A citation-based method for searching scientific literature

John P Grady, Sarah J Pickett, Yi Shiau Ng, Charlotte L Alston, Emma L Blakely, Steven A Hardy, Catherine L Feeney, Alexandra A Bright, Andrew M Schaefer, Gráinne S Gorman, Richard Jq McNally, Robert W Taylor, Doug M Turnbull, Robert McFarland. EMBO Mol Med 2018
Times Cited: 96







List of co-cited articles
1190 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Mitochondrial diseases.
Gráinne S Gorman, Patrick F Chinnery, Salvatore DiMauro, Michio Hirano, Yasutoshi Koga, Robert McFarland, Anu Suomalainen, David R Thorburn, Massimo Zeviani, Douglass M Turnbull. Nat Rev Dis Primers 2016
456
31

Prevalence of nuclear and mitochondrial DNA mutations related to adult mitochondrial disease.
Gráinne S Gorman, Andrew M Schaefer, Yi Ng, Nicholas Gomez, Emma L Blakely, Charlotte L Alston, Catherine Feeney, Rita Horvath, Patrick Yu-Wai-Man, Patrick F Chinnery,[...]. Ann Neurol 2015
404
23


Decrease of 3243 A-->G mtDNA mutation from blood in MELAS syndrome: a longitudinal study.
S Rahman, J Poulton, D Marchington, A Suomalainen. Am J Hum Genet 2001
162
18

Phenotypic heterogeneity in m.3243A>G mitochondrial disease: The role of nuclear factors.
Sarah J Pickett, John P Grady, Yi Shiau Ng, Gráinne S Gorman, Andrew M Schaefer, Ian J Wilson, Heather J Cordell, Doug M Turnbull, Robert W Taylor, Robert McFarland. Ann Clin Transl Neurol 2018
44
40


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
16

Clinical features and heteroplasmy in blood, urine and saliva in 34 Dutch families carrying the m.3243A > G mutation.
Paul de Laat, Saskia Koene, Lambert P W J van den Heuvel, Richard J T Rodenburg, Mirian C H Janssen, Jan A M Smeitink. J Inherit Metab Dis 2012
84
19

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy.
D C Wallace, G Singh, M T Lott, J A Hodge, T G Schurr, A M Lezza, L J Elsas, E K Nikoskelainen. Science 1988
15

The UK MRC Mitochondrial Disease Patient Cohort Study: clinical phenotypes associated with the m.3243A>G mutation--implications for diagnosis and management.
Victoria Nesbitt, Robert D S Pitceathly, Doug M Turnbull, Robert W Taylor, Mary G Sweeney, Ese E Mudanohwo, Shamima Rahman, Michael G Hanna, Robert McFarland. J Neurol Neurosurg Psychiatry 2013
120
15

MitoCarta2.0: an updated inventory of mammalian mitochondrial proteins.
Sarah E Calvo, Karl R Clauser, Vamsi K Mootha. Nucleic Acids Res 2016
752
14

Pathogenic mitochondrial DNA mutations are common in the general population.
Hannah R Elliott, David C Samuels, James A Eden, Caroline L Relton, Patrick F Chinnery. Am J Hum Genet 2008
357
14

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
14

Mitochondrial energy generation disorders: genes, mechanisms, and clues to pathology.
Ann E Frazier, David R Thorburn, Alison G Compton. J Biol Chem 2019
94
13

MELAS syndrome: Clinical manifestations, pathogenesis, and treatment options.
Ayman W El-Hattab, Adekunle M Adesina, Jeremy Jones, Fernando Scaglia. Mol Genet Metab 2015
228
13


Population prevalence of the MELAS A3243G mutation.
Neil Manwaring, Michael M Jones, Jie Jin Wang, Elena Rochtchina, Chris Howard, Paul Mitchell, Carolyn M Sue. Mitochondrion 2007
179
12


Melas: an original case and clinical criteria for diagnosis.
M Hirano, E Ricci, M R Koenigsberger, R Defendini, S G Pavlakis, D C DeVivo, S DiMauro, L P Rowland. Neuromuscul Disord 1992
241
12


