A citation-based method for searching scientific literature

Charles K Abrams, Steven S Scherer. Biochim Biophys Acta 2012
Times Cited: 82







List of co-cited articles
1233 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Transient central nervous system white matter abnormality in X-linked Charcot-Marie-Tooth disease.
Henry L Paulson, James Y Garbern, Timothy F Hoban, Karen M Krajewski, Richard A Lewis, Kenneth H Fischbeck, Robert I Grossman, Robert Lenkinski, John A Kamholz, Michael E Shy. Ann Neurol 2002
122
23

The CNS phenotype of X-linked Charcot-Marie-Tooth disease: more than a peripheral problem.
Robert A Taylor, Erin M Simon, Harold G Marks, Steven S Scherer. Neurology 2003
117
21

Connexins are critical for normal myelination in the CNS.
Daniela M Menichella, Daniel A Goodenough, Erich Sirkowski, Steven S Scherer, David L Paul. J Neurosci 2003
192
19

GJA1 mutations, variants, and connexin 43 dysfunction as it relates to the oculodentodigital dysplasia phenotype.
William A Paznekas, Barbara Karczeski, Sascha Vermeer, R Brian Lowry, Martin Delatycki, Faivre Laurence, Pasi A Koivisto, Lionel Van Maldergem, Simeon A Boyadjiev, Joann N Bodurtha,[...]. Hum Mutat 2009
190
19

Connexin 43 (GJA1) mutations cause the pleiotropic phenotype of oculodentodigital dysplasia.
William A Paznekas, Simeon A Boyadjiev, Robert E Shapiro, Otto Daniels, Bernd Wollnik, Catherine E Keegan, Jeffrey W Innis, Mary Beth Dinulos, Cathy Christian, Mark C Hannibal,[...]. Am J Hum Genet 2003
445
17

Connexin mutations in X-linked Charcot-Marie-Tooth disease.
J Bergoffen, S S Scherer, S Wang, M O Scott, L J Bone, D L Paul, K Chen, M W Lensch, P F Chance, K H Fischbeck. Science 1993
888
17

How do mutations in GJB1 cause X-linked Charcot-Marie-Tooth disease?
Kleopas A Kleopa, Charles K Abrams, Steven S Scherer. Brain Res 2012
67
20

Connexin32 is a myelin-related protein in the PNS and CNS.
S S Scherer, S M Deschênes, Y T Xu, J B Grinspan, K H Fischbeck, D L Paul. J Neurosci 1995
321
17

Transient, recurrent, white matter lesions in X-linked Charcot-Marie-Tooth disease with novel connexin 32 mutation.
C Oliver Hanemann, Carsten Bergmann, Jan Senderek, Klaus Zerres, Ann-Dorte Sperfeld. Arch Neurol 2003
88
15

Connexin32 mutations cause loss of function in Schwann cells and oligodendrocytes leading to PNS and CNS myelination defects.
Irene Sargiannidou, Natalie Vavlitou, Sophia Aristodemou, Andreas Hadjisavvas, Kyriacos Kyriacou, Steven S Scherer, Kleopas A Kleopa. J Neurosci 2009
83
14

Structure of the connexin 26 gap junction channel at 3.5 A resolution.
Shoji Maeda, So Nakagawa, Michihiro Suga, Eiki Yamashita, Atsunori Oshima, Yoshinori Fujiyoshi, Tomitake Tsukihara. Nature 2009
467
14

The impact of astrocytic gap junctional coupling on potassium buffering in the hippocampus.
Anke Wallraff, Rüdiger Köhling, Uwe Heinemann, Martin Theis, Klaus Willecke, Christian Steinhäuser. J Neurosci 2006
374
13


