A citation-based method for searching scientific literature

Max Borsche, Sandro L Pereira, Christine Klein, Anne Grünewald. J Parkinsons Dis 2021
Times Cited: 10







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



Times Cited
  Times     Co-cited
Similarity


Mitochondrial dysfunction in Parkinson's disease.
Anindita Bose, M Flint Beal. J Neurochem 2016
315
40

Parkinson disease.
R Balestrino, A H V Schapira. Eur J Neurol 2020
136
30

Parkinson's Disease in Women and Men: What's the Difference?
Silvia Cerri, Liudmila Mus, Fabio Blandini. J Parkinsons Dis 2019
62
20

Neurochemical and histologic characterization of striatal excitotoxic lesions produced by the mitochondrial toxin 3-nitropropionic acid.
M F Beal, E Brouillet, B G Jenkins, R J Ferrante, N W Kowall, J M Miller, E Storey, R Srivastava, B R Rosen, B T Hyman. J Neurosci 1993
784
20

Mitochondrial loss, dysfunction and altered dynamics in Huntington's disease.
Jinho Kim, Jennifer P Moody, Christina K Edgerly, Olivia L Bordiuk, Kerry Cormier, Karen Smith, M Flint Beal, Robert J Ferrante. Hum Mol Genet 2010
208
20

Mitochondrial defect in Huntington's disease caudate nucleus.
M Gu, M T Gash, V M Mann, F Javoy-Agid, J M Cooper, A H Schapira. Ann Neurol 1996
537
20

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology.
Alexander Zimprich, Saskia Biskup, Petra Leitner, Peter Lichtner, Matthew Farrer, Sarah Lincoln, Jennifer Kachergus, Mary Hulihan, Ryan J Uitti, Donald B Calne,[...]. Neuron 2004
20

Genetics of Parkinson's disease: An introspection of its journey towards precision medicine.
Sara Bandres-Ciga, Monica Diez-Fairen, Jonggeol Jeff Kim, Andrew B Singleton. Neurobiol Dis 2020
83
20

Parkin loss leads to PARIS-dependent declines in mitochondrial mass and respiration.
Daniel A Stevens, Yunjong Lee, Ho Chul Kang, Byoung Dae Lee, Yun-Il Lee, Aaron Bower, Haisong Jiang, Sung-Ung Kang, Shaida A Andrabi, Valina L Dawson,[...]. Proc Natl Acad Sci U S A 2015
144
20

PARIS (ZNF746) repression of PGC-1α contributes to neurodegeneration in Parkinson's disease.
Joo-Ho Shin, Han Seok Ko, Hochul Kang, Yunjong Lee, Yun-Il Lee, Olga Pletinkova, Juan C Troconso, Valina L Dawson, Ted M Dawson. Cell 2011
614
20

Damage in Mitochondrial DNA Associated with Parkinson's Disease.
Rebeca Martín-Jiménez, Olivier Lurette, Etienne Hebert-Chatelain. DNA Cell Biol 2020
10
20

Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease.
Coro Paisán-Ruíz, Shushant Jain, E Whitney Evans, William P Gilks, Javier Simón, Marcel van der Brug, Adolfo López de Munain, Silvia Aparicio, Angel Martínez Gil, Naheed Khan,[...]. Neuron 2004
20

Oxidative damage and metabolic dysfunction in Huntington's disease: selective vulnerability of the basal ganglia.
S E Browne, A C Bowling, U MacGarvey, M J Baik, S C Berger, M M Muqit, E D Bird, M F Beal. Ann Neurol 1997
631
20

alpha-Synuclein locus triplication causes Parkinson's disease.
A B Singleton, M Farrer, J Johnson, A Singleton, S Hague, J Kachergus, M Hulihan, T Peuralinna, A Dutra, R Nussbaum,[...]. Science 2003
20

Endogenous Parkin Preserves Dopaminergic Substantia Nigral Neurons following Mitochondrial DNA Mutagenic Stress.
Alicia M Pickrell, Chiu-Hui Huang, Scott R Kennedy, Alban Ordureau, Dionisia P Sideris, Jake G Hoekstra, J Wade Harper, Richard J Youle. Neuron 2015
196
20

