Medverkande i utredning : Peter Gustavsson

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Carlstedt, David, Chetry, Amit, Larsson, Carl, Purantagi, Ankeet Mohan, Gustavsson, Peter, Larsson, Fredrik och Asp, Leif, Multiscale modeling and calibration framework for predicting the mechanical response of Li-ion battery cell components, Journal of Power Sources, 2025, 659

Sahlin, Ellika, Gréen, Anna, Gustavsson, Peter, Lieden, Agne, Nordenskjold, Magnus, Papadogiannakis, Nikos, Pettersson, Karin, Nilsson, Daniel, Jonasson, Jon, Iwarsson, Erik, Sahlin, E, Green, A, Gustavsson, P, Lieden, A, Nordenskjold, M, Papadogiannakis, N, Pettersson, K, Nilsson, D, Jonasson, J, Iwarsson, E, Sahlin, E, Green, A, Gustavsson, P, Lieden, A, Nordenskjold, M, Papadogiannakis, N, Pettersson, K, Nilsson, D, Jonasson, J och Iwarsson, E, Identification of putative pathogenic single nucleotide variants (SNVs) in genes associated with heart disease in 290 cases of stillbirth, PLOS ONE, 2019, 14 nr 1, s. e0210017-e0210017, : Public Library of Science (PLoS)

Georgsson, Susanne, Sahlin, Ellika, Iwarsson, Moa, Nordenskjöld, Magnus, Gustavsson, Peter, Iwarsson, Erik, Georgsson, S, Sahlin, E, Iwarsson, M, Nordenskjold, M, Gustavsson, P och Iwarsson, E, Knowledge and Attitudes Regarding Non-Invasive Prenatal Testing (NIPT) and Preferences for Risk Information among High School Students in Sweden, JOURNAL OF GENETIC COUNSELING, 2017, 26 nr 3, s. 447–454, New York : Wiley

Nilsson, Daniel, Pettersson, Maria, Gustavsson, Peter, Förster, Alisa, Hofmeister, Wolfgang, Wincent, Josephine, Zachariadis, Vasilios, Anderlid, Britt-Marie, Nordgren, Ann, Mäkitie, Outi, Nilsson, D, Pettersson, M, Gustavsson, P, Forster, A, Hofmeister, W, Wincent, J, Zachariadis, V, Anderlid, B-M, Nordgren, A, Makitie, O, Nilsson, D, Pettersson, M, Gustavsson, P, Forster, A, Hofmeister, W, Wincent, J, Zachariadis, V, Anderlid, B-M, Nordgren, A, Makitie, O, Wirta, Valtteri, Käller, Max, Vezzi, Francesco, Lupski, James R., Nordenskjöld, Magnus, Lundberg, Elisabeth Syk, Carvalho, Claudia M. B. och Lindstrand, Anna, Whole-Genome Sequencing of Cytogenetically Balanced Chromosome Translocations Identifies Potentially Pathological Gene Disruptions and Highlights the Importance of Microhomology in the Mechanism of Formation, HUMAN MUTATION, 2017, 38 nr 2, s. 180–192, : Wiley

Sahlin, Ellika, Nordenskjöld, Magnus, Gustavsson, Peter, Wincent, Josephine, Georgsson, Susanne, Iwarsson, Erik, Sahlin, E, Nordenskjold, M, Gustavsson, P, Wincent, J, Georgsson, S och Iwarsson, E, Positive Attitudes towards Non-Invasive Prenatal Testing (NIPT) in a Swedish Cohort of 1,003 Pregnant Women, PLOS ONE, 2016, 11 nr 5, s. e0156088-e0156088, : Public Library of Science (PLoS)

Winberg, Johanna, Berggren, Håkan, Malm, Torsten, Johansson, Sune, Johansson, Jens, Nilsson, Boris, Liedén, Agne, Nordenskjöld, Agneta, Gustavsson, Peter, Nordgren, Ann, Winberg, J, Berggren, H, Malm, T, Johansson, S, Ramgren, JJ, Nilsson, B, Lieden, A, Nordenskjold, A, Gustavsson, P och Nordgren, A, No evidence for mosaic pathogenic copy number variations in cardiac tissue from patients with congenital heart malformations, EUROPEAN JOURNAL OF MEDICAL GENETICS, 2015, 58 nr 3, s. 129–133, : Elsevier BV

Gustavsson, Peter, Samhällskunskapsämnets kris, Vetenskapliga perspektiv på lärande, undervisning och utbildning i olika institutionella sammanhang utbildningsvetenskaplig forskning vid Lunds universitet, 2014,, s. 269–284, Lund : Institutionen för utbildningsvetenskap, Lunds universitet

Winberg, Johanna, Gustavsson, Peter, Papadogiannakis, Nikos, Sahlin, Ellika, Bradley, Frideborg, Nordenskjöld, Edvard, Svensson, Pär-Johan, Annerén, Göran, Iwarsson, Erik, Nordgren, Ann, Winberg, J, Gustavsson, P, Papadogiannakis, N, Sahlin, E, Bradley, F, Nordenskjold, E, Svensson, P-J, Anneren, G, Iwarsson, E, Nordgren, A, Winberg, J, Gustavsson, P, Papadogiannakis, N, Sahlin, E, Bradley, F, Nordenskjold, E, Svensson, P-J, Anneren, G, Iwarsson, E, Nordgren, A och Nordenskjöld, Agneta, Mutation Screening and Array Comparative Genomic Hybridization Using a 180K Oligonucleotide Array in VACTERL Association, PLOS ONE, 2014, 9 nr 1, s. e85313-e85313, : Public Library of Science (PLoS)

