A citation-based method for searching scientific literature

Petar Podlesniy, Margalida Puigròs, Núria Serra, Rubén Fernández-Santiago, Mario Ezquerra, Eduardo Tolosa, Ramon Trullas. EBioMedicine 2019
Times Cited: 9







List of co-cited articles
86 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
110
55

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
959
55

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
105
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
613
44

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
44

In D-loop: 40 years of mitochondrial 7S DNA.
Thomas J Nicholls, Michal Minczuk. Exp Gerontol 2014
108
44

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
100
33

Parkin and PINK1 mitigate STING-induced inflammation.
Danielle A Sliter, Jennifer Martinez, Ling Hao, Xi Chen, Nuo Sun, Tara D Fischer, Jonathon L Burman, Yan Li, Zhe Zhang, Derek P Narendra,[...]. Nature 2018
365
33

Mitochondrial dysfunction in Parkinson's disease.
Anindita Bose, M Flint Beal. J Neurochem 2016
286
33

LRRK2 mutations cause mitochondrial DNA damage in iPSC-derived neural cells from Parkinson's disease patients: reversal by gene correction.
Laurie H Sanders, Josée Laganière, Oliver Cooper, Sally K Mak, B Joseph Vu, Y Anne Huang, David E Paschon, Malini Vangipuram, Ramya Sundararajan, Fyodor D Urnov,[...]. Neurobiol Dis 2014
168
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
73
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
387
33

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
83
33

Genetics of Parkinson's disease.
Christine Klein, Ana Westenberger. Cold Spring Harb Perspect Med 2012
557
33

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
381
33

Mitochondrial DNA polymorphisms as risk factors for Parkinson's disease and Parkinson's disease dementia.
Jaana Autere, Jukka S Moilanen, Saara Finnilä, Hilkka Soininen, Arto Mannermaa, Päivi Hartikainen, Merja Hallikainen, Kari Majamaa. Hum Genet 2004
93
33

The unresolved role of mitochondrial DNA in Parkinson's disease: An overview of published studies, their limitations, and future prospects.
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
7
42

Mitophagy inhibits amyloid-β and tau pathology and reverses cognitive deficits in models of Alzheimer's disease.
Evandro F Fang, Yujun Hou, Konstantinos Palikaras, Bryan A Adriaanse, Jesse S Kerr, Beimeng Yang, Sofie Lautrup, Md Mahdi Hasan-Olive, Domenica Caponio, Xiuli Dan,[...]. Nat Neurosci 2019
325
33

Hereditary early-onset Parkinson's disease caused by mutations in PINK1.
Enza Maria Valente, Patrick M Abou-Sleiman, Viviana Caputo, Miratul M K Muqit, Kirsten Harvey, Suzana Gispert, Zeeshan Ali, Domenico Del Turco, Anna Rita Bentivoglio, Daniel G Healy,[...]. Science 2004
33

LRRK2 G2019S-induced mitochondrial DNA damage is LRRK2 kinase dependent and inhibition restores mtDNA integrity in Parkinson's disease.
Evan H Howlett, Nicholas Jensen, Frances Belmonte, Faria Zafar, Xiaoping Hu, Jillian Kluss, Birgitt Schüle, Brett A Kaufman, J T Greenamyre, Laurie H Sanders. Hum Mol Genet 2017
42
22

Mitochondrial DNA homeostasis is essential for nigrostriatal integrity.
Charalampos Tzoulis, Thomas Schwarzlmüller, Martin Biermann, Kristoffer Haugarvoll, Laurence A Bindoff. Mitochondrion 2016
22
22

Single-strand break repair and genetic disease.
Keith W Caldecott. Nat Rev Genet 2008
563
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
55
22

DNA damage in brain mitochondria caused by aging and MPTP treatment.
B S Mandavilli, S F Ali, B Van Houten. Brain Res 2000
60
22

POLG-related disorders and their neurological manifestations.
Shamima Rahman, William C Copeland. Nat Rev Neurol 2019
77
22

Expression of 8-oxoguanine DNA glycosylase (OGG1) in Parkinson's disease and related neurodegenerative disorders.
Jiro Fukae, Masashi Takanashi, Shin-ichiro Kubo, Ken-ichi Nishioka, Yusaku Nakabeppu, Hideo Mori, Yoshikuni Mizuno, Nobutaka Hattori. Acta Neuropathol 2005
87
22

Ageing and Parkinson's disease: why is advancing age the biggest risk factor?
Amy Reeve, Eve Simcox, Doug Turnbull. Ageing Res Rev 2014
312
22

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
266
22

Mitochondrial DNA damage induced autophagy, cell death, and disease.
Bennett Van Houten, Senyene E Hunter, Joel N Meyer. Front Biosci (Landmark Ed) 2016
72
22

Mitochondrial DNA Deletions Discriminate Affected from Unaffected LRRK2 Mutation Carriers.
Nassima Ouzren, Sylvie Delcambre, Jenny Ghelfi, Philip Seibler, Matthew J Farrer, Inke R König, Jan O Aasly, Joanne Trinh, Christine Klein, Anne Grünewald. Ann Neurol 2019
4
50