Tissue- and cell-type-specific manifestations of heteroplasmic mtDNA 3243A>G mutation in human induced pluripotent stem cell-derived disease model.
Riikka H Hämäläinen, Tuula Manninen, Hanna Koivumäki, Mikhail Kislin, Timo Otonkoski, Anu Suomalainen. Proc Natl Acad Sci U S A 2013
134
11

Growth differentiation factor 15 as a useful biomarker for mitochondrial disorders.
Shuichi Yatsuga, Yasunori Fujita, Akiko Ishii, Yoshihiro Fukumoto, Hajime Arahata, Tatsuyuki Kakuma, Toshio Kojima, Masafumi Ito, Masashi Tanaka, Reo Saiki,[...]. Ann Neurol 2015
128
11

Prediction of long-term prognosis by heteroplasmy levels of the m.3243A>G mutation in patients with the mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes syndrome.
A Fayssoil, P Laforêt, W Bougouin, C Jardel, A Lombès, H M Bécane, N Berber, T Stojkovic, A Béhin, B Eymard,[...]. Eur J Neurol 2017
26
42

Recent advances in understanding the molecular genetic basis of mitochondrial disease.
Kyle Thompson, Jack J Collier, Ruth I C Glasgow, Fiona M Robertson, Angela Pyle, Emma L Blakely, Charlotte L Alston, Monika Oláhová, Robert McFarland, Robert W Taylor. J Inherit Metab Dis 2020
58
18

mtDNA Variation and Analysis Using Mitomap and Mitomaster.
Marie T Lott, Jeremy N Leipzig, Olga Derbeneva, H Michael Xie, Dimitra Chalkia, Mahdi Sarmady, Vincent Procaccio, Douglas C Wallace. Curr Protoc Bioinformatics 2013
238
10

Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: a distinctive clinical syndrome.
S G Pavlakis, P C Phillips, S DiMauro, D C De Vivo, L P Rowland. Ann Neurol 1984
920
10

FGF21 is a biomarker for mitochondrial translation and mtDNA maintenance disorders.
Jenni M Lehtonen, Saara Forsström, Emanuela Bottani, Carlo Viscomi, Olivier R Baris, Helena Isoniemi, Krister Höckerstedt, Pia Österlund, Mikko Hurme, Juulia Jylhävä,[...]. Neurology 2016
98
10

The genetics and pathology of mitochondrial disease.
Charlotte L Alston, Mariana C Rocha, Nichola Z Lax, Doug M Turnbull, Robert W Taylor. J Pathol 2017
177
10

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
10

The m.3243A>G mitochondrial DNA mutation and related phenotypes. A matter of gender?
Michelangelo Mancuso, Daniele Orsucci, Corrado Angelini, Enrico Bertini, Valerio Carelli, Giacomo Pietro Comi, Alice Donati, Carlo Minetti, Maurizio Moggio, Tiziana Mongini,[...]. J Neurol 2014
68
14

Genome editing in mitochondria corrects a pathogenic mtDNA mutation in vivo.
Payam A Gammage, Carlo Viscomi, Marie-Lune Simard, Ana S H Costa, Edoardo Gaude, Christopher A Powell, Lindsey Van Haute, Beverly J McCann, Pedro Rebelo-Guiomar, Raffaele Cerutti,[...]. Nat Med 2018
110
10

MitoTALEN reduces mutant mtDNA load and restores tRNAAla levels in a mouse model of heteroplasmic mtDNA mutation.
Sandra R Bacman, Johanna H K Kauppila, Claudia V Pereira, Nadee Nissanka, Maria Miranda, Milena Pinto, Sion L Williams, Nils-Göran Larsson, James B Stewart, Carlos T Moraes. Nat Med 2018
96
10

Natural history of MELAS associated with mitochondrial DNA m.3243A>G genotype.
P Kaufmann, K Engelstad, Y Wei, R Kulikova, M Oskoui, D M Sproule, V Battista, D Y Koenigsberger, J M Pascual, S Shanske,[...]. Neurology 2011
88
11

Patient care standards for primary mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society.
Sumit Parikh, Amy Goldstein, Amel Karaa, Mary Kay Koenig, Irina Anselm, Catherine Brunel-Guitton, John Christodoulou, Bruce H Cohen, David Dimmock, Gregory M Enns,[...]. Genet Med 2017
92
10

Mitochondrial DNA mutations in human disease.
Robert W Taylor, Doug M Turnbull. Nat Rev Genet 2005
9

