A citation-based method for searching scientific literature

Kiyoshi Yamaguchi, Mitsuhiro Komura, Rui Yamaguchi, Seiya Imoto, Eigo Shimizu, Shinichi Kasuya, Tetsuo Shibuya, Seira Hatakeyama, Norihiko Takahashi, Tsuneo Ikenoue, Keisuke Hata, Giichiro Tsurita, Masaru Shinozaki, Yutaka Suzuki, Sumio Sugano, Satoru Miyano, Yoichi Furukawa. J Hum Genet 2015
Times Cited: 27







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



Times Cited
  Times     Co-cited
Similarity


Low-level APC mutational mosaicism is the underlying cause in a substantial fraction of unexplained colorectal adenomatous polyposis cases.
Isabel Spier, Dmitriy Drichel, Martin Kerick, Jutta Kirfel, Sukanya Horpaopan, Andreas Laner, Stefanie Holzapfel, Sophia Peters, Ronja Adam, Bixiao Zhao,[...]. J Med Genet 2016
28
33

Somatic APC mosaicism: an underestimated cause of polyposis coli.
F J Hes, M Nielsen, E C Bik, D Konvalinka, J T Wijnen, E Bakker, H F A Vasen, M H Breuning, C M J Tops. Gut 2008
95
25

Germline mutations affecting the proofreading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomas.
Claire Palles, Jean-Baptiste Cazier, Kimberley M Howarth, Enric Domingo, Angela M Jones, Peter Broderick, Zoe Kemp, Sarah L Spain, Estrella Guarino, Israel Salguero,[...]. Nat Genet 2013
565
25

Parallel sequencing used in detection of mosaic mutations: comparison with four diagnostic DNA screening techniques.
Anna Rohlin, Josephine Wernersson, Yvonne Engwall, Leif Wiklund, Jan Björk, Margareta Nordling. Hum Mutat 2009
107
25

High-resolution melting (HRM) re-analysis of a polyposis patients cohort reveals previously undetected heterozygous and mosaic APC gene mutations.
Astrid A Out, Ivonne J H M van Minderhout, Nienke van der Stoep, Lysette S R van Bommel, Irma Kluijt, Cora Aalfs, Marsha Voorendt, Rolf H A M Vossen, Maartje Nielsen, Hans F A Vasen,[...]. Fam Cancer 2015
11
54

Germline mutations in APC and MUTYH are responsible for the majority of families with attenuated familial adenomatous polyposis.
M Nielsen, F J Hes, F M Nagengast, M M Weiss, E M Mathus-Vliegen, H Morreau, M H Breuning, J T Wijnen, C M J Tops, H F A Vasen. Clin Genet 2007
97
22


The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data.
Aaron McKenna, Matthew Hanna, Eric Banks, Andrey Sivachenko, Kristian Cibulskis, Andrew Kernytsky, Kiran Garimella, David Altshuler, Stacey Gabriel, Mark Daly,[...]. Genome Res 2010
18

Somatic mosaicism: a cause for unexplained cases of FAP?
Thérèse M Tuohy, Randall W Burt. Gut 2008
20
25

Somatic APC mosaicism: a frequent cause of familial adenomatous polyposis (FAP).
Stefan Aretz, Dietlinde Stienen, Nicolaus Friedrichs, Susanne Stemmler, Siegfried Uhlhaas, Nils Rahner, Peter Propping, Waltraut Friedl. Hum Mutat 2007
88
18


ACG clinical guideline: Genetic testing and management of hereditary gastrointestinal cancer syndromes.
Sapna Syngal, Randall E Brand, James M Church, Francis M Giardiello, Heather L Hampel, Randall W Burt. Am J Gastroenterol 2015
624
18

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
893
18

Deep intronic APC mutations explain a substantial proportion of patients with familial or early-onset adenomatous polyposis.
Isabel Spier, Sukanya Horpaopan, Stefanie Vogt, Siegfried Uhlhaas, Monika Morak, Dietlinde Stienen, Markus Draaken, Michael Ludwig, Elke Holinski-Feder, Markus M Nöthen,[...]. Hum Mutat 2012
44
14

