A citation-based method for searching scientific literature

Concetta G A Marfella, Yasuyuki Ohkawa, Andrew H Coles, David S Garlick, Stephen N Jones, Anthony N Imbalzano. J Cell Physiol 2006
Times Cited: 63







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



Times Cited
  Times     Co-cited
Similarity


Mutations in a new member of the chromodomain gene family cause CHARGE syndrome.
Lisenka E L M Vissers, Conny M A van Ravenswaaij, Ronald Admiraal, Jane A Hurst, Bert B A de Vries, Irene M Janssen, Walter A van der Vliet, Erik H L P G Huys, Pieter J de Jong, Ben C J Hamel,[...]. Nat Genet 2004
760
36

Disruption of chromodomain helicase DNA binding protein 2 (CHD2) causes scoliosis.
Shashikant Kulkarni, Prabakaran Nagarajan, Jonathan Wall, Diana J Donovan, Robert L Donell, Azra H Ligon, Sundaresan Venkatachalam, Bradley J Quade. Am J Med Genet A 2008
39
53

Chd1 regulates open chromatin and pluripotency of embryonic stem cells.
Alexandre Gaspar-Maia, Adi Alajem, Fanny Polesso, Rupa Sridharan, Mike J Mason, Amy Heidersbach, João Ramalho-Santos, Michael T McManus, Kathrin Plath, Eran Meshorer,[...]. Nature 2009
349
31

Characterization of the CHD family of proteins.
T Woodage, M A Basrai, A D Baxevanis, P Hieter, F S Collins. Proc Natl Acad Sci U S A 1997
276
30

Role of chromodomain helicase DNA-binding protein 2 in DNA damage response signaling and tumorigenesis.
P Nagarajan, T M Onami, S Rajagopalan, S Kania, R Donnell, S Venkatachalam. Oncogene 2009
67
30

Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1.
Gemma L Carvill, Sinéad B Heavin, Simone C Yendle, Jacinta M McMahon, Brian J O'Roak, Joseph Cook, Adiba Khan, Michael O Dorschner, Molly Weaver, Sophie Calvert,[...]. Nat Genet 2013
402
28

The Chd family of chromatin remodelers.
Concetta G A Marfella, Anthony N Imbalzano. Mutat Res 2007
230
25

Chd2 interacts with H3.3 to determine myogenic cell fate.
Akihito Harada, Seiji Okada, Daijiro Konno, Jun Odawara, Tomohiko Yoshimi, Saori Yoshimura, Hiromi Kumamaru, Hirokazu Saiwai, Toshiaki Tsubota, Hitoshi Kurumizaka,[...]. EMBO J 2012
77
25

Chromatin remodelling in mammalian differentiation: lessons from ATP-dependent remodellers.
Ivana L de la Serna, Yasuyuki Ohkawa, Anthony N Imbalzano. Nat Rev Genet 2006
279
23


Chd1 chromodomain links histone H3 methylation with SAGA- and SLIK-dependent acetylation.
Marilyn G Pray-Grant, Jeremy A Daniel, David Schieltz, John R Yates, Patrick A Grant. Nature 2005
361
20

CHD5, a new member of the chromodomain gene family, is preferentially expressed in the nervous system.
Patricia M Thompson, Takahiro Gotoh, Marleen Kok, Peter S White, Garrett M Brodeur. Oncogene 2003
121
20

Human but not yeast CHD1 binds directly and selectively to histone H3 methylated at lysine 4 via its tandem chromodomains.
Robert J Sims, Chi-Fu Chen, Helena Santos-Rosa, Tony Kouzarides, Smita S Patel, Danny Reinberg. J Biol Chem 2005
269
19

CHD proteins: a diverse family with strong ties.
J Adam Hall, Philippe T Georgel. Biochem Cell Biol 2007
140
19

The biology of chromatin remodeling complexes.
Cedric R Clapier, Bradley R Cairns. Annu Rev Biochem 2009
19

Chromatin remodelling during development.
Lena Ho, Gerald R Crabtree. Nature 2010
692
19

De novo mutations in epileptic encephalopathies.
Andrew S Allen, Samuel F Berkovic, Patrick Cossette, Norman Delanty, Dennis Dlugos, Evan E Eichler, Michael P Epstein, Tracy Glauser, David B Goldstein, Yujun Han,[...]. Nature 2013
920
19

