Videnskabelige artikler (peer-review)

2020

Damsbo AG, Kraglund KL, Buttenschøn, Johnsen SP, Andersen G, Mortensen JK. Predictors for wellbeing and characteristics of mental health after stroke. J Affect Disord. 2020 Mar 1;264:358-364

Normann C, Buttenschøn HN. Gene-environment interactions between HPA-axis genes and childhood maltreatment in depression: a systematic review. Acta Neuropsychiatrica 2020 Jan 6:1-11 epub ahead of print

2019

Glanville KP, Coleman JRI, Hanscombe KB, Euesden J, Choi SW, Purves KL, Breen G, Air TM, Andlauer TFM, Baune BT, Binder EB, Blackwood DHR, Boomsma DI, Buttenschøn HN, Colodro-Conde L, Dannlowski U, Direk N, Dunn EC, Forstner AJ, de Geus EJC, Grabe HJ, Hamilton SP, Jones I, Jones LA, Knowles JA, Kutalik Z, Levinson DF, Lewis G, Lind PA, Lucae S, Magnusson PK, McGuffin P, McIntosh AM, Milaneschi Y, Mors O, Mostafavi S, Müller-Myhsok B, Pedersen NL, Penninx BWJH, Potash JB, Preisig M, Ripke S, Shi J, Shyn SI, Smoller JW, Streit F, Sullivan PF, Tiemeier H, Uher R, Van der Auwera S, Weissman MM; Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, O'Reilly PF, Lewis CM. Classical Human Leukocyte Antigen Alleles and C4 Haplotypes Are Not Significantly Associated With Depression. Biol Psychiatry. 2019 [Epub ahead of print] PMID: 31570195

Normann C, Buttenschon HN. Gene-environment interactions between HPA-axis genes and stressful life events in depression: a systematic review. Acta Neuropsychiatr 2019 May 20;31(4):186-192

Damsbo AG, Kraglund KL, Buttenschon HN, Johnsen SP, Andersen G, Mortensen JK. Serotonergic Regulation and Cognition after Stroke: The Role of Antidepressant Treatment and Genetic Variation. Cerebrovasc Dis 2019 Mar 7;47(1-2):72-79

2018

Mohammadnejad A, Brasch-Andersen C, Li W, Haagerup A, Baumbach J, Tan Q. A case-only genome-wide association study on gene-sex interaction in allergic rhinitis. Ann Allergy Asthma Immunol. 2018 Sep;121(3):366-367.e2.

Graversen L, Haagerup A, Andersen B, Petersen K, Gjørup V, Gumundsdottir G, Vogel I, Gregersen P. Novel TRPV4 mutation causes a severe form of metatropic dysplasia. Clin Case Report. 2018 Jul 20;6(9):1774-1778.

Ejerskov C, Krogh K, Ostergaard J, Joensson I, Haagerup A
Gastrointestinal Symptoms in Children and Adolescents With Neurofibromatosis Type 1. J Pediatr Gastroenterol Nutr. 2018 Jun;66(6):872-875.

2017

Doherty MA, Hertel NT, Hove HB, Haagerup A (2017). Neurological symptoms, evaluation and treatment in Danish patients with achondroplasia and hypochondroplasia. J Rare Dis Res Treat 2(4): 25-32 Open access.

Ejerskov C, Krogh K, Ostergaard JR, Fassov JL, Haagerup A (2017). Constipations in adults with neurofibromatosis type 1. Orphanet J Rare Dis 12: 139-143.

Elmholdt EM, Skewes J, Dietz, Møller A, Jensen MS, Roepsdorff, Wiech K, Jensen TS. (2017). Reduced Pain Sensation and Reduced BOLD Signal in Parietofrontal Networks during Religious Prayer. Front Hum Neurosci. 28;11:337

Jorgensen LB, Mikkelsen LR, Noe BB, Vesterby M, Uhd M, Fridlund B (2017). The psychosocial effect of web-based information in fast-track surgery. Health Informatics J 23: 304-18

Moosa S, Haagerup A, Gregersen PA, Kastbjerg K, Altmüller J, Thiele H, Nürnberg P, Cho TJ, Kim OH, Nishimura G, Wollnik B, Vogel I (2017). Confirmation of CAGSSS syndrome as a distinct entity in a Danish patient with a novel homozygous mutation in IARS2. Am J Med Genet 173:1102-08.

Noe BB, Stapelfeldt,C.M, Parner ET, Mikkelsen EM (2017). Survival after traumatic spinal cord injury in Denmark: a hospital-based study among patients injured in 1990-2012. Spinal Cord 55: 373-77

Parsons CE, Young KS, Petersen MV, Jegindoe Elmholdt EM, Vuust P, Stein A, Kringelbach ML (2017). Duration of motherhood has incremental effects on mothers' neural processing of infant vocal cues: a neuroimaging study of women. Scientific reports, 7(1):1727.

2016

Pedersen CE, Farholt S, Skovby F, Vestergaard EM, Haagerup A (2016). Twenty-three half-sibs from a mosaic neurofibromatosis type 1 sperm donor – a clinical presentation. Clin Genet 89:346-50.

Forskningsårsprojekt

Clinical and genetic evaluation of Danish patients with pyknodysostosis. Mia Aagaard Doherty, NIDO | danmark, Hospitalsenheden Vest and Department of Clinical Medicine, Aarhus University, 2017.

Ph.d.-afhandling

Gastrointestinal symptoms and NF1 mutational spectrum in neurofibromatosis type 1. Cecilie Ejerskov, NIDO | danmark, Staben, Hospitalsenheden Vest and Department of Clinical Medicine, Aarhus University, 2017.

Øvrige publikationer

Dialogisk dokumentation som metode og kommunikationsmiddel i hospice- og hospitalsvæsenet, Simon Berg. NIDO | danmark, Hospitalsenheden Vest og Institut for Kommunikation, Aalborg Universitet, bogkapitel, 2020.