Nature Search

The immunomodulating V and W proteins of Nipah virus determine disease course

Nipah virus (NiV) can be transmitted from bats and other animals to humans, causing severe encephalitis and respiratory disease. Here, Satterfield et al.show that the W protein of NiV modulates the host immune response and determines disease course in a ferret model of infection.

Benjamin A. Satterfield
Robert W. Cross
Chad E. Mire
ResearchOpen Access24 Jun 2015
Nature Communications

Volume: 6, P: 1-15
Author Correction: Common-variant and rare-variant genetic architecture of heart failure across the allele-frequency spectrum

David S. M. Lee
Kathleen M. Cardone
Scott M. Damrauer
Amendments and Corrections28 Nov 2025
Nature Genetics

Volume: 57, P: 3201
Common-variant and rare-variant genetic architecture of heart failure across the allele-frequency spectrum

Common-variant and rare-variant association analyses combining datasets from multiple populations yield insights into the genetic architecture of all-cause heart failure across the allele-frequency spectrum.

David S. M. Lee
Kathleen M. Cardone
Scott M. Damrauer
Research07 Apr 2025
Nature Genetics

Volume: 57, P: 829-838
Publisher Correction: Cardiac involvement in the long-term implications of COVID-19

Benjamin A. Satterfield
Deepak L. Bhatt
Bernard J. Gersh
Amendments and Corrections01 Nov 2021
Nature Reviews Cardiology

Volume: 19, P: 342
Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure

Heart failure is a major cause of cardiovascular morbidity and mortality. Here, the authors report results of a genome-wide association study meta-analysis, characterizing the role of common genetic variants in heart failure, finding overlap with common cardiovascular risk factors and imaging measures of cardiac structure/function.

Michael G. Levin
Noah L. Tsao
Scott M. Damrauer
ResearchOpen Access14 Nov 2022
Nature Communications

Volume: 13, P: 1-15
Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases

Fibromuscular dysplasia is a cardiovascular disease affecting mostly women with a mostly unknown genetic basis. Here the authors have performed a genome-wide association meta-analysis of Fibromuscular dysplasia to identify genetic loci, some of which are shared with common cardiovascular disease and traits.

Adrien Georges
Min-Lee Yang
Nabila Bouatia-Naji
ResearchOpen Access15 Oct 2021
Nature Communications

Volume: 12, P: 1-16
Cortical response selectivity derives from strength in numbers of synapses

Live neuron imaging and electron microscopy reconstruction shows that the selectivity of cortical neuron responses to visual stimuli arises from the total number of synapses activated rather than being dominated by a small number of strong synaptic inputs.

Benjamin Scholl
Connon I. Thomas
David Fitzpatrick
Research16 Dec 2020
Nature

Volume: 590, P: 111-114
Demographics shape public preferences for carbon dioxide removal and solar geoengineering interventions across 30 countries

Public support for solar geoengineering and carbon dioxide removal methods decreases with age, and gender has little effect overall, according to an analysis combining the survey of 30 844 participants from 30 countries and a statistical approach.

Benjamin K. Sovacool
Darrick Evensen
Sean Low
ResearchOpen Access29 Oct 2024
Communications Earth & Environment

Volume: 5, P: 1-17
Author Correction: Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases

Adrien Georges
Min-Lee Yang
Nabila Bouatia-Naji
Amendments and CorrectionsOpen Access20 Apr 2022
Nature Communications

Volume: 13, P: 1
A phenome-wide association study to discover pleiotropic effects of PCSK9, APOB, and LDLR

Maya S. Safarova
Benjamin A. Satterfield
Iftikhar J. Kullo
ResearchOpen Access11 Feb 2019
npj Genomic Medicine

Volume: 4, P: 1-9
Differential tuning of excitation and inhibition shapes direction selectivity in ferret visual cortex

Inhibition to the null direction of motion has a critical role in the direction selectivity of neurons in ferret primary visual cortex.

Daniel E. Wilson
Benjamin Scholl
David Fitzpatrick
Research25 Jul 2018
Nature

Volume: 560, P: 97-101
Cardiac involvement in the long-term implications of COVID-19

In this Perspectives article, the authors highlight what is known about cardiovascular sequelae in survivors of COVID-19 and discuss important questions that need to be addressed in prospective studies to understand and mitigate these lasting cardiovascular consequences, including in post-acute COVID-19 syndrome.

Benjamin A. Satterfield
Deepak L. Bhatt
Bernard J. Gersh
Reviews22 Oct 2021
Nature Reviews Cardiology

Volume: 19, P: 332-341
Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection

Kathleen Ferar
Taryn O. Hall
David R. Crosslin
ResearchOpen Access28 Oct 2023
Scientific Reports

Volume: 13, P: 1-15
Evaluation of the portability of computable phenotypes with natural language processing in the eMERGE network

Jennifer A. Pacheco
Luke V. Rasmussen
WeiQi Wei
ResearchOpen Access03 Feb 2023
Scientific Reports

Volume: 13, P: 1-11
Antagonism of STAT1 by Nipah virus P gene products modulates disease course but not lethal outcome in the ferret model

Benjamin A. Satterfield
Viktoriya Borisevich
Chad E. Mire
ResearchOpen Access13 Nov 2019
Scientific Reports

Volume: 9, P: 1-18
Pathogenic Differences between Nipah Virus Bangladesh and Malaysia Strains in Primates: Implications for Antibody Therapy

Chad E. Mire
Benjamin A. Satterfield
Thomas W. Geisbert
ResearchOpen Access03 Aug 2016
Scientific Reports

Volume: 6, P: 1-16
Author Correction: Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection

Kathleen Ferar
Taryn O. Hall
David R. Crosslin
Amendments and CorrectionsOpen Access15 Nov 2023
Scientific Reports

Volume: 13, P: 1

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The immunomodulating V and W proteins of Nipah virus determine disease course

Author Correction: Common-variant and rare-variant genetic architecture of heart failure across the allele-frequency spectrum

Common-variant and rare-variant genetic architecture of heart failure across the allele-frequency spectrum

Publisher Correction: Cardiac involvement in the long-term implications of COVID-19

Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure

Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases

Cortical response selectivity derives from strength in numbers of synapses

Demographics shape public preferences for carbon dioxide removal and solar geoengineering interventions across 30 countries

Author Correction: Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases

A phenome-wide association study to discover pleiotropic effects of PCSK9, APOB, and LDLR

Differential tuning of excitation and inhibition shapes direction selectivity in ferret visual cortex

Cardiac involvement in the long-term implications of COVID-19

Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection

Evaluation of the portability of computable phenotypes with natural language processing in the eMERGE network

Antagonism of STAT1 by Nipah virus P gene products modulates disease course but not lethal outcome in the ferret model

Pathogenic Differences between Nipah Virus Bangladesh and Malaysia Strains in Primates: Implications for Antibody Therapy

Author Correction: Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection

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