A citation-based method for searching scientific literature

Shahida Moosa, Bernd Wollnik. Semin Cell Dev Biol 2016
Times Cited: 20







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



Times Cited
  Times     Co-cited
Similarity



A population-based study of craniosynostosis in metropolitan Atlanta, 1989-2003.
Sheree L Boulet, Sonja A Rasmussen, Margaret A Honein. Am J Med Genet A 2008
173
30

Craniosynostosis.
David Johnson, Andrew O M Wilkie. Eur J Hum Genet 2011
230
20

Genetic study of nonsyndromic coronal craniosynostosis.
E Lajeunie, M Le Merrer, C Bonaïti-Pellie, D Marchac, D Renier. Am J Med Genet 1995
240
20

Tissue origins and interactions in the mammalian skull vault.
Xiaobing Jiang, Sachiko Iseki, Robert E Maxson, Henry M Sucov, Gillian M Morriss-Kay. Dev Biol 2002
484
20



Bent bone dysplasia-FGFR2 type, a distinct skeletal disorder, has deficient canonical FGF signaling.
Amy E Merrill, Anna Sarukhanov, Pavel Krejci, Brian Idoni, Natalia Camacho, Kristine D Estrada, Karen M Lyons, Hannah Deixler, Haynes Robinson, David Chitayat,[...]. Am J Hum Genet 2012
49
15

Understanding craniosynostosis as a growth disorder.
Kevin Flaherty, Nandini Singh, Joan T Richtsmeier. Wiley Interdiscip Rev Dev Biol 2016
47
15

Genetics of craniosynostosis.
Virginia Kimonis, June-Anne Gold, Trevor L Hoffman, Jayesh Panchal, Simeon A Boyadjiev. Semin Pediatr Neurol 2007
91
15

Fibroblast growth factor (FGF) signaling in development and skeletal diseases.
Chad M Teven, Evan M Farina, Jane Rivas, Russell R Reid. Genes Dis 2014
104
15

Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis.
Vikram P Sharma, Aimée L Fenwick, Mia S Brockop, Simon J McGowan, Jacqueline A C Goos, A Jeannette M Hoogeboom, Angela F Brady, Nu Owase Jeelani, Sally Ann Lynch, John B Mulliken,[...]. Nat Genet 2013
134
15

Genetic Syndromes Associated with Craniosynostosis.
Jung Min Ko. J Korean Neurosurg Soc 2016
30
15

Cellular signaling by fibroblast growth factor receptors.
V P Eswarakumar, I Lax, J Schlessinger. Cytokine Growth Factor Rev 2005
15


Mechanism of FGF receptor dimerization and activation.
Sarvenaz Sarabipour, Kalina Hristova. Nat Commun 2016
120
15


Inactivation of Msx1 and Msx2 in neural crest reveals an unexpected role in suppressing heterotopic bone formation in the head.
Paul G Roybal, Nancy L Wu, Jingjing Sun, Man-chun Ting, Christopher A Schafer, Robert E Maxson. Dev Biol 2010
56
15

Bent bone dysplasia (BBD)-FGFR2 type: the radiologic manifestations in early gestation.
Atsuhiko Handa, Yuka Okajima, Noriko Izumi, Michiko Yamanaka, Yasuyuki Kurihara. Pediatr Radiol 2016
3
66

Central nervous system malformations and deformations in FGFR2-related craniosynostosis.
Roman Hossein Khonsari, Anne-Lise Delezoide, Wenfei Kang, Jean M Hébert, Bettina Bessières, Valérie Bodiguel, Catherine Collet, Laurence Legeai-Mallet, Paul T Sharpe, Catherine Fallet-Bianco. Am J Med Genet A 2012
18
11


Prognosis for mental function in Apert's syndrome.
D Renier, E Arnaud, G Cinalli, G Sebag, M Zerah, D Marchac. J Neurosurg 1996
97
10

Abnormalities in cartilage and bone development in the Apert syndrome FGFR2(+/S252W) mouse.
Yingli Wang, Ran Xiao, Fan Yang, Baktiar O Karim, Anthony J Iacovelli, Juanliang Cai, Charles P Lerner, Joan T Richtsmeier, Jen M Leszl, Cheryl A Hill,[...]. Development 2005
135
10

Analysis of a gain-of-function FGFR2 Crouzon mutation provides evidence of loss of function activity in the etiology of cleft palate.
Alison K Snyder-Warwick, Chad A Perlyn, Jing Pan, Kai Yu, Lijuan Zhang, David M Ornitz. Proc Natl Acad Sci U S A 2010
51
10

Closing the Gap: Genetic and Genomic Continuum from Syndromic to Nonsyndromic Craniosynostoses.
Yann Heuzé, Gregory Holmes, Inga Peter, Joan T Richtsmeier, Ethylin Wang Jabs. Curr Genet Med Rep 2014
45
10


Management of craniosynostoses.
D Renier, E Lajeunie, E Arnaud, D Marchac. Childs Nerv Syst 2000
224
10

