A citation-based method for searching scientific literature

Smita Yadav, Juan A Oses-Prieto, Christian J Peters, Jing Zhou, Samuel J Pleasure, Alma L Burlingame, Lily Y Jan, Yuh-Nung Jan. Neuron 2017
Times Cited: 54







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



Times Cited
  Times     Co-cited
Similarity


Association between microdeletion and microduplication at 16p11.2 and autism.
Lauren A Weiss, Yiping Shen, Joshua M Korn, Dan E Arking, David T Miller, Ragnheidur Fossdal, Evald Saemundsen, Hreinn Stefansson, Manuel A R Ferreira, Todd Green,[...]. N Engl J Med 2008
37

Autism spectrum disorder susceptibility gene TAOK2 affects basal dendrite formation in the neocortex.
Froylan Calderon de Anda, Ana Lucia Rosario, Omer Durak, Tracy Tran, Johannes Gräff, Konstantinos Meletis, Damien Rei, Takahiro Soda, Ram Madabhushi, David D Ginty,[...]. Nat Neurosci 2012
99
31

Altered TAOK2 activity causes autism-related neurodevelopmental and cognitive abnormalities through RhoA signaling.
Melanie Richter, Nadeem Murtaza, Robin Scharrenberg, Sean H White, Ole Johanns, Susan Walker, Ryan K C Yuen, Birgit Schwanke, Bianca Bedürftig, Melad Henis,[...]. Mol Psychiatry 2019
46
32

Microduplications of 16p11.2 are associated with schizophrenia.
Shane E McCarthy, Vladimir Makarov, George Kirov, Anjene M Addington, Jon McClellan, Seungtai Yoon, Diana O Perkins, Diane E Dickel, Mary Kusenda, Olga Krastoshevsky,[...]. Nat Genet 2009
478
24

MST3 kinase phosphorylates TAO1/2 to enable Myosin Va function in promoting spine synapse development.
Sila K Ultanir, Smita Yadav, Nicholas T Hertz, Juan A Oses-Prieto, Suzanne Claxton, Alma L Burlingame, Kevan M Shokat, Lily Y Jan, Yuh-Nung Jan. Neuron 2014
37
35

The GTP-binding protein Septin 7 is critical for dendrite branching and dendritic-spine morphology.
Yunli Xie, John P Vessey, Anetta Konecna, Ralf Dahm, Paolo Macchi, Michael A Kiebler. Curr Biol 2007
174
22

Role of Septin cytoskeleton in spine morphogenesis and dendrite development in neurons.
Tomoko Tada, Alyson Simonetta, Matthew Batterton, Makoto Kinoshita, Dieter Edbauer, Morgan Sheng. Curr Biol 2007
191
22

KCTD13 is a major driver of mirrored neuroanatomical phenotypes of the 16p11.2 copy number variant.
Christelle Golzio, Jason Willer, Michael E Talkowski, Edwin C Oh, Yu Taniguchi, Sébastien Jacquemont, Alexandre Reymond, Mei Sun, Akira Sawa, James F Gusella,[...]. Nature 2012
235
20

Behavioral abnormalities and circuit defects in the basal ganglia of a mouse model of 16p11.2 deletion syndrome.
Thomas Portmann, Mu Yang, Rong Mao, Georgia Panagiotakos, Jacob Ellegood, Gul Dolen, Patrick L Bader, Brad A Grueter, Carleton Goold, Elaine Fisher,[...]. Cell Rep 2014
114
20


Dosage-dependent phenotypes in models of 16p11.2 lesions found in autism.
Guy Horev, Jacob Ellegood, Jason P Lerch, Young-Eun E Son, Lakshmi Muthuswamy, Hannes Vogel, Abba M Krieger, Andreas Buja, R Mark Henkelman, Michael Wigler,[...]. Proc Natl Acad Sci U S A 2011
170
18

Dendritic spine pathology in neuropsychiatric disorders.
Peter Penzes, Michael E Cahill, Kelly A Jones, Jon-Eric VanLeeuwen, Kevin M Woolfrey. Nat Neurosci 2011
864
16

Kctd13 deletion reduces synaptic transmission via increased RhoA.
Christine Ochoa Escamilla, Irina Filonova, Angela K Walker, Zhong X Xuan, Roopashri Holehonnur, Felipe Espinosa, Shunan Liu, Summer B Thyme, Isabel A López-García, Dorian B Mendoza,[...]. Nature 2017
49
18

The 16p11.2 deletion mouse model of autism exhibits altered cortical progenitor proliferation and brain cytoarchitecture linked to the ERK MAPK pathway.
Joanna Pucilowska, Joseph Vithayathil, Emmanuel J Tavares, Caitlin Kelly, J Colleen Karlo, Gary E Landreth. J Neurosci 2015
82
14

Recurrent 16p11.2 microdeletions in autism.
Ravinesh A Kumar, Samer KaraMohamed, Jyotsna Sudi, Donald F Conrad, Camille Brune, Judith A Badner, T Conrad Gilliam, Norma J Nowak, Edwin H Cook, William B Dobyns,[...]. Hum Mol Genet 2008
461
14



