A citation-based method for searching scientific literature

Beate Peter, Valentin Dinu, Li Liu, Matthew Huentelman, Marcus Naymik, Hope Lancaster, Caitlin Vose, Isabelle Schrauwen. Behav Genet 2019
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex Families.
Virpi M Leppa, Stephanie N Kravitz, Christa Lese Martin, Joris Andrieux, Cedric Le Caignec, Dominique Martin-Coignard, Christina DyBuncio, Stephan J Sanders, Jennifer K Lowe, Rita M Cantor,[...]. Am J Hum Genet 2016
75
75


Loss of Wwox Perturbs Neuronal Migration and Impairs Early Cortical Development.
Michele Iacomino, Simona Baldassari, Yuki Tochigi, Katarzyna Kośla, Francesca Buffelli, Annalaura Torella, Mariasavina Severino, Dario Paladini, Luana Mandarà, Antonella Riva,[...]. Front Neurosci 2020
4
50

WWOX Phosphorylation, Signaling, and Role in Neurodegeneration.
Chan-Chuan Liu, Pei-Chuan Ho, I-Ting Lee, Yu-An Chen, Chun-Hsien Chu, Chih-Chuan Teng, Sheng-Nan Wu, Chun-I Sze, Ming-Fu Chiang, Nan-Shan Chang. Front Neurosci 2018
18
50

WWOX protein expression in normal human tissues.
Maria I Nunez, John Ludes-Meyers, C Marcelo Aldaz. J Mol Histol 2006
54
50

A new form of childhood onset, autosomal recessive spinocerebellar ataxia and epilepsy is localized at 16q21-q23.
M Gribaa, M Salih, M Anheim, C Lagier-Tourenne, D H'mida, N Drouot, A Mohamed, S Elmalik, M Kabiraj, M Al-Rayess,[...]. Brain 2007
29
50

C6orf10 Low-Frequency and Rare Variants in Italian Multiple Sclerosis Patients.
Nicole Ziliotto, Giovanna Marchetti, Chiara Scapoli, Matteo Bovolenta, Silvia Meneghetti, Andrea Benazzo, Barbara Lunghi, Dario Balestra, Lorenza Anna Laino, Nicolò Bozzini,[...]. Front Genet 2019
4
50


Novel Homozygous Mutation in the WWOX Gene Causes Seizures and Global Developmental Delay: Report and Review.
Salleh N Ehaideb, Majed J Al-Bu Ali, Jaafer J Al-Obaid, Kareemah M Aljassim, Majid Alfadhel. Transl Neurosci 2018
9
50

The tumour suppressor gene WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardation.
Martial Mallaret, Matthis Synofzik, Jaeho Lee, Cari A Sagum, Muhammad Mahajnah, Rajech Sharkia, Nathalie Drouot, Mathilde Renaud, Fabrice A C Klein, Mathieu Anheim,[...]. Brain 2014
67
50

A spontaneous mutation of the Wwox gene and audiogenic seizures in rats with lethal dwarfism and epilepsy.
H Suzuki, K Katayama, M Takenaka, K Amakasu, K Saito, K Suzuki. Genes Brain Behav 2009
52
50

Loss of Wwox Causes Defective Development of Cerebral Cortex with Hypomyelination in a Rat Model of Lethal Dwarfism with Epilepsy.
Yuki Tochigi, Yutaka Takamatsu, Jun Nakane, Rika Nakai, Kentaro Katayama, Hiroetsu Suzuki. Int J Mol Sci 2019
8
50

The phenotypic spectrum of WWOX-related disorders: 20 additional cases of WOREE syndrome and review of the literature.
Juliette Piard, Lara Hawkes, Mathieu Milh, Laurent Villard, Renato Borgatti, Romina Romaniello, Melanie Fradin, Yline Capri, Delphine Héron, Marie-Christine Nougues,[...]. Genet Med 2019
16
50

Wwox deletion leads to reduced GABA-ergic inhibitory interneuron numbers and activation of microglia and astrocytes in mouse hippocampus.
Tabish Hussain, Hyunsuk Kil, Bharathi Hattiangady, Jaeho Lee, Maheedhar Kodali, Bing Shuai, Sahithi Attaluri, Yoko Takata, Jianjun Shen, Martin C Abba,[...]. Neurobiol Dis 2019
14
50

Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing.
Brian W Kunkle, Benjamin Grenier-Boley, Rebecca Sims, Joshua C Bis, Vincent Damotte, Adam C Naj, Anne Boland, Maria Vronskaya, Sven J van der Lee, Alexandre Amlie-Wolf,[...]. Nat Genet 2019
562
50

