Vogel, I., Andreasen, L., Balslev-Harder, M.
, Becher, N., Ernst, A., Gadsbøll, K., Hjortshøj, T. D., Hvidbjerg, M. S., Larsen, M.
, Lou, S., Bay Lund, I. C., Pedersen, L. H., Sønderberg Roos, L. K., Sperling, L.
, Sunde, L., Tørring, P. M., Vedel, C.
& Petersen, O. B. (2025).
Whole Genome Sequencing in Prenatal Diagnostics: The Danish Approach to Guideline Formation and Implementation Within Public Healthcare.
Prenatal Diagnosis. Advance online publication.
https://doi.org/10.1002/pd.6780
Zheng, H.-F., Forgetta, V., Hsu, Y.-H., Estrada, K., Rosello-Diez, A., Leo, P. J., Dahia, C. L., Park-Min, K. H., Tobias, J. H., Kooperberg, C., Kleinman, A., Styrkarsdottir, U., Liu, C.-T., Uggla, C., Evans, D. S., Nielson, C. M., Walter, K., Pettersson-Kymmer, U., McCarthy, S. ... AOGC Consortium (2015).
Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture.
Nature,
526(7571), 112-7.
https://doi.org/10.1038/nature14878Jelsig, A. M., van Overeem Hansen, T., Gede, L. B., Qvist, N.
, Christensen, L. L., Lautrup, C. K., Ljungmann, K., Christensen, L. T., Rønlund, K., Tørring, P. M., Bertelsen, B.
, Sunde, L. & Karstensen, J. G. (2023).
Whole genome sequencing and disease pattern in patients with juvenile polyposis syndrome: a nationwide study.
Familial Cancer,
22(4), 429-436.
https://doi.org/10.1007/s10689-023-00338-zKim, S. W., Lee, H., Song, D. Y., Lee, G. H., Ji, J., Park, J. W., Han, J. H., Lee, J. W., Byun, H. J., Son, J. H., Kim, Y. R., Lee, Y., Kim, J., Jung, A., Lee, J., Kim, E., Kim, S. H., Lee, J. H., Satterstrom, F. K. ... An, J. Y. (2024).
Whole genome sequencing analysis identifies sex differences of familial pattern contributing to phenotypic diversity in autism.
Genome Medicine,
16(1), Article 114.
https://doi.org/10.1186/s13073-024-01385-6Nordentoft, I., Lindskrog, S. V., Birkenkamp-Demtröder, K., Gonzalez, S., Kuzman, M., Levatic, J., Glavas, D., Ptashkin, R., Smadbeck, J., Afterman, D., Lauterman, T., Cohen, Y., Donenhirsh, Z., Tavassoly, I., Alon, U.
, Frydendahl, A., Rasmussen, M. H., Andersen, C. L., Lamy, P. ... Dyrskjøt, L. (2024).
Whole-genome Mutational Analysis for Tumor-informed Detection of Circulating Tumor DNA in Patients with Urothelial Carcinoma.
European Urology,
86(4), 301-311.
https://doi.org/10.1016/j.eururo.2024.05.014
McGuffin, P., Knight, J., Breen, G., Brewster, S., Boyd, PR., Craddock, N., Gill, M., Korszun, A., Maier, W., Middleton, L.
, Mors, O., Owen, MJ., Perry, J., Preisig, M., Reich, T., Rice, J., Rietschel, M., Jones, L., Sham, P. & Farmer, AE. (2005).
Whole Genome Linkage Scan of Recurrent Depressive Disorder From the Depression. Network (DeNt) Study.
Hum Mol Genet,
14, 3337-3345.
Stiehler, C.
, Bünger, C., Overall, R. W., Royer, L.
, Schroeder, M., Foss, M., Besenbacher, F., Kruhøffer, M., Kassem, M., Günther, K. P.
& Stiehler, M. (2013).
Whole-genome expression analysis of human mesenchymal stromal cells exposed to ultrasmooth tantalum vs. titanium oxide surfaces.
