A citation-based method for searching scientific literature

Anke Hoffmann, Dietmar Spengler. Front Genet 2019
Times Cited: 22







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



Times Cited
  Times     Co-cited
Similarity


Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.
Brian J O'Roak, Laura Vives, Santhosh Girirajan, Emre Karakoc, Niklas Krumm, Bradley P Coe, Roie Levy, Arthur Ko, Choli Lee, Joshua D Smith,[...]. Nature 2012
18

The Nucleosome Remodeling and Deacetylation Complex Modulates Chromatin Structure at Sites of Active Transcription to Fine-Tune Gene Expression.
Susanne Bornelöv, Nicola Reynolds, Maria Xenophontos, Sarah Gharbi, Ewan Johnstone, Robin Floyd, Meryem Ralser, Jason Signolet, Remco Loos, Sabine Dietmann,[...]. Mol Cell 2018
70
18

The chromatin remodeling enzyme Chd4 regulates genome architecture in the mouse brain.
Jared V Goodman, Tomoko Yamada, Yue Yang, Lingchun Kong, Dennis Y Wu, Guoyan Zhao, Harrison W Gabel, Azad Bonni. Nat Commun 2020
15
26

The structure of the core NuRD repression complex provides insights into its interaction with chromatin.
Christopher J Millard, Niranjan Varma, Almutasem Saleh, Kyle Morris, Peter J Watson, Andrew R Bottrill, Louise Fairall, Corinne J Smith, John W R Schwabe. Elife 2016
72
18

Genetic variation in the epigenetic machinery and mental health.
Chris Murgatroyd, Dietmar Spengler. Curr Psychiatry Rep 2012
27
13

Progress in iPSC-Based Modeling of Psychiatric Disorders.
Anke Hoffmann, Michael Ziller, Dietmar Spengler. Int J Mol Sci 2019
24
13

CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.
Lot Snijders Blok, Justine Rousseau, Joanna Twist, Sophie Ehresmann, Motoki Takaku, Hanka Venselaar, Lance H Rodan, Catherine B Nowak, Jessica Douglas, Kathryn J Swoboda,[...]. Nat Commun 2018
41
13

Synaptic, transcriptional and chromatin genes disrupted in autism.
Silvia De Rubeis, Xin He, Arthur P Goldberg, Christopher S Poultney, Kaitlin Samocha, A Erucment Cicek, Yan Kou, Li Liu, Menachem Fromer, Susan Walker,[...]. Nature 2014
13

Mechanisms of action and regulation of ATP-dependent chromatin-remodelling complexes.
Cedric R Clapier, Janet Iwasa, Bradley R Cairns, Craig L Peterson. Nat Rev Mol Cell Biol 2017
438
13

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
792
13

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
13

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
430
13

Analysis of the NuRD subunits reveals a histone deacetylase core complex and a connection with DNA methylation.
Y Zhang, H H Ng, H Erdjument-Bromage, P Tempst, A Bird, D Reinberg. Genes Dev 1999
877
13

Promoter decommissioning by the NuRD chromatin remodeling complex triggers synaptic connectivity in the mammalian brain.
Tomoko Yamada, Yue Yang, Martin Hemberg, Toshimi Yoshida, Ha Young Cho, J Patrick Murphy, Diasynou Fioravante, Wade G Regehr, Steven P Gygi, Katia Georgopoulos,[...]. Neuron 2014
61
13

FOG-1 recruits the NuRD repressor complex to mediate transcriptional repression by GATA-1.
Wei Hong, Minako Nakazawa, Ying-Yu Chen, Rajashree Kori, Christopher R Vakoc, Carrie Rakowski, Gerd A Blobel. EMBO J 2005
210
13

De novo variants in the Helicase-C domain of CHD8 are associated with severe phenotypes including autism, language disability and overgrowth.
Yu An, Linna Zhang, Wenwen Liu, Yunyun Jiang, Xue Chen, Xiaoping Lan, Gan Li, Qiang Hang, Jian Wang, James F Gusella,[...]. Hum Genet 2020
15
20

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
425
13

Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases.
Holly A F Stessman, Bo Xiong, Bradley P Coe, Tianyun Wang, Kendra Hoekzema, Michaela Fenckova, Malin Kvarnung, Jennifer Gerdts, Sandy Trinh, Nele Cosemans,[...]. Nat Genet 2017
285
13

