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



Times Cited
  Times     Co-cited
Similarity


Quantitative evaluation of the mitochondrial DNA depletion syndrome.
David Dimmock, Lin-Ya Tang, Eric S Schmitt, Lee-Jun C Wong. Clin Chem 2010
82
21

Number matters: control of mammalian mitochondrial DNA copy number.
Laura L Clay Montier, Janice J Deng, Yidong Bai. J Genet Genomics 2009
287
14

Mutations in the MPV17 gene are responsible for rapidly progressive liver failure in infancy.
Lee-Jun C Wong, Nicola Brunetti-Pierri, Qing Zhang, Nada Yazigi, Kevin E Bove, Beverly B Dahms, Michelle A Puchowicz, Ignacio Gonzalez-Gomez, Eric S Schmitt, Cavatina K Truong,[...]. Hepatology 2007
81
14

Mutation of RRM2B, encoding p53-controlled ribonucleotide reductase (p53R2), causes severe mitochondrial DNA depletion.
Alice Bourdon, Limor Minai, Valérie Serre, Jean-Philippe Jais, Emmanuelle Sarzi, Sophie Aubert, Dominique Chrétien, Pascale de Lonlay, Véronique Paquis-Flucklinger, Hirofumi Arakawa,[...]. Nat Genet 2007
375
11

Clinical and molecular features of mitochondrial DNA depletion due to mutations in deoxyguanosine kinase.
D P Dimmock, Q Zhang, C Dionisi-Vici, R Carrozzo, J Shieh, L-Y Tang, C Truong, E Schmitt, M Sifry-Platt, S Lucioli,[...]. Hum Mutat 2008
92
10

Quantitative PCR analysis of mitochondrial DNA content in patients with mitochondrial disease.
Ren-Kui Bai, Cherng-Lih Perng, Chang-Hung Hsu, Lee-Jun C Wong. Ann N Y Acad Sci 2004
85
11

Deficiency of the alpha subunit of succinate-coenzyme A ligase causes fatal infantile lactic acidosis with mitochondrial DNA depletion.
Elsebet Ostergaard, Ernst Christensen, Elisabeth Kristensen, Bodil Mogensen, Morten Duno, Eric A Shoubridge, Flemming Wibrand. Am J Hum Genet 2007
117
9

Deficiency of the ADP-forming succinyl-CoA synthase activity is associated with encephalomyopathy and mitochondrial DNA depletion.
Orly Elpeleg, Chaya Miller, Eli Hershkovitz, Maria Bitner-Glindzicz, Gili Bondi-Rubinstein, Shamima Rahman, Alistair Pagnamenta, Sharon Eshhar, Ann Saada. Am J Hum Genet 2005
214
9

Mitochondrial DNA copy number in peripheral blood cells declines with age and is associated with general health among elderly.
Jonas Mengel-From, Mikael Thinggaard, Christine Dalgård, Kirsten Ohm Kyvik, Kaare Christensen, Lene Christiansen. Hum Genet 2014
149
9


Reduced mitochondrial DNA copy number is correlated with tumor progression and prognosis in Chinese breast cancer patients.
Man Yu, Yunli Zhou, Yurong Shi, Liansheng Ning, Yi Yang, Xiyin Wei, Ning Zhang, Xishan Hao, Ruifang Niu. IUBMB Life 2007
163
8

Molecular and clinical genetics of mitochondrial diseases due to POLG mutations.
Lee-Jun C Wong, Robert K Naviaux, Nicola Brunetti-Pierri, Qing Zhang, Eric S Schmitt, Cavatina Truong, Margherita Milone, Bruce H Cohen, Beverly Wical, Jaya Ganesh,[...]. Hum Mutat 2008
181
8

Mitochondrial encephalomyopathy with elevated methylmalonic acid is caused by SUCLA2 mutations.
Elsebet Ostergaard, Flemming J Hansen, Nicolina Sorensen, Morten Duno, John Vissing, Pernille L Larsen, Oddmar Faeroe, Sigurdur Thorgrimsson, Flemming Wibrand, Ernst Christensen,[...]. Brain 2007
117
8

