Unexpectedly High Prevalence of Common Variable Immunodeficiency in Finland by Jannica S. Selenius, Jannica S. Selenius, Timi Martelius, Sampsa Pikkarainen, Sanna Siitonen, Eero Mattila, Risto Pietikäinen, Pekka Suomalainen, Arja H. Aalto, Arja H. Aalto, Janna Saarela, Elisabet Einarsdottir, Elisabet Einarsdottir, Elisabet Einarsdottir, Asko Järvinen, Martti Färkkilä, Juha Kere, Juha Kere, Juha Kere, Juha Kere, Mikko Seppänen, Mikko Seppänen

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Computational approach to evaluate scRNA-seq data quality and gene body coverage with SkewC by Imad Abugessaisa, Akira Hasegawa, Shintaro Katayama, Juha Kere, Takeya Kasukawa

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Complement in Human Pre-implantation Embryos: Attack and Defense by Martin P. Reichhardt, Martin P. Reichhardt, Karolina Lundin, A. Inkeri Lokki, A. Inkeri Lokki, Gaëlle Recher, Sanna Vuoristo, Shintaro Katayama, Juha S. Tapanainen, Juha S. Tapanainen, Juha Kere, Juha Kere, Juha Kere, Seppo Meri, Seppo Meri, Seppo Meri, Timo Tuuri

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Enrichment of rare CFTR variants in Finnish patients with congenital chloride diarrhea. by Satu Wedenoja, Jarmo Ritari, Jukka Partanen, Juha Kere, Kaija-Leena Kolho

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Congenital chloride diarrhea and Pendred syndrome: case report of siblings with two rare recessive disorders of SLC26 family genes by Eva Lindberg, Claes Moller, Juha Kere, Satu Wedenoja, Agneta Anderzén-Carlsson

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The zebrafish orthologue of the dyslexia candidate gene DYX1C1 is essential for cilia growth and function. by Gayathri Chandrasekar, Liselotte Vesterlund, Kjell Hultenby, Isabel Tapia-Páez, Juha Kere

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Case report: A novel de novo IGF2 missense variant in a Finnish patient with Silver-Russell syndrome by Petra Loid, Petra Loid, Petra Loid, Marita Lipsanen-Nyman, Marita Lipsanen-Nyman, Sirpa Ala-Mello, Katariina Hannula-Jouppi, Katariina Hannula-Jouppi, Katariina Hannula-Jouppi, Juha Kere, Juha Kere, Juha Kere, Outi Mäkitie, Outi Mäkitie, Outi Mäkitie, Outi Mäkitie, Mari Muurinen, Mari Muurinen, Mari Muurinen

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Expression analysis of the NLRP gene family suggests a role in human preimplantation development. by Pu Zhang, Morag Dixon, Marco Zucchelli, Fredwell Hambiliki, Lev Levkov, Outi Hovatta, Juha Kere

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A preliminary transcriptome analysis suggests a transitory effect of vitamin D on mitochondrial function in obese young Finnish subjects by Elisabet Einarsdottir, Minna Pekkinen, Kaarel Krjutškov, Shintaro Katayama, Juha Kere, Outi Mäkitie, Heli Viljakainen

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Genetic and protein interaction studies between the ciliary dyslexia candidate genes DYX1C1 and DCDC2 by Andrea Bieder, Gayathri Chandrasekar, Arpit Wason, Steffen Erkelenz, Jay Gopalakrishnan, Juha Kere, Isabel Tapia-Páez

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CRISPR/Cas9-mediated activation of NR5A1 steers female human embryonic stem cell-derived bipotential gonadal-like cells towards a steroidogenic cell fate by Laura Danti, Karolina Lundin, Kirsi Sepponen, Dawit A. Yohannes, Juha Kere, Timo Tuuri, Juha S. Tapanainen

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The axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexia. by Katariina Hannula-Jouppi, Nina Kaminen-Ahola, Mikko Taipale, Ranja Eklund, Jaana Nopola-Hemmi, Helena Kääriäinen, Juha Kere

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Gene-Expression Profiling Suggests Impaired Signaling via the Interferon Pathway in Cstb-/- Microglia. by Inken Körber, Shintaro Katayama, Elisabet Einarsdottir, Kaarel Krjutškov, Paula Hakala, Juha Kere, Anna-Elina Lehesjoki, Tarja Joensuu

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Pain in idiopathic scoliosis not associated with known genetic variants for pain by Tian Cheng, Elias Diarbakerli, Ane Simony, Mikkel Østerheden Andersen, Aina Danielsson, Juha Kere, Elisabet Einarsdottir, Paul Gerdhem

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Novel TMEM173 Mutation and the Role of Disease Modifying Alleles by Salla Keskitalo, Emma Haapaniemi, Emma Haapaniemi, Elisabet Einarsdottir, Elisabet Einarsdottir, Kristiina Rajamäki, Hannele Heikkilä, Mette Ilander, Mette Ilander, Minna Pöyhönen, Minna Pöyhönen, Ekaterina Morgunova, Kati Hokynar, Sonja Lagström, Sirpa Kivirikko, Sirpa Kivirikko, Satu Mustjoki, Satu Mustjoki, Kari Eklund, Kari Eklund, Janna Saarela, Juha Kere, Juha Kere, Juha Kere, Mikko R. J. Seppänen, Mikko R. J. Seppänen, Annamari Ranki, Katariina Hannula-Jouppi, Katariina Hannula-Jouppi, Markku Varjosalo

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High-throughput mutational screening adds clinically important information in myelodysplastic syndromes and secondary or therapy-related acute myeloid leukemia by Mohsen Karimi, Christer Nilsson, Marios Dimitriou, Monika Jansson, Hans Matsson, Per Unneberg, Sören Lehmann, Juha Kere, Eva Hellström-Lindberg

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Human pluripotent reprogramming with CRISPR activators by Jere Weltner, Diego Balboa, Shintaro Katayama, Maxim Bespalov, Kaarel Krjutškov, Eeva-Mari Jouhilahti, Ras Trokovic, Juha Kere, Timo Otonkoski

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Analysis of neuropeptide S receptor gene (NPSR1) polymorphism in rheumatoid arthritis. by Mauro D'Amato, Marco Zucchelli, Maria Seddighzadeh, Francesca Anedda, Staffan Lindblad, Juha Kere, Lars Alfredsson, Lars Klareskog, Leonid Padyukov

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Differential DNA methylation in purified human blood cells: implications for cell lineage and studies on disease susceptibility. by Lovisa E Reinius, Nathalie Acevedo, Maaike Joerink, Göran Pershagen, Sven-Erik Dahlén, Dario Greco, Cilla Söderhäll, Annika Scheynius, Juha Kere

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Primary cilia promote the differentiation of human neurons through the WNT signaling pathway by Andrea Coschiera, Masahito Yoshihara, Gilbert Lauter, Sini Ezer, Mariangela Pucci, Haonan Li, Alan Kavšek, Christian G. Riedel, Juha Kere, Peter Swoboda

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