A citation-based method for searching scientific literature

Angela Pyle, Haidyan Anugrha, Marzena Kurzawa-Akanbi, Alison Yarnall, David Burn, Gavin Hudson. Neurobiol Aging 2016
Times Cited: 107







List of co-cited articles
1030 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Defective mitochondrial DNA homeostasis in the substantia nigra in Parkinson disease.
Christian Dölle, Irene Flønes, Gonzalo S Nido, Hrvoje Miletic, Nelson Osuagwu, Stine Kristoffersen, Peer K Lilleng, Jan Petter Larsen, Ole-Bjørn Tysnes, Kristoffer Haugarvoll,[...]. Nat Commun 2016
112
25

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
972
23

Mitochondrial DNA Depletion in Respiratory Chain-Deficient Parkinson Disease Neurons.
Anne Grünewald, Karolina A Rygiel, Philippa D Hepplewhite, Christopher M Morris, Martin Picard, Doug M Turnbull. Ann Neurol 2016
109
18

Reduced cerebrospinal fluid mitochondrial DNA is a biomarker for early-stage Parkinson's disease.
Angela Pyle, Rebecca Brennan, Marzena Kurzawa-Akanbi, Alison Yarnall, Anais Thouin, Brit Mollenhauer, David Burn, Patrick F Chinnery, Gavin Hudson. Ann Neurol 2015
57
29

Mitochondrial DNA deletions are abundant and cause functional impairment in aged human substantia nigra neurons.
Yevgenya Kraytsberg, Elena Kudryavtseva, Ann C McKee, Changiz Geula, Neil W Kowall, Konstantin Khrapko. Nat Genet 2006
617
16

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
164
15

Evidence for polymerase gamma, POLG1 variation in reduced mitochondrial DNA copy number in Parkinson's disease.
Ya-Xing Gui, Zhong-Ping Xu, Wen Lv, Jin-Jia Zhao, Xing-Yue Hu. Parkinsonism Relat Disord 2015
24
62

Somatic mtDNA variation is an important component of Parkinson's disease.
Jonathan Coxhead, Marzena Kurzawa-Akanbi, Rafiqul Hussain, Angela Pyle, Patrick Chinnery, Gavin Hudson. Neurobiol Aging 2016
39
33

Number matters: control of mammalian mitochondrial DNA copy number.
Laura L Clay Montier, Janice J Deng, Yidong Bai. J Genet Genomics 2009
305
13

Association of Mitochondrial DNA Copy Number With Cardiovascular Disease.
Foram N Ashar, Yiyi Zhang, Ryan J Longchamps, John Lane, Anna Moes, Megan L Grove, Josyf C Mychaleckyj, Kent D Taylor, Josef Coresh, Jerome I Rotter,[...]. JAMA Cardiol 2017
78
16

Mitochondrial DNA copy numbers in pyramidal neurons are decreased and mitochondrial biogenesis transcriptome signaling is disrupted in Alzheimer's disease hippocampi.
Ann C Rice, Paula M Keeney, Norah K Algarzae, Amy C Ladd, Ravindar R Thomas, James P Bennett. J Alzheimers Dis 2014
55
21

Mitochondrial complex I deficiency in Parkinson's disease.
A H Schapira, J M Cooper, D Dexter, P Jenner, J B Clark, C D Marsden. Lancet 1989
12

Chronic Parkinsonism in humans due to a product of meperidine-analog synthesis.
J W Langston, P Ballard, J W Tetrud, I Irwin. Science 1983
11

Reduction in mitochondrial DNA copy number in peripheral leukocytes after onset of Huntington's disease.
Maria Hvidberg Petersen, Esben Budtz-Jørgensen, Sven Asger Sørensen, Jørgen Erik Nielsen, Lena Elisabeth Hjermind, Tua Vinther-Jensen, Signe Marie Borch Nielsen, Anne Nørremølle. Mitochondrion 2014
36
30

Low cerebrospinal fluid concentration of mitochondrial DNA in preclinical Alzheimer disease.
Petar Podlesniy, Joana Figueiro-Silva, Albert Llado, Anna Antonell, Raquel Sanchez-Valle, Daniel Alcolea, Alberto Lleo, Jose Luis Molinuevo, Nuria Serra, Ramon Trullas. Ann Neurol 2013
117
11


