A citation-based method for searching scientific literature

Xingbo Yang, Jiacheng Jiang, Zongyu Li, Jiayi Liang, Yaozu Xiang. Comput Struct Biotechnol J 2021
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity



A multicenter study on Leigh syndrome: disease course and predictors of survival.
Kalliopi Sofou, Irenaeus F M De Coo, Pirjo Isohanni, Elsebet Ostergaard, Karin Naess, Linda De Meirleir, Charalampos Tzoulis, Johanna Uusimaa, Isabell B De Angst, Tuula Lönnqvist,[...]. Orphanet J Rare Dis 2014
101
100

Leigh disease presenting in utero due to a novel missense mutation in the mitochondrial DNA-ND3.
Esther Leshinsky-Silver, Dorit Lev, Gustavo Malinger, Daniel Shapira, Sarit Cohen, Tally Lerman-Sagie, Ann Saada. Mol Genet Metab 2010
17
100

Novel mutation of ND4 gene identified by targeted next-generation sequencing in patient with Leigh syndrome.
Bing Xu, Xiyuan Li, Miaomiao Du, Chao Zhou, Hezhi Fang, Jianxin Lyu, Yanling Yang. J Hum Genet 2017
12
100

LRPPRC mutations cause a phenotypically distinct form of Leigh syndrome with cytochrome c oxidase deficiency.
François-Guillaume Debray, Charles Morin, Annie Janvier, Josée Villeneuve, Bruno Maranda, Rachel Laframboise, Jacques Lacroix, Jean-Claude Decarie, Yves Robitaille, Marie Lambert,[...]. J Med Genet 2011
51
100

Mitochondrial Genome and Longevity.
R A Zinovkin, M V Skulachev, V P Skulachev. Biochemistry (Mosc) 2016
3
100

Efficacy of idebenone for respiratory failure in a patient with Leigh syndrome: a long-term follow-up study.
Kazuhiro Haginoya, Shigeaki Miyabayashi, Masahiro Kikuchi, Akira Kojima, Katsuya Yamamoto, Kiyoshi Omura, Mitsugu Uematsu, Naomi Hino-Fukuyo, Soichiro Tanaka, Shigeru Tsuchiya. J Neurol Sci 2009
25
100

Late-Onset Leigh Syndrome due to NDUFV1 Mutation in a 10-Year-Old Boy Initially Presenting with Ataxia.
Faruk Incecik, Ozlem M Herguner, Seyda Besen, Sevcan T Bozdoğan, Neslihan O Mungan. J Pediatr Neurosci 2018
7
100

Normal oxidative damage to mitochondrial and nuclear DNA is extensive.
C Richter, J W Park, B N Ames. Proc Natl Acad Sci U S A 1988
100

A new mutation in MT-ND1 m.3928G>C p.V208L causes Leigh disease with infantile spasms.
Carter D Wray, Marisa W Friederich, Desiree du Sart, Sarah Pantaleo, Joél Smet, Cathlin Kucera, Laura Fenton, Gunter Scharer, Rudy Van Coster, Johan L K Van Hove. Mitochondrion 2013
11
100

MtDNA mutations are a common cause of severe disease phenotypes in children with Leigh syndrome.
Karin Naess, Christoph Freyer, Helene Bruhn, Rolf Wibom, Gunilla Malm, Inger Nennesmo, Ulrika von Döbeln, Nils-Göran Larsson. Biochim Biophys Acta 2009
33
100

Mitochondrial signaling: the retrograde response.
Ronald A Butow, Narayan G Avadhani. Mol Cell 2004
644
100

Combined enzymatic complex I and III deficiency associated with mutations in the nuclear encoded NDUFS4 gene.
S M Budde, L P van den Heuvel, A J Janssen, R J Smeets, C A Buskens, L DeMeirleir, R Van Coster, M Baethmann, T Voit, J M Trijbels,[...]. Biochem Biophys Res Commun 2000
152
100

Impact commentaries. Subacute necrotising encephalomyelopathy (Leigh's disease; Leigh syndrome).
P N Leigh, S Al-Sarraj, S DiMauro. J Neurol Neurosurg Psychiatry 2015
9
100

Molecular genetic aspects of human mitochondrial disorders.
N G Larsson, D A Clayton. Annu Rev Genet 1995
365
100


A novel neurological phenotype in mice lacking mitochondrial manganese superoxide dismutase.
S Melov, J A Schneider, B J Day, D Hinerfeld, P Coskun, S S Mirra, J D Crapo, D C Wallace. Nat Genet 1998
374
100

Hypoxia ameliorates brain hyperoxia and NAD+ deficiency in a murine model of Leigh syndrome.
Robert M H Grange, Rohit Sharma, Hardik Shah, Bryn Reinstadler, Olga Goldberger, Marissa K Cooper, Akito Nakagawa, Yusuke Miyazaki, Allyson G Hindle, Annabelle J Batten,[...]. Mol Genet Metab 2021
4
100

