A citation-based method for searching scientific literature

Kevin K L Lee, Philip Stanier, Erwin Pauws. Mol Syndromol 2019
Times Cited: 8







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



Times Cited
  Times     Co-cited
Similarity


Cell lineage in mammalian craniofacial mesenchyme.
Toshiyuki Yoshida, Philaiporn Vivatbutsiri, Gillian Morriss-Kay, Yumiko Saga, Sachiko Iseki. Mech Dev 2008
225
75

A Genetic-Pathophysiological Framework for Craniosynostosis.
Stephen R F Twigg, Andrew O M Wilkie. Am J Hum Genet 2015
105
62

Stem cells of the suture mesenchyme in craniofacial bone development, repair and regeneration.
Takamitsu Maruyama, Jaeim Jeong, Tzong-Jen Sheu, Wei Hsu. Nat Commun 2016
98
62

The suture provides a niche for mesenchymal stem cells of craniofacial bones.
Hu Zhao, Jifan Feng, Thach-Vu Ho, Weston Grimes, Mark Urata, Yang Chai. Nat Cell Biol 2015
175
62

Cell fate specification during calvarial bone and suture development.
Eva Lana-Elola, Ritva Rice, Agamemnon E Grigoriadis, David P C Rice. Dev Biol 2007
51
50




Postnatal Calvarial Skeletal Stem Cells Expressing PRX1 Reside Exclusively in the Calvarial Sutures and Are Required for Bone Regeneration.
Katarzyna Wilk, Shu-Chi A Yeh, Luke J Mortensen, Sasan Ghaffarigarakani, Courtney M Lombardo, Seyed Hossein Bassir, Zahra A Aldawood, Charles P Lin, Giuseppe Intini. Stem Cell Reports 2017
44
50

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
50

Regulation of cranial morphogenesis and cell fate at the neural crest-mesoderm boundary by engrailed 1.
Ron A Deckelbaum, Greg Holmes, Zhicheng Zhao, Chunxiang Tong, Claudio Basilico, Cynthia A Loomis. Development 2012
50
50

Skeletal analysis of the Fgfr3(P244R) mouse, a genetic model for the Muenke craniosynostosis syndrome.
Stephen R F Twigg, Chris Healy, Christian Babbs, Jacqueline A Sharpe, William G Wood, Paul T Sharpe, Gillian M Morriss-Kay, Andrew O M Wilkie. Dev Dyn 2009
56
37

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
37

Craniosynostosis.
David Johnson, Andrew O M Wilkie. Eur J Hum Genet 2011
230
37

Further analysis of the Crouzon mouse: effects of the FGFR2(C342Y) mutation are cranial bone-dependent.
Jin Liu, Hwa Kyung Nam, Estee Wang, Nan E Hatch. Calcif Tissue Int 2013
34
37


Twist1 homodimers enhance FGF responsiveness of the cranial sutures and promote suture closure.
Jeannette Connerney, Viktoria Andreeva, Yael Leshem, Miguel A Mercado, Karen Dowell, Xuehei Yang, Volkhard Lindner, Robert E Friesel, Douglas B Spicer. Dev Biol 2008
100
37


Comprehensive Integration of Single-Cell Data.
Tim Stuart, Andrew Butler, Paul Hoffman, Christoph Hafemeister, Efthymia Papalexi, William M Mauck, Yuhan Hao, Marlon Stoeckius, Peter Smibert, Rahul Satija. Cell 2019
37

The single-cell transcriptional landscape of mammalian organogenesis.
Junyue Cao, Malte Spielmann, Xiaojie Qiu, Xingfan Huang, Daniel M Ibrahim, Andrew J Hill, Fan Zhang, Stefan Mundlos, Lena Christiansen, Frank J Steemers,[...]. Nature 2019
489
37

Discovery of a periosteal stem cell mediating intramembranous bone formation.
Shawon Debnath, Alisha R Yallowitz, Jason McCormick, Sarfaraz Lalani, Tuo Zhang, Ren Xu, Na Li, Yifang Liu, Yeon Suk Yang, Mark Eiseman,[...]. Nature 2018
155
37

Mutations of the TWIST gene in the Saethre-Chotzen syndrome.
V el Ghouzzi, M Le Merrer, F Perrin-Schmitt, E Lajeunie, P Benit, D Renier, P Bourgeois, A L Bolcato-Bellemin, A Munnich, J Bonaventure. Nat Genet 1997
477
37


Increase of prevalence of craniosynostosis.
Martijn Cornelissen, Bianca den Ottelander, Dimitris Rizopoulos, René van der Hulst, Aebele Mink van der Molen, Chantal van der Horst, Hans Delye, Marie-Lise van Veelen, Gouke Bonsel, Irene Mathijssen. J Craniomaxillofac Surg 2016
69
37


The Development of the Calvarial Bones and Sutures and the Pathophysiology of Craniosynostosis.
Mamoru Ishii, Jingjing Sun, Man-Chun Ting, Robert E Maxson. Curr Top Dev Biol 2015
39
37