Opposing brain differences in 16p11.2 deletion and duplication carriers.
Abid Y Qureshi, Sophia Mueller, Abraham Z Snyder, Pratik Mukherjee, Jeffrey I Berman, Timothy P L Roberts, Srikantan S Nagarajan, John E Spiro, Wendy K Chung, Elliott H Sherr,[...]. J Neurosci 2014
90
12

Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size.
Marwan Shinawi, Pengfei Liu, Sung-Hae L Kang, Joseph Shen, John W Belmont, Daryl A Scott, Frank J Probst, William J Craigen, Brett H Graham, Amber Pursley,[...]. J Med Genet 2010
317
12

A Septin-Dependent Diffusion Barrier at Dendritic Spine Necks.
Helge Ewers, Tomoko Tada, Jennifer D Petersen, Bence Racz, Morgan Sheng, Daniel Choquet. PLoS One 2014
51
13

Prostate-derived sterile 20-like kinases (PSKs/TAOKs) phosphorylate tau protein and are activated in tangle-bearing neurons in Alzheimer disease.
Ignatius A Tavares, Dona Touma, Steven Lynham, Claire Troakes, Megan Schober, Mirsada Causevic, Ritu Garg, Wendy Noble, Richard Killick, Istvan Bodi,[...]. J Biol Chem 2013
38
18

Tao-1 is a negative regulator of microtubule plus-end growth.
Tao Liu, Jennifer L Rohn, Remigio Picone, Patricia Kunda, Buzz Baum. J Cell Sci 2010
33
21

Septin-driven coordination of actin and microtubule remodeling regulates the collateral branching of axons.
Jianli Hu, Xiaobo Bai, Jonathan R Bowen, Lee Dolat, Farida Korobova, Wenqian Yu, Peter W Baas, Tatyana Svitkina, Gianluca Gallo, Elias T Spiliotis. Curr Biol 2012
85
12

Reversal of dendritic phenotypes in 16p11.2 microduplication mouse model neurons by pharmacological targeting of a network hub.
Katherine D Blizinsky, Blanca Diaz-Castro, Marc P Forrest, Britta Schürmann, Anthony P Bach, Maria Dolores Martin-de-Saavedra, Lei Wang, John G Csernansky, Jubao Duan, Peter Penzes. Proc Natl Acad Sci U S A 2016
32
21

Septins: the fourth component of the cytoskeleton.
Serge Mostowy, Pascale Cossart. Nat Rev Mol Cell Biol 2012
400
12

Genetic deletion of SEPT7 reveals a cell type-specific role of septins in microtubule destabilization for the completion of cytokinesis.
Manoj B Menon, Akihiro Sawada, Anuhar Chaturvedi, Pooja Mishra, Karin Schuster-Gossler, Melanie Galla, Axel Schambach, Achim Gossler, Reinhold Förster, Michael Heuser,[...]. PLoS Genet 2014
55
12


A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders.
Flore Zufferey, Elliott H Sherr, Noam D Beckmann, Ellen Hanson, Anne M Maillard, Loyse Hippolyte, Aurélien Macé, Carina Ferrari, Zoltán Kutalik, Joris Andrieux,[...]. J Med Genet 2012
154
11

The 16p11.2 locus modulates brain structures common to autism, schizophrenia and obesity.
A M Maillard, A Ruef, F Pizzagalli, E Migliavacca, L Hippolyte, S Adaszewski, J Dukart, C Ferrari, P Conus, K Männik,[...]. Mol Psychiatry 2015
93
11

16p11.2 deletion and duplication: Characterizing neurologic phenotypes in a large clinically ascertained cohort.
Kyle J Steinman, Sarah J Spence, Melissa B Ramocki, Monica B Proud, Sudha K Kessler, Elysa J Marco, LeeAnne Green Snyder, Debra D'Angelo, Qixuan Chen, Wendy K Chung,[...]. Am J Med Genet A 2016
70
11

MARKK, a Ste20-like kinase, activates the polarity-inducing kinase MARK/PAR-1.
Thomas Timm, Xiao-Yu Li, Jacek Biernat, Jian Jiao, Eckhard Mandelkow, Joel Vandekerckhove, Eva-Maria Mandelkow. EMBO J 2003
137
11

Activity-induced protocadherin arcadlin regulates dendritic spine number by triggering N-cadherin endocytosis via TAO2beta and p38 MAP kinases.
Shin Yasuda, Hidekazu Tanaka, Hiroko Sugiura, Ko Okamura, Taiki Sakaguchi, Uyen Tran, Takako Takemiya, Akira Mizoguchi, Yoshiki Yagita, Takeshi Sakurai,[...]. Neuron 2007
132
11

