Medverkande i utredning : Katarina Lindahl

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Lindahl, Katarina, Att utveckla en högskolepedagogisk kurs om nätbaserad undervisning: design för engagemang och gemenskap, NU2026, 2026

Lindahl, Katarina, Reflektioner kring portföljarbetet och erfarenheter av att bli excellent lärare, Pedagogisk meritering i och för förändring. Red: Åsa Ryegård & Katarina Winka, 2025,, s. 189–201, : Mälardalens universitet

Lindahl, Katarina, Connecting Teacher Education to Research and Practice, ISSOTL 2023, Amsterdam, Nederländerna, 2023

Lindahl, Katarina, Collaborative writing in group work, Designing Courses with Digital Technologies, 2021,, s. 52–56, New York : Routledge

Lindahl, Katarina, Kollaborativa arbetsformer i nätbaserad undervisning, 2020

Lindahl, Katarina, Online teaching through information and communications technology, 2020

Lindahl, Katarina och Svensson, Joacim, Kurser på tillgängligt sätt genom modern teknik och god pedagogik, 2019

Lindahl, Katarina, Teaching Teacher Students through Innovative Teaching Approaches in Online Learning, 12th International Conference Innovation in Language Learning, 2019,, s. 386–389, Florence

Lindahl, Katarina, Engelskdidaktik i ett omvänt klassrum, Digitalisering av högre utbildning, 2018,, s. 163–167, Lund : Studentlitteratur AB

Lindahl, Katarina, Astrom, Eva, Dragomir, Anca, Symoens, Sofie, Coucke, Paul, Larsson, Sune, Paschalis, Eleftherios, Roschger, Paul, Gamsjaeger, Sonja, Klaushofer, Klaus, Fratzl-Zelman, Nadja och Kindmark, Andreas, Homozygosity for CREB3L1 premature stop codon in first case of recessive osteogenesis imperfecta associated with OASIS-deficiency to survive infancy, Bone, 2018, 114, s. 268–277, : Elsevier BV

Andersson, Kristofer, Dahllöf, Goran, Lindahl, Katarina, Kindmark, Andreas, Grigelioniene, Giedre, Åström, Eva, Malmgren, Barbro, Andersson, K, Dahllof, G, Lindahl, K, Kindmark, A, Grigelioniene, G, Astrom, E och Malmgren, B, Mutations in COL1A1 and COL1A2 and dental aberrations in children and adolescents with osteogenesis imperfecta – A retrospective cohort study, PLOS ONE, 2017, 12 nr 5, s. e0176466-e0176466, : Public Library of Science (PLoS)

Lindahl, Katarina, Vocational English : The gap between policy and practice, 2017

Malmgren, B., Andersson, K., Lindahl, Katarina, Kindmark, Andreas, Grigelioniene, G., Zachariadis, V., Dahllof, G, Astrom, E., Malmgren, B, Andersson, K, Lindahl, K, Kindmark, A, Grigelioniene, G, Zachariadis, V, Dahllof, G, Astrom, E, Malmgren, B, Andersson, K, Lindahl, K, Kindmark, A, Grigelioniene, G, Zachariadis, V, Dahllof, G, Astrom, E, Malmgren, B, Andersson, K, Lindahl, K, Kindmark, A, Grigelioniene, G, Zachariadis, V, Dahllof, G och Astrom, E, Tooth agenesis in osteogenesis imperfecta related to mutations in the collagen type I genes, ORAL DISEASES, 2017, 23 nr 1, s. 42–49, : Wiley

Lindahl, Katarina, Kindmark, Andreas, Rubin, Carl-Johan, Malmgren, B., Grigelioniene, G., Soderhall, S., Ljunggren, Östen, Åstrom, E., Lindahl, K, Kindmark, A, Rubin, C-J, Malmgren, B, Grigelioniene, G, Soderhall, S, Ljunggren, O, Astrom, E, Lindahl, K, Kindmark, A, Rubin, C-J, Malmgren, B, Grigelioniene, G, Soderhall, S, Ljunggren, O, Astrom, E, Lindahl, K, Kindmark, A, Rubin, C-J, Malmgren, B, Grigelioniene, G, Soderhall, S, Ljunggren, O och Astrom, E, Decreased fracture rate, pharmacogenetics and BMD response in 79 Swedish children with osteogenesis imperfecta types I, III and IV treated with Pamidronate, BONE, 2016, 87, s. 11–18, : Elsevier BV

