A citation-based method for searching scientific literature

Karla Terrazas, Jill Dixon, Paul A Trainor, Michael J Dixon. Wiley Interdiscip Rev Dev Biol 2017
Times Cited: 14







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



Times Cited
  Times     Co-cited
Similarity


Facial dysostoses: Etiology, pathogenesis and management.
Paul A Trainor, Brian T Andrews. Am J Med Genet C Semin Med Genet 2013
58
42

The Roles of RNA Polymerase I and III Subunits Polr1c and Polr1d in Craniofacial Development and in Zebrafish Models of Treacher Collins Syndrome.
Kristin E Noack Watt, Annita Achilleos, Cynthia L Neben, Amy E Merrill, Paul A Trainor. PLoS Genet 2016
47
35

Haploinsufficiency of SF3B4, a component of the pre-mRNA spliceosomal complex, causes Nager syndrome.
Francois P Bernier, Oana Caluseriu, Sarah Ng, Jeremy Schwartzentruber, Kati J Buckingham, A Micheil Innes, Ethylin Wang Jabs, Jeffrey W Innis, Jane L Schuette, Jerome L Gorski,[...]. Am J Hum Genet 2012
105
35

Clinical and mutation data in 12 patients with the clinical diagnosis of Nager syndrome.
J C Czeschik, C Voigt, Y Alanay, B Albrecht, S Avci, D Fitzpatrick, D R Goudie, U Hehr, A J Hoogeboom, H Kayserili,[...]. Hum Genet 2013
44
28

Human facial dysostoses.
D Wieczorek. Clin Genet 2013
41
28

Prevention of the neurocristopathy Treacher Collins syndrome through inhibition of p53 function.
Natalie C Jones, Megan L Lynn, Karin Gaudenz, Daisuke Sakai, Kazushi Aoto, Jean-Phillipe Rey, Earl F Glynn, Lacey Ellington, Chunying Du, Jill Dixon,[...]. Nat Med 2008
283
28

Nager syndrome: confirmation of SF3B4 haploinsufficiency as the major cause.
F Petit, F Escande, A S Jourdain, N Porchet, J Amiel, B Doray, M A Delrue, E Flori, C A Kim, S Marlin,[...]. Clin Genet 2014
37
28

Acrofacial Dysostosis, Cincinnati Type, a Mandibulofacial Dysostosis Syndrome with Limb Anomalies, Is Caused by POLR1A Dysfunction.
K Nicole Weaver, Kristin E Noack Watt, Robert B Hufnagel, Joaquin Navajas Acedo, Luke L Linscott, Kristen L Sund, Patricia L Bender, Rainer König, Charles M Lourenco, Ute Hehr,[...]. Am J Hum Genet 2015
37
21

The Treacher Collins syndrome (TCOF1) gene product is involved in pre-rRNA methylation.
Bianca Gonzales, Dale Henning, Rolando B So, Jill Dixon, Michael J Dixon, Benigno C Valdez. Hum Mol Genet 2005
87
21

A review of craniofacial disorders caused by spliceosomal defects.
D Lehalle, D Wieczorek, R M Zechi-Ceide, M R Passos-Bueno, S Lyonnet, J Amiel, C T Gordon. Clin Genet 2015
56
21

Mutations in genes encoding subunits of RNA polymerases I and III cause Treacher Collins syndrome.
Johannes G Dauwerse, Jill Dixon, Saskia Seland, Claudia A L Ruivenkamp, Arie van Haeringen, Lies H Hoefsloot, Dorien J M Peters, Agnes Clement-de Boers, Cornelia Daumer-Haas, Robert Maiwald,[...]. Nat Genet 2011
192
21

Sf3b4-depleted Xenopus embryos: A model to study the pathogenesis of craniofacial defects in Nager syndrome.
Arun Devotta, Hugo Juraver-Geslin, Jose Antonio Gonzalez, Chang-Soo Hong, Jean-Pierre Saint-Jeannet. Dev Biol 2016
33
21

The Treacher Collins syndrome (TCOF1) gene product is involved in ribosomal DNA gene transcription by interacting with upstream binding factor.
Benigno C Valdez, Dale Henning, Rolando B So, Jill Dixon, Michael J Dixon. Proc Natl Acad Sci U S A 2004
180
21

