A citation-based method for searching scientific literature

P L Townes, E R Brocks. J Pediatr 1972
Times Cited: 127







List of co-cited articles
577 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
55

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
42


Phenotypic variability in Townes-Brocks syndrome.
J Monteiro de Pina-Neto. Am J Med Genet 1984
36
75

Isolation, characterization, and organ-specific expression of two novel human zinc finger genes related to the Drosophila gene spalt.
J Kohlhase, R Schuh, G Dowe, R P Kühnlein, H Jäckle, B Schroeder, W Schulz-Schaeffer, H A Kretzschmar, A Köhler, U Müller,[...]. Genomics 1996
148
27

Townes-Brocks syndrome in two mentally retarded youngsters.
T H Cameron, A M Lachiewicz, A S Aylsworth. Am J Med Genet 1991
31
83

Townes-Brocks syndrome.
C M Powell, R C Michaelis. J Med Genet 1999
97
25

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
85

Townes-Brocks syndrome presenting as end stage renal failure.
W G Newman, M D Brunet, D Donnai. Clin Dysmorphol 1997
24
87

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
72

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
21

Hearing loss in Townes-Brocks syndrome.
D R Rossmiller, T R Pasic. Otolaryngol Head Neck Surg 1994
27
74

Townes-Brocks syndrome associated with mental retardation.
S Ishikiriyama, F Kudoh, N Shimojo, J Iwai, T Inoue. Am J Med Genet 1996
24
83

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
67


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
80



Familial and abnormality.
I S Reid, G Turner. J Pediatr 1976
27
51

[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
82

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
53

The Townes-Brocks syndrome.
M O'Callaghan, I D Young. J Med Genet 1990
29
44

Two cases of Townes-Brocks syndrome with previously undescribed anomalies.
S Marlin, J E Toublanc, C Petit. Clin Dysmorphol 1998
17
76

Townes-Brocks syndrome: detection of a SALL1 mutation hot spot and evidence for a position effect in one patient.
S Marlin, S Blanchard, R Slim, D Lacombe, F Denoyelle, J L Alessandri, E Calzolari, V Drouin-Garraud, F G Ferraz, A Fourmaintraux,[...]. Hum Mutat 1999
55
23

A population study of the VACTERL association: evidence for its etiologic heterogeneity.
M J Khoury, J F Cordero, F Greenberg, L M James, J D Erickson. Pediatrics 1983
238
12


Analysis of the VNTR locus D1S80 by the PCR followed by high-resolution PAGE.
B Budowle, R Chakraborty, A M Giusti, A J Eisenberg, R C Allen. Am J Hum Genet 1991
845
11

Donor splice-site mutations in WT1 are responsible for Frasier syndrome.
S Barbaux, P Niaudet, M C Gubler, J P Grünfeld, F Jaubert, F Kuttenn, C N Fékété, N Souleyreau-Therville, E Thibaud, M Fellous,[...]. Nat Genet 1997
492
11

SALL1 mutation analysis in Townes-Brocks syndrome: twelve novel mutations and expansion of the phenotype.
Elke M Botzenhart, Andrew Green, Helena Ilyina, Rainer König, R Brian Lowry, Ivan F M Lo, Mordechai Shohat, Leah Burke, Julie McGaughran, Ronit Chafai,[...]. Hum Mutat 2005
41
26

Townes-Brocks syndrome.
R König, U Schick, S Fuchs. Eur J Pediatr 1990
16
62

Autosomal glycogenosis of liver and muscle due to phosphorylase kinase deficiency is caused by mutations in the phosphorylase kinase beta subunit (PHKB).
B Burwinkel, A J Maichele, O Aagenaes, H D Bakker, A Lerner, Y S Shin, J A Strachan, M W Kilimann. Hum Mol Genet 1997
48
20

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
40

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
41


Trichothiodystrophy without associated neuroectodermal defects.
C Peter, J Tomczok, E Hoting, H Behrendt. Br J Dermatol 1998
18
55

Genetic alterations during colorectal-tumor development.
B Vogelstein, E R Fearon, S R Hamilton, S E Kern, A C Preisinger, M Leppert, Y Nakamura, R White, A M Smits, J L Bos. N Engl J Med 1988
10

The DCC gene: structural analysis and mutations in colorectal carcinomas.
K R Cho, J D Oliner, J W Simons, L Hedrick, E R Fearon, A C Preisinger, P Hedge, G A Silverman, B Vogelstein. Genomics 1994
218
10

Detection of 100% of the CFTR mutations in 63 CF families from Tyrol.
M Stuhrmann, T Dörk, M Frühwirth, A Golla, B Skawran, W Antonin, M Ebhardt, A Loos, H Ellemunter, J Schmidtke. Clin Genet 1997
28
35

Diaphragmatic hernia in Denys-Drash syndrome.
K Devriendt, E Deloof, P Moerman, E Legius, C Vanhole, F de Zegher, W Proesmans, H Devlieger. Am J Med Genet 1995
64
15

Lipids in keratinized tissues.
R D FRASER, T P MACRAE, G E ROGERS, B K FILSHIE. J Mol Biol 1963
39
25

Somatic alterations of the DPC4 gene in human colorectal cancers in vivo.
Y Takagi, H Kohmura, M Futamura, H Kida, H Tanemura, K Shimokawa, S Saji. Gastroenterology 1996
196
10

The nature of the defect in tyrosine metabolism in alcaptonuria.
B N LA DU, V G ZANNONI, L LASTER, J E SEEGMILLER. J Biol Chem 1958
269
10

Mutations in the TIGR gene in familial primary open-angle glaucoma in Japan.
Y Suzuki, S Shirato, F Taniguchi, K Ohara, K Nishimaki, S Ohta. Am J Hum Genet 1997
129
10

Defects in the DNA repair and transcription gene ERCC2(XPD) in trichothiodystrophy.
K Takayama, E P Salazar, B C Broughton, A R Lehmann, A Sarasin, L H Thompson, C A Weber. Am J Hum Genet 1996
94
10

Evaluation of candidate tumour suppressor genes on chromosome 18 in colorectal cancers.
S Thiagalingam, C Lengauer, F S Leach, M Schutte, S A Hahn, J Overhauser, J K Willson, S Markowitz, S R Hamilton, S E Kern,[...]. Nat Genet 1996
527
10

Mutational inactivation of transforming growth factor beta receptor type II in microsatellite stable colon cancers.
W M Grady, L L Myeroff, S E Swinler, A Rajput, S Thiagalingam, J D Lutterbaugh, A Neumann, M G Brattain, J Chang, S J Kim,[...]. Cancer Res 1999
309
10

Deletion 9p and sex reversal.
C P Bennett, Z Docherty, S A Robb, P Ramani, J R Hawkins, D Grant. J Med Genet 1993
138
10


Mutation and polymorphism analysis of the human homogentisate 1, 2-dioxygenase gene in alkaptonuria patients.
D Beltrán-Valero de Bernabé, B Granadino, I Chiarelli, B Porfirio, E Mayatepek, R Aquaron, M M Moore, J J Festen, R Sanmartí, M A Peñalva,[...]. Am J Hum Genet 1998
70
14



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.