A citation-based method for searching scientific literature

Tamara Vyshkina, Andrew Sylvester, Saud Sadiq, Eduardo Bonilla, Jeff A Canter, Andras Perl, Bernadette Kalman. Clin Immunol 2008
Times Cited: 48







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



Times Cited
  Times     Co-cited
Similarity


mtDNA nt13708A variant increases the risk of multiple sclerosis.
Xinhua Yu, Dirk Koczan, Anna-Maija Sulonen, Denis A Akkad, Antje Kroner, Manuel Comabella, Gianna Costa, Daniela Corongiu, Robert Goertsches, Montserrat Camina-Tato,[...]. PLoS One 2008
53
37

Mitochondrial hyperpolarization and ATP depletion in patients with systemic lupus erythematosus.
Peter Gergely, Craig Grossman, Brian Niland, Ferenc Puskas, Hom Neupane, Fatme Allam, Katalin Banki, Paul E Phillips, Andras Perl. Arthritis Rheum 2002
203
27

Mitochondrial DNA variants in Bulgarian patients affected by multiple sclerosis.
S M Mihailova, M I Ivanova, L M Quin, E J Naumova. Eur J Neurol 2007
18
61

Mitochondrial dysfunction as a cause of axonal degeneration in multiple sclerosis patients.
Ranjan Dutta, Jennifer McDonough, Xinghua Yin, John Peterson, Ansi Chang, Thalia Torres, Tatyana Gudz, Wendy B Macklin, David A Lewis, Robert J Fox,[...]. Ann Neurol 2006
576
22


Mitochondrial hyperpolarization: a checkpoint of T-cell life, death and autoimmunity.
Andras Perl, Peter Gergely, Gyorgy Nagy, Agnes Koncz, Katalin Banki. Trends Immunol 2004
159
18

Oxidative damage to mitochondrial DNA and activity of mitochondrial enzymes in chronic active lesions of multiple sclerosis.
F Lu, M Selak, J O'Connor, S Croul, C Lorenzana, C Butunoi, B Kalman. J Neurol Sci 2000
242
18

Mitochondrial DNA mutations in multiple sclerosis.
B Kalman, F D Lublin, H Alder. Mult Scler 1995
57
18

N-acetylcysteine reduces disease activity by blocking mammalian target of rapamycin in T cells from systemic lupus erythematosus patients: a randomized, double-blind, placebo-controlled trial.
Zhi-Wei Lai, Robert Hanczko, Eduardo Bonilla, Tiffany N Caza, Brandon Clair, Adam Bartos, Gabriella Miklossy, John Jimah, Edward Doherty, Hajra Tily,[...]. Arthritis Rheum 2012
200
18

Investigation of the role of mitochondrial DNA in multiple sclerosis susceptibility.
Maria Ban, Joanna Elson, Amie Walton, Douglas Turnbull, Alastair Compston, Patrick Chinnery, Stephen Sawcer. PLoS One 2008
32
25

Mitochondrial DNA mutations in multiple sclerosis patients with severe optic involvement.
U Mayr-Wohlfart, C Paulus, A Henneberg, G Rödel. Acta Neurol Scand 1996
59
16


Mitochondrial dysfunction in T cells of patients with systemic lupus erythematosus.
Andras Perl, Peter Gergely, Katalin Banki. Int Rev Immunol 2004
46
17

Diagnostic criteria for multiple sclerosis: 2010 revisions to the McDonald criteria.
Chris H Polman, Stephen C Reingold, Brenda Banwell, Michel Clanet, Jeffrey A Cohen, Massimo Filippi, Kazuo Fujihara, Eva Havrdova, Michael Hutchinson, Ludwig Kappos,[...]. Ann Neurol 2011
16

Mitochondrial DNA sequence variation in multiple sclerosis.
Gregory J Tranah, Adam Santaniello, Stacy J Caillier, Sandra D'Alfonso, Filippo Martinelli Boneschi, Stephen L Hauser, Jorge R Oksenberg. Neurology 2015
34
23

