A citation-based method for searching scientific literature

Jill Dixon, Paul Trainor, Michael J Dixon. Orthod Craniofac Res 2007
Times Cited: 55







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



Times Cited
  Times     Co-cited
Similarity


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
191
27

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
250
27

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
207
21

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
300
20

Genotyping in 46 patients with tentative diagnosis of Treacher Collins syndrome revealed unexpected phenotypic variation.
Ozge Altug Teber, Gabriele Gillessen-Kaesbach, Sven Fischer, Stefan Böhringer, Beate Albrecht, Angelika Albert, Mine Arslan-Kirchner, Eric Haan, Monika Hagedorn-Greiwe, Christof Hammans,[...]. Eur J Hum Genet 2004
99
20

Treacher Collins syndrome: etiology, pathogenesis and prevention.
Paul A Trainor, Jill Dixon, Michael J Dixon. Eur J Hum Genet 2009
117
18



Characterization of the nucleolar gene product, treacle, in Treacher Collins syndrome.
C Isaac, K L Marsh, W A Paznekas, J Dixon, M J Dixon, E W Jabs, U T Meier. Mol Biol Cell 2000
75
14

The mandibulofacial dysostosis; a new hereditary syndrome.
A FRANCESCHETTI, D KLEIN. Acta Ophthalmol (Copenh) 1949
126
12

High mutation detection rate in TCOF1 among Treacher Collins syndrome patients reveals clustering of mutations and 16 novel pathogenic changes.
A Splendore, E O Silva, L G Alonso, A Richieri-Costa, N Alonso, A Rosa, G Carakushanky, D P Cavalcanti, D Brunoni, M R Passos-Bueno. Hum Mutat 2000
80
10


Mandibulo-facial dysostosis. (Treacher-Collins syndrome).
L E Fazen, J Elmore, H L Nadler. Am J Dis Child 1967
65
10


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
93
9

Clinical features, treatment and genetic background of Treacher Collins syndrome.
Bozena Marszałek, Piotr Wójcicki, Kazimierz Kobus, Wiesław H Trzeciak. J Appl Genet 2002
45
11


Prenatal sonographic diagnosis of Treacher Collins syndrome: a case and review of the literature.
J Cohen, F Ghezzi, L Gonçalves, J D Fuentes, K J Paulyson, D M Sherer. Am J Perinatol 1995
24
20

The Treacher Collins syndrome. A clinical, radiological, and genetic linkage study on two pedigrees.
H A Marres, C W Cremers, M J Dixon, P L Huygen, F B Joosten. Arch Otolaryngol Head Neck Surg 1995
43
11


Prenatal diagnosis in Treacher Collins syndrome using combined linkage analysis and ultrasound imaging.
S J Edwards, A Fowlie, M P Cust, D T Liu, I D Young, M J Dixon. J Med Genet 1996
35
14


Prevalence of dental anomalies, ectopic eruption and associated oral malformations in subjects with Treacher Collins syndrome.
Gisele da Silva Dalben, Beatriz Costa, Marcia Ribeiro Gomide. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2006
20
25


Treacher Collins syndrome TCOF1 protein cooperates with NBS1 in the DNA damage response.
Alberto Ciccia, Jen-Wei Huang, Lior Izhar, Mathew E Sowa, J Wade Harper, Stephen J Elledge. Proc Natl Acad Sci U S A 2014
73
9

Combined deficiencies of Msx1 and Msx2 cause impaired patterning and survival of the cranial neural crest.
Mamoru Ishii, Jun Han, Hai-Yun Yen, Henry M Sucov, Yang Chai, Robert E Maxson. Development 2005
139
7

Another face of the Treacher Collins syndrome (TCOF1) gene: identification of additional exons.
Rolando B So, Bianca Gonzales, Dale Henning, Jill Dixon, Michael J Dixon, Benigno C Valdez. Gene 2004
33
12

TCOF1 mutation database: novel mutation in the alternatively spliced exon 6A and update in mutation nomenclature.
Alessandra Splendore, Roberto D Fanganiello, Cibele Masotti, Lucas S C Morganti, M Rita Passos-Bueno. Hum Mutat 2005
30
13

Multiple mutations in mouse Chd7 provide models for CHARGE syndrome.
Erika A Bosman, Andrew C Penn, John C Ambrose, Ross Kettleborough, Derek L Stemple, Karen P Steel. Hum Mol Genet 2005
151
7