Clinical and molecular features of mitochondrial DNA depletion syndromes.
A Spinazzola, F Invernizzi, F Carrara, E Lamantea, A Donati, M Dirocco, I Giordano, M Meznaric-Petrusa, E Baruffini, I Ferrero,[...]. J Inherit Metab Dis 2009
120
8

Biochemical assays of respiratory chain complex activity.
Denise M Kirby, David R Thorburn, Douglass M Turnbull, Robert W Taylor. Methods Cell Biol 2007
254
8


Variations in mitochondrial DNA copy numbers in MS brains.
Andrei Blokhin, Tamara Vyshkina, Samuel Komoly, Bernadette Kalman. J Mol Neurosci 2008
40
17

Mitochondrial DNA content: its genetic heritability and association with renal cell carcinoma.
Jinliang Xing, Meng Chen, Christopher G Wood, Jie Lin, Margaret R Spitz, Jianzhong Ma, Christopher I Amos, Peter G Shields, Neal L Benowitz, Jian Gu,[...]. J Natl Cancer Inst 2008
176
7

Twinkle helicase (PEO1) gene mutation causes mitochondrial DNA depletion.
Emmanuelle Sarzi, Steffi Goffart, Valérie Serre, Dominique Chrétien, Abdelhamid Slama, Arnold Munnich, Johannes N Spelbrink, Agnès Rötig. Ann Neurol 2007
121
7

Recessive Twinkle mutations in early onset encephalopathy with mtDNA depletion.
Anna H Hakonen, Pirjo Isohanni, Anders Paetau, Riitta Herva, Anu Suomalainen, Tuula Lönnqvist. Brain 2007
130
7

Utility of oligonucleotide array-based comparative genomic hybridization for detection of target gene deletions.
Lee-Jun C Wong, David Dimmock, Michael T Geraghty, Richard Quan, Uta Lichter-Konecki, Jing Wang, Ellen K Brundage, Fernando Scaglia, A Craig Chinault. Clin Chem 2008
61
11




Real-time quantitative PCR analysis of mitochondrial DNA content.
Victor Venegas, Jing Wang, David Dimmock, Lee-Jun Wong. Curr Protoc Hum Genet 2011
66
10

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
7

High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease.
Andreas Bender, Kim J Krishnan, Christopher M Morris, Geoffrey A Taylor, Amy K Reeve, Robert H Perry, Evelyn Jaros, Joshua S Hersheson, Joanne Betts, Thomas Klopstock,[...]. Nat Genet 2006
911
6


MPV17 encodes an inner mitochondrial membrane protein and is mutated in infantile hepatic mitochondrial DNA depletion.
Antonella Spinazzola, Carlo Viscomi, Erika Fernandez-Vizarra, Franco Carrara, Pio D'Adamo, Sarah Calvo, René Massimiliano Marsano, Claudia Donnini, Hans Weiher, Pietro Strisciuglio,[...]. Nat Genet 2006
282
6

SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness.
Rosalba Carrozzo, Carlo Dionisi-Vici, Ulrike Steuerwald, Simona Lucioli, Federica Deodato, Sivia Di Giandomenico, Enrico Bertini, Barbara Franke, Leo A J Kluijtmans, Maria Chiara Meschini,[...]. Brain 2007
118
6

Mitochondrial DNA as a non-invasive biomarker: accurate quantification using real time quantitative PCR without co-amplification of pseudogenes and dilution bias.
Afshan N Malik, Rojeen Shahni, Ana Rodriguez-de-Ledesma, Abas Laftah, Phil Cunningham. Biochem Biophys Res Commun 2011
77
7

Alterations of Mitochondrial DNA Copy Number and Telomere Length With Early Adversity and Psychopathology.
Audrey R Tyrka, Stephanie H Parade, Lawrence H Price, Hung-Teh Kao, Barbara Porton, Noah S Philip, Emma S Welch, Linda L Carpenter. Biol Psychiatry 2016
120
6


