A citation-based method for searching scientific literature

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
Times Cited: 48







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



Times Cited
  Times     Co-cited
Similarity


Startle syndromes.
Mirte J Bakker, J Gert van Dijk, Arn M J M van den Maagdenberg, Marina A J Tijssen. Lancet Neurol 2006
165
35

The genetics of hyperekplexia: more than startle!
Robert J Harvey, Maya Topf, Kirsten Harvey, Mark I Rees. Trends Genet 2008
142
35

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
95
33

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
158
33


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
57
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
35
34

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
40
30


A family with emotionally precipitated drop seizures.
L KIRSTEIN, B P SILFVERSKIOLD. Acta Psychiatr Neurol Scand 1958
70
18

Hyperekplexia: a treatable neurogenetic disease.
Lan Zhou, Kipp L Chillag, Michael A Nigro. Brain Dev 2002
77
18

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
190
16

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
18

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
16

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
25

Startle disease: an avoidable cause of sudden infant death.
F Vigevano, M Di Capua, B Dalla Bernardina. Lancet 1989
72
16


Clinical and genetic investigation of 17 Japanese patients with hyperekplexia.
Jun Mine, Takeshi Taketani, Kazushi Yoshida, Fusako Yokochi, Junpei Kobayashi, Koichi Maruyama, Etsuro Nanishi, Mayumi Ono, Atsushi Yokoyama, Hidee Arai,[...]. Dev Med Child Neurol 2015
15
46

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
12

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
12


The startle syndromes: physiology and treatment.
Yasmine E M Dreissen, Marina A J Tijssen. Epilepsia 2012
44
13

Startle disease or hyperekplexia: further delineation of the syndrome.
F Andermann, D L Keene, E Andermann, L F Quesney. Brain 1980
167
12

The effects of clonazepam and vigabatrin in hyperekplexia.
M A Tijssen, H C Schoemaker, P J Edelbroek, R A Roos, A F Cohen, J G van Dijk. J Neurol Sci 1997
39
15

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
21
28

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
279
10

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
18



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
17

The glycinergic inhibitory synapse.
P Legendre. Cell Mol Life Sci 2001
401
10

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
59
10

Presynaptic glycine receptors as a potential therapeutic target for hyperekplexia disease.
Wei Xiong, Shao-Rui Chen, Liming He, Kejun Cheng, Yi-Lin Zhao, Hong Chen, De-Pei Li, Gregg E Homanics, John Peever, Kenner C Rice,[...]. Nat Neurosci 2014
38
13

Fast synaptic inhibition in spinal sensory processing and pain control.
Hanns Ulrich Zeilhofer, Hendrik Wildner, Gonzalo E Yévenes. Physiol Rev 2012
223
10

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
230
10

Hyperekplexia: Report on phenotype and genotype of 16 Jordanian patients.
Amira Masri, Seo-Kyung Chung, Mark I Rees. Brain Dev 2017
9
55

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
8

The GLRA1 missense mutation W170S associates lack of Zn2+ potentiation with human hyperekplexia.
Ning Zhou, Chen-Hung Wang, Shu Zhang, Dong Chuan Wu. J Neurosci 2013
15
26

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
434
8


A 14-year-old girl with hyperekplexia having GLRB mutations.
Jun Mine, Takeshi Taketani, Shusuke Otsubo, Kazuko Kishi, Seiji Yamaguchi. Brain Dev 2013
6
66


Modulation by zinc ions of native rat and recombinant human inhibitory glycine receptors.
B Laube, J Kuhse, N Rundström, J Kirsch, V Schmieden, H Betz. J Physiol 1995
159
8

Novel mutation of GLRA1 in Omani families with hyperekplexia and mild mental retardation.
Amna Mohammed Al-Futaisi, Mohammed Nasser Al-Kindi, Al-Mundher Al-Mawali, Roshan Lal Koul, Samir Al-Adawi, Said Ali Al-Yahyaee. Pediatr Neurol 2012
14
28

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
14


Hyperekplexia associated with apnea and sudden infant death syndrome.
G P Giacoia, S G Ryan. Arch Pediatr Adolesc Med 1994
28
14

Hyperekplexia: treatment of a severe phenotype and review of the literature.
Aleksandra Mineyko, Sharon Whiting, Gail E Graham. Can J Neurol Sci 2011
10
40


Anaesthetic implications of hyperekplexia--'startle disease'.
R Garg, R Ramachandran, P Sharma. Anaesth Intensive Care 2008
5
80


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.