A citation-based method for searching scientific literature

P Edery, Y Manach, M Le Merrer, M Till, A Vignal, S Lyonnet, A Munnich. Am J Med Genet 1994
Times Cited: 16







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



Times Cited
  Times     Co-cited
Similarity


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
62

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
56

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
56


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
50

The ear deformities in mandibulofacial dysostosis (Treacher Collins syndrome).
P D Phelps, D Poswillo, G A Lloyd. Clin Otolaryngol Allied Sci 1981
75
43

Mild mandibulofacial dysostosis in a child with a deletion of 3p.
P H Arn, C Mankinen, E W Jabs. Am J Med Genet 1993
18
43

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
43

MANDIBULOFACIAL DYSOSTOSIS, A FAMILIAL STUDY OF FIVE GENERATIONS.
S ROVIN, S F DACHI, D B BORENSTEIN, W B COTTER. J Pediatr 1964
73
37


Association of Treacher Collins syndrome and translocation 6p21.31/16p13.11: exclusion of the locus from these candidate regions.
M J Dixon, E Haan, E Baker, D David, N McKenzie, R Williamson, J Mulley, M Farrall, D Callen. Am J Hum Genet 1991
22
37


Chromosomal deletion 4p15.32----p14 in a Treacher Collins syndrome patient: exclusion of the disease locus from and mapping of anonymous DNA sequences to this region.
E W Jabs, C A Coss, S J Hayflick, T E Whitmore, R M Pauli, S J Kirkpatrick, D A Meyers, R Goldberg, D W Day, K N Rosenbaum. Genomics 1991
21
37

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
37

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
37


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
31

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
31

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
55

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
25

Mandibulo-facial dysostosis. (Treacher-Collins syndrome).
L E Fazen, J Elmore, H L Nadler. Am J Dis Child 1967
65
25


Prenatal diagnosis of mandibulofacial dysostosis.
K H Nicolaides, D Johansson, D Donnai, C H Rodeck. Prenat Diagn 1984
19
25

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
25

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



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
18

The mandibulofacial dysostosis; a new hereditary syndrome.
A FRANCESCHETTI, D KLEIN. Acta Ophthalmol (Copenh) 1949
126
18

Anatomical abnormalities in mandibulofacial dysostosis.
S W Herring, U F Rowlatt, S Pruzansky. Am J Med Genet 1979
59
18

Isolation of genes from complex sources of mammalian genomic DNA using exon amplification.
D M Church, C J Stotler, J L Rutter, J R Murrell, J A Trofatter, A J Buckler. Nat Genet 1994
271
18

DNA sequencing with chain-terminating inhibitors.
F Sanger, S Nicklen, A R Coulson. Proc Natl Acad Sci U S A 1977
18


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
18



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
12

Treacher Collins syndrome.
M J Dixon. J Med Genet 1995
34
12

Treacher Collins syndrome with acute airway obstruction.
F A Shah, S Ramakrishna, V Ingle, J E Dada, M Al Khabori, P S Murty. Int J Pediatr Otorhinolaryngol 2000
6
33

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
12

Treacher Collins syndrome: etiology, pathogenesis and prevention.
Paul A Trainor, Jill Dixon, Michael J Dixon. Eur J Hum Genet 2009
117
12




Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia.
R Shiang, L M Thompson, Y Z Zhu, D M Church, T J Fielder, M Bocian, S T Winokur, J J Wasmuth. Cell 1994
937
12

Basic local alignment search tool.
S F Altschul, W Gish, W Miller, E W Myers, D J Lipman. J Mol Biol 1990
12

Primary structure of the human, membrane-associated Ca2+-binding protein p68 a novel member of a protein family.
M R Crompton, R J Owens, N F Totty, S E Moss, M D Waterfield, M J Crumpton. EMBO J 1988
157
12

Structure of the human annexin VI gene.
P D Smith, A Davies, M J Crumpton, S E Moss. Proc Natl Acad Sci U S A 1994
42
12

Developmental changes in heparan sulfate expression: in situ detection with mAbs.
G David, X M Bai, B Van der Schueren, J J Cassiman, H Van den Berghe. J Cell Biol 1992
415
12



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.