A citation-based method for searching scientific literature

Yi Shiau Ng, Laurence A Bindoff, Gráinne S Gorman, Thomas Klopstock, Cornelia Kornblum, Michelangelo Mancuso, Robert McFarland, Carolyn M Sue, Anu Suomalainen, Robert W Taylor, David R Thorburn, Doug M Turnbull. Lancet Neurol 2021
Times Cited: 6







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



Times Cited
  Times     Co-cited
Similarity


Mitochondrial Diseases: Hope for the Future.
Oliver M Russell, Gráinne S Gorman, Robert N Lightowlers, Doug M Turnbull. Cell 2020
68
83

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
66

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
50

Predisposition to infection and SIRS in mitochondrial disorders: 8 years' experience in an academic center.
Melissa A Walker, Nancy Slate, Alexandra Alejos, Stefano Volpi, Rajashri S Iyengar, David Sweetser, Katherine B Sims, Jolan E Walter. J Allergy Clin Immunol Pract 2014
22
33

The genetics of mitochondrial disease: dissecting mitochondrial pathology using multi-omic pipelines.
Charlotte L Alston, Sarah L Stenton, Gavin Hudson, Holger Prokisch, Robert W Taylor. J Pathol 2021
8
33

Genetics of mitochondrial diseases: Identifying mutations to help diagnosis.
Sarah L Stenton, Holger Prokisch. EBioMedicine 2020
37
33


Mitochondria as multifaceted regulators of cell death.
Florian J Bock, Stephen W G Tait. Nat Rev Mol Cell Biol 2020
293
33

Mitochondrial proteins: from biogenesis to functional networks.
Nikolaus Pfanner, Bettina Warscheid, Nils Wiedemann. Nat Rev Mol Cell Biol 2019
225
33

Mitochondrial diseases: the contribution of organelle stress responses to pathology.
Anu Suomalainen, Brendan J Battersby. Nat Rev Mol Cell Biol 2018
165
33

Retrospective natural history of thymidine kinase 2 deficiency.
Caterina Garone, Robert W Taylor, Andrés Nascimento, Joanna Poulton, Carl Fratter, Cristina Domínguez-González, Julie C Evans, Mariana Loos, Pirjo Isohanni, Anu Suomalainen,[...]. J Med Genet 2018
40
33

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
33

Moving towards clinical trials for mitochondrial diseases.
Robert D S Pitceathly, Nandaki Keshavan, Joyeeta Rahman, Shamima Rahman. J Inherit Metab Dis 2021
12
33

Pathogenic mtDNA mutations causing mitochondrial myopathy: The need for muscle biopsy.
Steven A Hardy, Emma L Blakely, Andrew I Purvis, Mariana C Rocha, Syeda Ahmed, Gavin Falkous, Joanna Poulton, Michael R Rose, Olivia O'Mahony, Niamh Bermingham,[...]. Neurol Genet 2016
14
33

Deoxynucleoside Therapy for Thymidine Kinase 2-Deficient Myopathy.
Cristina Domínguez-González, Marcos Madruga-Garrido, Fabiola Mavillard, Caterina Garone, Francisco Javier Aguirre-Rodríguez, M Alice Donati, Karin Kleinsteuber, Itxaso Martí, Elena Martín-Hernández, Juan P Morealejo-Aycinena,[...]. Ann Neurol 2019
34
33

Gene-environment interactions in Leber hereditary optic neuropathy.
Matthew Anthony Kirkman, Patrick Yu-Wai-Man, Alex Korsten, Miriam Leonhardt, Konstantin Dimitriadis, Ireneaus F De Coo, Thomas Klopstock, Patrick Francis Chinnery. Brain 2009
205
33

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
33

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
33

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
33

SURF1 deficiency: a multi-centre natural history study.
Yehani Wedatilake, Ruth M Brown, Robert McFarland, Joy Yaplito-Lee, Andrew A M Morris, Mike Champion, Phillip E Jardine, Antonia Clarke, David R Thorburn, Robert W Taylor,[...]. Orphanet J Rare Dis 2013
71
33

