Erratum

Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis (The American Journal of Human Genetics (2017) 101(2) (227–238), (S000292971730277X), (10.1016/j.ajhg.2017.06.014))

Despoina Manousaki, Tom Dudding, Simon Haworth, Yi Hsiang Hsu, Ching Ti Liu, Carolina Medina-Gómez, Trudy Voortman, Nathalie van der Velde, Håkan Melhus, Cassianne Robinson-Cohen, Diana L. Cousminer, Maria Nethander, Liesbeth Vandenput, Raymond Noordam, Vincenzo Forgetta, Celia M.T. Greenwood, Mary L. Biggs, Bruce M. Psaty, Jerome I. Rotter, Babette S. Zemel & 33 others Jonathan A. Mitchell, Bruce Taylor, Mattias Lorentzon, Magnus Karlsson, Vincent V.W. Jaddoe, Henning Tiemeier, Natalia Campos-Obando, Oscar H. Franco, Andre G. Utterlinden, Linda Broer, Natasja M. van Schoor, Annelies C. Ham, M. Arfan Ikram, David Karasik, Renée de Mutsert, Frits R. Rosendaal, Martin den Heijer, Thomas J. Wang, Lars Lind, Eric Orwoll, Dennis O. Mook-Kanamori, Karl Michaëlsson, Bryan Kestenbaum, Claes Ohlsson, Dan Mellström, Lisette C.P.G.M. de Groot, Struan F.A. Grant, Douglas P. Kiel, M. Carola Zillikens, Fernando Rivadeneira, Stephen Sawcer, Nicholas J. Timpson, J. Brent Richards

Research output: Contribution to journalComment/debate

1 Citation (Scopus)

Abstract

(The American Journal of Human Genetics 101, 227–238; August 3, 2017) The codon position p.Asp120Asp appearing in the abstract and in the first paragraph of the Results section is incorrect. The correct position is p.Asp353Asp. The authors apologize for this error and thank Dr. Michael Levine for bringing it to the attention of the authors.

Original languageEnglish (US)
Number of pages1
JournalAmerican Journal of Human Genetics
Volume103
Issue number6
DOIs
StatePublished - Dec 6 2018

Fingerprint

Medical Genetics
Vitamin D
Codon
Multiple Sclerosis

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

Erratum : Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis (The American Journal of Human Genetics (2017) 101(2) (227–238), (S000292971730277X), (10.1016/j.ajhg.2017.06.014)). / Manousaki, Despoina; Dudding, Tom; Haworth, Simon; Hsu, Yi Hsiang; Liu, Ching Ti; Medina-Gómez, Carolina; Voortman, Trudy; van der Velde, Nathalie; Melhus, Håkan; Robinson-Cohen, Cassianne; Cousminer, Diana L.; Nethander, Maria; Vandenput, Liesbeth; Noordam, Raymond; Forgetta, Vincenzo; Greenwood, Celia M.T.; Biggs, Mary L.; Psaty, Bruce M.; Rotter, Jerome I.; Zemel, Babette S.; Mitchell, Jonathan A.; Taylor, Bruce; Lorentzon, Mattias; Karlsson, Magnus; Jaddoe, Vincent V.W.; Tiemeier, Henning; Campos-Obando, Natalia; Franco, Oscar H.; Utterlinden, Andre G.; Broer, Linda; van Schoor, Natasja M.; Ham, Annelies C.; Ikram, M. Arfan; Karasik, David; de Mutsert, Renée; Rosendaal, Frits R.; den Heijer, Martin; Wang, Thomas J.; Lind, Lars; Orwoll, Eric; Mook-Kanamori, Dennis O.; Michaëlsson, Karl; Kestenbaum, Bryan; Ohlsson, Claes; Mellström, Dan; de Groot, Lisette C.P.G.M.; Grant, Struan F.A.; Kiel, Douglas P.; Zillikens, M. Carola; Rivadeneira, Fernando; Sawcer, Stephen; Timpson, Nicholas J.; Richards, J. Brent.

In: American Journal of Human Genetics, Vol. 103, No. 6, 06.12.2018.