Oxidative DNA damage in the parkinsonian brain: an apparent selective increase in 8-hydroxyguanine levels in substantia nigra.
Z I Alam, A Jenner, S E Daniel, A J Lees, N Cairns, C D Marsden, P Jenner, B Halliwell. J Neurochem 1997
582
22

Variations of the CAG trinucleotide repeat in DNA polymerase γ (POLG1) is associated with Parkinson's disease in Sweden.
Anna Anvret, Marie Westerlund, Olof Sydow, Thomas Willows, Charlotta Lind, Dagmar Galter, Andrea Carmine Belin. Neurosci Lett 2010
22
22

Loss of the Parkinson's disease-linked gene DJ-1 perturbs mitochondrial dynamics.
I Irrcher, H Aleyasin, E L Seifert, S J Hewitt, S Chhabra, M Phillips, A K Lutz, M W C Rousseaux, L Bevilacqua, A Jahani-Asl,[...]. Hum Mol Genet 2010
254
22

Reduced basal autophagy and impaired mitochondrial dynamics due to loss of Parkinson's disease-associated protein DJ-1.
Guido Krebiehl, Sabine Ruckerbauer, Lena F Burbulla, Nicole Kieper, Brigitte Maurer, Jens Waak, Hartwig Wolburg, Zemfira Gizatullina, Frank N Gellerich, Dirk Woitalla,[...]. PLoS One 2010
240
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
37
22

Progressive parkinsonism in mice with respiratory-chain-deficient dopamine neurons.
Mats I Ekstrand, Mügen Terzioglu, Dagmar Galter, Shunwei Zhu, Christoph Hofstetter, Eva Lindqvist, Sebastian Thams, Anita Bergstrand, Fredrik Sterky Hansson, Aleksandra Trifunovic,[...]. Proc Natl Acad Sci U S A 2007
373
22

Twinkle mutation in an Italian family with external progressive ophthalmoplegia and parkinsonism: a case report and an update on the state of art.
Lorenzo Kiferle, Daniele Orsucci, Michelangelo Mancuso, Annalisa Lo Gerfo, Lucia Petrozzi, Gabriele Siciliano, Roberto Ceravolo, Ubaldo Bonuccelli. Neurosci Lett 2013
19
22

Mitochondrial DNA polymerase gamma variants in idiopathic sporadic Parkinson disease.
P T Luoma, J Eerola, S Ahola, A H Hakonen, O Hellström, K T Kivistö, P J Tienari, A Suomalainen. Neurology 2007
102
22

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
22

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
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
7
28

Mitochondrial impairment in patients with Parkinson disease with the G2019S mutation in LRRK2.
Heather Mortiboys, Krisztina K Johansen, Jan O Aasly, Oliver Bandmann. Neurology 2010
185
22

Number of CAG repeats in POLG1 and its association with Parkinson disease in the Norwegian population.
Novin Balafkan, Charalampos Tzoulis, Bernd Müller, Kristoffer Haugarvoll, Ole-Bjørn Tysnes, Jan Petter Larsen, Laurence A Bindoff. Mitochondrion 2012
15
22

Cerebrospinal fluid mtDNA concentration is elevated in multiple sclerosis disease and responds to treatment.
Cyra E Leurs, Petar Podlesniy, Ramon Trullas, Lisanne Balk, Martijn D Steenwijk, Arjan Malekzadeh, Fredrik Piehl, Bernard Mj Uitdehaag, Joep Killestein, Jack van Horssen,[...]. Mult Scler 2018
17
22

Does uncoupling protein 2 expression qualify as marker of disease status in LRRK2-associated Parkinson's disease?
Anne Grünewald, Björn Arns, Britta Meier, Kathrin Brockmann, Vera Tadic, Christine Klein. Antioxid Redox Signal 2014
28
22

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
26
22

Mitochondrial DNA Haplogroups and the Risk of Sporadic Parkinson's Disease in Han Chinese.
Ya-Fang Chen, Wan-Jin Chen, Xiao-Zhen Lin, Qi-Jie Zhang, Jiang-Ping Cai, Chia-Wei Liou, Ning Wang. Chin Med J (Engl) 2015
11
22

Mitochondrial DNA polymorphisms and risk of Parkinson's disease in Spanish population.
Cecilia Huerta, Mónica G Castro, Eliecer Coto, Marta Blázquez, René Ribacoba, Luis M Guisasola, Carlos Salvador, Carmen Martínez, Carlos H Lahoz, Victoria Alvarez. J Neurol Sci 2005
74
22

Cellular processes associated with LRRK2 function and dysfunction.
Rebecca Wallings, Claudia Manzoni, Rina Bandopadhyay. FEBS J 2015
86
22

Ultradeep mapping of neuronal mitochondrial deletions in Parkinson's disease.
Gonzalo S Nido, Christian Dölle, Irene Flønes, Helen A Tuppen, Guido Alves, Ole-Bjørn Tysnes, Kristoffer Haugarvoll, Charalampos Tzoulis. Neurobiol Aging 2018
19
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.