Zobrazeno 1 - 10
of 73
pro vyhledávání: '"Jane H. Christensen"'
Autor:
Lise Bols Toustrup, Yan Zhou, Helene Kvistgaard, Niels Gregersen, Søren Rittig, Lars Aagaard, Thomas Juhl Corydon, Yonglun Luo, Jane H. Christensen
Publikováno v:
Stem Cell Research, Vol 19, Iss , Pp 37-42 (2017)
Autosomal dominant familial neurohypophyseal diabetes insipidus (adFNDI) is caused by variants in the arginine vasopressin (AVP) gene. Here we report the generation of induced pluripotent stem cells (iPSCs) from a 42-year-old man carrying an adFNDI c
Externí odkaz:
https://doaj.org/article/5ced2f43fe4c49b28bfe1a2e265051eb
Autor:
Raffaella Magnoni, Johan Palmfeldt, Jane H. Christensen, Majken Sand, Francesca Maltecca, Thomas J. Corydon, Mark West, Giorgio Casari, Peter Bross
Publikováno v:
Neurobiology of Disease, Vol 54, Iss , Pp 12-23 (2013)
Cells rely on efficient protein quality control systems (PQCs) to maintain proper activity of mitochondrial proteins. As part of this system, the mitochondrial chaperone Hsp60 assists folding of matrix proteins and it is an essential protein in all o
Externí odkaz:
https://doaj.org/article/91b06909bdc747fc8009aca9d0a4d561
Autor:
Per Qvist, Johan Palmfeldt, Jane H. Christensen, Anders Lade Nielsen, Ole N. Jensen, Pavel V. Shliaha, Anders D. Børglum, Julie G. Donskov, Ole Mors, Anders Valdemar Edhager, Veerle Paternoster
Publikováno v:
Paternoster, V, Edhager, A V, Qvist, P, Donskov, J G, Shliaha, P, Jensen, O N, Mors, O, Nielsen, A L, Børglum, A D, Palmfeldt, J & Christensen, J H 2021, ' Inactivation of the Schizophrenia-associated BRD1 gene in Brain Causes Failure-to-thrive, Seizure Susceptibility and Abnormal Histone H3 Acetylation and N-tail Clipping ', Molecular Neurobiology, vol. 58, no. 9, pp. 4495-4505 . https://doi.org/10.1007/s12035-021-02432-8
Genetic studies have repeatedly shown that the Bromodomain containing 1 gene, BRD1, is involved in determining mental health, and the importance of the BRD1 protein for normal brain function has been studied in both cell models and constitutive haplo
Autor:
Hreinn Stefansson, Esben Agerbo, Konstantinos Kamperis, Ole Mors, Viðar Örn Eðvarðsson, Thomas Werge, Ditte Demontis, Jane H. Christensen, Veera M. Rajagopal, Mette Nyegaard, Merete Nordentoft, Jakob Grove, Thomas Damm Als, Preben Bo Mortensen, Anders D. Børglum, Henriette Thisted Horsdal, Cecilie Siggaard Jørgensen, G. Bragi Walters, Kari Stefansson, David M. Hougaard, Søren Rittig
Publikováno v:
Jørgensen, C S, Horsdal, H T, Rajagopal, V M, Grove, J, Als, T D, Kamperis, K, Nyegaard, M, Walters, G B, Eðvarðsson, V Ö, Stefánsson, H, Nordentoft, M, Hougaard, D M, Werge, T, Mors, O, Mortensen, P B, Agerbo, E, Rittig, S, Stefánsson, K, Børglum, A D, Demontis, D & Christensen, J H 2021, ' Identification of genetic loci associated with nocturnal enuresis : a genome-wide association study ', The Lancet Child and Adolescent Health, vol. 5, no. 3, pp. 201-209 . https://doi.org/10.1016/S2352-4642(20)30350-3
Background: Nocturnal enuresis (bedwetting) is a common disorder affecting 10–16% of 7-year-old children globally. Nocturnal enuresis is highly heritable, but its genetic determinants remain unknown. We aimed to identify genetic variants associated
