Ngā hua rapu - Ann Nordgren

Whakamahine hua
  1. 1
    Reversed gender ratio of autism spectrum disorder in Smith-Magenis syndrome

    Reversed gender ratio of autism spectrum disorder in Smith-Magenis syndrome mā Heidi Elisabeth Nag, Ann Nordgren, Britt‐Marie Anderlid, Terje Nærland

    I whakaputaina 2018
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  2. 2
    A study of the interaction of omeprazole and warfarin in anticoagulated patients.

    A study of the interaction of omeprazole and warfarin in anticoagulated patients. mā Peter Unge, LE Svedberg, Ann Nordgren, Henry Blom, Tommy Andersson, P O Lagerström, JP Idström

    I whakaputaina 1992
    Whiwhi kuputuhi katoa
    Artigo
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  3. 3
    Comorbidities, Endocrine Medications, and Mortality in Prader–Willi Syndrome—A Swedish Register Study

    Comorbidities, Endocrine Medications, and Mortality in Prader–Willi Syndrome—A Swedish Register Study mā Julia Giesecke, Anna Oskarsson, Maria Petersson, Anna Skarin Nordenvall, Giorgio Tettamanti, Ann Nordgren, Charlotte Höybye

    I whakaputaina 2025
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    Artigo
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  4. 4
    Expanding the ataxia with oculomotor apraxia type 4 phenotype

    Expanding the ataxia with oculomotor apraxia type 4 phenotype mā Martin Paucar, Helena Malmgren, A. Malcolm R. Taylor, John J. Reynolds, Per Svenningsson, Rayomand Press, Ann Nordgren

    I whakaputaina 2016
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    Artigo
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  5. 5
    The cost-effectiveness of whole genome sequencing in neurodevelopmental disorders

    The cost-effectiveness of whole genome sequencing in neurodevelopmental disorders mā Hannes Runheim, Maria Pettersson, Anna Hammarsjö, Ann Nordgren, Martin Henriksson, Anna Lindstrand, Lars‐Åke Levin, Maria Soller

    I whakaputaina 2023
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    Artigo
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  6. 6
    p53 controls genomic stability and temporal differentiation of human neural stem cells and affects neural organization in human brain organoids

    p53 controls genomic stability and temporal differentiation of human neural stem cells and affects neural organization in human brain organoids mā Ana Marín Navarro, Robin Pronk, Astrid Tjitske van der Geest, Ganna Oliynyk, Ann Nordgren, Marie Arsenian‐Henriksson, Anna Falk, Margareta Wilhelm

    I whakaputaina 2020
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  7. 7
    The genomic landscape of high hyperdiploid childhood acute lymphoblastic leukemia

    The genomic landscape of high hyperdiploid childhood acute lymphoblastic leukemia mā Kajsa Paulsson, Henrik Lilljebjörn, Andrea Biloglav, Linda Olsson, Marianne Rissler, Anders Castor, Gisela Barbany, Linda Fogelstrand, Ann Nordgren, Helene Sjögren, Thoas Fioretos, Bertil Johansson

    I whakaputaina 2015
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    Artigo
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  8. 8
    The clinical impact of <i><scp>IKZF</scp>1</i> 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

    The clinical impact of <i><scp>IKZF</scp>1</i> deletions in paediatric B‐cell precursor acute lymphoblastic leukaemia is independent of minimal residual disease stratification in N... mā Linda Olsson, Ingegerd Öfverholm, Ulrika Norén‐Nyström, Vasilios Zachariadis, Jessica Nordlund, Helene Sjögren, Irina Golovleva, Ann Nordgren, Kajsa Paulsson, Mats Heyman, Gisela Barbany, Bertil Johansson

    I whakaputaina 2015
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    Artigo
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  9. 9
    Precision medicine in rare diseases: What is next?

