Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis (vol 101, pg 227, 2017)

Despoina Manousaki; Tom Dudding; Simon Haworth; Yi-Hsiang Hsu; Ching-Ti Liu; Carolina Medina-Gomez; Trudy Voortman; Nathalie van der Velde; Hakan 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; 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; Renee de Mutsert; Frits R. Rosendaal; Martin den Heijer; Thomas J. Wang; Lars Lind; Eric S. Orwoll; Dennis O. Mook-Kanamori; Karl Michaelsson; Bryan Kestenbaum; Claes Ohlsson; Dan Mellstrom; 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

doi:https://doi.org/10.1016/j.ajhg.2018.11.010

Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis (vol 101, pg 227, 2017)

Despoina Manousaki, Tom Dudding, Simon Haworth, Yi-Hsiang Hsu, Ching-Ti Liu, Carolina Medina-Gomez, Trudy Voortman, Nathalie van der Velde, Hakan 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. ZemelJonathan 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, Renee de Mutsert, Frits R. Rosendaal, Martin den Heijer, Thomas J. Wang, Lars Lind, Eric S. Orwoll, Dennis O. Mook-Kanamori, Karl Michaelsson, Bryan Kestenbaum, Claes Ohlsson, Dan Mellstrom, 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 journal › Article › Academic › peer-review

6 Citations (Scopus)

Original language	English
Pages (from-to)	1053-1053
Journal	American journal of human genetics
Volume	103
Issue number	6
DOIs	https://doi.org/10.1016/j.ajhg.2018.11.010
Publication status	Published - 6 Dec 2018

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https://doi.org/10.1016/j.ajhg.2018.11.010

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Manousaki, D., Dudding, T., Haworth, S., Hsu, Y.-H., Liu, C.-T., Medina-Gomez, C., Voortman, T., van der Velde, N., Melhus, H., Robinson-Cohen, C., Cousminer, D. L., Nethander, M., Vandenput, L., Noordam, R., Forgetta, V., Greenwood, C. M. T., Biggs, M. L., Psaty, B. M., Rotter, J. I., ... Richards, J. B. (2018). Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis (vol 101, pg 227, 2017). American journal of human genetics, 103(6), 1053-1053. https://doi.org/10.1016/j.ajhg.2018.11.010

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title = "Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis (vol 101, pg 227, 2017)",

author = "Despoina Manousaki and Tom Dudding and Simon Haworth and Yi-Hsiang Hsu and Ching-Ti Liu and Carolina Medina-Gomez and Trudy Voortman and {van der Velde}, Nathalie and Hakan 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}, Renee and Rosendaal, {Frits R.} and {den Heijer}, Martin and Wang, {Thomas J.} and Lars Lind and Orwoll, {Eric S.} and Mook-Kanamori, {Dennis O.} and Karl Michaelsson and Bryan Kestenbaum and Claes Ohlsson and Dan Mellstrom 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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Manousaki, D, Dudding, T, Haworth, S, Hsu, Y-H, Liu, C-T, Medina-Gomez, 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, ES, Mook-Kanamori, DO, Michaelsson, K, Kestenbaum, B, Ohlsson, C, Mellstrom, D, de Groot, LCPGM, Grant, SFA, Kiel, DP, Zillikens, MC, Rivadeneira, F, Sawcer, S, Timpson, NJ & Richards, JB 2018, 'Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis (vol 101, pg 227, 2017)', American journal of human genetics, vol. 103, no. 6, pp. 1053-1053. https://doi.org/10.1016/j.ajhg.2018.11.010

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T1 - Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis (vol 101, pg 227, 2017)

AU - Manousaki, Despoina

AU - Dudding, Tom

AU - Haworth, Simon

AU - Hsu, Yi-Hsiang

AU - Liu, Ching-Ti

AU - Medina-Gomez, Carolina

AU - Voortman, Trudy

AU - van der Velde, Nathalie

AU - Melhus, Hakan

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, Renee

AU - Rosendaal, Frits R.

AU - den Heijer, Martin

AU - Wang, Thomas J.

AU - Lind, Lars

AU - Orwoll, Eric S.

AU - Mook-Kanamori, Dennis O.

AU - Michaelsson, Karl

AU - Kestenbaum, Bryan

AU - Ohlsson, Claes

AU - Mellstrom, 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

U2 - https://doi.org/10.1016/j.ajhg.2018.11.010

DO - https://doi.org/10.1016/j.ajhg.2018.11.010

M3 - Article

C2 - 30526863

SN - 0002-9297

VL - 103

SP - 1053

EP - 1053

JO - American journal of human genetics

JF - American journal of human genetics

IS - 6

ER -