A citation-based method for searching scientific literature

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
Times Cited: 77







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



Times Cited
  Times     Co-cited
Similarity


p53 mutations in human lymphoid malignancies: association with Burkitt lymphoma and chronic lymphocytic leukemia.
G Gaidano, P Ballerini, J Z Gong, G Inghirami, A Neri, E W Newcomb, I T Magrath, D M Knowles, R Dalla-Favera. Proc Natl Acad Sci U S A 1991
895
23

p53 gene deletion predicts for poor survival and non-response to therapy with purine analogs in chronic B-cell leukemias.
H Döhner, K Fischer, M Bentz, K Hansen, A Benner, G Cabot, D Diehl, R Schlenk, J Coy, S Stilgenbauer. Blood 1995
565
22

Frequent deletions at 11q23 and 13q14 in B cell prolymphocytic leukemia (B-PLL).
D Lens, E Matutes, D Catovsky, L J Coignet. Leukemia 2000
28
53

Prolymphocytic leukaemia.
D A Galton, J M Goldman, E Wiltshaw, D Catovsky, K Henry, G J Goldenberg. Br J Haematol 1974
422
18


The immunological profile of B-cell disorders and proposal of a scoring system for the diagnosis of CLL.
E Matutes, K Owusu-Ankomah, R Morilla, J Garcia Marco, A Houlihan, T H Que, D Catovsky. Leukemia 1994
587
18

Proposals for the classification of chronic (mature) B and T lymphoid leukaemias. French-American-British (FAB) Cooperative Group.
J M Bennett, D Catovsky, M T Daniel, G Flandrin, D A Galton, H R Gralnick, C Sultan. J Clin Pathol 1989
685
16

B-prolymphocytic leukaemia with t(11;14) revisited: a splenomegalic form of mantle cell lymphoma evolving with leukaemia.
Rosa Ruchlemer, Nilima Parry-Jones, Vasantha Brito-Babapulle, Imma Attolico, Andrew C Wotherspoon, Estella Matutes, Daniel Catovsky. Br J Haematol 2004
45
28

Mutations of the p53 gene in B-cell chronic lymphocytic leukemia: a report on 39 cases with cytogenetic analysis.
P Fenaux, C Preudhomme, J L Laï, I Quiquandon, P Jonveaux, M Vanrumbeke, C Sartiaux, P Morel, M H Loucheux-Lefebvre, F Bauters. Leukemia 1992
133
15

Genomic aberrations and survival in chronic lymphocytic leukemia.
H Döhner, S Stilgenbauer, A Benner, E Leupolt, A Kröber, L Bullinger, K Döhner, M Bentz, P Lichter. N Engl J Med 2000
15

Clinical and laboratory features of 78 cases of T-prolymphocytic leukemia.
E Matutes, V Brito-Babapulle, J Swansbury, J Ellis, R Morilla, C Dearden, A Sempere, D Catovsky. Blood 1991
336
14

p53 expression in B-cell chronic lymphocytic leukemia: a marker of disease progression and poor prognosis.
I Cordone, S Masi, F R Mauro, S Soddu, O Morsilli, T Valentini, M L Vegna, C Guglielmi, F Mancini, S Giuliacci,[...]. Blood 1998
166
12

p53 mutations are associated with resistance to chemotherapy and short survival in hematologic malignancies.
E Wattel, C Preudhomme, B Hecquet, M Vanrumbeke, B Quesnel, I Dervite, P Morel, P Fenaux. Blood 1994
503
12

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
738
12

Alterations of a zinc finger-encoding gene, BCL-6, in diffuse large-cell lymphoma.
B H Ye, F Lista, F Lo Coco, D M Knowles, K Offit, R S Chaganti, R Dalla-Favera. Science 1993
597
12

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
12

p53 gene mutations and protein overexpression are associated with aggressive variants of mantle cell lymphomas.
L Hernandez, T Fest, M Cazorla, J Teruya-Feldstein, F Bosch, M A Peinado, M A Piris, E Montserrat, A Cardesa, E S Jaffe,[...]. Blood 1996
222
11



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
27

Hearing loss in Townes-Brocks syndrome.
D R Rossmiller, T R Pasic. Otolaryngol Head Neck Surg 1994
27
33



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
19

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
11


Townes-Brocks syndrome in two mentally retarded youngsters.
T H Cameron, A M Lachiewicz, A S Aylsworth. Am J Med Genet 1991
31
29


STAT6: its role in interleukin 4-mediated biological functions.
K Takeda, T Kishimoto, S Akira. J Mol Med (Berl) 1997
96
11


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
170
11



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
11

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
322
11

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

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
173
11

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
11

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
12

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
328
11


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
11

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

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
330
11

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
11


Anticipation: an old idea in new genes.
M G McInnis. Am J Hum Genet 1996
91
11


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.