TY - JOUR
T1 - Correction
T2 - Mitochondrial DNA variation in Alzheimer’s disease reveals a unique microprotein called SHMOOSE (Molecular Psychiatry, (2022), 10.1038/s41380-022-01769-3)
AU - for the Alzheimer's Disease Neuroimaging Initiative
AU - Miller, Brendan
AU - Kim, Su Jeong
AU - Mehta, Hemal H.
AU - Cao, Kevin
AU - Kumagai, Hiroshi
AU - Thumaty, Neehar
AU - Leelaprachakul, Naphada
AU - Braniff, Regina Gonzalez
AU - Jiao, Henry
AU - Vaughan, Joan
AU - Diedrich, Jolene
AU - Saghatelian, Alan
AU - Arpawong, Thalida E.
AU - Crimmins, Eileen M.
AU - Ertekin-Taner, Nilüfer
AU - Tubi, Meral A.
AU - Hare, Evan T.
AU - Braskie, Meredith N.
AU - Décarie-Spain, Léa
AU - Kanoski, Scott E.
AU - Grodstein, Francine
AU - Bennett, David A.
AU - Zhao, Lu
AU - Toga, Arthur W.
AU - Wan, Junxiang
AU - Yen, Kelvin
AU - Cohen, Pinchas
N1 - Funding Information:
In the Acknowledgements section of this article, the following text was missing: “Data collection and sharing for this project was funded by the Alzheimer’s Disease Neuroimaging Initiative (ADNI) (National Institutes of Health Grant U01 AG024904) and DOD ADNI (Department of Defense award number W81XWH-12-2-0012). ADNI is funded by the National Institute on Aging, the National Institute of Biomedical Imaging and Bioengineering, and through generous contributions from the following: AbbVie, Alzheimer’s Association; Alzheimer’s Drug Discovery Foundation; Araclon Biotech; BioClinica, Inc.; Biogen; Bristol-Myers Squibb Company; CereSpir, Inc.; Cogstate; Eisai Inc.; Elan Pharmaceuticals, Inc.; Eli Lilly and Company; EuroImmun; F. Hoffmann-La Roche Ltd and its affiliated company Genentech, Inc.; Fujirebio; GE Healthcare; IXICO Ltd.; Janssen Alzheimer Immunotherapy Research & Development, LLC.; Johnson & Johnson Pharmaceutical Research & Development LLC.; Lumosity; Lundbeck; Merck & Co., Inc.; Meso Scale Diagnostics, LLC.; NeuroRx Research; Neurotrack Technologies; Novartis Pharmaceuticals Corporation; Pfizer Inc.; Piramal Imaging; Servier; Takeda Pharmaceutical Company; and Transition Therapeutics. The Canadian Institutes of Health Research is providing funds to support ADNI clinical sites in Canada. Private sector contributions are facilitated by the Foundation for the National Institutes of Health ( www.fnih.org ). The grantee organization is the Northern California Institute for Research and Education, and the study is coordinated by the Alzheimer’s Therapeutic Research Institute at the University of Southern California. ADNI data are disseminated by the Laboratory for Neuro Imaging at the University of Southern California”.
Publisher Copyright:
© The Author(s), under exclusive licence to Springer Nature Limited 2023.
PY - 2023
Y1 - 2023
N2 - In the by-line of this article, the following phrase was missing: Include the phrase “for the Alzheimer’s Disease Neuroimaging Initiative”. In the by-line of this article, the following author was missing: Regina Gonzalez Braniff. In the methods section of this article, the following text was missing: “Data used in the preparation of this article were obtained from the Alzheimer’s Disease Neuroimaging Initiative (ADNI) database (adni.loni.usc.edu). The ADNI was launched in 2003 as a public-private partnership, led by Principal Investigator Michael W. Weiner, MD. The primary goal of ADNI has been to test whether serial magnetic resonance imaging (MRI), positron emission tomography (PET), other biological markers, and clinical and neuropsychological assessment can be combined to measure the progression of mild cognitive impairment (MCI) and early Alzheimer’s disease (AD)”. In the Acknowledgements section of this article, the following text was missing: “Data collection and sharing for this project was funded by the Alzheimer’s Disease Neuroimaging Initiative (ADNI) (National Institutes of Health Grant U01 AG024904) and DOD ADNI (Department of Defense award number W81XWH-12-2-0012). ADNI is funded by the National Institute on Aging, the National Institute of Biomedical Imaging and Bioengineering, and through generous contributions from the following: AbbVie, Alzheimer’s Association; Alzheimer’s Drug Discovery Foundation; Araclon Biotech; BioClinica, Inc.; Biogen; Bristol-Myers Squibb Company; CereSpir, Inc.; Cogstate; Eisai Inc.; Elan Pharmaceuticals, Inc.; Eli Lilly and Company; EuroImmun; F. Hoffmann-La Roche Ltd and its affiliated company