Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

View all journals
Search
Log in

nature
search

Search

Advanced search

Filter By:

Journal Check one or more journals to show results from those journals only.

European Journal of Human Genetics (4)
Scientific Reports (4)
Genetics in Medicine (1)
Nature (1)

Choose more journals

Article type Check one or more article types to show results from those article types only.

Research (9)
Amendments and Corrections (1)

Subject Check one or more subjects to show results from those subjects only.

Anatomy
Biological techniques
Biomarkers
Cancer
Computational biology and bioinformatics
Diseases
Genetics
Immunology
Mathematics and computing
Medical research
Pathogenesis
Rheumatology
Signs and symptoms

Date Choose a date option to show results from those dates only.

Today
Last 7 days
Last 30 days
Last 12 months
Last 2 years
Last 5 years

Custom date range

Clear all filters

Sort by:

Relevance

Date published (new to old)

Date published (old to new)

Showing 1–10 of 10 results

Advanced filters: Author: Magnus D Vigeland Clear advanced filters

PUF60 variants cause a syndrome of ID, short stature, microcephaly, coloboma, craniofacial, cardiac, renal and spinal features

Karen J Low
Morad Ansari
Sarah F Smithson
ResearchOpen Access22 Mar 2017
European Journal of Human Genetics

Volume: 25, P: 552-559
The Atlantic salmon genome provides insights into rediploidization

The genome sequence is presented for the Atlantic salmon (Salmo salar), providing information about a rediploidization following a salmonid-specific whole-genome duplication event that resulted in an autotetraploidization.

Sigbjørn Lien
Ben F. Koop
William S. Davidson
ResearchOpen Access18 Apr 2016
Nature

Volume: 533, P: 200-205
Correlation between gene expression and MRI STIR signals in patients with chronic low back pain and Modic changes indicates immune involvement

Maria Dehli Vigeland
Siri Tennebø Flåm
Vidar Rao
ResearchOpen Access07 Jan 2022
Scientific Reports

Volume: 12, P: 1-12
Publisher Correction: A 39 kb structural variant causing Lynch syndrome detected by optical genome mapping and nanopore sequencing

Pål Marius Bjørnstad
Ragnhild Aaløkken
Gregor D. Gilfillan
Amendments and CorrectionsOpen Access04 Jan 2024
European Journal of Human Genetics

Volume: 32, P: 601-602
A 39 kb structural variant causing Lynch Syndrome detected by optical genome mapping and nanopore sequencing

Pål Marius Bjørnstad
Ragnhild Aaløkken
Gregor D. Gilfillan
ResearchOpen Access29 Nov 2023
European Journal of Human Genetics

Volume: 32, P: 513-520
Joint DNA-based disaster victim identification

Magnus D. Vigeland
Thore Egeland
ResearchOpen Access01 Jul 2021
Scientific Reports

Volume: 11, P: 1-13
The invisible witness: air and dust as DNA evidence of human occupancy in indoor premises

Chiara Fantinato
Ane Elida Fonneløp
Peter Gill
ResearchOpen Access04 Nov 2023
Scientific Reports

Volume: 13, P: 1-16
Benefits of clinical criteria and high-throughput sequencing for diagnosing children with syndromic craniosynostosis

Elin Tønne
Bernt Johan Due-Tønnessen
Ketil Riddervold Heimdal
ResearchOpen Access07 Dec 2020
European Journal of Human Genetics

Volume: 29, P: 920-929
Phenotypic spectrum and transcriptomic profile associated with germline variants in TRAF7

Laura Castilla-Vallmanya
Kaja K. Selmer
Christopher T. Gordon
Research07 May 2020
Genetics in Medicine

Volume: 22, P: 1215-1226
Persistent pulmonary pathology after COVID-19 is associated with high viral load, weak antibody response, and high levels of matrix metalloproteinase-9

Tøri Vigeland Lerum
Niklas Nyboe Maltzahn
Ole Henning Skjønsberg
ResearchOpen Access01 Dec 2021
Scientific Reports

Volume: 11, P: 1-12