The spectrum of pyruvate dehydrogenase complex deficiency: clinical, biochemical and genetic features in 371 patients.
Kavi P Patel, Thomas W O'Brien, Sankarasubramon H Subramony, Jonathan Shuster, Peter W Stacpoole. Mol Genet Metab 2012
98
100

Recombinant mitochondrial transcription factor A with N-terminal mitochondrial transduction domain increases respiration and mitochondrial gene expression.
Shilpa Iyer, Ravindar R Thomas, Francisco R Portell, Lisa D Dunham, Caitlin K Quigley, James P Bennett. Mitochondrion 2009
44
100

Leigh syndrome caused by mutations in MTFMT is associated with a better prognosis.
Hannah Hayhurst, Irenaeus F M de Coo, Dorota Piekutowska-Abramczuk, Charlotte L Alston, Sunil Sharma, Kyle Thompson, Rocio Rius, Langping He, Sila Hopton, Rafal Ploski,[...]. Ann Clin Transl Neurol 2019
6
100

A novel frameshift mutation of the mtDNA COIII gene leads to impaired assembly of cytochrome c oxidase in a patient affected by Leigh-like syndrome.
V Tiranti, P Corona, M Greco, J W Taanman, F Carrara, E Lamantea, L Nijtmans, G Uziel, M Zeviani. Hum Mol Genet 2000
96
100

Strategies for fighting mitochondrial diseases.
C Viscomi, M Zeviani. J Intern Med 2020
19
100

High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency.
Sarah E Calvo, Elena J Tucker, Alison G Compton, Denise M Kirby, Gabriel Crawford, Noel P Burtt, Manuel Rivas, Candace Guiducci, Damien L Bruno, Olga A Goldberger,[...]. Nat Genet 2010
265
100

Live birth derived from oocyte spindle transfer to prevent mitochondrial disease.
John Zhang, Hui Liu, Shiyu Luo, Zhuo Lu, Alejandro Chávez-Badiola, Zitao Liu, Mingxue Yang, Zaher Merhi, Sherman J Silber, Santiago Munné,[...]. Reprod Biomed Online 2017
124
100

MT-ATP6 mitochondrial disease variants: Phenotypic and biochemical features analysis in 218 published cases and cohort of 14 new cases.
Rebecca D Ganetzky, Claudia Stendel, Elizabeth M McCormick, Zarazuela Zolkipli-Cunningham, Amy C Goldstein, Thomas Klopstock, Marni J Falk. Hum Mutat 2019
22
100

Leigh Syndrome Mouse Model Can Be Rescued by Interventions that Normalize Brain Hyperoxia, but Not HIF Activation.
Isha H Jain, Luca Zazzeron, Olga Goldberger, Eizo Marutani, Gregory R Wojtkiewicz, Tslil Ast, Hong Wang, Grigorij Schleifer, Anna Stepanova, Kathleen Brepoels,[...]. Cell Metab 2019
37
100

Two mtDNA mutations 14487T>C (M63V, ND6) and 12297T>C (tRNA Leu) in a Leigh syndrome family.
Jing Wang, Ariel Brautbar, Alicia K Chan, Tara Dzwiniel, Fang-Yuan Li, Paula J Waters, Brett H Graham, Lee-Jun Wong. Mol Genet Metab 2009
16
100

Leukoencephalopathy with accumulated succinate is indicative of SDHAF1 related complex II deficiency.
Andreas Ohlenbusch, Simon Edvardson, Johannes Skorpen, Alf Bjornstad, Ann Saada, Orly Elpeleg, Jutta Gärtner, Knut Brockmann. Orphanet J Rare Dis 2012
32
100


Mitochondria, energetics, epigenetics, and cellular responses to stress.
Daniel T Shaughnessy, Kimberly McAllister, Leroy Worth, Astrid C Haugen, Joel N Meyer, Frederick E Domann, Bennett Van Houten, Raul Mostoslavsky, Scott J Bultman, Andrea A Baccarelli,[...]. Environ Health Perspect 2014
138
100


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
520
100

Mitochondrial encephalopathies: molecular genetic diagnosis from blood samples.
S R Hammans, M G Sweeney, M Brockington, J A Morgan-Hughes, A E Harding. Lancet 1991
178
100

Severe infantile leigh syndrome associated with a rare mitochondrial ND6 mutation, m.14487T>C.
Mark Tarnopolsky, Brandon Meaney, Brian Robinson, Katherine Sheldon, Richard G Boles. Am J Med Genet A 2013
19
100

