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Author Correction: Two point mutations in protocadherin-1 disrupt hantavirus recognition and afford protection against lethal infection

Megan M. Slough
Rong Li
Kartik Chandran
Amendments and CorrectionsOpen Access22 Sept 2023
Nature Communications

Volume: 14, P: 1
Two point mutations in protocadherin-1 disrupt hantavirus recognition and afford protection against lethal infection

Protocadherin-1 (PCDH1) is a critical host factor for hantaviruses that can cause severe cardiopulmonary syndrome. Here, the authors map the binding site of the viral glycoprotein complex within PCDH1 and show that mutations engineered at this site can protect Syrian hamsters from viral challenge.

Megan M. Slough
Rong Li
Kartik Chandran
ResearchOpen Access24 Jul 2023
Nature Communications

Volume: 14, P: 1-17
GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19

An analysis of 24,202 critical cases of COVID-19 identifies potentially druggable targets in inflammatory signalling (JAK1), monocyte–macrophage activation and endothelial permeability (PDE4A), immunometabolism (SLC2A5 and AK5), and host factors required for viral entry and replication (TMPRSS2 and RAB2A).

Erola Pairo-Castineira
Konrad Rawlik
J. Kenneth Baillie
ResearchOpen Access17 May 2023
Nature

Volume: 617, P: 764-768
Correction: Corrigendum: Metabolomic profiles delineate potential role for sarcosine in prostate cancer progression

Arun Sreekumar
Laila M. Poisson
Arul M. Chinnaiyan
Amendments and Corrections05 Jun 2013
Nature

Volume: 499, P: 504
Whole-genome sequencing reveals host factors underlying critical COVID-19

Whole-genome sequencing, transcriptome-wide association and fine-mapping analyses in over 7,000 individuals with critical COVID-19 are used to identify 16 independent variants that are associated with severe illness in COVID-19.

Athanasios Kousathanas
Erola Pairo-Castineira
J. Kenneth Baillie
ResearchOpen Access07 Mar 2022
Nature

Volume: 607, P: 97-103
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
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
Multiple drivers of the North Atlantic warming hole

The North Atlantic ocean warming hole has been linked to reduced tropical heat import. Model simulations show an anthropogenically forced increased heat export poleward from the region, by overturning and gyre circulation, and shortwave cloud feedback control the warming hole formation and growth.

Paul Keil
Thorsten Mauritsen
Rohit Ghosh
Research29 Jun 2020
Nature Climate Change

Volume: 10, P: 667-671
Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci

Chiea Chuen Khor, Tin Aung, Francesca Pasutto, Janey Wiggs and colleagues report a global genome-wide association study of exfoliation syndrome and a fine-mapping analysis of a previously identified disease-associated locus, LOXL1. They identify a rare protective variant in LOXL1 exclusive to the Japanese population and five new common variant susceptibility loci.

Tin Aung
Mineo Ozaki
Chiea Chuen Khor
Research29 May 2017
Nature Genetics

Volume: 49, P: 993-1004
Correction: Corrigendum: A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome

Tin Aung
Mineo Ozaki
Chiea-Chuen Khor
Amendments and Corrections27 May 2015
Nature Genetics

Volume: 47, P: 689
Author Correction: GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19

Erola Pairo-Castineira
Konrad Rawlik
J. Kenneth Baillie
Amendments and CorrectionsOpen Access11 Jul 2023
Nature

Volume: 619, P: E61
Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma

Chiea Chuen Khor, Tin Aung and colleagues report the results of a large genome-wide association study of primary angle closure glaucoma. They identify five new susceptibility loci and provide insights into disease pathogenesis.

Chiea Chuen Khor
Tan Do
Tin Aung
Research04 Apr 2016
Nature Genetics

Volume: 48, P: 556-562
Metabolomic profiles delineate potential role for sarcosine in prostate cancer progression

A systematic analysis of metabolites in prostate cancer samples has led to the identification of sarcosine as a putative biomarker detectable in urine, which could potentially be used to aid prostate cancer diagnosis. Sarcosine promotes the invasion of prostate cancer cells and may play a role in metastasis.

Arun Sreekumar
Laila M. Poisson
Arul M. Chinnaiyan
Research01 Feb 2009
Nature

Volume: 457, P: 910-914
A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome

Tin Aung, Chiea-Chuen Khor and colleagues report the results of a genome-wide association study of exfoliation syndrome. They replicate a known association at LOXL1 and identify a previously unreported association at CACNA1A.