Mutations in a new member of the chromodomain gene family cause CHARGE syndrome.
Lisenka E L M Vissers, Conny M A van Ravenswaaij, Ronald Admiraal, Jane A Hurst, Bert B A de Vries, Irene M Janssen, Walter A van der Vliet, Erik H L P G Huys, Pieter J de Jong, Ben C J Hamel,[...]. Nat Genet 2004
785
7

Loss of Chd7 function in gene-trapped reporter mice is embryonic lethal and associated with severe defects in multiple developing tissues.
Elizabeth A Hurd, Patrice L Capers, Marsha N Blauwkamp, Meredith E Adams, Yehoash Raphael, Heather K Poucher, Donna M Martin. Mamm Genome 2007
111
7

Identification of the complete coding sequence and genomic organization of the Treacher Collins syndrome gene.
J Dixon, S J Edwards, I Anderson, A Brass, P J Scambler, M J Dixon. Genome Res 1997
60
7

TCOF1 gene encodes a putative nucleolar phosphoprotein that exhibits mutations in Treacher Collins Syndrome throughout its coding region.
C A Wise, L C Chiang, W A Paznekas, M Sharma, M M Musy, J A Ashley, M Lovett, E W Jabs. Proc Natl Acad Sci U S A 1997
116
7


Treacher Collins syndrome may result from insertions, deletions or splicing mutations, which introduce a termination codon into the gene.
A J Gladwin, J Dixon, S K Loftus, S Edwards, J J Wasmuth, R C Hennekam, M J Dixon. Hum Mol Genet 1996
60
7

Recurrence of Treacher Collins' syndrome with sonographic findings.
D A Milligan, F E Harlass, P Duff, J N Kopelman. Mil Med 1994
16
25

The ear deformities in mandibulofacial dysostosis (Treacher Collins syndrome).
P D Phelps, D Poswillo, G A Lloyd. Clin Otolaryngol Allied Sci 1981
75
7

Obstructive sleep apnea in Treacher Collins syndrome.
Harriet Akre, Britt Øverland, Pamela Åsten, Nina Skogedal, Ketil Heimdal. Eur Arch Otorhinolaryngol 2012
21
19

Treacher Collins syndrome: protocol management from birth to maturity.
James T Thompson, Peter J Anderson, David J David. J Craniofac Surg 2009
33
12

MANDIBULOFACIAL DYSOSTOSIS, A FAMILIAL STUDY OF FIVE GENERATIONS.
S ROVIN, S F DACHI, D B BORENSTEIN, W B COTTER. J Pediatr 1964
73
7

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
56
7

Treacher Collins syndrome: a clinical and molecular study based on a large series of patients.
Marie Vincent, David Geneviève, Agnès Ostertag, Sandrine Marlin, Didier Lacombe, Dominique Martin-Coignard, Christine Coubes, Albert David, Stanislas Lyonnet, Catheline Vilain,[...]. Genet Med 2016
72
7


Development of the upper lip: morphogenetic and molecular mechanisms.
Rulang Jiang, Jeffrey O Bush, Andrew C Lidral. Dev Dyn 2006
200
5

Fate of the mammalian cranial neural crest during tooth and mandibular morphogenesis.
Y Chai, X Jiang, Y Ito, P Bringas, J Han, D H Rowitch, P Soriano, A P McMahon, H M Sucov. Development 2000
965
5

Ribosome assembly in eukaryotes.
Micheline Fromont-Racine, Bruno Senger, Cosmin Saveanu, Franco Fasiolo. Gene 2003
457
5

Older paternal age and fresh gene mutation: data on additional disorders.
K L Jones, D W Smith, M A Harvey, B D Hall, L Quan. J Pediatr 1975
197
5


UBF levels determine the number of active ribosomal RNA genes in mammals.
Elaine Sanij, Gretchen Poortinga, Kerith Sharkey, Sandy Hung, Timothy P Holloway, Jaclyn Quin, Elysia Robb, Lee H Wong, Walter G Thomas, Victor Stefanovsky,[...]. J Cell Biol 2008
134
5

UBF binding in vivo is not restricted to regulatory sequences within the vertebrate ribosomal DNA repeat.
Audrey C O'Sullivan, Gareth J Sullivan, Brian McStay. Mol Cell Biol 2002
179
5


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.