A citation-based method for searching scientific literature

H Knoblauch, G Thiel, S Tinschert, H Körner, C Tennstedt, R Chaoui, J Kohlhase, C Dixkens, C Blanck. J Med Genet 2000
Times Cited: 4







List of co-cited articles
4 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
75

High resolution mapping of interstitial long arm deletions of chromosome 16: relationship to phenotype.
D F Callen, H Eyre, S Lane, Y Shen, I Hansmann, N Spinner, E Zackai, D McDonald-McGinn, S Schuffenhauer, J Wauters. J Med Genet 1993
42
50


Detection of heterozygous SALL1 deletions by quantitative real time PCR proves the contribution of a SALL1 dosage effect in the pathogenesis of Townes-Brocks syndrome.
Wiktor Borozdin, Katharina Steinmann, Beate Albrecht, Armand Bottani, Koenraad Devriendt, Michael Leipoldt, Jürgen Kohlhase. Hum Mutat 2006
33
50



Point mutations throughout the GLI3 gene cause Greig cephalopolysyndactyly syndrome.
M Kalff-Suske, A Wild, J Topp, M Wessling, E M Jacobsen, D Bornholdt, H Engel, H Heuer, C M Aalfs, M G Ausems,[...]. Hum Mol Genet 1999
110
25

GLI3 frameshift mutations cause autosomal dominant Pallister-Hall syndrome.
S Kang, J M Graham, A H Olney, L G Biesecker. Nat Genet 1997
358
25

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
25

Three novel SALL1 mutations extend the mutational spectrum in Townes-Brocks syndrome.
C Blanck, J Kohlhase, S Engels, P Burfeind, W Engel, A Bottani, M S Patel, H Y Kroes, J M Cobben. J Med Genet 2000
27
25


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



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
25

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
25


A SALL1 mutation causes a branchio-oto-renal syndrome-like phenotype.
S Engels, J Kohlhase, J McGaughran. J Med Genet 2000
49
25

Townes-Brocks syndrome and renal dysplasia: a novel mutation in the SALL1 gene.
A Salerno, J Kohlhase, B S Kaplan. Pediatr Nephrol 2000
27
25


Two distinct mechanisms for long-range patterning by Decapentaplegic in the Drosophila wing.
T Lecuit, W J Brook, M Ng, M Calleja, H Sun, S M Cohen. Nature 1996
538
25


spalt encodes an evolutionarily conserved zinc finger protein of novel structure which provides homeotic gene function in the head and tail region of the Drosophila embryo.
R P Kühnlein, G Frommer, M Friedrich, M Gonzalez-Gaitan, A Weber, J F Wagner-Bernholz, W J Gehring, H Jäckle, R Schuh. EMBO J 1994
224
25


Point mutations in human GLI3 cause Greig syndrome.
A Wild, M Kalff-Suske, A Vortkamp, D Bornholdt, R König, K H Grzeschik. Hum Mol Genet 1997
139
25


Molecular cloning, chromosomal localization, and expression of the murine SALL1 ortholog Sall1.
A Buck, L Archangelo, C Dixkens, J Kohlhase. Cytogenet Cell Genet 2000
34
25

Direct and long-range action of a DPP morphogen gradient.
D Nellen, R Burke, G Struhl, K Basler. Cell 1996
767
25


The phenotypic spectrum of GLI3 morphopathies includes autosomal dominant preaxial polydactyly type-IV and postaxial polydactyly type-A/B; No phenotype prediction from the position of GLI3 mutations.
U Radhakrishna, D Bornholdt, H S Scott, U C Patel, C Rossier, H Engel, A Bottani, D Chandal, J L Blouin, J V Solanki,[...]. Am J Hum Genet 1999
125
25

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
25

Mutation in GLI3 in postaxial polydactyly type A.
U Radhakrishna, A Wild, K H Grzeschik, S E Antonarakis. Nat Genet 1997
130
25

