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Published in Nature genetics (01.06.2015)
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Impact of IKZF1 deletions and PAX5 amplifications in pediatric B-cell precursor ALL treated according to NOPHO protocols
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Novel KIAA0753 mutations extend the phenotype of skeletal ciliopathies
Hammarsjö, A., Wang, Z., Vaz, R., Taylan, F., Sedghi, M., Girisha, K. M., Chitayat, D., Neethukrishna, K., Shannon, P., Godoy, R., Gowrishankar, K., Lindstrand, A., Nasiri, J., Baktashian, M., Newton, P. T., Guo, L., Hofmeister, W., Pettersson, M., Chagin, A. S., Nishimura, G., Yan, L., Matsumoto, N., Nordgren, A., Miyake, N., Grigelioniene, G., Ikegawa, S.
Published in Scientific reports (14.11.2017)
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Tree root and soil heterotrophic respiration as revealed by girdling of boreal Scots pine forest: extending observations beyond the first year
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Published in Plant, cell and environment (01.08.2003)
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The Roots of Autism and ADHD Twin Study in Sweden (RATSS)
Bölte, Sven, Willfors, Charlotte, Berggren, Steve, Norberg, Joakim, Poltrago, Lina, Mevel, Katell, Coco, Christina, Fransson, Peter, Borg, Jacqueline, Sitnikov, Rouslan, Toro, Roberto, Tammimies, Kristiina, Anderlid, Britt-Marie, Nordgren, Ann, Falk, Anna, Meyer, Urs, Kere, Juha, Landén, Mikael, Dalman, Christina, Ronald, Angelica, Anckarsäter, Henrik, Lichtenstein, Paul
Published in Twin research and human genetics (01.06.2014)
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The clinical impact of IKZF1 deletions in paediatric B‐cell precursor acute lymphoblastic leukaemia is independent of minimal residual disease stratification in Nordic Society for Paediatric Haematology and Oncology treatment protocols used between 1992 and 2013
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Published in British journal of haematology (2015)
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Identification of new TRIP12 variants and detailed clinical evaluation of individuals with non-syndromic intellectual disability with or without autism
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MLL2 mutation detection in 86 patients with Kabuki syndrome: a genotype-phenotype study
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Published in Clinical genetics (01.12.2013)
Published in Clinical genetics (01.12.2013)
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Maternal smoking during pregnancy and risk of phacomatoses: results from a Swedish register-based study
Tettamanti, Giorgio, Mogensen, Hanna, Nordgren, Ann, Feychting, Maria
Published in Clinical epidemiology (01.01.2019)
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Deformation mechanisms in a WC–Co based cemented carbide during creep
Yousfi, M.A., Weidow, J., Nordgren, A., Falk, L.K.L., Andrén, H.-O.
Published in International journal of refractory metals & hard materials (01.03.2015)
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Overexpression of chromatin remodeling and tyrosine kinase genes in iAMP21-positive acute lymphoblastic leukemia
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Medical history of discordant twins and environmental etiologies of autism
Willfors, C, Carlsson, T, Anderlid, B-M, Nordgren, A, Kostrzewa, E, Berggren, S, Ronald, A, Kuja-Halkola, R, Tammimies, K, Bölte, S
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Mutations in FLVCR2 associated with Fowler syndrome and survival beyond infancy
Kvarnung, M., Taylan, F., Nilsson, D., Albåge, M., Nordenskjöld, M., Anderlid, B.M., Nordgren, A., Syk Lundberg, E.
Published in Clinical genetics (01.01.2016)
Published in Clinical genetics (01.01.2016)
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From cytogenetics to cytogenomics: whole genome sequencing as a comprehensive genetic test in rare disease diagnostics
Nilsson, D., Eisfeldt, J., Lundin, J., Pettersson, M., Kvarnung, M., Lieden, A., Sahlin, E., Lagerstedt, K., Martin, M., Ygberg, S., Bjerin, O., Stranneheim, H., Wedell, A., Nordenskjold, M., Soller, M. Johansson, Nordgren, A., Wirta, Valtteri, Lindstrand, A.
Published in EUROPEAN JOURNAL OF HUMAN GENETICS (2019)
Published in EUROPEAN JOURNAL OF HUMAN GENETICS (2019)
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Conference Proceeding
High modal number and triple trisomies are highly correlated favorable factors in childhood B-cell precursor high hyperdiploid acute lymphoblastic leukemia treated according to the NOPHO ALL 1992/2000 protocols
Paulsson, Kajsa, Forestier, Erik, Andersen, Mette K, Autio, Kirsi, Barbany, Gisela, Borgström, Georg, Cavelier, Lucia, Golovleva, Irina, Heim, Sverre, Heinonen, Kristiina, Hovland, Randi, Johannsson, Johann H, Kjeldsen, Eigil, Nordgren, Ann, Palmqvist, Lars, Johansson, Bertil
Published in Haematologica (Roma) (01.09.2013)
Published in Haematologica (Roma) (01.09.2013)
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Relapsed childhood high hyperdiploid acute lymphoblastic leukemia: presence of preleukemic ancestral clones and the secondary nature of microdeletions and RTK-RAS mutations
Davidsson, J, Paulsson, K, Lindgren, D, Lilljebjörn, H, Chaplin, T, Forestier, E, Andersen, M K, Nordgren, A, Rosenquist, R, Fioretos, T, Young, B D, Johansson, B
Published in Leukemia (01.05.2010)
Published in Leukemia (01.05.2010)
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Short Stature in KBG Syndrome: First Responses to Growth Hormone Treatment
Reynaert, Nele, Ockeloen, C.W., Sävendahl, L., Beckers, D., Devriendt, K., Kleefstra, T., Carels, C.E.L., Grigelioniene, G., Nordgren, A., Francois, I., de Zegher, F., Casteels, K.
Published in Hormone research in paediatrics (01.01.2015)
Published in Hormone research in paediatrics (01.01.2015)
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The frequency and prognostic impact of dic(9;20)(p13.2;q11.2) in childhood B-cell precursor acute lymphoblastic leukemia: results from the NOPHO ALL-2000 trial
Zachariadis, V, Gauffin, F, Kuchinskaya, E, Heyman, M, Schoumans, J, Blennow, E, Gustafsson, B, Barbany, G, Golovleva, I, Ehrencrona, H, Cavelier, L, Palmqvist, L, Lönnerholm, G, Nordenskjöld, M, Johansson, B, Forestier, E, Nordgren, A
Published in Leukemia (01.04.2011)
Published in Leukemia (01.04.2011)
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