Rapamycin reduces disease activity and normalizes T cell activation-induced calcium fluxing in patients with systemic lupus erythematosus.
David Fernandez, Eduardo Bonilla, Naureen Mirza, Brian Niland, Andras Perl. Arthritis Rheum 2006
200
14

Activation of mammalian target of rapamycin controls the loss of TCRzeta in lupus T cells through HRES-1/Rab4-regulated lysosomal degradation.
David R Fernandez, Tiffany Telarico, Eduardo Bonilla, Qing Li, Sanjay Banerjee, Frank A Middleton, Paul E Phillips, Mary K Crow, Stefanie Oess, Werner Muller-Esterl,[...]. J Immunol 2009
151
14

Population screening for association of mitochondrial haplogroups BM, J, K and M with multiple sclerosis: interrelation between haplogroup J and MS in Persian patients.
M Houshmand, M H Sanati, F Babrzadeh, A Ardalan, M Teimori, M Vakilian, M Akuchekian, D Farhud, J Lotfi. Mult Scler 2005
17
41

Mitochondrial DNA polymorphisms are associated with susceptibility and phenotype of systemic lupus erythematosus.
A Jönsen, X Yu, L Truedsson, O Nived, G Sturfelt, S Ibrahim, Aa Bengtsson. Lupus 2009
17
35

Association of UCP2 -866 G/A polymorphism with chronic inflammatory diseases.
X Yu, S Wieczorek, A Franke, H Yin, M Pierer, C Sina, T H Karlsen, K M Boberg, A Bergquist, M Kunz,[...]. Genes Immun 2009
56
12

Systemic lupus erythematosus.
George C Tsokos. N Engl J Med 2011
12

Mitochondrial haplogroups in Basque multiple sclerosis patients.
D Otaegui, A Sáenz, M Martínez-Zabaleta, P Villoslada, I Fernández-Manchola, A Alvarez de Arcaya, J I Emparanza, A López de Munain. Mult Scler 2004
22
27

Leukocyte mitochondrial DNA alteration in systemic lupus erythematosus and its relevance to the susceptibility to lupus nephritis.
Hui-Ting Lee, Chen-Sung Lin, Wei-Sheng Chen, Hsien-Tzung Liao, Chang-Youh Tsai, Yau-Huei Wei. Int J Mol Sci 2012
24
25


Mitochondrial DNA mutations in human disease.
Robert W Taylor, Doug M Turnbull. Nat Rev Genet 2005
10

Nitric oxide-dependent mitochondrial biogenesis generates Ca2+ signaling profile of lupus T cells.
Gyorgy Nagy, Maureen Barcza, Nick Gonchoroff, Paul E Phillips, Andras Perl. J Immunol 2004
80
10


Rapamycin attenuates the severity of established nephritis in lupus-prone NZB/W F1 mice.
Sing Leung Lui, Ryan Tsang, Kwok Wah Chan, Florence Zhang, Sidney Tam, Susan Yung, Tak Mao Chan. Nephrol Dial Transplant 2008
56
10


The 1982 revised criteria for the classification of systemic lupus erythematosus.
E M Tan, A S Cohen, J F Fries, A T Masi, D J McShane, N F Rothfield, J G Schaller, N Talal, R J Winchester. Arthritis Rheum 1982
10

Mitochondrial D-loop variation in Persian multiple sclerosis patients: K and A haplogroups as a risk factor!!
Hassan Hassani-Kumleh, Massoud Houshmand, Mehdi Shafa Shariat Panahi, Gholam Hossein Riazi, Mohammad Hossein Sanati, Kurosh Gharagozli, Mojdeh Ghabaee. Cell Mol Neurobiol 2006
15
33

Murine lupus susceptibility locus Sle1c2 mediates CD4+ T cell activation and maps to estrogen-related receptor γ.
Daniel J Perry, Yiming Yin, Tiffany Telarico, Henry V Baker, Igor Dozmorov, Andras Perl, Laurence Morel. J Immunol 2012
35
14