Cellular and Molecular Bioengineering,
6(2), 199-209.
https://doi.org/10.1007/s12195-012-0255-6Qin, H., Samuels, J. F., Wang, Y., Zhu, Y., Grados, M. A., Riddle, M. A., Greenberg, B. D., Knowles, J. A., Fyer, A. J., McCracken, J. T., Murphy, D. L., Rasmussen, S. A., Cullen, B. A., Piacentini, J., Geller, D., Stewart, S. E., Pauls, D., Bienvenu, O. J., Goes, F. S. ... Shugart, Y. Y. (2015).
Whole-genome association analysis of treatment response in obsessive-compulsive disorder.
Molecular Psychiatry.
https://doi.org/10.1038/mp.2015.32Nordentoft, I. K., Lamy, P., Birkenkamp-Demtröder, K., Vang, S., Reinert, T., Hedegaard, J., Thorsen, K., Fristrup, N., Borre, M., Andersen, L. D., Pedersen, J. S. & Ørntoft, T. F. (2013).
Whole genome and transcriptome analysis reveals novel genomic alterations in bladder cancer. Poster session presented at American Association for Cancer Research, Washington, DC, United States.
Rosenquist, R., Ehrencrona, H.
, Hasle, H., Palle, J. & Kanduri, M. (2013).
Whole-genome-amplified DNA as a source for mutational analysis underestimates the frequency of mutations in pediatric acute myeloid leukemia.
Leukemia,
27(2), 510-512.
https://doi.org/10.1038/leu.2012.250Hokland, P., Simonsen, A. T., Hansen, M. C., Hindkjær, J.
& Aggerholm, A. (2016).
Whole Genome Amplification and Exome Sequencing at the Single Cell Level: A Way to Address Clonal Heterogeneity and Very Sparse Clinical Material. Abstract from 58th ASH Annual Meeting & Exposition, San Diego, United States.
Martín-Arana, J., Gimeno-Valiente, F.
, Henriksen, T. V., García-Micó, B., Martínez-Castedo, B., Gambardella, V., Martínez-Ciarpaglini, C., Palomar, B., Huerta, M., Camblor, D. G., García Bartolomé, M., Carbonell-Asins, J. A.
, Frydendahl, A., Gotchalck, K. A., Fleitas, T., Tébar-Martínez, R., Moro, D., Pla, V., Pérez-Santiago, L. ... Tarazona, N. (2025).
Whole-exome tumor-agnostic ctDNA analysis enhances minimal residual disease detection and reveals relapse mechanisms in localized colon cancer.
Nature Cancer,
6(6), 1000-1016. Article e0008476.
https://doi.org/10.1038/s43018-025-00960-zDemontis, D., Lescai, F., Børglum, A., Glerup, S., Østergaard, S. D., Mors, O., Li, Q., Liang, J., Jiang, H., Li, Y., Wang, J., Lesch, K.-P., Reif, A., Buitelaar, J. K. & Franke, B. (2016).
Whole-Exome Sequencing Reveals Increased Burden of Rare Functional and Disruptive Variants in Candidate Risk Genes in Individuals With Persistent Attention-Deficit/Hyperactivity Disorder.
Journal of the American Academy of Child and Adolescent Psychiatry,
55(6), 521-3.
https://doi.org/10.1016/j.jaac.2016.03.009
Heinz, J. L., Swagemakers, S. M. A., von Hofsten, J., Helleberg, M.
, Thomsen, M. M., De Keukeleere, K., de Boer, J. H., Ilginis, T., Verjans, G. M. G. M., van Hagen, P. M., van der Spek, P. J.
& Mogensen, T. H. (2023).
Whole exome sequencing of patients with varicella-zoster virus and herpes simplex virus induced acute retinal necrosis reveals rare disease-associated genetic variants.
Frontiers in Molecular Neuroscience,
16, Article 1253040.
https://doi.org/10.3389/fnmol.2023.1253040
Hait, A. S., Thomsen, M. M., Larsen, S. M., Helleberg, M.
, Mardahl, M., Barfod, T. S.
, Christiansen, M., Brandt, C.
& Mogensen, T. H. (2021).
Whole-Exome Sequencing of Patients With Recurrent HSV-2 Lymphocytic Mollaret Meningitis.
The Journal of Infectious Diseases,
223(10), 1776-1786.
https://doi.org/10.1093/infdis/jiaa589
Lescai, F., Als, T. D., Li, Q., Nyegaard, M., Andorsdottir, G., Biskopstø, M.
