A citation-based method for searching scientific literature

Laura Lammi, Sirpa Arte, Mirja Somer, Heikki Jarvinen, Paivi Lahermo, Irma Thesleff, Sinikka Pirinen, Pekka Nieminen. Am J Hum Genet 2004
Times Cited: 431







List of co-cited articles
1195 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


AXIN2-associated autosomal dominant ectodermal dysplasia and neoplastic syndrome.
Monica L Marvin, Serina M Mazzoni, Casey M Herron, Sean Edwards, Stephen B Gruber, Elizabeth M Petty. Am J Med Genet A 2011
58
39

A human MSX1 homeodomain missense mutation causes selective tooth agenesis.
H Vastardis, N Karimbux, S W Guthua, J G Seidman, C E Seidman. Nat Genet 1996
514
21

Loss-of-Function Mutations in the WNT Co-receptor LRP6 Cause Autosomal-Dominant Oligodontia.
Maarten P G Massink, Marijn A Créton, Francesca Spanevello, Willem M M Fennis, Marco S Cune, Sanne M C Savelberg, Isaäc J Nijman, Madelon M Maurice, Marie-José H van den Boogaard, Gijs van Haaften. Am J Hum Genet 2015
73
26

Mutations in AXIN2 cause colorectal cancer with defective mismatch repair by activating beta-catenin/TCF signalling.
W Liu, X Dong, M Mai, R S Seelan, K Taniguchi, K K Krishnadath, K C Halling, J M Cunningham, L A Boardman, C Qian,[...]. Nat Genet 2000
404
17

A novel AXIN2 germline variant associated with attenuated FAP without signs of oligondontia or ectodermal dysplasia.
B Rivera, J Perea, E Sánchez, M Villapún, E Sánchez-Tomé, F Mercadillo, M Robledo, J Benítez, M Urioste. Eur J Hum Genet 2014
33
51

Mutations in WNT10A are present in more than half of isolated hypodontia cases.
Marie-José van den Boogaard, Marijn Créton, Yvon Bronkhorst, Annemieke van der Hout, Eric Hennekam, Dick Lindhout, Marco Cune, Hans Kristian Ploos van Amstel. J Med Genet 2012
154
16

Mutation of PAX9 is associated with oligodontia.
D W Stockton, P Das, M Goldenberg, R N D'Souza, P I Patel. Nat Genet 2000
355
16

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
642
15

Mutations in WNT10B Are Identified in Individuals with Oligodontia.
Ping Yu, Wenli Yang, Dong Han, Xi Wang, Sen Guo, Jinchen Li, Fang Li, Xiaoxia Zhang, Sing-Wai Wong, Baojing Bai,[...]. Am J Hum Genet 2016
57
24

Wnt/beta-catenin signaling: components, mechanisms, and diseases.
Bryan T MacDonald, Keiko Tamai, Xi He. Dev Cell 2009
14


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
229
14

A meta-analysis of the prevalence of dental agenesis of permanent teeth.
Bart J Polder, Martin A Van't Hof, Frans P G M Van der Linden, Anne M Kuijpers-Jagtman. Community Dent Oral Epidemiol 2004
489
13

Isolated oligodontia associated with mutations in EDARADD, AXIN2, MSX1, and PAX9 genes.
Birgitta Bergendal, Joakim Klar, Christina Stecksén-Blicks, Johanna Norderyd, Niklas Dahl. Am J Med Genet A 2011
97
13

AXIN1 mutations in hepatocellular carcinomas, and growth suppression in cancer cells by virus-mediated transfer of AXIN1.
S Satoh, Y Daigo, Y Furukawa, T Kato, N Miwa, T Nishiwaki, T Kawasoe, H Ishiguro, M Fujita, T Tokino,[...]. Nat Genet 2000
818
13

