A citation-based method for searching scientific literature

Sadegheh Haghshenas, Pratibha Bhai, Erfan Aref-Eshghi, Bekim Sadikovic. Int J Mol Sci 2020
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


Evaluation of DNA Methylation Episignatures for Diagnosis and Phenotype Correlations in 42 Mendelian Neurodevelopmental Disorders.
Erfan Aref-Eshghi, Jennifer Kerkhof, Victor P Pedro, Mouna Barat-Houari, Nathalie Ruiz-Pallares, Jean-Christophe Andrau, Didier Lacombe, Julien Van-Gils, Patricia Fergelot, Christèle Dubourg,[...]. Am J Hum Genet 2020
41
100

DNA Methylation in the Diagnosis of Monogenic Diseases.
Flavia Cerrato, Angela Sparago, Francesca Ariani, Fulvia Brugnoletti, Luciano Calzari, Fabio Coppedè, Alessandro De Luca, Cristina Gervasini, Emiliano Giardina, Fiorella Gurrieri,[...]. Genes (Basel) 2020
13
50

Distribution, silencing potential and evolutionary impact of promoter DNA methylation in the human genome.
Michael Weber, Ines Hellmann, Michael B Stadler, Liliana Ramos, Svante Pääbo, Michael Rebhan, Dirk Schübeler. Nat Genet 2007
25

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
68
25


Three novel DNMT3B mutations in Japanese patients with ICF syndrome.
Hisao Shirohzu, Takeo Kubota, Azumi Kumazawa, Takashi Sado, Takahito Chijiwa, Kouichi Inagaki, Isao Suetake, Shoji Tajima, Keiko Wakui, Yuko Miki,[...]. Am J Med Genet 2002
75
25

Tandem repeats in the CpG islands of imprinted genes.
Barbara Hutter, Volkhard Helms, Martina Paulsen. Genomics 2006
48
25

Loss of ZBTB24 impairs nonhomologous end-joining and class-switch recombination in patients with ICF syndrome.
Angela Helfricht, Peter E Thijssen, Magdalena B Rother, Rashmi G Shah, Likun Du, Sanami Takada, Mélanie Rogier, Jacques Moritz, Hanna IJspeert, Chantal Stoepker,[...]. J Exp Med 2020
9
25

The Mendelian disorders of the epigenetic machinery.
Hans Tomas Bjornsson. Genome Res 2015
77
25

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
96
25

Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene.
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
831
25


Histone tails regulate DNA methylation by allosterically activating de novo methyltransferase.
Bin-Zhong Li, Zheng Huang, Qing-Yan Cui, Xue-Hui Song, Lin Du, Albert Jeltsch, Ping Chen, Guohong Li, En Li, Guo-Liang Xu. Cell Res 2011
80
25

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
133
25

Mendelian disorders of the epigenetic machinery: tipping the balance of chromatin states.
Jill A Fahrner, Hans T Bjornsson. Annu Rev Genomics Hum Genet 2014
57
25

Identification of distinct loci for de novo DNA methylation by DNMT3A and DNMT3B during mammalian development.
Masaki Yagi, Mio Kabata, Akito Tanaka, Tomoyo Ukai, Sho Ohta, Kazuhiko Nakabayashi, Masahito Shimizu, Kenichiro Hata, Alexander Meissner, Takuya Yamamoto,[...]. Nat Commun 2020
10
25

The histone mark H3K36me2 recruits DNMT3A and shapes the intergenic DNA methylation landscape.
Daniel N Weinberg, Simon Papillon-Cavanagh, Haifen Chen, Yuan Yue, Xiao Chen, Kartik N Rajagopalan, Cynthia Horth, John T McGuire, Xinjing Xu, Hamid Nikbakht,[...]. Nature 2019
123
25

A DNMT3A PWWP mutation leads to methylation of bivalent chromatin and growth retardation in mice.
Gintarė Sendžikaitė, Courtney W Hanna, Kathleen R Stewart-Morgan, Elena Ivanova, Gavin Kelsey. Nat Commun 2019
36
25

Genetics meets DNA methylation in rare diseases.
Guillaume Velasco, Claire Francastel. Clin Genet 2019
17
25

Chromatin methylation activity of Dnmt3a and Dnmt3a/3L is guided by interaction of the ADD domain with the histone H3 tail.
Yingying Zhang, Renata Jurkowska, Szabolcs Soeroes, Arumugam Rajavelu, Arunkumar Dhayalan, Ina Bock, Philipp Rathert, Ole Brandt, Richard Reinhardt, Wolfgang Fischle,[...]. Nucleic Acids Res 2010
222
25

DNA methylation dynamics of the human preimplantation embryo.
Zachary D Smith, Michelle M Chan, Kathryn C Humm, Rahul Karnik, Shila Mekhoubad, Aviv Regev, Kevin Eggan, Alexander Meissner. Nature 2014
334
25

The DNA methylation landscape of human early embryos.
Hongshan Guo, Ping Zhu, Liying Yan, Rong Li, Boqiang Hu, Ying Lian, Jie Yan, Xiulian Ren, Shengli Lin, Junsheng Li,[...]. Nature 2014
490
25

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
76
25


DNA methylation in human diseases.
Zelin Jin, Yun Liu. Genes Dis 2018
94
25

JmjC-domain-containing proteins and histone demethylation.
Robert J Klose, Eric M Kallin, Yi Zhang. Nat Rev Genet 2006
837
25

Clinical epigenetics: a primer for the practitioner.
Deniz Aygun, Hans T Bjornsson. Dev Med Child Neurol 2020
7
25

