A citation-based method for searching scientific literature

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, Frances M Cowan, Mireria Del Toro, Gail E Graham, Adnan Y Manzur, Amira Masri, Serge Rivera, Emmanuel Scalais, Rita Shiang, Kate Sinclair, Catriona A Stuart, Marina A J Tijssen, Grahame Wise, Sameer M Zuberi, Kirsten Harvey, Brian R Pearce, Maya Topf, Rhys H Thomas, Stéphane Supplisson, Mark I Rees, Robert J Harvey. J Biol Chem 2012
Times Cited: 59







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



Times Cited
  Times     Co-cited
Similarity


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
161
67

A novel dominant hyperekplexia mutation Y705C alters trafficking and biochemical properties of the presynaptic glycine transporter GlyT2.
Cecilio Giménez, Gonzalo Pérez-Siles, Jaime Martínez-Villarreal, Esther Arribas-González, Esperanza Jiménez, Enrique Núñez, Jaime de Juan-Sanz, Enrique Fernández-Sánchez, Noemí García-Tardón, Ignacio Ibáñez,[...]. J Biol Chem 2012
32
71

Deletion of the mouse glycine transporter 2 results in a hyperekplexia phenotype and postnatal lethality.
Jesús Gomeza, Koji Ohno, Swen Hülsmann, Wencke Armsen, Volker Eulenburg, Diethelm W Richter, Bodo Laube, Heinrich Betz. Neuron 2003
233
38

The genetics of hyperekplexia: more than startle!
Robert J Harvey, Maya Topf, Kirsten Harvey, Mark I Rees. Trends Genet 2008
144
35

Mutations within the human GLYT2 (SLC6A5) gene associated with hyperekplexia.
Volker Eulenburg, Kristina Becker, Jesús Gomeza, Bernhard Schmitt, Cord-Michael Becker, Heinrich Betz. Biochem Biophys Res Commun 2006
60
28

Pathophysiological mechanisms of dominant and recessive GLRA1 mutations in hyperekplexia.
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,[...]. J Neurosci 2010
99
27



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
39
35

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
51
25

Startle syndromes.
Mirte J Bakker, J Gert van Dijk, Arn M J M van den Maagdenberg, Marina A J Tijssen. Lancet Neurol 2006
167
20

Inactivation of the glycine transporter 1 gene discloses vital role of glial glycine uptake in glycinergic inhibition.
Jesús Gomeza, Swen Hülsmann, Koji Ohno, Volker Eulenburg, Katalin Szöke, Diethelm Richter, Heinrich Betz. Neuron 2003
238
20

Glycine transporters are differentially expressed among CNS cells.
F Zafra, C Aragón, L Olivares, N C Danbolt, C Giménez, J Storm-Mathisen. J Neurosci 1995
428
20

Molecular basis of the dominant negative effect of a glycine transporter 2 mutation associated with hyperekplexia.
Esther Arribas-González, Jaime de Juan-Sanz, Carmen Aragón, Beatriz López-Corcuera. J Biol Chem 2015
22
54


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
42
26

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
193
16

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
115
16

Endocytosis of the neuronal glycine transporter GLYT2: role of membrane rafts and protein kinase C-dependent ubiquitination.
Jaime de Juan-Sanz, Francisco Zafra, Beatriz López-Corcuera, Carmen Aragón. Traffic 2011
29
34

P2Y purinergic regulation of the glycine neurotransmitter transporters.
Esperanza Jiménez, Francisco Zafra, Raquel Pérez-Sen, Esmerilda G Delicado, Maria Teresa Miras-Portugal, Carmen Aragón, Beatriz López-Corcuera. J Biol Chem 2011
36
27



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
20

Glycine transporters: crucial roles of pharmacological interest revealed by gene deletion.
Carmen Aragón, Beatriz López-Corcuera. Trends Pharmacol Sci 2005
91
15

The glycinergic inhibitory synapse.
P Legendre. Cell Mol Life Sci 2001
403
15


Calnexin-assisted biogenesis of the neuronal glycine transporter 2 (GlyT2).
Esther Arribas-González, Pablo Alonso-Torres, Carmen Aragón, Beatriz López-Corcuera. PLoS One 2013
13
69