Bilateral visual improvement with unilateral gene therapy injection for Leber hereditary optic neuropathy.
Patrick Yu-Wai-Man, Nancy J Newman, Valerio Carelli, Mark L Moster, Valerie Biousse, Alfredo A Sadun, Thomas Klopstock, Catherine Vignal-Clermont, Robert C Sergott, Günther Rudolph,[...]. Sci Transl Med 2020
33
33

MitoCarta3.0: an updated mitochondrial proteome now with sub-organelle localization and pathway annotations.
Sneha Rath, Rohit Sharma, Rahul Gupta, Tslil Ast, Connie Chan, Timothy J Durham, Russell P Goodman, Zenon Grabarek, Mary E Haas, Wendy H W Hung,[...]. Nucleic Acids Res 2021
78
33

MtDNA-maintenance defects: syndromes and genes.
Carlo Viscomi, Massimo Zeviani. J Inherit Metab Dis 2017
84
33

Mitochondrial Functions in Infection and Immunity.
Varnesh Tiku, Man-Wah Tan, Ivan Dikic. Trends Cell Biol 2020
77
33

The m.5650G>A mitochondrial tRNAAla mutation is pathogenic and causes a phenotype of pure myopathy.
Robert McFarland, Helen Swalwell, Emma L Blakely, Langping He, Emma J Groen, Douglass M Turnbull, Kate M Bushby, Robert W Taylor. Neuromuscul Disord 2008
24
33

A tRNA(Ala) mutation causing mitochondrial myopathy clinically resembling myotonic dystrophy.
R Horváth, H Lochmüller, C Scharfe, B H Do, P J Oefner, J Müller-Höcker, B G Schoser, D Pongratz, D P Auer, M Jaksch. J Med Genet 2003
11
33

Leigh syndrome: One disorder, more than 75 monogenic causes.
Nicole J Lake, Alison G Compton, Shamima Rahman, David R Thorburn. Ann Neurol 2016
207
33

Assessment of Type I Interferon Signaling in Pediatric Inflammatory Disease.
Gillian I Rice, Isabelle Melki, Marie-Louise Frémond, Tracy A Briggs, Mathieu P Rodero, Naoki Kitabayashi, Anthony Oojageer, Brigitte Bader-Meunier, Alexandre Belot, Christine Bodemer,[...]. J Clin Immunol 2017
81
16

A type I interferon signature identifies bilateral striatal necrosis due to mutations in ADAR1.
John H Livingston, Jean-Pierre Lin, Russell C Dale, Deepak Gill, Paul Brogan, Arnold Munnich, Manju A Kurian, Victoria Gonzalez-Martinez, Christian G E L De Goede, Alastair Falconer,[...]. J Med Genet 2014
71
16

Mitochondrial transcript maturation and its disorders.
Lindsey Van Haute, Sarah F Pearce, Christopher A Powell, Aaron R D'Souza, Thomas J Nicholls, Michal Minczuk. J Inherit Metab Dis 2015
55
16

Mitochondrial dysfunction: a neglected component of skin diseases.
René G Feichtinger, Wolfgang Sperl, Johann W Bauer, Barbara Kofler. Exp Dermatol 2014
44
16

Mitochondrial Quality Control and Restraining Innate Immunity.
Andrew T Moehlman, Richard J Youle. Annu Rev Cell Dev Biol 2020
11
16

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
420
16

Neutrophil extracellular traps enriched in oxidized mitochondrial DNA are interferogenic and contribute to lupus-like disease.
Christian Lood, Luz P Blanco, Monica M Purmalek, Carmelo Carmona-Rivera, Suk S De Ravin, Carolyne K Smith, Harry L Malech, Jeffrey A Ledbetter, Keith B Elkon, Mariana J Kaplan. Nat Med 2016
602
16

Type I Interferons in the Pathogenesis and Treatment of Autoimmune Diseases.
Jiao Jiang, Ming Zhao, Christopher Chang, Haijing Wu, Qianjin Lu. Clin Rev Allergy Immunol 2020
20
16

