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.

Scientific Reports (24)
Nature Genetics (13)
Nature Communications (10)
Nature (3)
Cell Death and Differentiation (2)

Choose more journals

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

Research (63)
Amendments and Corrections (6)
Reviews (3)

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

Biochemistry
Biomarkers
Biotechnology
Cancer
Cell biology
Chemical biology
Computational biology and bioinformatics
Diseases
Genetics
Immunology
Medical research
Microbiology
Molecular biology
Molecular medicine
Nephrology
Neuroscience
Oncology
Rheumatology
Stem cells
Systems biology

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 1–50 of 72 results

Advanced filters: Author: Javier A. Neyra Clear advanced filters

Correction: Corrigendum: Functional variants in the B-cell gene BANK1 are associated with systemic lupus erythematosus

Sergey V Kozyrev
Anna-Karin Abelson
Marta E Alarcón-Riquelme
Amendments and Corrections01 Apr 2008
Nature Genetics

Volume: 40, P: 484
Trans-eQTL mapping prioritises USP18 as a negative regulator of interferon response at a lupus risk locus

Here the authors perform a trans expression quantitative trait locus meta-analysis study of over 3,700 people and link a USP18 variant to expression of 50 inflammation genes and lupus risk, highlighting how genetic regulation of immune responses drives autoimmune disease and informs new therapies.

Krista Freimann
Anneke Brümmer
Kaur Alasoo
ResearchOpen Access02 Oct 2025
Nature Communications

Volume: 16, P: 1-15
A second update on mapping the human genetic architecture of COVID-19

Masahiro Kanai
Shea J. Andrews
Matthew Solomonson
ResearchOpen Access06 Sept 2023
Nature

Volume: 621, P: E7-E26
Correction: Corrigendum: Analysis of the common genetic component of large-vessel vasculitides through a meta-Immunochip strategy

F. David Carmona
Patrick Coit
Steven R. Ytterberg
Amendments and CorrectionsOpen Access05 Apr 2017
Scientific Reports

Volume: 7, P: 1
Mapping the human genetic architecture of COVID-19

A global network of researchers was formed to investigate the role of human genetics in SARS-CoV-2 infection and COVID-19 severity; this paper reports 13 genome-wide significant loci and potentially actionable mechanisms in response to infection.

Mari E. K. Niemi
Juha Karjalainen
Chloe Donohue
ResearchOpen Access08 Jul 2021
Nature

Volume: 600, P: 472-477
COVID-19 progression and convalescence in common variable immunodeficiency patients show dysregulated adaptive immune responses and persistent type I interferon and inflammasome activation

Common variable immunodeficiency (CVID) is a prevalent primary immunodeficiency characterized by hypogammaglobulinemia, poor antibody responses, and enhanced susceptibility to infection. Here the authors examine CVID patients infected by SARS-CoV-2 and describe broad immune dysregulation, sustained type I IFN responses, altered B/T cell signaling, impaired NK cell differentiation, and persistent inflammasome activation.

Javier Rodríguez-Ubreva
Josep Calafell-Segura
Esteban Ballestar
ResearchOpen Access28 Nov 2024
Nature Communications

Volume: 15, P: 1-21
Change in platelet and leukocyte counts and hospital mortality in adults with acute kidney injury receiving continuous renal replacement therapy

Lan N. Bui
Joshua W. Lambert
Javier A. Neyra
ResearchOpen Access29 Sept 2025
Scientific Reports

Volume: 15, P: 1-10
Tailoring the natural rare sugars D-tagatose and L-sorbose to produce novel functional carbohydrates

Oswaldo Hernandez-Hernandez
Carlos Sabater
F. Javier Moreno
ResearchOpen Access04 Oct 2024
npj Science of Food

Volume: 8, P: 1-13
Single-cell Atlas of common variable immunodeficiency shows germinal center-associated epigenetic dysregulation in B-cell responses

Common variable immunodeficiency (CVID) is the most prevalent primary immunodeficiency. Here the authors perform single-cell omics analyses in CVID-discordant monozygotic twins and show epigenetic and transcriptional alterations associated with activation in memory B cells.