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
13

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
28
28

Subcellular localization of the neuronal glycine transporter GLYT2 in brainstem.
Enrique Núñez, Gonzalo Pérez-Siles, Lara Rodenstein, Pablo Alonso-Torres, Francisco Zafra, Esperanza Jiménez, Carmen Aragón, Beatriz López-Corcuera. Traffic 2009
26
30

Regional distribution and developmental variation of the glycine transporters GLYT1 and GLYT2 in the rat CNS.
F Zafra, J Gomeza, L Olivares, C Aragón, C Giménez. Eur J Neurosci 1995
230
13



Glycine transporters: essential regulators of neurotransmission.
Volker Eulenburg, Wencke Armsen, Heinrich Betz, Jesús Gomeza. Trends Biochem Sci 2005
245
13

Mutations in the carboxyl-terminal SEC24 binding motif of the serotonin transporter impair folding of the transporter.
Ali El-Kasaby, Herwig Just, Elisabeth Malle, Peggy C Stolt-Bergner, Harald H Sitte, Michael Freissmuth, Oliver Kudlacek. J Biol Chem 2010
49
16

Startle disease or hyperekplexia: further delineation of the syndrome.
F Andermann, D L Keene, E Andermann, L F Quesney. Brain 1980
167
11

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
281
11

Structure, function and regulation of glycine neurotransporters.
Carmen Aragón, Beatriz López-Corcuera. Eur J Pharmacol 2003
104
11

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
440
11

Glycinergic neurons expressing enhanced green fluorescent protein in bacterial artificial chromosome transgenic mice.
Hanns Ulrich Zeilhofer, Barbara Studler, Dimitrula Arabadzisz, Claude Schweizer, Seifollah Ahmadi, Beate Layh, Michael R Bösl, Jean-Marc Fritschy. J Comp Neurol 2005
238
11

The transporters GlyT2 and VIAAT cooperate to determine the vesicular glycinergic phenotype.
Karin R Aubrey, Francesco M Rossi, Raquel Ruivo, Silvia Alboni, Gian Carlo Bellenchi, Anne Le Goff, Bruno Gasnier, Stéphane Supplisson. J Neurosci 2007
58
12

Glycine transporter inhibitors as a novel drug discovery strategy for neuropathic pain.
Toshihiro Dohi, Katsuya Morita, Tomoya Kitayama, Naoyo Motoyama, Norimitsu Morioka. Pharmacol Ther 2009
80
11

Homozygous loss-of-function mutations in the gene encoding the dopamine transporter are associated with infantile parkinsonism-dystonia.
Manju A Kurian, Juan Zhen, Shu-Yuan Cheng, Yan Li, Santosh R Mordekar, Philip Jardine, Neil V Morgan, Esther Meyer, Louise Tee, Shanaz Pasha,[...]. J Clin Invest 2009
136
11

X-ray structure of dopamine transporter elucidates antidepressant mechanism.
Aravind Penmatsa, Kevin H Wang, Eric Gouaux. Nature 2013
399
11

Defining the blanks--pharmacochaperoning of SLC6 transporters and ABC transporters.
Peter Chiba, Michael Freissmuth, Thomas Stockner. Pharmacol Res 2014
30
23

Na+/K+-ATPase is a new interacting partner for the neuronal glycine transporter GlyT2 that downregulates its expression in vitro and in vivo.
Jaime de Juan-Sanz, Enrique Núñez, Lucía Villarejo-López, Daniel Pérez-Hernández, Alejo E Rodriguez-Fraticelli, Beatriz López-Corcuera, Jesús Vázquez, Carmen Aragón. J Neurosci 2013
29
24

Glycine transporter2 inhibitors: Getting the balance right.
Robert J Vandenberg, Shannon N Mostyn, Jane E Carland, Renae M Ryan. Neurochem Int 2016
15
46

Startle disease: an avoidable cause of sudden infant death.
F Vigevano, M Di Capua, B Dalla Bernardina. Lancet 1989
73
10


Clinical features and genetic analysis of children with hyperekplexia in Korea.
Cha Gon Lee, Min-Jung Kwon, Hee Joon Yu, Sook Hyun Nam, Jeehun Lee, Chang-Seok Ki, Munhyang Lee. J Child Neurol 2013
13
46


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.