Nature Search

Quality of TikTok videos on sudden cardiac death varies by video characteristics and health information accuracy

Mitansh Bansal
Ayesha Jalal
Rahul Kashyap
ResearchOpen Access23 Mar 2026
Scientific Reports

P: 1-10
Scalable and accurate rare variant meta-analysis with Meta-SAIGE

Meta-SAIGE is a computationally efficient method for meta-analysis of rare variant associations across cohorts. It effectively controls type I error rates and has power similar to analyses of pooled individual-level data.

Eunjae Park
Kisung Nam
Seunggeun Lee
ResearchOpen Access20 Nov 2025
Nature Genetics

Volume: 57, P: 3185-3192
The next phase in human genetics

Experimental haplotyping of whole genomes is now feasible, enabling new studies aimed at linking sequence variation to human phenotypes and disease susceptibility.

Vikas Bansal
Ryan Tewhey
Nicholas J Schork
News & Views01 Jan 2011
Nature Biotechnology

Volume: 29, P: 38-39
Impact of the indigenous rotavirus vaccine Rotavac in the Universal Immunization Program in India during 2016–2020

In this multicentered observational study, Rotavac, an indigenous, monovalent, live, attenuated, oral rotavirus vaccine, had an adjusted vaccine efficacy of 54% and protected against severe gastroenteritis in Indian children during its rollout between 2016 and 2020.

Nayana P. Nair
Samarasimha N. Reddy
Mahima Mittal
ResearchOpen Access07 Oct 2025
Nature Medicine

Volume: 31, P: 3871-3878
Statistical analysis strategies for association studies involving rare variants

There is increasing interest in investigating the influence of rare variants on common diseases, aided by high-throughput sequencing. However, the statistical approaches that are essential for analysing associations between rare variants and traits of interest are urgently in need of evaluation and refinement.

Vikas Bansal
Ondrej Libiger
Nicholas J. Schork
Reviews13 Oct 2010
Nature Reviews Genetics

Volume: 11, P: 773-785
The importance of phase information for human genomics

This Opinion article argues that capturing phase information in human genomics studies is crucial for important aims such as understanding how genotype contributes to phenotypes. existing approaches for phasing will need to be improved in order to meet this goal.

Ryan Tewhey
Vikas Bansal
Nicholas J. Schork
Reviews08 Feb 2011
Nature Reviews Genetics

Volume: 12, P: 215-223
Global, regional and national burden of dietary iron deficiency from 1990 to 2021: a Global Burden of Disease study

Systematic analysis from the Global Burden of Disease study reported that, despite global improvements from 1990 to 2021, dietary iron deficiency-associated disease burden remains high in women, children and residents in low socio-demographic index countries.

Sooji Lee
Yejun Son
Nicholas. J. Kassebaum
Research22 Apr 2025
Nature Medicine

Volume: 31, P: 1809-1829
Not so lost in the genetic crowd

Two new studies report improved statistics to predict whether an individual participated in a genome-wide association study based on aggregate allele or genotype frequency information. They demonstrate that it may be possible to release summary statistics for a subset of genetic markers in a study while maintaining individual privacy.

Nicholas J Schork
Vikas Bansal
News & Views01 Nov 2009
Nature Genetics

Volume: 41, P: 1163-1164
Thermal analysis of flat plate solar air heater system with radiation reflectors and W-shaped roughness: artificial neural network & machine learning approach

Piyush Kumar Jain
Kawal Lal Kurrey
Niraj Kumar Dewangan
ResearchOpen Access02 Mar 2026
Scientific Reports

Volume: 16, P: 1-20
Author Correction: Impact of the indigenous rotavirus vaccine Rotavac in the Universal Immunization Program in India during 2016–2020

Nayana P. Nair
Samarasimha N. Reddy
Mahima Mittal
Amendments and CorrectionsOpen Access27 Oct 2025
Nature Medicine

Volume: 31, P: 3931
JAK2V617F reprograms Hypoxia Inducible Factor-1 to induce a non-canonical hypoxia regulon in myeloproliferative neoplasms

David Kealy
Ruth Ellerington
Katherine S. Bridge
ResearchOpen Access02 Feb 2026
Leukemia

Volume: 40, P: 609-621
Robust and accurate estimation of paralog-specific copy number for duplicated genes using whole-genome sequencing

Low-copy repeats cover up to 5% of the human genome and are prone to extensive copy number variation. Here, the authors present a novel computational method to estimate paralog-specific copy number of such regions using whole-genome sequencing.

Timofey Prodanov
Vikas Bansal
ResearchOpen Access09 Jun 2022
Nature Communications

Volume: 13, P: 1-12
Functional hypoxia drives neuroplasticity and neurogenesis via brain erythropoietin

EPO treatment improves cognition, but underlying mechanisms were unknown. Here the authors describe a regulatory loop in which brain networks challenged by cognitive tasks drift into functional hypoxia that drives—via neuronal EPO synthesis—neurodifferentiation and dendritic spine formation.

Debia Wakhloo
Franziska Scharkowski
Hannelore Ehrenreich
ResearchOpen Access09 Mar 2020
Nature Communications

Volume: 11, P: 1-12
Realistic in silico generation and augmentation of single-cell RNA-seq data using generative adversarial networks

Low sample numbers often limit the robustness of analyses in biomedical research. Here, the authors introduce a method to generate realistic scRNA-seq data using GANs that learn gene expression dependencies from complex samples, and show that augmenting spare cell populations improves downstream analyses.

Matteo Marouf
Pierre Machart
Stefan Bonn
ResearchOpen Access09 Jan 2020
Nature Communications

Volume: 11, P: 1-12
A diploid assembly-based benchmark for variants in the major histocompatibility complex

Accurate, phased assemblies are a key tool in understanding the human genome, particularly in highly polymorphic regions like the medically important MHC. Here the authors provide an assembly-based benchmark for this difficult-to-characterize region.

