A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity


In-Depth Characterization and Validation of Human Urine Metabolomes Reveal Novel Metabolic Signatures of Lower Urinary Tract Symptoms.
Ling Hao, Tyler Greer, David Page, Yatao Shi, Chad M Vezina, Jill A Macoska, Paul C Marker, Dale E Bjorling, Wade Bushman, William A Ricke,[...]. Sci Rep 2016
25
100

The nuclear background influences the penetrance of the near-homoplasmic m.1630 A > G MELAS variant in a symptomatic proband and asymptomatic mother.
Martine Uittenbogaard, Hao Wang, Victor Wei Zhang, Lee-Jun Wong, Christine A Brantner, Andrea Gropman, Anne Chiaramello. Mol Genet Metab 2019
10
100

MELAS syndrome: Clinical manifestations, pathogenesis, and treatment options.
Ayman W El-Hattab, Adekunle M Adesina, Jeremy Jones, Fernando Scaglia. Mol Genet Metab 2015
263
100

Mutation in the mitochondrial tRNA(Val) causes mitochondrial encephalopathy, lactic acidosis and stroke-like episodes.
Catherine Glatz, Kristin D'Aco, Sabrina Smith, Neal Sondheimer. Mitochondrion 2011
20
100

An mtDNA mutation, 14453G-->A, in the NADH dehydrogenase subunit 6 associated with severe MELAS syndrome.
K Ravn, F Wibrand, F J Hansen, N Horn, T Rosenberg, M Schwartz. Eur J Hum Genet 2001
67
100

Innovation: Metabolomics: the apogee of the omics trilogy.
Gary J Patti, Oscar Yanes, Gary Siuzdak. Nat Rev Mol Cell Biol 2012
100

Glucose Metabolism and AMPK Signaling Regulate Dopaminergic Cell Death Induced by Gene (α-Synuclein)-Environment (Paraquat) Interactions.
Annadurai Anandhan, Shulei Lei, Roman Levytskyy, Aglaia Pappa, Mihalis I Panayiotidis, Ronald L Cerny, Oleh Khalimonchuk, Robert Powers, Rodrigo Franco. Mol Neurobiol 2017
28
50

Dopamine neuronal loss contributes to memory and reward dysfunction in a model of Alzheimer's disease.
Annalisa Nobili, Emanuele Claudio Latagliata, Maria Teresa Viscomi, Virve Cavallucci, Debora Cutuli, Giacomo Giacovazzo, Paraskevi Krashia, Francesca Romana Rizzo, Ramona Marino, Mauro Federici,[...]. Nat Commun 2017
180
50

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
518
50

Promising Metabolite Profiles in the Plasma and CSF of Early Clinical Parkinson's Disease.
Daniel Stoessel, Claudia Schulte, Marcia C Teixeira Dos Santos, Dieter Scheller, Irene Rebollo-Mesa, Christian Deuschle, Dirk Walther, Nicolas Schauer, Daniela Berg, Andre Nogueira da Costa,[...]. Front Aging Neurosci 2018
42
50



Atypical clinical presentations associated with the MELAS mutation at position 3243 of human mitochondrial DNA.
C T Moraes, F Ciacci, G Silvestri, S Shanske, M Sciacco, M Hirano, E A Schon, E Bonilla, S DiMauro. Neuromuscul Disord 1993
208
50

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
258
50



Mitochondrial metabolomics using high-resolution Fourier-transform mass spectrometry.
Young-Mi Go, Karan Uppal, Douglas I Walker, ViLinh Tran, Lauriane Dury, Frederick H Strobel, Hélène Baubichon-Cortay, Kurt D Pennell, James R Roede, Dean P Jones. Methods Mol Biol 2014
32
50

Urinary Amine Metabolomics Characterization with Custom 12-Plex Isobaric DiLeu Labeling.
Pingli Wei, Ling Hao, Samuel Thomas, Amanda Rae Buchberger, Laura Steinke, Paul C Marker, William A Ricke, Lingjun Li. J Am Soc Mass Spectrom 2020
5
50


Heteroplasmic mtDNA mutation (T----G) at 8993 can cause Leigh disease when the percentage of abnormal mtDNA is high.
Y Tatuch, J Christodoulou, A Feigenbaum, J T Clarke, J Wherret, C Smith, N Rudd, R Petrova-Benedict, B H Robinson. Am J Hum Genet 1992
400
50

Lysosomal perturbations in human dopaminergic neurons derived from induced pluripotent stem cells with PARK2 mutation.
Justyna Okarmus, Helle Bogetofte, Sissel Ida Schmidt, Matias Ryding, Silvia García-López, Brent James Ryan, Alberto Martínez-Serrano, Poul Hyttel, Morten Meyer. Sci Rep 2020
16
50

Metabolomics analysis for biomarker discovery: advances and challenges.
M S Monteiro, M Carvalho, M L Bastos, P Guedes de Pinho. Curr Med Chem 2013
139
50

Human SOD1-G93A specific distribution evidenced in murine brain of a transgenic model for amyotrophic lateral sclerosis by MALDI imaging mass spectrometry.
Elena Acquadro, Ilaria Caron, Massimo Tortarolo, Enrico M Bucci, Caterina Bendotti, Davide Corpillo. J Proteome Res 2014
20
50



