A citation-based method for searching scientific literature


List of co-cited articles
177 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
36

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
84


New finding of Schinzel-Giedion syndrome: a case with a malignant sacrococcygeal teratoma.
N H Robin, K Grace, T G DeSouza, D McDonald-McGinn, E H Zackai. Am J Med Genet 1993
31
83

Neurosonography and pathology in the Schinzel-Giedion syndrome.
A C Maclennan, D Doyle, R M Simpson. J Med Genet 1991
27
88

Schinzel-Giedion syndrome: autopsy report and additional clinical manifestations.
J I Rodríguez, J A Jiménez-Heffernan, J Leal. Am J Med Genet 1994
25
88

Three new cases of the Schinzel-Giedion syndrome and review of the literature.
P Labrune, S Lyonnet, V Zupan, M C Imbert, F Goutieres, P Hubert, M Le Merrer. Am J Med Genet 1994
26
84

Schinzel-Giedion syndrome: evidence for a neurodegenerative process.
A M Shah, M F Smith, P D Griffiths, O W Quarrell. Am J Med Genet 1999
22
90

Schinzel-Giedion syndrome.
A Verloes, D Moës, L Palumbo, C Elmer, A François, G Bricteux. Eur J Pediatr 1993
20
95

Schinzel-Giedion syndrome: report of two sibs.
J Antich, R Manzanares, F Camarasa, X Krauel, J Vila, V Cusi. Am J Med Genet 1995
21
85

SETBP1 mutations in two Thai patients with Schinzel-Giedion syndrome.
K Suphapeetiporn, C Srichomthong, V Shotelersuk. Clin Genet 2011
20
90

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
20

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
54

Sacral tumors in Schinzel-Giedion syndrome.
E McPherson, M Clemens, L Hoffner, U Surti. Am J Med Genet 1998
19
84

Schinzel-Giedion syndrome: further delineation of the phenotype.
A M Elliott, K Meagher-Villemure, K Oudjhane, V M der Kaloustian. Clin Dysmorphol 1996
17
88

The Schinzel-Giedion syndrome. A case report and review of the literature.
M Pul, N Yilmaz, B Komsuoglu. Clin Pediatr (Phila) 1990
15
93

Schinzel-Giedion syndrome and congenital megacalyces.
T E Herman, D A Sweetser, W H McAlister, S B Dowton. Pediatr Radiol 1993
19
73

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
60

Schinzel-Giedion syndrome with sacrococcygeal teratoma.
Alessandro Sandri, Andrea Domenco Manazza, Daniele Bertin, Margherita Silengo, Maria Eleonora Basso, Marco Forni, Enrico Madon. J Pediatr Hematol Oncol 2003
16
87

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
15

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
70

Agenesis of the corpus callosum in Schinzel-Giedion syndrome associated with 47,XXY karyotype.
F F Ozkinay, M Akisü, N Kültürsay, R Oral, N Tansug, G Sapmaz. Clin Genet 1996
17
76

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
50

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
13

Schinzel-Giedion syndrome.
H Touge, T Fujinaga, M Okuda, H Aoshi. Int J Urol 2001
14
78

Schinzel-Giedion syndrome: a further cause of West syndrome.
Salvatore Grosso, Caterina Pagano, Maddalena Cioni, Rosanna Maria Di Bartolo, Guido Morgese, Paolo Balestri. Brain Dev 2003
12
91


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
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
78

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
73

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
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
21

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
20

Schinzel-Giedion syndrome. A patient with hypothyroidism and diabetes insipidus.
H Santos, I Cordeiro, A Medeira, E Mendonça, N L Antunes, F C Rosa. Genet Couns 1994
9
100

A patient with Schinzel-Giedion syndrome and a review of 20 patients.
N Okamoto, M Takeuchi, H Kitajima, S Hosokawa. Jpn J Hum Genet 1995
12
75

A Croatian case of the Schinzel-Giedion syndrome.
V Culić, B Resic, J W Oorthuys, W C Overweg-Plandsoen, R C Hennekam. Genet Couns 1996
9
100


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
15

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
75

[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
90

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
75

Schinzel-Giedion syndrome.
S Alavi, A Kher, B A Bharucha. Indian Pediatr 1994
8
100

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
88

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
66

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
11

Schinzel-Giedion syndrome with severe deafness and neurodegenerative process.
Y Alembik, D Christmann, A de Saint Martin, M Eliot, H Dollfus, F Pauly, C Stoll. Ann Genet 1999
7
100

Hydronephrosis in Schinzel-Giedion syndrome: an important clue for the diagnosis.
Lilian Maria José Albano, Paula Priscila Ohara Sakae, Marta Maria Galli Bozzo Mataloun, Clea Rodrigues Leone, Débora R Bertola, Chong Ae Kim. Rev Hosp Clin Fac Med Sao Paulo 2004
10
70

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
7

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
7


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.