A citation-based method for searching scientific literature

Seo-Kyung Chung, Jean-François Vanbellinghen, Jonathan G L Mullins, Angela Robinson, Janina Hantke, Carrie L Hammond, Daniel F Gilbert, Michael Freilinger, Monique Ryan, Michael C Kruer, Amira Masri, Candan Gurses, Colin Ferrie, Kirsten Harvey, Rita Shiang, John Christodoulou, Frederick Andermann, Eva Andermann, Rhys H Thomas, Robert J Harvey, Joseph W Lynch, Mark I Rees. J Neurosci 2010
Times Cited: 95







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



Times Cited
  Times     Co-cited
Similarity



The genetics of hyperekplexia: more than startle!
Robert J Harvey, Maya Topf, Kirsten Harvey, Mark I Rees. Trends Genet 2008
142
38


Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease.
Mark I Rees, Kirsten Harvey, Brian R Pearce, Seo-Kyung Chung, Ian C Duguid, Philip Thomas, Sarah Beatty, Gail E Graham, Linlea Armstrong, Rita Shiang,[...]. Nat Genet 2006
157
29


The beta subunit determines the ligand binding properties of synaptic glycine receptors.
Joanna Grudzinska, Rudolf Schemm, Svenja Haeger, Annette Nicke, Guenther Schmalzing, Heinrich Betz, Bodo Laube. Neuron 2005
275
28


GlyR alpha3: an essential target for spinal PGE2-mediated inflammatory pain sensitization.
Robert J Harvey, Ulrike B Depner, Heinz Wässle, Seifollah Ahmadi, Cornelia Heindl, Heiko Reinold, Trevor G Smart, Kirsten Harvey, Burkhard Schütz, Osama M Abo-Salem,[...]. Science 2004
430
27

Novel missense mutations in the glycine receptor β subunit gene (GLRB) in startle disease.
Victoria M James, Anna Bode, Seo-Kyung Chung, Jennifer L Gill, Maartje Nielsen, Frances M Cowan, Mihailo Vujic, Rhys H Thomas, Mark I Rees, Kirsten Harvey,[...]. Neurobiol Dis 2013
39
66


Startle syndromes.
Mirte J Bakker, J Gert van Dijk, Arn M J M van den Maagdenberg, Marina A J Tijssen. Lancet Neurol 2006
164
23

GLRB is the third major gene of effect in hyperekplexia.
Seo-Kyung Chung, Anna Bode, Thomas D Cushion, Rhys H Thomas, Charlotte Hunt, Sian-Elin Wood, William O Pickrell, Cheney J G Drew, Sumimasa Yamashita, Rita Shiang,[...]. Hum Mol Genet 2013
35
54

Glycine receptor mechanism elucidated by electron cryo-microscopy.
Juan Du, Wei Lü, Shenping Wu, Yifan Cheng, Eric Gouaux. Nature 2015
255
20

New hyperekplexia mutations provide insight into glycine receptor assembly, trafficking, and activation mechanisms.
Anna Bode, Sian-Elin Wood, Jonathan G L Mullins, Angelo Keramidas, Thomas D Cushion, Rhys H Thomas, William O Pickrell, Cheney J G Drew, Amira Masri, Elizabeth A Jones,[...]. J Biol Chem 2013
28
64

The glycinergic system in human startle disease: a genetic screening approach.
Jeff S Davies, Seo-Kyung Chung, Rhys H Thomas, Angela Robinson, Carrie L Hammond, Jonathan G L Mullins, Eloisa Carta, Brian R Pearce, Kirsten Harvey, Robert J Harvey,[...]. Front Mol Neurosci 2010
43
39

Hyperekplexia associated with compound heterozygote mutations in the beta-subunit of the human inhibitory glycine receptor (GLRB).
Mark I Rees, Trevor M Lewis, John B J Kwok, Geert R Mortier, Paul Govaert, Russell G Snell, Peter R Schofield, Michael J Owen. Hum Mol Genet 2002
113
17

The GDP-GTP exchange factor collybistin: an essential determinant of neuronal gephyrin clustering.
Kirsten Harvey, Ian C Duguid, Melissa J Alldred, Sarah E Beatty, Hamish Ward, Nicholas H Keep, Sue E Lingenfelter, Brian R Pearce, Johan Lundgren, Michael J Owen,[...]. J Neurosci 2004
189
16

Genotype-phenotype correlations in hyperekplexia: apnoeas, learning difficulties and speech delay.
Rhys H Thomas, Seo-Kyung Chung, Sian E Wood, Thomas D Cushion, Cheney J G Drew, Carrie L Hammond, Jean-Francois Vanbellinghen, Jonathan G L Mullins, Mark I Rees. Brain 2013
47
34

Recessive hyperekplexia mutations of the glycine receptor alpha1 subunit affect cell surface integration and stability.
Carmen Villmann, Jana Oertel, Nima Melzer, Cord-Michael Becker. J Neurochem 2009
27
55

Mutations in the GlyT2 gene (SLC6A5) are a second major cause of startle disease.
Eloisa Carta, Seo-Kyung Chung, Victoria M James, Angela Robinson, Jennifer L Gill, Nathalie Remy, Jean-François Vanbellinghen, Cheney J G Drew, Sophie Cagdas, Duncan Cameron,[...]. J Biol Chem 2012
56
26

X-ray structure of a pentameric ligand-gated ion channel in an apparently open conformation.
Nicolas Bocquet, Hugues Nury, Marc Baaden, Chantal Le Poupon, Jean-Pierre Changeux, Marc Delarue, Pierre-Jean Corringer. Nature 2009
545
14

