A citation-based method for searching scientific literature

M Montera, F Piaggio, C Marchese, V Gismondi, A Stella, N Resta, L Varesco, G Guanti, C Mareni. J Med Genet 2001
Times Cited: 43







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



Times Cited
  Times     Co-cited
Similarity


Listening to silence and understanding nonsense: exonic mutations that affect splicing.
Luca Cartegni, Shern L Chew, Adrian R Krainer. Nat Rev Genet 2002
32

Familial adenomatous polyposis: aberrant splicing due to missense or silent mutations in the APC gene.
Stefan Aretz, Siegfried Uhlhaas, Yuli Sun, Constanze Pagenstecher, Elisabeth Mangold, Reiner Caspari, Gabriela Möslein, Karsten Schulmann, Peter Propping, Waltraut Friedl. Hum Mutat 2004
81
32

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
30

ESEfinder: A web resource to identify exonic splicing enhancers.
Luca Cartegni, Jinhua Wang, Zhengwei Zhu, Michael Q Zhang, Adrian R Krainer. Nucleic Acids Res 2003
30



Missense and nonsense mutations in codon 659 of MLH1 cause aberrant splicing of messenger RNA in HNPCC kindreds.
M Nyström-Lahti, M Holmberg, P Fidalgo, R Salovaara, A de la Chapelle, J Jiricny, P Peltomäki. Genes Chromosomes Cancer 1999
37
18

A "silent" polymorphism in the MDR1 gene changes substrate specificity.
Chava Kimchi-Sarfaty, Jung Mi Oh, In-Wha Kim, Zuben E Sauna, Anna Maria Calcagno, Suresh V Ambudkar, Michael M Gottesman. Science 2007
16


Predictive identification of exonic splicing enhancers in human genes.
William G Fairbrother, Ru-Fang Yeh, Phillip A Sharp, Christopher B Burge. Science 2002
792
13

BRCA2 T2722R is a deleterious allele that causes exon skipping.
James D Fackenthal, Luca Cartegni, Adrian R Krainer, Olufunmilayo I Olopade. Am J Hum Genet 2002
80
13

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
194
13

Synonymous mutations frequently act as driver mutations in human cancers.
Fran Supek, Belén Miñana, Juan Valcárcel, Toni Gabaldón, Ben Lehner. Cell 2014
306
13


A BRCA1 nonsense mutation causes exon skipping.
S Mazoyer, N Puget, L Perrin-Vidoz, H T Lynch, O M Serova-Sinilnikova, G M Lenoir. Am J Hum Genet 1998
88
11

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
895
11

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
239
11

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
495
11

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
11


Nontruncating APC germ-line mutations and mismatch repair deficiency play a minor role in APC mutation-negative polyposis.
K Heinimann, A Thompson, A Locher, T Furlanetto, E Bader, A Wolf, R Meier, K Walter, P Bauerfeind, G Marra,[...]. Cancer Res 2001
43
11

New type of disease causing mutations: the example of the composite exonic regulatory elements of splicing in CFTR exon 12.
Franco Pagani, Cristiana Stuani, Maria Tzetis, Emmanuel Kanavakis, Alexandra Efthymiadou, Stavros Doudounakis, Teresa Casals, Francisco E Baralle. Hum Mol Genet 2003
150
11

Aberrant splicing induced by missense mutations in BRCA1: clues from a humanized mouse model.
Yongping Yang, Srividya Swaminathan, Betty K Martin, Shyam K Sharan. Hum Mol Genet 2003
57
11

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
11

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
11

Molecular analysis of the APC gene in 105 Dutch kindreds with familial adenomatous polyposis: 67 germline mutations identified by DGGE, PTT, and southern analysis.
R B van der Luijt, P M Khan, H F Vasen, C M Tops, I S van Leeuwen-Cornelisse, J T Wijnen, H M van der Klift, R J Plug, G Griffioen, R Fodde. Hum Mutat 1997
105
11


The ABC of APC.
N S Fearnhead, M P Britton, W F Bodmer. Hum Mol Genet 2001
617
11

