Contribution of rare and common variants to intellectual disability in a sub-isolate of Northern Finland

Various types of genetic variation contribute to the etiology of intellectual disability (ID). Here, the authors study a cohort of ID patients enriched for mild ID from Finland, to investigate contributions of rare and common variants associated with ID of different levels of severity.

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Autores principales: Mitja I. Kurki, Elmo Saarentaus, Olli Pietiläinen, Padhraig Gormley, Dennis Lal, Sini Kerminen, Minna Torniainen-Holm, Eija Hämäläinen, Elisa Rahikkala, Riikka Keski-Filppula, Merja Rauhala, Satu Korpi-Heikkilä, Jonna Komulainen–Ebrahim, Heli Helander, Päivi Vieira, Minna Männikkö, Markku Peltonen, Aki S. Havulinna, Veikko Salomaa, Matti Pirinen, Jaana Suvisaari, Jukka S. Moilanen, Jarmo Körkkö, Outi Kuismin, Mark J. Daly, Aarno Palotie
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Publicado: Nature Portfolio 2019
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Acceso en línea:https://doaj.org/article/ab9e0271d0224acca582195c7d5d71d8
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spelling oai:doaj.org-article:ab9e0271d0224acca582195c7d5d71d82021-12-02T17:02:09ZContribution of rare and common variants to intellectual disability in a sub-isolate of Northern Finland10.1038/s41467-018-08262-y2041-1723https://doaj.org/article/ab9e0271d0224acca582195c7d5d71d82019-01-01T00:00:00Zhttps://doi.org/10.1038/s41467-018-08262-yhttps://doaj.org/toc/2041-1723Various types of genetic variation contribute to the etiology of intellectual disability (ID). Here, the authors study a cohort of ID patients enriched for mild ID from Finland, to investigate contributions of rare and common variants associated with ID of different levels of severity.Mitja I. KurkiElmo SaarentausOlli PietiläinenPadhraig GormleyDennis LalSini KerminenMinna Torniainen-HolmEija HämäläinenElisa RahikkalaRiikka Keski-FilppulaMerja RauhalaSatu Korpi-HeikkiläJonna Komulainen–EbrahimHeli HelanderPäivi VieiraMinna MännikköMarkku PeltonenAki S. HavulinnaVeikko SalomaaMatti PirinenJaana SuvisaariJukka S. MoilanenJarmo KörkköOuti KuisminMark J. DalyAarno PalotieNature PortfolioarticleScienceQENNature Communications, Vol 10, Iss 1, Pp 1-15 (2019)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Mitja I. Kurki
Elmo Saarentaus
Olli Pietiläinen
Padhraig Gormley
Dennis Lal
Sini Kerminen
Minna Torniainen-Holm
Eija Hämäläinen
Elisa Rahikkala
Riikka Keski-Filppula
Merja Rauhala
Satu Korpi-Heikkilä
Jonna Komulainen–Ebrahim
Heli Helander
Päivi Vieira
Minna Männikkö
Markku Peltonen
Aki S. Havulinna
Veikko Salomaa
Matti Pirinen
Jaana Suvisaari
Jukka S. Moilanen
Jarmo Körkkö
Outi Kuismin
Mark J. Daly
Aarno Palotie
Contribution of rare and common variants to intellectual disability in a sub-isolate of Northern Finland
description Various types of genetic variation contribute to the etiology of intellectual disability (ID). Here, the authors study a cohort of ID patients enriched for mild ID from Finland, to investigate contributions of rare and common variants associated with ID of different levels of severity.
format article
author Mitja I. Kurki
Elmo Saarentaus
Olli Pietiläinen
Padhraig Gormley
Dennis Lal
Sini Kerminen
Minna Torniainen-Holm
Eija Hämäläinen
Elisa Rahikkala
Riikka Keski-Filppula
Merja Rauhala
Satu Korpi-Heikkilä
Jonna Komulainen–Ebrahim
Heli Helander
Päivi Vieira
Minna Männikkö
Markku Peltonen
Aki S. Havulinna
Veikko Salomaa
Matti Pirinen
Jaana Suvisaari
Jukka S. Moilanen
Jarmo Körkkö
Outi Kuismin
Mark J. Daly
Aarno Palotie
author_facet Mitja I. Kurki
Elmo Saarentaus
Olli Pietiläinen
Padhraig Gormley
Dennis Lal
Sini Kerminen
Minna Torniainen-Holm
Eija Hämäläinen
Elisa Rahikkala
Riikka Keski-Filppula
Merja Rauhala
Satu Korpi-Heikkilä
Jonna Komulainen–Ebrahim
Heli Helander
Päivi Vieira
Minna Männikkö
Markku Peltonen
Aki S. Havulinna
Veikko Salomaa
Matti Pirinen
Jaana Suvisaari
Jukka S. Moilanen
Jarmo Körkkö
Outi Kuismin
Mark J. Daly
Aarno Palotie
author_sort Mitja I. Kurki
title Contribution of rare and common variants to intellectual disability in a sub-isolate of Northern Finland
title_short Contribution of rare and common variants to intellectual disability in a sub-isolate of Northern Finland
title_full Contribution of rare and common variants to intellectual disability in a sub-isolate of Northern Finland
title_fullStr Contribution of rare and common variants to intellectual disability in a sub-isolate of Northern Finland
title_full_unstemmed Contribution of rare and common variants to intellectual disability in a sub-isolate of Northern Finland
title_sort contribution of rare and common variants to intellectual disability in a sub-isolate of northern finland
publisher Nature Portfolio
publishDate 2019
url https://doaj.org/article/ab9e0271d0224acca582195c7d5d71d8
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