WWOX-related encephalopathies: delineation of the phenotypical spectrum and emerging genotype-phenotype correlation.
Cyril Mignot, Laetitia Lambert, Laurent Pasquier, Thierry Bienvenu, Andrée Delahaye-Duriez, Boris Keren, Jérémie Lefranc, Aline Saunier, Lila Allou, Virginie Roth,[...]. J Med Genet 2015
44
50


Genetic associations with brain cortical thickness in multiple sclerosis.
T Matsushita, L Madireddy, T Sprenger, P Khankhanian, S Magon, Y Naegelin, E Caverzasi, R L P Lindberg, L Kappos, S L Hauser,[...]. Genes Brain Behav 2015
19
50

Altered human oligodendrocyte heterogeneity in multiple sclerosis.
Sarah Jäkel, Eneritz Agirre, Ana Mendanha Falcão, David van Bruggen, Ka Wai Lee, Irene Knuesel, Dheeraj Malhotra, Charles Ffrench-Constant, Anna Williams, Gonçalo Castelo-Branco. Nature 2019
176
50

Down-regulation of WW domain-containing oxidoreductase induces Tau phosphorylation in vitro. A potential role in Alzheimer's disease.
Chun-I Sze, Meng Su, Subbiah Pugazhenthi, Purevsuren Jambal, Li-Jin Hsu, John Heath, Lori Schultz, Nan-Shan Chang. J Biol Chem 2004
91
50

Wwox deficiency leads to neurodevelopmental and degenerative neuropathies and glycogen synthase kinase 3β-mediated epileptic seizure activity in mice.
Ya-Yun Cheng, Ying-Tsen Chou, Feng-Jie Lai, Ming-Shiou Jan, Tsung-Hao Chang, I-Ming Jou, Pei-Shiuan Chen, Jui-Yen Lo, Shiang-Suo Huang, Nan-Shan Chang,[...]. Acta Neuropathol Commun 2020
8
50

Genome-wide association analysis identifies common variants influencing infant brain volumes.
K Xia, J Zhang, M Ahn, S Jha, J J Crowley, J Szatkiewicz, T Li, F Zou, H Zhu, D Hibar,[...]. Transl Psychiatry 2017
17
50

An integrated analysis of rare CNV and exome variation in Autism Spectrum Disorder using the Infinium PsychArray.
Elena Bacchelli, Cinzia Cameli, Marta Viggiano, Roberta Igliozzi, Alice Mancini, Raffaella Tancredi, Agatino Battaglia, Elena Maestrini. Sci Rep 2020
6
50

WWOX at the crossroads of cancer, metabolic syndrome related traits and CNS pathologies.
C Marcelo Aldaz, Brent W Ferguson, Martin C Abba. Biochim Biophys Acta 2014
65
50

Expression of WW domain-containing oxidoreductase WOX1 in the developing murine nervous system.
S T Chen, J I Chuang, J P Wang, M S Tsai, H Li, N-S Chang. Neuroscience 2004
45
50

Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis.
Ashley H Beecham, Nikolaos A Patsopoulos, Dionysia K Xifara, Mary F Davis, Anu Kemppinen, Chris Cotsapas, Tejas S Shah, Chris Spencer, David Booth, An Goris,[...]. Nat Genet 2013
791
50

The tumor suppressor gene WWOX links the canonical and noncanonical NF-κB pathways in HTLV-I Tax-mediated tumorigenesis.
Jing Fu, Zhaoxia Qu, Pengrong Yan, Chie Ishikawa, Rami I Aqeilan, Arnold B Rabson, Gutian Xiao. Blood 2011
54
50

Towards a theory of biological robustness.
Hiroaki Kitano. Mol Syst Biol 2007
328
25


A large-scale complex haploinsufficiency-based genetic interaction screen in Candida albicans: analysis of the RAM network during morphogenesis.
Nike Bharucha, Yeissa Chabrier-Rosello, Tao Xu, Cole Johnson, Sarah Sobczynski, Qingxuan Song, Craig J Dobry, Matthew J Eckwahl, Christopher P Anderson, Andrew J Benjamin,[...]. PLoS Genet 2011
40
25