Mutations in the gene encoding gap junction protein alpha 12 (connexin 46.6) cause Pelizaeus-Merzbacher-like disease.
Birgit Uhlenberg, Markus Schuelke, Franz Rüschendorf, Nico Ruf, Angela M Kaindl, Marco Henneke, Holger Thiele, Gisela Stoltenburg-Didinger, Fuat Aksu, Haluk Topaloğlu,[...]. Am J Hum Genet 2004
196
13

CMT1X phenotypes represent loss of GJB1 gene function.
M E Shy, C Siskind, E R Swan, K M Krajewski, T Doherty, D R Fuerst, P J Ainsworth, R A Lewis, S S Scherer, A F Hahn. Neurology 2007
117
13

X-linked hereditary motor sensory neuropathy (type 1) presenting with a stroke-like episode.
Geetha Anand, Nitin Maheshwari, David Roberts, Anuruddha Padeniya, Michele Hamilton-Ayers, Marjo van der Knaap, Carl Fratter, Sandeep Jayawant. Dev Med Child Neurol 2010
36
30

Neurological manifestations of the oculodentodigital dysplasia syndrome.
Tobias Loddenkemper, Kerstin Grote, Stefan Evers, Michael Oelerich, Florian Stögbauer. J Neurol 2002
123
12

Genetic and physiological evidence that oligodendrocyte gap junctions contribute to spatial buffering of potassium released during neuronal activity.
Daniela M Menichella, Marta Majdan, Rajeshwar Awatramani, Daniel A Goodenough, Erich Sirkowski, Steven S Scherer, David L Paul. J Neurosci 2006
119
12

Plasma membrane channels formed by connexins: their regulation and functions.
Juan C Saez, Viviana M Berthoud, Maria C Branes, Agustin D Martinez, Eric C Beyer. Physiol Rev 2003
862
12

Phenotypic and cellular expression of two novel connexin32 mutations causing CMT1X.
K A Kleopa, E Zamba-Papanicolaou, X Alevra, P Nicolaou, D-M Georgiou, A Hadjisavvas, T Kyriakides, K Christodoulou. Neurology 2006
41
24

Transient cerebral white matter lesions in a patient with connexin 32 missense mutation.
H J Schelhaas, B G M Van Engelen, A A W M Gabreëls-Festen, G Hageman, J H R Vliegen, M S Van Der Knaap, M J Zwarts. Neurology 2002
48
20

Central nervous system signs in X-linked Charcot-Marie-Tooth disease after hyperventilation.
Jayasri Srinivasan, Richard J Leventer, Andrew J Kornberg, Henrik H Dahl, Monique M Ryan. Pediatr Neurol 2008
28
35

Two distinct heterotypic channels mediate gap junction coupling between astrocyte and oligodendrocyte connexins.
Jennifer L Orthmann-Murphy, Mona Freidin, Esther Fischer, Steven S Scherer, Charles K Abrams. J Neurosci 2007
128
10

Connexin43 phosphorylation in brain, cardiac, endothelial and epithelial tissues.
Lucrecia Márquez-Rosado, Joell L Solan, Clarence A Dunn, Rachael P Norris, Paul D Lampe. Biochim Biophys Acta 2012
103
10

Changes in permeability caused by connexin 32 mutations underlie X-linked Charcot-Marie-Tooth disease.
S Oh, Y Ri, M V Bennett, E B Trexler, V K Verselis, T A Bargiello. Neuron 1997
203
10

Gap junction remodeling and cardiac arrhythmogenesis in a murine model of oculodentodigital dysplasia.
Nellie Kalcheva, Jiaxiang Qu, Nefthi Sandeep, Luis Garcia, Jie Zhang, Zhiyong Wang, Paul D Lampe, Sylvia O Suadicani, David C Spray, Glenn I Fishman. Proc Natl Acad Sci U S A 2007
96
10



Functional characterization of oculodentodigital dysplasia-associated Cx43 mutants.
Elizabeth McLachlan, Janet L Manias, Xiang-Qun Gong, Crystal S Lounsbury, Qing Shao, Suzanne M Bernier, Donglin Bai, Dale W Laird. Cell Commun Adhes 2005
53
16