Miciol, Frank-Gilles, Hur kulturen påverkar Svensk-Franska affärsrelationer : En studie av gemensamma industriella projekt mellan SAAB Aerospace i Linköping och Dassault Aviation i Paris, 2013, Linköping University Electronic Press, Linköping

Winberg, Johanna, Gustavsson, Peter, Lagerstedt-Robinson, Kristina, Blennow, Elisabeth, Lundin, Johanna, Iwarsson, Erik, Nordenström, Anna, Anderlid, Britt-Marie, Bondeson, Marie-Louise, Nordenskjöld, Agneta, Winberg, J, Gustavsson, P, Lagerstedt-Robinson, K, Blennow, E, Lundin, J, Iwarsson, E, Nordenstrom, A, Anderlid, B-M, Bondeson, M-L, Nordenskjold, A och Nordgren, Ann, Chimerism Resulting From Parthenogenetic Activation and Dispermic Fertilization, AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2010, 152A nr 9, s. 2277–2286, : Wiley

Gustavsson, Peter och Solymossy, Emeric, Maximizing Values through the ATLANTIS Program, Joint and double degree programs, 2009, New York : Freie Universität Berlin, Institute of International Education

Högberg, Örjan, Maktlösa makthavare : En studie om kommunalt chefskap, 2007, Linköping University Electronic Press, Linköping

Gustavsson, Peter, Klar, Joakim, Matsson, Hans, Forestier, Erik, Henter, Jan-Inge, Rao, Sreedhar, Seip, Martin, Skeppner, Gunnar och Dahl, Niklas, Familial transient erythroblastopenia of childhood is associated with the chromosome, Br J Haematol, 2002, 119 nr 1, s. 261–4

Gustavsson, Peter, Klar, Joakim, Matsson, Hans, Forestier, Erik, Henter, Jan-Inge, Rao, Sreedhar, Seip, Martin, Skeppner, Gunnar och Dahl, Niklas, Familial transient erythroblastopenia of childhood is associated with the chromosome 19q13.2 region but not caused by mutations in coding sequences of the ribosomal protein S19 (RPS19) gene, Br J Haematol och BRITISH JOURNAL OF HAEMATOLOGY, 2002, 119 nr 1, s. 261–264 och 119 nr 1, s. 261–264, : Wiley och : Wiley

Jonsson, Leif, Gustavsson, Peter, Arnell, Sven-Inge, Högberg, Örjan och Jonsson, Robert, Kommunchefers chefskap : ett lokalt präglat chefskap i politisk miljö, 2002, Nya Doxa, Nora

Calori, R, Melin, L, Atamer, T och Gustavsson, Peter, Innovative international strategies, Journal of World Business, 2000, 35 nr 4, s. 333–354

Carling, Tobias, Szabo, Eva, Bai, Mei, Ridefelt, Peter, Westin, Gunnar, Gustavsson, Peter, Trivedi, Sunita, Hellman, Per, Brown, Edward M., Dahl, Niklas och Rastad, Jonas, Familial hypercalcemia and hypercalciuria caused by a novel mutation in the cytoplasmic tail of the calcium receptor, Journal of Clinical Endocrinology and Metabolism, 2000, 85 nr 5, s. 2042–7

Gustavsson, Peter, Diamond-Blackfan anemia : Mapping and identification of the disease gene, 2000, Acta Universitatis Upsaliensis, Uppsala

Roland, Calori, Melin, Leif, Atamer, T och Gustavsson, Peter, Innovative international strategies, Journal of World Business, 2000, 35 nr 4, s. 333–354, : Elsevier BV

Tentler, Dmitry, Gustavsson, Peter, Elinder, Göran, Eklöf, Ole, Gordon, Laurie, Mandel, Ariane, Dahl, Niklas, Tentler, D, Gustavsson, P, Elinder, G, Eklöf, O, Gordon, L, Mandel, A och Dahl, N, A microdeletion in 19q13.2 associated with mental retardation, skeletal malformations, and Diamond-Blackfan anaemia suggests a novel contiguous gene syndrome, JOURNAL OF MEDICAL GENETICS, 2000, 37 nr 2, s. 128–131, : BMJ

Draptchinskaia, Natalia, Gustavsson, Peter, Andersson, Björn, Pettersson, Monica, Willig, Thiébaut-Noël, Dianzani, Irma, Ball, Sarah, Tchernia, Gil, Klar, Joakim, Matsson, Hans, Tentler, Dimitri, Mohandas, Narla, Carlsson, Birgit och Dahl, Niklas, The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemia, Nature Genetics, 1999, 21 nr 2, s. 169–75, : Springer Science and Business Media LLC

Matsson, Hans, Klar, Joakim, Darptchinskaia, Natalia, Gustavsson, Peter, Carlsson, Birgit, Bowers, Daniel, de Bont, Eveline och Dahl, Niklas, Truncating ribosomal protein S19 mutations and variable clinical expression in Diamond-Blackfan anemia, Human Genetics, 1999, 105, s. 496–500

Matsson, Hans, Klar, Joakim, Draptchinskaia, Natalia, Gustavsson, Peter, Carlsson, Birgit, Bowers, Daniel, de Bont, Eveline och Dahl, Niklas, Truncating ribosomal protein S19 mutations and variable clinical expression in Diamond-Blackfan anemia, Human Genetics, 1999, 105 nr 5, s. 496–500, : Springer Science and Business Media LLC

Gustavsson, Peter, Melin, Leif och Macdonald, S, Learning to Glocalize, Advances in Strategic Management, 1994, 10 B, s. 255–288

Gustavsson, Peter, Dadfar, Hossein och Wahlbin, Clas, Structural change and strategic behaviour within the Swedish building sector : the interaction between strategy, organization and environment in individual firms, 1994, Swedish Council for Building Research, Stockholm