Research output: Contribution to journalComment/debate

Manousaki, D, Dudding, T, Haworth, S, Hsu, YH, Liu, CT, Medina-Gómez, C, Voortman, T, van der Velde, N, Melhus, H, Robinson-Cohen, C, Cousminer, DL, Nethander, M, Vandenput, L, Noordam, R, Forgetta, V, Greenwood, CMT, Biggs, ML, Psaty, BM, Rotter, JI, Zemel, BS, Mitchell, JA, Taylor, B, Lorentzon, M, Karlsson, M, Jaddoe, VVW, Tiemeier, H, Campos-Obando, N, Franco, OH, Utterlinden, AG, Broer, L, van Schoor, NM, Ham, AC, Ikram, MA, Karasik, D, de Mutsert, R, Rosendaal, FR, den Heijer, M, Wang, TJ, Lind, L, Orwoll, E, Mook-Kanamori, DO, Michaëlsson, K, Kestenbaum, B, Ohlsson, C, Mellström, D, de Groot, LCPGM, Grant, SFA, Kiel, DP, Zillikens, MC, Rivadeneira, F, Sawcer, S, Timpson, NJ & Richards, JB 2018, 'Erratum: Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis (The American Journal of Human Genetics (2017) 101(2) (227–238), (S000292971730277X), (10.1016/j.ajhg.2017.06.014))', American Journal of Human Genetics, vol. 103, no. 6. https://doi.org/10.1016/j.ajhg.2018.11.010
Manousaki, Despoina ; Dudding, Tom ; Haworth, Simon ; Hsu, Yi Hsiang ; Liu, Ching Ti ; Medina-Gómez, Carolina ; Voortman, Trudy ; van der Velde, Nathalie ; Melhus, Håkan ; Robinson-Cohen, Cassianne ; Cousminer, Diana L. ; Nethander, Maria ; Vandenput, Liesbeth ; Noordam, Raymond ; Forgetta, Vincenzo ; Greenwood, Celia M.T. ; Biggs, Mary L. ; Psaty, Bruce M. ; Rotter, Jerome I. ; Zemel, Babette S. ; Mitchell, Jonathan A. ; Taylor, Bruce ; Lorentzon, Mattias ; Karlsson, Magnus ; Jaddoe, Vincent V.W. ; Tiemeier, Henning ; Campos-Obando, Natalia ; Franco, Oscar H. ; Utterlinden, Andre G. ; Broer, Linda ; van Schoor, Natasja M. ; Ham, Annelies C. ; Ikram, M. Arfan ; Karasik, David ; de Mutsert, Renée ; Rosendaal, Frits R. ; den Heijer, Martin ; Wang, Thomas J. ; Lind, Lars ; Orwoll, Eric ; Mook-Kanamori, Dennis O. ; Michaëlsson, Karl ; Kestenbaum, Bryan ; Ohlsson, Claes ; Mellström, Dan ; de Groot, Lisette C.P.G.M. ; Grant, Struan F.A. ; Kiel, Douglas P. ; Zillikens, M. Carola ; Rivadeneira, Fernando ; Sawcer, Stephen ; Timpson, Nicholas J. ; Richards, J. Brent. / Erratum : Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis (The American Journal of Human Genetics (2017) 101(2) (227–238), (S000292971730277X), (10.1016/j.ajhg.2017.06.014)). In: American Journal of Human Genetics. 2018 ; Vol. 103, No. 6.
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title = "Erratum: Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis (The American Journal of Human Genetics (2017) 101(2) (227–238), (S000292971730277X), (10.1016/j.ajhg.2017.06.014))",
abstract = "(The American Journal of Human Genetics 101, 227–238; August 3, 2017) The codon position p.Asp120Asp appearing in the abstract and in the first paragraph of the Results section is incorrect. The correct position is p.Asp353Asp. The authors apologize for this error and thank Dr. Michael Levine for bringing it to the attention of the authors.",
author = "Despoina Manousaki and Tom Dudding and Simon Haworth and Hsu, {Yi Hsiang} and Liu, {Ching Ti} and Carolina Medina-G{\'o}mez and Trudy Voortman and {van der Velde}, Nathalie and H{\aa}kan Melhus and Cassianne Robinson-Cohen and Cousminer, {Diana L.} and Maria Nethander and Liesbeth Vandenput and Raymond Noordam and Vincenzo Forgetta and Greenwood, {Celia M.T.} and Biggs, {Mary L.} and Psaty, {Bruce M.} and Rotter, {Jerome I.} and Zemel, {Babette S.} and Mitchell, {Jonathan A.} and Bruce Taylor and Mattias Lorentzon and Magnus Karlsson and Jaddoe, {Vincent V.W.} and Henning Tiemeier and Natalia Campos-Obando and Franco, {Oscar H.} and Utterlinden, {Andre G.} and Linda Broer and {van Schoor}, {Natasja M.} and Ham, {Annelies C.} and Ikram, {M. Arfan} and David Karasik and {de Mutsert}, Ren{\'e}e and Rosendaal, {Frits R.} and {den Heijer}, Martin and Wang, {Thomas J.} and Lars Lind and Eric Orwoll and Mook-Kanamori, {Dennis O.} and Karl Micha{\"e}lsson and Bryan Kestenbaum and Claes Ohlsson and Dan Mellstr{\"o}m and {de Groot}, {Lisette C.P.G.M.} and Grant, {Struan F.A.} and Kiel, {Douglas P.} and Zillikens, {M. Carola} and Fernando Rivadeneira and Stephen Sawcer and Timpson, {Nicholas J.} and Richards, {J. Brent}",
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language = "English (US)",
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TY - JOUR