Mitochondrial DNA deletions and neurodegeneration in multiple sclerosis.
Graham R Campbell, Iryna Ziabreva, Amy K Reeve, Kim J Krishnan, Richard Reynolds, Owen Howell, Hans Lassmann, Doug M Turnbull, Don J Mahad. Ann Neurol 2011
217
10

Is multiple sclerosis a mitochondrial disease?
Peizhong Mao, P Hemachandra Reddy. Biochim Biophys Acta 2010
146
10

Recent mitochondrial DNA mutations increase the risk of developing common late-onset human diseases.
Gavin Hudson, Aurora Gomez-Duran, Ian J Wilson, Patrick F Chinnery. PLoS Genet 2014
88
10

Shared signaling networks active in B cells isolated from genetically distinct mouse models of lupus.
Tianfu Wu, Xiangmei Qin, Zoran Kurepa, Kirthi Raman Kumar, Kui Liu, Hasna Kanta, Xin J Zhou, Anne B Satterthwaite, Laurie S Davis, Chandra Mohan. J Clin Invest 2007
64
8

Regulation of CD4 expression via recycling by HRES-1/RAB4 controls susceptibility to HIV infection.
Gyorgy Nagy, Jeffrey Ward, Dick D Mosser, Agnes Koncz, Peter Gergely, Christina Stancato, Yueming Qian, David Fernandez, Brian Niland, Craig E Grossman,[...]. J Biol Chem 2006
48
8

Review: Mitochondria and disease progression in multiple sclerosis.
D Mahad, H Lassmann, D Turnbull. Neuropathol Appl Neurobiol 2008
125
8

Mitochondrial changes within axons in multiple sclerosis.
Don J Mahad, Iryna Ziabreva, Graham Campbell, Nichola Lax, Katherine White, Peter S Hanson, Hans Lassmann, Douglass M Turnbull. Brain 2009
298
8

Estrogen and CD4+ T cells.
Alessandra B Pernis. Curr Opin Rheumatol 2007
76
8

Parent-of-origin effect in multiple sclerosis: observations in half-siblings.
G C Ebers, A D Sadovnick, D A Dyment, I M L Yee, C J Willer, Neil Risch. Lancet 2004
182
8

Sequence and organization of the human mitochondrial genome.
S Anderson, A T Bankier, B G Barrell, M H de Bruijn, A R Coulson, J Drouin, I C Eperon, D P Nierlich, B A Roe, F Sanger,[...]. Nature 1981
8

Leber's hereditary optic neuropathy mitochondrial DNA mutations in childhood multiple sclerosis.
F A Hanefeld, B P Ernst, E Wilichowski, H J Christen. Neuropediatrics 1994
40
10

A novel mitochondrial DNA point mutation in the tRNA(Ile) gene: studies in a patient presenting with chronic progressive external ophthalmoplegia and multiple sclerosis.
R W Taylor, P F Chinnery, M J Bates, M J Jackson, M A Johnson, R M Andrews, D M Turnbull. Biochem Biophys Res Commun 1998
45
8

The kinase mTOR regulates the differentiation of helper T cells through the selective activation of signaling by mTORC1 and mTORC2.
Greg M Delgoffe, Kristen N Pollizzi, Adam T Waickman, Emily Heikamp, David J Meyers, Maureen R Horton, Bo Xiao, Paul F Worley, Jonathan D Powell. Nat Immunol 2011
715
8


Cutting edge: distinct glycolytic and lipid oxidative metabolic programs are essential for effector and regulatory CD4+ T cell subsets.
Ryan D Michalek, Valerie A Gerriets, Sarah R Jacobs, Andrew N Macintyre, Nancie J MacIver, Emily F Mason, Sarah A Sullivan, Amanda G Nichols, Jeffrey C Rathmell. J Immunol 2011
8




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.