, Hedemand, A., Fiorentino, A., O'Brien, N. L., Jarram, A., Liang, T. J.
, Grove, J., Pallesen, J., Eickhardt, E., Mattheisen, M., Bolund, L., Demontis, D., Wang, A. G., McQuillin, A.
... Børglum, A. D. (2017).
Whole-exome sequencing of individuals from an isolated population implicates rare risk variants in bipolar disorder.
Translational Psychiatry,
7(2), e1034. Article 3.
https://doi.org/10.1038/tp.2017.3
Nissen, S. K., Christiansen, M., Helleberg, M.
, Kjær, K., Jørgensen, S. E., Gerstoft, J., Katzenstein, T. L., Benfield, T., Kronborg, G.
, Larsen, C. S., Laursen, A., Pedersen, G.
, Jakobsen, M. R., Tolstrup, M. & Mogensen, T. H. (2018).
Whole Exome Sequencing of HIV-1 long-term non-progressors identifies rare variants in genes encoding innate immune sensors and signaling molecules.
Scientific Reports,
8(1), 15253. Article 15253.
https://doi.org/10.1038/s41598-018-33481-0
Dembic, M., van Brakel Andersen, L., Larsen, M. J.
, Mechlenburg, I., Søballe, K. & Hertz, J. M. (2023).
Whole exome sequencing of 28 families of Danish descent reveals novel candidate genes and pathways in developmental dysplasia of the hip.
Molecular Genetics and Genomics,
298(2), 329-342.
https://doi.org/10.1007/s00438-022-01980-5Lohmueller, K. E., Sparsø, T. H., Li, Q., Andersson, E., Korneliussen, T. S., Albrechtsen, A., Banasik, K., Grarup, N., Hallgrimsdottir, I., Kiil, K., Kilpeläinen, T., Krarup, N. T., Pers, T. H., Sanchez, G., Hu, Y., Degiorgio, M., Jørgensen, T.
, Sandbæk, A., Lauritzen, T. ... Pedersen, O. (2013).
Whole-exome sequencing of 2,000 Danish individuals and the role of rare coding variants in type 2 diabetes.
American Journal of Human Genetics,
93(6), 1072-86.
https://doi.org/10.1016/j.ajhg.2013.11.005Gregersen, N., Lescai, F., Liang, J., Li, Q.
, Als, T. D., Buttenschøn, H. N., Hedemand, A., Biskopstø, M., Wang, J., Wang, A.
, Børglum, A., Mors, O. & Demontis, D. (2016).
Whole-exome sequencing implicates DGKH as a risk gene for panic disorder in the Faroese population.
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics,
171(8), 1013-1022.
https://doi.org/10.1002/ajmg.b.32464
Herlin, M. K., Le, V. Q., Højland, A. T., Ernst, A., Okkels, H., Petersen, A. C., Petersen, M. B. & Pedersen, I. S. (2019).
Whole-exome sequencing identifies a GREB1L variant in a three-generation family with Müllerian and renal agenesis: a novel candidate gene in Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome. A case report.
Human reproduction (Oxford, England),
34(9), 1838-1846.
https://doi.org/10.1093/humrep/dez126
Escrichs, A., Sanz Perl, Y., Fisher, P. M., Martínez-Molina, N., G-Guzman, E., Frokjaer, V. G.
, Kringelbach, M. L., Knudsen, G. M. & Deco, G. (2025).
Whole-brain turbulent dynamics predict responsiveness to pharmacological treatment in major depressive disorder.
Molecular Psychiatry,
30(3), 1069-1079. Article 110074.
https://doi.org/10.1038/s41380-024-02690-7Ferreri, A. J. M., Cwynarski, K.
, Pulczynski, E., Fox, C. P., Schorb, E., La Rosée, P., Binder, M., Fabbri, A., Torri, V., Minacapelli, E., Falautano, M., Ilariucci, F., Ambrosetti, A., Roth, A., Hemmaway, C., Johnson, P., Linton, K. M., Pukrop, T., Sønderskov Gørløv, J. ... International Extranodal Lymphoma Study Group (IELSG) (2017).
