Correction: The complex genetics of gait speed: Genome-wide metaanalysis approach [Aging, (Albany NY), 9, 1, (2017), (209-246)]doi 10.18632/aging.101151

Dan Ben-Avraham; David Karasik; Joe Verghese; Kathryn L. Lunetta; Jennifer A. Smith; John D. Eicher; Rotem Vered; Joris Deelen; Alice M. Arnold; Aron S. Buchman; Toshiko Tanaka; Jessica D. Faul; Maria Nethander; Myriam Fornage; Hieab H. Adams; Amy M. Matteini; Michele L. Callisaya; Albert V. Smith; Lei Yu; Philip L. De Jager; Denis A. Evans; Vilmundur Gudnason; Albert Hofman; Alison Pattie; Janie Corley; Lenore J. Launer; Davis S. Knopman; Neeta Parimi; Stephen T. Turner; Stefania Bandinelli; Marian Beekman; Danielle Gutman; Lital Sharvit; Simon P. Mooijaart; David C. Liewald; Jeanine J. Houwing-Duistermaat; Claes Ohlsson; Matthijs Moed; Vincent J. Verlinden; Dan Mellström; Jos N. van der Geest; Magnus Karlsson; Dena Hernandez; Rebekah McWhirter; Yongmei Liu; Russell Thomson; Gregory J. Tranah; Andre G. Uitterlinden; David R. Weir; Wei Zhao; John M. Starr; Andrew D. Johnson; M. Arfan Ikram; David A. Bennett; Steven R. Cummings; Ian J. Deary; Tamara B. Harris; Sharon L.R. Kardia; Thomas H. Mosley; Velandai K. Srikanth; Beverly G. Windham; Ann B. Newman; Jeremy D. Walston; Gail Davies; Daniel S. Evans; Eline P. Slagboom; Luigi Ferrucci; Douglas P. Kiel; Joanne M. Murabito; Gil Atzmon

doi:10.18632/aging.101260

Correction: The complex genetics of gait speed: Genome-wide metaanalysis approach [Aging, (Albany NY), 9, 1, (2017), (209-246)]doi 10.18632/aging.101151

Dan Ben-Avraham
, David Karasik
, Joe Verghese
, Kathryn L. Lunetta
, Jennifer A. Smith
, John D. Eicher
, Rotem Vered
, Joris Deelen
, Alice M. Arnold
, Aron S. Buchman
, Toshiko Tanaka
, Jessica D. Faul
, Maria Nethander
, Myriam Fornage
, Hieab H. Adams
, Amy M. Matteini
, Michele L. Callisaya
, Albert V. Smith
, Lei Yu
, Philip L. De Jager

Denis A. Evans, Vilmundur Gudnason, Albert Hofman, Alison Pattie, Janie Corley, Lenore J. Launer, Davis S. Knopman, Neeta Parimi, Stephen T. Turner, Stefania Bandinelli, Marian Beekman, Danielle Gutman, Lital Sharvit, Simon P. Mooijaart, David C. Liewald, Jeanine J. Houwing-Duistermaat, Claes Ohlsson, Matthijs Moed, Vincent J. Verlinden, Dan Mellström, Jos N. van der Geest, Magnus Karlsson, Dena Hernandez, Rebekah McWhirter, Yongmei Liu, Russell Thomson, Gregory J. Tranah, Andre G. Uitterlinden, David R. Weir, Wei Zhao, John M. Starr, Andrew D. Johnson, M. Arfan Ikram, David A. Bennett, Steven R. Cummings, Ian J. Deary, Tamara B. Harris, Sharon L.R. Kardia, Thomas H. Mosley, Velandai K. Srikanth, Beverly G. Windham, Ann B. Newman, Jeremy D. Walston, Gail Davies, Daniel S. Evans, Eline P. Slagboom, Luigi Ferrucci, Douglas P. Kiel, Joanne M. Murabito, Gil Atzmon