BAF restricts cGAS on nuclear DNA to prevent innate immune activation.
Baptiste Guey, Marilena Wischnewski, Alexiane Decout, Kristina Makasheva, Murat Kaynak, Mahmut S Sakar, Beat Fierz, Andrea Ablasser. Science 2020
35
16

The 3' addition of CCA to mitochondrial tRNASer(AGY) is specifically impaired in patients with mutations in the tRNA nucleotidyl transferase TRNT1.
Florin Sasarman, Isabelle Thiffault, Woranontee Weraarpachai, Steven Salomon, Catalina Maftei, Julie Gauthier, Benjamin Ellazam, Neil Webb, Hana Antonicka, Alexandre Janer,[...]. Hum Mol Genet 2015
45
16

BAK/BAX macropores facilitate mitochondrial herniation and mtDNA efflux during apoptosis.
Kate McArthur, Lachlan W Whitehead, John M Heddleston, Lucy Li, Benjamin S Padman, Viola Oorschot, Niall D Geoghegan, Stephane Chappaz, Sophia Davidson, Hui San Chin,[...]. Science 2018
256
16

Viral strategies for triggering and manipulating mitophagy.
Linliang Zhang, Yali Qin, Mingzhou Chen. Autophagy 2018
45
16

The AAA+ ATPase ATAD3A controls mitochondrial dynamics at the interface of the inner and outer membranes.
Benoît Gilquin, Emmanuel Taillebourg, Nadia Cherradi, Arnaud Hubstenberger, Olivia Gay, Nicolas Merle, Nicole Assard, Marie-Odile Fauvarque, Shiho Tomohiro, Osamu Kuge,[...]. Mol Cell Biol 2010
82
16

Influenza A virus M2 protein triggers mitochondrial DNA-mediated antiviral immune responses.
Miyu Moriyama, Takumi Koshiba, Takeshi Ichinohe. Nat Commun 2019
30
16

Mitochondrial DNA in innate immune responses and inflammatory pathology.
A Phillip West, Gerald S Shadel. Nat Rev Immunol 2017
334
16

Apoptotic caspases prevent the induction of type I interferons by mitochondrial DNA.
Anthony Rongvaux, Ruaidhrí Jackson, Christian C D Harman, Tuo Li, A Phillip West, Marcel R de Zoete, Youtong Wu, Brian Yordy, Saquib A Lakhani, Chia-Yi Kuan,[...]. Cell 2014
383
16


Cellular pyrimidine imbalance triggers mitochondrial DNA-dependent innate immunity.
Hans-Georg Sprenger, Thomas MacVicar, Amir Bahat, Kai Uwe Fiedler, Steffen Hermans, Denise Ehrentraut, Katharina Ried, Dusanka Milenkovic, Nina Bonekamp, Nils-Göran Larsson,[...]. Nat Metab 2021
7
16

cGAS drives noncanonical-inflammasome activation in age-related macular degeneration.
Nagaraj Kerur, Shinichi Fukuda, Daipayan Banerjee, Younghee Kim, Dongxu Fu, Ivana Apicella, Akhil Varshney, Reo Yasuma, Benjamin J Fowler, Elmira Baghdasaryan,[...]. Nat Med 2018
111
16

Phosphorylation and chromatin tethering prevent cGAS activation during mitosis.
Tuo Li, Tuozhi Huang, Mingjian Du, Xiang Chen, Fenghe Du, Junyao Ren, Zhijian J Chen. Science 2021
27
16

Mitochondrial disorder mimicking rheumatoid disease.
Josef Finsterer, Madleine Melichart-Kotig, Adelheid Woehrer. Z Rheumatol 2019
3
33

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
299
16

NAD+ supplementation prevents STING-induced senescence in ataxia telangiectasia by improving mitophagy.
Beimeng Yang, Xiuli Dan, Yujun Hou, Jong-Hyuk Lee, Noah Wechter, Sudarshan Krishnamurthy, Risako Kimura, Mansi Babbar, Tyler Demarest, Ross McDevitt,[...]. Aging Cell 2021
7
16


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.