A novel immunofluorescent assay to investigate oxidative phosphorylation deficiency in mitochondrial myopathy: understanding mechanisms and improving diagnosis.
Mariana C Rocha, John P Grady, Anne Grünewald, Amy Vincent, Philip F Dobson, Robert W Taylor, Doug M Turnbull, Karolina A Rygiel. Sci Rep 2015
68
13

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
216
9

MELAS: a nationwide prospective cohort study of 96 patients in Japan.
Shuichi Yatsuga, Nataliya Povalko, Junko Nishioka, Koju Katayama, Noriko Kakimoto, Toyojiro Matsuishi, Tatsuyuki Kakuma, Yasutoshi Koga. Biochim Biophys Acta 2012
130
9

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
138
9

Mutation in mitochondrial tRNA(Leu)(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness.
J M van den Ouweland, H H Lemkes, W Ruitenbeek, L A Sandkuijl, M F de Vijlder, P A Struyvenberg, J J van de Kamp, J A Maassen. Nat Genet 1992
924
9

Tissue specific distribution of the 3243A->G mtDNA mutation.
A L Frederiksen, P H Andersen, K O Kyvik, T D Jeppesen, J Vissing, M Schwartz. J Med Genet 2006
66
13

Progressive increase in mtDNA 3243A>G heteroplasmy causes abrupt transcriptional reprogramming.
Martin Picard, Jiangwen Zhang, Saege Hancock, Olga Derbeneva, Ryan Golhar, Pawel Golik, Sean O'Hearn, Shawn Levy, Prasanth Potluri, Maria Lvova,[...]. Proc Natl Acad Sci U S A 2014
164
9

A Phenotype-Driven Approach to Generate Mouse Models with Pathogenic mtDNA Mutations Causing Mitochondrial Disease.
Johanna H K Kauppila, Holly L Baines, Ana Bratic, Marie-Lune Simard, Christoph Freyer, Arnaud Mourier, Craig Stamp, Roberta Filograna, Nils-Göran Larsson, Laura C Greaves,[...]. Cell Rep 2016
59
15

Improving genetic diagnosis in Mendelian disease with transcriptome sequencing.
Beryl B Cummings, Jamie L Marshall, Taru Tukiainen, Monkol Lek, Sandra Donkervoort, A Reghan Foley, Veronique Bolduc, Leigh B Waddell, Sarah A Sandaradura, Gina L O'Grady,[...]. Sci Transl Med 2017
275
9

Genetic diagnosis of Mendelian disorders via RNA sequencing.
Laura S Kremer, Daniel M Bader, Christian Mertes, Robert Kopajtich, Garwin Pichler, Arcangela Iuso, Tobias B Haack, Elisabeth Graf, Thomas Schwarzmayr, Caterina Terrile,[...]. Nat Commun 2017
204
9

Whole exome sequencing of suspected mitochondrial patients in clinical practice.
Saskia B Wortmann, David A Koolen, Jan A Smeitink, Lambert van den Heuvel, Richard J Rodenburg. J Inherit Metab Dis 2015
121
9

Mitochondrial Diseases: Hope for the Future.
Oliver M Russell, Gráinne S Gorman, Robert N Lightowlers, Doug M Turnbull. Cell 2020
68
13

Mitochondrial threshold effects.
Rodrigue Rossignol, Benjamin Faustin, Christophe Rocher, Monique Malgat, Jean-Pierre Mazat, Thierry Letellier. Biochem J 2003
457
8

A randomized placebo-controlled trial of idebenone in Leber's hereditary optic neuropathy.
Thomas Klopstock, Patrick Yu-Wai-Man, Konstantinos Dimitriadis, Jacinthe Rouleau, Suzette Heck, Maura Bailie, Alaa Atawan, Sandip Chattopadhyay, Marion Schubert, Aylin Garip,[...]. Brain 2011
257
8

Use of whole-exome sequencing to determine the genetic basis of multiple mitochondrial respiratory chain complex deficiencies.
Robert W Taylor, Angela Pyle, Helen Griffin, Emma L Blakely, Jennifer Duff, Langping He, Tania Smertenko, Charlotte L Alston, Vivienne C Neeve, Andrew Best,[...]. JAMA 2014
213
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.