Leigh syndrome: clinical features and biochemical and DNA abnormalities.
S Rahman, R B Blok, H H Dahl, D M Danks, D M Kirby, C W Chow, J Christodoulou, D R Thorburn. Ann Neurol 1996
531
50

Mitochondrial respiratory dysfunction caused by a heteroplasmic mitochondrial DNA mutation blocks cellular reprogramming.
Mutsumi Yokota, Hideyuki Hatakeyama, Saki Okabe, Yasuha Ono, Yu-ichi Goto. Hum Mol Genet 2015
32
50

Lipidomics unveils lipid dyshomeostasis and low circulating plasmalogens as biomarkers in a monogenic mitochondrial disorder.
Matthieu Ruiz, Alexanne Cuillerier, Caroline Daneault, Sonia Deschênes, Isabelle Robillard Frayne, Bertrand Bouchard, Anik Forest, Julie Thompson Legault, Frederic M Vaz, John D Rioux,[...]. JCI Insight 2019
10
50

Parkin is recruited selectively to impaired mitochondria and promotes their autophagy.
Derek Narendra, Atsushi Tanaka, Der-Fen Suen, Richard J Youle. J Cell Biol 2008
50

Substrate specificity of human carnitine acetyltransferase: Implications for fatty acid and branched-chain amino acid metabolism.
Sara Violante, Lodewijk Ijlst, Jos Ruiter, Janet Koster, Henk van Lenthe, Marinus Duran, Isabel Tavares de Almeida, Ronald J A Wanders, Sander M Houten, Fátima V Ventura. Biochim Biophys Acta 2013
48
50

Huntington disease.
Gillian P Bates, Ray Dorsey, James F Gusella, Michael R Hayden, Chris Kay, Blair R Leavitt, Martha Nance, Christopher A Ross, Rachael I Scahill, Ronald Wetzel,[...]. Nat Rev Dis Primers 2015
629
50


Mitochondrial dynamics: Biological roles, molecular machinery, and related diseases.
Ayman W El-Hattab, Jehan Suleiman, Mohammed Almannai, Fernando Scaglia. Mol Genet Metab 2018
61
50


Extensive paternal mtDNA leakage in natural populations of Drosophila melanogaster.
Maria D S Nunes, Marlies Dolezal, Christian Schlötterer. Mol Ecol 2013
43
50


Therapeutic Options in Hereditary Optic Neuropathies.
Giulia Amore, Martina Romagnoli, Michele Carbonelli, Piero Barboni, Valerio Carelli, Chiara La Morgia. Drugs 2021
9
50

Alpha-synuclein and neurodegenerative diseases.
M Goedert. Nat Rev Neurosci 2001
969
50

Melatonin and the electron transport chain.
Rüdiger Hardeland. Cell Mol Life Sci 2017
60
50

Clinical presentation of mitochondrial disorders in childhood.
A Munnich, A Rötig, D Chretien, V Cormier, T Bourgeron, J P Bonnefont, J M Saudubray, P Rustin. J Inherit Metab Dis 1996
114
50

Metabolic features of the cell danger response.
Robert K Naviaux. Mitochondrion 2014
110
50

Alterations in energy/redox metabolism induced by mitochondrial and environmental toxins: a specific role for glucose-6-phosphate-dehydrogenase and the pentose phosphate pathway in paraquat toxicity.
Shulei Lei, Laura Zavala-Flores, Aracely Garcia-Garcia, Renu Nandakumar, Yuting Huang, Nandakumar Madayiputhiya, Robert C Stanton, Eric D Dodds, Robert Powers, Rodrigo Franco. ACS Chem Biol 2014
57
50

Mitochondrial endonuclease G mediates breakdown of paternal mitochondria upon fertilization.
Qinghua Zhou, Haimin Li, Hanzeng Li, Akihisa Nakagawa, Jason L J Lin, Eui-Seung Lee, Brian L Harry, Riley Robert Skeen-Gaar, Yuji Suehiro, Donna William,[...]. Science 2016
97
50


The role of mitochondria in apoptosis.
Seon-Yong Jeong, Dai-Wu Seol. BMB Rep 2008
346
50

New insights in the amyloid-Beta interaction with mitochondria.
Carlos Spuch, Saida Ortolano, Carmen Navarro. J Aging Res 2012
63
50

Amyloid-beta deposition in Alzheimer transgenic mice is associated with oxidative stress.
M A Smith, K Hirai, K Hsiao, M A Pappolla, P L Harris, S L Siedlak, M Tabaton, G Perry. J Neurochem 1998
454
50

Carnitine transport and fatty acid oxidation.
Nicola Longo, Marta Frigeni, Marzia Pasquali. Biochim Biophys Acta 2016
287
50


Universal heteroplasmy of human mitochondrial DNA.
Brendan A I Payne, Ian J Wilson, Patrick Yu-Wai-Man, Jonathan Coxhead, David Deehan, Rita Horvath, Robert W Taylor, David C Samuels, Mauro Santibanez-Koref, Patrick F Chinnery. Hum Mol Genet 2013
244
50


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.