Genentech, Inc.; Fujirebio; GE Healthcare; IXICO Ltd.; Janssen Alzheimer Immunotherapy Research & Development, LLC.; Johnson & Johnson Pharmaceutical Research & Development LLC.; Lumosity; Lundbeck; Merck & Co., Inc.; Meso Scale Diagnostics, LLC.; NeuroRx Research; Neurotrack Technologies; Novartis Pharmaceuticals Corporation; Pfizer Inc.; Piramal Imaging; Servier; Takeda Pharmaceutical Company; and Transition Therapeutics. The Canadian Institutes of Health Research is providing funds to support ADNI clinical sites in Canada. Private sector contributions are facilitated by the Foundation for the National Institutes of Health (www.fnih.org). The grantee organization is the Northern California Institute for Research and Education, and the study is coordinated by the Alzheimer’s Therapeutic Research Institute at the University of Southern California. ADNI data are disseminated by the Laboratory for Neuro Imaging at the University of Southern California”. In the sentence beginning “rs2853499 (henceforth referred to as SHMOOSE.D47N)…” in this article, the typo “from glutamine to aspartic acid” should read “from aspartic acid to asparagine”. The original article has been corrected.
AB - In the by-line of this article, the following phrase was missing: Include the phrase “for the Alzheimer’s Disease Neuroimaging Initiative”. In the by-line of this article, the following author was missing: Regina Gonzalez Braniff. In the methods section of this article, the following text was missing: “Data used in the preparation of this article were obtained from the Alzheimer’s Disease Neuroimaging Initiative (ADNI) database (adni.loni.usc.edu). The ADNI was launched in 2003 as a public-private partnership, led by Principal Investigator Michael W. Weiner, MD. The primary goal of ADNI has been to test whether serial magnetic resonance imaging (MRI), positron emission tomography (PET), other biological markers, and clinical and neuropsychological assessment can be combined to measure the progression of mild cognitive impairment (MCI) and early Alzheimer’s disease (AD)”. In the Acknowledgements section of this article, the following text was missing: “Data collection and sharing for this project was funded by the Alzheimer’s Disease Neuroimaging Initiative (ADNI) (National Institutes of Health Grant U01 AG024904) and DOD ADNI (Department of Defense award number W81XWH-12-2-0012). ADNI is funded by the National Institute on Aging, the National Institute of Biomedical Imaging and Bioengineering, and through generous contributions from the following: AbbVie, Alzheimer’s Association; Alzheimer’s Drug Discovery Foundation; Araclon Biotech; BioClinica, Inc.; Biogen; Bristol-Myers Squibb Company; CereSpir, Inc.; Cogstate; Eisai Inc.; Elan Pharmaceuticals, Inc.; Eli Lilly and Company; EuroImmun; F. Hoffmann-La Roche Ltd and its affiliated company Genentech, Inc.; Fujirebio; GE Healthcare; IXICO Ltd.; Janssen Alzheimer Immunotherapy Research & Development, LLC.; Johnson & Johnson Pharmaceutical Research & Development LLC.; Lumosity; Lundbeck; Merck & Co., Inc.; Meso Scale Diagnostics, LLC.; NeuroRx Research; Neurotrack Technologies; Novartis Pharmaceuticals Corporation; Pfizer Inc.; Piramal Imaging; Servier; Takeda Pharmaceutical Company; and Transition Therapeutics. The Canadian Institutes of Health Research is providing funds to support ADNI clinical sites in Canada. Private sector contributions are facilitated by the Foundation for the National Institutes of Health (www.fnih.org). The grantee organization is the Northern California Institute for Research and Education, and the study is coordinated by the Alzheimer’s Therapeutic Research Institute at the University of Southern California. ADNI data are disseminated by the Laboratory for Neuro Imaging at the University of Southern California”. In the sentence beginning “rs2853499 (henceforth referred to as SHMOOSE.D47N)…” in this article, the typo “from glutamine to aspartic acid” should read “from aspartic acid to asparagine”. The original article has been corrected.
UR - http://www.scopus.com/inward/record.url?scp=85146554555&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85146554555&partnerID=8YFLogxK
U2 - 10.1038/s41380-023-01956-w
DO - 10.1038/s41380-023-01956-w
M3 - Comment/debate
C2 - 36658336
AN - SCOPUS:85146554555
SN - 1359-4184
JO - Molecular Psychiatry
JF - Molecular Psychiatry
ER -