A citation-based method for searching scientific literature

Robert W Taylor, Martin J Barron, Gillian M Borthwick, Amy Gospel, Patrick F Chinnery, David C Samuels, Geoffrey A Taylor, Stefan M Plusa, Stephanie J Needham, Laura C Greaves, Thomas B L Kirkwood, Douglass M Turnbull. J Clin Invest 2003
Times Cited: 379







List of co-cited articles
1130 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
35

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
33

Mitochondrial DNA mutations are established in human colonic stem cells, and mutated clones expand by crypt fission.
Laura C Greaves, Sean L Preston, Paul J Tadrous, Robert W Taylor, Martin J Barron, Dahmane Oukrif, Simon J Leedham, Maesha Deheragoda, Peter Sasieni, Marco R Novelli,[...]. Proc Natl Acad Sci U S A 2006
211
23

Mechanisms of field cancerization in the human stomach: the expansion and spread of mutated gastric stem cells.
Stuart A C McDonald, Laura C Greaves, Lydia Gutierrez-Gonzalez, Manuel Rodriguez-Justo, Maesha Deheragoda, Simon J Leedham, Robert W Taylor, Chung Yin Lee, Sean L Preston, Matthew Lovell,[...]. Gastroenterology 2008
178
21

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
278
20


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
159
19

Random intracellular drift explains the clonal expansion of mitochondrial DNA mutations with age.
J L Elson, D C Samuels, D M Turnbull, P F Chinnery. Am J Hum Genet 2001
217
18

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
976
18

The hallmarks of aging.
Carlos López-Otín, Maria A Blasco, Linda Partridge, Manuel Serrano, Guido Kroemer. Cell 2013
16

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
619
14

Comparison of mitochondrial mutation spectra in ageing human colonic epithelium and disease: absence of evidence for purifying selection in somatic mitochondrial DNA point mutations.
Laura C Greaves, Joanna L Elson, Marco Nooteboom, John P Grady, Geoffrey A Taylor, Robert W Taylor, John C Mathers, Thomas B L Kirkwood, Doug M Turnbull. PLoS Genet 2012
49
28

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
169
14


Mitochondrial DNA mutations in human disease.
Robert W Taylor, Doug M Turnbull. Nat Rev Genet 2005
13

A methodological approach to tracing cell lineage in human epithelial tissues.
Tariq G Fellous, Stuart A C McDonald, Julia Burkert, Adam Humphries, Shahriar Islam, Nemantha M W De-Alwis, Lydia Gutierrez-Gonzalez, Paul J Tadrous, George Elia, Hemant M Kocher,[...]. Stem Cells 2009
54
24

Identification of stem cells in small intestine and colon by marker gene Lgr5.
Nick Barker, Johan H van Es, Jeroen Kuipers, Pekka Kujala, Maaike van den Born, Miranda Cozijnsen, Andrea Haegebarth, Jeroen Korving, Harry Begthel, Peter J Peters,[...]. Nature 2007
13


Accumulating mitochondrial DNA mutations drive premature hematopoietic aging phenotypes distinct from physiological stem cell aging.
Gudmundur L Norddahl, Cornelis J Pronk, Martin Wahlestedt, Gerd Sten, Jens M Nygren, Amol Ugale, Mikael Sigvardsson, David Bryder. Cell Stem Cell 2011
163
13

Somatic mitochondrial DNA mutations in mammalian aging.
Nils-Göran Larsson. Annu Rev Biochem 2010
317
13

Clonal expansion of early to mid-life mitochondrial DNA point mutations drives mitochondrial dysfunction during human ageing.
Laura C Greaves, Marco Nooteboom, Joanna L Elson, Helen A L Tuppen, Geoffrey A Taylor, Daniel M Commane, Ramesh P Arasaradnam, Konstantin Khrapko, Robert W Taylor, Thomas B L Kirkwood,[...]. PLoS Genet 2014
74
17

Defects in multiple complexes of the respiratory chain are present in ageing human colonic crypts.
Laura C Greaves, Martin J Barron, Stefan Plusa, Thomas B Kirkwood, John C Mathers, Robert W Taylor, Doug M Turnbull. Exp Gerontol 2010
36
36

Heteroplasmic mitochondrial DNA mutations in normal and tumour cells.
Yiping He, Jian Wu, Devin C Dressman, Christine Iacobuzio-Donahue, Sanford D Markowitz, Victor E Velculescu, Luis A Diaz, Kenneth W Kinzler, Bert Vogelstein, Nickolas Papadopoulos. Nature 2010
369
12