National study of microphthalmia, anophthalmia, and coloboma (MAC) in Scotland: investigation of genetic aetiology.
D Morrison, D FitzPatrick, I Hanson, K Williamson, V van Heyningen, B Fleck, I Jones, J Chalmers, H Campbell. J Med Genet 2002
176
25

The descriptive epidemiology of anophthalmia and microphthalmia.
B Källén, E Robert, J Harris. Int J Epidemiol 1996
95
25

Townes-Brocks syndrome: twenty novel SALL1 mutations in sporadic and familial cases and refinement of the SALL1 hot spot region.
Elke M Botzenhart, Gabriella Bartalini, Edward Blair, Angela F Brady, Frances Elmslie, Karen L Chong, Katie Christy, Wilfredo Torres-Martinez, Cesare Danesino, Matthew A Deardorff,[...]. Hum Mutat 2007
31
25

Recurrent de novo interstitial deletion of 16q in two mentally retarded sisters.
J J Hoo, R B Lowry, C C Lin, R H Haslam. Clin Genet 1985
31
25

SOX2 anophthalmia syndrome.
Nicola K Ragge, Birgit Lorenz, Adele Schneider, Kate Bushby, Luisa de Sanctis, Ugo de Sanctis, Alison Salt, J Richard O Collin, Anthony J Vivian, Samantha L Free,[...]. Am J Med Genet A 2005
164
25

Mutations in the calcium-related gene IL1RAPL1 are associated with autism.
Amélie Piton, Jacques L Michaud, Huashan Peng, Swaroop Aradhya, Julie Gauthier, Laurent Mottron, Nathalie Champagne, Ronald G Lafrenière, Fadi F Hamdan, Ridha Joober,[...]. Hum Mol Genet 2008
135
25


Congenital eye malformations: a descriptive epidemiologic study in about one million newborns in Italy.
M Clementi, R Tenconi, F Bianchi, L Botto, A Calabro, E Calzolari, D Cianciulli, I Mammi, P Mastroiacovo, P Meli,[...]. Birth Defects Orig Artic Ser 1996
23
25

Autosomal dominant granulomatous arthritis, uveitis, skin rash, and synovial cysts.
G M Pastores, V V Michels, G B Stickler, W P Su, A M Nelson, D A Bovenmyer. J Pediatr 1990
59
25

Interstitial deletion and ring chromosome derived from 16q.
C M Krauss, D Caldwell, L Atkins. J Med Genet 1987
32
25

Identification of a previously unrecognized microdeletion syndrome of 16q11.2q12.2.
B C Ballif, A Theisen, D M McDonald-McGinn, E H Zackai, J H Hersh, B A Bejjani, L G Shaffer. Clin Genet 2008
79
25

Human microphthalmia associated with mutations in the retinal homeobox gene CHX10.
E Ferda Percin, L A Ploder, J J Yu, K Arici, D J Horsford, A Rutherford, B Bapat, D W Cox, A M Duncan, V I Kalnins,[...]. Nat Genet 2000
208
25

Identification of a recurrent mutation in the CYLD gene in Brooke-Spiegler syndrome.
N Scheinfeld, G Hu, M Gill, C Austin, J T Celebi. Clin Exp Dermatol 2003
24
25

Small reciprocal insertion detected by spectral karyotyping (SKY) and delimited by array-CGH analysis.
Anja Matthaei, Walter Werner, Eva-Maria Gerlach, Ulrike Koerner, Sigrid Tinschert, Inna Nitz, Alexander Herr, Andreas Rump, Oliver Bartsch, Klaus G Hinkel,[...]. Eur J Med Genet 2005
7
25


CARD15 mutations in Blau syndrome.
C Miceli-Richard, S Lesage, M Rybojad, A M Prieur, S Manouvrier-Hanu, R Häfner, M Chamaillard, H Zouali, G Thomas, J P Hugot. Nat Genet 2001
691
25

Identification of the familial cylindromatosis tumour-suppressor gene.
G R Bignell, W Warren, S Seal, M Takahashi, E Rapley, R Barfoot, H Green, C Brown, P J Biggs, S R Lakhani,[...]. Nat Genet 2000
523
25



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.