A citation-based method for searching scientific literature

Amica C Müller-Nedebock, Rebecca R Brennan, Marianne Venter, Ilse S Pienaar, Francois H van der Westhuizen, Joanna L Elson, Owen A Ross, Soraya Bardien. Neurochem Int 2019
Times Cited: 9







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



Times Cited
  Times     Co-cited
Similarity


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
982
66

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
116
55

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
86
55

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
621
44

In D-loop: 40 years of mitochondrial 7S DNA.
Thomas J Nicholls, Michal Minczuk. Exp Gerontol 2014
120
44

Accumulation of mitochondrial 7S DNA in idiopathic and LRRK2 associated Parkinson's disease.
Petar Podlesniy, Margalida Puigròs, Núria Serra, Rubén Fernández-Santiago, Mario Ezquerra, Eduardo Tolosa, Ramon Trullas. EBioMedicine 2019
12
44

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
40
44

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
112
33

Parkinsonism, premature menopause, and mitochondrial DNA polymerase gamma mutations: clinical and molecular genetic study.
Petri Luoma, Atle Melberg, Juha O Rinne, Jyrki A Kaukonen, Nina N Nupponen, Richard M Chalmers, Anders Oldfors, Ilkka Rautakorpi, Leena Peltonen, Kari Majamaa,[...]. Lancet 2004
391
33

Expanding insights of mitochondrial dysfunction in Parkinson's disease.
Patrick M Abou-Sleiman, Miratul M K Muqit, Nicholas W Wood. Nat Rev Neurosci 2006
620
33

Mitochondrial DNA changes in pedunculopontine cholinergic neurons in Parkinson disease.
Alexander G Bury, Angela Pyle, Joanna L Elson, Laura Greaves, Christopher M Morris, Gavin Hudson, Ilse S Pienaar. Ann Neurol 2017
29
33

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
76
33

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
33

The Role of Astrocyte Dysfunction in Parkinson's Disease Pathogenesis.
Heather D E Booth, Warren D Hirst, Richard Wade-Martins. Trends Neurosci 2017
212
22

POLG-related disorders and their neurological manifestations.
Shamima Rahman, William C Copeland. Nat Rev Neurol 2019
90
22

A novel polymerase gamma mutation in a family with ophthalmoplegia, neuropathy, and Parkinsonism.
Michelangelo Mancuso, Massimiliano Filosto, Shin J Oh, Salvatore DiMauro. Arch Neurol 2004
79
22

Mitochondrial dysfunction in Parkinson's disease.
Anindita Bose, M Flint Beal. J Neurochem 2016
315
22

Early-onset familial parkinsonism due to POLG mutations.
Guido Davidzon, Paul Greene, Michelangelo Mancuso, Kevin J Klos, J Eric Ahlskog, Michio Hirano, Salvatore DiMauro. Ann Neurol 2006
164
22

Mitochondrial transcription factor A is necessary for mtDNA maintenance and embryogenesis in mice.
N G Larsson, J Wang, H Wilhelmsson, A Oldfors, P Rustin, M Lewandoski, G S Barsh, D A Clayton. Nat Genet 1998
22

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
174
22


Parkinsonism associated with the homozygous W748S mutation in the POLG1 gene.
A M Remes, R Hinttala, M Kärppä, H Soini, R Takalo, J Uusimaa, K Majamaa. Parkinsonism Relat Disord 2008
27
22

Genetic analysis of two Japanese families with progressive external ophthalmoplegia and parkinsonism.
Kazunori Sato, Ichiro Yabe, Hiroaki Yaguchi, Fumihito Nakano, Yasuyuki Kunieda, Shinji Saitoh, Hidenao Sasaki. J Neurol 2011
14
22

Alpha-synuclein pathology and Parkinsonism associated with POLG1 mutations and multiple mitochondrial DNA deletions.
J Betts-Henderson, E Jaros, K J Krishnan, R H Perry, A K Reeve, A M Schaefer, R W Taylor, D M Turnbull. Neuropathol Appl Neurobiol 2009
36
22

Parkinson's disease.
Lorraine V Kalia, Anthony E Lang. Lancet 2015
22

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
56
22

Mitochondrial DNA damage: molecular marker of vulnerable nigral neurons in Parkinson's disease.
Laurie H Sanders, Jennifer McCoy, Xiaoping Hu, Pier G Mastroberardino, Bryan C Dickinson, Christopher J Chang, Charleen T Chu, Bennett Van Houten, J T Greenamyre. Neurobiol Dis 2014
102
22