Javier Rodríguez-Ubreva
Anna Arutyunyan
Esteban Ballestar
ResearchOpen Access01 Apr 2022
Nature Communications

Volume: 13, P: 1-18
Evaluation of VDR gene polymorphisms in Trypanosoma cruzi infection and chronic Chagasic cardiomyopathy

Daniel A Leon Rodriguez
F David Carmona
Javier Martin
ResearchOpen Access09 Aug 2016
Scientific Reports

Volume: 6, P: 1-6
Mutational profile of rare variants in inflammasome-related genes in Behçet disease: A Next Generation Sequencing approach

Sergio Burillo-Sanz
Marco-Antonio Montes-Cano
María Francisca González-Escribano
ResearchOpen Access16 Aug 2017
Scientific Reports

Volume: 7, P: 1-9
Unraveling the molecular landscape of Erdheim–Chester disease: new insights from methylome and transcriptome integration

Miriam Cerván-Martín
Francesco Pegoraro
Javier Martín
ResearchOpen Access21 Aug 2025
Leukemia

Volume: 39, P: 2758-2766
Behçet’s disease and genetic interactions between HLA-B*51 and variants in genes of autoinflammatory syndromes

Sergio Burillo-Sanz
Marco-Antonio Montes-Cano
María Francisca González-Escribano
ResearchOpen Access26 Feb 2019
Scientific Reports

Volume: 9, P: 1-8
A new molecular classification to drive precision treatment strategies in primary Sjögren’s syndrome

Sjögren’s syndrome, a disease that primarily affects women, is poorly understood. Here, the authors combine data from a large cohort of patients and healthy controls to identify biomarkers that distinguish patient subgroups to improve our understanding of the disease and facilitate drug development.

Perrine Soret
Christelle Le Dantec
Jacques-Olivier Pers
ResearchOpen Access10 Jun 2021
Nature Communications

Volume: 12, P: 1-18
Association of a rare variant of the TNFSF13B gene with susceptibility to Rheumatoid Arthritis and Systemic Lupus Erythematosus

David González-Serna
Lourdes Ortiz-Fernández
Javier Martín
ResearchOpen Access29 May 2018
Scientific Reports

Volume: 8, P: 1-5
Genome-wide association study identifies Sjögren’s risk loci with functional implications in immune and glandular cells

The genetic architecture underlying Sjögren’s syndrome is not fully understood. Here, the authors perform a genome-wide association study to identify 10 new genetic risk regions, implicating genes involved in immune and salivary gland function.

Bhuwan Khatri
Kandice L. Tessneer
Christopher J. Lessard
ResearchOpen Access27 Jul 2022
Nature Communications

Volume: 13, P: 1-17
A genome-wide association study suggests the HLA Class II region as the major susceptibility locus for IgA vasculitis

Raquel López-Mejías
F. David Carmona
Miguel A. González-Gay
ResearchOpen Access11 Jul 2017
Scientific Reports

Volume: 7, P: 1-6
Publisher Correction: An international perspective on the future of systemic sclerosis research

David J. Abraham
Carol M. Black
Thomas Krieg
Amendments and Corrections03 Mar 2025
Nature Reviews Rheumatology

Volume: 21, P: 249
Expression of osteoprotegerin and its ligands, RANKL and TRAIL, in rheumatoid arthritis

Sara Remuzgo-Martínez
Fernanda Genre
Miguel A. González-Gay
ResearchOpen Access12 Jul 2016
Scientific Reports

Volume: 6, P: 1-5
Influence of elevated-CRP level-related polymorphisms in non-rheumatic Caucasians on the risk of subclinical atherosclerosis and cardiovascular disease in rheumatoid arthritis

Raquel López-Mejías
Fernanda Genre
Miguel A. González-Gay
ResearchOpen Access18 Aug 2016
Scientific Reports

Volume: 6, P: 1-7
Major histocompatibility complex associations of ankylosing spondylitis are complex and involve further epistasis with ERAP1

Ankylosing spondylitis is a common, highly inheritable inflammatory arthritis with poorly understood biology. Here Brown, Cortes and colleagues use fine mapping of the major histocompatibility complex and identify novel associations, and identify other HLA alleles that like HLA-B27 interact with ERAP1 variants to influence disease risk.

