A citation-based method for searching scientific literature

Daniela Pietrobon. Pflugers Arch 2010
Times Cited: 135







List of co-cited articles
1477 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Intracellular calcium release through IP3R or RyR contributes to secondary axonal degeneration.
Ben C Orem, Nicolas Pelisch, Joshua Williams, Jacqueline M Nally, David P Stirling. Neurobiol Dis 2017
13
7

Multiple sclerosis.
Massimo Filippi, Amit Bar-Or, Fredrik Piehl, Paolo Preziosa, Alessandra Solari, Sandra Vukusic, Maria A Rocca. Nat Rev Dis Primers 2018
277
1

Genetic and functional linkage of Kir5.1 and Kir2.1 channel subunits.
C Derst, C Karschin, E Wischmeyer, J R Hirsch, R Preisig-Müller, S Rajan, H Engel, K Grzeschik, J Daut, A Karschin. FEBS Lett 2001
44
2

KCNT1-related epilepsy: An international multicenter cohort of 27 pediatric cases.
Felippe Borlot, Ahmed Abushama, Nadine Morrison-Levy, Puneet Jain, Kollencheri Puthenveettil Vinayan, Musaad Abukhalid, Hesham M Aldhalaan, Hanin S Almuzaini, Sheffali Gulati, Tova Hershkovitz,[...]. Epilepsia 2020
15
6

Homo- and heterotetrameric architecture of the epithelial Ca2+ channels TRPV5 and TRPV6.
J G J Hoenderop, T Voets, S Hoefs, F Weidema, J Prenen, B Nilius, R J M Bindels. EMBO J 2003
245
1


ATP and glutamate released via astroglial connexin 43 hemichannels mediate neuronal death through activation of pannexin 1 hemichannels.
Juan A Orellana, Nicolas Froger, Pascal Ezan, Jean X Jiang, Michael V L Bennett, Christian C Naus, Christian Giaume, Juan C Sáez. J Neurochem 2011
246
1


Nimodipine fosters remyelination in a mouse model of multiple sclerosis and induces microglia-specific apoptosis.
Andrea Schampel, Oleg Volovitch, Tobias Koeniger, Claus-Jürgen Scholz, Stefanie Jörg, Ralf A Linker, Erhard Wischmeyer, Marie Wunsch, Johannes W Hell, Süleyman Ergün,[...]. Proc Natl Acad Sci U S A 2017
33
3

All four CatSper ion channel proteins are required for male fertility and sperm cell hyperactivated motility.
Huayu Qi, Magdalene M Moran, Betsy Navarro, Jayhong A Chong, Grigory Krapivinsky, Luba Krapivinsky, Yuriy Kirichok, I Scott Ramsey, Timothy A Quill, David E Clapham. Proc Natl Acad Sci U S A 2007
323
1

A new calcium channel antagonist, lomerizine, alleviates secondary retinal ganglion cell death after optic nerve injury in the rat.
Zahidul Karim, Akira Sawada, Hideaki Kawakami, Tetsuya Yamamoto, Takazumi Taniguchi. Curr Eye Res 2006
19
5


Axonal expression of sodium channels and neuropathology of the plaques in multiple sclerosis.
Adel Bouafia, Jean-Louis Golmard, Valerie Thuries, Veronique Sazdovitch, Jean Jacques Hauw, Betrand Fontaine, Danielle Seilhean. Neuropathol Appl Neurobiol 2014
14
7

L-type calcium channel CaV 1.2 in transgenic mice overexpressing human AbetaPP751 with the London (V717I) and Swedish (K670M/N671L) mutations.
Michael Willis, Walter A Kaufmann, Georg Wietzorrek, Birgit Hutter-Paier, Sven Moosmang, Christian Humpel, Franz Hofmann, Manfred Windisch, Hans-Günther Knaus, Josef Marksteiner. J Alzheimers Dis 2010
22
4



Kv2.1 cell surface clusters are insertion platforms for ion channel delivery to the plasma membrane.
Emily Deutsch, Aubrey V Weigel, Elizabeth J Akin, Phil Fox, Gentry Hansen, Christopher J Haberkorn, Rob Loftus, Diego Krapf, Michael M Tamkun. Mol Biol Cell 2012
68
1