Spectrum of CHD7 mutations in 110 individuals with CHARGE syndrome and genotype-phenotype correlation.
Seema R Lalani, Arsalan M Safiullah, Susan D Fernbach, Karine G Harutyunyan, Christina Thaller, Leif E Peterson, John D McPherson, Richard A Gibbs, Lisa D White, Margaret Hefner,[...]. Am J Hum Genet 2006
237
17


Double chromodomains cooperate to recognize the methylated histone H3 tail.
John F Flanagan, Li-Zhi Mi, Maksymilian Chruszcz, Marcin Cymborowski, Katrina L Clines, Youngchang Kim, Wladek Minor, Fraydoon Rastinejad, Sepideh Khorasanizadeh. Nature 2005
380
17

CHD5 defines a new subfamily of chromodomain-SWI2/SNF2-like helicases.
Eugene F Schuster, Reinhard Stöger. Mamm Genome 2002
39
28

CHD5 is a tumor suppressor at human 1p36.
Anindya Bagchi, Cristian Papazoglu, Ying Wu, Daniel Capurso, Michael Brodt, Dailia Francis, Markus Bredel, Hannes Vogel, Alea A Mills. Cell 2007
244
17

De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndrome.
Arvid Suls, Johanna A Jaehn, Angela Kecskés, Yvonne Weber, Sarah Weckhuysen, Dana C Craiu, Aleksandra Siekierska, Tania Djémié, Tatiana Afrikanova, Padhraig Gormley,[...]. Am J Hum Genet 2013
117
17

CHD2 haploinsufficiency is associated with developmental delay, intellectual disability, epilepsy and neurobehavioural problems.
Sébastien Chénier, Grace Yoon, Bob Argiropoulos, Julie Lauzon, Rachel Laframboise, Joo Wook Ahn, Caroline Mackie Ogilvie, Anath C Lionel, Christian R Marshall, Andrea K Vaags,[...]. J Neurodev Disord 2014
48
22

CHD2 is Required for Embryonic Neurogenesis in the Developing Cerebral Cortex.
Tianjin Shen, Fen Ji, Zengqiang Yuan, Jianwei Jiao. Stem Cells 2015
39
28


NURD, a novel complex with both ATP-dependent chromatin-remodeling and histone deacetylase activities.
Y Xue, J Wong, G T Moreno, M K Young, J Côté, W Wang. Mol Cell 1998
731
15

The ISWI ATPase Snf2h is required for early mouse development.
Tomas Stopka, Arthur I Skoultchi. Proc Natl Acad Sci U S A 2003
132
15

A Brg1 null mutation in the mouse reveals functional differences among mammalian SWI/SNF complexes.
S Bultman, T Gebuhr, D Yee, C La Mantia, J Nicholson, A Gilliam, F Randazzo, D Metzger, P Chambon, G Crabtree,[...]. Mol Cell 2000
612
15

CHD1 motor protein is required for deposition of histone variant H3.3 into chromatin in vivo.
Alexander Y Konev, Martin Tribus, Sung Yeon Park, Valerie Podhraski, Chin Yan Lim, Alexander V Emelyanov, Elena Vershilova, Vincenzo Pirrotta, James T Kadonaga, Alexandra Lusser,[...]. Science 2007
180
15

Loss of Chd7 function in gene-trapped reporter mice is embryonic lethal and associated with severe defects in multiple developing tissues.
Elizabeth A Hurd, Patrice L Capers, Marsha N Blauwkamp, Meredith E Adams, Yehoash Raphael, Heather K Poucher, Donna M Martin. Mamm Genome 2007
106
15

CHD8 suppresses p53-mediated apoptosis through histone H1 recruitment during early embryogenesis.
Masaaki Nishiyama, Kiyotaka Oshikawa, Yu-ichi Tsukada, Tadashi Nakagawa, Shun-ichiro Iemura, Tohru Natsume, Yuhong Fan, Akira Kikuchi, Arthur I Skoultchi, Keiichi I Nakayama. Nat Cell Biol 2009
119
15

Patterns and rates of exonic de novo mutations in autism spectrum disorders.
Benjamin M Neale, Yan Kou, Li Liu, Avi Ma'ayan, Kaitlin E Samocha, Aniko Sabo, Chiao-Feng Lin, Christine Stevens, Li-San Wang, Vladimir Makarov,[...]. Nature 2012
15