Tin Aung
Mineo Ozaki
Chiea-Chuen Khor
Research23 Feb 2015
Nature Genetics

Volume: 47, P: 387-392
Identification of novel predictive factors for post surgical corneal haze

Nimisha R. Kumar
Pooja Khamar
Arkasubhra Ghosh
ResearchOpen Access18 Nov 2019
Scientific Reports

Volume: 9, P: 1-14
Physical features of Adam’s Bridge interpreted from ICESat-2 based high-resolution digital bathymetric elevation model

Giribabu Dandabathula
Koushik Ghosh
Prakash Chauhan
ResearchOpen Access28 Jun 2024
Scientific Reports

Volume: 14, P: 1-19
Safety and efficacy of combination of suberoylamilide hydroxyamic acid and mitomycin C in reducing pro-fibrotic changes in human corneal epithelial cells

Rohit Shetty
Nimisha Rajiv Kumar
Debashish Das
ResearchOpen Access23 Feb 2021
Scientific Reports

Volume: 11, P: 1-18
Comprehensive assessment of TMPRSS2 and ETS family gene aberrations in clinically localized prostate cancer

Rohit Mehra
Scott A Tomlins
Rajal B Shah
Research02 Mar 2007
Modern Pathology

Volume: 20, P: 538-544
Correlation between tear levels of vascular endothelial growth factor and vitamin D at retinopathy of prematurity stages in preterm infants

Ponnalagu Murugeswari
Anand Vinekar
Debashish Das
ResearchOpen Access27 Sept 2023
Scientific Reports

Volume: 13, P: 1-11
Expanding repertoire of SARS-CoV-2 deletion mutations contributes to evolution of highly transmissible variants

A. J. Venkatakrishnan
Praveen Anand
Venky Soundararajan
ResearchOpen Access05 Jan 2023
Scientific Reports

Volume: 13, P: 1-11
Pre-analytical sample handling effects on tear fluid protein levels

Marlies Gijs
Sinthuja Arumugam
Rudy M. M. A. Nuijts
ResearchOpen Access24 Jan 2023
Scientific Reports

Volume: 13, P: 1-11
Keratoconus patients exhibit a distinct ocular surface immune cell and inflammatory profile

Sharon D’Souza
Archana Padmanabhan Nair
Swaminathan Sethu
ResearchOpen Access22 Oct 2021
Scientific Reports

Volume: 11, P: 1-16
Resveratrol reverses the adverse effects of bevacizumab on cultured ARPE-19 cells

Murali Subramani
Murugeswari Ponnalagu
Debashish Das
ResearchOpen Access25 Sept 2017
Scientific Reports

Volume: 7, P: 1-16
A High-Resolution Digital Bathymetric Elevation Model Derived from ICESat-2 for Adam’s Bridge

Giribabu Dandabathula
Rohit Hari
Prakash Chauhan
ResearchOpen Access27 Jun 2024
Scientific Data

Volume: 11, P: 1-18

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Author Correction: Two point mutations in protocadherin-1 disrupt hantavirus recognition and afford protection against lethal infection

Two point mutations in protocadherin-1 disrupt hantavirus recognition and afford protection against lethal infection

GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19

Correction: Corrigendum: Metabolomic profiles delineate potential role for sarcosine in prostate cancer progression

Whole-genome sequencing reveals host factors underlying critical COVID-19

Mapping the human genetic architecture of COVID-19

A second update on mapping the human genetic architecture of COVID-19

Multiple drivers of the North Atlantic warming hole

Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci

Correction: Corrigendum: A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome

Author Correction: GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19

Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma

Metabolomic profiles delineate potential role for sarcosine in prostate cancer progression

A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome

Identification of novel predictive factors for post surgical corneal haze

Physical features of Adam’s Bridge interpreted from ICESat-2 based high-resolution digital bathymetric elevation model

Safety and efficacy of combination of suberoylamilide hydroxyamic acid and mitomycin C in reducing pro-fibrotic changes in human corneal epithelial cells

Comprehensive assessment of TMPRSS2 and ETS family gene aberrations in clinically localized prostate cancer

Correlation between tear levels of vascular endothelial growth factor and vitamin D at retinopathy of prematurity stages in preterm infants

Expanding repertoire of SARS-CoV-2 deletion mutations contributes to evolution of highly transmissible variants

Pre-analytical sample handling effects on tear fluid protein levels

Keratoconus patients exhibit a distinct ocular surface immune cell and inflammatory profile

Resveratrol reverses the adverse effects of bevacizumab on cultured ARPE-19 cells

A High-Resolution Digital Bathymetric Elevation Model Derived from ICESat-2 for Adam’s Bridge

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