The role of transient receptor potential cation channels in Ca2+ signaling.
Maarten Gees, Barbara Colsoul, Bernd Nilius. Cold Spring Harb Perspect Biol 2010
265
1


Human skeletal muscle calcium channel alpha1S is expressed in the basal ganglia: distinctive expression pattern among L-type Ca2+ channels.
Yuji Takahashi, Seon-Yong Jeong, Katsuhisa Ogata, Jun Goto, Hideji Hashida, Kyoko Isahara, Yasuo Uchiyama, Ichiro Kanazawa. Neurosci Res 2003
18
5

[Clinical features and gene mutations in epilepsy of infancy with migrating focal seizures].
K W Shang, Y H Zhang, X L Yang, A J Liu, Z X Yang, X Y Liu, Y W Jiang, X R Wu. Zhonghua Er Ke Za Zhi 2016
3
33

Abnormal sodium channel distribution in optic nerve axons in a model of inflammatory demyelination.
Matthew J Craner, Albert C Lo, Joel A Black, Stephen G Waxman. Brain 2003
123
1

Dystonia as a network disorder: a concept in evolution.
Tommaso Schirinzi, Giuseppe Sciamanna, Nicola B Mercuri, Antonio Pisani. Curr Opin Neurol 2018
27
3

Novel CACNA1A variant may cause cervical dystonia and cerebellar ataxia syndrome.
A Fuerte-Hortigón, R Pérez-Noguera, J Dotor García-Soto, I Royo Boronat, S Álvarez de Andrés, J M García-Moreno. J Neurol Sci 2020
3
33

Paroxysmal movement disorders: An update.
A Méneret, E Roze. Rev Neurol (Paris) 2016
30
3

Advances in genetics of migraine.
Heidi G Sutherland, Cassie L Albury, Lyn R Griffiths. J Headache Pain 2019
37
2

Diagnostic and therapeutic aspects of hemiplegic migraine.
Vincenzo Di Stefano, Marianna Gabriella Rispoli, Noemi Pellegrino, Alessandro Graziosi, Eleonora Rotondo, Christian Napoli, Daniela Pietrobon, Filippo Brighina, Pasquale Parisi. J Neurol Neurosurg Psychiatry 2020
22
4

Detection of clinically relevant copy-number variants by exome sequencing in a large cohort of genetic disorders.
Rolph Pfundt, Marisol Del Rosario, Lisenka E L M Vissers, Michael P Kwint, Irene M Janssen, Nicole de Leeuw, Helger G Yntema, Marcel R Nelen, Dorien Lugtenberg, Erik-Jan Kamsteeg,[...]. Genet Med 2017
78
1

Benign paroxysmal torticollis of infancy: four new cases and linkage to CACNA1A mutation.
N J Giffin, S Benton, P J Goadsby. Dev Med Child Neurol 2002
99
1

A novel CACNA1A mutation associated with adult-onset, paroxysmal head tremor.
Anna Molloy, Okka Kimmich, Joanne Martindale, Helena Moore, Michael Hutchinson, Sean O'Riordan. Mov Disord 2013
6
16

Progressive Ataxia with Hemiplegic Migraines: a Phenotype of CACNA1A Missense Mutations, Not CAG Repeat Expansions.
Kevin R Duque, Luca Marsili, Andrea Sturchio, Abhimanyu Mahajan, Aristide Merola, Alberto J Espay, Marcelo A Kauffman. Cerebellum 2021
2
50

[Somatic polysaccharide-containing antigens of the plague bacterium].
E E Bakhrakh, V I Veĭnblat. Zh Mikrobiol Epidemiol Immunobiol 1972
63
1

[Editorial: Medical ethics in medical care services].
P Kassab. AMB Rev Assoc Med Bras 1973
83
1

CACNA1A-associated epilepsy: Electroclinical findings and treatment response on seizures in 18 patients.
Marie Le Roux, Magalie Barth, Sophie Gueden, Patrick Desbordes de Cepoy, Alec Aeby, Catheline Vilain, Edouard Hirsch, Anne de Saint Martin, Vincent des Portes, Gaëtan Lesca,[...]. Eur J Paediatr Neurol 2021
2
50

