A citation-based method for searching scientific literature

W A Paznekas, N Zhang, T Gridley, E W Jabs. Biochem Biophys Res Commun 1997
Times Cited: 11







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



Times Cited
  Times     Co-cited
Similarity



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
81


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
63




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
45


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
45


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
36

Canine TCOF1; cloning, chromosome assignment and genetic analysis in dogs with different head types.
K E Haworth, I Islam, M Breen, W Putt, E Makrinou, M Binns, D Hopkinson, Y Edwards. Mamm Genome 2001
32
36


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
36

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
36




Clinical features, treatment and genetic background of Treacher Collins syndrome.
Bozena Marszałek, Piotr Wójcicki, Kazimierz Kobus, Wiesław H Trzeciak. J Appl Genet 2002
45
27

Craniofacial, vestibular and bone defects in mice lacking the Distal-less-related gene Dlx5.
D Acampora, G R Merlo, L Paleari, B Zerega, M P Postiglione, S Mantero, E Bober, O Barbieri, A Simeone, G Levi. Development 1999
318
18


Dlx5 regulates regional development of the branchial arches and sensory capsules.
M J Depew, J K Liu, J E Long, R Presley, J J Meneses, R A Pedersen, J L Rubenstein. Development 1999
264
18

Cyclopia and defective axial patterning in mice lacking Sonic hedgehog gene function.
C Chiang, Y Litingtung, E Lee, K E Young, J L Corden, H Westphal, P A Beachy. Nature 1996
18

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
18

MANDIBULOFACIAL DYSOSTOSIS, A FAMILIAL STUDY OF FIVE GENERATIONS.
S ROVIN, S F DACHI, D B BORENSTEIN, W B COTTER. J Pediatr 1964
73
18


An early phase of embryonic Dlx5 expression defines the rostral boundary of the neural plate.
L Yang, H Zhang, G Hu, H Wang, C Abate-Shen, M M Shen. J Neurosci 1998
85
18



Mutations in the human Sonic Hedgehog gene cause holoprosencephaly.
E Roessler, E Belloni, K Gaudenz, P Jay, P Berta, S W Scherer, L C Tsui, M Muenke. Nat Genet 1996
859
18


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
18

Nonsense-mediated mRNA decay in health and disease.
P A Frischmeyer, H C Dietz. Hum Mol Genet 1999
811
18



Treacher Collins syndrome.
M J Dixon. Hum Mol Genet 1996
64
18

Transformation of tooth type induced by inhibition of BMP signaling.
A S Tucker, K L Matthews, P T Sharpe. Science 1998
320
18

Elevated blood pressure and craniofacial abnormalities in mice deficient in endothelin-1.
Y Kurihara, H Kurihara, H Suzuki, T Kodama, K Maemura, R Nagai, H Oda, T Kuwaki, W H Cao, N Kamada. Nature 1994
868
18




Barx1, a new mouse homeodomain transcription factor expressed in cranio-facial ectomesenchyme and the stomach.
J P Tissier-Seta, M L Mucchielli, M Mark, M G Mattei, C Goridis, J F Brunet. Mech Dev 1995
134
18

Signaling pathways crucial for craniofacial development revealed by endothelin-A receptor-deficient mice.
D E Clouthier, S C Williams, H Yanagisawa, M Wieduwilt, J A Richardson, M Yanagisawa. Dev Biol 2000
157
18

The triple origin of skull in higher vertebrates: a study in quail-chick chimeras.
G F Couly, P M Coltey, N M Le Douarin. Development 1993
722
18


Fgf-8 determines rostral-caudal polarity in the first branchial arch.
A S Tucker, G Yamada, M Grigoriou, V Pachnis, P T Sharpe. Development 1999
188
18

Dual genetic pathways of endothelin-mediated intercellular signaling revealed by targeted disruption of endothelin converting enzyme-1 gene.
H Yanagisawa, M Yanagisawa, R P Kapur, J A Richardson, S C Williams, D E Clouthier, D de Wit, N Emoto, R E Hammer. Development 1998
374
18

Cranial and cardiac neural crest defects in endothelin-A receptor-deficient mice.
D E Clouthier, K Hosoda, J A Richardson, S C Williams, H Yanagisawa, T Kuwaki, M Kumada, R E Hammer, M Yanagisawa. Development 1998
469
18



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.