Single-Cell Transcriptomic Analyses of the Developing Meninges Reveal Meningeal Fibroblast Diversity and Function.
John DeSisto, Rebecca O'Rourke, Hannah E Jones, Bradley Pawlikowski, Alexandra D Malek, Stephanie Bonney, Fabien Guimiot, Kenneth L Jones, Julie A Siegenthaler. Dev Cell 2020
21
37

The Osteogenic Potential of the Neural Crest Lineage May Contribute to Craniosynostosis.
Daniel Doro, Annie Liu, Agamemnon E Grigoriadis, Karen J Liu. Mol Syndromol 2019
13
37

Early onset of craniosynostosis in an Apert mouse model reveals critical features of this pathology.
Greg Holmes, Gerson Rothschild, Upal Basu Roy, Chu-Xia Deng, Alka Mansukhani, Claudio Basilico. Dev Biol 2009
68
37

Integrated Transcriptome and Network Analysis Reveals Spatiotemporal Dynamics of Calvarial Suturogenesis.
Greg Holmes, Ana S Gonzalez-Reiche, Na Lu, Xianxiao Zhou, Joshua Rivera, Divya Kriti, Robert Sebra, Anthony A Williams, Michael J Donovan, S Steven Potter,[...]. Cell Rep 2020
12
37

Altered bone growth dynamics prefigure craniosynostosis in a zebrafish model of Saethre-Chotzen syndrome.
Camilla S Teng, Man-Chun Ting, D'Juan T Farmer, Mia Brockop, Robert E Maxson, J Gage Crump. Elife 2018
23
37

BMP-IHH-mediated interplay between mesenchymal stem cells and osteoclasts supports calvarial bone homeostasis and repair.
Yuxing Guo, Yuan Yuan, Ling Wu, Thach-Vu Ho, Junjun Jing, Hideki Sugii, Jingyuan Li, Xia Han, Jifan Feng, Chuanbin Guo,[...]. Bone Res 2018
19
37


Analysis of the Fgfr2C342Y mouse model shows condensation defects due to misregulation of Sox9 expression in prechondrocytic mesenchyme.
Emma Peskett, Samin Kumar, William Baird, Janhvi Jaiswal, Ming Li, Priyanca Patel, Jonathan A Britto, Erwin Pauws. Biol Open 2017
11
25

Apoptosis in murine calvarial bone and suture development.
D P Rice, H J Kim, I Thesleff. Eur J Oral Sci 1999
83
25

Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome.
W Reardon, R M Winter, P Rutland, L J Pulleyn, B M Jones, S Malcolm. Nat Genet 1994
578
25

The homeoprotein engrailed 1 has pleiotropic functions in calvarial intramembranous bone formation and remodeling.
Ron A Deckelbaum, Amit Majithia, Thomas Booker, Janet E Henderson, Cynthia A Loomis. Development 2006
32
25

Attenuation of signaling pathways stimulated by pathologically activated FGF-receptor 2 mutants prevents craniosynostosis.
V P Eswarakumar, F Ozcan, E D Lew, J H Bae, F Tomé, C J Booth, D J Adams, I Lax, J Schlessinger. Proc Natl Acad Sci U S A 2006
77
25

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
25

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
25


Craniosynostosis in Twist heterozygous mice: a model for Saethre-Chotzen syndrome.
Ethan A Carver, Kathleen F Oram, Thomas Gridley. Anat Rec 2002
59
25

Understanding craniosynostosis as a growth disorder.
Kevin Flaherty, Nandini Singh, Joan T Richtsmeier. Wiley Interdiscip Rev Dev Biol 2016
47
25

Craniofacial shape variation in Twist1+/- mutant mice.
Trish E Parsons, Seth M Weinberg, Kameron Khaksarfard, R Nicole Howie, Mohammed Elsalanty, Jack C Yu, James J Cray. Anat Rec (Hoboken) 2014
19
25

Activation of p38 MAPK pathway in the skull abnormalities of Apert syndrome Fgfr2(+P253R) mice.
Yingli Wang, Miao Sun, Victoria L Uhlhorn, Xueyan Zhou, Inga Peter, Neus Martinez-Abadias, Cheryl A Hill, Christopher J Percival, Joan T Richtsmeier, David L Huso,[...]. BMC Dev Biol 2010
59
25


Mapping the Mouse Cell Atlas by Microwell-Seq.
Xiaoping Han, Renying Wang, Yincong Zhou, Lijiang Fei, Huiyu Sun, Shujing Lai, Assieh Saadatpour, Ziming Zhou, Haide Chen, Fang Ye,[...]. Cell 2018
433
25

The FaceBase Consortium: a comprehensive resource for craniofacial researchers.
James F Brinkley, Shannon Fisher, Matthew P Harris, Greg Holmes, Joan E Hooper, Ethylin Wang Jabs, Kenneth L Jones, Carl Kesselman, Ophir D Klein, Richard L Maas,[...]. Development 2016
27
25

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
25

A single-cell survey of the small intestinal epithelium.
Adam L Haber, Moshe Biton, Noga Rogel, Rebecca H Herbst, Karthik Shekhar, Christopher Smillie, Grace Burgin, Toni M Delorey, Michael R Howitt, Yarden Katz,[...]. Nature 2017
530
25


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.