Autosomal recessive GJA1 (Cx43) gene mutations cause oculodentodigital dysplasia by distinct mechanisms.
Tao Huang, Qing Shao, Andrew MacDonald, Li Xin, Robert Lorentz, Donglin Bai, Dale W Laird. J Cell Sci 2013
23
39

Structure and functional studies of N-terminal Cx43 mutants linked to oculodentodigital dysplasia.
Qing Shao, Qin Liu, Robert Lorentz, Xiang-Qun Gong, Donglin Bai, Gary S Shaw, Dale W Laird. Mol Biol Cell 2012
31
29




A V139M mutation also causes the reversible CNS phenotype in CMTX.
Michelle Halbrich, Jeffrey Barnes, Martin Bunge, Charuta Joshi. Can J Neurol Sci 2008
22
40

Recurrent stroke-like episodes in X-linked Charcot-Marie-Tooth disease.
A Basu, R Horvath, B Esisi, D Birchall, P F Chinnery. Neurology 2011
15
60

Charcot-Marie-Tooth disease masquerading as acute demyelinating encephalomyelitis-like illness.
Gun-Ha Kim, Kyoung Min Kim, Sang-Il Suh, Chang-Seok Ki, Baik-Lin Eun. Pediatrics 2014
17
52

Astroglial networks scale synaptic activity and plasticity.
Ulrike Pannasch, Lydia Vargová, Jürgen Reingruber, Pascal Ezan, David Holcman, Christian Giaume, Eva Syková, Nathalie Rouach. Proc Natl Acad Sci U S A 2011
243
9

Astroglial metabolic networks sustain hippocampal synaptic transmission.
Nathalie Rouach, Annette Koulakoff, Veronica Abudara, Klaus Willecke, Christian Giaume. Science 2008
557
9

Structural and functional diversity of connexin genes in the mouse and human genome.
Klaus Willecke, Jürgen Eiberger, Joachim Degen, Dominik Eckardt, Alessandro Romualdi, Martin Güldenagel, Urban Deutsch, Goran Söhl. Biol Chem 2002
893
9

Mutations in connexin genes and disease.
Anna Pfenniger, Annelise Wohlwend, Brenda R Kwak. Eur J Clin Invest 2011
109
9

Selective defects in channel permeability associated with Cx32 mutations causing X-linked Charcot-Marie-Tooth disease.
Massimiliano Bicego, Sabina Morassutto, Victor H Hernandez, Marcello Morgutti, Fabio Mammano, Paola D'Andrea, Roberto Bruzzone. Neurobiol Dis 2006
21
38

Cellular mechanisms of connexin32 mutations associated with CNS manifestations.
Kleopas A Kleopa, Sabrina W Yum, Steven S Scherer. J Neurosci Res 2002
91
9


Gap junction channel gating.
Feliksas F Bukauskas, Vytas K Verselis. Biochim Biophys Acta 2004
201
9



Oculodentodigital dysplasia connexin43 mutations result in non-functional connexin hemichannels and gap junctions in C6 glioma cells.
Albert Lai, Dung-Nghi Le, William A Paznekas, Wes D Gifford, Ethylin Wang Jabs, Andrew C Charles. J Cell Sci 2006
74
10

A Gja1 missense mutation in a mouse model of oculodentodigital dysplasia.
Ann M Flenniken, Lucy R Osborne, Nicole Anderson, Nadia Ciliberti, Craig Fleming, Joanne E I Gittens, Xiang-Qun Gong, Lois B Kelsey, Crystal Lounsbury, Luisa Moreno,[...]. Development 2005
187
9

Persistent CNS dysfunction in a boy with CMT1X.
Carly Siskind, Shawna M E Feely, Saunder Bernes, Michael E Shy, James Y Garbern. J Neurol Sci 2009
31
25


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.