Nature Search

Nannoplankton of Marine Origin from Great Bear Lake in the Northwest Territories of Canada

A. S. BURSA
L. JOHNSON
Research01 Apr 1967
Nature

Volume: 214, P: 528-529
Correction: Vitamin B₁₂ deficiency

Ralph Green
Lindsay H. Allen
Chittaranjan Yajnik
Amendments and Corrections20 Jul 2017
Nature Reviews Disease Primers

Volume: 3, P: 1
Insights from a century of data reveal global trends in ex situ living plant collections

The authors collate a meta-collection of ex situ living plant diversity held in 50 botanical collections worldwide, spanning a century of data and currently containing ~500,000 accessions. Their analyses examine the capacities and constraints within living plant collections, reveal the impact of the Convention on Biological Diversity and its consequences for material exchange and conservation, and call for the re-evaluation of strategic priorities.

Ángela Cano
Jake Powell
Samuel F. Brockington
ResearchOpen Access21 Jan 2025
Nature Ecology & Evolution

Volume: 9, P: 214-224
Erratum: A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4

Terri H Beaty
Jeffrey C Murray
Alan F Scott
Amendments and Corrections01 Aug 2010
Nature Genetics

Volume: 42, P: 727
Whole-brain annotation and multi-connectome cell typing of Drosophila

A consensus cell type atlas for the fly brain provides both an intellectual framework and open-source toolchains for brain-scale comparative connectomics.

Philipp Schlegel
Yijie Yin
Gregory S. X. E. Jefferis
ResearchOpen Access02 Oct 2024
Nature

Volume: 634, P: 139-152
GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture

Genome-wide association meta-analyses identify 26 risk loci for epilepsy, including 19 loci specific to genetic generalized epilepsy. Prioritized candidate genes implicate synaptic processes and overlap with targets of antiseizure medications.

Remi Stevelink
Ciarán Campbell
Quratulain Zulfiqar Ali
ResearchOpen Access31 Aug 2023
Nature Genetics

Volume: 55, P: 1471-1482
Maternal carriage of Prevotella during pregnancy associates with protection against food allergy in the offspring

Incidence of food allergy in westernized populations is associated with low abundance of Prevotella. Here, the authors analyse the microbiome of a mother-infant prebirth cohort and find that maternal carriage, but not infant carriage, of P. copri during pregnancy predicts the absence of food allergy in the offspring.

Peter J. Vuillermin
Martin O’Hely
Esther Bandala Sanchez
ResearchOpen Access24 Mar 2020
Nature Communications

Volume: 11, P: 1-7
Multi-laboratory assessment of reproducibility, qualitative and quantitative performance of SWATH-mass spectrometry

SWATH-mass spectrometry consists of a data-independent acquisition and a targeted data analysis strategy that aims to maintain the favorable quantitative characteristics on the scale of thousands of proteins. Here, using data generated by eleven groups worldwide, the authors show that SWATH-MS is capable of generating highly reproducible data across different laboratories.

Ben C. Collins
Christie L. Hunter
Ruedi Aebersold
ResearchOpen Access21 Aug 2017
Nature Communications

Volume: 8, P: 1-12
Confirmation of the R653Q polymorphism of the trifunctional C1-synthase enzyme as a maternal risk for neural tube defects in the Irish population

Anne Parle-McDermott
Peadar N Kirke
John M Scott
Research22 Mar 2006
European Journal of Human Genetics

Volume: 14, P: 768-772
Neuronal wiring diagram of an adult brain

FlyWire presents a neuronal wiring diagram of the whole fly brain with annotations for cell types, classes, nerves, hemilineages and predicted neurotransmitters, with data products and an open ecosystem to facilitate exploration and browsing.

Sven Dorkenwald
Arie Matsliah
Meet Zandawala
ResearchOpen Access02 Oct 2024
Nature

Volume: 634, P: 124-138
Analysis of the MTHFR 1298A→C and 677C→T polymorphisms as risk factors for neural tube defects

Anne Parle-McDermott
James L. Mills
Lawrence C. Brody
Research05 Mar 2003
Journal of Human Genetics

Volume: 48, P: 190-193
Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies

Epilepsies are common brain disorders and are classified based on clinical phenotyping, imaging and genetics. Here, the authors perform genome-wide association studies for 3 broad and 7 subtypes of epilepsy and identify 16 loci - 11 novel - that are further annotated by eQTL and partitioned heritability analyses.

