A citation-based method for searching scientific literature

K Pritchard-Jones, N Rahman, M Gerrard, D Variend, L King-Underwood. J Med Genet 2000
Times Cited: 12







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



Times Cited
  Times     Co-cited
Similarity


Familial Wilms' tumor associated with a WT1 zinc finger mutation.
C Kaplinsky, M Ghahremani, Y Frishberg, G Rechavi, J Pelletier. Genomics 1996
24
83

WT1 mutations contribute to abnormal genital system development and hereditary Wilms' tumour.
J Pelletier, W Bruening, F P Li, D A Haber, T Glaser, D E Housman. Nature 1991
408
58

Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation database.
C Jeanpierre, E Denamur, I Henry, M O Cabanis, S Luce, A Cécille, J Elion, M Peuchmaur, C Loirat, P Niaudet,[...]. Am J Hum Genet 1998
183
50

Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome.
J Pelletier, W Bruening, C E Kashtan, S M Mauer, J C Manivel, J E Striegel, D C Houghton, C Junien, R Habib, L Fouser. Cell 1991
761
50

Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping.
M Gessler, A Poustka, W Cavenee, R L Neve, S H Orkin, G A Bruns. Nature 1990
41

Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus.
K M Call, T Glaser, C Y Ito, A J Buckler, J Pelletier, D A Haber, E A Rose, A Kral, H Yeger, W H Lewis. Cell 1990
41

Wilms tumor genetics.
V Huff. Am J Med Genet 1998
105
41


The candidate Wilms' tumour gene is involved in genitourinary development.
K Pritchard-Jones, S Fleming, D Davidson, W Bickmore, D Porteous, C Gosden, J Bard, A Buckler, J Pelletier, D Housman. Nature 1990
803
33

Correlation of germ-line mutations and two-hit inactivation of the WT1 gene with Wilms tumors of stromal-predominant histology.
V Schumacher, S Schneider, A Figge, G Wildhardt, D Harms, D Schmidt, A Weirich, R Ludwig, B Royer-Pokora. Proc Natl Acad Sci U S A 1997
97
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
33

Spectrum of early onset nephrotic syndrome associated with WT1 missense mutations.
V Schumacher, K Schärer, E Wühl, H Altrogge, K E Bonzel, M Guschmann, T J Neuhaus, R M Pollastro, E Kuwertz-Bröking, M Bulla,[...]. Kidney Int 1998
111
33

Frequent association of beta-catenin and WT1 mutations in Wilms tumors.
S Maiti, R Alam, C I Amos, V Huff. Cancer Res 2000
165
33

Constitutional WT1 mutations in Wilms' tumor patients.
L Diller, M Ghahremani, J Morgan, P Grundy, C Reeves, N Breslow, D Green, D Neuberg, J Pelletier, F P Li. J Clin Oncol 1998
42
33

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
33


Twenty-four new cases of WT1 germline mutations and review of the literature: genotype/phenotype correlations for Wilms tumor development.
Brigitte Royer-Pokora, Manfred Beier, Markus Henzler, Rita Alam, Valérie Schumacher, Angela Weirich, Vicki Huff. Am J Med Genet A 2004
89
33

Novel familial WT1 read-through mutation associated with Wilms tumor and slow progressive nephropathy.
Birgit Zirn, Stefanie Wittmann, Manfred Gessler. Am J Kidney Dis 2005
15
33

Discordant expression of a new WT1 gene mutation in a family with monozygotic twins presenting with congenital nephrotic syndrome.
Filip Fencl, Michal Malina, Veronika Stará, Jakub Zieg, Dana Mixová, Tomáš Seeman, Květa Bláhová. Eur J Pediatr 2012
12
33

A clinical overview of WT1 gene mutations.
M Little, C Wells. Hum Mutat 1997
275
25

Alternative splicing and genomic structure of the Wilms tumor gene WT1.
D A Haber, R L Sohn, A J Buckler, J Pelletier, K M Call, D E Housman. Proc Natl Acad Sci U S A 1991
577
25


Inherited WT1 mutation in Denys-Drash syndrome.
M J Coppes, G J Liefers, M Higuchi, A B Zinn, J W Balfe, B R Williams. Cancer Res 1992
94
25

Nonrandom loss of maternal chromosome 11 alleles in Wilms tumors.
W T Schroeder, L Y Chao, D D Dao, L C Strong, S Pathak, V Riccardi, W H Lewis, G F Saunders. Am J Hum Genet 1987
245
25