Reciprocal Effects on Neurocognitive and Metabolic Phenotypes in Mouse Models of 16p11.2 Deletion and Duplication Syndromes.
Thomas Arbogast, Abdel-Mouttalib Ouagazzal, Claire Chevalier, Maksym Kopanitsa, Nurudeen Afinowi, Eugenia Migliavacca, Belinda S Cowling, Marie-Christine Birling, Marie-France Champy, Alexandre Reymond,[...]. PLoS Genet 2016
55
11

Septins promote dendrite and axon development by negatively regulating microtubule stability via HDAC6-mediated deacetylation.
Natsumi Ageta-Ishihara, Takaki Miyata, Chika Ohshima, Masahiko Watanabe, Yoshikatsu Sato, Yuki Hamamura, Tetsuya Higashiyama, Ralph Mazitschek, Haruhiko Bito, Makoto Kinoshita. Nat Commun 2013
68
11

The prostate-derived sterile 20-like kinase (PSK) regulates microtubule organization and stability.
Costas Mitsopoulos, Ceniz Zihni, Ritu Garg, Anne J Ridley, Jonathan D H Morris. J Biol Chem 2003
36
16

Dendritic structural plasticity and neuropsychiatric disease.
Marc P Forrest, Euan Parnell, Peter Penzes. Nat Rev Neurosci 2018
138
11

The sterile 20-like kinase Tao-1 controls tissue growth by regulating the Salvador-Warts-Hippo pathway.
Carole L C Poon, Jane I Lin, Xiaomeng Zhang, Kieran F Harvey. Dev Cell 2011
142
11

Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus.
Sébastien Jacquemont, Alexandre Reymond, Flore Zufferey, Louise Harewood, Robin G Walters, Zoltán Kutalik, Danielle Martinet, Yiping Shen, Armand Valsesia, Noam D Beckmann,[...]. Nature 2011
264
9

A copy number variation morbidity map of developmental delay.
Gregory M Cooper, Bradley P Coe, Santhosh Girirajan, Jill A Rosenfeld, Tiffany H Vu, Carl Baker, Charles Williams, Heather Stalker, Rizwan Hamid, Vickie Hannig,[...]. Nat Genet 2011
803
9

Transcriptional consequences of 16p11.2 deletion and duplication in mouse cortex and multiplex autism families.
Ian Blumenthal, Ashok Ragavendran, Serkan Erdin, Lambertus Klei, Aarathi Sugathan, Jolene R Guide, Poornima Manavalan, Julian Q Zhou, Vanessa C Wheeler, Joshua Z Levin,[...]. Am J Hum Genet 2014
66
9


Semiquantitative proteomic analysis of rat forebrain postsynaptic density fractions by mass spectrometry.
Junmin Peng, Myung Jong Kim, Dongmei Cheng, Duc M Duong, Steven P Gygi, Morgan Sheng. J Biol Chem 2004
344
9

Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder.
Ryan K C Yuen, Daniele Merico, Matt Bookman, Jennifer L Howe, Bhooma Thiruvahindrapuram, Rohan V Patel, Joe Whitney, Nicole Deflaux, Jonathan Bingham, Zhuozhi Wang,[...]. Nat Neurosci 2017
332
9

Spatiotemporal 16p11.2 protein network implicates cortical late mid-fetal brain development and KCTD13-Cul3-RhoA pathway in psychiatric diseases.
Guan Ning Lin, Roser Corominas, Irma Lemmens, Xinping Yang, Jan Tavernier, David E Hill, Marc Vidal, Jonathan Sebat, Lilia M Iakoucheva. Neuron 2015
77
9

Prostate-derived sterile 20-like kinase 1-alpha induces apoptosis. JNK- and caspase-dependent nuclear localization is a requirement for membrane blebbing.
Ceniz Zihni, Costas Mitsopoulos, Ignatius A Tavares, Buzz Baum, Anne J Ridley, Jonathan D H Morris. J Biol Chem 2007
23
21

Crystal structure of the TAO2 kinase domain: activation and specificity of a Ste20p MAP3K.
Tianjun Zhou, Malavika Raman, Yan Gao, Svetlana Earnest, Zhu Chen, Mischa Machius, Melanie H Cobb, Elizabeth J Goldsmith. Structure 2004
55
9

Common variant at 16p11.2 conferring risk of psychosis.
S Steinberg, S de Jong, M Mattheisen, J Costas, D Demontis, S Jamain, O P H Pietiläinen, K Lin, S Papiol, J Huttenlocher,[...]. Mol Psychiatry 2014
66
9

The Ste20 group kinases as regulators of MAP kinase cascades.
I Dan, N M Watanabe, A Kusumi. Trends Cell Biol 2001
467
9

The septin family of GTPases: architecture and dynamics.
Christine S Weirich, Jan P Erzberger, Yves Barral. Nat Rev Mol Cell Biol 2008
233
9

Prostate-derived sterile 20-like kinase 2 (PSK2) regulates apoptotic morphology via C-Jun N-terminal kinase and Rho kinase-1.
Ceniz Zihni, Costas Mitsopoulos, Ignatius A Tavares, Anne J Ridley, Jonathan D H Morris. J Biol Chem 2006
29
17


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.