Human Splicing Finder: an online bioinformatics tool to predict splicing signals.
François-Olivier Desmet, Dalil Hamroun, Marine Lalande, Gwenaëlle Collod-Béroud, Mireille Claustres, Christophe Béroud. Nucleic Acids Res 2009
11

Whole-genome sequencing identifies a recurrent functional synonymous mutation in melanoma.
Jared J Gartner, Stephen C J Parker, Todd D Prickett, Ken Dutton-Regester, Michael L Stitzel, Jimmy C Lin, Sean Davis, Vijaya L Simhadri, Sujata Jha, Nobuko Katagiri,[...]. Proc Natl Acad Sci U S A 2013
110
11

Understanding the contribution of synonymous mutations to human disease.
Zuben E Sauna, Chava Kimchi-Sarfaty. Nat Rev Genet 2011
527
11


Mutations affecting mRNA splicing are the most common molecular defects in patients with neurofibromatosis type 1.
E Ars, E Serra, J García, H Kruyer, A Gaona, C Lázaro, X Estivill. Hum Mol Genet 2000
241
9



Splicing defects in the ataxia-telangiectasia gene, ATM: underlying mutations and consequences.
S N Teraoka, M Telatar, S Becker-Catania, T Liang, S Onengüt, A Tolun, L Chessa, O Sanal, E Bernatowska, R A Gatti,[...]. Am J Hum Genet 1999
213
9

The APC variants I1307K and E1317Q are associated with colorectal tumors, but not always with a family history.
I M Frayling, N E Beck, M Ilyas, I Dove-Edwin, P Goodman, K Pack, J A Bell, C B Williams, S V Hodgson, H J Thomas,[...]. Proc Natl Acad Sci U S A 1998
148
9

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
9

Germ-line mutations of the APC gene in 53 familial adenomatous polyposis patients.
Y Miyoshi, H Ando, H Nagase, I Nishisho, A Horii, Y Miki, T Mori, J Utsunomiya, S Baba, G Petersen. Proc Natl Acad Sci U S A 1992
510
9

APC gene mutations and colorectal adenomatosis in familial adenomatous polyposis.
F Ficari, A Cama, R Valanzano, M C Curia, R Palmirotta, G Aceto, D L Esposito, S Crognale, A Lombardi, L Messerini,[...]. Br J Cancer 2000
67
9


Frequency and parental origin of de novo APC mutations in familial adenomatous polyposis.
Stefan Aretz, Siegfried Uhlhaas, Reiner Caspari, Elisabeth Mangold, Constanze Pagenstecher, Peter Propping, Waltraut Friedl. Eur J Hum Genet 2004
92
9

Comparative analysis identifies exonic splicing regulatory sequences--The complex definition of enhancers and silencers.
Amir Goren, Oren Ram, Maayan Amit, Hadas Keren, Galit Lev-Maor, Ida Vig, Tal Pupko, Gil Ast. Mol Cell 2006
231
9


An increased specificity score matrix for the prediction of SF2/ASF-specific exonic splicing enhancers.
Philip J Smith, Chaolin Zhang, Jinhua Wang, Shern L Chew, Michael Q Zhang, Adrian R Krainer. Hum Mol Genet 2006
358
9

Systematic identification and analysis of exonic splicing silencers.
Zefeng Wang, Michael E Rolish, Gene Yeo, Vivian Tung, Matthew Mawson, Christopher B Burge. Cell 2004
479
9

Clinical characterization and the mutation spectrum in Swedish adenomatous polyposis families.
Gunilla Kanter-Smoler, Kaisa Fritzell, Anna Rohlin, Yvonne Engwall, Birgitta Hallberg, Annika Bergman, Johan Meuller, Henrik Grönberg, Per Karlsson, Jan Björk,[...]. BMC Med 2008
30
13

Unclassified variants identified in BRCA1 exon 11: Consequences on splicing.
Olga Anczuków, Monique Buisson, Marie-Josèphe Salles, Sarah Triboulet, Michel Longy, Rosette Lidereau, Olga M Sinilnikova, Sylvie Mazoyer. Genes Chromosomes Cancer 2008
30
13

Familial adenomatous polyposis.
Polymnia Galiatsatos, William D Foulkes. Am J Gastroenterol 2006
325
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.