    Precision medicine in rare diseases: What is next? mā Bianca Tesi, Cathérine Boileau, Kym M. Boycott, Guillaume Canaud, Mark J. Caulfield, Daniela Choukair, Sue Hill, Malte Spielmann, Anna Wedell, Valtteri Wirta, Ann Nordgren, Anna Lindstrand

    I whakaputaina 2023
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Revisão
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  10. 10
    Dominant Mutations in KAT6A Cause Intellectual Disability with Recognizable Syndromic Features

    Dominant Mutations in KAT6A Cause Intellectual Disability with Recognizable Syndromic Features mā Emma Tham, Anna Lindstrand, Avni Santani, Helena Malmgren, Addie I. Nesbitt, Holly Dubbs, Elaine H. Zackai, Michael Parker, Francisca Millan, Kenneth N. Rosenbaum, Golder N. Wilson, Ann Nordgren

    I whakaputaina 2015
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    Artigo
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  11. 11
    Outcome of <i>ETV6/RUNX1</i>‐positive childhood acute lymphoblastic leukaemia in the NOPHO‐ALL‐1992 protocol: frequent late relapses but good overall survival

    Outcome of <i>ETV6/RUNX1</i>‐positive childhood acute lymphoblastic leukaemia in the NOPHO‐ALL‐1992 protocol: frequent late relapses but good overall survival mā Erik Forestier, Mats Heyman, Mette K. Andersen, K. Autio, Elisabeth Blennow, Georg Borgström, Irina Golovleva, Sverre Heim, Kristina Heinonen, Randi Hovland, Jóhann Heiðar Jóhannsson, Gitte Kerndrup, Ann Nordgren, Richard Rosenquist, Birgitta Swolin, Bertil Johansson

    I whakaputaina 2008
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    Artigo
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  12. 12
    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

    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... mā Kajsa Paulsson, Erik Forestier, Mette Klarskov Andersen, K. Autio, Gisela Barbany, G.H. Borgström, Lucia Cavelier, Irina Golovleva, Sverre Heim, Kristiina Heinonen, Randi Hovland, Jóhann Heiðar Jóhannsson, Eigil Kjeldsen, Ann Nordgren, Lars Palmqvist, Bertil Johansson

    I whakaputaina 2013
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    Artigo
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  13. 13
    Molecular and clinical delineation of the 17q22 microdeletion phenotype

    Molecular and clinical delineation of the 17q22 microdeletion phenotype mā Tobias Laurell, Johanna Lundin, Britt-Marie Anderlid, Jerome L. Gorski, Giedre Grigelioniené, Samantha J.L. Knight, Ana Cristina Victorino Krepischi, Agneta Nordenskjöld, Susan Price, Carla Rosenberg, Peter D. Turnpenny, Angela Maria Vianna‐Morgante, Ann Nordgren

    I whakaputaina 2013
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  14. 14
    The Roots of Autism and ADHD Twin Study in Sweden (RATSS)

    The Roots of Autism and ADHD Twin Study in Sweden (RATSS) mā Sven Bölte, Charlotte Willfors, Steve Berggren, Joakim Norberg, Lina Poltrago, Katell Mevel, Christina Coco, Peter Fransson, Jacqueline Borg, Rouslan Sitnikov, Roberto Toro, Kristiina Tammimies, Britt‐Marie Anderlid, Ann Nordgren, Anna Falk, Urs Meyer, Juha Kere, Mikael Landén, Christina Dalman, Angelica Ronald, Henrik Anckarsäter, Paul Lichtenstein

    I whakaputaina 2014
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    Artigo
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  15. 15
    DNA methylation-based subtype prediction for pediatric acute lymphoblastic leukemia

    DNA methylation-based subtype prediction for pediatric acute lymphoblastic leukemia mā Jessica Nordlund, Christofer Bäcklin, Vasilios Zachariadis, Lucia Cavelier, Johan Dahlberg, Ingegerd Öfverholm, Gisela Barbany, Ann Nordgren, Elin Övernäs, Jonas Abrahamsson, Trond Flægstad, Mats Heyman, Ólafur G. Jónsson, Jukka Kanerva, Rolf Larsson, Josefine Palle, Kjeld Schmiegelow, Mats G. Gustafsson, Gudmar Lönnerholm, Erik Forestier, Ann‐Christine Syvänen

    I whakaputaina 2015
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    Artigo
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  16. 16
    Gain-of-function mutation of microRNA-140 in human skeletal dysplasia

    Gain-of-function mutation of microRNA-140 in human skeletal dysplasia mā Giedre Grigelioniené, Hiroshi Suzuki, Fulya Taylan, Fatemeh Mirzamohammadi, Zvi Borochowitz, Ugur M. Ayturk, Shay Tzur, Eva Horemuzova, Anna Lindstrand, Mary Ann Weis, Gintautas Grigelionis, Anna Hammarsjö, Elin Marsk, Ann Nordgren, Magnus Nordenskjöld, David W. Eyre, Matthew L. Warman, Gen Nishimura, Phillip A. Sharp, Tatsuya Kobayashi

