Cited In for PMID: 20440652

Year	Number of Results
2010	1
2011	3
2012	5
2013	5
2014	4
2015	8
2016	9
2017	8
2018	10
2019	4
2020	7
2021	10
2022	5
2023	7
2024	3

1

Biochemical diagnosis of mitochondrial disorders.

Rodenburg RJ. Rodenburg RJ. J Inherit Metab Dis. 2011 Apr;34(2):283-92. doi: 10.1007/s10545-010-9081-y. Epub 2010 May 4. J Inherit Metab Dis. 2011. PMID: 20440652 Free PMC article. Review.

2

Platelet bioenergetic profiling uncovers a metabolic pattern of high dependency on mitochondrial fatty acid oxidation in type 2 diabetic patients who developed in-stent restenosis.

Wang XB, Cui NH, Fang ZQ, Gao MJ, Cai D. Wang XB, et al. Redox Biol. 2024 Apr 2;72:103146. doi: 10.1016/j.redox.2024.103146. Online ahead of print. Redox Biol. 2024. PMID: 38579589 Free PMC article.

3

Lack of mitochondrial complex I assembly factor NDUFAF2 results in a distinctive infantile-onset brainstem neurodegenerative disease with early lethality.

Abu Hanna F, Zehavi Y, Cohen-Barak E, Khayat M, Warwar N, Shreter R, Rodenburg RJ, Spiegel R. Abu Hanna F, et al. Orphanet J Rare Dis. 2024 Feb 28;19(1):92. doi: 10.1186/s13023-024-03094-0. Orphanet J Rare Dis. 2024. PMID: 38419071 Free PMC article. Review.

4

Endocrine features of primary mitochondrial diseases.

Romo L, Gold NB, Walker MA. Romo L, et al. Curr Opin Endocrinol Diabetes Obes. 2024 Feb 1;31(1):34-42. doi: 10.1097/MED.0000000000000848. Epub 2023 Dec 4. Curr Opin Endocrinol Diabetes Obes. 2024. PMID: 38047549 Free PMC article. Review.

5

Interplay of Impaired Cellular Bioenergetics and Autophagy in PMM2-CDG.

Ligezka AN, Budhraja R, Nishiyama Y, Fiesel FC, Preston G, Edmondson A, Ranatunga W, Van Hove JLK, Watzlawik JO, Springer W, Pandey A, Morava E, Kozicz T. Ligezka AN, et al. Genes (Basel). 2023 Aug 4;14(8):1585. doi: 10.3390/genes14081585. Genes (Basel). 2023. PMID: 37628636 Free PMC article.

6

Comparative Clustering (CompaCt) of eukaryote complexomes identifies novel interactions and sheds light on protein complex evolution.

van Strien J, Evers F, Lutikurti M, Berendsen SL, Garanto A, van Gemert GJ, Cabrera-Orefice A, Rodenburg RJ, Brandt U, Kooij TWA, Huynen MA. van Strien J, et al. PLoS Comput Biol. 2023 Aug 7;19(8):e1011090. doi: 10.1371/journal.pcbi.1011090. eCollection 2023 Aug. PLoS Comput Biol. 2023. PMID: 37549177 Free PMC article.

7

Uncharacterized protein C17orf80 - a novel interactor of human mitochondrial nucleoids.

Potter A, Hangas A, Goffart S, Huynen MA, Cabrera-Orefice A, Spelbrink JN. Potter A, et al. J Cell Sci. 2023 Aug 1;136(15):jcs260822. doi: 10.1242/jcs.260822. Epub 2023 Jul 31. J Cell Sci. 2023. PMID: 37401363 Free PMC article.

8

Mitochondrial complex III activity: from invasive muscle biopsies to patient-friendly buccal swab analysis.

Somers T, Allard NAE, Siddiqi S, Janssen MCM, Hopman MTE, Morshuis WJ, Russel FGM, Timmers S, Schirris TJJ. Somers T, et al. Sci Rep. 2023 Jun 14;13(1):9638. doi: 10.1038/s41598-023-36741-w. Sci Rep. 2023. PMID: 37316639 Free PMC article.

9

Recessive pathogenic variants in MCAT cause combined oxidative phosphorylation deficiency.

Webb BD, Nowinski SM, Solmonson A, Ganesh J, Rodenburg RJ, Leandro J, Evans A, Vu HS, Naidich TP, Gelb BD, DeBerardinis RJ, Rutter J, Houten SM. Webb BD, et al. Elife. 2023 Mar 7;12:e68047. doi: 10.7554/eLife.68047. Elife. 2023. PMID: 36881526 Free PMC article.

10

AAV-based gene therapy prevents and halts the progression of dilated cardiomyopathy in a mouse model of phosphoglucomutase 1 deficiency (PGM1-CDG).

Balakrishnan B, Altassan R, Budhraja R, Liou W, Lupo A, Bryant S, Mankouski A, Radenkovic S, Preston GJ, Pandey A, Boudina S, Kozicz T, Morava E, Lai K. Balakrishnan B, et al. Transl Res. 2023 Jul;257:1-14. doi: 10.1016/j.trsl.2023.01.004. Epub 2023 Jan 26. Transl Res. 2023. PMID: 36709920

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