A citation-based method for searching scientific literature

Michael J Keogh, Patrick F Chinnery. Biochim Biophys Acta 2015
Times Cited: 79







List of co-cited articles
957 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
18

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
13

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
13



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
633
11

Mitochondrial DNA mutations, oxidative stress, and apoptosis in mammalian aging.
G C Kujoth, A Hiona, T D Pugh, S Someya, K Panzer, S E Wohlgemuth, T Hofer, A Y Seo, R Sullivan, W A Jobling,[...]. Science 2005
10

Mitochondrial DNA deletions in human brain: regional variability and increase with advanced age.
M Corral-Debrinski, T Horton, M T Lott, J M Shoffner, M F Beal, D C Wallace. Nat Genet 1992
690
10


Germline mitochondrial DNA mutations aggravate ageing and can impair brain development.
Jaime M Ross, James B Stewart, Erik Hagström, Stefan Brené, Arnaud Mourier, Giuseppe Coppotelli, Christoph Freyer, Marie Lagouge, Barry J Hoffer, Lars Olson,[...]. Nature 2013
179
10

Somatic mitochondrial DNA mutations in mammalian aging.
Nils-Göran Larsson. Annu Rev Biochem 2010
327
10

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
10

Mitochondrial dysfunction in aging: Much progress but many unresolved questions.
Brendan A I Payne, Patrick F Chinnery. Biochim Biophys Acta 2015
189
8


Mechanisms linking mtDNA damage and aging.
Milena Pinto, Carlos T Moraes. Free Radic Biol Med 2015
95
8

Marked changes in mitochondrial DNA deletion levels in Alzheimer brains.
M Corral-Debrinski, T Horton, M T Lott, J M Shoffner, A C McKee, M F Beal, B H Graham, D C Wallace. Genomics 1994
230
8



Mitochondria, oxidants, and aging.
Robert S Balaban, Shino Nemoto, Toren Finkel. Cell 2005
7


Recent mitochondrial DNA mutations increase the risk of developing common late-onset human diseases.
Gavin Hudson, Aurora Gomez-Duran, Ian J Wilson, Patrick F Chinnery. PLoS Genet 2014
95
7

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
397
7


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
7

Super-resolution microscopy reveals that mammalian mitochondrial nucleoids have a uniform size and frequently contain a single copy of mtDNA.
Christian Kukat, Christian A Wurm, Henrik Spåhr, Maria Falkenberg, Nils-Göran Larsson, Stefan Jakobs. Proc Natl Acad Sci U S A 2011
312
7

Minimizing the damage: repair pathways keep mitochondrial DNA intact.
Lawrence Kazak, Aurelio Reyes, Ian J Holt. Nat Rev Mol Cell Biol 2012
226
7

Mitochondrial threshold effects.
Rodrigue Rossignol, Benjamin Faustin, Christophe Rocher, Monique Malgat, Jean-Pierre Mazat, Thierry Letellier. Biochem J 2003
477
7

The Mitochondrial Basis of Aging.
Nuo Sun, Richard J Youle, Toren Finkel. Mol Cell 2016
577
7

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
204
7


Mitochondria: in sickness and in health.
Jodi Nunnari, Anu Suomalainen. Cell 2012
7

Mammalian Mitochondria and Aging: An Update.
Timo E S Kauppila, Johanna H K Kauppila, Nils-Göran Larsson. Cell Metab 2017
267
7

The biologic clock: the mitochondria?
D Harman. J Am Geriatr Soc 1972
6

Dietary restriction, mitochondrial function and aging: from yeast to humans.
Andrea Ruetenik, Antoni Barrientos. Biochim Biophys Acta 2015
77
6

Mitochondrial dysfunction in neurodegenerative diseases.
Ashu Johri, M Flint Beal. J Pharmacol Exp Ther 2012
377
6

The hallmarks of aging.
Carlos López-Otín, Maria A Blasco, Linda Partridge, Manuel Serrano, Guido Kroemer. Cell 2013
6

Mitochondrial DNA-deletion mutations accumulate intracellularly to detrimental levels in aged human skeletal muscle fibers.
Entela Bua, Jody Johnson, Allen Herbst, Bridget Delong, Debbie McKenzie, Shahriar Salamat, Judd M Aiken. Am J Hum Genet 2006
284
6

Mitochondrial point mutations do not limit the natural lifespan of mice.
Marc Vermulst, Jason H Bielas, Gregory C Kujoth, Warren C Ladiges, Peter S Rabinovitch, Tomas A Prolla, Lawrence A Loeb. Nat Genet 2007
280
6

DNA deletions and clonal mutations drive premature aging in mitochondrial mutator mice.
Marc Vermulst, Jonathan Wanagat, Gregory C Kujoth, Jason H Bielas, Peter S Rabinovitch, Tomas A Prolla, Lawrence A Loeb. Nat Genet 2008
275
6

Somatic progenitor cell vulnerability to mitochondrial DNA mutagenesis underlies progeroid phenotypes in Polg mutator mice.
Kati J Ahlqvist, Riikka H Hämäläinen, Shuichi Yatsuga, Marko Uutela, Mügen Terzioglu, Alexandra Götz, Saara Forsström, Petri Salven, Alexandre Angers-Loustau, Outi H Kopra,[...]. Cell Metab 2012
168
6

Mitochondrial fusion is required for mtDNA stability in skeletal muscle and tolerance of mtDNA mutations.
Hsiuchen Chen, Marc Vermulst, Yun E Wang, Anne Chomyn, Tomas A Prolla, J Michael McCaffery, David C Chan. Cell 2010
729
6

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
246
6

Oxidative stress is not a major contributor to somatic mitochondrial DNA mutations.
Leslie S Itsara, Scott R Kennedy, Edward J Fox, Selina Yu, Joshua J Hewitt, Monica Sanchez-Contreras, Fernando Cardozo-Pelaez, Leo J Pallanck. PLoS Genet 2014
103
6

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
42
11

Mitochondrial genome changes and neurodegenerative diseases.
Milena Pinto, Carlos T Moraes. Biochim Biophys Acta 2014
46
10

The role of mitochondrial DNA mutation on neurodegenerative diseases.
Moon-Yong Cha, Dong Kyu Kim, Inhee Mook-Jung. Exp Mol Med 2015
76
6

Specific elimination of mutant mitochondrial genomes in patient-derived cells by mitoTALENs.
Sandra R Bacman, Siôn L Williams, Milena Pinto, Susana Peralta, Carlos T Moraes. Nat Med 2013
225
6

Mitochondrially targeted ZFNs for selective degradation of pathogenic mitochondrial genomes bearing large-scale deletions or point mutations.
Payam A Gammage, Joanna Rorbach, Anna I Vincent, Edward J Rebar, Michal Minczuk. EMBO Mol Med 2014
145
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.