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For: Rahman S. Mitochondrial disease in children. J Intern Med 2020;287:609-33. [PMID: 32176382 DOI: 10.1111/joim.13054] [Cited by in Crossref: 15] [Cited by in F6Publishing: 35] [Article Influence: 7.5] [Reference Citation Analysis]
Number Citing Articles
1 Valenti D, Vacca RA. Primary and Secondary Mitochondrial Diseases: Etiologies and Therapeutic Strategies. JCM 2022;11:4209. [DOI: 10.3390/jcm11144209] [Reference Citation Analysis]
2 Kirillova A, Mazunin I. Operation “mitochondrial wipeout” — clearing recipient mitochondria DNA during the cytoplasmic replacement therapy. J Assist Reprod Genet. [DOI: 10.1007/s10815-022-02561-6] [Reference Citation Analysis]
3 Abruzzo T, van den Berg R, Vadivelu S, Hetts SW, Dishop M, Cornejo P, Narayanan V, Ramsey KE, Coopwood C, Medici-van den Herik EG, Roosendaal SD, Lawton M, Bernes S. Arterioectatic Spinal Angiopathy of Childhood: Clinical, Imaging, Laboratory, Histologic, and Genetic Description of a Novel CNS Vascular Pathology. AJNR Am J Neuroradiol 2022. [PMID: 35772802 DOI: 10.3174/ajnr.A7551] [Reference Citation Analysis]
4 Aldossary AM, Tawfik EA, Alomary MN, Alsudir SA, Alfahad AJ, Alshehri AA, Almughem FA, Mohammed RY, Alzaydi MM. Recent Advances in Mitochondrial Diseases: from Molecular Insights to Therapeutic Perspectives. Saudi Pharmaceutical Journal 2022. [DOI: 10.1016/j.jsps.2022.05.011] [Reference Citation Analysis]
5 Smeitink J, van Maanen R, de Boer L, Ruiterkamp G, Renkema H. A randomised placebo-controlled, double-blind phase II study to explore the safety, efficacy, and pharmacokinetics of sonlicromanol in children with genetically confirmed mitochondrial disease and motor symptoms ("KHENERGYC"). BMC Neurol 2022;22:158. [PMID: 35477351 DOI: 10.1186/s12883-022-02685-3] [Reference Citation Analysis]
6 Chu CT. Mitochondria in neurodegeneration. Current Opinion in Physiology 2022. [DOI: 10.1016/j.cophys.2022.100532] [Reference Citation Analysis]
7 Candelise N, Salvatori I, Scaricamazza S, Nesci V, Zenuni H, Ferri A, Valle C. Mechanistic Insights of Mitochondrial Dysfunction in Amyotrophic Lateral Sclerosis: An Update on a Lasting Relationship. Metabolites 2022;12:233. [DOI: 10.3390/metabo12030233] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
8 Wikramanayake TC, Chéret J, Sevilla A, Birch-Machin M, Paus R. Targeting mitochondria in dermatological therapy: Beyond oxidative damage and skin aging. Expert Opin Ther Targets 2022. [PMID: 35249436 DOI: 10.1080/14728222.2022.2049756] [Reference Citation Analysis]
9 Fang H, Xie A, Du M, Li X, Yang K, Fu Y, Yuan X, Fan R, Yu W, Zhou Z, Sang T, Nie K, Li J, Zhao Q, Chen Z, Yang Y, Hong C, Lyu J. SERAC1 is a component of the mitochondrial serine transporter complex required for the maintenance of mitochondrial DNA. Sci Transl Med 2022;14:eabl6992. [PMID: 35235340 DOI: 10.1126/scitranslmed.abl6992] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
10 Chung J, Lee M, Chung J, Won H. Extremely Rare Case of Fetal Anemia Due to Mitochondrial Disease Managed with Intrauterine Transfusion. Medicina 2022;58:328. [DOI: 10.3390/medicina58030328] [Reference Citation Analysis]
11 Arena IG, Pugliese A, Volta S, Toscano A, Musumeci O. Molecular Genetics Overview of Primary Mitochondrial Myopathies. J Clin Med 2022;11:632. [PMID: 35160083 DOI: 10.3390/jcm11030632] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 3.0] [Reference Citation Analysis]
12 Wang W, Song J, Chuai Y, Chen F, Song C, Shu M, Wang Y, Li Y, Zhai X, Han S, Yao S, Shen K, Shang W, Zhang L. The mining and construction of a knowledge base for gene-disease association in mitochondrial diseases. Sci Rep 2021;11:23909. [PMID: 34903783 DOI: 10.1038/s41598-021-03249-0] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
