Baricitinib Blocks Cytokine-Mediated Downregulation of PAD1 in Human Keratinocytes: A Possible Molecular Link to the Effects of JAK Inhibitors in Atopic Dermatitis von Padhi, Avinash, Rekha, Rokeya Sultana, Benrejdal, Lisa, Grundeken, Marijke Elise, Lourda, Magda, Ehrström, Marcus, Eyerich, Kilian, Tapia-Páez, Isabel, Johansson, Emma K., Bradley, Maria, Bergman, Peter, Lysell, Josefin

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CTNND2—a candidate gene for reading problems and mild intellectual disability von Hofmeister, Wolfgang, Nilsson, Daniel, Topa, Alexandra, Anderlid, Britt-Marie, Darki, Fahimeh, Matsson, Hans, Tapia Páez, Isabel, Klingberg, Torkel, Samuelsson, Lena, Wirta, Valtteri, Vezzi, Francesco, Kere, Juha, Nordenskjöld, Magnus, Syk Lundberg, Elisabeth, Lindstrand, Anna

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Ciliary dyslexia candidate genes DYX1C1 and DCDC2 are regulated by Regulatory Factor X (RFX) transcription factors through X‐box promoter motifs von Tammimies, Kristiina, Bieder, Andrea, Lauter, Gilbert, Sugiaman‐Trapman, Debora, Torchet, Rachel, Hokkanen, Marie‐Estelle, Burghoorn, Jan, Castren, Eero, Kere, Juha, Tapia‐Páez, Isabel, Swoboda, Peter

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

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Dyslexia Candidate Gene and Ciliary Gene Expression Dynamics During Human Neuronal Differentiation von Bieder, Andrea, Yoshihara, Masahito, Katayama, Shintaro, Krjutškov, Kaarel, Falk, Anna, Kere, Juha, Tapia-Páez, Isabel

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Increased expression of the dyslexia candidate gene DCDC2 affects length and signaling of primary cilia in neurons von Massinen, Satu, Hokkanen, Marie-Estelle, Matsson, Hans, Tammimies, Kristiina, Tapia-Páez, Isabel, Dahlström-Heuser, Vanina, Kuja-Panula, Juha, Burghoorn, Jan, Jeppsson, Kristian E, Swoboda, Peter, Peyrard-Janvid, Myriam, Toftgård, Rune, Castrén, Eero, Kere, Juha

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

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Evaluation of Single Nucleotide Variants in Ethiopian Patients with Atopic Dermatitis von Asad, Samina, Tapia-Páez, Isabel, Montano Montes, Andrea, Wahlgren, Carl-Fredrik, Bilcha, Kassahun D, Nordenskjöld, Magnus, Bradley, Maria

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

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Genomic sequencing of a dyslexia susceptibility haplotype encompassing ROBO1 von Massinen, Satu, Wang, Jingwen, Laivuori, Krista, Bieder, Andrea, Tapia Paez, Isabel, Jiao, Hong, Kere, Juha

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Chromatin interactions in differentiating keratinocytes reveal novel atopic dermatitis– and psoriasis-associated genes von Sahlén, Pelin, Spalinskas, Rapolas, Asad, Samina, Mahapatra, Kunal Das, Höjer, Pontus, Anil, Anandashankar, Eisfeldt, Jesper, Srivastava, Ankit, Nikamo, Pernilla, Mukherjee, Anaya, Kim, Kyu-Han, Bergman, Otto, Ståhle, Mona, Sonkoly, Enikö, Pivarcsi, Andor, Wahlgren, Carl-Fredrik, Nordenskjöld, Magnus, Taylan, Fulya, Bradley, Maria, Tapia-Páez, Isabel

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DCDC2 Mutations Cause a Renal-Hepatic Ciliopathy by Disrupting Wnt Signaling von Schueler, Markus, Braun, Daniela A., Chandrasekar, Gayathri, Gee, Heon Yung, Klasson, Timothy D., Halbritter, Jan, Bieder, Andrea, Porath, Jonathan D., Airik, Rannar, Zhou, Weibin, LoTurco, Joseph J., Che, Alicia, Otto, Edgar A., Böckenhauer, Detlef, Sebire, Neil J., Honzik, Tomas, Harris, Peter C., Koon, Sarah J., Gunay-Aygun, Meral, Saunier, Sophie, Zerres, Klaus, Bruechle, Nadina Ortiz, Drenth, Joost P.H., Pelletier, Laurence, Tapia-Páez, Isabel, Lifton, Richard P., Giles, Rachel H., Kere, Juha, Hildebrandt, Friedhelm