Correlates of Peripheral Blood Mitochondrial DNA Content in a General Population.
Judita Knez, Ellen Winckelmans, Michelle Plusquin, Lutgarde Thijs, Nicholas Cauwenberghs, Yumei Gu, Jan A Staessen, Tim S Nawrot, Tatiana Kuznetsova. Am J Epidemiol 2016
53
18

Association between Mitochondrial DNA Copy Number in Peripheral Blood and Incident CKD in the Atherosclerosis Risk in Communities Study.
Adrienne Tin, Morgan E Grams, Foram N Ashar, John A Lane, Avi Z Rosenberg, Megan L Grove, Eric Boerwinkle, Elizabeth Selvin, Josef Coresh, Nathan Pankratz,[...]. J Am Soc Nephrol 2016
61
16

Mitochondrial import and accumulation of alpha-synuclein impair complex I in human dopaminergic neuronal cultures and Parkinson disease brain.
Latha Devi, Vijayendran Raghavendran, Badanavalu M Prabhu, Narayan G Avadhani, Hindupur K Anandatheerthavarada. J Biol Chem 2008
628
9

Mitochondrial DNA copy number variation across human cancers.
Ed Reznik, Martin L Miller, Yasin Şenbabaoğlu, Nadeem Riaz, Judy Sarungbam, Satish K Tickoo, Hikmat A Al-Ahmadie, William Lee, Venkatraman E Seshan, A Ari Hakimi,[...]. Elife 2016
214
9

Mitochondrial dysfunction in Parkinson's disease.
Anindita Bose, M Flint Beal. J Neurochem 2016
307
9

Functional Impairment in Miro Degradation and Mitophagy Is a Shared Feature in Familial and Sporadic Parkinson's Disease.
Chung-Han Hsieh, Atossa Shaltouki, Ashley E Gonzalez, Alexandre Bettencourt da Cruz, Lena F Burbulla, Erica St Lawrence, Birgitt Schüle, Dimitri Krainc, Theo D Palmer, Xinnan Wang. Cell Stem Cell 2016
219
9

Adjusting MtDNA Quantification in Whole Blood for Peripheral Blood Platelet and Leukocyte Counts.
Yamilee Hurtado-Roca, Marta Ledesma, Monica Gonzalez-Lazaro, Raquel Moreno-Loshuertos, Patricio Fernandez-Silva, Jose Antonio Enriquez, Martin Laclaustra. PLoS One 2016
39
23

Mitochondrial complex I deficiency in Parkinson's disease.
A H Schapira, J M Cooper, D Dexter, J B Clark, P Jenner, C D Marsden. J Neurochem 1990
8

Somatic mitochondrial DNA mutations in early Parkinson and incidental Lewy body disease.
Michael T Lin, Ippolita Cantuti-Castelvetri, Kangni Zheng, Katie E Jackson, Yong B Tan, Thomas Arzberger, Andrew J Lees, Rebecca A Betensky, M Flint Beal, David K Simon. Ann Neurol 2012
74
10


Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA.
R M Andrews, I Kubacka, P F Chinnery, R N Lightowlers, D M Turnbull, N Howell. Nat Genet 1999
8

Chronic systemic pesticide exposure reproduces features of Parkinson's disease.
R Betarbet, T B Sherer, G MacKenzie, M Garcia-Osuna, A V Panov, J T Greenamyre. Nat Neurosci 2000
8

Origin and functional consequences of the complex I defect in Parkinson's disease.
R H Swerdlow, J K Parks, S W Miller, J B Tuttle, P A Trimmer, J P Sheehan, J P Bennett, R E Davis, W D Parker. Ann Neurol 1996
517
8

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism.
T Kitada, S Asakawa, N Hattori, H Matsumine, Y Yamamura, S Minoshima, M Yokochi, Y Mizuno, N Shimizu. Nature 1998
8

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
108
8

Assessing Mitochondrial DNA Variation and Copy Number in Lymphocytes of ~2,000 Sardinians Using Tailored Sequencing Analysis Tools.
Jun Ding, Carlo Sidore, Thomas J Butler, Mary Kate Wing, Yong Qian, Osorio Meirelles, Fabio Busonero, Lam C Tsoi, Andrea Maschio, Andrea Angius,[...]. PLoS Genet 2015
56
14

Association of mitochondrial DNA levels with frailty and all-cause mortality.
Foram N Ashar, Anna Moes, Ann Z Moore, Megan L Grove, Paulo H M Chaves, Josef Coresh, Anne B Newman, Amy M Matteini, Karen Bandeen-Roche, Eric Boerwinkle,[...]. J Mol Med (Berl) 2015
89
8


