Disease Systems Biology Program

Research output

Research output per year 2007 2017 2018 2019 2024

• 349 Journal article
• 14 Comment/debate
• 14 Review
• 12 Book chapter
• 32 More
  • 12 Conference abstract in journal
  • 9 Letter
  • 4 Conference article
  • 4 Editorial
  • 2 Preprint
  • 1 Paper

Research output per year

Research output per year

Search results

• 2023

  A second update on mapping the human genetic architecture of COVID-19

  Kanai, M., Andrews, S., Cordioli, M., Stevens, C., Neale, B. M., Daly, M., Ganna, A., Pathak, G. A., Ellinghaus, D., Banasik, K., Brunak, S., Pedersen, O. B., Westergaard, D., Sequeros, C. B., Nissen, J., Feldt-Rasmussen, U., Grønbæk, K., Ostrowski, S. R., Guindo-Martinez, M., Garcia, S. M. & 70 others, Hjalgrim, H., Admin team lead, Admin team member, Analysis team lead, Analysis team member, Data collection lead, Data collection member, Manuscript analysis team lead, Manuscript analysis team members: Mendelian randomization, Manuscript analysis team members: methods development, Manuscript analysis team members: phenome-wide association study, Manuscript analysis team members: principal component projection, gene prioritization, Project management lead, Scientific communication lead, Scientific communication member, Writing group lead, Writing group member, 23andMe, Adolescent brain and cognitive development study, Analysis group, Armenia_Covid-19hg, Assessment of the influence of clinical, functional, immunological and genetic factors on the severity of the course of coronavirus infection with SARS-CoV-2 and post-COVID syndrome, Avon Longitudinal Study of Parents and Children (ALSPAC), BelCovid, Biobanque Quebec COVID19, BioVU, Bonn Study of COVID-19 Genetics, CGEn HostSeq—Canadian COVID-19 Human Host Genome Sequencing Databank, Colorado Center for Personalized Medicine—CCPM, COMRI/Virology Study, Covid19 Ioannina Biobank, COVID19-Host(a)ge, Covid19hg-CL, Danish COVID-19 Genomic Consortium, Egypt hgCOVID hub, EraCORE, FinnGen, French hgCOVID, GCAT. Genomes For Life, Genes & Health, Genetic influences on severity of COVID-19 illness in Korea, GenOMICC, Genotek COVID-19 study, Helix Exome+ COVID-19 Phenotypes, Host Genetic Factors for COVID-19 Severity and Outcome in Western Indian Population, Host Genetics in COVID Cohorts of Mixed ancestry from Mexico, Japan Coronavirus Taskforce, Japan NCGM-COVID19, Jordan COVID-19 Host Genomics Initiative (JCHGI), Leadership, Lung eQTL Consortium, Mass General Brigham—Host Vulnerability to COVID-19, MexGen-COVID, Pa-COVID-19, Project management group, Project management support, Qatar Genome Program, SARS-CoV-2 and Host Genome sequencing, Scientific communication group, Search for Genomic Markers Predicting the Severity of the response to COVID-19, Spanish COalition to Unlock Research on host GEnetics on COVID-19 (SCOURGE), The Danish Blood Donor Study, The Genetic Predisposition to severe COVID-19, Tirschenreuth Study (TiKoco), UCLA Precision Health COVID-19 Host Genomics Biobank, UK Biobank, Variability in Immune Response Genes and Severity of SARS-CoV-2 Infection (INMUNGEN-CoV2 study), Website development, Writing Group & The COVID-19 Host Genetics Initiative, 2023, In: Nature. 621, 7977, p. E7-E26 23 p.

  Research output: Contribution to journal › Comment/debate › Research › peer-review

  Open Access

  File
  25 Citations (Scopus)

  9 Downloads (Pure)

• DanMAC5: a browser of aggregated sequence variants from 8,671 whole genome sequenced Danish individuals

  Banasik, K., Møller, P. L., Techlo, T. R., Holm, P. C., Walters, G. B., Ingason, A., Rosengren, A., Rohde, P. D., Kogelman, L. J. A., Westergaard, D., Siggaard, T., Chmura, P. J., Chalmer, M. A., Magnússon, Ó., Þórisson, G., Stefánsson, H., Guðbjartsson, D. F., Stefánsson, K., Olesen, J., Winther, S. & 5 others, Bøttcher, M., Brunak, S., Werge, T., Nyegaard, M. & Hansen, T. F., 2023, In: BMC Genomic Data. 24, 1, 4 p., 30.

  Research output: Contribution to journal › Comment/debate › Research › peer-review

  Open Access

  File
  2 Citations (Scopus)

  19 Downloads (Pure)
• 2022

  Machine Learning to Identify Patients at Risk of Inappropriate Dosing for Renal Risk Medications: A Critical Comment on Kaas-Hansen et al [Response to Letter]

  Kaas-Hansen, B. S., Leal Rodríguez, C., Placido, D., Thorsen-Meyer, H-C., Nielsen, A. P., Dérian, N., Brunak, S. & Andersen, S. E., 2022, In: Clinical Epidemiology. 14, p. 765-766 2 p.