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T2 - Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis (The American Journal of Human Genetics (2017) 101(2) (227–238), (S000292971730277X), (10.1016/j.ajhg.2017.06.014))

AU - Manousaki, Despoina

AU - Dudding, Tom

AU - Haworth, Simon

AU - Hsu, Yi Hsiang

AU - Liu, Ching Ti

AU - Medina-Gómez, Carolina

AU - Voortman, Trudy

AU - van der Velde, Nathalie

AU - Melhus, Håkan

AU - Robinson-Cohen, Cassianne

AU - Cousminer, Diana L.

AU - Nethander, Maria

AU - Vandenput, Liesbeth

AU - Noordam, Raymond

AU - Forgetta, Vincenzo

AU - Greenwood, Celia M.T.

AU - Biggs, Mary L.

AU - Psaty, Bruce M.

AU - Rotter, Jerome I.

AU - Zemel, Babette S.

AU - Mitchell, Jonathan A.

AU - Taylor, Bruce

AU - Lorentzon, Mattias

AU - Karlsson, Magnus

AU - Jaddoe, Vincent V.W.

AU - Tiemeier, Henning

AU - Campos-Obando, Natalia

AU - Franco, Oscar H.

AU - Utterlinden, Andre G.

AU - Broer, Linda

AU - van Schoor, Natasja M.

AU - Ham, Annelies C.

AU - Ikram, M. Arfan

AU - Karasik, David

AU - de Mutsert, Renée

AU - Rosendaal, Frits R.

AU - den Heijer, Martin

AU - Wang, Thomas J.

AU - Lind, Lars

AU - Orwoll, Eric

AU - Mook-Kanamori, Dennis O.

AU - Michaëlsson, Karl

AU - Kestenbaum, Bryan

AU - Ohlsson, Claes

AU - Mellström, Dan

AU - de Groot, Lisette C.P.G.M.

AU - Grant, Struan F.A.

AU - Kiel, Douglas P.

AU - Zillikens, M. Carola

AU - Rivadeneira, Fernando

AU - Sawcer, Stephen

AU - Timpson, Nicholas J.

AU - Richards, J. Brent

PY - 2018/12/6

Y1 - 2018/12/6

N2 - (The American Journal of Human Genetics 101, 227–238; August 3, 2017) The codon position p.Asp120Asp appearing in the abstract and in the first paragraph of the Results section is incorrect. The correct position is p.Asp353Asp. The authors apologize for this error and thank Dr. Michael Levine for bringing it to the attention of the authors.

AB - (The American Journal of Human Genetics 101, 227–238; August 3, 2017) The codon position p.Asp120Asp appearing in the abstract and in the first paragraph of the Results section is incorrect. The correct position is p.Asp353Asp. The authors apologize for this error and thank Dr. Michael Levine for bringing it to the attention of the authors.

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U2 - 10.1016/j.ajhg.2018.11.010

DO - 10.1016/j.ajhg.2018.11.010

M3 - Comment/debate

VL - 103

JO - American Journal of Human Genetics

JF - American Journal of Human Genetics

SN - 0002-9297

IS - 6

ER -