    I whakaputaina 2019
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    Artigo
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  17. 17
    The transcriptional regulator <i>ADNP</i> links the BAF (SWI/SNF) complexes with autism

    The transcriptional regulator <i>ADNP</i> links the BAF (SWI/SNF) complexes with autism mā Geert Vandeweyer, Céline Helsmoortel, Anke Van Dijck, Anneke T. Vulto‐van Silfhout, Bradley P. Coe, Raphael Bernier, Jennifer Gerdts, Liesbeth Rooms, Jenneke van den Ende, Madhura Bakshi, Meredith Wilson, Ann Nordgren, Laura G. Hendon, Omar Abdul‐Rahman, Corrado Romano, Bert B.A. de Vries, Tjitske Kleefstra, Evan E. Eichler, Nathalie Van der Aa, R. Frank Kooy

    I whakaputaina 2014
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    Artigo
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  18. 18
    Small 6q16.1 Deletions Encompassing POU3F2 Cause Susceptibility to Obesity and Variable Developmental Delay with Intellectual Disability

    Small 6q16.1 Deletions Encompassing POU3F2 Cause Susceptibility to Obesity and Variable Developmental Delay with Intellectual Disability mā Paul R. Kasher, Katherine E. Schertz, Megan Thomas, Adam Jackson, Silvia Annunziata, María Juliana Ballesta‐Martínez, Philippe M. Campeau, Peter Clayton, Jennifer L. Eaton, Tiziana Granata, Encarna Guillén‐Navarro, Cristina Hernándo, Caroline E. Laverriere, Agne Liedén, Olaya Villa-Marcos, Meriel McEntagart, Ann Nordgren, Chiara Pantaleoni, Céline Pebrel‐Richard, Catherine Sarret, Francesca L. Sciacca, Ronnie Wright, Bronwyn Kerr, Eric Glasgow, Siddharth Banka

    I whakaputaina 2016
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    Artigo
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  19. 19
    From cytogenetics to cytogenomics: whole-genome sequencing as a first-line test comprehensively captures the diverse spectrum of disease-causing genetic variation underlying intellectual disability

    From cytogenetics to cytogenomics: whole-genome sequencing as a first-line test comprehensively captures the diverse spectrum of disease-causing genetic variation underlying intell... mā Anna Lindstrand, Jesper Eisfeldt, Maria Pettersson, Claudia M.B. Carvalho, Malin Kvarnung, Giedre Grigelioniené, Britt‐Marie Anderlid, Olof Bjerin, Peter Gustavsson, Anna Hammarsjö, Patrik Georgii‐Hemming, Erik Iwarsson, Maria Soller, Kristina Lagerstedt‐Robinson, Agne Liedén, Måns Magnusson, Marcel Martin, Helena Malmgren, Magnus Nordenskjöld, Ameli Norling, Ellika Sahlin, Henrik Stranneheim, Emma Tham, Josephine Wincent, Sofia Ygberg, Anna Wedell, Valtteri Wirta, Ann Nordgren, Johanna Lundin, Daniel Nilsson

    I whakaputaina 2019
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    Artigo
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  20. 20
    Neu-Laxova Syndrome Is a Heterogeneous Metabolic Disorder Caused by Defects in Enzymes of the L-Serine Biosynthesis Pathway

    Neu-Laxova Syndrome Is a Heterogeneous Metabolic Disorder Caused by Defects in Enzymes of the L-Serine Biosynthesis Pathway mā Rocío Acuña‐Hidalgo, Denny Schanze, Ariana Kariminejad, Ann Nordgren, Mohamad Hasan Kariminejad, Peter Conner, Giedre Grigelioniené, Daniel Nilsson, Magnus Nordenskjöld, Anna Wedell, Christoph Freyer, Anna Wredenberg, Dagmar Wieczorek, Gabriele Gillessen‐Kaesbach, Hülya Kayserili, Nursel Elçioğlu, Siavash Ghaderi‐Sohi, Payman Goodarzi, Hamidreza Setayesh, Maartje van de Vorst, Marloes Steehouwer, Rolph Pfundt, Birgit Krabichler, Cynthia J. Curry, Malcolm G. MacKenzie, Kym M. Boycott, Christian Gilissen, Andreas Janecke, Alexander Hoischen, Martin Zenker

    I whakaputaina 2014
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    Artigo
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