Reduced mitochondrial DNA copy number is a biomarker of Parkinson's disease.
Angela Pyle, Haidyan Anugrha, Marzena Kurzawa-Akanbi, Alison Yarnall, David Burn, Gavin Hudson. Neurobiol Aging 2016
98
6

Liver mtDNA content increases during development: a comparison of methods and the importance of age- and tissue-specific controls for the diagnosis of mtDNA depletion.
Karl J Morten, Neil Ashley, Frits Wijburg, Nedim Hadzic, Jeremy Parr, Sandeep Jayawant, Susan Adams, Laurence Bindoff, Henk D Bakker, Giorgina Mieli-Vergani,[...]. Mitochondrion 2007
42
11

The deoxyguanosine kinase gene is mutated in individuals with depleted hepatocerebral mitochondrial DNA.
H Mandel, R Szargel, V Labay, O Elpeleg, A Saada, A Shalata, Y Anbinder, D Berkowitz, C Hartman, M Barak,[...]. Nat Genet 2001
354
5

Disorders of nuclear-mitochondrial intergenomic communication.
Antonella Spinazzola, Massimo Zeviani. Biosci Rep 2007
41
12

Inherited mitochondrial diseases of DNA replication.
William C Copeland. Annu Rev Med 2008
180
5

mtDNA depletion with variable tissue expression: a novel genetic abnormality in mitochondrial diseases.
C T Moraes, S Shanske, H J Tritschler, J R Aprille, F Andreetta, E Bonilla, E A Schon, S DiMauro. Am J Hum Genet 1991
409
5

Mitochondrial neurogastrointestinal encephalopathy due to mutations in RRM2B.
Aziz Shaibani, Oleg A Shchelochkov, Shulin Zhang, Panagiotis Katsonis, Olivier Lichtarge, Lee-Jun Wong, Marwan Shinawi. Arch Neurol 2009
66
7

Compensatory amplification of mtDNA in a patient with a novel deletion/duplication and high mutant load.
L-J C Wong, C-L Perng, C-H Hsu, R-K Bai, S Schelley, G D Vladutiu, H Vogel, G M Enns. J Med Genet 2003
31
16

Mitochondrial DNA mutations in human disease.
Robert W Taylor, Doug M Turnbull. Nat Rev Genet 2005
974
5

Molecular analysis for mitochondrial DNA disorders.
Sara Shanske, Lee-Jun C Wong. Mitochondrion 2004
27
18

DNA extraction procedures meaningfully influence qPCR-based mtDNA copy number determination.
Wen Guo, Lan Jiang, Shalender Bhasin, Shaharyar M Khan, Russell H Swerdlow. Mitochondrion 2009
102
5

Mitochondrial dysfunction in autism.
Cecilia Giulivi, Yi-Fan Zhang, Alicja Omanska-Klusek, Catherine Ross-Inta, Sarah Wong, Irva Hertz-Picciotto, Flora Tassone, Isaac N Pessah. JAMA 2010
221
5


Leukocyte mitochondrial DNA (mtDNA) content is associated with depression in old women.
Moo-Young Kim, Ji-Won Lee, Hee-Cheol Kang, Eosu Kim, Duk-Chul Lee. Arch Gerontol Geriatr 2011
47
10

The relationship between leukocyte mitochondrial DNA copy number and telomere length in community-dwelling elderly women.
Jung-Ha Kim, Hye Kyung Kim, Jae-Hong Ko, Hyoweon Bang, Duk-Chul Lee. PLoS One 2013
54
9

Telomere dysfunction induces metabolic and mitochondrial compromise.
Ergün Sahin, Simona Colla, Marc Liesa, Javid Moslehi, Florian L Müller, Mira Guo, Marcus Cooper, Darrell Kotton, Attila J Fabian, Carl Walkey,[...]. Nature 2011
740
5

Origins and functional consequences of somatic mitochondrial DNA mutations in human cancer.
Young Seok Ju, Ludmil B Alexandrov, Moritz Gerstung, Inigo Martincorena, Serena Nik-Zainal, Manasa Ramakrishna, Helen R Davies, Elli Papaemmanuil, Gunes Gundem, Adam Shlien,[...]. Elife 2014
189
5


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.