Skull base and calvarial deformities: association with intracranial changes in craniofacial syndromes.
A M Tokumaru, A J Barkovich, S F Ciricillo, M S Edwards. AJNR Am J Neuroradiol 1996
82
10


Craniosynostosis: imaging review and primer on computed tomography.
Chaitra A Badve, Mallikarjunappa M K, Ramesh S Iyer, Gisele E Ishak, Paritosh C Khanna. Pediatr Radiol 2013
37
10

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
116
10

Apert syndrome with preaxial polydactyly showing the typical mutation Ser252Trp in the FGFR2 gene.
J M Mantilla-Capacho, L Arnaud, M Díaz-Rodriguez, P Barros-Núñez. Genet Couns 2005
13
15

Hydrocephalus and craniosynostosis.
G Cinalli, C Sainte-Rose, E M Kollar, M Zerah, F Brunelle, P Chumas, E Arnaud, D Marchac, A Pierre-Kahn, D Renier. J Neurosurg 1998
120
10

Identical Twins Discordant for Metopic Craniosynostosis: Evidence of Epigenetic Influences.
Suresh N Magge, Kendall Snyder, Aparna Sajja, Tiffani A DeFreitas, Sean E Hofherr, Richard E Broth, Robert F Keating, Gary F Rogers. J Craniofac Surg 2017
8
25

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
674
10

Prevalence and complications of single-gene and chromosomal disorders in craniosynostosis.
Andrew O M Wilkie, Jo C Byren, Jane A Hurst, Jayaratnam Jayamohan, David Johnson, Samantha J L Knight, Tracy Lester, Peter G Richards, Stephen R F Twigg, Steven A Wall. Pediatrics 2010
155
10

Expanding the mutation spectrum in 182 Spanish probands with craniosynostosis: identification and characterization of novel TCF12 variants.
Beatriz Paumard-Hernández, Julia Berges-Soria, Eva Barroso, Carlos I Rivera-Pedroza, Virginia Pérez-Carrizosa, Sara Benito-Sanz, Eva López-Messa, Fernando Santos, Ignacio I García-Recuero, Ana Romance,[...]. Eur J Hum Genet 2015
36
10

A Genetic-Pathophysiological Framework for Craniosynostosis.
Stephen R F Twigg, Andrew O M Wilkie. Am J Hum Genet 2015
105
10

Craniosynostosis: molecular pathways and future pharmacologic therapy.
Kshemendra Senarath-Yapa, Michael T Chung, Adrian McArdle, Victor W Wong, Natalina Quarto, Michael T Longaker, Derrick C Wan. Organogenesis 2012
38
10

Mutation screening in patients with syndromic craniosynostoses indicates that a limited number of recurrent FGFR2 mutations accounts for severe forms of Pfeiffer syndrome.
Elisabeth Lajeunie, Solange Heuertz, Vincent El Ghouzzi, Jelena Martinovic, Dominique Renier, Martine Le Merrer, Jacky Bonaventure. Eur J Hum Genet 2006
86
10

Apert syndrome mutations in fibroblast growth factor receptor 2 exhibit increased affinity for FGF ligand.
J Anderson, H D Burns, P Enriquez-Harris, A O Wilkie, J K Heath. Hum Mol Genet 1998
193
10

Soluble form of FGFR2 with S252W partially prevents craniosynostosis of the apert mouse model.
Jumpei Morita, Masataka Nakamura, Yukiho Kobayashi, Chu-Xia Deng, Noriko Funato, Keiji Moriyama. Dev Dyn 2014
23
10

FGFR2c-mediated ERK-MAPK activity regulates coronal suture development.
Miles J Pfaff, Ke Xue, Li Li, Mark C Horowitz, Derek M Steinbacher, Jacob V P Eswarakumar. Dev Biol 2016
20
10

Identification of a new fibroblast growth factor receptor, FGFR5.
M Sleeman, J Fraser, M McDonald, S Yuan, D White, P Grandison, K Kumble, J D Watson, J G Murison. Gene 2001
185
10

RNA interference and inhibition of MEK-ERK signaling prevent abnormal skeletal phenotypes in a mouse model of craniosynostosis.
Vivek Shukla, Xavier Coumoul, Rui-Hong Wang, Hyun-Seok Kim, Chu-Xia Deng. Nat Genet 2007
135
10

Fibroblast growth factor receptor 2 promotes osteogenic differentiation in mesenchymal cells via ERK1/2 and protein kinase C signaling.
Hichem Miraoui, Karim Oudina, Hervé Petite, Yukiho Tanimoto, Keiji Moriyama, Pierre J Marie. J Biol Chem 2009
108
10

Craniosynostosis: genes and mechanisms.
A O Wilkie. Hum Mol Genet 1997
372
10

Craniosynostosis update 1987.
M M Cohen. Am J Med Genet Suppl 1988
79
10

Fetal constraint as a potential risk factor for craniosynostosis.
Pedro A Sanchez-Lara, Suzan L Carmichael, John M Graham, Edward J Lammer, Gary M Shaw, Chen Ma, Sonja A Rasmussen. Am J Med Genet A 2010
54
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.