Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities

Kaitlyn M. Price; Karen G. Wigg; Else Eising; Yu Feng; Kirsten Blokland; Margaret Wilkinson; Elizabeth N. Kerr; Sharon L. Guger; Filippo Abbondanza; Andrea G. Allegrini; Till F.M. Andlauer; Timothy C. Bates; Manon Bernard; Milene Bonte; Dorret I. Boomsma; Thomas Bourgeron; Daniel Brandeis; Manuel Carreiras; Fabiola Ceroni; Valéria Csépe; Philip S. Dale; John C. DeFries; Peter F. de Jong; Jean Francois Démonet; Eveline L. de Zeeuw; Marie Christine J. Franken; Clyde Francks; Margot Gerritse; Alessandro Gialluisi; Scott D. Gordon; Jeffrey R. Gruen; Marianna E. Hayiou-Thomas; Juan Hernández-Cabrera; Jouke Jan Hottenga; Charles Hulme; Philip R. Jansen; Juha Kere; Tanner Koomar; Karin Landerl; Gabriel T. Leonard; Zhijie Liao; Michelle Luciano; Heikki Lyytinen; Nicholas G. Martin; Angela Martinelli; Urs Maurer; Jacob J. Michaelson; Nazanin Mirza-Schreiber; Kristina Moll; Kaili Rimfeld

doi:10.1038/s41398-022-02250-z

Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities

Kaitlyn M. Price
, Karen G. Wigg
, Else Eising
, Yu Feng
, Kirsten Blokland
, Margaret Wilkinson
, Elizabeth N. Kerr
, Sharon L. Guger
, Filippo Abbondanza
, Andrea G. Allegrini
, Till F.M. Andlauer
, Timothy C. Bates
, Manon Bernard
, Milene Bonte
, Dorret I. Boomsma
, Thomas Bourgeron
, Daniel Brandeis
, Manuel Carreiras
, Fabiola Ceroni
, Valéria Csépe

Philip S. Dale, John C. DeFries, Peter F. de Jong, Jean Francois Démonet, Eveline L. de Zeeuw, Marie Christine J. Franken, Clyde Francks, Margot Gerritse, Alessandro Gialluisi, Scott D. Gordon, Jeffrey R. Gruen, Marianna E. Hayiou-Thomas, Juan Hernández-Cabrera, Jouke Jan Hottenga, Charles Hulme, Philip R. Jansen, Juha Kere, Tanner Koomar, Karin Landerl, Gabriel T. Leonard, Zhijie Liao, Michelle Luciano, Heikki Lyytinen, Nicholas G. Martin, Angela Martinelli, Urs Maurer, Jacob J. Michaelson, Nazanin Mirza-Schreiber, Kristina Moll, Kaili Rimfeld

Research output: Contribution to journal › Article › peer-review

Original language	English
Article number	495
Journal	Translational Psychiatry
Volume	12
Issue number	1
Early online date	29 Nov 2022
DOIs	https://doi.org/10.1038/s41398-022-02250-z
Publication status	E-pub ahead of print - 29 Nov 2022

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

SDG 3 Good Health and Well-being

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Price, K. M., Wigg, K. G., Eising, E., Feng, Y., Blokland, K., Wilkinson, M., Kerr, E. N., Guger, S. L., Abbondanza, F., Allegrini, A. G., Andlauer, T. F. M., Bates, T. C., Bernard, M., Bonte, M., Boomsma, D. I., Bourgeron, T., Brandeis, D., Carreiras, M., Ceroni, F., ... Rimfeld, K. (2022). Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities. Translational Psychiatry, 12(1), Article 495. Advance online publication. https://doi.org/10.1038/s41398-022-02250-z

@article{2470b456a6be403bb0dc9d1d4159c5ff,

title = "Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities",

author = "Price, \{Kaitlyn M.\} and Wigg, \{Karen G.\} and Else Eising and Yu Feng and Kirsten Blokland and Margaret Wilkinson and Kerr, \{Elizabeth N.\} and Guger, \{Sharon L.\} and Filippo Abbondanza and Allegrini, \{Andrea G.\} and Andlauer, \{Till F.M.\} and Bates, \{Timothy C.\} and Manon Bernard and Milene Bonte and Boomsma, \{Dorret I.\} and Thomas Bourgeron and Daniel Brandeis and Manuel Carreiras and Fabiola Ceroni and Val{\'e}ria Cs{\'e}pe and Dale, \{Philip S.\} and DeFries, \{John C.\} and \{de Jong\}, \{Peter F.\} and D{\'e}monet, \{Jean Francois\} and \{de Zeeuw\}, \{Eveline L.\} and Franken, \{Marie Christine J.\} and Clyde Francks and Margot Gerritse and Alessandro Gialluisi and Gordon, \{Scott D.\} and Gruen, \{Jeffrey R.\} and Hayiou-Thomas, \{Marianna E.\} and Juan Hern{\'a}ndez-Cabrera and Hottenga, \{Jouke Jan\} and Charles Hulme and Jansen, \{Philip R.\} and Juha Kere and Tanner Koomar and Karin Landerl and Leonard, \{Gabriel T.\} and Zhijie Liao and Michelle Luciano and Heikki Lyytinen and Martin, \{Nicholas G.\} and Angela Martinelli and Urs Maurer and Michaelson, \{Jacob J.\} and Nazanin Mirza-Schreiber and Kristina Moll and Kaili Rimfeld",

