A citation-based method for searching scientific literature

E W Jabs, X Li, C A Coss, E W Taylor, D A Meyers, J L Weber. Genomics 1991
Times Cited: 53







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



Times Cited
  Times     Co-cited
Similarity


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
54

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
43

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
73


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
46

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
24

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
40

MANDIBULOFACIAL DYSOSTOSIS, A FAMILIAL STUDY OF FIVE GENERATIONS.
S ROVIN, S F DACHI, D B BORENSTEIN, W B COTTER. J Pediatr 1964
73
22

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
54

The ear deformities in mandibulofacial dysostosis (Treacher Collins syndrome).
P D Phelps, D Poswillo, G A Lloyd. Clin Otolaryngol Allied Sci 1981
75
20


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
52

Radiation hybrid map of 13 loci on the long arm of chromosome 5.
J A Warrington, L V Hall, L M Hinton, J N Miller, J J Wasmuth, M Lovett. Genomics 1991
59
20

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
34

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
16

Apparent genetic homogeneity of the Treacher Collins-Franceschetti syndrome.
P Edery, Y Manach, M Le Merrer, M Till, A Vignal, S Lyonnet, A Munnich. Am J Med Genet 1994
16
56

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
16


Anatomical abnormalities in mandibulofacial dysostosis.
S W Herring, U F Rowlatt, S Pruzansky. Am J Med Genet 1979
59
16

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
26


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
21

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
88

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
38

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
16

The mandibulofacial dysostosis; a new hereditary syndrome.
A FRANCESCHETTI, D KLEIN. Acta Ophthalmol (Copenh) 1949
126
13

Mandibulo-facial dysostosis. (Treacher-Collins syndrome).
L E Fazen, J Elmore, H L Nadler. Am J Dis Child 1967
64
13

Prenatal diagnosis of mandibulofacial dysostosis.
K H Nicolaides, D Johansson, D Donnai, C H Rodeck. Prenat Diagn 1984
19
36


Prenatal mandibulofacial dysostosis (Treacher Collins syndrome).
R G Behrents, J A McNamara, J K Avery. Cleft Palate J 1977
50
12

The gene for an inherited form of deafness maps to chromosome 5q31.
P E Leon, H Raventos, E Lynch, J Morrow, M C King. Proc Natl Acad Sci U S A 1992
143
11




Recurrence of Treacher Collins' syndrome with sonographic findings.
D A Milligan, F E Harlass, P Duff, J N Kopelman. Mil Med 1994
16
37

DNA sequencing with chain-terminating inhibitors.
F Sanger, S Nicklen, A R Coulson. Proc Natl Acad Sci U S A 1977
11


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
9


Mapping of human chromosome 5 microsatellite DNA polymorphisms.
J L Weber, M H Polymeropoulos, P E May, A E Kwitek, H Xiao, J D McPherson, J J Wasmuth. Genomics 1991
95
9

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
9

The skeletal anatomy of mandibulofacial dysostosis (Treacher Collins syndrome).
J L Marsh, S E Celin, M W Vannier, M Gado. Plast Reconstr Surg 1986
61
9

An x-radiocephalometric study of mandibulofacial dysostosis in man.
F G Roberts, S Pruzansky, H Aduss. Arch Oral Biol 1975
55
9

Basic local alignment search tool.
S F Altschul, W Gish, W Miller, E W Myers, D J Lipman. J Mol Biol 1990
9

A radiation hybrid map of 18 growth factor, growth factor receptor, hormone receptor, or neurotransmitter receptor genes on the distal region of the long arm of chromosome 5.
J A Warrington, S K Bailey, E Armstrong, O Aprelikova, K Alitalo, G M Dolganov, A S Wilcox, J M Sikela, S F Wolfe, M Lovett. Genomics 1992
98
9







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.