Nature Search

Towards fair decentralized benchmarking of healthcare AI algorithms with the Federated Tumor Segmentation (FeTS) challenge

Federated learning (FL) algorithms have emerged as a promising solution to train models for healthcare imaging across institutions while preserving privacy. Here, the authors describe the Federated Tumor Segmentation (FeTS) challenge for the decentralised benchmarking of FL algorithms and evaluation of Healthcare AI algorithm generalizability in real-world cancer imaging datasets.

Maximilian Zenk
Ujjwal Baid
Spyridon Bakas
ResearchOpen Access08 Jul 2025
Nature Communications

Volume: 16, P: 1-20
Characterising acute and chronic care needs: insights from the Global Burden of Disease Study 2019

Chronic care manages long-term, progressive conditions, while acute care handles short-term ones. Here, authors show chronic conditions account for most of the global health burden, with 68% of DALYs and 93% of YLDs attributed to chronic care needs.

Cecilia Anza-Ramirez
J. Jaime Miranda
Yves Miel H. Zuniga
ResearchOpen Access07 May 2025
Nature Communications

Volume: 16, P: 1-36
Conformational changes in intact dengue virus reveal serotype-specific expansion

Temperature differences between mosquitoes and humans trigger structural changes in dengue virus 2 (DENV2) particles, but not in other DENV serotypes. Here, using HDXMS, the authors describe serotype-specific expansion of intact viral particles of DENV1 and DENV2 at 28 °C (mosquitoes), 37 °C (humans) and 40 °C (fever).

Xin-Xiang Lim
Arun Chandramohan
Ganesh S. Anand
ResearchOpen Access10 Feb 2017
Nature Communications

Volume: 8, P: 1-13
Stroke metrics during the first year of the COVID-19 pandemic, a tale of two comprehensive stroke centers

Lara Carvalho de Oliveira
Ana Ponciano
Aravind Ganesh
ResearchOpen Access11 Oct 2023
Scientific Reports

Volume: 13, P: 1-11
Ligand-mediated changes in conformational dynamics of NpmA: implications for ribosomal interactions

Nilofer Husain
Nikhil Kumar Tulsian
J. Sivaraman
ResearchOpen Access15 Nov 2016
Scientific Reports

Volume: 6, P: 1-8
Genomic autopsy to identify underlying causes of pregnancy loss and perinatal death

In a new study including 200 families who experienced perinatal death, adding genomic analyses to standard autopsies improved the identification of underlying pathogenic causes and informed genetic counseling.

Alicia B. Byrne
Peer Arts
Hamish S. Scott
ResearchOpen Access19 Jan 2023
Nature Medicine

Volume: 29, P: 180-189
CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

Chromodomain Helicase DNA-binding (CHD) proteins have been implicated in neurodevelopmental processes. Here, the authors identify missense variants in CHD3 that disturb its chromatin remodeling activities and cause a neurodevelopmental disorder with macrocephaly and speech and language impairment.

Lot Snijders Blok
Justine Rousseau
Philippe M. Campeau
ResearchOpen Access05 Nov 2018
Nature Communications

Volume: 9, P: 1-12
Prevalence and architecture of de novo mutations in developmental disorders

Whole-exome analysis of individuals with developmental disorders shows that de novo mutations can equally cause loss or altered protein function, but that most mutations causing altered protein function have not yet been described.

Jeremy F. McRae
Stephen Clayton
Matthew E. Hurles
Research25 Jan 2017
Nature

Volume: 542, P: 433-438
Estimating best nanomaterial for energy harvesting through reinforcement learning DQN coupled with fuzzy PROMETHEE under road-based conditions

Sekar Kidambi Raju
Ganesh Karthikeyan Varadarajan
S. K. Towfek
ResearchOpen Access14 Oct 2024
Scientific Reports

Volume: 14, P: 1-23
Recommendations for performing, interpreting and reporting hydrogen deuterium exchange mass spectrometry (HDX-MS) experiments

Members of the hydrogen deuterium exchange mass spectrometry (HDX-MS) community provide their ‘best practices’ recommendations for HDX-MS data collection, analysis and reporting.