Whole-brain radiotherapy or autologous stem-cell transplantation as consolidation strategies after high-dose methotrexate-based chemoimmunotherapy in patients with primary CNS lymphoma: results of the second randomisation of the International Extranodal Lymphoma Study Group-32 phase 2 trial.
The Lancet Haematology,
4(11), 510-523.
https://doi.org/10.1016/S2352-3026(17)30174-6Deco, G., Cruzat, J.
, Cabral, J., Knudsen, G. M., Carhart-Harris, R. L., Whybrow, P. C., Logothetis, N. K.
& Kringelbach, M. L. (2018).
Whole-Brain Multimodal Neuroimaging Model Using Serotonin Receptor Maps Explains Non-linear Functional Effects of LSD.
Current Biology,
28(19), 3065-+.
https://doi.org/10.1016/j.cub.2018.07.083Mindlin, I., Herzog, R., Belloli, L., Manasova, D., Monge-Asensio, M., Vohryzek, J., Escrichs, A., Alnagger, N., Núñez, P., Gosseries, O.
, Kringelbach, M. L., Deco, G., Tagliazucchi, E., Naccache, L., Rohaut, B., Sitt, J. D. & Sanz Perl, Y. (2024).
Whole brain modelling for simulating pharmacological interventions on patients with disorders of consciousness.
Communications Biology,
7(1), Article 1176.
https://doi.org/10.1038/s42003-024-06852-9Patow, G., Martin, I., Sanz Perl, Y.
, Kringelbach, M. L. & Deco, G. (2024).
Whole-brain modelling: an essential tool for understanding brain dynamics.
Nature Reviews Methods Primers,
4, Article 53.
https://doi.org/10.1038/s43586-024-00336-0Uribe, C., Escrichs, A., de Filippi, E., Sanz-Perl, Y., Junque, C., Gomez-Gil, E.
, Kringelbach, M. L., Guillamon, A. & Deco, G. (2022).
Whole-brain dynamics differentiate among cisgender and transgender individuals.
Human Brain Mapping,
43(13), 4103-4115.
https://doi.org/10.1002/hbm.25905Bonetti, L., Carlomagno, F., Kliuchko, M., Gold, B. P., Palva, S.
, Trusbak Haumann, N., Tervaniemi, M., Huotilainen, M.
, Vuust, P. & Brattico, E. (2022).
Whole-brain computation of cognitive versus acoustic errors in music: A mismatch negativity study.
NeuroImage: Reports,
2(4), Article 100145.
https://doi.org/10.1016/j.ynirp.2022.100145
Jochumsen, M. R., Christensen, N. L., Iversen, P., Gormsen, L. C., Sørensen, J. & Tolbod, L. P. (2024).
Whole-body parametric mapping of tumour perfusion in metastatic prostate cancer using long axial field-of-view [15O]H2O PET. European Journal of Nuclear Medicine and Molecular Imaging,
51(13), 4134-4140.
https://doi.org/10.1007/s00259-024-06799-3
Fraum, T. J., Sari, H.
, Dias, A. H., Munk, O. L., Pyka, T., Smith, A. M., Mawlawi, O. R., Laforest, R. & Wang, G. (2024).
Whole-Body Multiparametric PET in Clinical Oncology: Current Status, Challenges, and Opportunities.
American Journal of Roentgenology,
223(5), Article e2431712.
https://doi.org/10.2214/AJR.24.31712Sivesgaard, K., Jöhnk, M. L.
, Larsen, L. P. S., Sørensen, M., Kramer, S.
, Hansen, F. & Pedersen, E. M. (2015).
Whole Body MRI Could Aid in the Detection of Extra-Hepatic Colorectal Cancer Metastases. Poster session presented at Ph.d.-day, Aarhus, Denmark.
Sivesgaard, K., Larsen, L. P., Sørensen, M., Kramer, S., Schlander, S., Amanavicius, N., Mortensen, F. V. & Pedersen, E. M. (2020).
Whole-body MRI added to gadoxetic acid-enhanced liver MRI for detection of extrahepatic disease in patients considered eligible for hepatic resection and/or local ablation of colorectal cancer liver metastases.