Neurology

Stony Brook University

Albert Einstein College of Medicine
Harvard University
Bar-Ilan University
The National Heart Lung and Blood Institute's Framingham Heart Study
Boston University
University of Michigan, Ann Arbor
National Institutes of Health
University of Haifa
Leiden University
Max Planck Institute for Biology of Ageing
University of Washington
Rush University
University of Gothenburg
University of Texas Health Science Center at Houston
Erasmus University Rotterdam
Johns Hopkins University
Peninsula Health
University of Tasmania
University of Iceland
Brigham and Women’s Hospital
Rush Institute for Healthy Aging
University of Edinburgh
Mayo Clinic Rochester, MN
California Pacific Medical Center
Azienda Sanitaria Firenze (ASF)
University of Leeds
Lund University
Wake Forest University
Western Sydney University
Netherlands Genomics Initiative
University of Mississippi
University of Pittsburgh
Broad Institute

Research output: Contribution to journal › Comment/debate

2 Scopus citations

Abstract

Applying HaploReg v4.1 analysis to the 536 variants resulted in 9 categories (Supplementary Table 8): miscRNA (1 variant); snoRNA (2 variants); microRNA (4 variants); snRNA (9 variants); pseudogenes (14 variants); sequencing in progress (43 variants); LINC RNA (86 variants); and 372 variants within protein coding genes. In addition, some variants annotate to the same gene resulting in a total of 139 genes (protein-coding or non-coding). Of those genes, 6 are exceptionally long, containing over a million base-pairs, the longest of which is PTPRT coded by 1117219bp. The shortest genes are the ones coding for micro (MIR3143) or small nuclear (U7) RNAs at 63bp each. There is only partial information regarding the chromatin state of each variant. However, from the information gathered in the analysis we observed 14 transcription start sites and 245 enhancers (Supplementary Table 8).

Original language	English
Pages (from-to)	1844-1846
Number of pages	3
Journal	Aging
Volume	9
Issue number	7
DOIs	https://doi.org/10.18632/aging.101260
State	Published - Jul 1 2017

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Ben-Avraham, D., Karasik, D., Verghese, J., Lunetta, K. L., Smith, J. A., Eicher, J. D., Vered, R., Deelen, J., Arnold, A. M., Buchman, A. S., Tanaka, T., Faul, J. D., Nethander, M., Fornage, M., Adams, H. H., Matteini, A. M., Callisaya, M. L., Smith, A. V., Yu, L., ... Atzmon, G. (2017). Correction: The complex genetics of gait speed: Genome-wide metaanalysis approach [Aging, (Albany NY), 9, 1, (2017), (209-246)]doi 10.18632/aging.101151. Aging, 9(7), 1844-1846. https://doi.org/10.18632/aging.101260

@article{0d635fe4b92048768bf47fc3d5dff31a,

title = "Correction: The complex genetics of gait speed: Genome-wide metaanalysis approach [Aging, (Albany NY), 9, 1, (2017), (209-246)]doi 10.18632/aging.101151",

abstract = "Applying HaploReg v4.1 analysis to the 536 variants resulted in 9 categories (Supplementary Table 8): miscRNA (1 variant); snoRNA (2 variants); microRNA (4 variants); snRNA (9 variants); pseudogenes (14 variants); sequencing in progress (43 variants); LINC RNA (86 variants); and 372 variants within protein coding genes. In addition, some variants annotate to the same gene resulting in a total of 139 genes (protein-coding or non-coding). Of those genes, 6 are exceptionally long, containing over a million base-pairs, the longest of which is PTPRT coded by 1117219bp. The shortest genes are the ones coding for micro (MIR3143) or small nuclear (U7) RNAs at 63bp each. There is only partial information regarding the chromatin state of each variant. However, from the information gathered in the analysis we observed 14 transcription start sites and 245 enhancers (Supplementary Table 8).",

