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

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

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Working memory brain activity and capacity link MAOA polymorphism to aggressive behavior during development von Ziermans, T, Dumontheil, I, Roggeman, C, Peyrard-Janvid, M, Matsson, H, Kere, J, Klingberg, T

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P-110 Evaluation of a high throughput mutation-screening strategy in myelodysplastic syndrome patients and acute myeloid leukemia using Halogenomics™ targeted-gene enrichment techn... von Karimi, M, Dimitriou, M, Nilsson, C, Jansson, M, Matsson, H, Unneberg, P, Lehmann, S, Kere, J, Hellström-Lindberg, E

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Influence of the COMT Genotype on Working Memory and Brain Activity Changes During Development von Dumontheil, Iroise, Roggeman, Chantal, Ziermans, Tim, Peyrard-Janvid, Myriam, Matsson, Hans, Kere, Juha, Klingberg, Torkel

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Polymorphisms in the Dopamine Receptor 2 Gene Region Influence Improvements during Working Memory Training in Children and Adolescents von Söderqvist, Stina, Matsson, Hans, Peyrard-Janvid, Myriam, Kere, Juha, Klingberg, Torkel

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Erythropoiesis in the Rps19 disrupted mouse: Analysis of erythropoietin response and biochemical markers for Diamond-Blackfan anemia von Matsson, H., Davey, E.J., Fröjmark, A.S., Miyake, K., Utsugisawa, T., Flygare, J., Zahou, E., Byman, I., Landin, B., Ronquist, G., Karlsson, S., Dahl, N.

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X-box promoter motif searches: from C. elegans to humans to novel candidate ciliopathies von Lauter, G, Tammimies, K, Bieder, A, Torchet, R, Matsson, H, Peyrard, M, Burghoorn, J, Castren, E, Kere, J, Tapia-Páez, I, Swoboda, P

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DCDC2 polymorphism is associated with left temporoparietal gray and white matter structures during development von Darki, Fahimeh, Peyrard-Janvid, Myriam, Matsson, Hans, Kere, Juha, Klingberg, Torkel

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[P2.28]: From dyslexia candidate genes to molecular pathways in brain development von Tammimies, K., Tapia‐Páez, I., Massinen, S., Hokkanen, M.E., Matsson, H., Peyrard‐Janvid, M.

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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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Dopamine, Working Memory, and Training Induced Plasticity: Implications for Developmental Research von Söderqvist, Stina, Bergman Nutley, Sissela, Peyrard-Janvid, Myriam, Matsson, Hans, Humphreys, Keith, Kere, Juha, Klingberg, Torkel

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Genome-wide meta-analysis identifies BARX1 and EML4-MTA3 as new loci associated with infantile hypertrophic pyloric stenosis von Fadista, João, Skotte, Line, Geller, Frank, Bybjerg-Grauholm, Jonas, Gørtz, Sanne, Romitti, Paul A, Caggana, Michele, Kay, Denise M, Matsson, Hans, Boyd, Heather A, Hougaard, David M, Nordenskjöld, Agneta, Mills, James L, Melbye, Mads, Feenstra, Bjarke

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Variant Profiling of Candidate Genes in Pancreatic Ductal Adenocarcinoma von Huang, Jiaqi, Löhr, Johannes-Matthias, Nilsson, Magnus, Segersvärd, Ralf, Matsson, Hans, Verbeke, Caroline, Heuchel, Rainer, Kere, Juha, Iafrate, A John, Zheng, Zongli, Ye, Weimin

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Genome-wide association study of Hirschsprung disease detects a novel low-frequency variant at the RET locus von Fadista, João, Lund, Marie, Skotte, Line, Geller, Frank, Nandakumar, Priyanka, Chatterjee, Sumantra, Matsson, Hans, Granström, Anna Löf, Wester, Tomas, Salo, Perttu, Virtanen, Valtter, Carstensen, Lisbeth, Bybjerg-Grauholm, Jonas, Hougaard, David Michael, Pakarinen, Mikko, Perola, Markus, Nordenskjöld, Agneta, Chakravarti, Aravinda, Melbye, Mads, Feenstra, Bjarke

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Three Dyslexia Susceptibility Genes, DYX1C1 , DCDC2 , and KIAA0319, Affect Temporo-Parietal White Matter Structure von Darki, Fahimeh, Peyrard-Janvid, Myriam, Matsson, Hans, Kere, Juha, Klingberg, Torkel

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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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Alpha-cardiac actin mutations produce atrial septal defects von Matsson, Hans, Eason, Jacqueline, Bookwalter, Carol S., Klar, Joakim, Gustavsson, Peter, Sunnegårdh, Jan, Enell, Henrik, Jonzon, Anders, Vikkula, Miikka, Gutierrez, Ilse, Granados-Riveron, Javier, Pope, Mark, Bu’Lock, Frances, Cox, Jane, Robinson, Thelma E, Song, Feifei, Brook, David J, Marston, Steven, Trybus, Kathleen M., Dahl, Niklas

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The SNAP25 Gene Is Linked to Working Memory Capacity and Maturation of the Posterior Cingulate Cortex During Childhood von Söderqvist, Stina, McNab, Fiona, Peyrard-Janvid, Myriam, Matsson, Hans, Humphreys, Keith, Kere, Juha, Klingberg, Torkel

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Mutation in CEP63 co-segregating with developmental dyslexia in a Swedish family von Einarsdottir, Elisabet, Svensson, Idor, Darki, Fahimeh, Peyrard-Janvid, Myriam, Lindvall, Jessica M., Ameur, Adam, Jacobsson, Christer, Klingberg, Torkel, Kere, Juha, Matsson, Hans

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