Adrian Cortes
Sara L. Pulit
Matthew A. Brown
ResearchOpen Access21 May 2015
Nature Communications

Volume: 6, P: 1-8
Multi-ancestry genome-wide association analyses identify novel genetic mechanisms in rheumatoid arthritis

Multi-ancestry genome-wide association analyses identify 124 risk loci for rheumatoid arthritis, of which 34 are novel. A polygenic risk score based on multi-ancestry data showed comparable performance between populations of European and East Asian ancestries.

Kazuyoshi Ishigaki
Saori Sakaue
Soumya Raychaudhuri
Research04 Nov 2022
Nature Genetics

Volume: 54, P: 1640-1651
GWAS for systemic sclerosis identifies multiple risk loci and highlights fibrotic and vasculopathy pathways

Systemic sclerosis (SSc) is a heterogeneous chronic autoimmune disease that affects the connective tissue. Here, López-Isac et al. identify 13 new risk loci for SSc as well as loci specific for limited cutaneous and diffuse SSc and, defining credible sets and performing functional annotation, highlight key pathways and cell types for SSc.

Elena López-Isac
Marialbert Acosta-Herrera
Javier Martin
ResearchOpen Access31 Oct 2019
Nature Communications

Volume: 10, P: 1-14
Transancestral mapping and genetic load in systemic lupus erythematosus

Systemic lupus erythematosus (SLE) is an autoimmune disease with a strong ethnic and gender bias. In a transancestral genetic association study, Langefeldet al. identify 24 novel regions associated with risk to lupus and propose a cumulative hits hypothesis for loci conferring risk to SLE.

Carl D. Langefeld
Hannah C. Ainsworth
Timothy J. Vyse
ResearchOpen Access17 Jul 2017
Nature Communications

Volume: 8, P: 1-18
Specific association of a CLEC16A/KIAA0350 polymorphism with NOD2/CARD15⁻ Crohn's disease patients

Ana Márquez
Jezabel Varadé
Elena Urcelay
Research01 Apr 2009
European Journal of Human Genetics

Volume: 17, P: 1304-1308
Transcriptomic profiling reveals Agave Lechuguilla extract as a multi-target pre-emergent bioherbicide candidate against Chenopodium album

Adrián Esteban Velázquez-Lizárraga
Leopoldo Javier Rios-González
Ana G. Reyes
ResearchOpen Access14 Oct 2025
Scientific Reports

Volume: 15, P: 1-17
Functional variants in the B-cell gene BANK1 are associated with systemic lupus erythematosus

Sergey V Kozyrev
Anna-Karin Abelson
Marta E Alarcón-Riquelme
Research20 Jan 2008
Nature Genetics

Volume: 40, P: 211-216
Discovery of core genes for systemic lupus erythematosus via genome-wide aggregated trans-effects analysis

Andrii Iakovliev
Olivia Castellini-Pérez
Athina Spiliopoulou
ResearchOpen Access03 Sept 2025
Genes & Immunity

Volume: 26, P: 497-508
Author Correction: Genome-wide association study identifies Sjögren’s risk loci with functional implications in immune and glandular cells

Bhuwan Khatri
Kandice L. Tessneer
Christopher J. Lessard
Amendments and CorrectionsOpen Access03 Feb 2023
Nature Communications

Volume: 14, P: 1-3
Protein tyrosine phosphatase non-receptor 22 and C-Src tyrosine kinase genes are down-regulated in patients with rheumatoid arthritis