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
14

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
14

Advances in understanding cancer genomes through second-generation sequencing.
Matthew Meyerson, Stacey Gabriel, Gad Getz. Nat Rev Genet 2010
726
14

Exome sequencing can detect pathogenic mosaic mutations present at low allele frequencies.
Alistair T Pagnamenta, Stefano Lise, Victoria Harrison, Helen Stewart, Sandeep Jayawant, Gerardine Quaghebeur, Alexander T Deng, Valerie Elizabeth Murphy, Elham Sadighi Akha, Andy Rimmer,[...]. J Hum Genet 2012
46
14

A genomic view of mosaicism and human disease.
Leslie G Biesecker, Nancy B Spinner. Nat Rev Genet 2013
321
14

Analysis of protein-coding genetic variation in 60,706 humans.
Monkol Lek, Konrad J Karczewski, Eric V Minikel, Kaitlin E Samocha, Eric Banks, Timothy Fennell, Anne H O'Donnell-Luria, James S Ware, Andrew J Hill, Beryl B Cummings,[...]. Nature 2016
14

Familial adenomatous polyposis (FAP): frequency, penetrance, and mutation rate.
M L Bisgaard, K Fenger, S Bülow, E Niebuhr, J Mohr. Hum Mutat 1994
280
14

Attenuated familial adenomatous polyposis (AFAP). A review of the literature.
Anne Lyster Knudsen, Marie Luise Bisgaard, Steffen Bülow. Fam Cancer 2003
172
14

Distinct Patterns of Somatic Mosaicism in the APC Gene in Neoplasms From Patients With Unexplained Adenomatous Polyposis.
Anne M L Jansen, Stijn Crobach, Willemina R R Geurts-Giele, Brendy E W M van den Akker, Marina Ventayol Garcia, Dina Ruano, Maartje Nielsen, Carli M J Tops, Juul T Wijnen, Frederik J Hes,[...]. Gastroenterology 2017
18
22

Gonadal mosaicism and familial adenomatous polyposis.
Angela L Schwab, Thérèse M F Tuohy, Michelle Condie, Deborah W Neklason, Randall W Burt. Fam Cancer 2008
18
16


Parental somatic mosaicism is underrecognized and influences recurrence risk of genomic disorders.
Ian M Campbell, Bo Yuan, Caroline Robberecht, Rolph Pfundt, Przemyslaw Szafranski, Meriel E McEntagart, Sandesh C S Nagamani, Ayelet Erez, Magdalena Bartnik, Barbara Wiśniowiecka-Kowalnik,[...]. Am J Hum Genet 2014
140
11

Prevalence and phenotypes of APC and MUTYH mutations in patients with multiple colorectal adenomas.
Shilpa Grover, Fay Kastrinos, Ewout W Steyerberg, E Francis Cook, Akriti Dewanwala, Lynn Anne Burbidge, Richard J Wenstrup, Sapna Syngal. JAMA 2012
100
11

PTEN mosaicism with features of Cowden syndrome.
A Gammon, K Jasperson, R Pilarski, Tw Prior, S Kuwada. Clin Genet 2013
14
21

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
11

Detection of APC germ line mosaicism in patients with de novo familial adenomatous polyposis: a plea for the protein truncation test.
Judith Necker, Michal Kovac, Michèle Attenhofer, Bruno Reichlin, Karl Heinimann. J Med Genet 2011
16
18

ACMG clinical laboratory standards for next-generation sequencing.
Heidi L Rehm, Sherri J Bale, Pinar Bayrak-Toydemir, Jonathan S Berg, Kerry K Brown, Joshua L Deignan, Michael J Friez, Birgit H Funke, Madhuri R Hegde, Elaine Lyon. Genet Med 2013
526
11

Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasma.
Rossa W K Chiu, K C Allen Chan, Yuan Gao, Virginia Y M Lau, Wenli Zheng, Tak Y Leung, Chris H F Foo, Bin Xie, Nancy B Y Tsui, Fiona M F Lun,[...]. Proc Natl Acad Sci U S A 2008
556
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
256
11

Clinical implications of the colorectal cancer risk associated with MUTYH mutation.
Steven J Lubbe, Maria Chiara Di Bernardo, Ian P Chandler, Richard S Houlston. J Clin Oncol 2009
121
11

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
11

The ABC of APC.
N S Fearnhead, M P Britton, W F Bodmer. Hum Mol Genet 2001
615
11

Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples.
Kristian Cibulskis, Michael S Lawrence, Scott L Carter, Andrey Sivachenko, David Jaffe, Carrie Sougnez, Stacey Gabriel, Matthew Meyerson, Eric S Lander, Gad Getz. Nat Biotechnol 2013
11

Sequencing technologies - the next generation.
Michael L Metzker. Nat Rev Genet 2010
11

A germline homozygous mutation in the base-excision repair gene NTHL1 causes adenomatous polyposis and colorectal cancer.
Robbert D A Weren, Marjolijn J L Ligtenberg, C Marleen Kets, Richarda M de Voer, Eugène T P Verwiel, Liesbeth Spruijt, Wendy A G van Zelst-Stams, Marjolijn C Jongmans, Christian Gilissen, Jayne Y Hehir-Kwa,[...]. Nat Genet 2015
188
11

Fundic gland polyp dysplasia is common in familial adenomatous polyposis.
Laura K Bianchi, Carol A Burke, Ana E Bennett, Rocio Lopez, Hennie Hasson, James M Church. Clin Gastroenterol Hepatol 2008
93
11

Amplicon Resequencing Identified Parental Mosaicism for Approximately 10% of "de novo" SCN1A Mutations in Children with Dravet Syndrome.
Xiaojing Xu, Xiaoxu Yang, Qixi Wu, Aijie Liu, Xiaoling Yang, Adam Yongxin Ye, August Yue Huang, Jiarui Li, Meng Wang, Zhe Yu,[...]. Hum Mutat 2015
65
11

Duodenal adenomatosis in familial adenomatous polyposis.
S Bülow, J Björk, I J Christensen, O Fausa, H Järvinen, F Moesgaard, H F A Vasen. Gut 2004
216
11

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
11

Somatic APC mosaicism and oligogenic inheritance in genetically unsolved colorectal adenomatous polyposis patients.
Michele Ciavarella, Sara Miccoli, Anna Prossomariti, Tommaso Pippucci, Elena Bonora, Francesco Buscherini, Flavia Palombo, Roberta Zuntini, Tiziana Balbi, Claudio Ceccarelli,[...]. Eur J Hum Genet 2018
15
20

ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007.
C Sue Richards, Sherri Bale, Daniel B Bellissimo, Soma Das, Wayne W Grody, Madhuri R Hegde, Elaine Lyon, Brian E Ward. Genet Med 2008
517
7

A framework for variation discovery and genotyping using next-generation DNA sequencing data.
Mark A DePristo, Eric Banks, Ryan Poplin, Kiran V Garimella, Jared R Maguire, Christopher Hartl, Anthony A Philippakis, Guillermo del Angel, Manuel A Rivas, Matt Hanna,[...]. Nat Genet 2011
7

Familial adenomatous polyposis.
Polymnia Galiatsatos, William D Foulkes. Am J Gastroenterol 2006
324
7

Exploring the variation within.
Evan Z Macosko, Steven A McCarroll. Nat Genet 2012
13
15

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data.
Kai Wang, Mingyao Li, Hakon Hakonarson. Nucleic Acids Res 2010
7

Role of MUTYH in human cancer.
Filomena Mazzei, Alessandra Viel, Margherita Bignami. Mutat Res 2013
58
7


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.