A citation-based method for searching scientific literature

Irene H Hung, Gary C Schoenwolf, Mark Lewandoski, David M Ornitz. Dev Biol 2016
Times Cited: 29







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



Times Cited
  Times     Co-cited
Similarity



The Fibroblast Growth Factor signaling pathway.
David M Ornitz, Nobuyuki Itoh. Wiley Interdiscip Rev Dev Biol 2015
896
44



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
327
37

Coordination of chondrogenesis and osteogenesis by fibroblast growth factor 18.
Zhonghao Liu, Jingsong Xu, Jennifer S Colvin, David M Ornitz. Genes Dev 2002
338
37

FGF signaling in the osteoprogenitor lineage non-autonomously regulates postnatal chondrocyte proliferation and skeletal growth.
Kannan Karuppaiah, Kai Yu, Joohyun Lim, Jianquan Chen, Craig Smith, Fanxin Long, David M Ornitz. Development 2016
38
31

Development of the endochondral skeleton.
Fanxin Long, David M Ornitz. Cold Spring Harb Perspect Biol 2013
299
24





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
688
17


Conditional inactivation of FGF receptor 2 reveals an essential role for FGF signaling in the regulation of osteoblast function and bone growth.
Kai Yu, Jingsong Xu, Zhonghao Liu, Drazen Sosic, Jiansu Shao, Eric N Olson, Dwight A Towler, David M Ornitz. Development 2003
456
17

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
837
17

Male-to-female sex reversal in mice lacking fibroblast growth factor 9.
J S Colvin, R P Green, J Schmahl, B Capel, D M Ornitz. Cell 2001
408
17

FGF9 monomer-dimer equilibrium regulates extracellular matrix affinity and tissue diffusion.
Masayo Harada, Hirotaka Murakami, Akihiko Okawa, Noriaki Okimoto, Shuichi Hiraoka, Taka Nakahara, Ryogo Akasaka, Yo-Ichi Shiraishi, Noriyuki Futatsugi, Yoko Mizutani-Koseki,[...]. Nat Genet 2009
83
17

FGF9 can induce endochondral ossification in cranial mesenchyme.
Venkatesh Govindarajan, Paul A Overbeek. BMC Dev Biol 2006
42
17

Unique expression pattern of the FGF receptor 3 gene during mouse organogenesis.
K Peters, D Ornitz, S Werner, L Williams. Dev Biol 1993
409
13



A novel homozygous mutation in FGFR3 causes tall stature, severe lateral tibial deviation, scoliosis, hearing impairment, camptodactyly, and arachnodactyly.
Periklis Makrythanasis, Samia Temtamy, Mona S Aglan, Ghada A Otaify, Hanan Hamamy, Stylianos E Antonarakis. Hum Mutat 2014
38
13


Achondroplasia.
William A Horton, Judith G Hall, Jacqueline T Hecht. Lancet 2007
280
13

Snail1 is a transcriptional effector of FGFR3 signaling during chondrogenesis and achondroplasias.
Cristina A de Frutos, Sonia Vega, Miguel Manzanares, Juana M Flores, Hector Huertas, M Luisa Martínez-Frías, M Angela Nieto. Dev Cell 2007
65
13

Developmental expression of two murine fibroblast growth factor receptors, flg and bek.
A Orr-Urtreger, D Givol, A Yayon, Y Yarden, P Lonai. Development 1991
356
13

Skeletal dysplasia and defective chondrocyte differentiation by targeted overexpression of fibroblast growth factor 9 in transgenic mice.
S Garofalo, M Kliger-Spatz, J L Cooke, O Wolstin, G P Lunstrum, S M Moshkovitz, W A Horton, A Yayon. J Bone Miner Res 1999
75
13

Genomic organization and embryonic expression of the mouse fibroblast growth factor 9 gene.
J S Colvin, B Feldman, J H Nadeau, M Goldfarb, D M Ornitz. Dev Dyn 1999
169
13


The IIIc alternative of Fgfr2 is a positive regulator of bone formation.
Vereragavan P Eswarakumar, Efrat Monsonego-Ornan, Mark Pines, Ileana Antonopoulou, Gillian M Morriss-Kay, Peter Lonai. Development 2002
192
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
253
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
798
13

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
200
13

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
13

Direct interactions of Runx2 and canonical Wnt signaling induce FGF18.
Martina I Reinhold, Michael C Naski. J Biol Chem 2007
78
13

Genetic insights into the mechanisms of Fgf signaling.
J Richard Brewer, Pierre Mazot, Philippe Soriano. Genes Dev 2016
105
13

A gain-of-function mutation of Fgfr2c demonstrates the roles of this receptor variant in osteogenesis.
Veraragavan P Eswarakumar, Mark C Horowitz, Rachel Locklin, Gillian M Morriss-Kay, Peter Lonai. Proc Natl Acad Sci U S A 2004
140
13


Multiple synostoses syndrome is due to a missense mutation in exon 2 of FGF9 gene.
Xiao-Lin Wu, Ming-Min Gu, Lei Huang, Xue-Song Liu, Hong-Xin Zhang, Xiao-Yi Ding, Jian-Qiang Xu, Bin Cui, Long Wang, Shun-Yuan Lu,[...]. Am J Hum Genet 2009
60
13

FGF-18, a novel member of the fibroblast growth factor family, stimulates hepatic and intestinal proliferation.
M C Hu, W R Qiu, Y P Wang, D Hill, B D Ring, S Scully, B Bolon, M DeRose, R Luethy, W S Simonet,[...]. Mol Cell Biol 1998
103
13

A point mutation in Fgf9 impedes joint interzone formation leading to multiple synostoses syndrome.
Lingyun Tang, Xiaolin Wu, Hongxin Zhang, Shunyuan Lu, Min Wu, Chunling Shen, Xuejiao Chen, Yicheng Wang, Weigang Wang, Yan Shen,[...]. Hum Mol Genet 2017
14
28

Roles of FGFR3 during morphogenesis of Meckel's cartilage and mandibular bones.
Bruce A Havens, Dimitris Velonis, Mark S Kronenberg, Alex C Lichtler, Bonnie Oliver, Mina Mina. Dev Biol 2008
27
11




Developmental regulation of the growth plate.
Henry M Kronenberg. Nature 2003
10


A single-base change in the tyrosine kinase II domain of ovine FGFR3 causes hereditary chondrodysplasia in sheep.
J E Beever, M A Smit, S N Meyers, T S Hadfield, C Bottema, J Albretsen, N E Cockett. Anim Genet 2006
38
10

Shared role of the pRB-related p130 and p107 proteins in limb development.
D Cobrinik, M H Lee, G Hannon, G Mulligan, R T Bronson, N Dyson, E Harlow, D Beach, R A Weinberg, T Jacks. Genes Dev 1996
356
10


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.