A citation-based method for searching scientific literature

D M Eccles, R van der Luijt, C Breukel, H Bullman, D Bunyan, A Fisher, J Barber, C du Boulay, J Primrose, J Burn, R Fodde. Am J Hum Genet 1996
Times Cited: 152







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



Times Cited
  Times     Co-cited
Similarity


Familial infiltrative fibromatosis (desmoid tumours) (MIM135290) caused by a recurrent 3' APC gene mutation.
R J Scott, N J Froggatt, R C Trembath, D G Evans, S V Hodgson, E R Maher. Hum Mol Genet 1996
111
56

Familial adenomatous polyposis: desmoid tumours and lack of ophthalmic lesions (CHRPE) associated with APC mutations beyond codon 1444.
R Caspari, S Olschwang, W Friedl, M Mandl, C Boisson, T Böker, A Augustin, M Kadmon, G Möslein, G Thomas. Hum Mol Genet 1995
291
34


Mutations of adenomatous polyposis coli (APC) gene are uncommon in sporadic desmoid tumours.
M Giarola, D Wells, P Mondini, S Pilotti, P Sala, A Azzarelli, L Bertario, M A Pierotti, J D Delhanty, P Radice. Br J Cancer 1998
71
42

Alleles of the APC gene: an attenuated form of familial polyposis.
L Spirio, S Olschwang, J Groden, M Robertson, W Samowitz, G Joslyn, L Gelbert, A Thliveris, M Carlson, B Otterud. Cell 1993
496
30

Desmoid tumours in familial adenomatous polyposis.
A K Gurbuz, F M Giardiello, G M Petersen, A J Krush, G J Offerhaus, S V Booker, M C Kerr, S R Hamilton. Gut 1994
237
25

Predominance of beta-catenin mutations and beta-catenin dysregulation in sporadic aggressive fibromatosis (desmoid tumor).
S Tejpar, F Nollet, C Li, J S Wunder, G Michils, P dal Cin, E Van Cutsem, B Bapat, F van Roy, J J Cassiman,[...]. Oncogene 1999
232
25

Identification and characterization of the familial adenomatous polyposis coli gene.
J Groden, A Thliveris, W Samowitz, M Carlson, L Gelbert, H Albertsen, G Joslyn, J Stevens, L Spirio, M Robertson. Cell 1991
25

Identification of FAP locus genes from chromosome 5q21.
K W Kinzler, M C Nilbert, L K Su, B Vogelstein, T M Bryan, D B Levy, K J Smith, A C Preisinger, P Hedge, D McKechnie. Science 1991
25

Genotype and phenotype factors as determinants of desmoid tumors in patients with familial adenomatous polyposis.
L Bertario, A Russo, P Sala, M Eboli, M Giarola, F D'amico, V Gismondi, L Varesco, M A Pierotti, P Radice. Int J Cancer 2001
135
24


Hereditary desmoid disease in a family with a germline Alu I repeat mutation of the APC gene.
K C Halling, C R Lazzaro, R Honchel, J A Bufill, S M Powell, C A Arndt, N M Lindor. Hum Hered 1999
55
38


Desmoid tumours complicating familial adenomatous polyposis.
S K Clark, K F Neale, J C Landgrebe, R K Phillips. Br J Surg 1999
166
19

Genotype-phenotype correlations in attenuated adenomatous polyposis coli.
C Soravia, T Berk, L Madlensky, A Mitri, H Cheng, S Gallinger, Z Cohen, B Bapat. Am J Hum Genet 1998
240
19

Severe Gardner syndrome in families with mutations restricted to a specific region of the APC gene.
D R Davies, J G Armstrong, N Thakker, K Horner, S P Guy, T Clancy, P Sloan, V Blair, C Dodd, T W Warnes. Am J Hum Genet 1995
116
19

Can APC mutation analysis contribute to therapeutic decisions in familial adenomatous polyposis? Experience from 680 FAP families.
W Friedl, R Caspari, M Sengteller, S Uhlhaas, C Lamberti, M Jungck, M Kadmon, M Wolf, J Fahnenstich, J Gebert,[...]. Gut 2001
197
18

Mortality in patients with familial adenomatous polyposis.
M L Arvanitis, D G Jagelman, V W Fazio, I C Lavery, E McGannon. Dis Colon Rectum 1990
309
17



Surgical management of intra-abdominal desmoid tumours.
A J Smith, J J Lewis, N B Merchant, D H Leung, J M Woodruff, M F Brennan. Br J Surg 2000
123
16

Germline mutations in the 3' part of APC exon 15 do not result in truncated proteins and are associated with attenuated adenomatous polyposis coli.
R B van der Luijt, P Meera Khan, H F Vasen, C Breukel, C M Tops, R J Scott, R Fodde. Hum Genet 1996
125
16

