98 and the SET binding protein 1 (SETBP1) gene in a paediatric acute T cell lymphoblastic leukaemia with t(11;18)(p15;q12).
Ioannis Panagopoulos, Gitte Kerndrup, Niels Carlsen, Bodil Strömbeck, Margareth Isaksson, Bertil Johansson. Br J Haematol 2007
34
23

PP2A impaired activity is a common event in acute myeloid leukemia and its activation by forskolin has a potent anti-leukemic effect.
I Cristóbal, L Garcia-Orti, C Cirauqui, M M Alonso, M J Calasanz, M D Odero. Leukemia 2011
97
16

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
16

Mutations in SETBP1 are recurrent in myelodysplastic syndromes and often coexist with cytogenetic markers associated with disease progression.
Marta Fernandez-Mercado, Andrea Pellagatti, Cristina Di Genua, Maria Jose Larrayoz, Nils Winkelmann, Paula Aranaz, Adam Burns, Anna Schuh, Maria Jose Calasanz, Nicholas C P Cross,[...]. Br J Haematol 2013
33
24

Overlapping SETBP1 gain-of-function mutations in Schinzel-Giedion syndrome and hematologic malignancies.
Rocio Acuna-Hidalgo, Pelagia Deriziotis, Marloes Steehouwer, Christian Gilissen, Sarah A Graham, Sipko van Dam, Julie Hoover-Fong, Aida B Telegrafi, Anne Destree, Robert Smigiel,[...]. PLoS Genet 2017
17
41

Clonal architecture of secondary acute myeloid leukemia.
Matthew J Walter, Dong Shen, Li Ding, Jin Shao, Daniel C Koboldt, Ken Chen, David E Larson, Michael D McLellan, David Dooling, Rachel Abbott,[...]. N Engl J Med 2012
528
12

Gain-of-function of mutated C-CBL tumour suppressor in myeloid neoplasms.
Masashi Sanada, Takahiro Suzuki, Lee-Yung Shih, Makoto Otsu, Motohiro Kato, Satoshi Yamazaki, Azusa Tamura, Hiroaki Honda, Mamiko Sakata-Yanagimoto, Keiki Kumano,[...]. Nature 2009
308
12

Genomic and epigenomic landscapes of adult de novo acute myeloid leukemia.
Timothy J Ley, Christopher Miller, Li Ding, Benjamin J Raphael, Andrew J Mungall, A Gordon Robertson, Katherine Hoadley, Timothy J Triche, Peter W Laird, Jack D Baty,[...]. N Engl J Med 2013
12

Schinzel-Giedion syndrome in two Brazilian patients: Report of a novel mutation in SETBP1 and literature review of the clinical features.
Ellaine Carvalho, Rachel Honjo, Monize Magalhães, Guilherme Yamamoto, Katia Rocha, Michel Naslavsky, Mayana Zatz, Maria Rita Passos-Bueno, Chong Kim, Debora Bertola. Am J Med Genet A 2015
14
42

Progressive brain atrophy in Schinzel-Giedion syndrome with a SETBP1 mutation.
Akihito Takeuchi, Nobuhiko Okamoto, Shoko Fujinaga, Hirosuke Morita, Junya Shimizu, Tomoyuki Akiyama, Shinsuke Ninomiya, Jun-ichi Takanashi, Toshihide Kubo. Eur J Med Genet 2015
15
40

SETBP1 induces transcription of a network of development genes by acting as an epigenetic hub.
Rocco Piazza, Vera Magistroni, Sara Redaelli, Mario Mauri, Luca Massimino, Alessandro Sessa, Marco Peronaci, Maciej Lalowski, Rabah Soliymani, Caterina Mezzatesta,[...]. Nat Commun 2018
19
31

Schinzel-Giedion syndrome: report of splenopancreatic fusion and proposed diagnostic criteria.
Anna M Lehman, Deborah McFadden, Denise Pugash, Karan Sangha, William T Gibson, Millan S Patel. Am J Med Genet A 2008
31
16

The tumor suppressor PP2A is functionally inactivated in blast crisis CML through the inhibitory activity of the BCR/ABL-regulated SET protein.
Paolo Neviani, Ramasamy Santhanam, Rossana Trotta, Mario Notari, Bradley W Blaser, Shujun Liu, Hsiaoyin Mao, Ji Suk Chang, Annamaria Galietta, Ashwin Uttam,[...]. Cancer Cell 2005
367
10

Frequent CBL mutations associated with 11q acquired uniparental disomy in myeloproliferative neoplasms.
Francis H Grand, Claire E Hidalgo-Curtis, Thomas Ernst, Katerina Zoi, Christine Zoi, Carolann McGuire, Sebastian Kreil, Amy Jones, Joannah Score, Georgia Metzgeroth,[...]. Blood 2009
289
10

Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disorders.
Thomas Ernst, Andrew J Chase, Joannah Score, Claire E Hidalgo-Curtis, Catherine Bryant, Amy V Jones, Katherine Waghorn, Katerina Zoi, Fiona M Ross, Andreas Reiter,[...]. Nat Genet 2010
806
10

