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
Published 2005-10-01

Skin Microbiota and Clinical Associations in Netherton Syndrome

by Veera Sillanpää, Tatiany Aparecida Teixeira Soratto, Elina Eränkö, Mauricio Barrientos-Somarribas, Katariina Hannula-Jouppi, Björn Andersson, Annamari Ranki
Published 2021-06-01

Immune cell phenotype and functional defects in Netherton syndrome

by Elina Eränkö, Mette Ilander, Mirja Tuomiranta, Antti Mäkitie, Tea Lassila, Anna Kreutzman, Paula Klemetti, Satu Mustjoki, Katariina Hannula-Jouppi, Annamari Ranki
Published 2018-11-01

Altered Methylation of IGF2 Locus 20 Years after Preterm Birth at Very Low Birth Weight.

by Karoliina Wehkalampi, Mari Muurinen, Sara Bruce Wirta, Katariina Hannula-Jouppi, Petteri Hovi, Anna-Liisa Järvenpää, Johan G Eriksson, Sture Andersson, Juha Kere, Eero Kajantie
Published 2013-01-01

Genetic susceptibility to non-necrotizing erysipelas/cellulitis.

by Katariina Hannula-Jouppi, Satu Massinen, Tuula Siljander, Siru Mäkelä, Katja Kivinen, Rasko Leinonen, Hong Jiao, Päivi Aitos, Matti Karppelin, Jaana Vuopio, Jaana Syrjänen, Juha Kere
Published 2013-01-01

Phenotypic Variability with SLURP1 Mutations and Diffuse Palmoplantar Keratoderma

by Liisa Harjama, Kaisa Kettunen, Outi Elomaa, Elisabet Einarsdottir, Hannele Heikkilä, Sirpa Kivirikko, Katriina Lappalainen, Janna Saarela, Caroline Alby, Annamari Ranki, Juha Kere, Smail Hadj-Rabia, Katariina Hannula-Jouppi
Published 2020-02-01

Novel DSP Spectrin 6 Region Variant Causes Neonatal Erythroderma, Failure to Thrive, Severe Herpes Simplex Infections and Brain Lesions

by Svetlana Vakkilainen, Laura Puhakka, Paula Klemetti, Kaarina Heiskanen, Mikko Seppänen, Mikko Muona, Celine Posseme, Darragh Duffy, Timo Väisänen, Outi Elomaa, Maarit Palomäki, Harri Saxén, Annamari Ranki, Katariina Hannula-Jouppi
Published 2019-06-01

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
Published 2019-12-01

Meta-Analysis of Mutations in <i>ALOX12B</i> or <i>ALOXE3</i> Identified in a Large Cohort of 224 Patients

by Alrun Hotz, Julia Kopp, Emmanuelle Bourrat, Vinzenz Oji, Katalin Komlosi, Kathrin Giehl, Bakar Bouadjar, Anette Bygum, Iliana Tantcheva-Poor, Maritta Hellström Pigg, Cristina Has, Zhou Yang, Alan D. Irvine, Regina C. Betz, Giovanna Zambruno, Gianluca Tadini, Kira Süßmuth, Robert Gruber, Matthias Schmuth, Juliette Mazereeuw-Hautier, Natalie Jonca, Sophie Guez, Michela Brena, Angela Hernandez-Martin, Peter van den Akker, Maria C. Bolling, Katariina Hannula-Jouppi, Andreas D. Zimmer, Svenja Alter, Anders Vahlquist, Judith Fischer
Published 2021-01-01