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Research | 16 February 2011
Multiple independent variants in 6q21-22 associated with susceptibility to celiac disease in the Dutch, Finnish and Hungarian populations
- elisabet.einarsdottir@helsinki.fi
- Elisabet Einarsdottir
- , Marianna R Bevova
- , Alexandra Zhernakova
- , Alienke Monsuur
- , Lotta LE Koskinen
- , Ruben van't Slot
- , Chris Mulder
- , M Luisa Mearin
- , Ilma R Korponay-Szabo
- , Katri Kaukinen
- , Kalle Kurppa
- , Juha Kere
- , Markku Mäki
- , Cisca Wijmenga
- & Päivi Saavalainen
European Journal of Human Genetics 19 , 682–686

Rights & permissionsfor article Multiple independent variants in 6q21-22 associated with susceptibility to celiac disease in the Dutch, Finnish and Hungarian populations . Opens in a new window.
Research | 17 May 2012
Association of celiac disease genes with inflammatory bowel disease in Finnish and Swedish patients
- elisabet.einarsdottir@helsinki.fi
- A S Parmar
- , M Lappalainen
- , P Paavola-Sakki
- , L Halme
- , M Färkkilä
- , U Turunen
- , K Kontula
- , A Aromaa
- , V Salomaa
- , L Peltonen
- , J Halfvarson
- , L Törkvist
- , M D'Amato
- , P Saavalainen
- & E Einarsdottir
Genes & Immunity 13 , 474–480

Rights & permissionsfor article Association of celiac disease genes with inflammatory bowel disease in Finnish and Swedish patients . Opens in a new window.
Research | 24 August 2017 | Open
Identification of NCAN as a candidate gene for developmental dyslexia
- elisabet.einarsdottir@ki.se
- 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
Scientific Reports 7 , 1–11

Rights & permissionsfor article Identification of <i>NCAN</i> as a candidate gene for developmental dyslexia . Opens in a new window.
Research | 16 September 2016 | Open
Genome-wide association analysis reveals variants on chromosome 19 that contribute to childhood risk of chronic otitis media with effusion
- elisabet.einarsdottir@ki.se
- Elisabet Einarsdottir
- , Lena Hafrén
- , Eira Leinonen
- , Mahmood F. Bhutta
- , Erna Kentala
- , Juha Kere
- & Petri S. Mattila
Scientific Reports 6 , 1–11

Rights & permissionsfor article Genome-wide association analysis reveals variants on chromosome 19 that contribute to childhood risk of chronic otitis media with effusion . Opens in a new window.

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