Lindahl, Katarina, Astrom, Eva, Rubin, Carl-Johan, Grigelioniene, Giedre, Malmgren, Barbro, Ljunggren, Östen, Kindmark, Andreas, Lindahl, K, Astrom, E, Rubin, C-J, Grigelioniene, G, Malmgren, B, Ljunggren, O, Kindmark, A, Lindahl, K, Astrom, E, Rubin, C-J, Grigelioniene, G, Malmgren, B, Ljunggren, O, Kindmark, A, Lindahl, K, Astrom, E, Rubin, C-J, Grigelioniene, G, Malmgren, B, Ljunggren, O och Kindmark, A, Genetic epidemiology, prevalence, and genotype-phenotype correlations in the Swedish population with osteogenesis imperfecta, EUROPEAN JOURNAL OF HUMAN GENETICS, 2015, 23 nr 8, s. 1042–1050, : Springer Science and Business Media LLC

Lindahl, Katarina, Vocational English in policy and practice, 2015, Göteborgs universitet, Göteborg

Lindahl, Katarina, Langdahl, Bente, Ljunggren, Östen och Kindmark, Andreas, Therapy of Endocrine Disease : Treatment of osteogenesis imperfecta in adults, European Journal of Endocrinology, 2014, 171 nr 2, s. R79-R90, : Oxford University Press (OUP)

Lindahl, Katarina, Kindmark, Andreas, Laxman, Navya, Åström, Eva, Rubin, Carl-Johan och Ljunggren, Östen, Allele Dependent Silencing of Collagen Type I Using Small Interfering RNAs Targeting 3'UTR Indels : a Novel Therapeutic Approach in Osteogenesis Imperfecta, International Journal of Medical Sciences, 2013, 10 nr 10, s. 1333–1343, : Ivyspring International Publisher

Lindahl, Katarina, Osteogenesis Imperfecta : Genetic and Therapeutic Studies, 2013, Acta Universitatis Upsaliensis, Uppsala

Lindahl, Katarina, Rubin, Carl-Johan, Astrom, E., Malmgren, B., Kindmark, Andreas och Ljunggren, Östen, Genotype-phenotype correlations and pharmacogenetic studies in 140 Swedish families with osteogenesis imperfecta, Bone, 2012, 50, s. S109-S109, : Elsevier BV

Lindahl, Katarina, Barnes, Aileen M., Fratzl-Zelman, Nadja, Whyte, Michael P., Hefferan, Theresa E., Makareeva, Elena, Brusel, Marina, Yaszemski, Michael J., Rubin, Carl-Johan, Kindmark, Andreas, Roschger, Paul, Klaushofer, Klaus, McAlister, William H., Mumm, Steven, Leikin, Sergey, Kessler, Efrat, Boskey, Adele L., Ljunggren, Östen och Marini, Joan C., COL1 C-Propeptide Cleavage Site Mutations Cause High Bone Mass Osteogenesis Imperfecta, Human Mutation, 2011, 32 nr 6, s. 598–609, : Hindawi Limited

Ljunggren, Östen, Lindahl, Katarina, Rubin, Carl-Johan och Kindmark, Andreas, Allele-Specific Gene Silencing in Osteogenesis Imperfecta, Cartilage and Bone Development and Its Disorders och Endocrine Development, 2011, 21, s. 85–90 och 21, s. 85–90, : S. Karger AG och : S. Karger AG

Lindahl, Katarina, Rubin, Carl-Johan, Brändström, Helena, Karlsson, Magnus K., Holmberg, Anna H, Ohlsson, Claes, Mellström, Dan, Orwoll, Eric, Mallmin, Hans, Kindmark, Andreas och Ljunggren, Östen, Heterozygosity for a coding SNP in COL1A2 confers a lower BMD and an increased stroke risk., Biochemical and biophysical research communications, 2009, 384 nr 4, s. 501–5, : Elsevier BV

Lindahl, Katarina, Rubin, Carl-Johan, Kindmark, Andreas och Ljunggren, Östen, Allele dependent silencing of COL1A2 using small interfering RNAs, International Journal of Medical Sciences, 2008, 5 nr 6, s. 361–365

Lindahl, Katarina, Åström, Eva, Rubin, Carl-Johan, Söderhäll, Stefan, Malmgren, Barbro, Kindmark, Andreas och Ljunggren, Östen, Genotype-Phenotype Correlations, Response to Bisphosphonate Treatment and Pharmaco-genetics in 150 Swedish Families with Osteogenesis Imperfecta (Type I, IV and III)