A citation-based method for searching scientific literature

Yvan Herenger, Corinne Stoetzel, Elise Schaefer, Sophie Scheidecker, Marie-Cécile Manière, Valérie Pelletier, Yves Alembik, Dominique Christmann, Jean-Michel Clavert, Joelle Terzic, Michel Fischbach, Anne De Saint Martin, Hélène Dollfus. Eur J Med Genet 2015
Times Cited: 12







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



Times Cited
  Times     Co-cited
Similarity


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
83

SETBP1 mutations in two Thai patients with Schinzel-Giedion syndrome.
K Suphapeetiporn, C Srichomthong, V Shotelersuk. Clin Genet 2011
20
75

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
321
75


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
66

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
58

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

[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
60

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
50

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
242
50

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
171
50

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
41

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
41

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
41

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
149
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
22
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

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
33

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
25

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
25


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
112
25

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
158
25

Schinzel-Giedion syndrome.
H Touge, T Fujinaga, M Okuda, H Aoshi. Int J Urol 2001
14
25

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
25

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
25

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
25

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
25

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
25

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
25

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
25

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
25

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
25

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

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
325
16

Analysis of protein-coding genetic variation in 60,706 humans.
Monkol Lek, Konrad J Karczewski, Eric V Minikel, Kaitlin E Samocha, Eric Banks, Timothy Fennell, Anne H O'Donnell-Luria, James S Ware, Andrew J Hill, Beryl B Cummings,[...]. Nature 2016
16

Atypical chronic myeloid leukemia with concomitant CSF3R T618I and SETBP1 mutations unresponsive to the JAK inhibitor ruxolitinib.
Emanuele Ammatuna, Matthias Eefting, Kirsten van Lom, François G Kavelaars, Peter J M Valk, Ivo P Touw. Ann Hematol 2015
24
16

A case of Schinzel-Giedion syndrome complicated with progressive severe gingival hyperplasia and progressive brain atrophy.
T Kondoh, N Kamimura, A Tsuru, T Matsumoto, T Matsuzaka, H Moriuchi. Pediatr Int 2001
15
16

Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profiles.
Aravind Subramanian, Pablo Tamayo, Vamsi K Mootha, Sayan Mukherjee, Benjamin L Ebert, Michael A Gillette, Amanda Paulovich, Scott L Pomeroy, Todd R Golub, Eric S Lander,[...]. Proc Natl Acad Sci U S A 2005
16

ASXL1 mutations are frequent and prognostically detrimental in CSF3R-mutated chronic neutrophilic leukemia.
Michelle A Elliott, Animesh Pardanani, Curtis A Hanson, Terra L Lasho, Christy M Finke, Alem A Belachew, Ayalew Tefferi. Am J Hematol 2015
44
16

Prioritization of neurodevelopmental disease genes by discovery of new mutations.
Alexander Hoischen, Niklas Krumm, Evan E Eichler. Nat Neurosci 2014
104
16

CSF3R, SETBP1 and CALR mutations in chronic neutrophilic leukemia.
Yajuan Cui, Bing Li, Robert Peter Gale, Qian Jiang, Zefeng Xu, Tiejun Qin, Peihong Zhang, Yue Zhang, Zhijian Xiao. J Hematol Oncol 2014
30
16

Further clinical and sensorial delineation of Schinzel-Giedion syndrome: report of two cases.
David Minn, Dominique Christmann, Anne De Saint-Martin, Yves Alembik, Mylène Eliot, Geneviève Mack, Michel Fischbach, Jacques Flament, Francis Veillon, Hélène Dollfus. Am J Med Genet 2002
23
16

Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2.
Michael I Love, Wolfgang Huber, Simon Anders. Genome Biol 2014
16


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.