A citation-based method for searching scientific literature


List of co-cited articles
1538 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia.
R Shiang, L M Thompson, Y Z Zhu, D M Church, T J Fielder, M Bocian, S T Winokur, J J Wasmuth. Cell 1994
916
35

Cellular signaling by fibroblast growth factor receptors.
V P Eswarakumar, I Lax, J Schlessinger. Cytokine Growth Factor Rev 2005
26

Thanatophoric dysplasia (types I and II) caused by distinct mutations in fibroblast growth factor receptor 3.
P L Tavormina, R Shiang, L M Thompson, Y Z Zhu, D J Wilkin, R S Lachman, W R Wilcox, D L Rimoin, D H Cohn, J J Wasmuth. Nat Genet 1995
476
26

Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia.
F Rousseau, J Bonaventure, L Legeai-Mallet, A Pelet, J M Rozet, P Maroteaux, M Le Merrer, A Munnich. Nature 1994
649
24

Achondroplasia.
William A Horton, Judith G Hall, Jacqueline T Hecht. Lancet 2007
268
23

Frequent activating mutations of FGFR3 in human bladder and cervix carcinomas.
D Cappellen, C De Oliveira, D Ricol, S de Medina, J Bourdin, X Sastre-Garau, D Chopin, J P Thiery, F Radvanyi. Nat Genet 1999
524
22

Skeletal overgrowth and deafness in mice lacking fibroblast growth factor receptor 3.
J S Colvin, B A Bohne, G W Harding, D G McEwen, D M Ornitz. Nat Genet 1996
687
22

Fibroblast growth factor receptor 3 is a negative regulator of bone growth.
C Deng, A Wynshaw-Boris, F Zhou, A Kuo, P Leder. Cell 1996
834
20


Constitutive activation of MEK1 in chondrocytes causes Stat1-independent achondroplasia-like dwarfism and rescues the Fgfr3-deficient mouse phenotype.
Shunichi Murakami, Gener Balmes, Sandra McKinney, Zhaoping Zhang, David Givol, Benoit de Crombrugghe. Genes Dev 2004
198
17

A neonatal lethal mutation in FGFR3 uncouples proliferation and differentiation of growth plate chondrocytes in embryos.
T Iwata, L Chen, C Li, D A Ovchinnikov, R R Behringer, C A Francomano, C X Deng. Hum Mol Genet 2000
157
16


A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia.
G A Bellus, I McIntosh, E A Smith, A S Aylsworth, I Kaitila, W A Horton, G A Greenhaw, J T Hecht, C A Francomano. Nat Genet 1995
332
16

Achondroplasia is defined by recurrent G380R mutations of FGFR3.
G A Bellus, T W Hefferon, R I Ortiz de Luna, J T Hecht, W A Horton, M Machado, I Kaitila, I McIntosh, C A Francomano. Am J Hum Genet 1995
335
15



Fibroblast growth factor signalling: from development to cancer.
Nicholas Turner, Richard Grose. Nat Rev Cancer 2010
15


Distinct missense mutations of the FGFR3 lys650 codon modulate receptor kinase activation and the severity of the skeletal dysplasia phenotype.
G A Bellus, E B Spector, P W Speiser, C A Weaver, A T Garber, C R Bryke, J Israel, S S Rosengren, M K Webster, D J Donoghue,[...]. Am J Hum Genet 2000
114
14


Antibody-based targeting of FGFR3 in bladder carcinoma and t(4;14)-positive multiple myeloma in mice.
Jing Qing, Xiangnan Du, Yongmei Chen, Pamela Chan, Hao Li, Ping Wu, Scot Marsters, Scott Stawicki, Janet Tien, Klara Totpal,[...]. J Clin Invest 2009
169
14

Overexpression of CNP in chondrocytes rescues achondroplasia through a MAPK-dependent pathway.
Akihiro Yasoda, Yasato Komatsu, Hideki Chusho, Takashi Miyazawa, Ami Ozasa, Masako Miura, Tatsuya Kurihara, Tomohiro Rogi, Shoji Tanaka, Michio Suda,[...]. Nat Med 2004
262
14

Evaluation of the therapeutic potential of a CNP analog in a Fgfr3 mouse model recapitulating achondroplasia.
Florence Lorget, Nabil Kaci, Jeff Peng, Catherine Benoist-Lasselin, Emilie Mugniery, Todd Oppeneer, Dan J Wendt, Sean M Bell, Sherry Bullens, Stuart Bunting,[...]. Am J Hum Genet 2012
101
14


Cell responses to FGFR3 signalling: growth, differentiation and apoptosis.
Corine G M L'Hôte, Margaret A Knowles. Exp Cell Res 2005
157
13

Receptor specificity of the fibroblast growth factor family. The complete mammalian FGF family.
Xiuqin Zhang, Omar A Ibrahimi, Shaun K Olsen, Hisashi Umemori, Moosa Mohammadi, David M Ornitz. J Biol Chem 2006
781
13

Coordination of chondrogenesis and osteogenesis by fibroblast growth factor 18.
Zhonghao Liu, Jingsong Xu, Jennifer S Colvin, David M Ornitz. Genes Dev 2002
337
13


