A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity


The molecular and phenotypic spectrum of IQSEC2-related epilepsy.
Ayelet Zerem, Kazuhiro Haginoya, Dorit Lev, Lubov Blumkin, Sara Kivity, Ilan Linder, Cheryl Shoubridge, Elizabeth Emma Palmer, Michael Field, Jackie Boyle,[...]. Epilepsia 2016
37
31

Bidirectional regulation of synaptic transmission by BRAG1/IQSEC2 and its requirement in long-term depression.
Joshua C Brown, Amber Petersen, Ling Zhong, Miranda L Himelright, Jessica A Murphy, Randall S Walikonis, Nashaat Z Gerges. Nat Commun 2016
23
31

IQ Motif and SEC7 Domain-containing Protein 3 (IQSEC3) Interacts with Gephyrin to Promote Inhibitory Synapse Formation.
Ji Won Um, Gayoung Choii, Dongseok Park, Dongwook Kim, Sangmin Jeon, Hyeyeon Kang, Takuma Mori, Theofilos Papadopoulos, Taesun Yoo, Yeunkum Lee,[...]. J Biol Chem 2016
20
31


IQ-ArfGEF/BRAG1 is a guanine nucleotide exchange factor for Arf6 that interacts with PSD-95 at postsynaptic density of excitatory synapses.
Hiroyuki Sakagami, Masashi Sanda, Masahiro Fukaya, Taisuke Miyazaki, Jun Sukegawa, Teruyuki Yanagisawa, Tatsuo Suzuki, Kohji Fukunaga, Masahiko Watanabe, Hisatake Kondo. Neurosci Res 2008
57
26

The postsynaptic density protein, IQ-ArfGEF/BRAG1, can interact with IRSp53 through its proline-rich sequence.
Masashi Sanda, Akifumi Kamata, Osamu Katsumata, Kohji Fukunaga, Masahiko Watanabe, Hisatake Kondo, Hiroyuki Sakagami. Brain Res 2009
24
26

Subunit-selective N-Methyl-d-aspartate (NMDA) Receptor Signaling through Brefeldin A-resistant Arf Guanine Nucleotide Exchange Factors BRAG1 and BRAG2 during Synapse Maturation.
Mohammad Nael Elagabani, Dušica Briševac, Michael Kintscher, Jörg Pohle, Georg Köhr, Dietmar Schmitz, Hans-Christian Kornau. J Biol Chem 2016
22
26

Mutations in the guanine nucleotide exchange factor gene IQSEC2 cause nonsyndromic intellectual disability.
Cheryl Shoubridge, Patrick S Tarpey, Fatima Abidi, Sarah L Ramsden, Sinitdhorn Rujirabanjerd, Jessica A Murphy, Jackie Boyle, Marie Shaw, Alison Gardner, Anne Proos,[...]. Nat Genet 2010
102
21

AMPA receptor signaling through BRAG2 and Arf6 critical for long-term synaptic depression.
Ralf Scholz, Sven Berberich, Louisa Rathgeber, Alexander Kolleker, Georg Köhr, Hans-Christian Kornau. Neuron 2010
105
21

Arf6-GEF BRAG1 regulates JNK-mediated synaptic removal of GluA1-containing AMPA receptors: a new mechanism for nonsyndromic X-linked mental disorder.
Kenneth R Myers, Guangfu Wang, Yanghui Sheng, Kathryn K Conger, James E Casanova, J Julius Zhu. J Neurosci 2012
50
21

The balancing act of GABAergic synapse organizers.
Jaewon Ko, Gayoung Choii, Ji Won Um. Trends Mol Med 2015
56
21

Diagnostic exome sequencing identifies two novel IQSEC2 mutations associated with X-linked intellectual disability with seizures: implications for genetic counseling and clinical diagnosis.
Stephanie K Gandomi, K D Farwell Gonzalez, M Parra, L Shahmirzadi, J Mancuso, P Pichurin, R Temme, S Dugan, W Zeng, Sha Tang. J Genet Couns 2014
37
15

Mutations in epilepsy and intellectual disability genes in patients with features of Rett syndrome.
Heather E Olson, Dimira Tambunan, Christopher LaCoursiere, Marti Goldenberg, Rebecca Pinsky, Emilie Martin, Eugenia Ho, Omar Khwaja, Walter E Kaufmann, Annapurna Poduri. Am J Med Genet A 2015
56
15


