A citation-based method for searching scientific literature

K L Jones, D W Smith, M A Harvey, B D Hall, L Quan. J Pediatr 1975
Times Cited: 197







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



Times Cited
  Times     Co-cited
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MANDIBULOFACIAL DYSOSTOSIS, A FAMILIAL STUDY OF FIVE GENERATIONS.
S ROVIN, S F DACHI, D B BORENSTEIN, W B COTTER. J Pediatr 1964
73
21


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
25

The ear deformities in mandibulofacial dysostosis (Treacher Collins syndrome).
P D Phelps, D Poswillo, G A Lloyd. Clin Otolaryngol Allied Sci 1981
75
18


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
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
32

Treacher Collins syndrome: correlation between clinical and genetic linkage studies.
M J Dixon, H A Marres, S J Edwards, J Dixon, C W Cremers. Clin Dysmorphol 1994
37
35

Mandibulo-facial dysostosis. (Treacher-Collins syndrome).
L E Fazen, J Elmore, H L Nadler. Am J Dis Child 1967
64
18

The gene for Treacher Collins syndrome maps to the long arm of chromosome 5.
M J Dixon, A P Read, D Donnai, A Colley, J Dixon, R Williamson. Am J Hum Genet 1991
67
17

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
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
34
32


Narrowing the position of the Treacher Collins syndrome locus to a small interval between three new microsatellite markers at 5q32-33.1.
M J Dixon, J Dixon, T Houseal, M Bhatt, D C Ward, K Klinger, G M Landes. Am J Hum Genet 1993
51
19

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
16

Parental age and mutation.
L S PENROSE. Lancet 1955
275
10



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
10


Mapping the Treacher Collins syndrome locus to 5q31.3----q33.3.
E W Jabs, X Li, C A Coss, E W Taylor, D A Meyers, J L Weber. Genomics 1991
53
16

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
11

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
9



Mutations in fibroblast growth-factor receptor 3 in sporadic cases of achondroplasia occur exclusively on the paternally derived chromosome.
D J Wilkin, J K Szabo, R Cameron, S Henderson, G A Bellus, M L Mack, I Kaitila, J Loughlin, A Munnich, B Sykes,[...]. Am J Hum Genet 1998
147
8

Advancing paternal age and the risk of schizophrenia.
D Malaspina, S Harlap, S Fennig, D Heiman, D Nahon, D Feldman, E S Susser. Arch Gen Psychiatry 2001
361
8

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
10

A combined genetic and radiation hybrid map surrounding the Treacher Collins syndrome locus on chromosome 5q.
S K Loftus, S J Edwards, T Scherpbier-Heddema, K H Buetow, J J Wasmuth, M J Dixon. Hum Mol Genet 1993
23
30

The high spontaneous mutation rate: is it a health risk?
J F Crow. Proc Natl Acad Sci U S A 1997
275
7

Birth prevalence, mutation rate, sex ratio, parents' age, and ethnicity in Apert syndrome.
M M Tolarova, J A Harris, D E Ordway, K Vargervik. Am J Med Genet 1997
87
8


The observed human sperm mutation frequency cannot explain the achondroplasia paternal age effect.
Irene Tiemann-Boege, William Navidi, Raji Grewal, Dan Cohn, Brenda Eskenazi, Andrew J Wyrobek, Norman Arnheim. Proc Natl Acad Sci U S A 2002
103
7

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
7

Anatomical abnormalities in mandibulofacial dysostosis.
S W Herring, U F Rowlatt, S Pruzansky. Am J Med Genet 1979
59
11

Transcriptional map of the Treacher Collins candidate gene region.
S K Loftus, J Dixon, K Koprivnikar, M J Dixon, J J Wasmuth. Genome Res 1996
9
77

Genetic and physical mapping of the Treacher Collins syndrome locus with respect to loci in the chromosome 5q3 region.
E W Jabs, X Li, M Lovett, L H Yamaoka, E Taylor, M C Speer, C Coss, R Cadle, B Hall, K Brown. Genomics 1993
32
21

Parent-of-origin effects in multiple endocrine neoplasia type 2B.
K M Carlson, J Bracamontes, C E Jackson, R Clark, A Lacroix, S A Wells, P J Goodfellow. Am J Hum Genet 1994
170
6

Spontaneous mutation and parental age in humans.
N Risch, E W Reich, M M Wishnick, J G McCarthy. Am J Hum Genet 1987
173
6

Paternal age and the occurrence of birth defects.
Z H Lian, M M Zack, J D Erickson. Am J Hum Genet 1986
91
6

The mandibulofacial dysostosis; a new hereditary syndrome.
A FRANCESCHETTI, D KLEIN. Acta Ophthalmol (Copenh) 1949
126
6


Mutation testing in Treacher Collins Syndrome.
P E Ellis, M Dawson, M J Dixon. J Orthod 2002
24
25

Acrodysostosis. A syndrome of peripheral dysostosis, nasal hypoplasia, and mental retardation.
M Robinow, R A Pfeiffer, R J Gorlin, V A McKusick, A W Renuart, G F Johnson, R L Summitt. Am J Dis Child 1971
67
8

Advancing paternal age and autism.
Abraham Reichenberg, Raz Gross, Mark Weiser, Michealine Bresnahan, Jeremy Silverman, Susan Harlap, Jonathan Rabinowitz, Cory Shulman, Dolores Malaspina, Gad Lubin,[...]. Arch Gen Psychiatry 2006
369
6

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
6

Genetic and physical mapping of the Treacher Collins syndrome locus: refinement of the localization to chromosome 5q32-33.2.
M J Dixon, J Dixon, D Raskova, M M Le Beau, R Williamson, K Klinger, G M Landes. Hum Mol Genet 1992
32
18

A YAC contig encompassing the Treacher Collins syndrome critical region at 5q31.3-32.
J Dixon, A J Gladwin, S K Loftus, J H Riley, R Perveen, J J Wasmuth, R Anand, M J Dixon. Am J Hum Genet 1994
29
20


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.