Novel mutation in GLRB in a large family with hereditary hyperekplexia.
M Al-Owain, D Colak, A Al-Bakheet, N Al-Hashmi, T Shuaib, A Al-Hemidan, H Aldhalaan, Z Rahbeeni, M Al-Sayed, B Al-Younes,[...]. Clin Genet 2012
27
51






Mutational analysis of familial and sporadic hyperekplexia.
R Shiang, S G Ryan, Y Z Zhu, T J Fielder, R J Allen, A Fryer, S Yamashita, P O'Connell, J J Wasmuth. Ann Neurol 1995
100
13

Serotonin receptor 1A-modulated phosphorylation of glycine receptor α3 controls breathing in mice.
Till Manzke, Marcus Niebert, Uwe R Koch, Alex Caley, Steffen Vogelgesang, Swen Hülsmann, Evgeni Ponimaskin, Ulrike Müller, Trevor G Smart, Robert J Harvey,[...]. J Clin Invest 2010
68
19

Isoform heterogeneity of the human gephyrin gene (GPHN), binding domains to the glycine receptor, and mutation analysis in hyperekplexia.
Mark I Rees, Kirsten Harvey, Hamish Ward, Julia H White, Luc Evans, Ian C Duguid, Cynthia C-H Hsu, Sharon L Coleman, Jan Miller, Kristin Baer,[...]. J Biol Chem 2003
87
14

A yellow fluorescent protein-based assay for high-throughput screening of glycine and GABAA receptor chloride channels.
Wade Kruger, Daniel Gilbert, Rebecca Hawthorne, Deanne H Hryciw, Stephan Frings, Philip Poronnik, Joseph W Lynch. Neurosci Lett 2005
45
28

Crystal structure of human glycine receptor-α3 bound to antagonist strychnine.
Xin Huang, Hao Chen, Klaus Michelsen, Stephen Schneider, Paul L Shaffer. Nature 2015
145
13

Two novel mutations of the glycine receptor gene in a Taiwanese hyperekplexia family.
C H Tsai, F C Chang, Y C Su, F J Tsai, M K Lu, C C Lee, C C Kuo, Y W Yang, C S Lu. Neurology 2004
28
42


Binding, activation and modulation of Cys-loop receptors.
Paul S Miller, Trevor G Smart. Trends Pharmacol Sci 2010
214
12


Stoichiometry and subunit arrangement of α1β glycine receptors as determined by atomic force microscopy.
Zhe Yang, Elena Taran, Timothy I Webb, Joseph W Lynch. Biochemistry 2012
39
30

Disturbed neuronal ER-Golgi sorting of unassembled glycine receptors suggests altered subcellular processing is a cause of human hyperekplexia.
Natascha Schaefer, Christoph J Kluck, Kerry L Price, Heike Meiselbach, Nadine Vornberger, Stephan Schwarzinger, Stephanie Hartmann, Georg Langlhofer, Solveig Schulz, Nadja Schlegel,[...]. J Neurosci 2015
20
60


Properties of human glycine receptors containing the hyperekplexia mutation alpha1(K276E), expressed in Xenopus oocytes.
T M Lewis, L G Sivilotti, D Colquhoun, R M Gardiner, R Schoepfer, M Rees. J Physiol 1998
87
12

A GLRA1 null mutation in recessive hyperekplexia challenges the functional role of glycine receptors.
W Brune, R G Weber, B Saul, M von Knebel Doeberitz, C Grond-Ginsbach, K Kellerman, H M Meinck, C M Becker. Am J Hum Genet 1996
70
15


Conformational variability of the glycine receptor M2 domain in response to activation by different agonists.
Stephan A Pless, Mohammed I Dibas, Henry A Lester, Joseph W Lynch. J Biol Chem 2007
61
18

Hyperekplexia: a treatable neurogenetic disease.
Lan Zhou, Kipp L Chillag, Michael A Nigro. Brain Dev 2002
77
14

Hyperekplexia phenotype of glycine receptor alpha1 subunit mutant mice identifies Zn(2+) as an essential endogenous modulator of glycinergic neurotransmission.
Klaus Hirzel, Ulrike Müller, A Tobias Latal, Swen Hülsmann, Joanna Grudzinska, Mathias W Seeliger, Heinrich Betz, Bodo Laube. Neuron 2006
92
11


Startle disease or hyperekplexia: further delineation of the syndrome.
F Andermann, D L Keene, E Andermann, L F Quesney. Brain 1980
166
11

Cannabinoids suppress inflammatory and neuropathic pain by targeting α3 glycine receptors.
Wei Xiong, Tanxing Cui, Kejun Cheng, Fei Yang, Shao-Rui Chen, Dan Willenbring, Yun Guan, Hui-Lin Pan, Ke Ren, Yan Xu,[...]. J Exp Med 2012
135
11

Functional complementation of Glra1(spd-ot), a glycine receptor subunit mutant, by independently expressed C-terminal domains.
Carmen Villmann, Jana Oertel, Zhan-Lu Ma-Högemeier, Michael Hollmann, Rolf Sprengel, Kristina Becker, Hans-Georg Breitinger, Cord-Michael Becker. J Neurosci 2009
24
45

Hyperekplexia phenotype due to compound heterozygosity for GLRA1 gene mutations.
M N Vergouwe, M A Tijssen, A C Peters, R Wielaard, R R Frants. Ann Neurol 1999
45
24


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.