A citation-based method for searching scientific literature

Joseph W Lynch. Physiol Rev 2004
Times Cited: 544



R Shiang, S G Ryan, Y Z Zhu, A F Hahn, P O'Connell, J J Wasmuth. Nat Genet 1993
Times Cited: 391




List of shared articles



Times cited

The startle disease mutation α1S270T predicts shortening of glycinergic synaptic currents.
Zhiyi Wu, Remigijus Lape, Lea Jopp-Saile, Benjamin J O'Callaghan, Timo Greiner, Lucia G Sivilotti. J Physiol 2020
0

Identification of the hypertension drug niflumic acid as a glycine receptor inhibitor.
Daishi Ito, Yoshinori Kawazoe, Ayato Sato, Motonari Uesugi, Hiromi Hirata. Sci Rep 2020
1


Variable colocalisation of GABAA receptor subunits and glycine receptors on neurons in the human hypoglossal nucleus.
H J Waldvogel, F M Biggins, A Singh, C J Arasaratnam, R L M Faull. J Chem Neuroanat 2019
4

Clinical features and genetic analysis of two siblings with startle disease in an Italian family: a case report.
Teresa Sprovieri, Carmine Ungaro, Serena Sivo, Michela Quintiliani, Ilaria Contaldo, Chiara Veredice, Luigi Citrigno, Maria Muglia, Francesca Cavalcanti, Sebastiano Cavallaro,[...]. BMC Med Genet 2019
2

Mutations affecting glycinergic neurotransmission in hyperekplexia increase pain sensitivity.
Pascal Henri Vuilleumier, Raphael Fritsche, Jürg Schliessbach, Bernhard Schmitt, Lars Arendt-Nielsen, Hanns Ulrich Zeilhofer, Michele Curatolo. Brain 2018
12

A Missense Mutation A384P Associated with Human Hyperekplexia Reveals a Desensitization Site of Glycine Receptors.
Chen-Hung Wang, Ciria C Hernandez, Junyi Wu, Ning Zhou, Hsin-Yu Hsu, Mei-Lin Shen, Yi-Ching Wang, Robert L Macdonald, Dong Chuan Wu. J Neurosci 2018
5