note = "Publisher Copyright: {\textcopyright} 2022, The Author(s).",

year = "2022",

month = nov,

day = "29",

doi = "10.1038/s41398-022-02250-z",

language = "English",

volume = "12",

journal = "Translational Psychiatry",

issn = "2158-3188",

publisher = "Nature Publishing Group",

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Price, KM, Wigg, KG, Eising, E, Feng, Y, Blokland, K, Wilkinson, M, Kerr, EN, Guger, SL, Abbondanza, F, Allegrini, AG, Andlauer, TFM, Bates, TC, Bernard, M, Bonte, M, Boomsma, DI, Bourgeron, T, Brandeis, D, Carreiras, M, Ceroni, F, Csépe, V, Dale, PS, DeFries, JC, de Jong, PF, Démonet, JF, de Zeeuw, EL, Franken, MCJ, Francks, C, Gerritse, M, Gialluisi, A, Gordon, SD, Gruen, JR, Hayiou-Thomas, ME, Hernández-Cabrera, J, Hottenga, JJ, Hulme, C, Jansen, PR, Kere, J, Koomar, T, Landerl, K, Leonard, GT, Liao, Z, Luciano, M, Lyytinen, H, Martin, NG, Martinelli, A, Maurer, U, Michaelson, JJ, Mirza-Schreiber, N, Moll, K & Rimfeld, K 2022, 'Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities', Translational Psychiatry, vol. 12, no. 1, 495. https://doi.org/10.1038/s41398-022-02250-z

TY - JOUR

T1 - Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities

AU - Price, Kaitlyn M.

AU - Wigg, Karen G.

AU - Eising, Else

AU - Feng, Yu

AU - Blokland, Kirsten

AU - Wilkinson, Margaret

AU - Kerr, Elizabeth N.

AU - Guger, Sharon L.

AU - Abbondanza, Filippo

AU - Allegrini, Andrea G.

AU - Andlauer, Till F.M.

AU - Bates, Timothy C.

AU - Bernard, Manon

AU - Bonte, Milene

AU - Boomsma, Dorret I.

AU - Bourgeron, Thomas

AU - Brandeis, Daniel

AU - Carreiras, Manuel

AU - Ceroni, Fabiola

AU - Csépe, Valéria

AU - Dale, Philip S.

AU - DeFries, John C.

AU - de Jong, Peter F.

AU - Démonet, Jean Francois

AU - de Zeeuw, Eveline L.

AU - Franken, Marie Christine J.

AU - Francks, Clyde

AU - Gerritse, Margot

AU - Gialluisi, Alessandro

AU - Gordon, Scott D.

AU - Gruen, Jeffrey R.

AU - Hayiou-Thomas, Marianna E.

AU - Hernández-Cabrera, Juan

AU - Hottenga, Jouke Jan

AU - Hulme, Charles

AU - Jansen, Philip R.

AU - Kere, Juha

AU - Koomar, Tanner

AU - Landerl, Karin

AU - Leonard, Gabriel T.

AU - Liao, Zhijie

AU - Luciano, Michelle

AU - Lyytinen, Heikki

AU - Martin, Nicholas G.

AU - Martinelli, Angela

AU - Maurer, Urs

AU - Michaelson, Jacob J.

AU - Mirza-Schreiber, Nazanin

AU - Moll, Kristina

AU - Rimfeld, Kaili

PY - 2022/11/29

Y1 - 2022/11/29

UR - https://www.scopus.com/pages/publications/85142921133

U2 - 10.1038/s41398-022-02250-z

DO - 10.1038/s41398-022-02250-z

M3 - Article

C2 - 36446759

AN - SCOPUS:85142921133

SN - 2158-3188

VL - 12

JO - Translational Psychiatry

JF - Translational Psychiatry

IS - 1

M1 - 495

ER -

Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities

UN SDGs

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