Skip to main content

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.

Advertisement

Nature

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.

Nature Communications (46)
Nature Genetics (34)
Nature (33)
Scientific Reports (15)
Nature Physics (6)

Choose more journals

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

Research (137)
Amendments and Corrections (32)
Correspondence (2)
Reviews (2)

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

Biochemistry
Biological techniques
Biomarkers
Cancer
Cardiology
Cell biology
Computational biology and bioinformatics
Diseases
Ecology
Endocrinology
Evolution
Genetics
Health care
Medical research
Microbiology
Neuroscience
Oncology
Optics and photonics
Physics
Physiology

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 101–150 of 173 results

Advanced filters: Author: Jonas B Nielsen Clear advanced filters

Model-based assessment of replicability for genome-wide association meta-analysis

In genome-wide association meta-analysis, it is often difficult to find an independent dataset of sufficient size to replicate associations. Here, the authors have developed MAMBA to calculate the probability of replicability based on consistency between datasets within the meta-analysis.

Daniel McGuire
Yu Jiang
Dajiang J. Liu
ResearchOpen Access30 Mar 2021
Nature Communications

Volume: 12, P: 1-14
A novel computational approach to pain perception modelling within a Bayesian framework using quantitative sensory testing

Armin Drusko
David Baumeister
Jonas Tesarz
ResearchOpen Access23 Feb 2023
Scientific Reports

Volume: 13, P: 1-14
Author Correction: Combined burden and functional impact tests for cancer driver discovery using DriverPower

Shimin Shuai
Federico Abascal
Christian von Mering
Amendments and CorrectionsOpen Access08 Dec 2022
Nature Communications

Volume: 13, P: 1
Machine learning reveals limited contribution of trans-only encoded variants to the HLA-DQ immunopeptidome

The analysis integrating immunoinformatics data mining models with large volumes of high-quality HLA-DQ specific immunopeptidomics data reveals trans-only HLA-DQ variants have a limited to no contribution to the overall HLA-DQ immunopeptidome.

Jonas Birkelund Nilsson
Saghar Kaabinejadian
Morten Nielsen
ResearchOpen Access21 Apr 2023
Communications Biology

Volume: 6, P: 1-13
A common Greenlandic TBC1D4 variant confers muscle insulin resistance and type 2 diabetes

An association mapping study of type-2-diabetes-related quantitative traits in the Greenlandic population identified a common variant in TBC1D4 that increases plasma glucose levels and serum insulin levels after an oral glucose load and type 2 diabetes risk, with effect sizes several times larger than any previous findings of large-scale genome-wide association studies for these traits.

Ida Moltke
Niels Grarup
Torben Hansen
Research18 Jun 2014
Nature

Volume: 512, P: 190-193
Author Correction: Pathway and network analysis of more than 2500 whole cancer genomes

Matthew A. Reyna
David Haan
Christian von Mering
Amendments and CorrectionsOpen Access08 Dec 2022
Nature Communications

Volume: 13, P: 1
Author Correction: Integrative pathway enrichment analysis of multivariate omics data

Marta Paczkowska
Jonathan Barenboim
Christian von Mering
Amendments and CorrectionsOpen Access08 Dec 2022
Nature Communications

Volume: 13, P: 1
Author Correction: High-coverage whole-genome analysis of 1220 cancers reveals hundreds of genes deregulated by rearrangement-mediated cis-regulatory alterations

Yiqun Zhang
Fengju Chen
Christian von Mering
Amendments and CorrectionsOpen Access08 Dec 2022
Nature Communications

Volume: 13, P: 1
Author Correction: A deep learning system accurately classifies primary and metastatic cancers using passenger mutation patterns

Wei Jiao
Gurnit Atwal
Christian von Mering
Amendments and CorrectionsOpen Access08 Dec 2022
Nature Communications

Volume: 13, P: 1
Time-restricted eating in people at high diabetes risk does not affect mitochondrial bioenergetics in peripheral blood mononuclear cells and platelets

Joana Mendes Lopes de Melo
Martin Bæk Blond
Joachim Størling
ResearchOpen Access24 Mar 2025
Scientific Reports

Volume: 15, P: 1-10
Author Correction: Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples

Matthew H. Bailey
William U. Meyerson
Christian von Mering
Amendments and CorrectionsOpen Access30 Nov 2020
Nature Communications

Volume: 11, P: 1
Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies

SAIGE (Scalable and Accurate Implementation of GEneralized mixed model) is a generalized mixed model association test that can efficiently analyze large data sets while controlling for unbalanced case-control ratios and sample relatedness, as shown by applying SAIGE to the UK Biobank data for > 1,400 binary phenotypes.