Sara Remuzgo-Martínez
Fernanda Genre
Miguel A. González-Gay
ResearchOpen Access05 Sept 2017
Scientific Reports

Volume: 7, P: 1-7
Author Correction: Genome-wide association study identifies Sjögren’s risk loci with functional implications in immune and glandular cells

Bhuwan Khatri
Kandice L. Tessneer
Christopher J. Lessard
Amendments and CorrectionsOpen Access31 Oct 2022
Nature Communications

Volume: 13, P: 1
Influence of coronary artery disease and subclinical atherosclerosis related polymorphisms on the risk of atherosclerosis in rheumatoid arthritis

Raquel López-Mejías
Alfonso Corrales
Miguel A. González-Gay
ResearchOpen Access06 Jan 2017
Scientific Reports

Volume: 7, P: 1-6
Development, implementation and outcomes of a quality assurance system for the provision of continuous renal replacement therapy in the intensive care unit

Eloy F. Ruiz
Victor M. Ortiz-Soriano
Jillian M. Kouns
ResearchOpen Access26 Nov 2020
Scientific Reports

Volume: 10, P: 1-10
Widespread non-additive and interaction effects within HLA loci modulate the risk of autoimmune diseases

Soumya Raychaudhuri, Paul de Bakker and colleagues test the non-additive disease contributions of classical HLA alleles to five common autoimmune diseases. In four of the five diseases, they observe highly significant non-additive dominance and interaction effects.

Tobias L Lenz
Aaron J Deutsch
Soumya Raychaudhuri
Research10 Aug 2015
Nature Genetics

Volume: 47, P: 1085-1090
Role of the IL33 and IL1RL1 pathway in the pathogenesis of Immunoglobulin A vasculitis

Diana Prieto-Peña
Sara Remuzgo-Martínez
Raquel López-Mejías
ResearchOpen Access09 Aug 2021
Scientific Reports

Volume: 11, P: 1-8
BAFF, APRIL and BAFFR on the pathogenesis of Immunoglobulin-A vasculitis

Diana Prieto-Peña
Fernanda Genre
Raquel López-Mejías
ResearchOpen Access01 Jun 2021
Scientific Reports

Volume: 11, P: 1-7
Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci

Matthew Brown and colleagues identify multiple susceptibility variants for ankylosing spondylitis through an association study based on high-density genotyping of immune-related loci. Their findings implicate numerous biological pathways in the pathogenesis of this disease and highlight shared risk factors with other autoimmune diseases.

Adrian Cortes
Johanna Hadler
Matthew A Brown
Research09 Jun 2013
Nature Genetics

Volume: 45, P: 730-738
Author Correction: BAFF, APRIL and BAFFR on the pathogenesis of Immunoglobulin-A vasculitis

Diana Prieto-Peña
Fernanda Genre
Raquel López-Mejías
Amendments and CorrectionsOpen Access16 Aug 2021
Scientific Reports

Volume: 11, P: 1
Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus

Timothy Radstake and Maureen Mayes and colleagues report results of a genome-wide association study of systemic sclerosis. They identify a new susceptibility locus at CD247.

Timothy R D J Radstake
Olga Gorlova
Maureen D Mayes
Research11 Apr 2010
Nature Genetics

Volume: 42, P: 426-429
Genetic association analyses implicate aberrant regulation of innate and adaptive immunity genes in the pathogenesis of systemic lupus erythematosus

Timothy Vyse and colleagues report the results of a large-scale association study of systemic lupus erythematosus (SLE). They identify ten new susceptibility loci and implicate aberrant regulation of innate and adaptive immunity genes in disease pathogenesis.

James Bentham
David L Morris
Timothy J Vyse
Research26 Oct 2015
Nature Genetics

Volume: 47, P: 1457-1464
High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis

Jane Worthington and colleagues use a high-density genotyping chip to identify new susceptibility loci for rheumatoid arthritis and examine genetic overlap with other autoimmune diseases. Their results increase the number of confirmed rheumatoid arthritis risk loci in individuals of European ancestry and refine the location of many previously identified association signals to single genes.