Autor:
Sara A. Paciga, Richard M. Weinshilboum, Andrew M. McIntosh, Tim B. Bigdeli, Stephanie H. Witt, Sven Cichon, Glyn Lewis, Henning Teismann, Brenda W.J.H. Penninx, Gerome Breen, Roseann E. Peterson, Saira Saeed Mirza, Diego Albani, Lisa Jones, Andreas J. Forstner, Sara Mostafavi, Julien Bryois, Qingqin S. Li, Kenneth S. Kendler, Thomas Damm Als, Fernando S. Goes, Marie Bækvad-Hansen, Nancy L. Pedersen, Gianluigi Forloni, Per Qvist, Carsten Horn, Per Hoffmann, Steven P. Hamilton, Georg Homuth, Michael Gill, Julien Mendlewicz, Katharina Domschke, Volker Arolt, Adrian I. Campos, Christine Søholm Hansen, Scott D. Gordon, Hogni Oskarsson, Peter McGuffin, Oliver Pain, Eric Jorgenson, Victoria S. Marshe, Stacy Steinberg, Bertram Müller-Myhsok, Mark Adams, J. Raymond DePaulo, Rick Jansen, Katherine J. Aitchison, Vassily Trubetskoy, Henry Völzke, Manuel Mattheisen, Bernard Ng, James A. Knowles, Dorret I. Boomsma, Tracy Air, Elisabeth B. Binder, Ian B. Hickie, Christel M. Middeldorp, Tõnu Esko, David M. Hougaard, E.J.C. de Geus, Toni-Kim Clarke, Helena Gaspar, Bernhard T. Baune, Abdel Abdellaoui, Engilbert Sigurdsson, Andres Metspalu, Klaus Berger, Jorge A. Quiroz, Patrick F. Sullivan, Aartjan T.F. Beekman, Thomas Hansen, Panagiotis Ferentinos, Jürgen Wellmann, Miguel E. Rentería, Daniel Umbricht, Marcella Rietschel, Stanley I. Shyn, Chiara Fabbri, Hreinn Stefansson, Jerome C. Foo, Daniel Souery, Zoltán Kutalik, Yu-Li Liu, Paul F. O'Reilly, Michael John Owen, Nese Direk, Douglas F. Levinson, Stuart Montgomery, Hamdi Mbarek, David M. Howard, Guido Bondolfi, Lucía Colodro-Conde, Pippa A. Thomson, Merete Nordentoft, Stefan Kloiber, Yunpeng Wang, Michael Conlon O'Donovan, Grant C.B. Sinnamon, Alexander Viktorin, Hilary K. Finucane, Esben Agerbo, Stefan Herms, Markus M. Nöthen, Till F. M. Andlauer, Divya Mehta, Bradley T. Webb, Joanna M. Biernacka, David J. Porteous, Jordan W. Smoller, Jonathan R. I. Coleman, Dean F. MacKinnon, Farnush Farhadi Hassan Kiadeh, Baptiste Couvy-Duchesne, Evelin Mihailov, Eleanor M. Wigmore, Franziska Degenhardt, Jianxin Shi, Dale R. Nyholt, Enda M. Byrne, Stephan Ripke, Ole Mors, Patrik K. E. Magnusson, Eric J. Lenze, Warren W. Kretzschmar, Masaki Kato, Marcus Ising, Ian Jones, Lynsey S. Hall, Wouter J. Peyrot, Ling Shen, Nader Perroud, Na Cai, Maciej Trzaskowski, Matthias Nauck, Isaac S. Kohane, Enrico Domenici, Fabian Streit, James L. Kennedy, Peter M. Visscher, Valentina Escott-Price, Donald J. MacIntyre, Enrique Castelao, Margarita Rivera, Mojca Z. Dernovsek, John P. Rice, Joseph Zohar, Gail Davies, Andrew C. Heath, Josef Frank, Wesley K. Thompson, Caroline Hayward, Penelope A. Lind, Thorgeir E. Thorgeirsson, Rudolf Uher, Jana Strohmaier, Henriette N. Buttenschøn, Erin C. Dunn, Jonas Bybjerg-Grauholm, Alexander Teumer, Jakob Grove, Eske M. Derks, Nicholas G. Martin, Jodie N. Painter, Myrna M. Weissman, Preben Bo Mortensen, Michel G. Nivard, Catherine Schaefer, Yihan Li, Daniel J. Smith, Shih-Jen Tsai, Niamh Mullins, Jian Yang, Marianne Giørtz Pedersen, Dan Rujescu, Thomas G. Schulze, Lili Milani, Yuri Milaneschi, Giorgio Pistis, James B. Potash, Neven Henigsberg, Nicholas John Craddock, Karen Hodgson, Silviu-Alin Bacanu, Shantel Weinsheimer, Charles