A randomized, double-blind, placebo-controlled trial of coenzyme Q10 in Huntington disease.
Andrew McGarry, Michael McDermott, Karl Kieburtz, Elisabeth A de Blieck, Flint Beal, Karen Marder, Christopher Ross, Ira Shoulson, Peter Gilbert, William M Mallonee,[...]. Neurology 2017
66
20

Mutant Twinkle increases dopaminergic neurodegeneration, mtDNA deletions and modulates Parkin expression.
Lanying Song, Yuxi Shan, K C Kent Lloyd, Gino A Cortopassi. Hum Mol Genet 2012
26
20


Defects in adaptive energy metabolism with CNS-linked hyperactivity in PGC-1alpha null mice.
Jiandie Lin, Pei-Hsuan Wu, Paul T Tarr, Katrin S Lindenberg, Julie St-Pierre, Chen-Yu Zhang, Vamsi K Mootha, Sibylle Jäger, Claudia R Vianna, Richard M Reznick,[...]. Cell 2004
901
20

Genotype-Phenotype Relations for the Parkinson's Disease Genes Parkin, PINK1, DJ1: MDSGene Systematic Review.
Meike Kasten, Corinna Hartmann, Jennie Hampf, Susen Schaake, Ana Westenberger, Eva-Juliane Vollstedt, Alexander Balck, Aloysius Domingo, Franca Vulinovic, Marija Dulovic,[...]. Mov Disord 2018
97
20



PPARγ as a therapeutic target to rescue mitochondrial function in neurological disease.
Juan Carlos Corona, Michael R Duchen. Free Radic Biol Med 2016
95
20

Mitochondrial Dysfunction in Huntington's Disease; Interplay Between HSF1, p53 and PGC-1α Transcription Factors.
Taylor A Intihar, Elisa A Martinez, Rocio Gomez-Pastor. Front Cell Neurosci 2019
27
20

Mutant huntingtin and mitochondrial dysfunction.
Ella Bossy-Wetzel, Alejandra Petrilli, Andrew B Knott. Trends Neurosci 2008
150
20

Mechanisms controlling mitochondrial biogenesis and respiration through the thermogenic coactivator PGC-1.
Z Wu, P Puigserver, U Andersson, C Zhang, G Adelmant, V Mootha, A Troy, S Cinti, B Lowell, R C Scarpulla,[...]. Cell 1999
20

Mitochondriopathies as a Clue to Systemic Disorders-Analytical Tools and Mitigating Measures in Context of Predictive, Preventive, and Personalized (3P) Medicine.
Alena Liskova, Marek Samec, Lenka Koklesova, Erik Kudela, Peter Kubatka, Olga Golubnitschaja. Int J Mol Sci 2021
11
20

Tangeretin: a mechanistic review of its pharmacological and therapeutic effects.
Milad Ashrafizadeh, Zahra Ahmadi, Reza Mohammadinejad, Elham Ghasemipour Afshar. J Basic Clin Physiol Pharmacol 2020
15
20

Flavonoids against the Warburg phenotype-concepts of predictive, preventive and personalised medicine to cut the Gordian knot of cancer cell metabolism.
Marek Samec, Alena Liskova, Lenka Koklesova, Samson Mathews Samuel, Kevin Zhai, Constanze Buhrmann, Elizabeth Varghese, Mariam Abotaleb, Tawar Qaradakhi, Anthony Zulli,[...]. EPMA J 2020
43
20

Genoprotective activities of plant natural substances in cancer and chemopreventive strategies in the context of 3P medicine.
Lenka Koklesova, Alena Liskova, Marek Samec, Tawar Qaradakhi, Anthony Zulli, Karel Smejkal, Karol Kajo, Jana Jakubikova, Payam Behzadi, Martin Pec,[...]. EPMA J 2020
23
20

Management of Measurable Variable Cardiovascular Disease' Risk Factors.
Sonja Francula-Zaninovic, Iskra A Nola. Curr Cardiol Rev 2018
37
20

Mitochondrial γ-secretase participates in the metabolism of mitochondria-associated amyloid precursor protein.
Pavel F Pavlov, Birgitta Wiehager, Jun Sakai, Susanne Frykman, Homira Behbahani, Bengt Winblad, Maria Ankarcrona. FASEB J 2011
89
20

