A citation-based method for searching scientific literature

G L Xu, T H Bestor, D Bourc'his, C L Hsieh, N Tommerup, M Bugge, M Hulten, X Qu, J J Russo, E Viegas-Péquignot. Nature 1999
Times Cited: 823







List of co-cited articles
1228 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity



The DNMT3B DNA methyltransferase gene is mutated in the ICF immunodeficiency syndrome.
R S Hansen, C Wijmenga, P Luo, A M Stanek, T K Canfield, C M Weemaes, S M Gartler. Proc Natl Acad Sci U S A 1999
518
40

Mutations in CDCA7 and HELLS cause immunodeficiency-centromeric instability-facial anomalies syndrome.
Peter E Thijssen, Yuya Ito, Giacomo Grillo, Jun Wang, Guillaume Velasco, Hirohisa Nitta, Motoko Unoki, Minako Yoshihara, Mikita Suyama, Yu Sun,[...]. Nat Commun 2015
85
37

Mutations in ZBTB24 are associated with immunodeficiency, centromeric instability, and facial anomalies syndrome type 2.
Jessica C de Greef, Jun Wang, Judit Balog, Johan T den Dunnen, Rune R Frants, Kirsten R Straasheijm, Caner Aytekin, Mirjam van der Burg, Laurence Duprez, Alina Ferster,[...]. Am J Hum Genet 2011
95
32

Genomic profiling of DNA methyltransferases reveals a role for DNMT3B in genic methylation.
Tuncay Baubec, Daniele F Colombo, Christiane Wirbelauer, Juliane Schmidt, Lukas Burger, Arnaud R Krebs, Altuna Akalin, Dirk Schübeler. Nature 2015
331
18

Converging disease genes in ICF syndrome: ZBTB24 controls expression of CDCA7 in mammals.
Haoyu Wu, Peter E Thijssen, Eleonora de Klerk, Kelly K D Vonk, Jun Wang, Bianca den Hamer, Caner Aytekin, Silvère M van der Maarel, Lucia Daxinger. Hum Mol Genet 2016
26
65

Immunodeficiency, centromeric region instability, facial anomalies syndrome (ICF).
Melanie Ehrlich, Kelly Jackson, Corry Weemaes. Orphanet J Rare Dis 2006
71
22

Heterogeneous clinical presentation in ICF syndrome: correlation with underlying gene defects.
Corry M R Weemaes, Maarten J D van Tol, Jun Wang, Monique M van Ostaijen-ten Dam, Marja C J A van Eggermond, Peter E Thijssen, Caner Aytekin, Nicola Brunetti-Pierri, Mirjam van der Burg, E Graham Davies,[...]. Eur J Hum Genet 2013
66
24


HELLS and CDCA7 comprise a bipartite nucleosome remodeling complex defective in ICF syndrome.
Christopher Jenness, Simona Giunta, Manuel M Müller, Hiroshi Kimura, Tom W Muir, Hironori Funabiki. Proc Natl Acad Sci U S A 2018
45
33

Comparative methylome analysis of ICF patients identifies heterochromatin loci that require ZBTB24, CDCA7 and HELLS for their methylated state.
Guillaume Velasco, Giacomo Grillo, Nizar Touleimat, Laure Ferry, Ivana Ivkovic, Florence Ribierre, Jean-François Deleuze, Sophie Chantalat, Capucine Picard, Claire Francastel. Hum Mol Genet 2018
25
60


DNA methylation: roles in mammalian development.
Zachary D Smith, Alexander Meissner. Nat Rev Genet 2013
13

DNMT3L connects unmethylated lysine 4 of histone H3 to de novo methylation of DNA.
Steen K T Ooi, Chen Qiu, Emily Bernstein, Keqin Li, Da Jia, Zhe Yang, Hediye Erdjument-Bromage, Paul Tempst, Shau-Ping Lin, C David Allis,[...]. Nature 2007
949
13


Mutations in the DNA methyltransferase gene DNMT3A cause an overgrowth syndrome with intellectual disability.
Katrina Tatton-Brown, Sheila Seal, Elise Ruark, Jenny Harmer, Emma Ramsay, Silvana Del Vecchio Duarte, Anna Zachariou, Sandra Hanks, Eleanor O'Brien, Lise Aksglaede,[...]. Nat Genet 2014
162
13