Constitutional mutations in the WT1 gene in patients with Denys-Drash syndrome.
P N Baird, A Santos, N Groves, L Jadresic, J K Cowell. Hum Mol Genet 1992
83
25

Familial Wilms' tumor: a descriptive study.
N E Breslow, J Olson, J Moksness, J B Beckwith, P Grundy. Med Pediatr Oncol 1996
65
25


Germline intronic and exonic mutations in the Wilms' tumour gene (WT1) affecting urogenital development.
W Bruening, N Bardeesy, B L Silverman, R A Cohn, G A Machin, A J Aronson, D Housman, J Pelletier. Nat Genet 1992
189
25

Frasier syndrome is caused by defective alternative splicing of WT1 leading to an altered ratio of WT1 +/-KTS splice isoforms.
B Klamt, A Koziell, F Poulat, P Wieacker, P Scambler, P Berta, M Gessler. Hum Mol Genet 1998
236
25

Mother-to-child transmitted WT1 splice-site mutation is responsible for distinct glomerular diseases.
E Denamur, N Bocquet, B Mougenot, F Da Silva, L Martinat, C Loirat, J Elion, A Bensman, P M Ronco. J Am Soc Nephrol 1999
64
25

Vertical transmission of a mutation in exon 1 of the WT1 gene: lessons for genetic counseling.
Miriam Regev, Richard Kirk, Maya Mashevich, Zvi Bistritzer, Orit Reish. Am J Med Genet A 2008
13
25

Evidence for a familial Wilms' tumour gene (FWT1) on chromosome 17q12-q21.
N Rahman, L Arbour, P Tonin, J Renshaw, J Pelletier, S Baruchel, K Pritchard-Jones, M R Stratton, S A Narod. Nat Genet 1996
99
16

Mutation and cancer: statistical study of retinoblastoma.
A G Knudson. Proc Natl Acad Sci U S A 1971
16

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
16

Genetics of Wilms' tumor.
E Matsunaga. Hum Genet 1981
224
16

WT1 proteins: functions in growth and differentiation.
V Scharnhorst, A J van der Eb, A G Jochemsen. Gene 2001
253
16

Confirmation of FWT1 as a Wilms' tumour susceptibility gene and phenotypic characteristics of Wilms' tumour attributable to FWT1.
N Rahman, F Abidi, D Ford, L Arbour, E Rapley, P Tonin, D Barton, G Batcup, J Berry, F Cotter,[...]. Hum Genet 1998
24
16

Linkage of familial Wilms' tumor predisposition to chromosome 19 and a two-locus model for the etiology of familial tumors.
J M McDonald, E C Douglass, R Fisher, C F Geiser, C E Krill, L C Strong, D Virshup, V Huff. Cancer Res 1998
79
16

Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5.
A Koufos, P Grundy, K Morgan, K A Aleck, T Hadro, B C Lampkin, A Kalbakji, W K Cavenee. Am J Hum Genet 1989
431
16

WT1-mediated transcriptional activation is inhibited by dominant negative mutant proteins.
J C Reddy, J C Morris, J Wang, M A English, D A Haber, Y Shi, J D Licht. J Biol Chem 1995
147
16


A novel WT1 gene mutation associated with wilms' tumor and congenital male genitourinary malformation.
J Sakamoto, A Takata, R Fukuzawa, H Kikuchi, M Sugiyama, Y Kanamori, K Hashizume, J I Hata. Pediatr Res 2001
10
20


Equivalent expression of paternally and maternally inherited WT1 alleles in normal fetal tissue and Wilms' tumours.
M H Little, R Dunn, J A Byrne, A Seawright, P J Smith, K Pritchard-Jones, V van Heyningen, N D Hastie. Oncogene 1992
60
16

Mutations/deletions of the WT1 gene, loss of heterozygosity on chromosome arms 11p and 11q, chromosome ploidy and histology in Wilms' tumors in Japan.
H Nakadate, K Yokomori, N Watanabe, T Tsuchiya, T Namiki, H Kobayshi, S Suita, Y Tsunematsu, Y Horikoshi, Y Hatae,[...]. Int J Cancer 2001
22
16


[Glomerulopathy in Denys-Drash syndrome. Case report of a model disease].
T Stallmach, T J Neuhaus, R Kösters, S Hailemariam. Pathologe 1998
4
50


Two molecular subgroups of Wilms' tumors with or without WT1 mutations.
Valérie Schumacher, Stefanie Schuhen, Sandra Sonner, Angela Weirich, Ivo Leuschner, Dieter Harms, Jonathan Licht, Stefan Roberts, Brigitte Royer-Pokora. Clin Cancer Res 2003
46
16


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.