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
13

Exome Sequencing Identifies Biallelic MSH3 Germline Mutations as a Recessive Subtype of Colorectal Adenomatous Polyposis.
Ronja Adam, Isabel Spier, Bixiao Zhao, Michael Kloth, Jonathan Marquez, Inga Hinrichsen, Jutta Kirfel, Aylar Tafazzoli, Sukanya Horpaopan, Siegfried Uhlhaas,[...]. Am J Hum Genet 2016
129
13

Genetic analysis: Wnt and other pathways in nonsyndromic tooth agenesis.
Miao Yu, Sing-Wai Wong, Dong Han, Tao Cai. Oral Dis 2019
45
26



Hereditary mixed polyposis syndrome is caused by a 40-kb upstream duplication that leads to increased and ectopic expression of the BMP antagonist GREM1.
Emma Jaeger, Simon Leedham, Annabelle Lewis, Stefania Segditsas, Martin Becker, Pedro Rodenas Cuadrado, Hayley Davis, Kulvinder Kaur, Karl Heinimann, Kimberley Howarth,[...]. Nat Genet 2012
151
11

Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-tumor Phenotype.
Judith E Grolleman, Richarda M de Voer, Fadwa A Elsayed, Maartje Nielsen, Robbert D A Weren, Claire Palles, Marjolijn J L Ligtenberg, Janet R Vos, Sanne W Ten Broeke, Noel F C C de Miranda,[...]. Cancer Cell 2019
80
13

Mutations in AXIN2 gene as a risk factor for tooth agenesis and cancer: A review.
Alena Hlouskova, Peter Bielik, Ondrej Bonczek, Vladimir J Balcar, Omar Šerý. Neuro Endocrinol Lett 2017
13
84

The Wnt signaling pathway in development and disease.
Catriona Y Logan, Roel Nusse. Annu Rev Cell Dev Biol 2004
10

Genetic basis of tooth agenesis.
Pekka Nieminen. J Exp Zool B Mol Dev Evol 2009
149
10

Wnt/beta-catenin signaling directs multiple stages of tooth morphogenesis.
Fei Liu, Emily Y Chu, Brenda Watt, Yuhang Zhang, Natalie M Gallant, Thomas Andl, Steven H Yang, Min-Min Lu, Stefano Piccolo, Ruth Schmidt-Ullrich,[...]. Dev Biol 2008
269
10

Wnt/beta-catenin/Tcf signaling induces the transcription of Axin2, a negative regulator of the signaling pathway.
Eek-hoon Jho, Tong Zhang, Claire Domon, Choun-Ki Joo, Jean-Noel Freund, Frank Costantini. Mol Cell Biol 2002
10

Phenotypic confirmation of oligodontia, colorectal polyposis and cancer in a family carrying an exon 7 nonsense variant in the AXIN2 gene.
Catherine Beard, Rebecca Purvis, Ingrid M Winship, Finlay A Macrae, Daniel D Buchanan. Fam Cancer 2019
13
76

WNT10A variants are associated with non-syndromic tooth agenesis in the general population.
Shujuan Song, Ruiying Zhao, Huiying He, Jin Zhang, Hailan Feng, Liyun Lin. Hum Genet 2014
51
17


Novel EDA mutation resulting in X-linked non-syndromic hypodontia and the pattern of EDA-associated isolated tooth agenesis.
Dong Han, Yu Gong, Hua Wu, Xiaoxia Zhang, Ming Yan, Xiaozhu Wang, Hong Qu, Hailan Feng, Shujuan Song. Eur J Med Genet 2008
60
15

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
9

Wnt pathway inhibition via the targeting of Frizzled receptors results in decreased growth and tumorigenicity of human tumors.
Austin Gurney, Fumiko Axelrod, Christopher J Bond, Jennifer Cain, Cecile Chartier, Lucas Donigan, Marcus Fischer, Aurélie Chaudhari, May Ji, Ann M Kapoun,[...]. Proc Natl Acad Sci U S A 2012
391
9

