A citation-based method for searching scientific literature

T H Cameron, A M Lachiewicz, A S Aylsworth. Am J Med Genet 1991
Times Cited: 31







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



Times Cited
  Times     Co-cited
Similarity



Mutations in the SALL1 putative transcription factor gene cause Townes-Brocks syndrome.
J Kohlhase, A Wischermann, H Reichenbach, U Froster, W Engel. Nat Genet 1998
331
70

Townes-Brocks syndrome associated with mental retardation.
S Ishikiriyama, F Kudoh, N Shimojo, J Iwai, T Inoue. Am J Med Genet 1996
24
87

Townes syndrome. A distinct multiple malformation syndrome resembling VACTERL association.
J H Hersh, M Jaworski, R E Solinger, B Weisskopf, J Donat. Clin Pediatr (Phila) 1986
28
60

Townes-Brocks syndrome presenting as end stage renal failure.
W G Newman, M D Brunet, D Donnai. Clin Dysmorphol 1997
24
70

Phenotypic variability in Townes-Brocks syndrome.
J Monteiro de Pina-Neto. Am J Med Genet 1984
36
54

Molecular analysis of SALL1 mutations in Townes-Brocks syndrome.
J Kohlhase, P E Taschner, P Burfeind, B Pasche, B Newman, C Blanck, M H Breuning, L P ten Kate, P Maaswinkel-Mooy, B Mitulla,[...]. Am J Hum Genet 1999
127
54

Hearing loss in Townes-Brocks syndrome.
D R Rossmiller, T R Pasic. Otolaryngol Head Neck Surg 1994
27
59

Townes-Brocks syndrome in an infant with translocation t (5;16).
F Serville, D Lacombe, R Saura, C Billeaud, M P Sergent. Genet Couns 1993
29
51

Townes-Brocks syndrome.
C M Powell, R C Michaelis. J Med Genet 1999
97
48


[Clinical heterogeneity of Townes-Brocks syndrome].
P Parent, M Bensaid, H Le Guern, A Colin, L Broussine, A Chabarot, A Cozic, B Jehannin, L de Parscau. Arch Pediatr 1995
17
76

Description of a patient with difficult nosological classification: Goldenhar syndrome or Townes-Brocks syndrome?
O Gabrielli, V Bonifazi, A M Offidani, A Cellini, G V Coppa, P L Giorgi. Minerva Pediatr 1993
26
46


A new family with the Townes-Brocks syndrome.
M A de Vries-Van der Weerd, P J Willems, H M Mandema, L P ten Kate. Clin Genet 1988
28
39

Two cases of Townes-Brocks syndrome with previously undescribed anomalies.
S Marlin, J E Toublanc, C Petit. Clin Dysmorphol 1998
17
64

The Townes-Brocks syndrome.
M O'Callaghan, I D Young. J Med Genet 1990
29
34

Interstitial 16q deletion with typical dysmorphic syndrome.
J P Fryns, W Proesmans, G Van Hoey, H Van den Berghe. Ann Genet 1981
30
33

WT-1 is required for early kidney development.
J A Kreidberg, H Sariola, J M Loring, M Maeda, J Pelletier, D Housman, R Jaenisch. Cell 1993
32

Townes-Brocks syndrome. Report of a case and review of the literature.
F G Ferraz, L Nunes, M E Ferraz, J P Sousa, M Santos, C Carvalho, P Maroteaux. Ann Genet 1989
21
42



Association of the FcepsilonRIbeta gene with bronchial hyper-responsiveness in an Italian population.
E Trabetti, V Cusin, G Malerba, L C Martinati, A Casartelli, A L Boner, P F Pignatti. J Med Genet 1998
33
29



Variability of biochemical and clinical phenotype in X-linked liver glycogenosis with mutations in the phosphorylase kinase PHKA2 gene.
B Burwinkel, L Amat, R G Gray, N Matsuo, K Muroya, K Narisawa, R J Sokol, M A Vilaseca, M W Kilimann. Hum Genet 1998
46
29

Evidence that WT1 mutations in Denys-Drash syndrome patients may act in a dominant-negative fashion.
M H Little, K A Williamson, M Mannens, A Kelsey, C Gosden, N D Hastie, V van Heyningen. Hum Mol Genet 1993
127
29



p53 abnormalities in B-cell prolymphocytic leukemia.
D Lens, P J De Schouwer, R A Hamoudi, M Abdul-Rauf, N Farahat, E Matutes, T Crook, M J Dyer, D Catovsky. Blood 1997
78
29