author = "Dan Ben-Avraham and David Karasik and Joe Verghese and Lunetta, \{Kathryn L.\} and Smith, \{Jennifer A.\} and Eicher, \{John D.\} and Rotem Vered and Joris Deelen and Arnold, \{Alice M.\} and Buchman, \{Aron S.\} and Toshiko Tanaka and Faul, \{Jessica D.\} and Maria Nethander and Myriam Fornage and Adams, \{Hieab H.\} and Matteini, \{Amy M.\} and Callisaya, \{Michele L.\} and Smith, \{Albert V.\} and Lei Yu and \{De Jager\}, \{Philip L.\} and Evans, \{Denis A.\} and Vilmundur Gudnason and Albert Hofman and Alison Pattie and Janie Corley and Launer, \{Lenore J.\} and Knopman, \{Davis S.\} and Neeta Parimi and Turner, \{Stephen T.\} and Stefania Bandinelli and Marian Beekman and Danielle Gutman and Lital Sharvit and Mooijaart, \{Simon P.\} and Liewald, \{David C.\} and Houwing-Duistermaat, \{Jeanine J.\} and Claes Ohlsson and Matthijs Moed and Verlinden, \{Vincent J.\} and Dan Mellstr{\"o}m and \{van der Geest\}, \{Jos N.\} and Magnus Karlsson and Dena Hernandez and Rebekah McWhirter and Yongmei Liu and Russell Thomson and Tranah, \{Gregory J.\} and Uitterlinden, \{Andre G.\} and Weir, \{David R.\} and Wei Zhao and Starr, \{John M.\} and Johnson, \{Andrew D.\} and \{Arfan Ikram\}, M. and Bennett, \{David A.\} and Cummings, \{Steven R.\} and Deary, \{Ian J.\} and Harris, \{Tamara B.\} and Kardia, \{Sharon L.R.\} and Mosley, \{Thomas H.\} and Srikanth, \{Velandai K.\} and Windham, \{Beverly G.\} and Newman, \{Ann B.\} and Walston, \{Jeremy D.\} and Gail Davies and Evans, \{Daniel S.\} and Slagboom, \{Eline P.\} and Luigi Ferrucci and Kiel, \{Douglas P.\} and Murabito, \{Joanne M.\} and Gil Atzmon",

year = "2017",

month = jul,

day = "1",

doi = "10.18632/aging.101260",

language = "English",

volume = "9",

pages = "1844--1846",

journal = "Aging",

issn = "1945-4589",

number = "7",

}

Ben-Avraham, D, Karasik, D, Verghese, J, Lunetta, KL, Smith, JA, Eicher, JD, Vered, R, Deelen, J, Arnold, AM, Buchman, AS, Tanaka, T, Faul, JD, Nethander, M, Fornage, M, Adams, HH, Matteini, AM, Callisaya, ML, Smith, AV, Yu, L, De Jager, PL, Evans, DA, Gudnason, V, Hofman, A, Pattie, A, Corley, J, Launer, LJ, Knopman, DS, Parimi, N, Turner, ST, Bandinelli, S, Beekman, M, Gutman, D, Sharvit, L, Mooijaart, SP, Liewald, DC, Houwing-Duistermaat, JJ, Ohlsson, C, Moed, M, Verlinden, VJ, Mellström, D, van der Geest, JN, Karlsson, M, Hernandez, D, McWhirter, R, Liu, Y, Thomson, R, Tranah, GJ, Uitterlinden, AG, Weir, DR, Zhao, W, Starr, JM, Johnson, AD, Arfan Ikram, M, Bennett, DA, Cummings, SR, Deary, IJ, Harris, TB, Kardia, SLR, Mosley, TH, Srikanth, VK, Windham, BG, Newman, AB, Walston, JD, Davies, G, Evans, DS, Slagboom, EP, Ferrucci, L, Kiel, DP, Murabito, JM & Atzmon, G 2017, 'Correction: The complex genetics of gait speed: Genome-wide metaanalysis approach [Aging, (Albany NY), 9, 1, (2017), (209-246)]doi 10.18632/aging.101151', Aging, vol. 9, no. 7, pp. 1844-1846. https://doi.org/10.18632/aging.101260

TY - JOUR

T1 - Correction

T2 - The complex genetics of gait speed: Genome-wide metaanalysis approach [Aging, (Albany NY), 9, 1, (2017), (209-246)]doi 10.18632/aging.101151

AU - Ben-Avraham, Dan

AU - Karasik, David

AU - Verghese, Joe

AU - Lunetta, Kathryn L.

AU - Smith, Jennifer A.

AU - Eicher, John D.

AU - Vered, Rotem

AU - Deelen, Joris

AU - Arnold, Alice M.

AU - Buchman, Aron S.

AU - Tanaka, Toshiko

AU - Faul, Jessica D.

AU - Nethander, Maria

AU - Fornage, Myriam

AU - Adams, Hieab H.

