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

Year Number of Results
1952 1
1958 1
1963 1
1972 1
1973 2
1974 1
1975 1
1982 1
2001 1
2002 1
2003 1
2004 3
2005 2
2006 1
2007 1
2010 4
2011 1
2012 1
2013 2
2014 2
2015 2
2016 4
2017 4
2018 6
2019 2
2020 4
2021 7
2022 5
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Search Results

57 results
Results by year
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Page 1
Genetic Basis of Severe Childhood-Onset Cardiomyopathies.
Vasilescu C, Ojala TH, Brilhante V, Ojanen S, Hinterding HM, Palin E, Alastalo TP, Koskenvuo J, Hiippala A, Jokinen E, Jahnukainen T, Lohi J, Pihkala J, Tyni TA, Carroll CJ, Suomalainen A. Vasilescu C, et al. Among authors: carroll cj. J Am Coll Cardiol. 2018 Nov 6;72(19):2324-2338. doi: 10.1016/j.jacc.2018.08.2171. J Am Coll Cardiol. 2018. PMID: 30384889 Free article.
SUCLA2 mutations cause global protein succinylation contributing to the pathomechanism of a hereditary mitochondrial disease.
Gut P, Matilainen S, Meyer JG, Pällijeff P, Richard J, Carroll CJ, Euro L, Jackson CB, Isohanni P, Minassian BA, Alkhater RA, Østergaard E, Civiletto G, Parisi A, Thevenet J, Rardin MJ, He W, Nishida Y, Newman JC, Liu X, Christen S, Moco S, Locasale JW, Schilling B, Suomalainen A, Verdin E. Gut P, et al. Among authors: carroll cj. Nat Commun. 2020 Nov 23;11(1):5927. doi: 10.1038/s41467-020-19743-4. Nat Commun. 2020. PMID: 33230181 Free PMC article.
MED27 Variants Cause Developmental Delay, Dystonia, and Cerebellar Hypoplasia.
Meng L, Isohanni P, Shao Y, Graham BH, Hickey SE, Brooks S, Suomalainen A, Joset P, Steindl K, Rauch A, Hackenberg A, High FA, Armstrong-Javors A, Mencacci NE, Gonzàlez-Latapi P, Kamel WA, Al-Hashel JY, Bustos BI, Hernandez AV, Krainc D, Lubbe SJ, Van Esch H, De Luca C, Ballon K, Ravelli C, Burglen L, Qebibo L, Calame DG, Mitani T, Marafi D, Pehlivan D, Saadi NW, Sahin Y, Maroofian R, Efthymiou S, Houlden H, Maqbool S, Rahman F, Gu S, Posey JE, Lupski JR, Hunter JV, Wangler MF, Carroll CJ, Yang Y. Meng L, et al. Among authors: carroll cj. Ann Neurol. 2021 Apr;89(4):828-833. doi: 10.1002/ana.26019. Epub 2021 Feb 8. Ann Neurol. 2021. PMID: 33443317 Free article.
Next-generation sequencing for mitochondrial disorders.
Carroll CJ, Brilhante V, Suomalainen A. Carroll CJ, et al. Br J Pharmacol. 2014 Apr;171(8):1837-53. doi: 10.1111/bph.12469. Br J Pharmacol. 2014. PMID: 24138576 Free PMC article. Review.
Resolving the Dust Bowl paradox of grassland responses to extreme drought.
Knapp AK, Chen A, Griffin-Nolan RJ, Baur LE, Carroll CJW, Gray JE, Hoffman AM, Li X, Post AK, Slette IJ, Collins SL, Luo Y, Smith MD. Knapp AK, et al. Among authors: carroll cjw. Proc Natl Acad Sci U S A. 2020 Sep 8;117(36):22249-22255. doi: 10.1073/pnas.1922030117. Epub 2020 Aug 24. Proc Natl Acad Sci U S A. 2020. PMID: 32839346 Free PMC article.
Genetic background of ataxia in children younger than 5 years in Finland.
Ignatius E, Isohanni P, Pohjanpelto M, Lahermo P, Ojanen S, Brilhante V, Palin E, Suomalainen A, Lönnqvist T, Carroll CJ. Ignatius E, et al. Among authors: carroll cj. Neurol Genet. 2020 Jun 5;6(4):e444. doi: 10.1212/NXG.0000000000000444. eCollection 2020 Aug. Neurol Genet. 2020. PMID: 32637629 Free PMC article.
57 results