A citation-based method for searching scientific literature

L Spirio, S Olschwang, J Groden, M Robertson, W Samowitz, G Joslyn, L Gelbert, A Thliveris, M Carlson, B Otterud. Cell 1993
Times Cited: 496







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



Times Cited
  Times     Co-cited
Similarity


Inherited variants of MYH associated with somatic G:C-->T:A mutations in colorectal tumors.
Nada Al-Tassan, Nikolas H Chmiel, Julie Maynard, Nick Fleming, Alison L Livingston, Geraint T Williams, Angela K Hodges, D Rhodri Davies, Sheila S David, Julian R Sampson,[...]. Nat Genet 2002
898
42

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
36

Multiple colorectal adenomas, classic adenomatous polyposis, and germ-line mutations in MYH.
Oliver M Sieber, Lara Lipton, Michael Crabtree, Karl Heinimann, Paulo Fidalgo, Robin K S Phillips, Marie-Luise Bisgaard, Torben F Orntoft, Lauri A Aaltonen, Shirley V Hodgson,[...]. N Engl J Med 2003
560
34

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
32

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
23

Attenuated familial adenomatous polyposis (AFAP). A review of the literature.
Anne Lyster Knudsen, Marie Luise Bisgaard, Steffen Bülow. Fam Cancer 2003
173
23

Autosomal recessive colorectal adenomatous polyposis due to inherited mutations of MYH.
Julian R Sampson, Sunil Dolwani, Sian Jones, Diana Eccles, Anthony Ellis, D Gareth Evans, Ian Frayling, Sheila Jordan, Eamonn R Maher, Tony Mak,[...]. Lancet 2003
291
22

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
289
22

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
195
20



Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability.
Asad Umar, C Richard Boland, Jonathan P Terdiman, Sapna Syngal, Albert de la Chapelle, Josef Rüschoff, Richard Fishel, Noralane M Lindor, Lawrence J Burgart, Richard Hamelin,[...]. J Natl Cancer Inst 2004
17

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
17

Guidelines for the clinical management of familial adenomatous polyposis (FAP).
H F A Vasen, G Möslein, A Alonso, S Aretz, I Bernstein, L Bertario, I Blanco, S Bülow, J Burn, G Capella,[...]. Gut 2008
385
17

Familial adenomatous polyposis: mutation at codon 1309 and early onset of colon cancer.
R Caspari, W Friedl, M Mandl, G Möslein, M Kadmon, M Knapp, K H Jacobasch, K W Ecker, D Kreissler-Haag, G Timmermanns. Lancet 1994
166
16

Hereditary colorectal cancer.
Henry T Lynch, Albert de la Chapelle. N Engl J Med 2003
16

Multiple approach to the exploration of genotype-phenotype correlations in familial adenomatous polyposis.
L Bertario, A Russo, P Sala, L Varesco, M Giarola, P Mondini, M Pierotti, P Spinelli, P Radice. J Clin Oncol 2003
131
16

Association between biallelic and monoallelic germline MYH gene mutations and colorectal cancer risk.
Marina E Croitoru, Sean P Cleary, Nando Di Nicola, Michael Manno, Teresa Selander, Melyssa Aronson, Mark Redston, Michelle Cotterchio, Julia Knight, Robert Gryfe,[...]. J Natl Cancer Inst 2004
176
16

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
15

Localization of the gene for familial adenomatous polyposis on chromosome 5.
W F Bodmer, C J Bailey, J Bodmer, H J Bussey, A Ellis, P Gorman, F C Lucibello, V A Murday, S H Rider, P Scambler. Nature 1987
15


The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC).
H F Vasen, J P Mecklin, P M Khan, H T Lynch. Dis Colon Rectum 1991
14

Attenuated familial adenomatous polyposis (AFAP). A phenotypically and genotypically distinctive variant of FAP.
H T Lynch, T Smyrk, T McGinn, S Lanspa, J Cavalieri, J Lynch, S Slominski-Castor, M C Cayouette, I Priluck, M C Luce. Cancer 1995
179
14

Familial adenomatous polyposis (FAP): frequency, penetrance, and mutation rate.
M L Bisgaard, K Fenger, S Bülow, E Niebuhr, J Mohr. Hum Mutat 1994
282
14

Genetic testing and phenotype in a large kindred with attenuated familial adenomatous polyposis.
Randall W Burt, Mark F Leppert, Martha L Slattery, Wade S Samowitz, Lisa N Spirio, Richard A Kerber, Scott K Kuwada, Deborah W Neklason, James A Disario, Elaine Lyon,[...]. Gastroenterology 2004
101
14

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
17

The ABC of APC.
N S Fearnhead, M P Britton, W F Bodmer. Hum Mol Genet 2001
620
13

Germline susceptibility to colorectal cancer due to base-excision repair gene defects.
Susan M Farrington, Albert Tenesa, Rebecca Barnetson, Alice Wiltshire, James Prendergast, Mary Porteous, Harry Campbell, Malcolm G Dunlop. Am J Hum Genet 2005
186
12