13 Shi Y, Chen G, Sun D, Hu C, Liu Z, Shen D, Wang J, Song T, Zhang W, Li J, Ren X, Han T, Ding C, Wang Y, Fang F. Phenotypes and genotypes of mitochondrial diseases with mtDNA variations in Chinese children: A multi-center study. Mitochondrion 2022;62:139-50. [PMID: 34800692 DOI: 10.1016/j.mito.2021.11.006] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 4.0] [Reference Citation Analysis]
14 Terburgh K, Lindeque JZ, van der Westhuizen FH, Louw R. Cross-comparison of systemic and tissue-specific metabolomes in a mouse model of Leigh syndrome. Metabolomics 2021;17:101. [PMID: 34792662 DOI: 10.1007/s11306-021-01854-8] [Reference Citation Analysis]
15 Olimpio C, Tiet MY, Horvath R. Primary mitochondrial myopathies in childhood. Neuromuscul Disord 2021;31:978-87. [PMID: 34736635 DOI: 10.1016/j.nmd.2021.08.005] [Reference Citation Analysis]
16 Pagano G, Pallardó FV, Lyakhovich A, Tiano L, Trifuoggi M. Mitigating the pro-oxidant state and melanogenesis of Retinitis pigmentosa: by counteracting mitochondrial dysfunction. Cell Mol Life Sci 2021;78:7491-503. [PMID: 34718826 DOI: 10.1007/s00018-021-04007-1] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
17 Hikmat O, Isohanni P, Keshavan N, Ferla MP, Fassone E, Abbott MA, Bellusci M, Darin N, Dimmock D, Ghezzi D, Houlden H, Invernizzi F, Kamarus Jaman NB, Kurian MA, Morava E, Naess K, Ortigoza-Escobar JD, Parikh S, Pennisi A, Barcia G, Tylleskär KB, Brackman D, Wortmann SB, Taylor JC, Bindoff LA, Fellman V, Rahman S. Expanding the phenotypic spectrum of BCS1L-related mitochondrial disease. Ann Clin Transl Neurol 2021;8:2155-65. [PMID: 34662929 DOI: 10.1002/acn3.51470] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
18 Gayathri N, Deepha S, Sharma S. Diagnosis of primary mitochondrial disorders -Emphasis on myopathological aspects. Mitochondrion 2021;61:69-84. [PMID: 34592422 DOI: 10.1016/j.mito.2021.09.007] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
19 Bakare AB, Dean J, Chen Q, Thorat V, Huang Y, LaFramboise T, Lesnefsky EJ, Iyer S. Evaluating the Bioenergetics Health Index Ratio in Leigh Syndrome Fibroblasts to Understand Disease Severity. Int J Mol Sci 2021;22:10344. [PMID: 34638685 DOI: 10.3390/ijms221910344] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
20 Luciani A, Denley MCS, Govers LP, Sorrentino V, Froese DS. Mitochondrial disease, mitophagy, and cellular distress in methylmalonic acidemia. Cell Mol Life Sci 2021;78:6851-67. [PMID: 34524466 DOI: 10.1007/s00018-021-03934-3] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
21 Bonekamp NA, Jiang M, Motori E, Garcia Villegas R, Koolmeister C, Atanassov I, Mesaros A, Park CB, Larsson NG. High levels of TFAM repress mammalian mitochondrial DNA transcription in vivo. Life Sci Alliance 2021;4:e202101034. [PMID: 34462320 DOI: 10.26508/lsa.202101034] [Cited by in F6Publishing: 13] [Reference Citation Analysis]
22 Guo L, Engelen BPH, Hemel IMGM, de Coo IFM, Vreeburg M, Sallevelt SCEH, Hellebrekers DMEI, Jacobs EH, Sadeghi-Niaraki F, van Tienen FHJ, Smeets HJM, Gerards M. Pathogenic SLIRP variants as a novel cause of autosomal recessive mitochondrial encephalomyopathy with complex I and IV deficiency. Eur J Hum Genet 2021;29:1789-95. [PMID: 34426662 DOI: 10.1038/s41431-021-00947-1] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
23 Tolomeo D, Orsucci D, Nesti C, Baldacci J, Battini R, Bruno C, Bruno G, Cassandrini D, Doccini S, Donati MA, Ferrari A, Fiori S, Fiorillo C, Guerrini R, Mari F, Montomoli M, Pochiero F, Procopio E, Ruggiero L, Sampaolo S, Sicca F, Ticci C, Rubegni A, Santorelli FM. The Diagnostic Approach to Mitochondrial Disorders in Children in the Era of Next-Generation Sequencing: A 4-Year Cohort Study. J Clin Med 2021;10:3222. [PMID: 34362006 DOI: 10.3390/jcm10153222] [Reference Citation Analysis]