Cancer Susceptibility Gene Mutations in Individuals With Colorectal Cancer.
Matthew B Yurgelun, Matthew H Kulke, Charles S Fuchs, Brian A Allen, Hajime Uno, Jason L Hornick, Chinedu I Ukaegbu, Lauren K Brais, Philip G McNamara, Robert J Mayer,[...]. J Clin Oncol 2017
240
9

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
800
9



Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: the odonto-onycho-dermal dysplasia.
Lynn Adaimy, Eliane Chouery, Hala Megarbane, Salman Mroueh, Valerie Delague, Elsa Nicolas, Hanen Belguith, Philippe de Mazancourt, Andre Megarbane. Am J Hum Genet 2007
163
8

Taurodontism, variations in tooth number, and misshapened crowns in Wnt10a null mice and human kindreds.
Jie Yang, Shih-Kai Wang, Murim Choi, Bryan M Reid, Yuanyuan Hu, Yuan-Ling Lee, Curtis R Herzog, Hera Kim-Berman, Moses Lee, Paul J Benke,[...]. Mol Genet Genomic Med 2015
60
13

GREMLIN 2 Mutations and Dental Anomalies.
P N Kantaputra, M Kaewgahya, A Hatsadaloi, P Vogel, K Kawasaki, A Ohazama, J R Ketudat Cairns. J Dent Res 2015
38
21

Tooth agenesis: from molecular genetics to molecular dentistry.
E Matalova, J Fleischmannova, P T Sharpe, A S Tucker. J Dent Res 2008
123
8

WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes.
Axel Bohring, Thomas Stamm, Christiane Spaich, Claudia Haase, Kerstin Spree, Ute Hehr, Mandy Hoffmann, Susanne Ledig, Saadettin Sel, Peter Wieacker,[...]. Am J Hum Genet 2009
142
8

Axis inhibition protein 2 (AXIN2) polymorphisms and tooth agenesis.
N Callahan, A Modesto, R Meira, F Seymen, A Patir, A R Vieira. Arch Oral Biol 2009
47
17

Tumour suppressor RNF43 is a stem-cell E3 ligase that induces endocytosis of Wnt receptors.
Bon-Kyoung Koo, Maureen Spit, Ingrid Jordens, Teck Y Low, Daniel E Stange, Marc van de Wetering, Johan H van Es, Shabaz Mohammed, Albert J R Heck, Madelon M Maurice,[...]. Nature 2012
588
8

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
8

Germline mutation of RPS20, encoding a ribosomal protein, causes predisposition to hereditary nonpolyposis colorectal carcinoma without DNA mismatch repair deficiency.
Taina T Nieminen, Marie-Françoise O'Donohue, Yunpeng Wu, Hannes Lohi, Stephen W Scherer, Andrew D Paterson, Pekka Ellonen, Wael M Abdel-Rahman, Satu Valo, Jukka-Pekka Mecklin,[...]. Gastroenterology 2014
113
8

Germline Genetic Features of Young Individuals With Colorectal Cancer.
Elena M Stoffel, Erika Koeppe, Jessica Everett, Peter Ulintz, Mark Kiel, Jenae Osborne, Linford Williams, Kristen Hanson, Stephen B Gruber, Laura S Rozek. Gastroenterology 2018
135
8

Prevalence and Spectrum of Germline Cancer Susceptibility Gene Mutations Among Patients With Early-Onset Colorectal Cancer.
Rachel Pearlman, Wendy L Frankel, Benjamin Swanson, Weiqiang Zhao, Ahmet Yilmaz, Kristin Miller, Jason Bacher, Christopher Bigley, Lori Nelsen, Paul J Goodfellow,[...]. JAMA Oncol 2017
341
8

Small-molecule antagonists of the oncogenic Tcf/beta-catenin protein complex.
Maina Lepourcelet, Ying-Nan P Chen, Dennis S France, Huisheng Wang, Phillip Crews, Frank Petersen, Charles Bruseo, Alexander W Wood, Ramesh A Shivdasani. Cancer Cell 2004
525
8

Can we safely target the WNT pathway?
Michael Kahn. Nat Rev Drug Discov 2014
681
8


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.