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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2005 1
2008 2
2009 2
2010 5
2011 2
2012 5
2013 3
2014 2
2016 1
2017 3
2018 3
2019 8
2020 8
2021 14
2022 6
2023 4
2024 3

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65 results

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Page 1
How to treat a "sweetheart" in mitochondrial cardiomyopathy.
Lin HP, Narendra DP. Lin HP, et al. Among authors: narendra dp. EMBO Mol Med. 2024 May 9. doi: 10.1038/s44321-024-00070-w. Online ahead of print. EMBO Mol Med. 2024. PMID: 38724624 Free article. No abstract available.
Genotype-phenotype correlation in PRKN-associated Parkinson's disease.
Menon PJ, Sambin S, Criniere-Boizet B, Courtin T, Tesson C, Casse F, Ferrien M, Mariani LL, Carvalho S, Lejeune FX, Rebbah S, Martet G, Houot M, Lanore A, Mangone G, Roze E, Vidailhet M, Aasly J, Gan Or Z, Yu E, Dauvilliers Y, Zimprich A, Tomantschger V, Pirker W, Álvarez I, Pastor P, Di Fonzo A, Bhatia KP, Magrinelli F, Houlden H, Real R, Quattrone A, Limousin P, Korlipara P, Foltynie T, Grosset D, Williams N, Narendra D, Lin HP, Jovanovic C, Svetel M, Lynch T, Gallagher A, Vandenberghe W, Gasser T, Brockmann K, Morris HR, Borsche M, Klein C, Corti O, Brice A, Lesage S, Corvol JC; French Parkinson disease Genetics Study Group (PDG). Menon PJ, et al. Among authors: narendra d. NPJ Parkinsons Dis. 2024 Mar 29;10(1):72. doi: 10.1038/s41531-024-00677-3. NPJ Parkinsons Dis. 2024. PMID: 38553467 Free PMC article.
NeuroBooster Array: A Genome-Wide Genotyping Platform to Study Neurological Disorders Across Diverse Populations.
Bandres-Ciga S, Faghri F, Majounie E, Koretsky MJ, Kim J, Levine KS, Leonard H, Makarious MB, Iwaki H, Crea PW, Hernandez DG, Arepalli S, Billingsley K, Lohmann K, Klein C, Lubbe SJ, Jabbari E, Saffie-Awad P, Narendra D, Reyes-Palomares A, Quinn JP, Schulte C, Morris HR, Traynor BJ, Scholz SW, Houlden H, Hardy J, Dumanis S, Riley E, Blauwendraat C, Singleton A, Nalls M, Jeff J, Vitale D. Bandres-Ciga S, et al. Among authors: narendra d. medRxiv [Preprint]. 2023 Nov 14:2023.11.06.23298176. doi: 10.1101/2023.11.06.23298176. medRxiv. 2023. PMID: 37986980 Free PMC article. Preprint.
A mitochondrial iron-responsive pathway regulated by DELE1.
Sekine Y, Houston R, Eckl EM, Fessler E, Narendra DP, Jae LT, Sekine S. Sekine Y, et al. Among authors: narendra dp. Mol Cell. 2023 Jun 15;83(12):2059-2076.e6. doi: 10.1016/j.molcel.2023.05.031. Mol Cell. 2023. PMID: 37327776
OMA1 mediates local and global stress responses against protein misfolding in CHCHD10 mitochondrial myopathy.
Shammas MK, Huang X, Wu BP, Fessler E, Song IY, Randolph NP, Li Y, Bleck CK, Springer DA, Fratter C, Barbosa IA, Powers AF, Quirós PM, Lopez-Otin C, Jae LT, Poulton J, Narendra DP. Shammas MK, et al. Among authors: narendra dp. J Clin Invest. 2022 Jul 15;132(14):e157504. doi: 10.1172/JCI157504. J Clin Invest. 2022. PMID: 35700042 Free PMC article.
Heterozygous PRKN mutations are common but do not increase the risk of Parkinson's disease.
Zhu W, Huang X, Yoon E, Bandres-Ciga S, Blauwendraat C, Billingsley KJ, Cade JH, Wu BP, Williams VH, Schindler AB, Brooks J, Gibbs JR, Hernandez DG, Ehrlich D, Singleton AB, Narendra DP. Zhu W, et al. Among authors: narendra dp. Brain. 2022 Jun 30;145(6):2077-2091. doi: 10.1093/brain/awab456. Brain. 2022. PMID: 35640906 Free PMC article.
65 results