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
12

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
12

APC mutation in the alternatively spliced region of exon 9 associated with late onset familial adenomatous polyposis.
R B van der Luijt, H F Vasen, C M Tops, C Breukel, R Fodde, P Meera Khan. Hum Genet 1995
96
12

Genetic analysis of an inherited predisposition to colon cancer in a family with a variable number of adenomatous polyps.
M Leppert, R Burt, J P Hughes, W Samowitz, Y Nakamura, S Woodward, E Gardner, J M Lalouel, R White. N Engl J Med 1990
250
12

Mutations in the SMAD4/DPC4 gene in juvenile polyposis.
J R Howe, S Roth, J C Ringold, R W Summers, H J Järvinen, P Sistonen, I P Tomlinson, R S Houlston, S Bevan, F A Mitros,[...]. Science 1998
656
12

Large deletions of the APC gene in 15% of mutation-negative patients with classical polyposis (FAP): a Belgian study.
Geneviève Michils, Sabine Tejpar, Reinhilde Thoelen, Eric van Cutsem, Joris Robert Vermeesch, Jean-Pierre Fryns, Eric Legius, Gert Matthijs. Hum Mutat 2005
83
14


Germline APC variants in patients with multiple colorectal adenomas, with evidence for the particular importance of E1317Q.
H Lamlum, N Al Tassan, E Jaeger, I Frayling, O Sieber, F B Reza, M Eckert, A Rowan, E Barclay, W Atkin,[...]. Hum Mol Genet 2000
99
11


Prevalence of the Y165C, G382D and 1395delGGA germline mutations of the MYH gene in Italian patients with adenomatous polyposis coli and colorectal adenomas.
Viviana Gismondi, Maurizio Meta, Luigina Bonelli, Paolo Radice, Paola Sala, Lucio Bertario, Alessandra Viel, Mara Fornasarig, Arrigo Arrigoni, Mattia Gentile,[...]. Int J Cancer 2004
124
11

Multiplicity in polyp count and extracolonic manifestations in 40 Dutch patients with MYH associated polyposis coli (MAP).
M Nielsen, P F Franken, T H C M Reinards, M M Weiss, A Wagner, H van der Klift, S Kloosterman, J J Houwing-Duistermaat, C M Aalfs, M G E M Ausems,[...]. J Med Genet 2005
134
11


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
10

Attenuated familial adenomatous polyposis: an evolving and poorly understood entity.
Gerald S Hernegger, Harvey G Moore, Jose G Guillem. Dis Colon Rectum 2002
99
10

MYH mutations in patients with attenuated and classic polyposis and with young-onset colorectal cancer without polyps.
Liang Wang, Linnea M Baudhuin, Lisa A Boardman, Kelle J Steenblock, Gloria M Petersen, Kevin C Halling, Amy J French, Ruth A Johnson, Lawrence J Burgart, Kari Rabe,[...]. Gastroenterology 2004
148
10

Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancer.
H J Järvinen, M Aarnio, H Mustonen, K Aktan-Collan, L A Aaltonen, P Peltomäki, A De La Chapelle, J P Mecklin. Gastroenterology 2000
920
10

Biallelic germline mutations in MYH predispose to multiple colorectal adenoma and somatic G:C-->T:A mutations.
Siân Jones, Paul Emmerson, Julie Maynard, Jacqueline M Best, Sheila Jordan, Geraint T Williams, Julian R Sampson, Jeremy P Cheadle. Hum Mol Genet 2002
280
10

Large submicroscopic genomic APC deletions are a common cause of typical familial adenomatous polyposis.
S Aretz, D Stienen, S Uhlhaas, C Pagenstecher, E Mangold, R Caspari, P Propping, W Friedl. J Med Genet 2005
63
15

Whole-gene APC deletions cause classical familial adenomatous polyposis, but not attenuated polyposis or "multiple" colorectal adenomas.
O M Sieber, H Lamlum, M D Crabtree, A J Rowan, E Barclay, L Lipton, S Hodgson, H J W Thomas, K Neale, R K S Phillips,[...]. Proc Natl Acad Sci U S A 2002
97
10

Upper gastrointestinal cancer in patients with familial adenomatous polyposis.
A D Spigelman, C B Williams, I C Talbot, P Domizio, R K Phillips. Lancet 1989
490
10

Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer).
Heather Hampel, Wendy L Frankel, Edward Martin, Mark Arnold, Karamjit Khanduja, Philip Kuebler, Hidewaki Nakagawa, Kaisa Sotamaa, Thomas W Prior, Judith Westman,[...]. N Engl J Med 2005
910
9

A serine/threonine kinase gene defective in Peutz-Jeghers syndrome.
A Hemminki, D Markie, I Tomlinson, E Avizienyte, S Roth, A Loukola, G Bignell, W Warren, M Aminoff, P Höglund,[...]. Nature 1998
9


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.