Reduced expression by SETBP1 haploinsufficiency causes developmental and expressive language delay indicating a phenotype distinct from Schinzel-Giedion syndrome.
Isabel Filges, Keiko Shimojima, Nobuhiko Okamoto, Benno Röthlisberger, Peter Weber, Andreas R Huber, Tsutomu Nishizawa, Alexandre N Datta, Peter Miny, Toshiyuki Yamamoto. J Med Genet 2011
46
10

SETBP1 and miR_4319 dysregulation in primary myelofibrosis progression to acute myeloid leukemia.
Francesco Albano, Luisa Anelli, Antonella Zagaria, Nicoletta Coccaro, Paola Casieri, Angela Minervini, Giorgina Specchia. J Hematol Oncol 2012
19
26

Mutations of polycomb-associated gene ASXL1 in myelodysplastic syndromes and chronic myelomonocytic leukaemia.
Véronique Gelsi-Boyer, Virginie Trouplin, José Adélaïde, Julien Bonansea, Nathalie Cervera, Nadine Carbuccia, Arnaud Lagarde, Thomas Prebet, Meyer Nezri, Danielle Sainty,[...]. Br J Haematol 2009
415
10

Mutation in TET2 in myeloid cancers.
François Delhommeau, Sabrina Dupont, Véronique Della Valle, Chloé James, Severine Trannoy, Aline Massé, Olivier Kosmider, Jean-Pierre Le Couedic, Fabienne Robert, Antonio Alberdi,[...]. N Engl J Med 2009
10

Evi-1 is a critical regulator for hematopoietic stem cells and transformed leukemic cells.
Susumu Goyama, Go Yamamoto, Munetake Shimabe, Tomohiko Sato, Motoshi Ichikawa, Seishi Ogawa, Shigeru Chiba, Mineo Kurokawa. Cell Stem Cell 2008
186
10

Correction of X-linked chronic granulomatous disease by gene therapy, augmented by insertional activation of MDS1-EVI1, PRDM16 or SETBP1.
Marion G Ott, Manfred Schmidt, Kerstin Schwarzwaelder, Stefan Stein, Ulrich Siler, Ulrike Koehl, Hanno Glimm, Klaus Kühlcke, Andrea Schilz, Hana Kunkel,[...]. Nat Med 2006
842
10

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
782
10

The role of mutations in epigenetic regulators in myeloid malignancies.
Alan H Shih, Omar Abdel-Wahab, Jay P Patel, Ross L Levine. Nat Rev Cancer 2012
487
10

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
10

SETBP1 mutations in juvenile myelomonocytic leukaemia and myelodysplastic syndrome but not in paediatric acute myeloid leukaemia.
Norio Shiba, Kentaro Ohki, Myoung-Ja Park, Manabu Sotomatsu, Kazuko Kudo, Etsuro Ito, Masahiro Sako, Hirokazu Arakawa, Yasuhide Hayashi. Br J Haematol 2014
9
55

Clinical implications of the SETBP1 mutation in patients with primary myelodysplastic syndrome and its stability during disease progression.
Hsin-An Hou, Yuan-Yeh Kuo, Jih-Luh Tang, Wen-Chien Chou, Ming Yao, Yan-Jun Lai, Chien-Chin Lin, Chien-Yuan Chen, Chieh-Yu Liu, Mei-Hsuan Tseng,[...]. Am J Hematol 2014
48
10

A new player SETs in myeloid malignancy.
Thomas Trimarchi, Panagiotis Ntziachristos, Iannis Aifantis. Nat Genet 2013
12
41

Subclonal mutations in SETBP1 confer a poor prognosis in juvenile myelomonocytic leukemia.
Elliot Stieglitz, Camille B Troup, Laura C Gelston, John Haliburton, Eric D Chow, Kristie B Yu, Jon Akutagawa, Amaro N Taylor-Weiner, Y Lucy Liu, Yong-Dong Wang,[...]. Blood 2015
45
11

Long term follow up of two independent patients with Schinzel-Giedion carrying SETBP1 mutations.
Yvan Herenger, Corinne Stoetzel, Elise Schaefer, Sophie Scheidecker, Marie-Cécile Manière, Valérie Pelletier, Yves Alembik, Dominique Christmann, Jean-Michel Clavert, Joelle Terzic,[...]. Eur J Med Genet 2015
12
41

SETBP1 mutations in two Thai patients with Schinzel-Giedion syndrome.
K Suphapeetiporn, C Srichomthong, V Shotelersuk. Clin Genet 2011
20
25

Sequential gain of mutations in severe congenital neutropenia progressing to acute myeloid leukemia.
Renée Beekman, Marijke G Valkhof, Mathijs A Sanders, Paulette M H van Strien, Jurgen R Haanstra, Lianne Broeders, Wendy M Geertsma-Kleinekoort, Anjo J P Veerman, Peter J M Valk, Roel G Verhaak,[...]. Blood 2012
115
8


Patterns of missplicing due to somatic U2AF1 mutations in myeloid neoplasms.
Bartlomiej Przychodzen, Andres Jerez, Kathryn Guinta, Mikkael A Sekeres, Richard Padgett, Jaroslaw P Maciejewski, Hideki Makishima. Blood 2013
109
8

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
825
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.