Somatic mtDNA mutations cause aging phenotypes without affecting reactive oxygen species production.
Aleksandra Trifunovic, Anna Hansson, Anna Wredenberg, Anja T Rovio, Eric Dufour, Ivan Khvorostov, Johannes N Spelbrink, Rolf Wibom, Howard T Jacobs, Nils-Göran Larsson. Proc Natl Acad Sci U S A 2005
379
12

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
98
12

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
12


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
683
11

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
234
11

The biologic clock: the mitochondria?
D Harman. J Am Geriatr Soc 1972
11

Locating the stem cell niche and tracing hepatocyte lineages in human liver.
Tariq G Fellous, Shahriar Islam, Paul J Tadrous, George Elia, Hemant M Kocher, Satyajit Bhattacharya, Lisa Mears, Douglas M Turnbull, Robert W Taylor, Laura C Greaves,[...]. Hepatology 2009
103
11

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
694
11

Mammalian Mitochondria and Aging: An Update.
Timo E S Kauppila, Johanna H K Kauppila, Nils-Göran Larsson. Cell Metab 2017
240
11


Role of mitochondrial DNA mutations in human aging: implications for the central nervous system and muscle.
E J Brierley, M A Johnson, R N Lightowlers, O F James, D M Turnbull. Ann Neurol 1998
220
10

Ageing muscle: clonal expansions of mitochondrial DNA point mutations and deletions cause focal impairment of mitochondrial function.
Guillemette Fayet, Monica Jansson, Damien Sternberg, Ali Reza Moslemi, Patricia Blondy, Anne Lombès, Michel Fardeau, Anders Oldfors. Neuromuscul Disord 2002
128
10

Quantification of crypt and stem cell evolution in the normal and neoplastic human colon.
Ann-Marie Baker, Biancastella Cereser, Samuel Melton, Alexander G Fletcher, Manuel Rodriguez-Justo, Paul J Tadrous, Adam Humphries, George Elia, Stuart A C McDonald, Nicholas A Wright,[...]. Cell Rep 2014
112
10

Intestinal crypt homeostasis results from neutral competition between symmetrically dividing Lgr5 stem cells.
Hugo J Snippert, Laurens G van der Flier, Toshiro Sato, Johan H van Es, Maaike van den Born, Carla Kroon-Veenboer, Nick Barker, Allon M Klein, Jacco van Rheenen, Benjamin D Simons,[...]. Cell 2010
10

Ultra-deep sequencing of mouse mitochondrial DNA: mutational patterns and their origins.
Adam Ameur, James B Stewart, Christoph Freyer, Erik Hagström, Max Ingman, Nils-Göran Larsson, Ulf Gyllensten. PLoS Genet 2011
117
10

Strong purifying selection in transmission of mammalian mitochondrial DNA.
James Bruce Stewart, Christoph Freyer, Joanna L Elson, Anna Wredenberg, Zekiye Cansu, Aleksandra Trifunovic, Nils-Göran Larsson. PLoS Biol 2008
323
10

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
275
10


Similar patterns of clonally expanded somatic mtDNA mutations in the colon of heterozygous mtDNA mutator mice and ageing humans.
Holly L Baines, James B Stewart, Craig Stamp, Anze Zupanic, Thomas B L Kirkwood, Nils-Göran Larsson, Douglass M Turnbull, Laura C Greaves. Mech Ageing Dev 2014
23
43

Origins and functional consequences of somatic mitochondrial DNA mutations in human cancer.
Young Seok Ju, Ludmil B Alexandrov, Moritz Gerstung, Inigo Martincorena, Serena Nik-Zainal, Manasa Ramakrishna, Helen R Davies, Elli Papaemmanuil, Gunes Gundem, Adam Shlien,[...]. Elife 2014
207
10

Intestinal stem cell replacement follows a pattern of neutral drift.
Carlos Lopez-Garcia, Allon M Klein, Benjamin D Simons, Douglas J Winton. Science 2010
408
10

Mitochondrial DNA polymerase editing mutation, PolgD257A, disturbs stem-progenitor cell cycling in the small intestine and restricts excess fat absorption.
Raymond G Fox, Scott Magness, Gregory C Kujoth, Tomas A Prolla, Nobuyo Maeda. Am J Physiol Gastrointest Liver Physiol 2012
35
28




Aging-dependent large accumulation of point mutations in the human mtDNA control region for replication.
Y Michikawa, F Mazzucchelli, N Bresolin, G Scarlato, G Attardi. Science 1999
530
8


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.