A citation-based method for searching scientific literature

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
Times Cited: 113







List of co-cited articles
991 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
155
48

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
86
50

Compound heterozygosity and nonsense mutations in the alpha(1)-subunit of the inhibitory glycine receptor in hyperekplexia.
M I Rees, T M Lewis, B Vafa, C Ferrie, P Corry, F Muntoni, H Jungbluth, J B Stephenson, M Kerr, R G Snell,[...]. Hum Genet 2001
60
56


The genetics of hyperekplexia: more than startle!
Robert J Harvey, Maya Topf, Kirsten Harvey, Mark I Rees. Trends Genet 2008
139
31


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
273
28

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
187
28

Startle syndromes.
Mirte J Bakker, J Gert van Dijk, Arn M J M van den Maagdenberg, Marina A J Tijssen. Lancet Neurol 2006
164
26

The spastic mouse: aberrant splicing of glycine receptor beta subunit mRNA caused by intronic insertion of L1 element.
C Mülhardt, M Fischer, P Gass, D Simon-Chazottes, J L Guénet, J Kuhse, H Betz, C M Becker. Neuron 1994
153
25

Hyperekplexia: a treatable neurogenetic disease.
Lan Zhou, Kipp L Chillag, Michael A Nigro. Brain Dev 2002
77
31

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
23

Glycine receptor beta-subunit gene mutation in spastic mouse associated with LINE-1 element insertion.
S F Kingsmore, B Giros, D Suh, M Bieniarz, M G Caron, M F Seldin. Nat Genet 1994
181
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
228
22

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
428
22

Startle disease or hyperekplexia: further delineation of the syndrome.
F Andermann, D L Keene, E Andermann, L F Quesney. Brain 1980
166
20


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
33


Dual requirement for gephyrin in glycine receptor clustering and molybdoenzyme activity.
G Feng, H Tintrup, J Kirsch, M C Nichol, J Kuhse, H Betz, J R Sanes. Science 1998
319
17

A missense mutation in the gene encoding the alpha 1 subunit of the inhibitory glycine receptor in the spasmodic mouse.
S G Ryan, M S Buckwalter, J W Lynch, C A Handford, L Segura, R Shiang, J J Wasmuth, S A Camper, P Schofield, P O'Connell. Nat Genet 1994
151
17

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
94
18

Startle disease: an avoidable cause of sudden infant death.
F Vigevano, M Di Capua, B Dalla Bernardina. Lancet 1989
72
22

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

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
33

A novel recessive hyperekplexia allele GLRA1 (S231R): genotyping by MALDI-TOF mass spectrometry and functional characterisation as a determinant of cellular glycine receptor trafficking.
Andreas Humeny, Thomas Bonk, Kristina Becker, Mehrdad Jafari-Boroujerdi, Ulrich Stephani, Klaus Reuter, Cord-Michael Becker. Eur J Hum Genet 2002
34
44

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
21

A family with emotionally precipitated drop seizures.
L KIRSTEIN, B P SILFVERSKIOLD. Acta Psychiatr Neurol Scand 1958
70
21

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
55


The glycinergic inhibitory synapse.
P Legendre. Cell Mol Life Sci 2001
395
14


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
233
14

Glycine transporters: essential regulators of neurotransmission.
Volker Eulenburg, Wencke Armsen, Heinrich Betz, Jesús Gomeza. Trends Biochem Sci 2005
240
14


Point mutation of glycine receptor alpha 1 subunit in the spasmodic mouse affects agonist responses.
B Saul, V Schmieden, C Kling, C Mülhardt, P Gass, J Kuhse, C M Becker. FEBS Lett 1994
92
14


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
30


A nonsense mutation in the alpha1 subunit of the inhibitory glycine receptor associated with bovine myoclonus.
K D Pierce, C A Handford, R Morris, B Vafa, J A Dennis, P J Healy, P R Schofield. Mol Cell Neurosci 2001
30
40


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
33
36

Molecular genetic reevaluation of the Dutch hyperekplexia family.
M A Tijssen, R Shiang, J van Deutekom, R H Boerman, J J Wasmuth, L A Sandkuijl, R R Frants, G W Padberg. Arch Neurol 1995
47
23

Hyperekplexia: a syndrome of pathological startle responses.
E Sáenz-Lope, F J Herranz-Tanarro, J C Masdeu, J R Chacón Peña. Ann Neurol 1984
93
11


A mutation (V260M) in the middle of the M2 pore-lining domain of the glycine receptor causes hereditary hyperekplexia.
E M del Giudice, G Coppola, G Bellini, G Cirillo, G Scuccimarra, A Pascotto. Eur J Hum Genet 2001
22
50

Hyperekplexia in neonates.
V Praveen, S K Patole, J S Whitehall. Postgrad Med J 2001
41
26

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
39

Zebrafish bandoneon mutants display behavioral defects due to a mutation in the glycine receptor beta-subunit.
Hiromi Hirata, Louis Saint-Amant, Gerald B Downes, Wilson W Cui, Weibin Zhou, Michael Granato, John Y Kuwada. Proc Natl Acad Sci U S A 2005
75
14


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.