Acta Radiologica,
61(2), 156-167.
https://doi.org/10.1177/0284185119855184
Christensen, B., Nellemann, B., Larsen, M. S., Thams, L., Sieljacks, P., Vestergaard, P. F., Bibby, B. M., Vissing, K., Stødkilde-Jørgensen, H., Pedersen, S. B., Møller, N., Nielsen, S., Jessen, N. & Jørgensen, J. O. L. (2013).
Whole body metabolic effects of prolonged endurance training in combination with erythropoietin treatment in humans: a randomized placebo controlled study.
A J P: Endocrinology and Metabolism (Online),
305(7), E879-889.
https://doi.org/10.1152/ajpendo.00269.2013
Giraudo, C., Lecouvet, F. E., Cotten, A., Eshed, I., Jans, L.
, Jurik, A. G., Maas, M., Weber, M. & Sudoł-Szopińska, I. (2021).
Whole-body magnetic resonance imaging in inflammatory diseases: Where are we now? Results of an International Survey by the European Society of Musculoskeletal Radiology.
European Journal of Radiology,
136, Article 109533.
https://doi.org/10.1016/j.ejrad.2021.109533Brix, L., Ejlersen, J. A., Fledelius, J., Makieva, I., Thylin, E. S. G., Hansen, J., Kieu Ha, L., Gerke, O.
& Isaksen, C. R. G. (2020).
Whole-body magnetic resonance imaging for detection of malignant disease: a head-to-head-comparison with whole-body 18F-FDG-PET/CT as the reference standard.
Journal of Radiology and Imaging,
4(3), 17-24.
https://doi.org/10.14312/2399-8172.2020-3
Christensen, N. L., Jakobsen, S., Schacht, A. C., Munk, O. L., Alstrup, A. K. O., Tolbod, L. P., Harms, H. J., Nielsen, S. & Gormsen, L. C. (2017).
Whole-body biodistribution, dosimetry and metabolite correction of [11C]palmitate: A PET tracer for imaging of fatty acid metabolism.
Molecular Imaging,
16.
Dollerup, M. R., Alstrup, A. K. O., Gormsen, L. C., Nielsen, E. N., Falborg, L., Vendelbo, M., Luong, T. V. & Simonsen, M. I. T. (2022).
Whole body biodistribution and myocardial kinetics of the ketone PET radiotracer 3-[11C]OHB: A pilot study in domestic pigs. Poster session presented at The World Molecular Imaging Congress 2022, Miami, United States.
Nielsen, A. W., van Praagh, G. D., van der Geest, K. S. M.
, Hansen, I. T., Nielsen, B. D., Kjær, S. G., Blegvad-Nissen, J., Rewers, K.
, Sørensen, C. M., Brouwer, E.
, Hauge, E. M., Gormsen, L. C., Slart, R. H. J. A.
& Keller, K. K. (2025).
Whole-body and site specific [18F]FDG uptake patterns on PET/CT have limited value in differentiating between polymyalgia rheumatica and other inflammatory diseases: two cohorts of treatment-naïve suspected polymyalgia rheumatica.
EJNMMI research,
15(1), Article 51.
https://doi.org/10.1186/s13550-025-01233-7
Theodorou, K., van der Vorst, E. P. C., Gijbels, M. J., Wolfs, I. M. J., Jeurissen, M., Theelen, T. L., Sluimer, J. C., Wijnands, E., Cleutjens, J. P., Li, Y., Jansen, Y., Weber, C., Ludwig, A.
, Bentzon, J. F., Bartsch, J. W., Biessen, E. A. L. & Donners, M. M. P. C. (2017).
Whole body and hematopoietic ADAM8 deficiency does not influence advanced atherosclerotic lesion development, despite its association with human plaque progression.
Scientific Reports,
7(1), Article 11670.
https://doi.org/10.1038/s41598-017-10549-xRiis, AL., Jørgensen, JO., Gjedde, S., Nørrelund, H.
, Jurik, A. G., Nair, KS., Ivarsen, P.
, Weeke, J. & Møller, N. (2005).
Whole body and forearm substrate metabolism in hyperthyroidism: Evidence of increased basal muscle protein breakdown. Am J Phys Endocrin Metabol,
288, 1067-73.