A distinct neurodevelopmental syndrome with intellectual disability, autism spectrum disorder, characteristic facies, and macrocephaly is caused by defects in CHD8.
Heba Yasin, William T Gibson, Sylvie Langlois, Robert M Stowe, Erica S Tsang, Leora Lee, Jenny Poon, Grant Tran, Christine Tyson, Chi Kin Wong,[...]. J Hum Genet 2019
19
15

De novo genic mutations among a Chinese autism spectrum disorder cohort.
Tianyun Wang, Hui Guo, Bo Xiong, Holly A F Stessman, Huidan Wu, Bradley P Coe, Tychele N Turner, Yanling Liu, Wenjing Zhao, Kendra Hoekzema,[...]. Nat Commun 2016
183
13

De novo mutations revealed by whole-exome sequencing are strongly associated with autism.
Stephan J Sanders, Michael T Murtha, Abha R Gupta, John D Murdoch, Melanie J Raubeson, A Jeremy Willsey, A Gulhan Ercan-Sencicek, Nicholas M DiLullo, Neelroop N Parikshak, Jason L Stein,[...]. Nature 2012
13


BCL11B functionally associates with the NuRD complex in T lymphocytes to repress targeted promoter.
Valeriu B Cismasiu, Karen Adamo, Jennifer Gecewicz, Javier Duque, Qishan Lin, Dorina Avram. Oncogene 2005
125
13

Fast gapped-read alignment with Bowtie 2.
Ben Langmead, Steven L Salzberg. Nat Methods 2012
13

MBD2/NuRD and MBD3/NuRD, two distinct complexes with different biochemical and functional properties.
Xavier Le Guezennec, Michiel Vermeulen, Arie B Brinkman, Wieteke A M Hoeijmakers, Adrian Cohen, Edwin Lasonder, Hendrik G Stunnenberg. Mol Cell Biol 2006
241
13

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
13

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
636
13

Super-enhancers in the control of cell identity and disease.
Denes Hnisz, Brian J Abraham, Tong Ihn Lee, Ashley Lau, Violaine Saint-André, Alla A Sigova, Heather A Hoke, Richard A Young. Cell 2013
13

Histone H3K27ac separates active from poised enhancers and predicts developmental state.
Menno P Creyghton, Albert W Cheng, G Grant Welstead, Tristan Kooistra, Bryce W Carey, Eveline J Steine, Jacob Hanna, Michael A Lodato, Garrett M Frampton, Phillip A Sharp,[...]. Proc Natl Acad Sci U S A 2010
13

Complex Oscillatory Waves Emerging from Cortical Organoids Model Early Human Brain Network Development.
Cleber A Trujillo, Richard Gao, Priscilla D Negraes, Jing Gu, Justin Buchanan, Sebastian Preissl, Allen Wang, Wei Wu, Gabriel G Haddad, Isaac A Chaim,[...]. Cell Stem Cell 2019
256
9

An in vivo model of functional and vascularized human brain organoids.
Abed AlFatah Mansour, J Tiago Gonçalves, Cooper W Bloyd, Hao Li, Sarah Fernandes, Daphne Quang, Stephen Johnston, Sarah L Parylak, Xin Jin, Fred H Gage. Nat Biotechnol 2018
467
9

A Single-Cell Transcriptomic Atlas of Human Neocortical Development during Mid-gestation.
Damon Polioudakis, Luis de la Torre-Ubieta, Justin Langerman, Andrew G Elkins, Xu Shi, Jason L Stein, Celine K Vuong, Susanne Nichterwitz, Melinda Gevorgian, Carli K Opland,[...]. Neuron 2019
152
9

Individual brain organoids reproducibly form cell diversity of the human cerebral cortex.
Silvia Velasco, Amanda J Kedaigle, Sean K Simmons, Allison Nash, Marina Rocha, Giorgia Quadrato, Bruna Paulsen, Lan Nguyen, Xian Adiconis, Aviv Regev,[...]. Nature 2019
343
9

New considerations for hiPSC-based models of neuropsychiatric disorders.
Gabriel E Hoffman, Nadine Schrode, Erin Flaherty, Kristen J Brennand. Mol Psychiatry 2019
46
9

