A citation-based method for searching scientific literature

Cheng Zhang, Lulu Xu, Xueping Zheng, Shiguo Liu, Fengyuan Che. Dev Neurobiol 2021
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


Nuclear punctate distribution of ALL-1 is conferred by distinct elements at the N terminus of the protein.
T Yano, T Nakamura, J Blechman, C Sorio, C V Dang, B Geiger, E Canaani. Proc Natl Acad Sci U S A 1997
82
50



The DNA sequence and biological annotation of human chromosome 1.
S G Gregory, K F Barlow, K E McLay, R Kaul, D Swarbreck, A Dunham, C E Scott, K L Howe, K Woodfine, C C A Spencer,[...]. Nature 2006
126
50



Sequence variants in SLITRK1 are associated with Tourette's syndrome.
Jesse F Abelson, Kenneth Y Kwan, Brian J O'Roak, Danielle Y Baek, Althea A Stillman, Thomas M Morgan, Carol A Mathews, David L Pauls, Mladen-Roko Rasin, Murat Gunel,[...]. Science 2005
641
50

De novo loss-of-function variants of ASH1L are associated with an emergent neurodevelopmental disorder.
Wei Shen, Patti Krautscheid, Audrey M Rutz, Pinar Bayrak-Toydemir, Sarah L Dugan. Eur J Med Genet 2019
8
50


Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome.
Alden Y Huang, Dongmei Yu, Lea K Davis, Jae Hoon Sul, Fotis Tsetsos, Vasily Ramensky, Ivette Zelaya, Eliana Marisa Ramos, Lisa Osiecki, Jason A Chen,[...]. Neuron 2017
71
50

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
219
50


Shared Brain Connectivity Issues, Symptoms, and Comorbidities in Autism Spectrum Disorder, Attention Deficit/Hyperactivity Disorder, and Tourette Syndrome.
Janet K Kern, David A Geier, Paul G King, Lisa K Sykes, Jyutika A Mehta, Mark R Geier. Brain Connect 2015
43
50

Symplekin, a novel type of tight junction plaque protein.
B H Keon, S Schäfer, C Kuhn, C Grund, W W Franke. J Cell Biol 1996
245
50

The hubs of the human connectome are generally implicated in the anatomy of brain disorders.
Nicolas A Crossley, Andrea Mechelli, Jessica Scott, Francesco Carletti, Peter T Fox, Philip McGuire, Edward T Bullmore. Brain 2014
570
50

Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples.
Jack A Kosmicki, Kaitlin E Samocha, Daniel P Howrigan, Stephan J Sanders, Kamil Slowikowski, Monkol Lek, Konrad J Karczewski, David J Cutler, Bernie Devlin, Kathryn Roeder,[...]. Nat Genet 2017
152
50

Gilles de la Tourette syndrome and disruptive behavior disorders: prevalence, associations, and explanation of the relationships.
Mary M Robertson, Andrea E Cavanna, Valsamma Eapen. J Neuropsychiatry Clin Neurosci 2015
29
50

Control networks in paediatric Tourette syndrome show immature and anomalous patterns of functional connectivity.
Jessica A Church, Damien A Fair, Nico U F Dosenbach, Alexander L Cohen, Francis M Miezin, Steven E Petersen, Bradley L Schlaggar. Brain 2009
176
50

Histone Lysine Methylases and Demethylases in the Landscape of Human Developmental Disorders.
Víctor Faundes, William G Newman, Laura Bernardini, Natalie Canham, Jill Clayton-Smith, Bruno Dallapiccola, Sally J Davies, Michelle K Demos, Amy Goldman, Harinder Gill,[...]. Am J Hum Genet 2018
77
50

Neuroimaging Applications in Tourette's Syndrome.
Davide Martino, Christos Ganos, Yulia Worbe. Int Rev Neurobiol 2018
10
50

Familial Risks of Tourette Syndrome and Chronic Tic Disorders. A Population-Based Cohort Study.
David Mataix-Cols, Kayoko Isomura, Ana Pérez-Vigil, Zheng Chang, Christian Rück, K Johan Larsson, James F Leckman, Eva Serlachius, Henrik Larsson, Paul Lichtenstein. JAMA Psychiatry 2015
59
50

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
50

Trithorax and ASH1 interact directly and associate with the trithorax group-responsive bxd region of the Ultrabithorax promoter.
T Rozovskaia, S Tillib, S Smith, Y Sedkov, O Rozenblatt-Rosen, S Petruk, T Yano, T Nakamura, L Ben-Simchon, J Gildea,[...]. Mol Cell Biol 1999
57
50

H3K36 methyltransferases as cancer drug targets: rationale and perspectives for inhibitor development.
David S Rogawski, Jolanta Grembecka, Tomasz Cierpicki. Future Med Chem 2016
15
50

Activity-dependent BDNF release via endocytic pathways is regulated by synaptotagmin-6 and complexin.
Yu-Hui Wong, Chia-Ming Lee, Wenjun Xie, Bianxiao Cui, Mu-ming Poo. Proc Natl Acad Sci U S A 2015
41
50

Mammalian ASH1L is a histone methyltransferase that occupies the transcribed region of active genes.
Gregory D Gregory, Christopher R Vakoc, Tanya Rozovskaia, Xingwu Zheng, Shetal Patel, Tatsuya Nakamura, Eli Canaani, Gerd A Blobel. Mol Cell Biol 2007
126
50