Mitochondrial DNA haplogroups and subhaplogroups are associated with Parkinson's disease risk in a Polish PD cohort.
Katarzyna Gaweda-Walerych, Aleksandra Maruszak, Krzysztof Safranow, Monika Bialecka, Gabriela Klodowska-Duda, Krzysztof Czyzewski, Jaroslaw Slawek, Monika Rudzinska, Maria Styczynska, Grzegorz Opala,[...]. J Neural Transm (Vienna) 2008
38
22

Mitochondrial DNA haplogroups and APOE4 allele are non-independent variables in sporadic Alzheimer's disease.
G Carrieri, M Bonafè, M De Luca, G Rose, O Varcasia, A Bruni, R Maletta, B Nacmias, S Sorbi, F Corsonello,[...]. Hum Genet 2001
132
22

Lewy body pathology is associated with mitochondrial DNA damage in Parkinson's disease.
Sarina K Müller, Andreas Bender, Christoph Laub, Tobias Högen, Falk Schlaudraff, Birgit Liss, Thomas Klopstock, Matthias Elstner. Neurobiol Aging 2013
31
22

The mitochondrial common deletion in Parkinson's disease and related movement disorders.
J Zhang, T J Montine, M A Smith, S L Siedlak, G Gu, D Robertson, G Perry. Parkinsonism Relat Disord 2002
25
22

Mitochondrial DNA deletions/rearrangements in parkinson disease and related neurodegenerative disorders.
Guangyu Gu, Patricio E Reyes, Gregory T Golden, Randall L Woltjer, Christine Hulette, Thomas J Montine, Jing Zhang. J Neuropathol Exp Neurol 2002
78
22

Mitochondrial DNA variants modulate genetic susceptibility to Parkinson's disease in Han Chinese.
Hong-Mei Wu, Ting Li, Zhen-Feng Wang, Shi-Shi Huang, Zi-Qiang Shao, Ke Wang, Hai-Qing Zhong, Song-Fang Chen, Xiong Zhang, Jian-Hong Zhu. Neurobiol Dis 2018
8
25

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
111
22

Catecholamine metabolism drives generation of mitochondrial DNA deletions in dopaminergic neurons.
Johannes F G Neuhaus, Olivier R Baris, Simon Hess, Natasha Moser, Hannsjörg Schröder, Shankar J Chinta, Julie K Andersen, Peter Kloppenburg, Rudolf J Wiesner. Brain 2014
26
22


Investigation of mitochondrial biogenesis defects in single substantia nigra neurons using post-mortem human tissues.
Chun Chen, Amy E Vincent, Alasdair P Blain, Anna L Smith, Doug M Turnbull, Amy K Reeve. Neurobiol Dis 2020
15
22


Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients.
J M Shoffner, M D Brown, A Torroni, M T Lott, M F Cabell, S S Mirra, M F Beal, C C Yang, M Gearing, R Salvo. Genomics 1993
384
22

Enhanced ROS production and antioxidant defenses in cybrids harbouring mutations in mtDNA.
Cristofol Vives-Bauza, Ricardo Gonzalo, Giovanni Manfredi, Elena Garcia-Arumi, Antonio L Andreu. Neurosci Lett 2006
77
22

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
22

Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup background.
Gavin Hudson, Valerio Carelli, Liesbeth Spruijt, Mike Gerards, Catherine Mowbray, Alessandro Achilli, Angela Pyle, Joanna Elson, Neil Howell, Chiara La Morgia,[...]. Am J Hum Genet 2007
260
22

Mitochondrial genetic medicine.
Douglas C Wallace. Nat Genet 2018
101
22

Mitochondrial polymorphisms significantly reduce the risk of Parkinson disease.
Joelle M van der Walt, Kristin K Nicodemus, Eden R Martin, William K Scott, Martha A Nance, Ray L Watts, Jean P Hubble, Jonathan L Haines, William C Koller, Kelly Lyons,[...]. Am J Hum Genet 2003
413
22

Low platelet mitochondrial complex I and complex II/III activity in early untreated Parkinson's disease.
R H Haas, F Nasirian, K Nakano, D Ward, M Pay, R Hill, C W Shults. Ann Neurol 1995
323
22

High frequency of mitochondrial complex I mutations in Parkinson's disease and aging.
Rafal Smigrodzki, Janice Parks, W Davis Parker. Neurobiol Aging 2004
106
22


Human mitochondrial transcription revisited: only TFAM and TFB2M are required for transcription of the mitochondrial genes in vitro.
Dmitry Litonin, Marina Sologub, Yonghong Shi, Maria Savkina, Michael Anikin, Maria Falkenberg, Claes M Gustafsson, Dmitry Temiakov. J Biol Chem 2010
124
22

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
22

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
22


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.