  Research output: Contribution to journal › Comment/debate › Research

  Open Access

  File
  27 Downloads (Pure)
• 2019

  Author Correction: Leveraging European infrastructures to access 1 million human genomes by 2022

  Saunders, G., Baudis, M., Becker, R., Beltran, S., Béroud, C., Birney, E., Brooksbank, C., Brunak, S., Van den Bulcke, M., Drysdale, R., Capella-Gutierrez, S., Flicek, P., Florindi, F., Goodhand, P., Gut, I., Heringa, J., Holub, P., Hooyberghs, J., Juty, N., Keane, T. M. & 21 others, Korbel, J. O., Lappalainen, I., Leskosek, B., Matthijs, G., Mayrhofer, M. T., Metspalu, A., Navarro, A., Newhouse, S., Nyrönen, T., Page, A., Persson, B., Palotie, A., Parkinson, H., Rambla, J., Salgado, D., Steinfelder, E., Swertz, M. A., Valencia, A., Varma, S., Blomberg, N. & Scollen, S., Nov 2019, In: Nature Reviews. Genetics. 20, 11, p. 702

  Research output: Contribution to journal › Comment/debate › Research
  1 Citation (Scopus)

• Identifying Sepsis Phenotypes

  Moseley, P. L. & Brunak, S., 2019, In: J A M A: The Journal of the American Medical Association. 322, 14, p. 1416-1417 2 p.

  Research output: Contribution to journal › Comment/debate › Research
  4 Citations (Scopus)

• Roadmap for a precision-medicine initiative in the Nordic region

  Njølstad, P. R., Andreassen, O. A., Brunak, S., Børglum, A. D., Dillner, J., Esko, T., Franks, P. W., Freimer, N., Groop, L., Heimer, H., Hougaard, D. M., Hovig, E., Hveem, K., Jalanko, A., Kaprio, J., Knudsen, G. P., Melbye, M., Metspalu, A., Mortensen, P. B., Palmgren, J. & 11 others, Palotie, A., Reed, W., Stefánsson, H., Stitziel, N. O., Sullivan, P. F., Thorsteinsdóttir, U., Vaudel, M., Vuorio, E., Werge, T., Stoltenberg, C. & Stefánsson, K., 2019, In: Nature Genetics. 51, p. 924-930

  Research output: Contribution to journal › Comment/debate › Research
  20 Citations (Scopus)

• SnapShot: S-Phase Entry and Exit

  Burgess, A., Vuong, J., Marzec, K. A., de Lichtenberg, U. N., O'Donoghue, S. I. & Jensen, L. J., 2019, In: Cell. 179, 3, p. 802-802.e1 2 p.

  Research output: Contribution to journal › Comment/debate › Research › peer-review
  2 Citations (Scopus)

• The first step towards personalized risk prediction for common epilepsies

  Hansen, T. F. & Møller, R. S., 2019, In: Brain. 142, p. 3316-3318 3 p.

  Research output: Contribution to journal › Comment/debate › Research
  1 Citation (Scopus)
• 2018

  A Novel Familial Cardiac Arrhythmia Syndrome with Widespread ST-Segment Depression

  Bundgård, H., Jøns, C., Lodder, E. M., Izarzugaza, J. M. G., Romero Herrera, J. A., Pehrson, S., Tfelt-Hansen, J., Ahlberg, G., Olesen, M. S., Holst, A. G., Wellens, H., de Villiers, C., Hastings, R., Stuart, G., Brunak, S., Wilde, A. A. M., Watkins, H. & Christensen, A. H., 2018, In: The New England Journal of Medicine. 379, 18, p. 1780-1781 2 p.

  Research output: Contribution to journal › Comment/debate › Research
  15 Citations (Scopus)
• 2017

  Corrigendum: Disentangling type 2 diabetes and metformin treatment signatures in the human gut microbiota

  Forslund, K., Hildebrand, F., Nielsen, T., Falony, G., Le Chatelier, E., Sunagawa, S., Prifti, E., Vieira-Silva, S., Gudmundsdottir, V., Pedersen, H. K., Arumugam, M., Kristiansen, K., Voigt, A. Y., Vestergaard, H., Hercog, R., Costea, P. I., Kultima, J. R., Li, J., Jørgensen, T., Levenez, F. & 10 others, Doré, J., Nielsen, H. B., Brunak, S., Raes, J., Hansen, T., Wang, J., Ehrlich, S. D., Bork, P., Pedersen, O. & MetaHIT consortium, 3 May 2017, In: Nature. 545, 116, 1 p., 22318.

  Research output: Contribution to journal › Comment/debate › Research
  51 Citations (Scopus)

• Nomenclature for alleles of the human carboxylesterase 1 gene

  INDICES Consortium, 1 Jan 2017, In: Pharmacogenetics and Genomics. 27, 2, p. 78-80 3 p.

  Research output: Contribution to journal › Comment/debate › Research › peer-review
  5 Citations (Scopus)
• 2015

  Avoiding abundance bias in the functional annotation of posttranslationally modified proteins

  Schölz, C., Lyon, D., Refsgaard, J. C., Jensen, L. J., Choudhary, C. R. & Weinert, B. T., Nov 2015, In: Nature Methods. 12, p. 1003-4 2 p.

  Research output: Contribution to journal › Comment/debate › Research › peer-review
  55 Citations (Scopus)
• 2013

  Reply to 'Mining electronic health records: An additional perspective'

  Jensen, P. B., Jensen, L. J. & Brunak, S., 1 Jan 2013, In: Nature Reviews. Genetics. 14, 1 p.

  Research output: Contribution to journal › Comment/debate › Research › peer-review
  5 Citations (Scopus)
• 2008

  Biochemistry. Not comparable, but complementary

  Jensen, L. J. & Bork, P., 3 Oct 2008, In: Science (New York, N.Y.). 322, 5898, p. 56-7 2 p.

  Research output: Contribution to journal › Comment/debate › Research › peer-review
  49 Citations (Scopus)