Bassel Abou-Khalil
Pauls Auce
Fritz Zimprich
ResearchOpen Access10 Dec 2018
Nature Communications

Volume: 9, P: 1-15
Effect of Cortisol on Gene Expression of the Renin-Angiotensin System in Fetal Sheep

Jeffrey L Segar
Kurt Bedell
Jean E Robillard
Research01 Jun 1995
Pediatric Research

Volume: 37, P: 741-746
A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4

Terri Beaty and colleagues report a genome-wide association study of cleft lip with/without cleft palate. They identified variants near MAFB and ABCA4 associated with risk of this birth defect in case-parent trios of European and Asian ancestry.

Terri H Beaty
Jeffrey C Murray
Alan F Scott
Research02 May 2010
Nature Genetics

Volume: 42, P: 525-529
Vitamin B₁₂ deficiency

Vitamin B₁₂ (also known as cobalamin) is a B vitamin that has an important role in cellular metabolism, especially in DNA synthesis, methylation and mitochondrial metabolism. In this Primer, Green et al. describe the causes, consequences and management of vitamin B₁₂ deficiency.

Ralph Green
Lindsay H. Allen
Chittaranjan Yajnik
Reviews29 Jun 2017
Nature Reviews Disease Primers

Volume: 3, P: 1-20
At-admission prediction of mortality and pulmonary embolism in an international cohort of hospitalised patients with COVID-19 using statistical and machine learning methods

Munib Mesinovic
Xin Ci Wong
David Zucman
ResearchOpen Access16 Jul 2024
Scientific Reports

Volume: 14, P: 1-43
Sustained translational repression by eIF2α-P mediates prion neurodegeneration

Accumulation of prion protein during prion replication causes persistent translational repression of global protein synthesis, which is mediated by eIF2α-P and is associated with synaptic failure and neuronal loss in prion-diseased mice; promoting translational recovery in hippocampi of prion-infected mice is neuroprotective.

Julie A. Moreno
Helois Radford
Giovanna R. Mallucci
Research06 May 2012
Nature

Volume: 485, P: 507-511
RBM3 mediates structural plasticity and protective effects of cooling in neurodegeneration

Structural synaptic plasticity and remodelling are features of the healthy adult brain and are seen during hibernation; a hibernation-inspired model of mouse cooling used to study synaptic regeneration has identified the ‘cold-shock’ RNA-binding protein, RBM3, as a regulator of synaptic assembly, deficiency of which contributes to synapse loss in neurodegenerative disease.

Diego Peretti
Amandine Bastide
Giovanna R. Mallucci
Research14 Jan 2015
Nature

Volume: 518, P: 236-239
Directed evolution of human T-cell receptors with picomolar affinities by phage display

Yi Li
Ruth Moysey
Jonathan M Boulter
Research20 Feb 2005
Nature Biotechnology

Volume: 23, P: 349-354
A genetic perspective on the recent demographic history of Ireland and Britain

Ashwini Shanmugam
Michael Merrigan
Edmund H. Gilbert
ResearchOpen Access05 Feb 2025
European Journal of Human Genetics

Volume: 33, P: 538-545
Low folate predicts accelerated cognitive decline: 8-year follow-up of 3140 older adults in Ireland

Deirdre M. A. O’Connor
Siobhan Scarlett
Rose Anne Kenny
Research13 Jan 2022
European Journal of Clinical Nutrition

Volume: 76, P: 950-957
The Newfoundland and Labrador mosaic founder population descends from an Irish and British diaspora from 300 years ago

An analysis of the population genetic structure of Newfoundland and Labrador identifies close genetic links between this population and South England and South Ireland, with a strong bottleneck roughly 300 years ago.

Edmund Gilbert
Heather Zurel
Michael S. Phillips
ResearchOpen Access28 Apr 2023
Communications Biology

Volume: 6, P: 1-12
Heterozygous and homozygous variants in STX1A cause a neurodevelopmental disorder with or without epilepsy

Johannes Luppe
Heinrich Sticht
Konrad Platzer
ResearchOpen Access23 Dec 2022
European Journal of Human Genetics

Volume: 31, P: 345-352
Disrupted brain functional connectivity as early signature in cognitively healthy individuals with pathological CSF amyloid/tau

This study reveals disrupted brain functional connectivity as an early biomarker in cognitively healthy individuals with pathological CSF amyloid/tau, aiding early Alzheimer’s detection.