Tcof1/Treacle is required for neural crest cell formation and proliferation deficiencies that cause craniofacial abnormalities.
Jill Dixon, Natalie C Jones, Lisa L Sandell, Sachintha M Jayasinghe, Jennifer Crane, Jean-Philippe Rey, Michael J Dixon, Paul A Trainor. Proc Natl Acad Sci U S A 2006
236
21

Splicing factor 3b subunit 4 binds BMPR-IA and inhibits osteochondral cell differentiation.
Hiroki Watanabe, Masafumi Shionyu, Tomoatsu Kimura, Koji Kimata, Hideto Watanabe. J Biol Chem 2007
36
21

Prevention of Treacher Collins syndrome craniofacial anomalies in mouse models via maternal antioxidant supplementation.
Daisuke Sakai, Jill Dixon, Annita Achilleos, Michael Dixon, Paul A Trainor. Nat Commun 2016
49
21

Treacher Collins Syndrome: A Systematic Review of Evidence-Based Treatment and Recommendations.
Raul G Plomp, Manouk J S van Lieshout, Koen F M Joosten, Eppo B Wolvius, Marc P van der Schroeff, Sarah L Versnel, René M L Poublon, Irene M J Mathijssen. Plast Reconstr Surg 2016
38
21

Mandible and Tongue Development.
Carolina Parada, Yang Chai. Curr Top Dev Biol 2015
62
21

The emerging roles of ribosome biogenesis in craniofacial development.
Adam P Ross, Konstantinos S Zarbalis. Front Physiol 2014
23
14

The NBS1-Treacle complex controls ribosomal RNA transcription in response to DNA damage.
Dorthe H Larsen, Flurina Hari, Julie A Clapperton, Myriam Gwerder, Katrin Gutsche, Matthias Altmeyer, Stephanie Jungmichel, Luis I Toledo, Daniel Fink, Maj-Britt Rask,[...]. Nat Cell Biol 2014
84
14


CHD7, the gene mutated in CHARGE syndrome, regulates genes involved in neural crest cell guidance.
Yvonne Schulz, Peter Wehner, Lennart Opitz, Gabriela Salinas-Riester, Ernie M H F Bongers, Conny M A van Ravenswaaij-Arts, Josephine Wincent, Jacqueline Schoumans, Jürgen Kohlhase, Annette Borchers,[...]. Hum Genet 2014
72
14

Embryonic bauplans and the developmental origins of facial diversity and constraint.
Nathan M Young, Diane Hu, Alexis J Lainoff, Francis J Smith, Raul Diaz, Abigail S Tucker, Paul A Trainor, Richard A Schneider, Benedikt Hallgrímsson, Ralph S Marcucio. Development 2014
80
14

CHD7 cooperates with PBAF to control multipotent neural crest formation.
Ruchi Bajpai, Denise A Chen, Alvaro Rada-Iglesias, Junmei Zhang, Yiqin Xiong, Jill Helms, Ching-Pin Chang, Yingming Zhao, Tomek Swigut, Joanna Wysocka. Nature 2010
375
14


Ribosomopathies: Global process, tissue specific defects.
Pamela C Yelick, Paul A Trainor. Rare Dis 2015
55
14

Spliceosome structure and function.
Cindy L Will, Reinhard Lührmann. Cold Spring Harb Perspect Biol 2011
862
14

Altered mRNA Splicing, Chondrocyte Gene Expression and Abnormal Skeletal Development due to SF3B4 Mutations in Rodriguez Acrofacial Dysostosis.
Felipe Marques, Jessica Tenney, Ivan Duran, Jorge Martin, Lisette Nevarez, Robert Pogue, Deborah Krakow, Daniel H Cohn, Bing Li. PLoS Genet 2016
19
14

A new syndrome with growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate.
Maria Leine Guion-Almeida, Roseli Maria Zechi-Ceide, Siulan Vendramini, Alfredo Tabith Ju Nior. Clin Dysmorphol 2006
33
14

Tissue-selective effects of nucleolar stress and rDNA damage in developmental disorders.
Eliezer Calo, Bo Gu, Margot E Bowen, Fardin Aryan, Antoine Zalc, Jialiang Liang, Ryan A Flynn, Tomek Swigut, Howard Y Chang, Laura D Attardi,[...]. Nature 2018
61
14


The basics of epithelial-mesenchymal transition.
Raghu Kalluri, Robert A Weinberg. J Clin Invest 2009
14

