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

Year Number of Results
1968 1
1980 1
1982 1
1984 1
1986 1
1987 2
1990 1
1991 1
1993 1
1998 1
2004 1
2013 1
2014 1
2015 3
2016 6
2017 7
2018 16
2019 9
2020 8
2021 11
2022 9
2023 7

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78 results

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Page 1
Primary Pyruvate Dehydrogenase Complex Deficiency Overview.
Ganetzky R, McCormick EM, Falk MJ. Ganetzky R, et al. Among authors: mccormick em. 2021 Jun 17. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2023. 2021 Jun 17. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2023. PMID: 34138529 Free Books & Documents. Review.
Specifications of the ACMG/AMP standards and guidelines for mitochondrial DNA variant interpretation.
McCormick EM, Lott MT, Dulik MC, Shen L, Attimonelli M, Vitale O, Karaa A, Bai R, Pineda-Alvarez DE, Singh LN, Stanley CM, Wong S, Bhardwaj A, Merkurjev D, Mao R, Sondheimer N, Zhang S, Procaccio V, Wallace DC, Gai X, Falk MJ. McCormick EM, et al. Hum Mutat. 2020 Dec;41(12):2028-2057. doi: 10.1002/humu.24107. Epub 2020 Nov 10. Hum Mutat. 2020. PMID: 32906214 Free PMC article.
Methodological considerations for developmental longitudinal fMRI research.
Telzer EH, McCormick EM, Peters S, Cosme D, Pfeifer JH, van Duijvenvoorde ACK. Telzer EH, et al. Among authors: mccormick em. Dev Cogn Neurosci. 2018 Oct;33:149-160. doi: 10.1016/j.dcn.2018.02.004. Epub 2018 Feb 7. Dev Cogn Neurosci. 2018. PMID: 29456104 Free PMC article. Review.
Mitochondrial function requires NGLY1.
Kong J, Peng M, Ostrovsky J, Kwon YJ, Oretsky O, McCormick EM, He M, Argon Y, Falk MJ. Kong J, et al. Among authors: mccormick em. Mitochondrion. 2018 Jan;38:6-16. doi: 10.1016/j.mito.2017.07.008. Epub 2017 Jul 25. Mitochondrion. 2018. PMID: 28750948 Free PMC article.
Diagnosis of 'possible' mitochondrial disease: an existential crisis.
Parikh S, Karaa A, Goldstein A, Bertini ES, Chinnery PF, Christodoulou J, Cohen BH, Davis RL, Falk MJ, Fratter C, Horvath R, Koenig MK, Mancuso M, McCormack S, McCormick EM, McFarland R, Nesbitt V, Schiff M, Steele H, Stockler S, Sue C, Tarnopolsky M, Thorburn DR, Vockley J, Rahman S. Parikh S, et al. Among authors: mccormick em. J Med Genet. 2019 Mar;56(3):123-130. doi: 10.1136/jmedgenet-2018-105800. Epub 2019 Jan 25. J Med Genet. 2019. PMID: 30683676 Review.
78 results