A citation-based method for searching scientific literature

Akihito Takeuchi, Nobuhiko Okamoto, Shoko Fujinaga, Hirosuke Morita, Junya Shimizu, Tomoyuki Akiyama, Shinsuke Ninomiya, Jun-ichi Takanashi, Toshihide Kubo. Eur J Med Genet 2015
Times Cited: 15







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



Times Cited
  Times     Co-cited
Similarity


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
80


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
83

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
71

SETBP1 mutations in two Thai patients with Schinzel-Giedion syndrome.
K Suphapeetiporn, C Srichomthong, V Shotelersuk. Clin Genet 2011
20
66

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
60

Distinct neurological features in a patient with Schinzel-Giedion syndrome caused by a recurrent SETBP1 mutation.
Jung Min Ko, Byung Chan Lim, Ki Joong Kim, Yong Seung Hwang, Hye Won Ryu, Jung Ho Lee, Jon Su Kim, Jong-Hee Chae. Childs Nerv Syst 2013
20
53

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
53

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
46

[Schinzel-Giedion syndrome: a new mutation in SETBP1].
V López-González, M R Domingo-Jiménez, L Burglen, M J Ballesta-Martínez, S Whalen, J A Piñero-Fernández, E Guillén-Navarro. An Pediatr (Barc) 2015
10
70

West syndrome in a patient with Schinzel-Giedion syndrome.
Fuyu Miyake, Yukiko Kuroda, Takuya Naruto, Ikuko Ohashi, Kyoko Takano, Kenji Kurosawa. J Child Neurol 2015
12
50

Setbp1 promotes the self-renewal of murine myeloid progenitors via activation of Hoxa9 and Hoxa10.
Kevin Oakley, Yufen Han, Bandana A Vishwakarma, Su Chu, Ravi Bhatia, Kristbjorn O Gudmundsson, Jonathan Keller, Xiongfong Chen, Vasyl Vasko, Nancy A Jenkins,[...]. Blood 2012
49
40

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
40

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
40

Refining analyses of copy number variation identifies specific genes associated with developmental delay.
Bradley P Coe, Kali Witherspoon, Jill A Rosenfeld, Bregje W M van Bon, Anneke T Vulto-van Silfhout, Paolo Bosco, Kathryn L Friend, Carl Baker, Serafino Buono, Lisenka E L M Vissers,[...]. Nat Genet 2014
323
33

Whole-Exome Sequencing in the Clinic: Lessons from Six Consecutive Cases from the Clinician's Perspective.
Amber Volk, Erin Conboy, Beverly Wical, Marc Patterson, Salman Kirmani. Mol Syndromol 2015
21
33

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
33

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
33

372 kb microdeletion in 18q12.3 causing SETBP1 haploinsufficiency associated with mild mental retardation and expressive speech impairment.
Giuseppina Marseglia, Maria Rosaria Scordo, Chiara Pescucci, Genni Nannetti, Elisabetta Biagini, Valeria Scandurra, Francesca Gerundino, Alberto Magi, Matteo Benelli, Francesca Torricelli. Eur J Med Genet 2012
32
33

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
26

Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study.
Anita Rauch, Dagmar Wieczorek, Elisabeth Graf, Thomas Wieland, Sabine Endele, Thomas Schwarzmayr, Beate Albrecht, Deborah Bartholdi, Jasmin Beygo, Nataliya Di Donato,[...]. Lancet 2012
657
20

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 in 106 patients with therapy-related myeloid neoplasms.
Emiliano Fabiani, Giulia Falconi, Luana Fianchi, Marianna Criscuolo, Giuseppe Leone, Maria Teresa Voso. Haematologica 2014
12
25

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
20


Unusual neuroradiological features in Schinzel-Giedion syndrome: a novel case.
Jodi Marianne Lestner, Wui K Chong, Amaka Offiiah, Jonathan Kefas, Anthony M Vandersteen. Clin Dysmorphol 2012
9
33

