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

por Cheng, Tian, Einarsdottir, Elisabet, Kere, Juha, Gerdhem, Paul
Publicado 2022

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

por Katayama, Shintaro, Skoog, Tiina, Söderhäll, Cilla, Einarsdottir, Elisabet, Krjutškov, Kaarel, Kere, Juha
Publicado 2019

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

por Einarsdottir, Elisabet, Pekkinen, Minna, Krjutškov, Kaarel, Katayama, Shintaro, Kere, Juha, Mäkitie, Outi, Viljakainen, Heli
Publicado 2019

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

por Einarsdottir, Elisabet, Hafrén, Lena, Leinonen, Eira, Bhutta, Mahmood F., Kentala, Erna, Kere, Juha, Mattila, Petri S.
Publicado 2016

Gene-Expression Profiling Suggests Impaired Signaling via the Interferon Pathway in Cstb(-/-) Microglia

por Körber, Inken, Katayama, Shintaro, Einarsdottir, Elisabet, Krjutškov, Kaarel, Hakala, Paula, Kere, Juha, Lehesjoki, Anna-Elina, Joensuu, Tarja
Publicado 2016

Pleomorphic Adenoma Gene 1 Is Needed For Timely Zygotic Genome Activation and Early Embryo Development

por Madissoon, Elo, Damdimopoulos, Anastasios, Katayama, Shintaro, Krjutškov, Kaarel, Einarsdottir, Elisabet, Mamia, Katariina, De Groef, Bert, Hovatta, Outi, Kere, Juha, Damdimopoulou, Pauliina
Publicado 2019

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

por Einarsdottir, Elisabet, Svensson, Idor, Darki, Fahimeh, Peyrard-Janvid, Myriam, Lindvall, Jessica M., Ameur, Adam, Jacobsson, Christer, Klingberg, Torkel, Kere, Juha, Matsson, Hans
Publicado 2015

Investigation of rare and low-frequency variants using high-throughput sequencing with pooled DNA samples

por Wang, Jingwen, Skoog, Tiina, Einarsdottir, Elisabet, Kaartokallio, Tea, Laivuori, Hannele, Grauers, Anna, Gerdhem, Paul, Hytönen, Marjo, Lohi, Hannes, Kere, Juha, Jiao, Hong
Publicado 2016

A mouse-to-man candidate gene study identifies association of chronic otitis media with the loci TGIF1 and FBXO11

por Bhutta, Mahmood F., Lambie, Jane, Hobson, Lindsey, Goel, Anuj, Hafrén, Lena, Einarsdottir, Elisabet, Mattila, Petri S., Farrall, Martin, Brown, Steve, Burton, Martin J.
Publicado 2017

Mlh1 deficiency in normal mouse colon mucosa associates with chromosomally unstable colon cancer

por Pussila, Marjaana, Törönen, Petri, Einarsdottir, Elisabet, Katayama, Shintaro, Krjutškov, Kaarel, Holm, Liisa, Kere, Juha, Peltomäki, Päivi, Mäkinen, Markus J, Linden, Jere, Nyström, Minna
Publicado 2018

Viral infection‐related gene upregulation in monocytes in children with signs of β‐cell autoimmunity

por Valta, Milla, Yoshihara, Masahito, Einarsdottir, Elisabet, Pahkuri, Sirpa, Ezer, Sini, Katayama, Shintaro, Knip, Mikael, Veijola, Riitta, Toppari, Jorma, Ilonen, Jorma, Kere, Juha, Lempainen, Johanna
Publicado 2022

Ketogenic diet attenuates hepatopathy in mouse model of respiratory chain complex III deficiency caused by a Bcs1l mutation

por Purhonen, Janne, Rajendran, Jayasimman, Mörgelin, Matthias, Uusi-Rauva, Kristiina, Katayama, Shintaro, Krjutskov, Kaarel, Einarsdottir, Elisabet, Velagapudi, Vidya, Kere, Juha, Jauhiainen, Matti, Fellman, Vineta, Kallijärvi, Jukka
Publicado 2017