Glenn R. Masson
John E. Burke
Kasper D. Rand
ReviewsOpen Access27 Jun 2019
Nature Methods

Volume: 16, P: 595-602
A phase III randomized-controlled study of safety and immunogenicity of DTwP-HepB-IPV-Hib vaccine (HEXASIIL^®) in infants

Hitt Sharma
Sameer Parekh
Sunil Gairola
ResearchOpen Access22 Feb 2024
npj Vaccines

Volume: 9, P: 1-9
The role of electron correlations in the electronic structure of putative Chern magnet TbMn₆Sn₆

Abdulgani Annaberdiyev
Subhasish Mandal
Panchapakesan Ganesh
ResearchOpen Access27 Sept 2023
npj Quantum Materials

Volume: 8, P: 1-13
Author Correction: Genomic autopsy to identify underlying causes of pregnancy loss and perinatal death

Alicia B. Byrne
Peer Arts
Hamish S. Scott
Amendments and Corrections10 Jul 2023
Nature Medicine

Volume: 30, P: 302
Machine-learned interatomic potentials by active learning: amorphous and liquid hafnium dioxide

Ganesh Sivaraman
Anand Narayanan Krishnamoorthy
Álvaro Vázquez-Mayagoitia
ResearchOpen Access23 Jul 2020
npj Computational Materials

Volume: 6, P: 1-8
Prolonged warm ischemia time leads to severe renal dysfunction of donation-after-cardiac death kidney grafts

Peter Urbanellis
Laura Mazilescu
Markus Selzner
ResearchOpen Access09 Sept 2021
Scientific Reports

Volume: 11, P: 1-11
Molecular interaction between natural IgG and ficolin – mechanistic insights on adaptive-innate immune crosstalk

Saswati Panda
Jing Zhang
Jeak L. Ding
ResearchOpen Access14 Jan 2014
Scientific Reports

Volume: 4, P: 1-12
β-subunit myristoylation functions as an energy sensor by modulating the dynamics of AMP-activated Protein Kinase

Nada Ali
Naomi Ling
Paul R. Gooley
ResearchOpen Access21 Dec 2016
Scientific Reports

Volume: 6, P: 1-8
Small peptide inhibitor from the sequence of RUNX3 disrupts PAK1–RUNX3 interaction and abrogates its phosphorylation-dependent oncogenic function

Rahul Kanumuri
Aruna Kumar Chelluboyina
Suresh K. Rayala
Research12 Jul 2021
Oncogene

Volume: 40, P: 5327-5341
Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

Lot Snijders Blok
Justine Rousseau
Philippe M. Campeau
Amendments and CorrectionsOpen Access15 Feb 2019
Nature Communications

Volume: 10, P: 1-4
Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

Lot Snijders Blok
Justine Rousseau
Philippe M. Campeau
Amendments and CorrectionsOpen Access02 May 2019
Nature Communications

Volume: 10, P: 1-4
Altered transcriptional regulatory proteins in glioblastoma and YBX1 as a potential regulator of tumor invasion

Manoj Kumar Gupta
Ravindra Varma Polisetty
Ravi Sirdeshmukh
ResearchOpen Access29 Jul 2019
Scientific Reports

Volume: 9, P: 1-15
ISARIC-COVID-19 dataset: A Prospective, Standardized, Global Dataset of Patients Hospitalized with COVID-19

Ali Abbas
Sheryl Ann Abdukahil
Luis Felipe Reyes
ResearchOpen Access30 Jul 2022
Scientific Data

Volume: 9, P: 1-22

Search

Towards fair decentralized benchmarking of healthcare AI algorithms with the Federated Tumor Segmentation (FeTS) challenge

Characterising acute and chronic care needs: insights from the Global Burden of Disease Study 2019

Conformational changes in intact dengue virus reveal serotype-specific expansion

Stroke metrics during the first year of the COVID-19 pandemic, a tale of two comprehensive stroke centers

Ligand-mediated changes in conformational dynamics of NpmA: implications for ribosomal interactions

Genomic autopsy to identify underlying causes of pregnancy loss and perinatal death

CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

Prevalence and architecture of de novo mutations in developmental disorders

Estimating best nanomaterial for energy harvesting through reinforcement learning DQN coupled with fuzzy PROMETHEE under road-based conditions

Recommendations for performing, interpreting and reporting hydrogen deuterium exchange mass spectrometry (HDX-MS) experiments

A phase III randomized-controlled study of safety and immunogenicity of DTwP-HepB-IPV-Hib vaccine (HEXASIIL^®) in infants

The role of electron correlations in the electronic structure of putative Chern magnet TbMn₆Sn₆

Author Correction: Genomic autopsy to identify underlying causes of pregnancy loss and perinatal death

Machine-learned interatomic potentials by active learning: amorphous and liquid hafnium dioxide

Prolonged warm ischemia time leads to severe renal dysfunction of donation-after-cardiac death kidney grafts

Molecular interaction between natural IgG and ficolin – mechanistic insights on adaptive-innate immune crosstalk

β-subunit myristoylation functions as an energy sensor by modulating the dynamics of AMP-activated Protein Kinase

Small peptide inhibitor from the sequence of RUNX3 disrupts PAK1–RUNX3 interaction and abrogates its phosphorylation-dependent oncogenic function

Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

Altered transcriptional regulatory proteins in glioblastoma and YBX1 as a potential regulator of tumor invasion

ISARIC-COVID-19 dataset: A Prospective, Standardized, Global Dataset of Patients Hospitalized with COVID-19

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