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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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.