A citation-based method for searching scientific literature

Robert J Harvey, Maya Topf, Kirsten Harvey, Mark I Rees. Trends Genet 2008
Times Cited: 143







List of co-cited articles
1004 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
158
36

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


Startle syndromes.
Mirte J Bakker, J Gert van Dijk, Arn M J M van den Maagdenberg, Marina A J Tijssen. Lancet Neurol 2006
165
22

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
229
22


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
35

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
19

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
432
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
189
17

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
48
35

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
277
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
37



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
17

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
38


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
234
14

Glycine receptor mechanism elucidated by electron cryo-microscopy.
Juan Du, Wei Lü, Shenping Wu, Yifan Cheng, Eric Gouaux. Nature 2015
258
14

Hyperekplexia: a treatable neurogenetic disease.
Lan Zhou, Kipp L Chillag, Michael A Nigro. Brain Dev 2002
77
16

Gephyrin: a master regulator of neuronal function?
Shiva K Tyagarajan, Jean-Marc Fritschy. Nat Rev Neurosci 2014
228
13

Startle disease in Irish wolfhounds associated with a microdeletion in the glycine transporter GlyT2 gene.
Jennifer L Gill, Deborah Capper, Jean-François Vanbellinghen, Seo-Kyung Chung, Robert J Higgins, Mark I Rees, G Diane Shelton, Robert J Harvey. Neurobiol Dis 2011
31
38

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

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

Startle disease: an avoidable cause of sudden infant death.
F Vigevano, M Di Capua, B Dalla Bernardina. Lancet 1989
72
15

The glycinergic inhibitory synapse.
P Legendre. Cell Mol Life Sci 2001
400
11


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
18

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
34

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
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
11


Fast synaptic inhibition in spinal sensory processing and pain control.
Hanns Ulrich Zeilhofer, Hendrik Wildner, Gonzalo E Yévenes. Physiol Rev 2012
222
10


A family with emotionally precipitated drop seizures.
L KIRSTEIN, B P SILFVERSKIOLD. Acta Psychiatr Neurol Scand 1958
70
12

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
33

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
9

Highly effective SNP-based association mapping and management of recessive defects in livestock.
Carole Charlier, Wouter Coppieters, Frédéric Rollin, Daniel Desmecht, Jorgen S Agerholm, Nadine Cambisano, Eloisa Carta, Sabrina Dardano, Marc Dive, Corinne Fasquelle,[...]. Nat Genet 2008
171
9

Crystal structure of a bacterial homologue of Na+/Cl--dependent neurotransmitter transporters.
Atsuko Yamashita, Satinder K Singh, Toshimitsu Kawate, Yan Jin, Eric Gouaux. Nature 2005
9


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
136
9


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
17


Behavioral characterization of knockin mice with mutations M287L and Q266I in the glycine receptor α1 subunit.
Yuri A Blednov, Jill M Benavidez, Gregg E Homanics, R Adron Harris. J Pharmacol Exp Ther 2012
29
27

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
29

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
40
20

Molecular basis for zinc potentiation at strychnine-sensitive glycine receptors.
Paul S Miller, Helena M A Da Silva, Trevor G Smart. J Biol Chem 2005
69
11

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


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.