The clinical spectrum of the m.10191T>C mutation in complex I-deficient Leigh syndrome.
Victoria Nesbitt, Patrick J Morrison, Ellen Crushell, Deirdre E Donnelly, Charlotte L Alston, Langping He, Robert McFarland, Robert W Taylor. Dev Med Child Neurol 2012
26
100

Delineating MT-ATP6-associated disease: From isolated neuropathy to early onset neurodegeneration.
Claudia Stendel, Christiane Neuhofer, Elisa Floride, Shi Yuqing, Rebecca D Ganetzky, Joohyun Park, Peter Freisinger, Cornelia Kornblum, Stephanie Kleinle, Ludger Schöls,[...]. Neurol Genet 2020
27
100

C. elegans longevity pathways converge to decrease mitochondrial membrane potential.
Bernard D Lemire, Maciej Behrendt, Adrienne DeCorby, Dana Gásková. Mech Ageing Dev 2009
54
100

Long-term outcome of Leigh syndrome caused by the NARP-T8993C mtDNA mutation.
François-Guillaume Debray, Marie Lambert, Anne Lortie, Michel Vanasse, Grant A Mitchell. Am J Med Genet A 2007
33
100

Respiratory chain complex I deficiency due to NDUFA12 mutations as a new cause of Leigh syndrome.
Elsebet Ostergaard, Richard J Rodenburg, Mariël van den Brand, Lise Lykke Thomsen, Morten Duno, Mustafa Batbayli, Flemming Wibrand, Leo Nijtmans. J Med Genet 2011
38
100

Impaired complex IV activity in response to loss of LRPPRC function can be compensated by mitochondrial hyperfusion.
Stéphane G Rolland, Elisa Motori, Nadin Memar, Jürgen Hench, Stephan Frank, Konstanze F Winklhofer, Barbara Conradt. Proc Natl Acad Sci U S A 2013
44
100


Metabolic rescue in pluripotent cells from patients with mtDNA disease.
Hong Ma, Clifford D L Folmes, Jun Wu, Robert Morey, Sergio Mora-Castilla, Alejandro Ocampo, Li Ma, Joanna Poulton, Xinjian Wang, Riffat Ahmed,[...]. Nature 2015
113
100

The mutation at nt 8993 of mitochondrial DNA is a common cause of Leigh's syndrome.
F M Santorelli, S Shanske, A Macaya, D C DeVivo, S DiMauro. Ann Neurol 1993
205
100

NDUFS4 deletion triggers loss of NDUFA12 in Ndufs4-/- mice and Leigh syndrome patients: A stabilizing role for NDUFAF2.
Merel J W Adjobo-Hermans, Ria de Haas, Peter H G M Willems, Aleksandra Wojtala, Sjenet E van Emst-de Vries, Jori A Wagenaars, Mariel van den Brand, Richard J Rodenburg, Jan A M Smeitink, Leo G Nijtmans,[...]. Biochim Biophys Acta Bioenerg 2020
7
100

Cell-permeable succinate prodrugs rescue mitochondrial respiration in cellular models of acute acetaminophen overdose.
Sarah Piel, Imen Chamkha, Adam Kozak Dehlin, Johannes K Ehinger, Fredrik Sjövall, Eskil Elmér, Magnus J Hansson. PLoS One 2020
7
100

Mitochondrial gene therapy improves respiration, biogenesis, and transcription in G11778A Leber's hereditary optic neuropathy and T8993G Leigh's syndrome cells.
Shilpa Iyer, Kristen Bergquist, Kisha Young, Erich Gnaiger, Raj R Rao, James P Bennett. Hum Gene Ther 2012
32
100

NAD(+)-dependent activation of Sirt1 corrects the phenotype in a mouse model of mitochondrial disease.
Raffaele Cerutti, Eija Pirinen, Costanza Lamperti, Silvia Marchet, Anthony A Sauve, Wei Li, Valerio Leoni, Eric A Schon, Françoise Dantzer, Johan Auwerx,[...]. Cell Metab 2014
207
100

Leigh syndrome in individuals bearing m.9185T>C MTATP6 variant. Is hyperventilation a factor which starts its development?
Dorota Piekutowska-Abramczuk, Rafał Rutyna, Elżbieta Czyżyk, Elżbieta Jurkiewicz, Katarzyna Iwanicka-Pronicka, Dariusz Rokicki, Sylwia Stachowicz, Joanna Strzemecka, Wiesław Guz, Michał Gawroński,[...]. Metab Brain Dis 2018
6
100

EPI-743 reverses the progression of the pediatric mitochondrial disease--genetically defined Leigh Syndrome.
Diego Martinelli, Michela Catteruccia, Fiorella Piemonte, Anna Pastore, Giulia Tozzi, Carlo Dionisi-Vici, Giuseppe Pontrelli, Tiziana Corsetti, Susanna Livadiotti, Viktoria Kheifets,[...]. Mol Genet Metab 2012
115
100


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.