Wei Zhou
Jonas B. Nielsen
Seunggeun Lee
Research13 Aug 2018
Nature Genetics

Volume: 50, P: 1335-1341
Brugada syndrome risk loci seem protective against atrial fibrillation

Laura Andreasen
Jonas B Nielsen
Morten S Olesen
Research26 Mar 2014
European Journal of Human Genetics

Volume: 22, P: 1357-1361
Author Correction: Genetic effects on the timing of parturition and links to fetal birth weight

Pol Solé-Navais
Christopher Flatley
Bo Jacobsson
Amendments and CorrectionsOpen Access10 May 2023
Nature Genetics

Volume: 55, P: 1250
The nightscape of the Arctic winter shapes the diving behavior of a marine predator

Philippine Chambault
Jonas Teilmann
Mads Peter Heide-Jørgensen
ResearchOpen Access16 Feb 2024
Scientific Reports

Volume: 14, P: 1-9
GWAS of serum ALT and AST reveals an association of SLC30A10 Thr95Ile with hypermanganesemia symptoms

Circulating liver enzymes, like alanine aminotransferase (ALT) and aspartate aminotransferase (AST), are highly heritable and predictive of disease. Here, the authors perform a genome-wide association study on ALT and AST, revealing a rare variant in SLC30A10 associated with elevated ALT and AST.

Lucas D. Ward
Ho-Chou Tu
Paul Nioi
ResearchOpen Access27 Jul 2021
Nature Communications

Volume: 12, P: 1-14
Author Correction: Disruption of chromatin folding domains by somatic genomic rearrangements in human cancer

Kadir C. Akdemir
Victoria T. Le
Christian von Mering
Amendments and CorrectionsOpen Access21 Mar 2023
Nature Genetics

Volume: 55, P: 1079
Biological activity and safety of adenoviral vector-expressed wild-type p53 after intratumoral injection in melanoma and breast cancer patients with p53-overexpressing tumors

Reinhard Dummer
Jonas Bergh
Susanne Osanto
Research15 Jul 2000
Cancer Gene Therapy

Volume: 7, P: 1069-1076
Author Correction: Pan-cancer analysis of whole genomes

Lauri A. Aaltonen
Federico Abascal
Christian von Mering
Amendments and CorrectionsOpen Access25 Jan 2023
Nature

Volume: 614, P: E39
Author Correction: The landscape of viral associations in human cancers

Marc Zapatka
Ivan Borozan
Christian von Mering
Amendments and CorrectionsOpen Access21 Mar 2023
Nature Genetics

Volume: 55, P: 1077
Author Correction: The repertoire of mutational signatures in human cancer

Ludmil B. Alexandrov
Jaegil Kim
Christian von Mering
Amendments and CorrectionsOpen Access25 Jan 2023
Nature

Volume: 614, P: E41
Author Correction: Comprehensive molecular characterization of mitochondrial genomes in human cancers

Yuan Yuan
Young Seok Ju
Christian von Mering
Amendments and CorrectionsOpen Access21 Mar 2023
Nature Genetics

Volume: 55, P: 1078
Author Correction: Patterns of somatic structural variation in human cancer genomes

Yilong Li
Nicola D. Roberts
Christian von Mering
Amendments and CorrectionsOpen Access25 Jan 2023
Nature

Volume: 614, P: E38
Author Correction: Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing

Isidro Cortés-Ciriano
Jake June-Koo Lee
Christian von Mering
Amendments and CorrectionsOpen Access21 Mar 2023
Nature Genetics

Volume: 55, P: 1076
Author Correction: A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease

Douglas P. Wightman
Iris E. Jansen
Danielle Posthuma
Amendments and Corrections20 Jun 2022
Nature Genetics

Volume: 54, P: 1062
Exploring and visualizing large-scale genetic associations by using PheWeb

Sarah A. Gagliano Taliun
Peter VandeHaar
Gonçalo R. Abecasis
Correspondence05 Jun 2020
Nature Genetics

Volume: 52, P: 550-552
Author Correction: A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease

Douglas P. Wightman
Iris E. Jansen
Danielle Posthuma
Amendments and Corrections12 Nov 2021
Nature Genetics