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A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applications von Buckley, Patrick G., Mantripragada, Kiran K., Benetkiewicz, Magdalena, Tapia-Páez, Isabel, Diaz de Ståhl, Teresita, Rosenquist, Magnus, Ali, Haider, Jarbo, Caroline, de Bustos, Cecilía, Hirvelä, Carina, Sinder Wilén, Birgitta, Fransson, Ingegerd, Thyr, Charlotte, Johnsson, Britt-Inger, Bruder, Carl E.G., Menzel, Uwe, Hergersberg, Martin, Mandahl, Nils, Blennow, Elisabeth, Wedell, Anna, Beare, David M., Collins, John E., Dunham, Ian, Albertson, Donna, Pinkel, Daniel, Bastian, Boris C., Faruqi, A. Fawad, Lasken, Roger S., Ichimura, Koichi, Collins, V. Peter, Dumanski, Jan P.

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Rare coding variants in NOX4 link high ROS levels to psoriatic arthritis mutilans von Wang, Sailan, Nikamo, Pernilla, Laasonen, Leena, Gudbjornsson, Bjorn, Ejstrup, Leif, Iversen, Lars, Lindqvist, Ulla, Alm, Jessica J, Eisfeldt, Jesper, Zheng, Xiaowei, Catrina, Sergiu-Bogdan, Taylan, Fulya, Vaz, Raquel, Ståhle, Mona, Tapia-Paez, Isabel

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

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complex of TFII-I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexia von Tapia-Páez, Isabel, Tammimies, Kristiina, Massinen, Satu, Roy, Ananda L, Kere, Juha

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Uncommon Variants in FLG2 and NOD2 Are Associated with Atopic Dermatitis in the Ethiopian Population von Wang, Sailan, Elmgren, Julia K., Eisfeldt, Jesper, Asad, Samina, Ek, Marlene, Bilcha, Kassahun, Befekadu, Annisa, Wahlgren, Carl-Fredrik, Nordenskjöld, Magnus, Taylan, Fulya, Tapia-Paez, Isabel, Bradley, Maria

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Molecular Networks of DYX1C1 Gene Show Connection to Neuronal Migration Genes and Cytoskeletal Proteins von Tammimies, Kristiina, Vitezic, Morana, Matsson, Hans, Le Guyader, Sylvie, Bürglin, Thomas R, Öhman, Tiina, Strömblad, Staffan, Daub, Carsten O, Nyman, Tuula A, Kere, Juha, Tapia-Páez, Isabel

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The Aromatase Gene CYP19A1: Several Genetic and Functional Lines of Evidence Supporting a Role in Reading, Speech and Language von Anthoni, Heidi, Sucheston, Lara E., Lewis, Barbara A., Tapia-Páez, Isabel, Fan, Xiaotang, Zucchelli, Marco, Taipale, Mikko, Stein, Catherine M., Hokkanen, Marie-Estelle, Castrén, Eero, Pennington, Bruce F., Smith, Shelley D., Olson, Richard K., Tomblin, J. Bruce, Schulte-Körne, Gerd, Nöthen, Markus, Schumacher, Johannes, Müller-Myhsok, Bertram, Hoffmann, Per, Gilger, Jeffrey W., Hynd, George W., Nopola-Hemmi, Jaana, Leppanen, Paavo H. T., Lyytinen, Heikki, Schoumans, Jacqueline, Nordenskjöld, Magnus, Spencer, Jason, Stanic, Davor, Boon, Wah Chin, Simpson, Evan, Mäkelä, Sari, Gustafsson, Jan-Åke, Peyrard-Janvid, Myriam, Iyengar, Sudha, Kere, Juha

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Functional interaction of DYX1C1 with estrogen receptors suggests involvement of hormonal pathways in dyslexia von Massinen, Satu, Tammimies, Kristiina, Tapia-Páez, Isabel, Matsson, Hans, Hokkanen, Marie-Estelle, Söderberg, Ola, Landegren, Ulf, Castrén, Eero, Gustafsson, Jan-Åke, Treuter, Eckardt, Kere, Juha

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