Identification of NCAN as a candidate gene for developmental dyslexia

Elisabet Einarsdottir; Myriam Peyrard-Janvid; Fahimeh Darki; Jetro J. Tuulari; Harri Merisaari; Linnea Karlsson; Noora M. Scheinin; Jani Saunavaara; Riitta Parkkola; Katri Kantojarvi; Antti-Jussi Ammala; Nancy Yiu-Lin Yu; Hans Matsson; Jaana Nopola-Hemmi; Hasse Karlsson; Tiina Paunio; Torkel Klingberg; Eira Leinonen; Juha Kere

doi:10.1038/s41598-017-10175-7

Identification of NCAN as a candidate gene for developmental dyslexia

Elisabet Einarsdottir, Myriam Peyrard-Janvid, Fahimeh Darki, Jetro J. Tuulari, Harri Merisaari, Linnea Karlsson, Noora M. Scheinin, Jani Saunavaara, Riitta Parkkola, Katri Kantojarvi, Antti-Jussi Ammala, Nancy Yiu-Lin Yu, Hans Matsson, Jaana Nopola-Hemmi, Hasse Karlsson, Tiina Paunio, Torkel Klingberg, Eira Leinonen, Juha Kere

Forskningsoutput: Tidskriftsbidrag › Artikel › Vetenskaplig › Peer review

Originalspråk	engelska
Artikelnummer	9294
Tidskrift	Scientific Reports
Volym	7
Antal sidor	11
ISSN	2045-2322
DOI	https://doi.org/10.1038/s41598-017-10175-7
Status	Publicerad - 24 aug. 2017
MoE-publikationstyp	A1 Tidskriftsartikel-refererad

Vetenskapsgrenar

3111 Biomedicinska vetenskaper

Åtkomst av dokument

10.1038/s41598-017-10175-7

Identification of NCANSlutlig publicerad version, 1,78 MBLicens: CC BY

Citera det här

Einarsdottir, E., Peyrard-Janvid, M., Darki, F., Tuulari, J. J., Merisaari, H., Karlsson, L., Scheinin, N. M., Saunavaara, J., Parkkola, R., Kantojarvi, K., Ammala, A.-J., Yu, N. Y.-L., Matsson, H., Nopola-Hemmi, J., Karlsson, H., Paunio, T., Klingberg, T., Leinonen, E., & Kere, J. (2017). Identification of NCAN as a candidate gene for developmental dyslexia. Scientific Reports, 7, Artikel 9294. https://doi.org/10.1038/s41598-017-10175-7

@article{1a8eb71d426f4eafa6a279d4d45f6db0,

title = "Identification of NCAN as a candidate gene for developmental dyslexia",

keywords = "RISK VARIANT RS10503253, GENOME-WIDE ASSOCIATION, VOXEL BASED MORPHOMETRY, WHITE-MATTER STRUCTURE, BIPOLAR DISORDER, READING-ABILITY, COMMON VARIATION, HEALTHY-SUBJECTS, BRAIN, SCHIZOPHRENIA, 3111 Biomedicine",

author = "Elisabet Einarsdottir and Myriam Peyrard-Janvid and Fahimeh Darki and Tuulari, {Jetro J.} and Harri Merisaari and Linnea Karlsson and Scheinin, {Noora M.} and Jani Saunavaara and Riitta Parkkola and Katri Kantojarvi and Antti-Jussi Ammala and Yu, {Nancy Yiu-Lin} and Hans Matsson and Jaana Nopola-Hemmi and Hasse Karlsson and Tiina Paunio and Torkel Klingberg and Eira Leinonen and Juha Kere",

year = "2017",

month = aug,

day = "24",

doi = "10.1038/s41598-017-10175-7",

language = "English",

volume = "7",

journal = "Scientific Reports",

issn = "2045-2322",

publisher = "Nature Publishing Group",

}

Einarsdottir, E, Peyrard-Janvid, M, Darki, F, Tuulari, JJ, Merisaari, H, Karlsson, L, Scheinin, NM, Saunavaara, J, Parkkola, R, Kantojarvi, K, Ammala, A-J, Yu, NY-L, Matsson, H, Nopola-Hemmi, J, Karlsson, H, Paunio, T, Klingberg, T, Leinonen, E & Kere, J 2017, 'Identification of NCAN as a candidate gene for developmental dyslexia', Scientific Reports, vol. 7, 9294. https://doi.org/10.1038/s41598-017-10175-7

TY - JOUR

T1 - Identification of NCAN as a candidate gene for developmental dyslexia

AU - Einarsdottir, Elisabet

AU - Peyrard-Janvid, Myriam

AU - Darki, Fahimeh

AU - Tuulari, Jetro J.

AU - Merisaari, Harri

AU - Karlsson, Linnea

AU - Scheinin, Noora M.

AU - Saunavaara, Jani

AU - Parkkola, Riitta

AU - Kantojarvi, Katri

AU - Ammala, Antti-Jussi

AU - Yu, Nancy Yiu-Lin

AU - Matsson, Hans

AU - Nopola-Hemmi, Jaana

AU - Karlsson, Hasse

AU - Paunio, Tiina

AU - Klingberg, Torkel

AU - Leinonen, Eira

AU - Kere, Juha

PY - 2017/8/24

Y1 - 2017/8/24

KW - RISK VARIANT RS10503253

KW - GENOME-WIDE ASSOCIATION

KW - VOXEL BASED MORPHOMETRY

KW - WHITE-MATTER STRUCTURE

KW - BIPOLAR DISORDER

KW - READING-ABILITY

KW - COMMON VARIATION

KW - HEALTHY-SUBJECTS

KW - BRAIN

KW - SCHIZOPHRENIA

KW - 3111 Biomedicine

U2 - 10.1038/s41598-017-10175-7

DO - 10.1038/s41598-017-10175-7

M3 - Article

SN - 2045-2322

VL - 7

JO - Scientific Reports

JF - Scientific Reports

M1 - 9294

ER -