Volume: 53, P: 1722
Author Correction: Divergent mutational processes distinguish hypoxic and normoxic tumours

Vinayak Bhandari
Constance H. Li
Christian von Mering
Amendments and CorrectionsOpen Access08 Dec 2022
Nature Communications

Volume: 13, P: 1
Author Correction: Genomic footprints of activated telomere maintenance mechanisms in cancer

Lina Sieverling
Chen Hong
Christian von Mering
Amendments and CorrectionsOpen Access08 Dec 2022
Nature Communications

Volume: 13, P: 1
Author Correction: GWAS of thyroid stimulating hormone highlights the pleiotropic effects and inverse association with thyroid cancer

Wei Zhou
Ben Brumpton
Bjørn Olav Åsvold
Amendments and CorrectionsOpen Access16 Dec 2021
Nature Communications

Volume: 12, P: 1-2
Scalable generalized linear mixed model for region-based association tests in large biobanks and cohorts

SAIGE-GENE is a scalable generalized mixed-model region-based association test that can analyze large datasets while accounting for sample relatedness and unbalanced case–control ratios for binary traits.

Wei Zhou
Zhangchen Zhao
Seunggeun Lee
Research18 May 2020
Nature Genetics

Volume: 52, P: 634-639
Author Correction: Genotyping, sequencing and analysis of 140,000 adults from Mexico City

Andrey Ziyatdinov
Jason Torres
Roberto Tapia-Conyer
Amendments and CorrectionsOpen Access08 Feb 2024
Nature

Volume: 626, P: E18
Publisher Correction: Stroke genetics informs drug discovery and risk prediction across ancestries

Aniket Mishra
Rainer Malik
Stephanie Debette
Amendments and CorrectionsOpen Access14 Nov 2022
Nature

Volume: 612, P: E7
Analysis of rare genetic variation underlying cardiometabolic diseases and traits among 200,000 individuals in the UK Biobank

Analysis of whole-exome sequencing data from over 200,000 individuals in the UK Biobank provides new insights into the contribution of rare variants to cardiometabolic diseases and traits.

Sean J. Jurgens
Seung Hoan Choi
Patrick T. Ellinor
Research17 Feb 2022
Nature Genetics

Volume: 54, P: 240-250
Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology

This large-scale genome-wide association analysis of subjects with asthma, hay fever or eczema provides insights into the shared genetic basis of these allergic diseases. The findings suggest that these diseases partly co-occur because they share many genetic risk variants that dysregulate the expression of immune-related genes.

Manuel A Ferreira
Judith M Vonk
Lavinia Paternoster
Research30 Oct 2017
Nature Genetics

Volume: 49, P: 1752-1757
Distributed quantum sensing in a continuous-variable entangled network

Experiments demonstrate quantum phase sensing with a four-mode entangled state, reaching a measurement precision that is beyond what can be achieved by separate individual probes.

Xueshi Guo
Casper R. Breum
Ulrik L. Andersen
Research23 Dec 2019
Nature Physics

Volume: 16, P: 281-284
Shotgun-based proteomics of extracellular vesicles in Alzheimer’s disease reveals biomarkers involved in immunological and coagulation pathways

Jonas Ellegaard Nielsen
Bent Honoré
Shona Pedersen
ResearchOpen Access16 Sept 2021
Scientific Reports

Volume: 11, P: 1-15
Age-dependent transition from islet insulin hypersecretion to hyposecretion in mice with the long QT-syndrome loss-of-function mutation Kcnq1-A340V

Anniek F. Lubberding
Jinyi Zhang
Signe S. Torekov
ResearchOpen Access10 Jun 2021
Scientific Reports

Volume: 11, P: 1-14
Transit detection of the long-period volatile-rich super-Earth ν² Lupi d with CHEOPS

Three planets orbit the Sun-like star ν² Lupi. CHEOPS data show that all of them are transiting and show remarkable diversity. In particular, dry and gas-poor inner planet b has experienced extensive atmospheric loss, while planets c and d are water rich and have a small gaseous envelope of primordial origin.

Laetitia Delrez
David Ehrenreich
Nicholas A. Walton
Research28 Jun 2021
Nature Astronomy

Volume: 5, P: 775-787
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use

Association studies of up to 1.2 million individuals identify 566 genetic variants in 406 loci associated with tobacco use and addiction (initiation, cessation, and heaviness) as well as alcohol use, with 150 loci showing pleiotropic association.

