A citation-based method for searching scientific literature

Katsumi Horiuchi, Tadashi Ariga, Hirotaka Fujioka, Kunihiro Kawashima, Yuhei Yamamoto, Hiroharu Igawa, Tsuneki Sugihara, Yukio Sakiyama. Am J Med Genet A 2005
Times Cited: 14







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



Times Cited
  Times     Co-cited
Similarity


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
79
64


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
57

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
42


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
42

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
115
42


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
248
42

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
35

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
189
35


Identification of mutations in TCOF1: use of molecular analysis in the pre- and postnatal diagnosis of Treacher Collins syndrome.
Jill Dixon, Ian Ellis, Armand Bottani, Karen Temple, Michael James Dixon. Am J Med Genet A 2004
27
28



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
28

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
28

Mutation testing in Treacher Collins Syndrome.
P E Ellis, M Dawson, M J Dixon. J Orthod 2002
24
28

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
202
28



Novel mutations of TCOF1 gene in European patients with Treacher Collins syndrome.
Chiara Conte, Maria Rosaria D'Apice, Fabrizio Rinaldi, Stefano Gambardella, Federica Sangiuolo, Giuseppe Novelli. BMC Med Genet 2011
21
21


Treacher Collins syndrome with craniosynostosis, choanal atresia, and esophageal regurgitation caused by a novel nonsense mutation in TCOF1.
Katsumi Horiuchi, Tadashi Ariga, Hirotaka Fujioka, Kunihiro Kawashima, Yuhei Yamamoto, Hiroharu Igawa, Yukio Sakiyama, Tsuneki Sugihara. Am J Med Genet A 2004
9
22



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
14

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
92
14

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
14

MANDIBULOFACIAL DYSOSTOSIS, A FAMILIAL STUDY OF FIVE GENERATIONS.
S ROVIN, S F DACHI, D B BORENSTEIN, W B COTTER. J Pediatr 1964
73
14

Treacher Collins syndrome.
M J Dixon. Hum Mol Genet 1996
64
14

The structure of the N-terminal domain of the product of the lissencephaly gene Lis1 and its functional implications.
Myung Hee Kim, David R Cooper, Arkadiusz Oleksy, Yancho Devedjiev, Urszula Derewenda, Orly Reiner, Jacek Otlewski, Zygmunt S Derewenda. Structure 2004
83
14



Craniofacial morphology in Treacher Collins syndrome.
M Arvystas, R J Shprintzen. Cleft Palate Craniofac J 1991
38
14

Defects in middle ear cavitation cause conductive hearing loss in the Tcof1 mutant mouse.
Carol A Richter, Susan Amin, Jennifer Linden, Jill Dixon, Michael J Dixon, Abigail S Tucker. Hum Mol Genet 2010
30
14

Mandibulofacial dysostosis (Treacher Collins syndrome): a new proposal for its pathogenesis.
K K Sulik, M C Johnston, S J Smiley, H S Speight, B E Jarvis. Am J Med Genet 1987
122
14

Mosaicism of a TCOF1 mutation in an individual clinically unaffected with Treacher Collins syndrome.
Brenda A Shoo, Elizabeth McPherson, Ethylin Wang Jabs. Am J Med Genet A 2004
12
16

Treacher Collins syndrome.
Jill Dixon, Paul Trainor, Michael J Dixon. Orthod Craniofac Res 2007
55
14

Reduced transcription of TCOF1 in adult cells of Treacher Collins syndrome patients.
Cibele Masotti, Camila C Ornelas, Alessandra Splendore-Gordonos, Ricardo Moura, Têmis M Félix, Nivaldo Alonso, Anamaria A Camargo, Maria Rita Passos-Bueno. BMC Med Genet 2009
14
14

Treacher Collins syndrome: clinical implications for the paediatrician--a new mutation in a severely affected newborn and comparison with three further patients with the same mutation, and review of the literature.
Jan-Ulrich Schlump, Anja Stein, Ute Hehr, Tanja Karen, Claudia Möller-Hartmann, Nursel H Elcioglu, Nadja Bogdanova, Hartmut Fritz Woike, Dietmar R Lohmann, Ursula Felderhoff-Mueser,[...]. Eur J Pediatr 2012
14
14

A novel silent deletion, an insertion mutation and a nonsense mutation in the TCOF1 gene found in two Chinese cases of Treacher Collins syndrome.
Yan Wang, Xiao-Juan Yin, Tao Han, Wei Peng, Hong-Lin Wu, Xin Liu, Zhi-Chun Feng. Mol Genet Genomics 2014
8
25

[Clinical and genetic analysis of a patient with Treacher Collins syndrome in TCOF1 gene].
Hongbo Li, Xu Zhang, Zhenyue Li, Jing Chen, Yu Lu, Jingjie Jia, Huijun Yuan, Dongyi Han. Lin Chung Er Bi Yan Hou Tou Jing Wai Ke Za Zhi 2012
6
33

Gross deletions in TCOF1 are a cause of Treacher-Collins-Franceschetti syndrome.
Michael Bowman, Michael Oldridge, Caroline Archer, Anthony O'Rourke, Joanna McParland, Roel Brekelmans, Anneke Seller, Tracy Lester. Eur J Hum Genet 2012
34
14

Facial dysostoses: Etiology, pathogenesis and management.
Paul A Trainor, Brian T Andrews. Am J Med Genet C Semin Med Genet 2013
61
14

A novel mutation in the TCOF1 gene found in two Chinese cases of Treacher Collins syndrome.
Xu Zhang, Yue Fan, Ying Zhang, Huadan Xue, Xiaowei Chen. Int J Pediatr Otorhinolaryngol 2013
9
22

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
41
14

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
51
14

Treacher collins syndrome.
Christopher C Chang, Derek M Steinbacher. Semin Plast Surg 2012
31
14

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
71
14


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.