Mapping and analysis of chromatin state dynamics in nine human cell types.
Jason Ernst, Pouya Kheradpour, Tarjei S Mikkelsen, Noam Shoresh, Lucas D Ward, Charles B Epstein, Xiaolan Zhang, Li Wang, Robbyn Issner, Michael Coyne,[...]. Nature 2011
25

Epigenomic analysis of multilineage differentiation of human embryonic stem cells.
Wei Xie, Matthew D Schultz, Ryan Lister, Zhonggang Hou, Nisha Rajagopal, Pradipta Ray, John W Whitaker, Shulan Tian, R David Hawkins, Danny Leung,[...]. Cell 2013
471
25

DNA Methylation Profiling of Uniparental Disomy Subjects Provides a Map of Parental Epigenetic Bias in the Human Genome.
Ricky S Joshi, Paras Garg, Noah Zaitlen, Tuuli Lappalainen, Corey T Watson, Nidha Azam, Daniel Ho, Xin Li, Stylianos E Antonarakis, Han G Brunner,[...]. Am J Hum Genet 2016
33
25

limma powers differential expression analyses for RNA-sequencing and microarray studies.
Matthew E Ritchie, Belinda Phipson, Di Wu, Yifang Hu, Charity W Law, Wei Shi, Gordon K Smyth. Nucleic Acids Res 2015
25

Epigenetic inactivation of the Sotos overgrowth syndrome gene histone methyltransferase NSD1 in human neuroblastoma and glioma.
María Berdasco, Santiago Ropero, Fernando Setien, Mario F Fraga, Pablo Lapunzina, Régine Losson, Miguel Alaminos, Nai-Kong Cheung, Nazneen Rahman, Manel Esteller. Proc Natl Acad Sci U S A 2009
141
25

Regulation of growth and metabolism by imprinted genes.
F M Smith, A S Garfield, A Ward. Cytogenet Genome Res 2006
126
25

ChAMP: 450k Chip Analysis Methylation Pipeline.
Tiffany J Morris, Lee M Butcher, Andrew Feber, Andrew E Teschendorff, Ankur R Chakravarthy, Tomasz K Wojdacz, Stephan Beck. Bioinformatics 2014
416
25

DNA methyltransferase expression in the mouse germ line during periods of de novo methylation.
Diane J Lees-Murdock, Tanya C Shovlin, Tom Gardiner, Massimo De Felici, Colum P Walsh. Dev Dyn 2005
63
25

Depletion of H3K36me2 recapitulates epigenomic and phenotypic changes induced by the H3.3K36M oncohistone mutation.
Kartik N Rajagopalan, Xiao Chen, Daniel N Weinberg, Haifen Chen, Jacek Majewski, C David Allis, Chao Lu. Proc Natl Acad Sci U S A 2021
6
25



Genome-wide analysis in the mouse embryo reveals the importance of DNA methylation for transcription integrity.
Thomas Dahlet, Andrea Argüeso Lleida, Hala Al Adhami, Michael Dumas, Ambre Bender, Richard P Ngondo, Manon Tanguy, Judith Vallet, Ghislain Auclair, Anaïs F Bardet,[...]. Nat Commun 2020
24
25

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
317
25

Genome-wide signatures of differential DNA methylation in pediatric acute lymphoblastic leukemia.
Jessica Nordlund, Christofer L Bäcklin, Per Wahlberg, Stephan Busche, Eva C Berglund, Maija-Leena Eloranta, Trond Flaegstad, Erik Forestier, Britt-Marie Frost, Arja Harila-Saari,[...]. Genome Biol 2013
189
25

Genome-wide DNA methylation patterns in LSH mutant reveals de-repression of repeat elements and redundant epigenetic silencing pathways.
Weishi Yu, Carl McIntosh, Ryan Lister, Iris Zhu, Yixing Han, Jianke Ren, David Landsman, Eunice Lee, Victorino Briones, Minoru Terashima,[...]. Genome Res 2014
62
25

NSD1 mutations are the major cause of Sotos syndrome and occur in some cases of Weaver syndrome but are rare in other overgrowth phenotypes.
Jenny Douglas, Sandra Hanks, I Karen Temple, Sally Davies, Alexandra Murray, Meena Upadhyaya, Susan Tomkins, Helen E Hughes, Trevor R P Cole, Nazneen Rahman. Am J Hum Genet 2003
184
25


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
31
25

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
25

Gain-of-function DNMT3A mutations cause microcephalic dwarfism and hypermethylation of Polycomb-regulated regions.
Patricia Heyn, Clare V Logan, Adeline Fluteau, Rachel C Challis, Tatsiana Auchynnikava, Carol-Anne Martin, Joseph A Marsh, Francesca Taglini, Fiona Kilanowski, David A Parry,[...]. Nat Genet 2019
50
25

Growth disrupting mutations in epigenetic regulatory molecules are associated with abnormalities of epigenetic aging.
Aaron R Jeffries, Reza Maroofian, Claire G Salter, Barry A Chioza, Harold E Cross, Michael A Patton, Emma Dempster, I Karen Temple, Deborah J G Mackay, Faisal I Rezwan,[...]. Genome Res 2019
16
25

Paradoxical NSD1 mutations in Beckwith-Wiedemann syndrome and 11p15 anomalies in Sotos syndrome.
Geneviève Baujat, Marlène Rio, Sylvie Rossignol, Damien Sanlaville, Stanislas Lyonnet, Martine Le Merrer, Arnold Munnich, Christine Gicquel, Valérie Cormier-Daire, Laurence Colleaux. Am J Hum Genet 2004
79
25



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.