A citation-based method for searching scientific literature

Q Yue, J C Jen, S F Nelson, R W Baloh. Am J Hum Genet 1997
Times Cited: 102







List of co-cited articles
1009 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4.
R A Ophoff, G M Terwindt, M N Vergouwe, R van Eijk, P J Oefner, S M Hoffman, J E Lamerdin, H W Mohrenweiser, D E Bulman, M Ferrari,[...]. Cell 1996
78

Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel.
O Zhuchenko, J Bailey, P Bonnen, T Ashizawa, D W Stockton, C Amos, W B Dobyns, S H Subramony, H Y Zoghbi, C C Lee. Nat Genet 1997
969
71

Episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) due to CAG repeat expansion in the CACNA1A gene on chromosome 19p.
C Jodice, E Mantuano, L Veneziano, F Trettel, G Sabbadini, L Calandriello, A Francia, M Spadaro, F Pierelli, F Salvi,[...]. Hum Mol Genet 1997
173
45

High prevalence of CACNA1A truncations and broader clinical spectrum in episodic ataxia type 2.
C Denier, A Ducros, K Vahedi, A Joutel, P Thierry, A Ritz, G Castelnovo, T Deonna, P Gérard, J L Devoize,[...]. Neurology 1999
118
32

A novel nonsense mutation in CACNA1A causes episodic ataxia and hemiplegia.
J Jen, Q Yue, S F Nelson, H Yu, M Litt, J Nutt, R W Baloh. Neurology 1999
74
39

Absence epilepsy in tottering mutant mice is associated with calcium channel defects.
C F Fletcher, C M Lutz, T N O'Sullivan, J D Shaughnessy, R Hawkes, W N Frankel, N G Copeland, N A Jenkins. Cell 1996
505
26

Familial hemiplegic migraine mutations change alpha1A Ca2+ channel kinetics.
R L Kraus, M J Sinnegger, H Glossmann, S Hering, J Striessnig. J Biol Chem 1998
132
26

Functional consequences of mutations in the human alpha1A calcium channel subunit linked to familial hemiplegic migraine.
M Hans, S Luvisetto, M E Williams, M Spagnolo, A Urrutia, A Tottene, P F Brust, E C Johnson, M M Harpold, K A Stauderman,[...]. J Neurosci 1999
153
26

A new CACNA1A gene mutation in acetazolamide-responsive familial hemiplegic migraine and ataxia.
S Battistini, S Stenirri, M Piatti, C Gelfi, P G Righetti, R Rocchi, F Giannini, N Battistini, G C Guazzi, M Ferrari,[...]. Neurology 1999
115
24

Complete loss of P/Q calcium channel activity caused by a CACNA1A missense mutation carried by patients with episodic ataxia type 2.
S Guida, F Trettel, S Pagnutti, E Mantuano, A Tottene, L Veneziano, T Fellin, M Spadaro, K Stauderman, M Williams,[...]. Am J Hum Genet 2001
95
25

The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel.
A Ducros, C Denier, A Joutel, M Cecillon, C Lescoat, K Vahedi, F Darcel, E Vicaut, M G Bousser, E Tournier-Lasserve. N Engl J Med 2001
301
24

Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia.
A Ducros, C Denier, A Joutel, K Vahedi, A Michel, F Darcel, M Madigand, D Guerouaou, F Tison, J Julien,[...]. Am J Hum Genet 1999
96
23

De novo mutation in CACNA1A caused acetazolamide-responsive episodic ataxia.
Q Yue, J C Jen, M M Thwe, S F Nelson, R W Baloh. Am J Med Genet 1998
49
46

Primary structure and functional expression from complementary DNA of a brain calcium channel.
Y Mori, T Friedrich, M S Kim, A Mikami, J Nakai, P Ruth, E Bosse, F Hofmann, V Flockerzi, T Furuichi. Nature 1991
603
22

Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1.
D L Browne, S T Gancher, J G Nutt, E R Brunt, E A Smith, P Kramer, M Litt. Nat Genet 1994
446
21


Ablation of P/Q-type Ca(2+) channel currents, altered synaptic transmission, and progressive ataxia in mice lacking the alpha(1A)-subunit.
K Jun, E S Piedras-Rentería, S M Smith, D B Wheeler, S B Lee, T G Lee, H Chin, M E Adams, R H Scheller, R W Tsien,[...]. Proc Natl Acad Sci U S A 1999
321
19

Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHM.
K L Friend, D Crimmins, T G Phan, C M Sue, A Colley, V S Fung, J G Morris, G R Sutherland, R I Richards. Hum Genet 1999
47
40

Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel.
A Jouvenceau, L H Eunson, A Spauschus, V Ramesh, S M Zuberi, D M Kullmann, M G Hanna. Lancet 2001
221
19

Immunochemical identification and subcellular distribution of the alpha 1A subunits of brain calcium channels.
R E Westenbroek, T Sakurai, E M Elliott, J W Hell, T V Starr, T P Snutch, W A Catterall. J Neurosci 1995
386
18

Single tottering mutations responsible for the neuropathic phenotype of the P-type calcium channel.
M Wakamori, K Yamazaki, H Matsunodaira, T Teramoto, I Tanaka, T Niidome, K Sawada, Y Nishizawa, N Sekiguchi, E Mori,[...]. J Biol Chem 1998
156
17


Genetic heterogeneity in Italian families with familial hemiplegic migraine.
P Carrera, M Piatti, S Stenirri, L M Grimaldi, E Marchioni, M Curcio, P G Righetti, M Ferrari, C Gelfi. Neurology 1999
58
27

