A citation-based method for searching scientific literature

William T Gibson, Rebecca L Hood, Shing Hei Zhan, Dennis E Bulman, Anthony P Fejes, Richard Moore, Andrew J Mungall, Patrice Eydoux, Riyana Babul-Hirji, Jianghong An, Marco A Marra, David Chitayat, Kym M Boycott, David D Weaver, Steven J M Jones. Am J Hum Genet 2012
Times Cited: 160







List of co-cited articles
1418 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Germline mutations in the oncogene EZH2 cause Weaver syndrome and increased human height.
Katrina Tatton-Brown, Sandra Hanks, Elise Ruark, Anna Zachariou, Silvana Del Vecchio Duarte, Emma Ramsay, Katie Snape, Anne Murray, Elizabeth R Perdeaux, Sheila Seal,[...]. Oncotarget 2011
101
43

A novel mutation in EED associated with overgrowth.
Ana S A Cohen, Beyhan Tuysuz, Yaoqing Shen, Sanjiv K Bhalla, Steven J M Jones, William T Gibson. J Hum Genet 2015
42
69

Weaver syndrome and EZH2 mutations: Clarifying the clinical phenotype.
Katrina Tatton-Brown, Anne Murray, Sandra Hanks, Jenny Douglas, Ruth Armstrong, Siddharth Banka, Lynne M Bird, Carol L Clericuzio, Valerie Cormier-Daire, Tom Cushing,[...]. Am J Med Genet A 2013
75
36

Role of histone H3 lysine 27 methylation in Polycomb-group silencing.
Ru Cao, Liangjun Wang, Hengbin Wang, Li Xia, Hediye Erdjument-Bromage, Paul Tempst, Richard S Jones, Yi Zhang. Science 2002
26

Weaver Syndrome-Associated EZH2 Protein Variants Show Impaired Histone Methyltransferase Function In Vitro.
Ana S A Cohen, Damian B Yap, M E Suzanne Lewis, Chieko Chijiwa, Maria A Ramos-Arroyo, Natália Tkachenko, Valentina Milano, Mélanie Fradin, Margaret L McKinnon, Katelin N Townsend,[...]. Hum Mutat 2016
36
66

Mutations in genes encoding polycomb repressive complex 2 subunits cause Weaver syndrome.
Eri Imagawa, Ken Higashimoto, Yasunari Sakai, Chikahiko Numakura, Nobuhiko Okamoto, Satoko Matsunaga, Akihide Ryo, Yoshinori Sato, Masafumi Sanefuji, Kenji Ihara,[...]. Hum Mutat 2017
44
54

Novel EED mutation in patient with Weaver syndrome.
Erin Cooney, Weimin Bi, Alan E Schlesinger, Sherry Vinson, Lorraine Potocki. Am J Med Genet A 2017
36
63

EED-associated overgrowth in a second male patient.
Ana Sa Cohen, William T Gibson. J Hum Genet 2016
31
74

The polycomb-group gene Ezh2 is required for early mouse development.
D O'Carroll, S Erhardt, M Pagani, S C Barton, M A Surani, T Jenuwein. Mol Cell Biol 2001
634
23

Mutations in Epigenetic Regulation Genes Are a Major Cause of Overgrowth with Intellectual Disability.
Katrina Tatton-Brown, Chey Loveday, Shawn Yost, Matthew Clarke, Emma Ramsay, Anna Zachariou, Anna Elliott, Harriet Wylie, Anna Ardissone, Olaf Rittinger,[...]. Am J Hum Genet 2017
91
23

Haploinsufficiency of NSD1 causes Sotos syndrome.
Naohiro Kurotaki, Kiyoshi Imaizumi, Naoki Harada, Mitsuo Masuno, Tatsuro Kondoh, Toshiro Nagai, Hirofumi Ohashi, Kenji Naritomi, Masato Tsukahara, Yoshio Makita,[...]. Nat Genet 2002
390
20

Suz12 is essential for mouse development and for EZH2 histone methyltransferase activity.
Diego Pasini, Adrian P Bracken, Michael R Jensen, Eros Lazzerini Denchi, Kristian Helin. EMBO J 2004
618
19


The Polycomb complex PRC2 and its mark in life.
Raphaël Margueron, Danny Reinberg. Nature 2011
17

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
176
16

Mutations in SETD2 cause a novel overgrowth condition.
Armelle Luscan, Ingrid Laurendeau, Valérie Malan, Christine Francannet, Sylvie Odent, Fabienne Giuliano, Didier Lacombe, Renaud Touraine, Michel Vidaud, Eric Pasmant,[...]. J Med Genet 2014
58
27

Somatic mutations altering EZH2 (Tyr641) in follicular and diffuse large B-cell lymphomas of germinal-center origin.
Ryan D Morin, Nathalie A Johnson, Tesa M Severson, Andrew J Mungall, Jianghong An, Rodrigo Goya, Jessica E Paul, Merrill Boyle, Bruce W Woolcock, Florian Kuchenbauer,[...]. Nat Genet 2010
15

Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome.
Sarah B Ng, Abigail W Bigham, Kati J Buckingham, Mark C Hannibal, Margaret J McMillin, Heidi I Gildersleeve, Anita E Beck, Holly K Tabor, Gregory M Cooper, Heather C Mefford,[...]. Nat Genet 2010
863
14

Histone methyltransferase activity associated with a human multiprotein complex containing the Enhancer of Zeste protein.
Andrei Kuzmichev, Kenichi Nishioka, Hediye Erdjument-Bromage, Paul Tempst, Danny Reinberg. Genes Dev 2002
14


Novel SUZ12 mutations in Weaver-like syndrome.
Eri Imagawa, Edoarda V A Albuquerque, Bertrand Isidor, Satomi Mitsuhashi, Takeshi Mizuguchi, Satoko Miyatake, Atsushi Takata, Noriko Miyake, Margaret C S Boguszewski, César L Boguszewski,[...]. Clin Genet 2018
20
65

Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disorders.
Thomas Ernst, Andrew J Chase, Joannah Score, Claire E Hidalgo-Curtis, Catherine Bryant, Amy V Jones, Katherine Waghorn, Katerina Zoi, Fiona M Ross, Andreas Reiter,[...]. Nat Genet 2010
835
12

The eed mutation disrupts anterior mesoderm production in mice.
C Faust, A Schumacher, B Holdener, T Magnuson. Development 1995
210
12

EZH1 mediates methylation on histone H3 lysine 27 and complements EZH2 in maintaining stem cell identity and executing pluripotency.
Xiaohua Shen, Yingchun Liu, Yu-Jung Hsu, Yuko Fujiwara, Jonghwan Kim, Xiaohong Mao, Guo-Cheng Yuan, Stuart H Orkin. Mol Cell 2008
650
12

Role of the polycomb protein EED in the propagation of repressive histone marks.
Raphael Margueron, Neil Justin, Katsuhito Ohno, Miriam L Sharpe, Jinsook Son, William J Drury, Philipp Voigt, Stephen R Martin, William R Taylor, Valeria De Marco,[...]. Nature 2009
753
11

Ezh2 Mutations Found in the Weaver Overgrowth Syndrome Cause a Partial Loss of H3K27 Histone Methyltransferase Activity.
Julian C Lui, Kevin M Barnes, Lijin Dong, Shanna Yue, Evan Graber, Robert Rapaport, Andrew Dauber, Ola Nilsson, Jeffrey Baron. J Clin Endocrinol Metab 2018
19
57

Genome Regulation by Polycomb and Trithorax: 70 Years and Counting.
Bernd Schuettengruber, Henri-Marc Bourbon, Luciano Di Croce, Giacomo Cavalli. Cell 2017
412
11

Loss-of-function mutations in euchromatin histone methyl transferase 1 (EHMT1) cause the 9q34 subtelomeric deletion syndrome.
Tjitske Kleefstra, Han G Brunner, Jeanne Amiel, Astrid R Oudakker, Willy M Nillesen, Alex Magee, David Geneviève, Valérie Cormier-Daire, Hilde van Esch, Jean-Pierre Fryns,[...]. Am J Hum Genet 2006
248
10

Disruption of an EHMT1-associated chromatin-modification module causes intellectual disability.
Tjitske Kleefstra, Jamie M Kramer, Kornelia Neveling, Marjolein H Willemsen, Tom S Koemans, Lisenka E L M Vissers, Willemijn Wissink-Lindhout, Michaela Fenckova, Willem M R van den Akker, Nael Nadif Kasri,[...]. Am J Hum Genet 2012
150
10

Polycomb complexes repress developmental regulators in murine embryonic stem cells.
Laurie A Boyer, Kathrin Plath, Julia Zeitlinger, Tobias Brambrink, Lea A Medeiros, Tong Ihn Lee, Stuart S Levine, Marius Wernig, Adriana Tajonar, Mridula K Ray,[...]. Nature 2006
10

Control of developmental regulators by Polycomb in human embryonic stem cells.
Tong Ihn Lee, Richard G Jenner, Laurie A Boyer, Matthew G Guenther, Stuart S Levine, Roshan M Kumar, Brett Chevalier, Sarah E Johnstone, Megan F Cole, Kyo-ichi Isono,[...]. Cell 2006
10

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
188
10

Brief Report: SETD2 Mutation in a Child with Autism, Intellectual Disabilities and Epilepsy.
Heidi S Lumish, Julia Wynn, Orrin Devinsky, Wendy K Chung. J Autism Dev Disord 2015
37
27

MTF2 recruits Polycomb Repressive Complex 2 by helical-shape-selective DNA binding.
Matteo Perino, Guido van Mierlo, Ino D Karemaker, Siebe van Genesen, Michiel Vermeulen, Hendrik Marks, Simon J van Heeringen, Gert Jan C Veenstra. Nat Genet 2018
89
11