F. Reynolds, Johannes H. Smit, Gonneke Willemsen, Futao Zhang, Henning Tiemeier, Grant W. Montgomery, Martin Preisig, Udo Dannlowski, Thalia C. Eley, Thomas Werge, Katherine E. Tansey, Jane H. Christensen, Julia Kraft, Ian J. Deary, Cathryn M. Lewis, Sarah E. Medland, André G. Uitterlinden, Daniel J. Müller, Carsten Bøcker Pedersen, Gustavo Turecki, Hans J. Grabe, Matthew Traylor, Brien P. Riley, Roy H. Perlis, Patrick J. McGrath, Conor V. Dolan, Hualin S. Xi, Jonathan Marchini, Robert A. Schoevers, Albert M. van Hemert, Anders D. Børglum, Susanne Lucae, Jouke-Jan Hottenga, Kari Stefansson, Benoit H. Mulsant, Francis M. Mondimore, Naomi R. Wray, Yang Wu, Wolfgang Maier, Danielle Posthuma, Annamaria Cattaneo, Gregory E. Crawford, Siegfried Kasper, Alessandro Serretti, Tania Carrillo-Roa, Robert Maier, Pamela A. F. Madden, Eva C. Schulte, Jens Treutlein, Joanna Hauser, Sandra Van der Auwera
Publikováno v:
GSRD Consortium & Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium 2022, ' Identifying the Common Genetic Basis of Antidepressant Response ', Biological Psychiatry Global Open Science, vol. 2, no. 2, pp. 115-126 . https://doi.org/10.1016/j.bpsgos.2021.07.008
Pain, O, Hodgson, K, Trubetskoy, V, Ripke, S, Marshe, V S, Adams, M J, Byrne, E M, Campos, A I, Carrillo-Roa, T, Cattaneo, A, Als, T D, Souery, D, Dernovsek, M Z, Fabbri, C, Hayward, C, Henigsberg, N, Hauser, J, Kennedy, J L, Lenze, E J, Lewis, G, Müller, D J, Martin, N G, Mulsant, B H, Mors, O, Perroud, N, Porteous, D J, Rentería, M E, Reynolds, C F, Rietschel, M, Uher, R, Wigmore, E M, Maier, W, Wray, N R, Aitchison, K J, Arolt, V, Baune, B T, Biernacka, J M, Bondolfi, G, Domschke, K, Kato, M, Li, Q S, Liu, Y-L, Serretti, A, Tsai, S-J, Turecki, G & Weinshilboum, R & McIntosh, A M & Lewis, C M 2022, ' Identifying the Common Genetic Basis of Antidepressant Response ', Biological psychiatry global open science, vol. 2, no. 2, pp. 115-126 . https://doi.org/10.1016/j.bpsgos.2021.07.008
Biological Psychiatry Global Open Science, 2(2), 115-126. Elsevier BV
McIntosh, A M, Lewis, C M, GSRD Consortium & Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium 2022, ' Identifying the Common Genetic Basis of Antidepressant Response ', Biological Psychiatry: Global Open Science, vol. 2, no. 2, pp. 115-126 . https://doi.org/10.1016/j.bpsgos.2021.07.008
Biological psychiatry: global open science 2(2), 115-126 (2022). doi:10.1016/j.bpsgos.2021.07.008
Biological Psychiatry Global Open Science, 2(2), 115-126
Biological Psychiatry Global Open Science, 2(2), 115-126. Elsevier
Pain, O, Hodgson, K, Trubetskoy, V, Ripke, S, Marshe, V S, Adams, M J, Byrne, E M, Campos, A I, Carrillo-Roa, T, Cattaneo, A, Als, T D, Souery, D, Dernovsek, M Z, Fabbri, C, Hayward, C, Henigsberg, N, Hauser, J, Kennedy, J L, Lenze, E J, Lewis, G, Müller, D J, Martin, N G, Mulsant, B H, Mors, O, Perroud, N, Porteous, D J, Rentería, M E, Reynolds, C F, Rietschel, M, Uher, R, Wigmore, E M, Maier, W, Wray, N R, Aitchison, K J, Arolt, V, Baune, B T, Biernacka, J M, Bondolfi, G, Domschke, K, Kato, M, Li, Q S, Liu, Y-L, Serretti, A, Tsai, S-J, Turecki, G & Weinshilboum, R & McIntosh, A M & Lewis, C M 2022, ' Identifying the Common Genetic Basis of Antidepressant Response ', Biological psychiatry global open science, vol. 2, no. 2, pp. 115-126 . https://doi.org/10.1016/j.bpsgos.2021.07.008