A novel skeletal dysplasia with developmental delay and acanthosis nigricans is caused by a Lys650Met mutation in the fibroblast growth factor receptor 3 gene.
P L Tavormina, G A Bellus, M K Webster, M J Bamshad, A E Fraley, I McIntosh, J Szabo, W Jiang, E W Jabs, W R Wilcox,[...]. Am J Hum Genet 1999
115
13


Activation of Stat1 by mutant fibroblast growth-factor receptor in thanatophoric dysplasia type II dwarfism.
W C Su, M Kitagawa, N Xue, B Xie, S Garofalo, J Cho, C Deng, W A Horton, X Y Fu. Nature 1997
251
13

Receptor specificity of the fibroblast growth factor family.
D M Ornitz, J Xu, J S Colvin, D G McEwen, C A MacArthur, F Coulier, G Gao, M Goldfarb. J Biol Chem 1996
12

A novel mutation in FGFR3 causes camptodactyly, tall stature, and hearing loss (CATSHL) syndrome.
Reha M Toydemir, Anna E Brassington, Pinar Bayrak-Toydemir, Patrycja A Krakowiak, Lynn B Jorde, Frank G Whitby, Nicola Longo, David H Viskochil, John C Carey, Michael J Bamshad. Am J Hum Genet 2006
85
14

A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome.
M Muenke, U Schell, A Hehr, N H Robin, H W Losken, A Schinzel, L J Pulleyn, P Rutland, W Reardon, S Malcolm. Nat Genet 1994
488
12

FGF18 is required for normal cell proliferation and differentiation during osteogenesis and chondrogenesis.
Norihiko Ohbayashi, Masaki Shibayama, Yoko Kurotaki, Mayumi Imanishi, Toshihiko Fujimori, Nobuyuki Itoh, Shinji Takada. Genes Dev 2002
326
12


Proline to arginine mutations in FGF receptors 1 and 3 result in Pfeiffer and Muenke craniosynostosis syndromes through enhancement of FGF binding affinity.
Omar A Ibrahimi, Fuming Zhang, Anna V Eliseenkova, Robert J Linhardt, Moosa Mohammadi. Hum Mol Genet 2004
100
12

A molecular brake in the kinase hinge region regulates the activity of receptor tyrosine kinases.
Huaibin Chen, Jinghong Ma, Wanqing Li, Anna V Eliseenkova, Chongfeng Xu, Thomas A Neubert, W Todd Miller, Moosa Mohammadi. Mol Cell 2007
164
12

Analysis of STAT1 activation by six FGFR3 mutants associated with skeletal dysplasia undermines dominant role of STAT1 in FGFR3 signaling in cartilage.
Pavel Krejci, Lisa Salazar, Tamara A Kashiwada, Katarina Chlebova, Alena Salasova, Leslie Michels Thompson, Vitezslav Bryja, Alois Kozubik, William R Wilcox. PLoS One 2008
32
37

Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome.
A O Wilkie, S F Slaney, M Oldridge, M D Poole, G J Ashworth, A D Hockley, R D Hayward, D J David, L J Pulleyn, P Rutland. Nat Genet 1995
672
12


Novel fibroblast growth factor receptor 3 (FGFR3) mutations in bladder cancer previously identified in non-lethal skeletal disorders.
Bas W G van Rhijn, Angela A G van Tilborg, Irene Lurkin, Jacky Bonaventure, Annie de Vries, Jean-Paul Thiery, Theodorus H van der Kwast, Ellen C Zwarthoff, Francois Radvanyi. Eur J Hum Genet 2002
119
11

Spatio-temporal expression of FGFR 1, 2 and 3 genes during human embryo-fetal ossification.
A L Delezoide, C Benoist-Lasselin, L Legeai-Mallet, M Le Merrer, A Munnich, M Vekemans, J Bonaventure. Mech Dev 1998
136
11

Clinical spectrum of fibroblast growth factor receptor mutations.
M R Passos-Bueno, W R Wilcox, E W Jabs, A L Sertié, L G Alonso, H Kitoh. Hum Mutat 1999
221
11

FGFR3-related dwarfism and cell signaling.
Daisuke Harada, Yoshitaka Yamanaka, Koso Ueda, Hiroyuki Tanaka, Yoshiki Seino. J Bone Miner Metab 2009
25
44

Activating mutations in FGFR3 and HRAS reveal a shared genetic origin for congenital disorders and testicular tumors.
Anne Goriely, Ruth M S Hansen, Indira B Taylor, Inge A Olesen, Grete Krag Jacobsen, Simon J McGowan, Susanne P Pfeifer, Gilean A T McVean, Ewa Rajpert-De Meyts, Andrew O M Wilkie. Nat Genet 2009
142
11


Regulation of rate of cartilage differentiation by Indian hedgehog and PTH-related protein.
A Vortkamp, K Lee, B Lanske, G V Segre, H M Kronenberg, C J Tabin. Science 1996
11


Defective lysosomal targeting of activated fibroblast growth factor receptor 3 in achondroplasia.
Jay Y Cho, Changsheng Guo, Monica Torello, Gregory P Lunstrum, Tomoko Iwata, Chuxia Deng, William A Horton. Proc Natl Acad Sci U S A 2004
91
12


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.