The Drosophila kismet gene is related to chromatin-remodeling factors and is required for both segmentation and segment identity.
G Daubresse, R Deuring, L Moore, O Papoulas, I Zakrajsek, W R Waldrip, M P Scott, J A Kennison, J W Tamkun. Development 1999
113
14

Multiple mutations in mouse Chd7 provide models for CHARGE syndrome.
Erika A Bosman, Andrew C Penn, John C Ambrose, Ross Kettleborough, Derek L Stemple, Karen P Steel. Hum Mol Genet 2005
144
14

CHARGE syndrome: the phenotypic spectrum of mutations in the CHD7 gene.
M C J Jongmans, R J Admiraal, K P van der Donk, L E L M Vissers, A F Baas, L Kapusta, J M van Hagen, D Donnai, T J de Ravel, J A Veltman,[...]. J Med Genet 2006
252
14

The SANT domain: a unique histone-tail-binding module?
Laurie A Boyer, Robert R Latek, Craig L Peterson. Nat Rev Mol Cell Biol 2004
243
14

Definition and characterization of a region of 1p36.3 consistently deleted in neuroblastoma.
Peter S White, Patricia M Thompson, Takahiro Gotoh, Erin R Okawa, Jun Igarashi, Marleen Kok, Cynthia Winter, Simon G Gregory, Michael D Hogarty, John M Maris,[...]. Oncogene 2005
112
14

The chromatin remodeler Mi-2beta is required for CD4 expression and T cell development.
Christine J Williams, Taku Naito, Pablo Gómez-Del Arco, John R Seavitt, Susan M Cashman, Beverly De Souza, Xiaoqing Qi, Piper Keables, Ulrich H Von Andrian, Katia Georgopoulos. Immunity 2004
172
14

DNA-binding and chromatin localization properties of CHD1.
D G Stokes, R P Perry. Mol Cell Biol 1995
109
14

In vivo association of CReMM/CHD9 with promoters in osteogenic cells.
I Shur, R Socher, D Benayahu. J Cell Physiol 2006
35
25

Distinct activities of CHD1 and ACF in ATP-dependent chromatin assembly.
Alexandra Lusser, Debra L Urwin, James T Kadonaga. Nat Struct Mol Biol 2005
196
14

Identification of multiple distinct Snf2 subfamilies with conserved structural motifs.
Andrew Flaus, David M A Martin, Geoffrey J Barton, Tom Owen-Hughes. Nucleic Acids Res 2006
434
14

Early embryonic death in mice lacking the beta-catenin-binding protein Duplin.
Masaaki Nishiyama, Keiko Nakayama, Ryosuke Tsunematsu, Tadasuke Tsukiyama, Akira Kikuchi, Keiichi I Nakayama. Mol Cell Biol 2004
48
18

A mutation in the mouse Chd2 chromatin remodeling enzyme results in a complex renal phenotype.
Concetta G A Marfella, Nils Henninger, Scott E LeBlanc, Namrata Krishnan, David S Garlick, Lawrence B Holzman, Anthony N Imbalzano. Kidney Blood Press Res 2008
20
45

Human CHD2 is a chromatin assembly ATPase regulated by its chromo- and DNA-binding domains.
Jessica C Liu, Catarina G Ferreira, Timur Yusufzai. J Biol Chem 2015
21
42

Disruptive CHD8 mutations define a subtype of autism early in development.
Raphael Bernier, Christelle Golzio, Bo Xiong, Holly A Stessman, Bradley P Coe, Osnat Penn, Kali Witherspoon, Jennifer Gerdts, Carl Baker, Anneke T Vulto-van Silfhout,[...]. Cell 2014
386
14

Transcription-coupled recruitment of human CHD1 and CHD2 influences chromatin accessibility and histone H3 and H3.3 occupancy at active chromatin regions.
Lee Siggens, Lina Cordeddu, Michelle Rönnerblad, Andreas Lennartsson, Karl Ekwall. Epigenetics Chromatin 2015
31
29

Phenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human development.
D Sanlaville, H C Etchevers, M Gonzales, J Martinovic, M Clément-Ziza, A-L Delezoide, M-C Aubry, A Pelet, S Chemouny, C Cruaud,[...]. J Med Genet 2006
156
12

Chromatin deacetylation by an ATP-dependent nucleosome remodelling complex.
J K Tong, C A Hassig, G R Schnitzler, R E Kingston, S L Schreiber. Nature 1998
517
12


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.