Biological Psychiatry Global Open Science, 2(2), 115-126. Elsevier BV
McIntosh, A M, Lewis, C M, GSRD Consortium & Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium 2022, ' Identifying the Common Genetic Basis of Antidepressant Response ', Biological Psychiatry: Global Open Science, vol. 2, no. 2, pp. 115-126 . https://doi.org/10.1016/j.bpsgos.2021.07.008
Biological psychiatry: global open science 2(2), 115-126 (2022). doi:10.1016/j.bpsgos.2021.07.008
Biological Psychiatry Global Open Science, 2(2), 115-126
Biological Psychiatry Global Open Science, 2(2), 115-126. Elsevier
Background: Antidepressants are a first-line treatment for depression. However, only a third of individuals experience remission after the first treatment. Common genetic variation, in part, likely regulates antidepressant response, yet the success o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c907fa773f30e9647559b297edd74e1d
https://pure.au.dk/portal/da/publications/identifying-the-common-genetic-basis-of-antidepressant-response(7255846b-ac58-462b-be46-77e5e1468621).html
https://pure.au.dk/portal/da/publications/identifying-the-common-genetic-basis-of-antidepressant-response(7255846b-ac58-462b-be46-77e5e1468621).html
Autor:
Antonio Brunetti, Eusebio Chiefari, Jane Hagelskjær Knudsen, Daniela Foti, Vera Tocci, Maria Mirabelli, Jane H. Christensen, Antonio Aversa, Domenico La Torre, Helene Kvistgaard, Stefania Giuliano
Publikováno v:
Tocci, V, Mirabelli, M, Giuliano, S, Chiefari, E, Knudsen, J H, Kvistgaard, H, La Torre, D, Aversa, A, Foti, D P, Christensen, J H & Brunetti, A 2021, ' A Partial Phenotype of adFNDI Related to the Signal Peptide c.55G >A Variant of the AVP Gene ', Endocrines, vol. 2, no. 1, pp. 37-43 . https://doi.org/10.3390/endocrines2010004
Endocrines, Vol 2, Iss 4, Pp 37-43 (2021)
Endocrines, Vol 2, Iss 4, Pp 37-43 (2021)
The autosomal dominant familial form of neurohypophyseal diabetes insipidus (adFNDI) is a rare inherited endocrine disorder characterized by hypotonic polyuria, severe thirst and polydipsia, which results from a deficient neurosecretion of the antidi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1bd83ad389703e084b5fee966916bf43
https://pure.au.dk/portal/da/publications/a-partial-phenotype-of-adfndi-related-to-the-signal-peptide-c55ga-variant-of-the-avp-gene(28819d0c-8c01-4f66-b58a-6621b30f1c8d).html
https://pure.au.dk/portal/da/publications/a-partial-phenotype-of-adfndi-related-to-the-signal-peptide-c55ga-variant-of-the-avp-gene(28819d0c-8c01-4f66-b58a-6621b30f1c8d).html
Autor:
Anders D. Børglum, Jane H. Christensen
Publikováno v:
Christensen, J H & Børglum, A D 2019, ' Modeling the cooperativity of schizophrenia risk genes ', Nature Genetics, vol. 51, no. 10, pp. 1434-1436 . https://doi.org/10.1038/s41588-019-0508-6
Common genetic variants increase the risk of schizophrenia, but the downstream biological mechanisms are largely unknown. A new study demonstrates that schizophrenia risk genes cause neuronal dysfunction and have synergistic effects on gene expressio
Autor:
Anders D. Børglum, Simon Fristed Eskildsen, Jens R. Nyengaard, Mohammad Baragji, Gregers Wegener, Veerle Paternoster, Jane H. Christensen, Jolien Roovers, Brian Benjamin Hansen, Thomas J. Corydon, Hans Stødkilde-Jørgensen, Simon Glerup, Ole Mors, Simon Molgaard, Steffen Ringgaard, Per Qvist
Publikováno v:
Scientific Reports, Vol 8, Iss 1, Pp 1-12 (2018)
Scientific Reports
Qvist, P, Eskildsen, S F, Hansen, B, Baragji, M, Ringgaard, S, Roovers, J, Paternoster, V, Molgaard, S, Corydon, T J, Stødkilde-Jørgensen, H, Glerup, S, Mors, O, Wegener, G, Nyengaard, J R, Børglum, A D & Christensen, J H 2018, ' Brain volumetric alterations accompanied with loss of striatal medium-sized spiny neurons and cortical parvalbumin expressing interneurons in Brd1+/-mice ', Scientific Reports, vol. 8, no. 1, pp. 16486 . https://doi.org/10.1038/s41598-018-34729-5
Scientific Reports
Qvist, P, Eskildsen, S F, Hansen, B, Baragji, M, Ringgaard, S, Roovers, J, Paternoster, V, Molgaard, S, Corydon, T J, Stødkilde-Jørgensen, H, Glerup, S, Mors, O, Wegener, G, Nyengaard, J R, Børglum, A D & Christensen, J H 2018, ' Brain volumetric alterations accompanied with loss of striatal medium-sized spiny neurons and cortical parvalbumin expressing interneurons in Brd1+/-mice ', Scientific Reports, vol. 8, no. 1, pp. 16486 . https://doi.org/10.1038/s41598-018-34729-5
Schizophrenia is a common and severe mental disorder arising from complex gene-environment interactions affecting brain development and functioning. While a consensus on the neuroanatomical correlates of schizophrenia is emerging, much of its fundame
Autor:
Arne Mørk, Ross Lazarus, Mette Nyegaard, Tue Fryland, Nico Liebenberg, Anders D. Børglum, Jonatan Pallesen, Michael Didriksen, Gregers Wegener, Veerle Paternoster, Bente Pakkenberg, Johan Palmfeldt, Kim Fejgin, Anto P. Rajkumar, Jens R. Nyengaard, Nicoletta Nava, Jane H. Christensen, Per Qvist, Gudrun Winther, Sanne H la Cour, Julie G. Donskov, Ole Mors
Publikováno v:
Rajkumar, A P, Qvist, P, Donskov, J G, Lazarus, R, Pallesen, J, Nava, N, Winther, G, Liebenberg, N, Cour, S H L, Paternoster, V, Fryland, T, Palmfeldt, J, Fejgin, K, Mørk, A, Nyegaard, M, Pakkenberg, B, Didriksen, M, Nyengaard, J R, Wegener, G, Mors, O, Christensen, J H & Børglum, A D 2020, ' Reduced Brd1 expression leads to reversible depression-like behaviors and gene-expression changes in female mice ', Translational Psychiatry, vol. 10, 239 . https://doi.org/10.1038/s41398-020-00914-2
Rajkumar, A P, Qvist, P, Donskov, J G, Lazarus, R, Pallesen, J, Nava, N, Winther, G, Liebenberg, N, Cour, S H L, Paternoster, V, Fryland, T, Palmfeldt, J, Fejgin, K, Mørk, A, Nyegaard, M, Pakkenberg, B, Didriksen, M, Nyengaard, J R, Wegener, G, Mors, O, Christensen, J H & Børglum, A D 2020, ' Reduced Brd1 expression leads to reversible depression-like behaviors and gene-expression changes in female mice ', Translational Psychiatry, vol. 10, no. 1, 239 . https://doi.org/10.1038/s41398-020-00914-2
Translational Psychiatry, Vol 10, Iss 1, Pp 1-14 (2020)
Translational Psychiatry