DNMT3B mutations and DNA methylation defect define two types of ICF syndrome.
Y L Jiang, M Rigolet, D Bourc'his, F Nigon, I Bokesoy, J P Fryns, M Hultén, P Jonveaux, P Maraschio, A Mégarbané,[...]. Hum Mutat 2005
74
17


Intragenic DNA methylation prevents spurious transcription initiation.
Francesco Neri, Stefania Rapelli, Anna Krepelova, Danny Incarnato, Caterina Parlato, Giulia Basile, Mara Maldotti, Francesca Anselmi, Salvatore Oliviero. Nature 2017
262
12

Human DNA methylomes at base resolution show widespread epigenomic differences.
Ryan Lister, Mattia Pelizzola, Robert H Dowen, R David Hawkins, Gary Hon, Julian Tonti-Filippini, Joseph R Nery, Leonard Lee, Zhen Ye, Que-Minh Ngo,[...]. Nature 2009
12

Telomeres in ICF syndrome cells are vulnerable to DNA damage due to elevated DNA:RNA hybrids.
Shira Sagie, Shir Toubiana, Stella R Hartono, Hagar Katzir, Aya Tzur-Gilat, Shany Havazelet, Claire Francastel, Guillaume Velasco, Frédéric Chédin, Sara Selig. Nat Commun 2017
52
23


An embryonic-like methylation pattern of classical satellite DNA is observed in ICF syndrome.
M Jeanpierre, C Turleau, A Aurias, M Prieur, F Ledeist, A Fischer, E Viegas-Pequignot. Hum Mol Genet 1993
215
12

Subtelomeric methylation distinguishes between subtypes of Immunodeficiency, Centromeric instability and Facial anomalies syndrome.
Shir Toubiana, Guillaume Velasco, Adi Chityat, Angela M Kaindl, Noam Hershtig, Aya Tzur-Gilat, Claire Francastel, Sara Selig. Hum Mol Genet 2018
18
66

Roles for Dnmt3b in mammalian development: a mouse model for the ICF syndrome.
Yoshihide Ueda, Masaki Okano, Christine Williams, Taiping Chen, Katia Georgopoulos, En Li. Development 2006
122
12

CDCA7 and HELLS mutations undermine nonhomologous end joining in centromeric instability syndrome.
Motoko Unoki, Hironori Funabiki, Guillaume Velasco, Claire Francastel, Hiroyuki Sasaki. J Clin Invest 2019
29
41

Structural insight into autoinhibition and histone H3-induced activation of DNMT3A.
Xue Guo, Ling Wang, Jie Li, Zhanyu Ding, Jianxiong Xiao, Xiaotong Yin, Shuang He, Pan Shi, Liping Dong, Guohong Li,[...]. Nature 2015
174
11

Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss.
Christopher J Klein, Maria-Victoria Botuyan, Yanhong Wu, Christopher J Ward, Garth A Nicholson, Simon Hammans, Kaori Hojo, Hiromitch Yamanishi, Adam R Karpf, Douglas C Wallace,[...]. Nat Genet 2011
239
11

Clinical spectrum of immunodeficiency, centromeric instability and facial dysmorphism (ICF syndrome).
M M Hagleitner, A Lankester, P Maraschio, M Hultén, J P Fryns, C Schuetz, G Gimelli, E G Davies, A Gennery, B H Belohradsky,[...]. J Med Genet 2008
73
15

DNA methyltransferase 3B (DNMT3B) mutations in ICF syndrome lead to altered epigenetic modifications and aberrant expression of genes regulating development, neurogenesis and immune function.
Bilian Jin, Qian Tao, Jinrong Peng, Hui Meng Soo, Wei Wu, Jianming Ying, C Robert Fields, Amber L Delmas, Xuefeng Liu, Jingxin Qiu,[...]. Hum Mol Genet 2008
161
11


The molecular hallmarks of epigenetic control.
C David Allis, Thomas Jenuwein. Nat Rev Genet 2016
878
10