Acute doses of caffeine shift nervous system cell expression profiles toward promotion of neuronal projection growth

por Yu, Nancy Y., Bieder, Andrea, Raman, Amitha, Mileti, Enrichetta, Katayama, Shintaro, Einarsdottir, Elisabet, Fredholm, Bertil B., Falk, Anna, Tapia-Páez, Isabel, Daub, Carsten O., Kere, Juha
Publicado 2017

The human long non-coding RNA gene RMRP has pleiotropic effects and regulates cell-cycle progression at G2

por Vakkilainen, Svetlana, Skoog, Tiina, Einarsdottir, Elisabet, Middleton, Anna, Pekkinen, Minna, Öhman, Tiina, Katayama, Shintaro, Krjutškov, Kaarel, Kovanen, Panu E., Varjosalo, Markku, Lindqvist, Arne, Kere, Juha, Mäkitie, Outi
Publicado 2019

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

por Bieder, Andrea, Einarsdottir, Elisabet, Matsson, Hans, Nilsson, Harriet E., Eisfeldt, Jesper, Dragomir, Anca, Paucar, Martin, Granberg, Tobias, Li, Tie-Qiang, Lindstrand, Anna, Kere, Juha, Tapia-Páez, Isabel
Publicado 2020

Globin mRNA reduction for whole-blood transcriptome sequencing

por Krjutškov, Kaarel, Koel, Mariann, Roost, Anne Mari, Katayama, Shintaro, Einarsdottir, Elisabet, Jouhilahti, Eeva-Mari, Söderhäll, Cilla, Jaakma, Ülle, Plaas, Mario, Vesterlund, Liselotte, Lohi, Hannes, Salumets, Andres, Kere, Juha
Publicado 2016

Targeted high-throughput sequencing of candidate genes for chronic obstructive pulmonary disease

por Matsson, Hans, Söderhäll, Cilla, Einarsdottir, Elisabet, Lamontagne, Maxime, Gudmundsson, Sanna, Backman, Helena, Lindberg, Anne, Rönmark, Eva, Kere, Juha, Sin, Don, Postma, Dirkje S., Bossé, Yohan, Lundbäck, Bo, Klar, Joakim
Publicado 2016

Phenotypic Variability with SLURP1 Mutations and Diffuse Palmoplantar Keratoderma*

por HARJAMA, Liisa, KETTUNEN, Kaisa, ELOMAA, Outi, EINARSDOTTIR, Elisabet, HEIKKILÄ, Hannele, KIVIRIKKO, Sirpa, LAPPALAINEN, Katriina, SAARELA, Janna, ALBY, Caroline, RANKI, Annamari, KERE, Juha, HADJ-RABIA, Smail, HANNULA-JOUPPI, Katariina
Publicado 2020

Unexpectedly High Prevalence of Common Variable Immunodeficiency in Finland

por Selenius, Jannica S., Martelius, Timi, Pikkarainen, Sampsa, Siitonen, Sanna, Mattila, Eero, Pietikäinen, Risto, Suomalainen, Pekka, Aalto, Arja H., Saarela, Janna, Einarsdottir, Elisabet, Järvinen, Asko, Färkkilä, Martti, Kere, Juha, Seppänen, Mikko
Publicado 2017

Characterization and target genes of nine human PRD-like homeobox domain genes expressed exclusively in early embryos

por Madissoon, Elo, Jouhilahti, Eeva-Mari, Vesterlund, Liselotte, Töhönen, Virpi, Krjutškov, Kaarel, Petropoulous, Sophie, Einarsdottir, Elisabet, Linnarsson, Sten, Lanner, Fredrik, Månsson, Robert, Hovatta, Outi, Bürglin, Thomas R., Katayama, Shintaro, Kere, Juha
Publicado 2016