Clinical spectrum of episodic ataxia type 2.
J Jen, G W Kim, R W Baloh. Neurology 2004
147
16

The mouse stargazer gene encodes a neuronal Ca2+-channel gamma subunit.
V A Letts, R Felix, G H Biddlecome, J Arikkath, C L Mahaffey, A Valenzuela, F S Bartlett, Y Mori, K P Campbell, W N Frankel. Nat Genet 1998
384
15

Three new familial hemiplegic migraine mutants affect P/Q-type Ca(2+) channel kinetics.
R L Kraus, M J Sinnegger, A Koschak, H Glossmann, S Stenirri, P Carrera, J Striessnig. J Biol Chem 2000
92
16

Loss-of-function EA2 mutations are associated with impaired neuromuscular transmission.
J Jen, J Wan, M Graves, H Yu, A F Mock, C J Coulin, G Kim, Q Yue, D M Papazian, R W Baloh. Neurology 2001
84
17

Spinocerebellar ataxia type 6. Frequency of the mutation and genotype-phenotype correlations.
D H Geschwind, S Perlman, K P Figueroa, J Karrim, R W Baloh, S M Pulst. Neurology 1997
103
14

A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns.
N A Singh, C Charlier, D Stauffer, B R DuPont, R J Leach, R Melis, G M Ronen, I Bjerre, T Quattlebaum, J V Murphy,[...]. Nat Genet 1998
741
14

Coding and noncoding variation of the human calcium-channel beta4-subunit gene CACNB4 in patients with idiopathic generalized epilepsy and episodic ataxia.
A Escayg, M De Waard, D D Lee, D Bichet, P Wolf, T Mayer, J Johnston, R Baloh, T Sander, M H Meisler. Am J Hum Genet 2000
229
14

A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family.
C Charlier, N A Singh, S G Ryan, T B Lewis, B E Reus, R J Leach, M Leppert. Nat Genet 1998
610
13


Molecular features of the CAG repeats of spinocerebellar ataxia 6 (SCA6).
Z Matsuyama, H Kawakami, H Maruyama, Y Izumi, O Komure, F Udaka, M Kameyama, T Nishio, Y Kuroda, M Nishimura,[...]. Hum Mol Genet 1997
102
13

Missense CACNA1A mutation causing episodic ataxia type 2.
C Denier, A Ducros, A Durr, B Eymard, B Chassande, E Tournier-Lasserve. Arch Neurol 2001
40
32

Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.
H T Orr, M Y Chung, S Banfi, T J Kwiatkowski, A Servadio, A L Beaudet, A E McCall, L A Duvick, L P Ranum, H Y Zoghbi. Nat Genet 1993
12

A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsy.
S M Zuberi, L H Eunson, A Spauschus, R De Silva, J Tolmie, N W Wood, R C McWilliam, J B Stephenson, D M Kullmann, M G Hanna. Brain 1999
213
12

Spinocerebellar ataxia type 6 mutation alters P-type calcium channel function.
S Toru, T Murakoshi, K Ishikawa, H Saegusa, H Fujigasaki, T Uchihara, S Nagayama, M Osanai, H Mizusawa, T Tanabe. J Biol Chem 2000
66
18

Dystonia and cerebellar atrophy in Cacna1a null mice lacking P/Q calcium channel activity.
C F Fletcher, A Tottene, V A Lennon, S M Wilson, S J Dubel, R Paylor, D A Hosford, L Tessarollo, M W McEnery, D Pietrobon,[...]. FASEB J 2001
125
12

Delayed cerebral edema and fatal coma after minor head trauma: role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine.
E E Kors, G M Terwindt, F L Vermeulen, R B Fitzsimons, P E Jardine, P Heywood, S Love, A M van den Maagdenberg, J Haan, R R Frants,[...]. Ann Neurol 2001
198
12

Altered calcium channel currents in Purkinje cells of the neurological mutant mouse leaner.
N M Lorenzon, C M Lutz, W N Frankel, K G Beam. J Neurosci 1998
108
11



Abundant expression and cytoplasmic aggregations of [alpha]1A voltage-dependent calcium channel protein associated with neurodegeneration in spinocerebellar ataxia type 6.
K Ishikawa, H Fujigasaki, H Saegusa, K Ohwada, T Fujita, H Iwamoto, Y Komatsuzaki, S Toru, H Toriyama, M Watanabe,[...]. Hum Mol Genet 1999
114
11


Early onset, non fluctuating spinocerebellar ataxia and a novel missense mutation in CACNA1A gene.
Alessandra Tonelli, Maria Grazia D'Angelo, Roberto Salati, Laura Villa, Chiara Germinasi, Tiziano Frattini, Giovanni Meola, Anna Carla Turconi, Nereo Bresolin, Maria Teresa Bassi. J Neurol Sci 2006
31
35

A gene for hereditary paroxysmal cerebellar ataxia maps to chromosome 19p.
K Vahedi, A Joutel, P Van Bogaert, A Ducros, J Maciazeck, J F Bach, M G Bousser, E Tournier-Lasserve. Ann Neurol 1995
59
16


Dihydropyridine receptor mutations cause hypokalemic periodic paralysis.
L J Ptácek, R Tawil, R C Griggs, A G Engel, R B Layzer, H Kwieciński, P G McManis, L Santiago, M Moore, G Fouad. Cell 1994
260
10


Direct alteration of the P/Q-type Ca2+ channel property by polyglutamine expansion in spinocerebellar ataxia 6.
Z Matsuyama, M Wakamori, Y Mori, H Kawakami, S Nakamura, K Imoto. J Neurosci 1999
61
16


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.