Rajkumar, A P, Qvist, P, Donskov, J G, Lazarus, R, Pallesen, J, Nava, N, Winther, G, Liebenberg, N, Cour, S H L, Paternoster, V, Fryland, T, Palmfeldt, J, Fejgin, K, Mørk, A, Nyegaard, M, Pakkenberg, B, Didriksen, M, Nyengaard, J R, Wegener, G, Mors, O, Christensen, J H & Børglum, A D 2020, ' Reduced Brd1 expression leads to reversible depression-like behaviors and gene-expression changes in female mice ', Translational Psychiatry, vol. 10, no. 1, 239 . https://doi.org/10.1038/s41398-020-00914-2
Translational Psychiatry, Vol 10, Iss 1, Pp 1-14 (2020)
Translational Psychiatry
The schizophrenia-associated gene, BRD1, encodes an epigenetic regulator in which chromatin interactome is enriched with genes implicated in mental health. Alterations in histone modifications and epigenetic regulation contribute to brain transcripto
Autor:
Jane H. Christensen, Ulf Simonsen, Guillem Pintos-Morell, Susie Mogensen, Ole Hilberg, Ilaria Campo, Are Martin Holm, Francesca Mariani, Maria Del Mar Martinez-Colls, Bruno Crestani, Camille Taillé, Amparo Escribano-Montaner, Elizabeth J. Kopras, Åsa Lina M Jönsson, Elisabeth Bendstrup, Francis X. McCormack
Publikováno v:
Jönsson, Å L M, Bendstrup, E, Mogensen, S, Kopras, E J, McCormack, F X, Campo, I, Mariani, F, Escribano-Montaner, A, Holm, A M, Martinez-Colls, M D M, Pintos-Morell, G, Taillé, C, Crestani, B, Hilberg, O, Hvarregaard Christensen, J & Simonsen, U 2020, ' Eight novel variants in the SLC34A2 gene in pulmonary alveolar microlithiasis ', European Respiratory Journal, vol. 55, no. 2 . https://doi.org/10.1183/13993003.00806-2019
Jönsson, Å L M, Bendstrup, E, Mogensen, S, Kopras, E J, McCormack, F X, Campo, I, Mariani, F, Escribano-Montaner, A, Holm, A M, Martinez-Colls, M D M, Pintos-Morell, G, Taillé, C, Crestani, B, Hilberg, O, Hvarregaard Christensen, J & Simonsen, U 2020, ' Eight novel variants in the SLC34A2 gene in pulmonary alveolar microlithiasis ', The European Respiratory Journal, vol. 55, no. 2, 1900806 . https://doi.org/10.1183/13993003.00806-2019
European Respiratory Journal
r-IGTP: Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
Institut de Recerca Germans Trias i Pujol (IGTP)
r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
Universidad de Alicante (UA)
Jönsson, Å L M, Bendstrup, E, Mogensen, S, Kopras, E J, McCormack, F X, Campo, I, Mariani, F, Escribano-Montaner, A, Holm, A M, Martinez-Colls, M D M, Pintos-Morell, G, Taillé, C, Crestani, B, Hilberg, O, Hvarregaard Christensen, J & Simonsen, U 2020, ' Eight novel variants in the SLC34A2 gene in pulmonary alveolar microlithiasis ', The European Respiratory Journal, vol. 55, no. 2, 1900806 . https://doi.org/10.1183/13993003.00806-2019
European Respiratory Journal
r-IGTP: Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
Institut de Recerca Germans Trias i Pujol (IGTP)
r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
Universidad de Alicante (UA)
BackgroundPulmonary alveolar microlithiasis (PAM) is caused by genetic variants in the SLC34A2 gene, which encodes the sodium-dependent phosphate transport protein 2B (NaPi-2b). PAM is characterised by deposition of calcium phosphate concretions (mic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7883ebd77469718aec1ca5e4170d1b08
https://findresearcher.sdu.dk:8443/ws/files/161754488/13993003.00806_2019.full.pdf
https://findresearcher.sdu.dk:8443/ws/files/161754488/13993003.00806_2019.full.pdf