STAT6: its role in interleukin 4-mediated biological functions.
K Takeda, T Kishimoto, S Akira. J Mol Med (Berl) 1997
96
29


Regulation of tissue-specific expression of alternative peripheral myelin protein-22 (PMP22) gene transcripts by two promoters.
U Suter, G J Snipes, R Schoener-Scott, A A Welcher, S Pareek, J R Lupski, R A Murphy, E M Shooter, P I Patel. J Biol Chem 1994
171
29



Charcot-Marie-Tooth disease type 1A. Association with a spontaneous point mutation in the PMP22 gene.
B B Roa, C A Garcia, U Suter, D A Kulpa, C A Wise, J Mueller, A A Welcher, G J Snipes, E M Shooter, P I Patel,[...]. N Engl J Med 1993
327
29

A gene for the mouse pink-eyed dilution locus and for human type II oculocutaneous albinism.
E M Rinchik, S J Bultman, B Horsthemke, S T Lee, K M Strunk, R A Spritz, K M Avidano, M T Jong, R D Nicholls. Nature 1993
323
29

Phosphorylase b kinase deficiency glycogenosis with cirrhosis of the liver.
A F Kagalwalla, Y A Kagalwalla, S al Ajaji, W Gorka, M A Ali. J Pediatr 1995
20
45

Control of inflammation, cytokine expression, and germinal center formation by BCL-6.
A L Dent, A L Shaffer, X Yu, D Allman, L M Staudt. Science 1997
740
29

Smith-Lemli-Opitz syndrome: a variable clinical and biochemical phenotype.
A K Ryan, K Bartlett, P Clayton, S Eaton, L Mills, D Donnai, R M Winter, J Burn. J Med Genet 1998
174
29

Essential role of Stat6 in IL-4 signalling.
K Takeda, T Tanaka, W Shi, M Matsumoto, M Minami, S Kashiwamura, K Nakanishi, N Yoshida, T Kishimoto, S Akira. Nature 1996
29

Molecular and clinical study of 61 Angelman syndrome patients.
S Saitoh, N Harada, Y Jinno, K Hashimoto, K Imaizumi, Y Kuroki, Y Fukushima, T Sugimoto, M Renedo, J Wagstaff. Am J Med Genet 1994
72
29

Retinitis pigmentosa caused by a homozygous mutation in the Stargardt disease gene ABCR.
A Martínez-Mir, E Paloma, R Allikmets, C Ayuso, T del Rio, M Dean, L Vilageliu, R Gonzàlez-Duarte, S Balcells. Nat Genet 1998
329
29


DNA duplication associated with Charcot-Marie-Tooth disease type 1A.
J R Lupski, R M de Oca-Luna, S Slaugenhaupt, L Pentao, V Guzzetta, B J Trask, O Saucedo-Cardenas, D F Barker, J M Killian, C A Garcia,[...]. Cell 1991
29

Homozygosity mapping of autosomal recessive retinitis pigmentosa locus (RP22) on chromosome 16p12.1-p12.3.
U Finckh, S Xu, G Kumaramanickavel, M Schürmann, J K Mukkadan, S T Fernandez, S John, J L Weber, M J Denton, A Gal. Genomics 1998
25
36

Partial monosomy of the long arm of chromosome 16: a distinct clinical entity?
J P Fryns, J Bande-Knops, H Van Den Berghe. Hum Genet 1979
28
32

Autosomal recessive phosphorylase kinase deficiency in liver, caused by mutations in the gene encoding the beta subunit (PHKB).
I E van den Berg, E A van Beurden, J B de Klerk, O P van Diggelen, H E Malingré, M M Boer, R Berger. Am J Hum Genet 1997
24
37

16q21 is critical for 16q deletion syndrome.
K Naritomi, N Shiroma, Y Izumikawa, K Sameshima, S Ohdo, K Hirayama. Clin Genet 1988
26
34

A genome-wide search for linkage to asthma. German Asthma Genetics Group.
M Wjst, G Fischer, T Immervoll, M Jung, K Saar, F Rueschendorf, A Reis, M Ulbrecht, M Gomolka, E H Weiss,[...]. Genomics 1999
289
29


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.