The genetic architecture of mitochondrial dysfunction in Parkinson's disease.
S B Larsen, Z Hanss, R Krüger. Cell Tissue Res 2018
76
20

Cell-free nucleic acid patterns in disease prediction and monitoring-hype or hope?
Adriana Torres Crigna, Marek Samec, Lenka Koklesova, Alena Liskova, Frank A Giordano, Peter Kubatka, Olga Golubnitschaja. EPMA J 2020
30
20

The Mitochondrial Basis of Aging.
Nuo Sun, Richard J Youle, Toren Finkel. Mol Cell 2016
534
20

Risks associated with the stroke predisposition at young age: facts and hypotheses in light of individualized predictive and preventive approach.
Jiri Polivka, Jiri Polivka, Martin Pesta, Vladimir Rohan, Libuse Celedova, Smit Mahajani, Ondrej Topolcan, Olga Golubnitschaja. EPMA J 2019
30
20


Neuron-Astrocyte Interactions in Parkinson's Disease.
Ikuko Miyazaki, Masato Asanuma. Cells 2020
10
20

Mitochondrial genetic medicine.
Douglas C Wallace. Nat Genet 2018
101
20

Targeting Mitochondrial Impairment in Parkinson's Disease: Challenges and Opportunities.
Jannik Prasuhn, Ryan L Davis, Kishore R Kumar. Front Cell Dev Biol 2021
8
25

Drosophila pink1 is required for mitochondrial function and interacts genetically with parkin.
Ira E Clark, Mark W Dodson, Changan Jiang, Joseph H Cao, Jun R Huh, Jae Hong Seol, Soon Ji Yoo, Bruce A Hay, Ming Guo. Nature 2006
20

Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy.
Suzanne Lesage, Valérie Drouet, Elisa Majounie, Vincent Deramecourt, Maxime Jacoupy, Aude Nicolas, Florence Cormier-Dequaire, Sidi Mohamed Hassoun, Claire Pujol, Sorana Ciura,[...]. Am J Hum Genet 2016
190
20

PINK1-linked parkinsonism is associated with Lewy body pathology.
Lluís Samaranch, Oswaldo Lorenzo-Betancor, José M Arbelo, Isidre Ferrer, Elena Lorenzo, Jaione Irigoyen, Maria A Pastor, Carmen Marrero, Concepción Isla, Joanna Herrera-Henriquez,[...]. Brain 2010
156
20

Cytosolic proteostasis through importing of misfolded proteins into mitochondria.
Linhao Ruan, Chuankai Zhou, Erli Jin, Andrei Kucharavy, Ying Zhang, Zhihui Wen, Laurence Florens, Rong Li. Nature 2017
218
20

The Overcrowded Crossroads: Mitochondria, Alpha-Synuclein, and the Endo-Lysosomal System Interaction in Parkinson's Disease.
Kai-Jung Lin, Kai-Lieh Lin, Shang-Der Chen, Chia-Wei Liou, Yao-Chung Chuang, Hung-Yu Lin, Tsu-Kung Lin. Int J Mol Sci 2019
35
20

PINK1 and Parkin target Miro for phosphorylation and degradation to arrest mitochondrial motility.
Xinnan Wang, Dominic Winter, Ghazaleh Ashrafi, Julia Schlehe, Yao Liang Wong, Dennis Selkoe, Sarah Rice, Judith Steen, Matthew J LaVoie, Thomas L Schwarz. Cell 2011
746
20

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
20

Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study.
Daniel G Healy, Mario Falchi, Sean S O'Sullivan, Vincenzo Bonifati, Alexandra Durr, Susan Bressman, Alexis Brice, Jan Aasly, Cyrus P Zabetian, Stefano Goldwurm,[...]. Lancet Neurol 2008
927
20

Genetics in Parkinson disease: Mendelian versus non-Mendelian inheritance.
Dena G Hernandez, Xylena Reed, Andrew B Singleton. J Neurochem 2016
252
20

A mutation in VPS35, encoding a subunit of the retromer complex, causes late-onset Parkinson disease.
Alexander Zimprich, Anna Benet-Pagès, Walter Struhal, Elisabeth Graf, Sebastian H Eck, Marc N Offman, Dietrich Haubenberger, Sabine Spielberger, Eva C Schulte, Peter Lichtner,[...]. Am J Hum Genet 2011
546
20


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.