Novel Missense Mutation A789V in IQSEC2 Underlies X-Linked Intellectual Disability in the MRX78 Family.
Vera M Kalscheuer, Victoria M James, Miranda L Himelright, Philip Long, Renske Oegema, Corinna Jensen, Melanie Bienek, Hao Hu, Stefan A Haas, Maya Topf,[...]. Front Mol Neurosci 2016
18
16

ARF6 and EFA6A regulate the development and maintenance of dendritic spines.
Seungwon Choi, Jaewon Ko, Jae-Ran Lee, Hyun Woo Lee, Karam Kim, Hye Sun Chung, Hyun Kim, Eunjoon Kim. J Neurosci 2006
83
15

Xp11.2 microduplications including IQSEC2, TSPYL2 and KDM5C genes in patients with neurodevelopmental disorders.
Ching Moey, Susan J Hinze, Louise Brueton, Jenny Morton, Dominic J McMullan, Benjamin Kamien, Christopher P Barnett, Nicola Brunetti-Pierri, Jillian Nicholl, Jozef Gecz,[...]. Eur J Hum Genet 2016
30
15

SynArfGEF is a guanine nucleotide exchange factor for Arf6 and localizes preferentially at post-synaptic specializations of inhibitory synapses.
Masahiro Fukaya, Akifumi Kamata, Yoshinobu Hara, Hideaki Tamaki, Osamu Katsumata, Naoki Ito, Shin'ichi Takeda, Yutaka Hata, Tatsuo Suzuki, Masahiko Watanabe,[...]. J Neurochem 2011
40
15

ARF family G proteins and their regulators: roles in membrane transport, development and disease.
Julie G Donaldson, Catherine L Jackson. Nat Rev Mol Cell Biol 2011
549
15

Incorrect dosage of IQSEC2, a known intellectual disability and epilepsy gene, disrupts dendritic spine morphogenesis.
S J Hinze, M R Jackson, S Lie, L Jolly, M Field, S C Barry, R J Harvey, C Shoubridge. Transl Psychiatry 2017
21
15

Neuroligins/LRRTMs prevent activity- and Ca2+/calmodulin-dependent synapse elimination in cultured neurons.
Jaewon Ko, Gilberto J Soler-Llavina, Marc V Fuccillo, Robert C Malenka, Thomas C Südhof. J Cell Biol 2011
71
15


Hippocampal GABAergic Inhibitory Interneurons.
Kenneth A Pelkey, Ramesh Chittajallu, Michael T Craig, Ludovic Tricoire, Jason C Wester, Chris J McBain. Physiol Rev 2017
297
15

The small GTPase ARF6 regulates GABAergic synapse development.
Hyeonho Kim, Hyeji Jung, Hyunsu Jung, Seok-Kyu Kwon, Jaewon Ko, Ji Won Um. Mol Brain 2020
6
50

Loss of IQSEC3 Disrupts GABAergic Synapse Maintenance and Decreases Somatostatin Expression in the Hippocampus.
Seungjoon Kim, Hyeonho Kim, Dongseok Park, Jinhu Kim, Joohyeon Hong, Jae Seong Kim, Hyeji Jung, Dongwook Kim, Eunji Cheong, Jaewon Ko,[...]. Cell Rep 2020
7
42

Role of LRRTMs in synapse development and plasticity.
Reiko T Roppongi, Benyamin Karimi, Tabrez J Siddiqui. Neurosci Res 2017
27
10

Diagnostic exome sequencing provides a molecular diagnosis for a significant proportion of patients with epilepsy.
Katherine L Helbig, Kelly D Farwell Hagman, Deepali N Shinde, Cameron Mroske, Zöe Powis, Shuwei Li, Sha Tang, Ingo Helbig. Genet Med 2016
182
10

Next-generation sequencing in X-linked intellectual disability.
Andreas Tzschach, Ute Grasshoff, Stefanie Beck-Woedl, Claudia Dufke, Claudia Bauer, Martin Kehrer, Christina Evers, Ute Moog, Barbara Oehl-Jaschkowitz, Nataliya Di Donato,[...]. Eur J Hum Genet 2015
85
10

Rett-like phenotypes: expanding the genetic heterogeneity to the KCNA2 gene and first familial case of CDKL5-related disease.
L Allou, S Julia, D Amsallem, S El Chehadeh, L Lambert, J Thevenon, Y Duffourd, A Saunier, P Bouquet, S Pere,[...]. Clin Genet 2017
34
10

Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study.
Anita Rauch, Dagmar Wieczorek, Elisabeth Graf, Thomas Wieland, Sabine Endele, Thomas Schwarzmayr, Beate Albrecht, Deborah Bartholdi, Jasmin Beygo, Nataliya Di Donato,[...]. Lancet 2012
692
10

Efficient strategy for the molecular diagnosis of intellectual disability using targeted high-throughput sequencing.
Claire Redin, Bénédicte Gérard, Julia Lauer, Yvan Herenger, Jean Muller, Angélique Quartier, Alice Masurel-Paulet, Marjolaine Willems, Gaétan Lesca, Salima El-Chehadeh,[...]. J Med Genet 2014
170
10

Neuronal activity-regulated gene transcription in synapse development and cognitive function.
Anne E West, Michael E Greenberg. Cold Spring Harb Perspect Biol 2011
330
10



A glutamic finger in the guanine nucleotide exchange factor ARNO displaces Mg2+ and the beta-phosphate to destabilize GDP on ARF1.
S Béraud-Dufour, S Robineau, P Chardin, S Paris, M Chabre, J Cherfils, B Antonny. EMBO J 1998
152
10

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
955
10

Predominant localization of EFA6A, a guanine nucleotide exchange factor for ARF6, at the perisynaptic photoreceptor processes.
Osamu Katsumata, Takashi Honma, Masashi Sanda, Akifumi Kamata, Shin'ichi Takeda, Hisatake Kondo, Hiroyuki Sakagami. Brain Res 2008
4
50

Distinct synaptic localization patterns of brefeldin A-resistant guanine nucleotide exchange factors BRAG2 and BRAG3 in the mouse retina.
Hiroyuki Sakagami, Osamu Katsumata, Yoshinobu Hara, Hideaki Tamaki, Masahiko Watanabe, Robert J Harvey, Masahiro Fukaya. J Comp Neurol 2013
20
10

ARF proteins: roles in membrane traffic and beyond.
Crislyn D'Souza-Schorey, Philippe Chavrier. Nat Rev Mol Cell Biol 2006
978
10

GEP100/BRAG2: activator of ADP-ribosylation factor 6 for regulation of cell adhesion and actin cytoskeleton via E-cadherin and alpha-catenin.
Toyoko Hiroi, Akimasa Someya, Walter Thompson, Joel Moss, Martha Vaughan. Proc Natl Acad Sci U S A 2006
59
10

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
348
10

Disruption of the IQSEC2 transcript in a female with X;autosome translocation t(X;20)(p11.2;q11.2) and a phenotype resembling X-linked infantile spasms (ISSX) syndrome.
Manuela Morleo, Daniela Iaconis, David Chitayat, Ivana Peluso, Rosalia Marzella, Alessandra Renieri, Francesca Mari, Brunella Franco. Mol Med Rep 2008
19
10

IQSEC2 and X-linked syndromal intellectual disability.
Aaron F Alexander-Bloch, Christopher J McDougle, Zhanna Ullman, David A Sweetser. Psychiatr Genet 2016
11
18

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
10

Expanding the phenotype of IQSEC2 mutations: truncating mutations in severe intellectual disability.
Frederic Tran Mau-Them, Marjolaine Willems, Beate Albrecht, Elodie Sanchez, Jacques Puechberty, Sabine Endele, Anouck Schneider, Nathalie Ruiz Pallares, Chantal Missirian, Francois Rivier,[...]. Eur J Hum Genet 2014
29
10


Genes that escape from X inactivation.
Joel B Berletch, Fan Yang, Jun Xu, Laura Carrel, Christine M Disteche. Hum Genet 2011
202
10


Dynamic microtubules regulate dendritic spine morphology and synaptic plasticity.
Jacek Jaworski, Lukas C Kapitein, Susana Montenegro Gouveia, Bjorn R Dortland, Phebe S Wulf, Ilya Grigoriev, Paola Camera, Samantha A Spangler, Paola Di Stefano, Jeroen Demmers,[...]. Neuron 2009
448
10

Molecular characterization and comparison of the components and multiprotein complexes in the postsynaptic proteome.
Mark O Collins, Holger Husi, Lu Yu, Julia M Brandon, Chris N G Anderson, Walter P Blackstock, Jyoti S Choudhary, Seth G N Grant. J Neurochem 2006
314
10


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.