Abdulhakim Al-Ezzi
Rebecca J. Arechavala
Xianghong Arakaki
ResearchOpen Access23 Aug 2024
Communications Biology

Volume: 7, P: 1-15
PI3K/mTOR inhibition of IDH1 mutant glioma leads to reduced 2HG production that is associated with increased survival

Georgios Batsios
Pavithra Viswanath
Sabrina M. Ronen
ResearchOpen Access19 Jul 2019
Scientific Reports

Volume: 9, P: 1-15
The Irish DNA Atlas: Revealing Fine-Scale Population Structure and History within Ireland

Edmund Gilbert
Seamus O’Reilly
Gianpiero L. Cavalleri
ResearchOpen Access08 Dec 2017
Scientific Reports

Volume: 7, P: 1-11
The genetic landscape of polycystic kidney disease in Ireland

Katherine A. Benson
Susan L. Murray
Peter Conlon
Research16 Jan 2021
European Journal of Human Genetics

Volume: 29, P: 827-838
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
Author Correction: The Irish DNA Atlas: Revealing Fine-Scale Population Structure and History within Ireland

Edmund Gilbert
Seamus O’Reilly
Gianpiero L. Cavalleri
Amendments and CorrectionsOpen Access03 May 2018
Scientific Reports

Volume: 8, P: 1-2
Bronchiolitis: evidence-based management in high-risk infants in the intensive care setting

Ruth Walsh
Liam Costello
Eleanor Molloy
ReviewsOpen Access20 Jun 2024
Pediatric Research

Volume: 96, P: 1560-1567
Neutrophil and monocyte toll-like receptor 4, CD11b and reactive oxygen intermediates, and neuroimaging outcomes in preterm infants

Fiona M. O’Hare
William Watson
Eleanor J. Molloy
Research31 Mar 2015
Pediatric Research

Volume: 78, P: 82-90

Search

Nannoplankton of Marine Origin from Great Bear Lake in the Northwest Territories of Canada

Correction: Vitamin B₁₂ deficiency

Insights from a century of data reveal global trends in ex situ living plant collections

Erratum: A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4

Whole-brain annotation and multi-connectome cell typing of Drosophila

GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture

Maternal carriage of Prevotella during pregnancy associates with protection against food allergy in the offspring

Multi-laboratory assessment of reproducibility, qualitative and quantitative performance of SWATH-mass spectrometry

Confirmation of the R653Q polymorphism of the trifunctional C1-synthase enzyme as a maternal risk for neural tube defects in the Irish population

Neuronal wiring diagram of an adult brain

Analysis of the MTHFR 1298A→C and 677C→T polymorphisms as risk factors for neural tube defects

Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies

Effect of Cortisol on Gene Expression of the Renin-Angiotensin System in Fetal Sheep

A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4

Vitamin B₁₂ deficiency

At-admission prediction of mortality and pulmonary embolism in an international cohort of hospitalised patients with COVID-19 using statistical and machine learning methods

Sustained translational repression by eIF2α-P mediates prion neurodegeneration

RBM3 mediates structural plasticity and protective effects of cooling in neurodegeneration

Directed evolution of human T-cell receptors with picomolar affinities by phage display

A genetic perspective on the recent demographic history of Ireland and Britain

Low folate predicts accelerated cognitive decline: 8-year follow-up of 3140 older adults in Ireland

The Newfoundland and Labrador mosaic founder population descends from an Irish and British diaspora from 300 years ago

Heterozygous and homozygous variants in STX1A cause a neurodevelopmental disorder with or without epilepsy

Disrupted brain functional connectivity as early signature in cognitively healthy individuals with pathological CSF amyloid/tau

PI3K/mTOR inhibition of IDH1 mutant glioma leads to reduced 2HG production that is associated with increased survival

The Irish DNA Atlas: Revealing Fine-Scale Population Structure and History within Ireland

The genetic landscape of polycystic kidney disease in Ireland

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

Author Correction: The Irish DNA Atlas: Revealing Fine-Scale Population Structure and History within Ireland

Bronchiolitis: evidence-based management in high-risk infants in the intensive care setting

Neutrophil and monocyte toll-like receptor 4, CD11b and reactive oxygen intermediates, and neuroimaging outcomes in preterm infants

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