Haploinsufficiency of a spliceosomal GTPase encoded by EFTUD2 causes mandibulofacial dysostosis with microcephaly.
Matthew A Lines, Lijia Huang, Jeremy Schwartzentruber, Stuart L Douglas, Danielle C Lynch, Chandree Beaulieu, Maria Leine Guion-Almeida, Roseli Maria Zechi-Ceide, Blanca Gener, Gabriele Gillessen-Kaesbach,[...]. Am J Hum Genet 2012
123
14


A primary cilia-dependent etiology for midline facial disorders.
Samantha A Brugmann, Nancy C Allen, Aaron W James, Zesemayat Mekonnen, Elena Madan, Jill A Helms. Hum Mol Genet 2010
94
14

Development of the upper lip: morphogenetic and molecular mechanisms.
Rulang Jiang, Jeffrey O Bush, Andrew C Lidral. Dev Dyn 2006
190
14

Disrupting hedgehog and WNT signaling interactions promotes cleft lip pathogenesis.
Hiroshi Kurosaka, Angelo Iulianella, Trevor Williams, Paul A Trainor. J Clin Invest 2014
67
14

Fishing the molecular bases of Treacher Collins syndrome.
Andrea M J Weiner, Nadia L Scampoli, Nora B Calcaterra. PLoS One 2012
31
14

Mouse Models of Rare Craniofacial Disorders.
Annita Achilleos, Paul A Trainor. Curr Top Dev Biol 2015
5
40

New directions in craniofacial morphogenesis.
Heather L Szabo-Rogers, Lucy E Smithers, Wardati Yakob, Karen J Liu. Dev Biol 2010
87
14


Spliceosomal protein eftud2 mutation leads to p53-dependent apoptosis in zebrafish neural progenitors.
Lei Lei, Shou-Yu Yan, Ran Yang, Jia-Yu Chen, Yumei Li, Ye Bu, Nannan Chang, Qinchao Zhou, Xiaojun Zhu, Chuan-Yun Li,[...]. Nucleic Acids Res 2017
36
14

Zebrafish Craniofacial Development: A Window into Early Patterning.
Lindsey Mork, Gage Crump. Curr Top Dev Biol 2015
59
14

WNT5A mutations in patients with autosomal dominant Robinow syndrome.
Anthony D Person, Soraya Beiraghi, Christine M Sieben, Spencer Hermanson, Ann N Neumann, Mara E Robu, J Robert Schleiffarth, Charles J Billington, Hans van Bokhoven, Jeannette M Hoogeboom,[...]. Dev Dyn 2010
149
14

Autosomal recessive inheritance of Nager acrofacial dysostosis.
J Chemke, B M Mogilner, I Ben-Itzhak, L Zurkowski, D Ophir. J Med Genet 1988
44
14

Convergent extension movements and ciliary function are mediated by ofd1, a zebrafish orthologue of the human oral-facial-digital type 1 syndrome gene.
Maria I Ferrante, Leila Romio, Silvia Castro, John E Collins, David A Goulding, Derek L Stemple, Adrian S Woolf, Stephen W Wilson. Hum Mol Genet 2009
96
14

The skeletal dysplasias.
Deborah Krakow, David L Rimoin. Genet Med 2010
109
14

Obstructive sleep apnoea in Treacher Collins syndrome: prevalence, severity and cause.
R G Plomp, H H Bredero-Boelhouwer, K F M Joosten, E B Wolvius, H L J Hoeve, R M L Poublon, I M J Mathijssen. Int J Oral Maxillofac Surg 2012
40
14

Nosology and classification of genetic skeletal disorders: 2019 revision.
Geert R Mortier, Daniel H Cohn, Valerie Cormier-Daire, Christine Hall, Deborah Krakow, Stefan Mundlos, Gen Nishimura, Stephen Robertson, Luca Sangiorgi, Ravi Savarirayan,[...]. Am J Med Genet A 2019
179
14

4H Leukodystrophy: A Brain Magnetic Resonance Imaging Scoring System.
Suzanne Vrij-van den Bos, Janna A Hol, Roberta La Piana, Inga Harting, Adeline Vanderver, Frederik Barkhof, Ferdy Cayami, Wessel N van Wieringen, Petra J W Pouwels, Marjo S van der Knaap,[...]. Neuropediatrics 2017
9
11


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.