Steve Eyre
John Bowes
Jane Worthington
Research11 Nov 2012
Nature Genetics

Volume: 44, P: 1336-1340
An international perspective on the future of systemic sclerosis research

The diagnosis, treatment and management of systemic sclerosis (SSc) remains challenging, owing to the complexity of this disease. In this Perspective, an international group of experts discuss the future of SSc research and how the advent of innovative technologies will advance research into and understanding of SSc.

David J. Abraham
Carol M. Black
Thomas Krieg
Reviews14 Feb 2025
Nature Reviews Rheumatology

Volume: 21, P: 174-187
Impact of early initiation of renal replacement therapy in patients on venoarterial ECMO using target trial emulation with Japanese nationwide data

Toshihiro Kubo
Tomonori Takeuchi
Kenji Wakabayashi
ResearchOpen Access07 Jan 2025
Scientific Reports

Volume: 15, P: 1-9
Acute kidney injury in patients with burns

Here, the authors discuss the pathophysiology of acute kidney injury (AKI) in patients with burns, approaches to prevention and management of AKI in this population and the application of AKI biomarkers and artificial intelligence approaches to guide treatment and predict short-term and long-term outcomes.

Matthieu Legrand
Audra T. Clark
Marlies Ostermann
Reviews27 Sept 2023
Nature Reviews Nephrology

Volume: 20, P: 188-200
A cross-disease meta-GWAS identifies four new susceptibility loci shared between systemic sclerosis and Crohn’s disease

David González-Serna
Eguzkine Ochoa
Armando Gabrielli
ResearchOpen Access05 Feb 2020
Scientific Reports

Volume: 10, P: 1-11
Intradialytic hypotension and hemodynamic phenotypes in children following continuous renal replacement therapy initiation

Sameer Thadani
Christin Silos
Javier A. Neyra
Research11 Sept 2025
Pediatric Research

P: 1-8
Analysis of the common genetic component of large-vessel vasculitides through a meta-Immunochip strategy

F. David Carmona
Patrick Coit
Steven R. Ytterberg
ResearchOpen Access09 Mar 2017
Scientific Reports

Volume: 7, P: 1-11
Dopaminergic control of ADAMTS2 expression through cAMP/CREB and ERK: molecular effects of antipsychotics

Fulgencio Ruso-Julve
Ana Pombero
Benedicto Crespo-Facorro
ResearchOpen Access18 Nov 2019
Translational Psychiatry

Volume: 9, P: 1-12
Digital health and acute kidney injury: consensus report of the 27th Acute Disease Quality Initiative workgroup

In this Consensus Statement, the authors discuss a framework for the development, validation and implementation of digital health technologies across the acute kidney injury continuum — risk prediction, prevention, detection and management.

Kianoush B. Kashani
Linda Awdishu
Ravindra L. Mehta
Reviews14 Aug 2023
Nature Reviews Nephrology

Volume: 19, P: 807-818
A method to decipher pleiotropy by detecting underlying heterogeneity driven by hidden subgroups applied to autoimmune and neuropsychiatric diseases

Soumya Raychaudhuri, Buhm Han and colleagues present a statistical method to distinguish whether shared genetic risk variants among complex traits are driven by whole-group pleiotropy or a subset of individuals who constitute a genetically heterogeneous subgroup. They use the method to examine genetic sharing among autoimmune diseases and between major depressive disorder and schizophrenia and find that most genetic sharing cannot be explained by subgroup heterogeneity but that, in contrast, seronegative rheumatoid arthritis is a heterogeneous condition.

Buhm Han
Jennie G Pouget
Soumya Raychaudhuri
Research16 May 2016
Nature Genetics

Volume: 48, P: 803-810

Previous page
page 1
page 2
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 Awards
Nature Careers
Nature Conferences

Regional websites

Nature Africa
Nature China
Nature India
Nature Japan
Nature Middle East

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

© 2026 Springer Nature Limited