De novo missense variants in PPP2R5D are associated with intellectual disability, macrocephaly, hypotonia, and autism.
Linshan Shang, Lindsay B Henderson, Megan T Cho, Donald S Petrey, Chin-To Fong, Katrina M Haude, Natasha Shur, Julie Lundberg, Natalie Hauser, Jason Carmichael,[...]. Neurogenetics 2016
30
25

Harnessing synthetic lethal interactions in anticancer drug discovery.
Denise A Chan, Amato J Giaccia. Nat Rev Drug Discov 2011
182
25

Germline Chd8 haploinsufficiency alters brain development in mouse.
Andrea L Gompers, Linda Su-Feher, Jacob Ellegood, Nycole A Copping, M Asrafuzzaman Riyadh, Tyler W Stradleigh, Michael C Pride, Melanie D Schaffler, A Ayanna Wade, Rinaldo Catta-Preta,[...]. Nat Neurosci 2017
99
25

Mechanisms underlying the rapid induction and sustained expression of synaptic homeostasis.
C Andrew Frank, Matthew J Kennedy, Carleton P Goold, Kurt W Marek, Graeme W Davis. Neuron 2006
246
25


Firing rate homeostasis in visual cortex of freely behaving rodents.
Keith B Hengen, Mary E Lambo, Stephen D Van Hooser, Donald B Katz, Gina G Turrigiano. Neuron 2013
157
25

Homeostatic Plasticity and STDP: Keeping a Neuron's Cool in a Fluctuating World.
Alanna J Watt, Niraj S Desai. Front Synaptic Neurosci 2010
81
25


RIM controls homeostatic plasticity through modulation of the readily-releasable vesicle pool.
Martin Müller, Karen Suk Yin Liu, Stephan J Sigrist, Graeme W Davis. J Neurosci 2012
113
25

AKT/PKB Signaling: Navigating the Network.
Brendan D Manning, Alex Toker. Cell 2017
25

Mutations in the PP2A regulatory subunit B family genes PPP2R5B, PPP2R5C and PPP2R5D cause human overgrowth.
Chey Loveday, Katrina Tatton-Brown, Matthew Clarke, Isaac Westwood, Anthony Renwick, Emma Ramsay, Andrea Nemeth, Jennifer Campbell, Shelagh Joss, McKinlay Gardner,[...]. Hum Mol Genet 2015
41
25

A postsynaptic PI3K-cII dependent signaling controller for presynaptic homeostatic plasticity.
Anna G Hauswirth, Kevin J Ford, Tingting Wang, Richard D Fetter, Amy Tong, Graeme W Davis. Elife 2018
12
25

Proteome-wide search for PP2A substrates in fission yeast.
Manuel Bernal, Jacob Zhurinsky, Ana B Iglesias-Romero, Maria A Sanchez-Romero, Ignacio Flor-Parra, Laura Tomas-Gallardo, Antonio J Perez-Pulido, Juan Jimenez, Rafael R Daga. Proteomics 2014
6
25

TOR is required for the retrograde regulation of synaptic homeostasis at the Drosophila neuromuscular junction.
Jay Penney, Kazuya Tsurudome, Edward H Liao, Fatima Elazzouzi, Mark Livingstone, Miranda Gonzalez, Nahum Sonenberg, A Pejmun Haghighi. Neuron 2012
63
25

Principles for the buffering of genetic variation.
J L Hartman, B Garvik, L Hartwell. Science 2001
516
25

The contribution of de novo coding mutations to autism spectrum disorder.
Ivan Iossifov, Brian J O'Roak, Stephan J Sanders, Michael Ronemus, Niklas Krumm, Dan Levy, Holly A Stessman, Kali T Witherspoon, Laura Vives, Karynne E Patterson,[...]. Nature 2014
25


Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci.
Stephan J Sanders, Xin He, A Jeremy Willsey, A Gulhan Ercan-Sencicek, Kaitlin E Samocha, A Ercument Cicek, Michael T Murtha, Vanessa H Bal, Somer L Bishop, Shan Dong,[...]. Neuron 2015
601
25

Local presynaptic activity gates homeostatic changes in presynaptic function driven by dendritic BDNF synthesis.
Sonya K Jakawich, Hassan B Nasser, Michael J Strong, Amber J McCartney, Amanda S Perez, Neal Rakesh, Cynthia J L Carruthers, Michael A Sutton. Neuron 2010
121
25

PP2A and GSK-3beta act antagonistically to regulate active zone development.
Natasha M Viquez, Petra Füger, Vera Valakh, Richard W Daniels, Tobias M Rasse, Aaron DiAntonio. J Neurosci 2009
26
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.