The Dnmt3a PWWP domain reads histone 3 lysine 36 trimethylation and guides DNA methylation.
Arunkumar Dhayalan, Arumugam Rajavelu, Philipp Rathert, Raluca Tamas, Renata Z Jurkowska, Sergey Ragozin, Albert Jeltsch. J Biol Chem 2010
305
10


DNMT3A mutations in acute myeloid leukemia.
Timothy J Ley, Li Ding, Matthew J Walter, Michael D McLellan, Tamara Lamprecht, David E Larson, Cyriac Kandoth, Jacqueline E Payton, Jack Baty, John Welch,[...]. N Engl J Med 2010
9

Lsh is involved in de novo methylation of DNA.
Heming Zhu, Theresa M Geiman, Sichuan Xi, Qiong Jiang, Anja Schmidtmann, Taiping Chen, En Li, Kathrin Muegge. EMBO J 2006
117
9

Conversion of 5-methylcytosine to 5-hydroxymethylcytosine in mammalian DNA by MLL partner TET1.
Mamta Tahiliani, Kian Peng Koh, Yinghua Shen, William A Pastor, Hozefa Bandukwala, Yevgeny Brudno, Suneet Agarwal, Lakshminarayan M Iyer, David R Liu, L Aravind,[...]. Science 2009
9

Whole-genome methylation scan in ICF syndrome: hypomethylation of non-satellite DNA repeats D4Z4 and NBL2.
T Kondo, M P Bobek, R Kuick, B Lamb, X Zhu, A Narayan, D Bourc'his, E Viegas-Péquignot, M Ehrlich, S M Hanash. Hum Mol Genet 2000
130
9

TERRA, CpG methylation and telomere heterochromatin: lessons from ICF syndrome cells.
Zhong Deng, Amy E Campbell, Paul M Lieberman. Cell Cycle 2010
64
14

RNaseH1 regulates TERRA-telomeric DNA hybrids and telomere maintenance in ALT tumour cells.
Rajika Arora, Yongwoo Lee, Harry Wischnewski, Catherine M Brun, Tobias Schwarz, Claus M Azzalin. Nat Commun 2014
196
9

Whole-genome bisulfite DNA sequencing of a DNMT3B mutant patient.
Holger Heyn, Enrique Vidal, Sergi Sayols, Jose V Sanchez-Mut, Sebastian Moran, Ignacio Medina, Juan Sandoval, Laia Simó-Riudalbas, Karolina Szczesna, Dori Huertas,[...]. Epigenetics 2012
49
18

Three novel ZBTB24 mutations identified in Japanese and Cape Verdean type 2 ICF syndrome patients.
Hirohisa Nitta, Motoko Unoki, Kenji Ichiyanagi, Tomoki Kosho, Tomonari Shigemura, Hiroshi Takahashi, Guillaume Velasco, Claire Francastel, Capucine Picard, Takeo Kubota,[...]. J Hum Genet 2013
30
30

DNA methylation pathways and their crosstalk with histone methylation.
Jiamu Du, Lianna M Johnson, Steven E Jacobsen, Dinshaw J Patel. Nat Rev Mol Cell Biol 2015
397
8

Structure of Dnmt3a bound to Dnmt3L suggests a model for de novo DNA methylation.
Da Jia, Renata Z Jurkowska, Xing Zhang, Albert Jeltsch, Xiaodong Cheng. Nature 2007
512
8



Establishment and maintenance of genomic methylation patterns in mouse embryonic stem cells by Dnmt3a and Dnmt3b.
Taiping Chen, Yoshihide Ueda, Jonathan E Dodge, Zhenjuan Wang, En Li. Mol Cell Biol 2003
510
8

Suv39h-mediated histone H3 lysine 9 methylation directs DNA methylation to major satellite repeats at pericentric heterochromatin.
Bernhard Lehnertz, Yoshihide Ueda, Alwin A H A Derijck, Ulrich Braunschweig, Laura Perez-Burgos, Stefan Kubicek, Taiping Chen, En Li, Thomas Jenuwein, Antoine H F M Peters. Curr Biol 2003
851
8

The DNA methyltransferases of mammals.
T H Bestor. Hum Mol Genet 2000
8

DNA methylation and human disease.
Keith D Robertson. Nat Rev Genet 2005
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.