24 Herbst A, Lee CC, Vandiver AR, Aiken JM, McKenzie D, Hoang A, Allison D, Liu N, Wanagat J. Mitochondrial DNA deletion mutations increase exponentially with age in human skeletal muscle. Aging Clin Exp Res 2021;33:1811-20. [PMID: 32965609 DOI: 10.1007/s40520-020-01698-7] [Cited by in Crossref: 9] [Cited by in F6Publishing: 8] [Article Influence: 9.0] [Reference Citation Analysis]
25 Friedrich VK, Rubel MA, Schurr TG. Mitochondrial genetic variation in human bioenergetics, adaptation, and adult disease. Am J Hum Biol 2021;:e23629. [PMID: 34146380 DOI: 10.1002/ajhb.23629] [Reference Citation Analysis]
26 Finsterer J. Secondary manifestations of mitochondrial disorders. J Zhejiang Univ Sci B 2020;21:590-2. [PMID: 32633113 DOI: 10.1631/jzus.B2000010] [Cited by in Crossref: 1] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
27 Forny P, Footitt E, Davison JE, Lam A, Woodward CE, Batzios S, Bhate S, Chakrapani A, Cleary M, Gissen P, Grunewald S, Hurst JA, Scott R, Heales S, Jacques TS, Cullup T, Rahman S. Diagnosing Mitochondrial Disorders Remains Challenging in the Omics Era. Neurol Genet 2021;7:e597. [PMID: 34056100 DOI: 10.1212/NXG.0000000000000597] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
28 Erchova I, Sun S, Votruba M. A Perspective on Accelerated Aging Caused by the Genetic Deficiency of the Metabolic Protein, OPA1. Front Neurol 2021;12:641259. [PMID: 33927681 DOI: 10.3389/fneur.2021.641259] [Reference Citation Analysis]
29 Loos MA, Gomez G, Mayorga L, Caraballo RH, Eiroa HD, Obregon MG, Rugilo C, Lubieniecki F, Taratuto AL, Saccoliti M, Alonso CN, Aráoz HV. Clinical and molecular characterization of mitochondrial DNA disorders in a group of Argentinian pediatric patients. Mol Genet Metab Rep 2021;27:100733. [PMID: 33717984 DOI: 10.1016/j.ymgmr.2021.100733] [Reference Citation Analysis]
30 Klein IL, van de Loo KFE, Smeitink JAM, Janssen MCH, Kessels RPC, van Karnebeek CD, van der Veer E, Custers JAE, Verhaak CM. Cognitive functioning and mental health in mitochondrial disease: A systematic scoping review. Neurosci Biobehav Rev 2021;125:57-77. [PMID: 33582231 DOI: 10.1016/j.neubiorev.2021.02.004] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
31 Rath S, Sharma R, Gupta R, Ast T, Chan C, Durham TJ, Goodman RP, Grabarek Z, Haas ME, Hung WHW, Joshi PR, Jourdain AA, Kim SH, Kotrys AV, Lam SS, McCoy JG, Meisel JD, Miranda M, Panda A, Patgiri A, Rogers R, Sadre S, Shah H, Skinner OS, To TL, Walker MA, Wang H, Ward PS, Wengrod J, Yuan CC, Calvo SE, Mootha VK. MitoCarta3.0: an updated mitochondrial proteome now with sub-organelle localization and pathway annotations. Nucleic Acids Res 2021;49:D1541-7. [PMID: 33174596 DOI: 10.1093/nar/gkaa1011] [Cited by in Crossref: 59] [Cited by in F6Publishing: 152] [Article Influence: 59.0] [Reference Citation Analysis]
32 Filograna R, Mennuni M, Alsina D, Larsson NG. Mitochondrial DNA copy number in human disease: the more the better? FEBS Lett 2021;595:976-1002. [PMID: 33314045 DOI: 10.1002/1873-3468.14021] [Cited by in Crossref: 11] [Cited by in F6Publishing: 54] [Article Influence: 5.5] [Reference Citation Analysis]
33 Schlieben LD, Prokisch H. The Dimensions of Primary Mitochondrial Disorders. Front Cell Dev Biol 2020;8:600079. [PMID: 33324649 DOI: 10.3389/fcell.2020.600079] [Cited by in Crossref: 6] [Cited by in F6Publishing: 16] [Article Influence: 3.0] [Reference Citation Analysis]
34 Pitceathly RDS, Keshavan N, Rahman J, Rahman S. Moving towards clinical trials for mitochondrial diseases. J Inherit Metab Dis 2021;44:22-41. [PMID: 32618366 DOI: 10.1002/jimd.12281] [Cited by in Crossref: 5] [Cited by in F6Publishing: 12] [Article Influence: 2.5] [Reference Citation Analysis]
35 Larsson NG, Wedell A. Mitochondria in human disease. J Intern Med 2020;287:589-91. [PMID: 32406555 DOI: 10.1111/joim.13088] [Reference Citation Analysis]