Elisabet Einarsdottir

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2015-2024
Publications (10 Years): 12

Top Venues

Scientific reports

EFORT open reviews

American journal of human biology : the official journal of the Human Biology Council

PloS one

This page only lists publications with an associated author ORCID identifier.

Publications

Xuan Li, Suvratha Jayaprasad, Elisabet Einarsdottir, Steven J B Cooper, Alexander Suh, Takeshi Kawakami, Octavio Manuel Palacios-Gimenez
Chromosome-level genome assembly of the morabine grasshopper Vandiemenella viatica19. Scientific data 11 (1) (2024)
Signe Altmäe, Abel Plaza-Florido, Francisco J Esteban, Augusto Anguita-Ruiz, Kaarel Krjutškov, Shintaro Katayama, Elisabet Einarsdottir, Juha Kere, Shlomit Radom-Aizik, Francisco B Ortega
Effects of exercise on whole-blood transcriptome profile in children with overweight/obesity. American journal of human biology : the official journal of the Human Biology Council (2023)
Tian Cheng, Elisabet Einarsdottir, Juha Kere, Lovisa Gerdhem
Idiopathic scoliosis: a systematic review and meta-analysis of heritability. EFORT open reviews 7 (6) (2022)
Svetlana Vakkilainen, Tiina Skoog, Elisabet Einarsdottir, Anna Middleton, Minna Pekkinen, Tiina Öhman, Shintaro Katayama, Kaarel Krjutškov, Panu E Kovanen, Markku Varjosalo, Arne Lindqvist, Juha Kere, Outi Mäkitie
The human long non-coding RNA gene RMRP has pleiotropic effects and regulates cell-cycle progression at G2. Scientific reports 9 (1) (2019)
Kazuki Takeda, Ikuyo Kou, Nao Otomo, Anna Grauers, Yan-Hui Fan, Yoji Ogura, Yohei Takahashi, Yukihide Momozawa, Elisabet Einarsdottir, Juha Kere, null null, Morio Matsumoto, Yong Qiu, You-Qiang Song, Paul Gerdhem, Kota Watanabe, Shiro Ikegawa
A multiethnic meta-analysis defined the association of rs12946942 with severe adolescent idiopathic scoliosis. Journal of human genetics 64 (5) (2019)
Ikuyo Kou, Kota Watanabe, Yohei Takahashi, Yukihide Momozawa, Anas Khanshour, Anna Grauers, Hang Zhou, Gang Liu, Yan-Hui Fan, Kazuki Takeda, Yoji Ogura, Taifeng Zhou, Yusuke Iwasaki, Michiaki Kubo, Zhihong Wu, Morio Matsumoto, null null, null null, Elisabet Einarsdottir, Juha Kere, Dongsheng Huang, Guixing Qiu, Yong Qiu, Carol A Wise, You-Qiang Song, Nan Wu, Peiqiang Su, Paul Gerdhem, Shiro Ikegawa
A multi-ethnic meta-analysis confirms the association of rs6570507 with adolescent idiopathic scoliosis. Scientific reports 8 (1) (2018)
Yoji Ogura, Kazuki Takeda, Ikuyo Kou, Anas Khanshour, Anna Grauers, Hang Zhou, Gang Liu, Yan-Hui Fan, Taifeng Zhou, Zhihong Wu, Yohei Takahashi, Morio Matsumoto, null null, null null, Elisabet Einarsdottir, Juha Kere, Dongsheng Huang, Guixing Qiu, Leilei Xu, Yong Qiu, Carol A Wise, You-Qiang Song, Nan Wu, Peiqiang Su, Paul Gerdhem, Kota Watanabe, Shiro Ikegawa
An international meta-analysis confirms the association of BNC2 with adolescent idiopathic scoliosis. Scientific reports 8 (1) (2018)
Janne Purhonen, Jayasimman Rajendran, Matthias Mörgelin, Kristiina Uusi-Rauva, Shintaro Katayama, Kaarel Krjutskov, Elisabet Einarsdottir, Vidya Velagapudi, Juha Kere, Matti Jauhiainen, Vineta Fellman, Jukka Kallijärvi
Ketogenic diet attenuates hepatopathy in mouse model of respiratory chain complex III deficiency caused by a Bcs1l mutation. Scientific reports 7 (1) (2017)
Elisabet Einarsdottir, Anna Grauers, Jingwen Wang, Hong Jiao, Stefan A Escher, Aina Danielsson, Ane Simony, Mikkel Andersen, Steen Bach Christensen, Kristina Åkesson, Ikuyo Kou, Anas M Khanshour, Acke Ohlin, Carol Wise, Shiro Ikegawa, Juha Kere, Paul Gerdhem
CELSR2 is a candidate susceptibility gene in idiopathic scoliosis. PloS one 12 (12) (2017)
Nancy Yiu-Lin Yu, Andrea Bieder, Amitha Raman, Enrichetta Mileti, Shintaro Katayama, Elisabet Einarsdottir, Bertil B Fredholm, Anna Falk, Isabel Tapia-Páez, Carsten O Daub, Juha Kere
Acute doses of caffeine shift nervous system cell expression profiles toward promotion of neuronal projection growth. Scientific reports 7 (1) (2017)
Elisabet Einarsdottir, Myriam Peyrard-Janvid, Fahimeh Darki, Jetro J Tuulari, Harri Merisaari, Linnea Karlsson, Noora M Scheinin, Jani Saunavaara, Riitta Parkkola, Katri Kantojärvi, Antti-Jussi Ämmälä, Nancy Yiu-Lin Yu, Hans Matsson, Jaana Nopola-Hemmi, Hasse Karlsson, Tiina Paunio, Torkel Klingberg, Eira Leinonen, Juha Kere
Identification of NCAN as a candidate gene for developmental dyslexia. Scientific reports 7 (1) (2017)
Mahmood F Bhutta, Jane Lambie, Lindsey Hobson, Anuj Goel, Lena Hafrén, Elisabet Einarsdottir, Petri S Mattila, Martin Farrall, Steve Brown, Martin J Burton
A mouse-to-man candidate gene study identifies association of chronic otitis media with the loci TGIF1 and FBXO11. Scientific reports 7 (1) (2017)
Elisabet Einarsdottir, Idor Svensson, Fahimeh Darki, Myriam Peyrard-Janvid, Jessica M Lindvall, Adam Ameur, Christer Jacobsson, Torkel Klingberg, Juha Kere, Hans Matsson
Mutation in CEP63 co-segregating with developmental dyslexia in a Swedish family. Human genetics 134 (11-12) (2015)

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Publication Activity (10 Years)

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Elisabet Einarsdottir