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
20

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
20

Schinzel-Giedion syndrome.
H Touge, T Fujinaga, M Okuda, H Aoshi. Int J Urol 2001
14
21

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
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
20

Clinical and radiological findings in Schinzel-Giedion syndrome.
Mudaffer Al-Mudaffer, Christine Oley, Sue Price, Ian Hayes, Alison Stewart, Christine M Hall, William Reardon. Eur J Pediatr 2008
12
25

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
20

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
33

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
20

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
20

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
21

Refractory sacrococcygeal germ cell tumor in Schinzel-Giedion syndrome.
Kenji Kishimoto, Ryoji Kobayashi, Nozomi Yonemaru, Hiroshi Yamamoto, Takao Tsujioka, Hirozumi Sano, Daisuke Suzuki, Kazue Yasuda, Masahiko Suzuki, Akiko Ando,[...]. J Pediatr Hematol Oncol 2015
5
60

Malignant retroperitoneal tumor arising in a multicystic dysplastic kidney of a girl with Schinzel-Giedion syndrome.
Fumi Matsumoto, Akira Tohda, Kenji Shimada, Nobuhiko Okamoto. Int J Urol 2005
12
25

Schinzel-Giedion syndrome: further delineation of the phenotype.
A M Elliott, K Meagher-Villemure, K Oudjhane, V M der Kaloustian. Clin Dysmorphol 1996
17
20

Delineation of a critical region on chromosome 18 for the del(18)(q12.2q21.1) syndrome.
Karen Buysse, Björn Menten, Ann Oostra, Sylvie Tavernier, Geert R Mortier, Frank Speleman. Am J Med Genet A 2008
25
20

Extradural ependymal tumor with myxopapillary and ependymoblastic differentiation in a case of Schinzel-Giedion syndrome.
Rudi Beschorner, Manfred Wehrmann, Ulrike Ernemann, Michael Bonin, Veronka Horber, Barbara Oehl-Jaschkowitz, Richard Meyermann, Andreas Dufke. Acta Neuropathol 2007
24
20

Interstitial deletion of the long arm of chromosome 18, del(18)(q12.2q21.1): a report of three cases of an autosomal deletion with a mild phenotype.
A Schinzel, F Binkert, D M Lillington, M Sands, R J Stocks, R H Lindenbaum, H Matthews, H Sheridan. J Med Genet 1991
32
20

The Schinzel-Giedion syndrome.
L I al-Gazali, P Farndon, J Burn, D B Flannery, C Davison, R F Mueller. J Med Genet 1990
33
20

Schinzel-Giedion syndrome: a further cause of early myoclonic encephalopathy and vacuolating myelinopathy.
Shuei Watanabe, Akitoshi Murayama, Kazuhiro Haginoya, Soichiro Tanaka, Noriko Togashi, Daiki Abukawa, Atsushi Sato, Masue Imaizumi, Hideto Yoshikawa, Rumiko Takayama,[...]. Brain Dev 2012
12
25

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
20

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
20

Synaptic, transcriptional and chromatin genes disrupted in autism.
Silvia De Rubeis, Xin He, Arthur P Goldberg, Christopher S Poultney, Kaitlin Samocha, A Erucment Cicek, Yan Kou, Li Liu, Menachem Fromer, Susan Walker,[...]. Nature 2014
13

Whole-exome sequencing improves the diagnosis yield in sporadic infantile spasm syndrome.
S Dimassi, A Labalme, D Ville, A Calender, C Mignot, N Boutry-Kryza, J de Bellescize, C Rivier-Ringenbach, E Bourel-Ponchel, D Cheillan,[...]. Clin Genet 2016
51
13

De novo genic mutations among a Chinese autism spectrum disorder cohort.
Tianyun Wang, Hui Guo, Bo Xiong, Holly A F Stessman, Huidan Wu, Bradley P Coe, Tychele N Turner, Yanling Liu, Wenjing Zhao, Kendra Hoekzema,[...]. Nat Commun 2016
147
13


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.