AU - Matteini, Amy M.

AU - Callisaya, Michele L.

AU - Smith, Albert V.

AU - Yu, Lei

AU - De Jager, Philip L.

AU - Evans, Denis A.

AU - Gudnason, Vilmundur

AU - Hofman, Albert

AU - Pattie, Alison

AU - Corley, Janie

AU - Launer, Lenore J.

AU - Knopman, Davis S.

AU - Parimi, Neeta

AU - Turner, Stephen T.

AU - Bandinelli, Stefania

AU - Beekman, Marian

AU - Gutman, Danielle

AU - Sharvit, Lital

AU - Mooijaart, Simon P.

AU - Liewald, David C.

AU - Houwing-Duistermaat, Jeanine J.

AU - Ohlsson, Claes

AU - Moed, Matthijs

AU - Verlinden, Vincent J.

AU - Mellström, Dan

AU - van der Geest, Jos N.

AU - Karlsson, Magnus

AU - Hernandez, Dena

AU - McWhirter, Rebekah

AU - Liu, Yongmei

AU - Thomson, Russell

AU - Tranah, Gregory J.

AU - Uitterlinden, Andre G.

AU - Weir, David R.

AU - Zhao, Wei

AU - Starr, John M.

AU - Johnson, Andrew D.

AU - Arfan Ikram, M.

AU - Bennett, David A.

AU - Cummings, Steven R.

AU - Deary, Ian J.

AU - Harris, Tamara B.

AU - Kardia, Sharon L.R.

AU - Mosley, Thomas H.

AU - Srikanth, Velandai K.

AU - Windham, Beverly G.

AU - Newman, Ann B.

AU - Walston, Jeremy D.

AU - Davies, Gail

AU - Evans, Daniel S.

AU - Slagboom, Eline P.

AU - Ferrucci, Luigi

AU - Kiel, Douglas P.

AU - Murabito, Joanne M.

AU - Atzmon, Gil

PY - 2017/7/1

Y1 - 2017/7/1

N2 - Applying HaploReg v4.1 analysis to the 536 variants resulted in 9 categories (Supplementary Table 8): miscRNA (1 variant); snoRNA (2 variants); microRNA (4 variants); snRNA (9 variants); pseudogenes (14 variants); sequencing in progress (43 variants); LINC RNA (86 variants); and 372 variants within protein coding genes. In addition, some variants annotate to the same gene resulting in a total of 139 genes (protein-coding or non-coding). Of those genes, 6 are exceptionally long, containing over a million base-pairs, the longest of which is PTPRT coded by 1117219bp. The shortest genes are the ones coding for micro (MIR3143) or small nuclear (U7) RNAs at 63bp each. There is only partial information regarding the chromatin state of each variant. However, from the information gathered in the analysis we observed 14 transcription start sites and 245 enhancers (Supplementary Table 8).

AB - Applying HaploReg v4.1 analysis to the 536 variants resulted in 9 categories (Supplementary Table 8): miscRNA (1 variant); snoRNA (2 variants); microRNA (4 variants); snRNA (9 variants); pseudogenes (14 variants); sequencing in progress (43 variants); LINC RNA (86 variants); and 372 variants within protein coding genes. In addition, some variants annotate to the same gene resulting in a total of 139 genes (protein-coding or non-coding). Of those genes, 6 are exceptionally long, containing over a million base-pairs, the longest of which is PTPRT coded by 1117219bp. The shortest genes are the ones coding for micro (MIR3143) or small nuclear (U7) RNAs at 63bp each. There is only partial information regarding the chromatin state of each variant. However, from the information gathered in the analysis we observed 14 transcription start sites and 245 enhancers (Supplementary Table 8).

UR - https://www.scopus.com/pages/publications/85026669383

U2 - 10.18632/aging.101260

DO - 10.18632/aging.101260

M3 - Comment/debate

C2 - 28696945

SN - 1945-4589

VL - 9

SP - 1844

EP - 1846

JO - Aging

JF - Aging

IS - 7

ER -

Correction: The complex genetics of gait speed: Genome-wide metaanalysis approach [Aging, (Albany NY), 9, 1, (2017), (209-246)]doi 10.18632/aging.101151

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