Cell diversity and network dynamics in photosensitive human brain organoids.
Giorgia Quadrato, Tuan Nguyen, Evan Z Macosko, John L Sherwood, Sung Min Yang, Daniel R Berger, Natalie Maria, Jorg Scholvin, Melissa Goldman, Justin P Kinney,[...]. Nature 2017
568
9


Childhood-Onset Schizophrenia: Insights from Induced Pluripotent Stem Cells.
Anke Hoffmann, Michael Ziller, Dietmar Spengler. Int J Mol Sci 2018
14
14



The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin-Siris syndrome.
Pleuntje J van der Sluijs, Sandra Jansen, Samantha A Vergano, Miho Adachi-Fukuda, Yasemin Alanay, Adila AlKindy, Anwar Baban, Allan Bayat, Stefanie Beck-Wödl, Katherine Berry,[...]. Genet Med 2019
45
9

Mice lacking the chromodomain helicase DNA-binding 5 chromatin remodeler display autism-like characteristics.
M T Pisansky, A E Young, M B O'Connor, I I Gottesman, A Bagchi, J C Gewirtz. Transl Psychiatry 2017
16
12

Mutations in SWI/SNF chromatin remodeling complex gene ARID1B cause Coffin-Siris syndrome.
Gijs W E Santen, Emmelien Aten, Yu Sun, Rowida Almomani, Christian Gilissen, Maartje Nielsen, Sarina G Kant, Irina N Snoeck, Els A J Peeters, Yvonne Hilhorst-Hofstee,[...]. Nat Genet 2012
237
9

Mutations in ARID2 are associated with intellectual disabilities.
Linshan Shang, Megan T Cho, Kyle Retterer, Leandra Folk, Jennifer Humberson, Luis Rohena, Alpa Sidhu, Sheila Saliganan, Alejandro Iglesias, Patrik Vitazka,[...]. Neurogenetics 2015
38
9

Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism.
F Kyle Satterstrom, Jack A Kosmicki, Jiebiao Wang, Michael S Breen, Silvia De Rubeis, Joon-Yong An, Minshi Peng, Ryan Collins, Jakob Grove, Lambertus Klei,[...]. Cell 2020
642
9

An essential switch in subunit composition of a chromatin remodeling complex during neural development.
Julie Lessard, Jiang I Wu, Jeffrey A Ranish, Mimi Wan, Monte M Winslow, Brett T Staahl, Hai Wu, Ruedi Aebersold, Isabella A Graef, Gerald R Crabtree. Neuron 2007
493
9

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
162
9

A Functional Switch of NuRD Chromatin Remodeling Complex Subunits Regulates Mouse Cortical Development.
Justyna Nitarska, Jacob G Smith, William T Sherlock, Michele M G Hillege, Alexi Nott, William D Barshop, Ajay A Vashisht, James A Wohlschlegel, Richard Mitter, Antonella Riccio. Cell Rep 2016
72
9

Mutations in the BAF-Complex Subunit DPF2 Are Associated with Coffin-Siris Syndrome.
Georgia Vasileiou, Silvia Vergarajauregui, Sabine Endele, Bernt Popp, Christian Büttner, Arif B Ekici, Marion Gerard, Nuria C Bramswig, Beate Albrecht, Jill Clayton-Smith,[...]. Am J Hum Genet 2018
44
9

Expanding the Spectrum of BAF-Related Disorders: De Novo Variants in SMARCC2 Cause a Syndrome with Intellectual Disability and Developmental Delay.
Keren Machol, Justine Rousseau, Sophie Ehresmann, Thomas Garcia, Thi Tuyet Mai Nguyen, Rebecca C Spillmann, Jennifer A Sullivan, Vandana Shashi, Yong-Hui Jiang, Nicholas Stong,[...]. Am J Hum Genet 2019
32
9

Heterozygous missense mutations in SMARCA2 cause Nicolaides-Baraitser syndrome.
Jeroen K J Van Houdt, Beata Anna Nowakowska, Sérgio B Sousa, Barbera D C van Schaik, Eve Seuntjens, Nelson Avonce, Alejandro Sifrim, Omar A Abdul-Rahman, Marie-José H van den Boogaard, Armand Bottani,[...]. Nat Genet 2012
162
9


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.