Mitochondrial DNA and primary mitochondrial dysfunction in Parkinson's disease.
Maria Pia Giannoccaro, Chiara La Morgia, Giovanni Rizzo, Valerio Carelli. Mov Disord 2017
78
10

Mitochondrial DNA point mutations and relative copy number in 1363 disease and control human brains.
Wei Wei, Michael J Keogh, Ian Wilson, Jonathan Coxhead, Sarah Ryan, Sara Rollinson, Helen Griffin, Marzena Kurzawa-Akanbi, Mauro Santibanez-Koref, Kevin Talbot,[...]. Acta Neuropathol Commun 2017
39
20

Premature ageing in mice expressing defective mitochondrial DNA polymerase.
Aleksandra Trifunovic, Anna Wredenberg, Maria Falkenberg, Johannes N Spelbrink, Anja T Rovio, Carl E Bruder, Mohammad Bohlooly-Y, Sebastian Gidlöf, Anders Oldfors, Rolf Wibom,[...]. Nature 2004
8

Mitochondrial DNA in CSF distinguishes LRRK2 from idiopathic Parkinson's disease.
Petar Podlesniy, Dolores Vilas, Peggy Taylor, Leslie M Shaw, Eduard Tolosa, Ramon Trullas. Neurobiol Dis 2016
28
25

Two-stage association study and meta-analysis of mitochondrial DNA variants in Parkinson disease.
Gavin Hudson, Mike Nalls, Jonathan R Evans, David P Breen, Sophie Winder-Rhodes, Karen E Morrison, Huw R Morris, Caroline H Williams-Gray, Roger A Barker, Andrew B Singleton,[...]. Neurology 2013
85
8


Mitochondrial dysfunction in Drosophila PINK1 mutants is complemented by parkin.
Jeehye Park, Sung Bae Lee, Sungkyu Lee, Yongsung Kim, Saera Song, Sunhong Kim, Eunkyung Bae, Jaeseob Kim, Minho Shong, Jin-Man Kim,[...]. Nature 2006
7

Severe nigrostriatal degeneration without clinical parkinsonism in patients with polymerase gamma mutations.
Charalampos Tzoulis, Gia Tuong Tran, Thomas Schwarzlmüller, Karsten Specht, Kristoffer Haugarvoll, Novin Balafkan, Peer K Lilleng, Hrvoje Miletic, Martin Biermann, Laurence A Bindoff. Brain 2013
55
12


Quantification of mitochondrial DNA copy number: pre-analytical factors.
Antonio L Andreu, Ramiro Martinez, Ramon Marti, Elena García-Arumí. Mitochondrion 2009
88
7

Age-Related and Heteroplasmy-Related Variation in Human mtDNA Copy Number.
Manja Wachsmuth, Alexander Hübner, Mingkun Li, Burkhard Madea, Mark Stoneking. PLoS Genet 2016
75
9

High aggregate burden of somatic mtDNA point mutations in aging and Alzheimer's disease brain.
Michael T Lin, David K Simon, Colette H Ahn, Lauren M Kim, M Flint Beal. Hum Mol Genet 2002
236
7

Mitochondrial Dysfunction in Parkinson's Disease: New Mechanistic Insights and Therapeutic Perspectives.
Jin-Sung Park, Ryan L Davis, Carolyn M Sue. Curr Neurol Neurosci Rep 2018
168
7

α-Synuclein is localized to mitochondria-associated ER membranes.
Cristina Guardia-Laguarta, Estela Area-Gomez, Cornelia Rüb, Yuhui Liu, Jordi Magrané, Dorothea Becker, Wolfgang Voos, Eric A Schon, Serge Przedborski. J Neurosci 2014
279
6

Mutation in the alpha-synuclein gene identified in families with Parkinson's disease.
M H Polymeropoulos, C Lavedan, E Leroy, S E Ide, A Dehejia, A Dutra, B Pike, H Root, J Rubenstein, R Boyer,[...]. Science 1997
6

LRRK2 regulates mitochondrial dynamics and function through direct interaction with DLP1.
Xinglong Wang, Michael H Yan, Hisashi Fujioka, Jun Liu, Amy Wilson-Delfosse, Shu G Chen, George Perry, Gemma Casadesus, Xiongwei Zhu. Hum Mol Genet 2012
270
6


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.