The language of covalent histone modifications.
B D Strahl, C D Allis. Nature 2000
9

NSD1 is essential for early post-implantation development and has a catalytically active SET domain.
Geetha Vani Rayasam, Olivia Wendling, Pierre-Olivier Angrand, Manuel Mark, Karen Niederreither, Luyan Song, Thierry Lerouge, Gordon L Hager, Pierre Chambon, Régine Losson. EMBO J 2003
239
9

EZH2 inhibition as a therapeutic strategy for lymphoma with EZH2-activating mutations.
Michael T McCabe, Heidi M Ott, Gopinath Ganji, Susan Korenchuk, Christine Thompson, Glenn S Van Aller, Yan Liu, Alan P Graves, Anthony Della Pietra, Elsie Diaz,[...]. Nature 2012
9

Genetic inactivation of the polycomb repressive complex 2 in T cell acute lymphoblastic leukemia.
Panagiotis Ntziachristos, Aristotelis Tsirigos, Pieter Van Vlierberghe, Jelena Nedjic, Thomas Trimarchi, Maria Sol Flaherty, Dolors Ferres-Marco, Vanina da Ros, Zuojian Tang, Jasmin Siegle,[...]. Nat Med 2012
341
9

Ezh2 is required for neural crest-derived cartilage and bone formation.
Daniel Schwarz, Sandra Varum, Martina Zemke, Anne Schöler, Arianna Baggiolini, Kalina Draganova, Haruhiko Koseki, Dirk Schübeler, Lukas Sommer. Development 2014
78
11

Ezh2, the histone methyltransferase of PRC2, regulates the balance between self-renewal and differentiation in the cerebral cortex.
João D Pereira, Stephen N Sansom, James Smith, Marc-Werner Dobenecker, Alexander Tarakhovsky, Frederick J Livesey. Proc Natl Acad Sci U S A 2010
260
9

Histone methyltransferase activity of a Drosophila Polycomb group repressor complex.
Jürg Müller, Craig M Hart, Nicole J Francis, Marcus L Vargas, Aditya Sengupta, Brigitte Wild, Ellen L Miller, Michael B O'Connor, Robert E Kingston, Jeffrey A Simon. Cell 2002
9

Molecular architecture of human polycomb repressive complex 2.
Claudio Ciferri, Gabriel C Lander, Alessio Maiolica, Franz Herzog, Ruedi Aebersold, Eva Nogales. Elife 2012
172
9

Ezh1 and Ezh2 maintain repressive chromatin through different mechanisms.
Raphael Margueron, Guohong Li, Kavitha Sarma, Alexandre Blais, Jiri Zavadil, Christopher L Woodcock, Brian D Dynlacht, Danny Reinberg. Mol Cell 2008
543
9

NSD1 mutations generate a genome-wide DNA methylation signature.
S Choufani, C Cytrynbaum, B H Y Chung, A L Turinsky, D Grafodatskaya, Y A Chen, A S A Cohen, L Dupuis, D T Butcher, M T Siu,[...]. Nat Commun 2015
91
9

Polycomb-like proteins link the PRC2 complex to CpG islands.
Haojie Li, Robert Liefke, Junyi Jiang, Jesse Vigoda Kurland, Wei Tian, Pujuan Deng, Weidi Zhang, Qian He, Dinshaw J Patel, Martha L Bulyk,[...]. Nature 2017
143
9

Mutations affecting components of the SWI/SNF complex cause Coffin-Siris syndrome.
Yoshinori Tsurusaki, Nobuhiko Okamoto, Hirofumi Ohashi, Tomoki Kosho, Yoko Imai, Yumiko Hibi-Ko, Tadashi Kaname, Kenji Naritomi, Hiroshi Kawame, Keiko Wakui,[...]. Nat Genet 2012
317
8

Deletion of KDM6A, a histone demethylase interacting with MLL2, in three patients with Kabuki syndrome.
Damien Lederer, Bernard Grisart, Maria Cristina Digilio, Valérie Benoit, Marianne Crespin, Sophie Claire Ghariani, Isabelle Maystadt, Bruno Dallapiccola, Christine Verellen-Dumoulin. Am J Hum Genet 2012
225
8

The NSD1 and EZH2 overgrowth genes, similarities and differences.
Katrina Tatton-Brown, Nazneen Rahman. Am J Med Genet C Semin Med Genet 2013
47
17

Inhibition of PRC2 activity by a gain-of-function H3 mutation found in pediatric glioblastoma.
Peter W Lewis, Manuel M Müller, Matthew S Koletsky, Francisco Cordero, Shu Lin, Laura A Banaszynski, Benjamin A Garcia, Tom W Muir, Oren J Becher, C David Allis. Science 2013
751
8

Ezh2 requires PHF1 to efficiently catalyze H3 lysine 27 trimethylation in vivo.
Kavitha Sarma, Raphael Margueron, Alexey Ivanov, Vincenzo Pirrotta, Danny Reinberg. Mol Cell Biol 2008
204
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.