Mengzhen Liu
Yu Jiang
Scott Vrieze
Research14 Jan 2019
Nature Genetics

Volume: 51, P: 237-244
Climate actions by climate and non-climate researchers

Fabian Dablander
Maien S. M. Sachisthal
Jonas M. B. Haslbeck
ResearchOpen Access19 Nov 2024
npj Climate Action

Volume: 3, P: 1-4
DNA-thioguanine concentration and relapse risk in children and young adults with acute lymphoblastic leukemia: an IPD meta-analysis

Linea N. Toksvang
Kathrine Grell
Kjeld Schmiegelow
Research26 Jun 2021
Leukemia

Volume: 36, P: 33-41
New population-based exome data are questioning the pathogenicity of previously cardiomyopathy-associated genetic variants

Charlotte Andreasen
Jonas B Nielsen
Morten S Olesen
ResearchOpen Access09 Jan 2013
European Journal of Human Genetics

Volume: 21, P: 918-928
Why we thrive beneath a northern sky – genomic signals of selection in apple for adaptation to northern Sweden

J. Skytte af Sätra
L. Garkava-Gustavsson
P. K. Ingvarsson
ResearchOpen Access04 Jun 2024
Heredity

Volume: 133, P: 67-77
Divergence of cuticular hydrocarbons in two sympatric grasshopper species and the evolution of fatty acid synthases and elongases across insects

Jonas Finck
Emma L. Berdan
Sven Geiselhardt
ResearchOpen Access28 Sept 2016
Scientific Reports

Volume: 6, P: 1-13
Hybrid discrete- and continuous-variable quantum information

The traditional approaches to quantum information processing using either discrete or continuous variables can be combined in hybrid protocols for tasks including quantum teleportation, computation, entanglement distillation or Bell tests.

Ulrik L. Andersen
Jonas S. Neergaard-Nielsen
Akira Furusawa
Reviews01 Sept 2015
Nature Physics

Volume: 11, P: 713-719
Targeting transferrin receptors at the blood-brain barrier improves the uptake of immunoliposomes and subsequent cargo transport into the brain parenchyma

Kasper Bendix Johnsen
Annette Burkhart
Torben Moos
ResearchOpen Access04 Sept 2017
Scientific Reports

Volume: 7, P: 1-13
Biofilms can act as plasmid reserves in the absence of plasmid specific selection

Henriette Lyng Røder
Urvish Trivedi
Jonas Stenløkke Madsen
ResearchOpen Access07 Oct 2021
npj Biofilms and Microbiomes

Volume: 7, P: 1-6
Microscopic colitis

This Primer reviews the epidemiology, pathophysiology, diagnosis and management of microscopic colitis (MC), a type of inflammatory bowel disease that causes persistent watery diarrhoea. This Primer also discusses the effect of MC on patient quality of life and future research priorities in this field.

Kristin E. Burke
Mauro D’Amato
Hamed Khalili
Reviews10 Jun 2021
Nature Reviews Disease Primers

Volume: 7, P: 1-17
High prevalence of genetic variants previously associated with LQT syndrome in new exome data

Lena Refsgaard
Anders G Holst
Morten S Olesen
ResearchOpen Access29 Feb 2012
European Journal of Human Genetics

Volume: 20, P: 905-908

Previous page
page 1
page 2
page 3
page 4
Next page

Search

Search articles by subject, keyword or author

Show results from

Advanced search

Quick links

Explore articles by subject
Find a job
Guide to authors
Editorial policies

Nature.com

nature.com sitemap

About Nature Portfolio

About us
Press releases
Press office
Contact us

Discover content

Journals A-Z
Articles by subject
protocols.io
Nature Index

Publishing policies

Nature portfolio policies
Open access

Author & Researcher services

Reprints & permissions
Research data
Language editing
Scientific editing
Nature Masterclasses
Research Solutions

Libraries & institutions

Librarian service & tools
Librarian portal
Open research
Recommend to library

Advertising & partnerships

Advertising
Partnerships & Services
Media kits
Branded content

Professional development

Nature Careers
Nature Conferences

Regional websites

Nature Africa
Nature China
Nature India
Nature Italy
Nature Japan
Nature Middle East

Privacy Policy
Use of cookies
Legal notice
Accessibility statement
Terms & Conditions
Your US state privacy rights

© 2025 Springer Nature Limited