Chen-Shan Chin
Justin Wagner
Justin M. Zook
ResearchOpen Access22 Sept 2020
Nature Communications

Volume: 11, P: 1-9
Longshot enables accurate variant calling in diploid genomes from single-molecule long read sequencing

Single-molecule sequencing (SMS) such as Pacific Biosciences and Oxford Nanopore generate long reads with high error rate. Here, the authors develop Longshot, a computational method that detects and phases single nucleotide variants (SNV) in diploid genomes using SMS data.

Peter Edge
Vikas Bansal
ResearchOpen Access11 Oct 2019
Nature Communications

Volume: 10, P: 1-10
Multi-locus genome-wide association studies (ML-GWAS) reveal novel genomic regions associated with seedling and adult plant stage leaf rust resistance in bread wheat (Triticum aestivum L.)

V. K. Vikas
Anjan Kumar Pradhan
Sundeep Kumar
Research13 Apr 2022
Heredity

Volume: 128, P: 434-449
Forebrain-specific loss of erythropoietin provokes compensatory upregulation of different EPO receptors

Umer Javed Butt
Umut Çakır
Hannelore Ehrenreich
ResearchOpen Access30 Sept 2025
Molecular Psychiatry

Volume: 31, P: 1241-1252
Medin co-aggregates with vascular amyloid-β in Alzheimer’s disease

Medin promotes the formation of vascular aggregates with amyloid-β in mouse models and in human patients with Alzheimer’s disease, and is associated with vascular defects and cognitive decline.

Jessica Wagner
Karoline Degenhardt
Jonas J. Neher
ResearchOpen Access16 Nov 2022
Nature

Volume: 612, P: 123-131
Reliability of Allen Ferguson classification versus subaxial injury classification and severity scale for subaxial cervical spine injuries: a psychometrics study

Vijayanth Kanagaraju
P. K. Karthik Yelamarthy
Vikas Tandon
Research08 Aug 2018
Spinal Cord

Volume: 57, P: 26-32
Dynamics of the human and viral m⁶A RNA methylomes during HIV-1 infection of T cells

Infection with HIV-1 triggers an increase in N⁶-methyladenosine (m⁶A) modification of both viral and host mRNAs, which impacts viral replication and nuclear export of viral RNA.

Gianluigi Lichinchi
Shang Gao
Tariq M. Rana
Research22 Feb 2016
Nature Microbiology

Volume: 1, P: 1-9
Whole-genome haplotype reconstruction using proximity-ligation and shotgun sequencing

Genetic variants are grouped into chromosome-spanning haplotypes with the help of chromatin-interaction data.

Siddarth Selvaraj
Jesse R Dixon
Bing Ren
Research01 Dec 2013
Nature Biotechnology

Volume: 31, P: 1111-1118
Whole-genome sequencing of multiple related individuals with type 2 diabetes reveals an atypical likely pathogenic mutation in the PAX6 gene

Bernhard O. Boehm
Wolfgang Kratzer
Vikas Bansal
ResearchOpen Access07 Oct 2022
European Journal of Human Genetics

Volume: 31, P: 89-96
Violent aggression predicted by multiple pre-adult environmental hits

Marina Mitjans
Jan Seidel
Hannelore Ehrenreich
ResearchOpen Access24 May 2018
Molecular Psychiatry

Volume: 24, P: 1549-1564

Search

Quality of TikTok videos on sudden cardiac death varies by video characteristics and health information accuracy

Scalable and accurate rare variant meta-analysis with Meta-SAIGE

The next phase in human genetics

Impact of the indigenous rotavirus vaccine Rotavac in the Universal Immunization Program in India during 2016–2020

Statistical analysis strategies for association studies involving rare variants

The importance of phase information for human genomics

Global, regional and national burden of dietary iron deficiency from 1990 to 2021: a Global Burden of Disease study

Not so lost in the genetic crowd

Thermal analysis of flat plate solar air heater system with radiation reflectors and W-shaped roughness: artificial neural network & machine learning approach

Author Correction: Impact of the indigenous rotavirus vaccine Rotavac in the Universal Immunization Program in India during 2016–2020

JAK2V617F reprograms Hypoxia Inducible Factor-1 to induce a non-canonical hypoxia regulon in myeloproliferative neoplasms

Robust and accurate estimation of paralog-specific copy number for duplicated genes using whole-genome sequencing

Functional hypoxia drives neuroplasticity and neurogenesis via brain erythropoietin

Realistic in silico generation and augmentation of single-cell RNA-seq data using generative adversarial networks

A diploid assembly-based benchmark for variants in the major histocompatibility complex

Longshot enables accurate variant calling in diploid genomes from single-molecule long read sequencing

Multi-locus genome-wide association studies (ML-GWAS) reveal novel genomic regions associated with seedling and adult plant stage leaf rust resistance in bread wheat (Triticum aestivum L.)

Forebrain-specific loss of erythropoietin provokes compensatory upregulation of different EPO receptors

Medin co-aggregates with vascular amyloid-β in Alzheimer’s disease

Reliability of Allen Ferguson classification versus subaxial injury classification and severity scale for subaxial cervical spine injuries: a psychometrics study

Dynamics of the human and viral m⁶A RNA methylomes during HIV-1 infection of T cells

Whole-genome haplotype reconstruction using proximity-ligation and shotgun sequencing

Whole-genome sequencing of multiple related individuals with type 2 diabetes reveals an atypical likely pathogenic mutation in the PAX6 gene

Violent aggression predicted by multiple pre-adult environmental hits

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