Two distinct phenotypes, hemiplegic migraine and episodic Ataxia type 2, caused by a novel common CACNA1A variant.
Rosaria Nardello, Giorgia Plicato, Giuseppe Donato Mangano, Elena Gennaro, Salvatore Mangano, Filippo Brighina, Vincenzo Raieli, Antonina Fontana. BMC Neurol 2020
5
20

The electrophysiological footprint of CACNA1A disorders.
Elisabetta Indelicato, Iris Unterberger, Wolfgang Nachbauer, Andreas Eigentler, Matthias Amprosi, Fiona Zeiner, Edda Haberlandt, Manuela Kaml, Elke Gizewski, Sylvia Boesch. J Neurol 2021
4
25

Benign paroxysmal torticollis, benign paroxysmal vertigo, and benign tonic upward gaze are not benign disorders.
Véronique Humbertclaude, Benjamin Krams, Erika Nogue, Nicolas Nagot, Daniel Annequin, Barbara Tourniaire, Elisabeth Tournier-Lasserve, Florence Riant, Agathe Roubertie. Dev Med Child Neurol 2018
8
12

Genetics of the SCA6 gene in a large family segregating an autosomal dominant "pure" cerebellar ataxia.
J García-Planells, A Cuesta, J J Vilchez, F Martínez, F Prieto, F Palau. J Med Genet 1999
8
12

Visualization, quantification and correlation of brain atrophy with clinical symptoms in spinocerebellar ataxia types 1, 3 and 6.
Jörg B Schulz, Johannes Borkert, Stefanie Wolf, Tanja Schmitz-Hübsch, Maryla Rakowicz, Caterina Mariotti, Ludger Schöls, Dagmar Timmann, Bart van de Warrenburg, Alexandra Dürr,[...]. Neuroimage 2010
111
1

Large CACNA1A deletion in a family with episodic ataxia type 2.
Florence Riant, Reda Mourtada, Pascale Saugier-Veber, Elisabeth Tournier-Lasserve. Arch Neurol 2008
31
3

Epilepsy and episodic ataxia type 2: family study and review of the literature.
Lorenzo Verriello, Giada Pauletto, Annacarmen Nilo, Incoronata Lonigro, Elena Betto, Mariarosaria Valente, Francesco Curcio, Gian Luigi Gigli. J Neurol 2021
1
100

Two cases with postural axial tremor: Consider a genetic origin.
R Zutt, J W Elting, P Santens, G J R Luijckx, M A J Tijssen. Parkinsonism Relat Disord 2020
2
50

Transient benign paroxysmal movement disorders in infancy.
Emilio Fernández-Alvarez. Eur J Paediatr Neurol 2018
10
10


A post-hoc comparison of the utility of sanger sequencing and exome sequencing for the diagnosis of heterogeneous diseases.
Kornelia Neveling, Ilse Feenstra, Christian Gilissen, Lies H Hoefsloot, Erik-Jan Kamsteeg, Arjen R Mensenkamp, Richard J T Rodenburg, Helger G Yntema, Liesbeth Spruijt, Sascha Vermeer,[...]. Hum Mutat 2013
222
1

The Genetic Homogeneity of CAPOS Syndrome: Four New Patients With the c.2452G>A (p.Glu818Lys) Mutation in the ATP1A3 Gene.
Roderick P P W M Maas, Jolanda H Schieving, Meyke Schouten, Erik-Jan Kamsteeg, Bart P C van de Warrenburg. Pediatr Neurol 2016
28
3

Paroxysmal tonic upgaze: A heterogeneous clinical condition responsive to carbonic anhydrase inhibition.
Annegret Quade, Anne Thiel, Ingo Kurth, Manuel Holtgrewe, Miriam Elbracht, Dieter Beule, Katja Eggermann, Ute I Scholl, Martin Häusler. Eur J Paediatr Neurol 2020
6
16

Copy number variation detection and genotyping from exome sequence data.
Niklas Krumm, Peter H Sudmant, Arthur Ko, Brian J O'Roak, Maika Malig, Bradley P Coe, Aaron R Quinlan, Deborah A Nickerson, Evan E Eichler. Genome Res 2012
368
1



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.