Einarsdóttir E - Search Results

1

Developmental dyslexia susceptibility genes DNAAF4, DCDC2, and NRSN1 are associated with brain function in fluently reading adolescents and young adults.

Rinne N, Wikman P, Sahari E, Salmi J, Einarsdóttir E, Kere J, Alho K. Rinne N, et al. Among authors: einarsdottir e. Cereb Cortex. 2024 Apr 1;34(4):bhae144. doi: 10.1093/cercor/bhae144. Cereb Cortex. 2024. PMID: 38610086 Free PMC article.

2

Polymorphisms in DCDC2 and S100B associate with developmental dyslexia.

Matsson H, Huss M, Persson H, Einarsdottir E, Tiraboschi E, Nopola-Hemmi J, Schumacher J, Neuhoff N, Warnke A, Lyytinen H, Schulte-Körne G, Nöthen MM, Leppänen PH, Peyrard-Janvid M, Kere J. Matsson H, et al. Among authors: einarsdottir e. J Hum Genet. 2015 Jul;60(7):399-401. doi: 10.1038/jhg.2015.37. Epub 2015 Apr 16. J Hum Genet. 2015. PMID: 25877001 Free PMC article.

3

Rare variants in dynein heavy chain genes in two individuals with situs inversus and developmental dyslexia: a case report.

Bieder A, Einarsdottir E, Matsson H, Nilsson HE, Eisfeldt J, Dragomir A, Paucar M, Granberg T, Li TQ, Lindstrand A, Kere J, Tapia-Páez I. Bieder A, et al. Among authors: einarsdottir e. BMC Med Genet. 2020 May 1;21(1):87. doi: 10.1186/s12881-020-01020-2. BMC Med Genet. 2020. PMID: 32357925 Free PMC article.

4

Mutation in CEP63 co-segregating with developmental dyslexia in a Swedish family.

Einarsdottir E, Svensson I, Darki F, Peyrard-Janvid M, Lindvall JM, Ameur A, Jacobsson C, Klingberg T, Kere J, Matsson H. Einarsdottir E, et al. Hum Genet. 2015 Nov;134(11-12):1239-48. doi: 10.1007/s00439-015-1602-1. Epub 2015 Sep 23. Hum Genet. 2015. PMID: 26400686 Free PMC article.

5

Identification of NCAN as a candidate gene for developmental dyslexia.

Einarsdottir E, Peyrard-Janvid M, Darki F, Tuulari JJ, Merisaari H, Karlsson L, Scheinin NM, Saunavaara J, Parkkola R, Kantojärvi K, Ämmälä AJ, Yiu-Lin Yu N, Matsson H, Nopola-Hemmi J, Karlsson H, Paunio T, Klingberg T, Leinonen E, Kere J. Einarsdottir E, et al. Sci Rep. 2017 Aug 24;7(1):9294. doi: 10.1038/s41598-017-10175-7. Sci Rep. 2017. PMID: 28839234 Free PMC article.

6

Idiopathic scoliosis: a systematic review and meta-analysis of heritability.

Cheng T, Einarsdottir E, Kere J, Gerdhem P. Cheng T, et al. Among authors: einarsdottir e. EFORT Open Rev. 2022 May 31;7(6):414-421. doi: 10.1530/EOR-22-0026. EFORT Open Rev. 2022. PMID: 35638601 Free PMC article. Review.

7

A preliminary transcriptome analysis suggests a transitory effect of vitamin D on mitochondrial function in obese young Finnish subjects.

Einarsdottir E, Pekkinen M, Krjutškov K, Katayama S, Kere J, Mäkitie O, Viljakainen H. Einarsdottir E, et al. Endocr Connect. 2019 May 1;8(5):559-570. doi: 10.1530/EC-18-0537. Endocr Connect. 2019. PMID: 30965285 Free PMC article.

8

Genome-wide association analysis reveals variants on chromosome 19 that contribute to childhood risk of chronic otitis media with effusion.

Einarsdottir E, Hafrén L, Leinonen E, Bhutta MF, Kentala E, Kere J, Mattila PS. Einarsdottir E, et al. Sci Rep. 2016 Sep 16;6:33240. doi: 10.1038/srep33240. Sci Rep. 2016. PMID: 27632927 Free PMC article.

9

ABO Genotype and Blood Type Are Associated with Otitis Media.

Wiesen BM, Hafrén L, Einarsdottir E, Kere J, Mattila PS, Santos-Cortez RLP. Wiesen BM, et al. Among authors: einarsdottir e. Genet Test Mol Biomarkers. 2019 Nov;23(11):823-827. doi: 10.1089/gtmb.2019.0135. Genet Test Mol Biomarkers. 2019. PMID: 31693456 Free PMC article.

10

Guide for library design and bias correction for large-scale transcriptome studies using highly multiplexed RNAseq methods.

Katayama S, Skoog T, Söderhäll C, Einarsdottir E, Krjutškov K, Kere J. Katayama S, et al. Among authors: einarsdottir e. BMC Bioinformatics. 2019 Aug 13;20(1):418. doi: 10.1186/s12859-019-3017-9. BMC Bioinformatics. 2019. PMID: 31409293 Free PMC article.

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