Correlation between the location of germ-line mutations in the APC gene and the number of colorectal polyps in familial adenomatous polyposis patients.
H Nagase, Y Miyoshi, A Horii, T Aoki, M Ogawa, J Utsunomiya, S Baba, T Sasazuki, Y Nakamura. Cancer Res 1992
290
16

Molecular genetic tests as a guide to surgical management of familial adenomatous polyposis.
H F Vasen, R B van der Luijt, J F Slors, E Buskens, P de Ruiter, C G Baeten, W R Schouten, H J Oostvogel, J H Kuijpers, C M Tops,[...]. Lancet 1996
152
15


Evidence for genetic predisposition to desmoid tumours in familial adenomatous polyposis independent of the germline APC mutation.
N J H Sturt, M C Gallagher, P Bassett, C R Philp, K F Neale, I P M Tomlinson, A R J Silver, R K S Phillips. Gut 2004
91
16

Mesenteric fibromatosis complicating familial adenomatous polyposis: predisposing factors and results of treatment.
A M Lotfi, R R Dozois, H Gordon, L S Hruska, L H Weiland, P W Carryer, R D Hurt. Int J Colorectal Dis 1989
97
14

Desmoids in familial adenomatous polyposis.
S K Clark, R K Phillips. Br J Surg 1996
217
13

Desmoid tumors in familial polyposis coli.
I T Jones, D G Jagelman, V W Fazio, I C Lavery, F L Weakley, E McGannon. Ann Surg 1986
176
13

Variable phenotype of familial adenomatous polyposis in pedigrees with 3' mutation in the APC gene.
J D Brensinger, S J Laken, M C Luce, S M Powell, G H Vance, D J Ahnen, G M Petersen, S R Hamilton, F M Giardiello. Gut 1998
80
16

The molecular basis of Turcot's syndrome.
S R Hamilton, B Liu, R E Parsons, N Papadopoulos, J Jen, S M Powell, A J Krush, T Berk, Z Cohen, B Tetu. N Engl J Med 1995
737
13

The ABC of APC.
N S Fearnhead, M P Britton, W F Bodmer. Hum Mol Genet 2001
624
13

The type of somatic mutation at APC in familial adenomatous polyposis is determined by the site of the germline mutation: a new facet to Knudson's 'two-hit' hypothesis.
H Lamlum, M Ilyas, A Rowan, S Clark, V Johnson, J Bell, I Frayling, J Efstathiou, K Pack, S Payne,[...]. Nat Med 1999
257
12

Activation of beta-catenin-Tcf signaling in colon cancer by mutations in beta-catenin or APC.
P J Morin, A B Sparks, V Korinek, N Barker, H Clevers, B Vogelstein, K W Kinzler. Science 1997
12

Desmoid disease in patients with familial adenomatous polyposis.
C Soravia, T Berk, R S McLeod, Z Cohen. Dis Colon Rectum 2000
115
12


Mutations of chromosome 5q21 genes in FAP and colorectal cancer patients.
I Nishisho, Y Nakamura, Y Miyoshi, Y Miki, H Ando, A Horii, K Koyama, J Utsunomiya, S Baba, P Hedge. Science 1991
12



ICF syndrome: a new case and review of the literature.
D F Smeets, U Moog, C M Weemaes, G Vaes-Peeters, G F Merkx, J P Niehof, G Hamers. Hum Genet 1994
88
13



Non-participation in predictive testing for Huntington's disease: individual decision-making, personality and avoidant behaviour in the family.
M Decruyenaere, G Evers-Kiebooms, A Boogaerts, T Cloostermans, J J Cassiman, K Demyttenaere, R Dom, J P Fryns, H Van den Berghe. Eur J Hum Genet 1997
52
23


Disruption of a new forkhead/winged-helix protein, scurfin, results in the fatal lymphoproliferative disorder of the scurfy mouse.
M E Brunkow, E W Jeffery, K A Hjerrild, B Paeper, L B Clark, S A Yasayko, J E Wilkinson, D Galas, S F Ziegler, F Ramsdell. Nat Genet 2001
12



A Japanese family of X-linked auto-immune enteropathy with haemolytic anaemia and polyendocrinopathy.
N Satake, M Nakanishi, M Okano, K Tomizawa, A Ishizaka, K Kojima, M Onodera, T Ariga, A Satake, Y Sakiyama. Eur J Pediatr 1993
65
18

Predictive testing for Huntington's disease with use of a linked DNA marker.
G J Meissen, R H Myers, C A Mastromauro, W J Koroshetz, K W Klinger, L A Farrer, P A Watkins, J F Gusella, E D Bird, J B Martin. N Engl J Med 1988
154
12

Unstable DNA sequence in myotonic dystrophy.
H G Harley, S A Rundle, W Reardon, J Myring, S Crow, J D Brook, P S Harper, D J Shaw. Lancet 1992
181
12


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.