Meta-Analysis of Tourette Syndrome and Attention Deficit Hyperactivity Disorder Provides Support for a Shared Genetic Basis.
Fotis Tsetsos, Shanmukha S Padmanabhuni, John Alexander, Iordanis Karagiannidis, Margaritis Tsifintaris, Apostolia Topaloudi, Dimitrios Mantzaris, Marianthi Georgitsi, Petros Drineas, Peristera Paschou. Front Neurosci 2016
15
50

The genetic basis of Gilles de la Tourette Syndrome.
Peristera Paschou. Neurosci Biobehav Rev 2013
56
50

Trithorax group proteins: switching genes on and keeping them active.
Bernd Schuettengruber, Anne-Marie Martinez, Nicola Iovino, Giacomo Cavalli. Nat Rev Mol Cell Biol 2011
274
50

Familial clustering of tic disorders and obsessive-compulsive disorder.
Heidi A Browne, Stefan N Hansen, Joseph D Buxbaum, Shannon L Gair, Judith B Nissen, Kathrine H Nikolajsen, Diana E Schendel, Abraham Reichenberg, Erik T Parner, Dorothy E Grice. JAMA Psychiatry 2015
33
50

The bromodomain: a chromatin-targeting module?
F Winston, C D Allis. Nat Struct Biol 1999
207
50

Widespread abnormality of the γ-aminobutyric acid-ergic system in Tourette syndrome.
Alicja Lerner, Anto Bagic, Janine M Simmons, Zoltan Mari, Omer Bonne, Ben Xu, Diane Kazuba, Peter Herscovitch, Richard E Carson, Dennis L Murphy,[...]. Brain 2012
109
50

Trithorax-group protein ASH1 methylates histone H3 lysine 36.
Yujiro Tanaka, Zen-Ichiro Katagiri, Koji Kawahashi, Dimitris Kioussis, Shigetaka Kitajima. Gene 2007
107
50


Antagonism between MES-4 and Polycomb repressive complex 2 promotes appropriate gene expression in C. elegans germ cells.
Laura J Gaydos, Andreas Rechtsteiner, Thea A Egelhofer, Coleen R Carroll, Susan Strome. Cell Rep 2012
83
50

Novel MCA/ID syndrome with ASH1L mutation.
Nobuhiko Okamoto, Fuyuki Miya, Tatsuhiko Tsunoda, Mitsuhiro Kato, Shinji Saitoh, Mami Yamasaki, Yonehiro Kanemura, Kenjiro Kosaki. Am J Med Genet A 2017
8
50

Lifetime prevalence, age of risk, and genetic relationships of comorbid psychiatric disorders in Tourette syndrome.
Matthew E Hirschtritt, Paul C Lee, David L Pauls, Yves Dion, Marco A Grados, Cornelia Illmann, Robert A King, Paul Sandor, William M McMahon, Gholson J Lyon,[...]. JAMA Psychiatry 2015
225
50

Unleashing the Power of ASH1L Methyltransferase.
Inessa De, Christoph W Müller. Structure 2019
1
100

Histone H3K36 mutations promote sarcomagenesis through altered histone methylation landscape.
Chao Lu, Siddhant U Jain, Dominik Hoelper, Denise Bechet, Rosalynn C Molden, Leili Ran, Devan Murphy, Sriram Venneti, Meera Hameed, Bruce R Pawel,[...]. Science 2016
185
50


Autism and the synapse: emerging mechanisms and mechanism-based therapies.
Darius Ebrahimi-Fakhari, Mustafa Sahin. Curr Opin Neurol 2015
90
50

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
310
50

Mrg15 stimulates Ash1 H3K36 methyltransferase activity and facilitates Ash1 Trithorax group protein function in Drosophila.
Chang Huang, Fu Yang, Zhuqiang Zhang, Jing Zhang, Gaihong Cai, Lin Li, Yong Zheng, She Chen, Rongwen Xi, Bing Zhu. Nat Commun 2017
21
50

Dual function of histone H3 lysine 36 methyltransferase ASH1 in regulation of Hox gene expression.
Yujiro Tanaka, Koji Kawahashi, Zen-Ichiro Katagiri, Yasuhiro Nakayama, Milind Mahajan, Dimitris Kioussis. PLoS One 2011
29
50


The Inheritance of Tourette Disorder: A review.
David L Pauls, Thomas V Fernandez, Carol A Mathews, Matthew W State, Jeremiah M Scharf. J Obsessive Compuls Relat Disord 2014
40
50

Dendritic spine pathology in schizophrenia.
J R Glausier, D A Lewis. Neuroscience 2013
291
50

Acute BDNF and cortisol response to low intensity exercise and following ramp incremental exercise to exhaustion in humans.
Sandra Rojas Vega, Heiko K Strüder, Bertha Vera Wahrmann, Annette Schmidt, Wilhelm Bloch, Wildor Hollmann. Brain Res 2006
217
50

Excess of rare, inherited truncating mutations in autism.
Niklas Krumm, Tychele N Turner, Carl Baker, Laura Vives, Kiana Mohajeri, Kali Witherspoon, Archana Raja, Bradley P Coe, Holly A Stessman, Zong-Xiao He,[...]. Nat Genet 2015
274
50



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.