Nature Search

African swine fever outbreaks in German pig holdings – experiences, epidemiological considerations and genome sequences

Katja Schulz
Sten Calvelage
Carola Sauter-Louis
ResearchOpen Access29 Jan 2026
Scientific Reports

Volume: 16, P: 1-15
An intersectional approach to examine low birthweight by migration status in Sweden using register data

Sooz Romero
Andrea Dunlavy
Sol P. Juárez
ResearchOpen Access04 Nov 2025
Scientific Reports

Volume: 15, P: 1-8
COVID-19: living guidelines help fix cracks in evidence pipeline

Per Olav Vandvik
Lisa Askie
Thomas Agoritsas
Correspondence06 Jul 2021
Nature

Volume: 595, P: 172
Synthetic chaperone based on Hsp90-Tau interaction inhibits Tau aggregation and rescues physiological Tau-Microtubule interaction

Tau aggregation, a hallmark of Alzheimer’s disease, disrupts neuron structure. Aging weakens chaperone defenses like Hsp90. This study designs β-Hsp90, a small peptide mimicking Hsp90, to prevent Tau aggregation, offering promise for new amyloid disease drugs.

Davide Di Lorenzo
Nicolo Bisi
Sandrine Ongeri
ResearchOpen Access01 Oct 2025
Nature Communications

Volume: 16, P: 1-18
Identification and mutation analysis of the complete gene for Chediak–Higashi syndrome

Deborah L. Nagle
Mohammad A. Karim
Karen J. Moore
Research01 Nov 1996
Nature Genetics

Volume: 14, P: 307-311
Students step up

Universities and institutions in the United States are getting ready to celebrate nanotechnology and its achievements for National Nanotechnology Day. Lisa Friedersdorf, Quinn Spadola and Brendan Ryan share students' plans for the occasion.

Lisa E. Friedersdorf
Quinn A. Spadola
Brendan Ryan
Comments & Opinion06 Oct 2017
Nature Nanotechnology

Volume: 12, P: 1016
The corneal thickness profile in different forms of glaucoma

Lisa Ramm
Wienke Fleischer
Karin R. Pillunat
ResearchOpen Access07 Nov 2025
Scientific Reports

Volume: 15, P: 1-10
Naloxone Potentiates Epinephrine Release during Hypoxia in Fetal Sheep: Dose Response and Cardiovascular Effects

Alma Martinez
James Padbury
James Humme
Research01 Apr 1988
Pediatric Research

Volume: 23, P: 343-347
Correction: Corrigendum: Genome-wide association study identifies variants at 16p13 associated with survival in multiple myeloma patients

Elad Ziv
Eric Dean
Celine Vachon
Amendments and Corrections09 Dec 2015
Nature Communications

Volume: 6, P: 1
Scattered tree death contributes to substantial forest loss in California

Tree mortality due to climate change and other disturbances is on the rise. Here, the authors use high-resolution remote sensing data, ground observations and deep learning to quantify individual dead trees and potential drivers across California in the year 2020, encompassing 91.4 million dead trees.

Yan Cheng
Stefan Oehmcke
Stéphanie Horion
ResearchOpen Access20 Jan 2024
Nature Communications

Volume: 15, P: 1-13
H5N1 clade 2.3.4.4b dynamics in experimentally infected calves and cows

Infection studies on highly pathogenic avian influenza virus clade 2.3.4.4b H5N1 on calves and lactating cows indicate that transmission occurs primarily via milk and milking procedures rather than respiratory routes.

Nico Joel Halwe
Konner Cool
Juergen A. Richt
ResearchOpen Access25 Sept 2024
Nature

Volume: 637, P: 903-912
Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa

Genome-wide analyses identify eight independent loci associated with anorexia nervosa. Genetic correlations implicate both psychiatric and metabolic components in the etiology of this disorder, even after adjusting for the effects of common variants associated with body mass index.

Hunna J. Watson
Zeynep Yilmaz
Cynthia M. Bulik
Research15 Jul 2019
Nature Genetics

Volume: 51, P: 1207-1214
Genome sequence of the Brown Norway rat yields insights into mammalian evolution

Richard A. Gibbs
George M. Weinstock
Francis Collins
Research01 Apr 2004
Nature

Volume: 428, P: 493-521
Genome-wide association study identifies variants at 16p13 associated with survival in multiple myeloma patients

Multiple myeloma is an incurable blood cancer with family history being a strong contributing risk factor. Here Ziv et al.perform a genome-wide association study for genetic variation associated with myeloma survival, identifying FOPNL variants associated with worse clinical outcomes.

Elad Ziv
Eric Dean
Celine Vachon
Research22 Jul 2015
Nature Communications

Volume: 6, P: 1-9
A safe, effective and adaptable live-attenuated SARS-CoV-2 vaccine to reduce disease and transmission using one-to-stop genome modifications

A live-attenuated SARS-CoV-2 vaccine based on one-to-stop codon modifications can elicit broad, systemic and mucosal immunity, as well as reduced transmission of SARS-CoV-2 in vivo.

Jacob Schön
G. Tuba Barut
Volker Thiel
ResearchOpen Access12 Jul 2024
Nature Microbiology

Volume: 9, P: 2099-2112
To which world regions does the valence–dominance model of social perception apply?

Jones et al. examine the generalizability of the valence–dominance model of social judgements of faces in 41 countries across 11 world regions. They find evidence of both generalizability and variation, depending on the analytical method.

Benedict C. Jones
Lisa M. DeBruine
Nicholas A. Coles
Research04 Jan 2021
Nature Human Behaviour

Volume: 5, P: 159-169
Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia

Susan Slager and colleagues report a meta-analysis of genome-wide association studies for chronic lymphocytic leukemia (CLL). They identify nine loci newly associated with CLL.

Sonja I Berndt
Christine F Skibola
Susan L Slager
Research16 Jun 2013
Nature Genetics

Volume: 45, P: 868-876
Repetitive transcranial magnetic stimulation reveals a causal role of the human precuneus in spatial updating

Notger G. Müller
Martin Riemer
Thomas Wolbers
ResearchOpen Access05 Jul 2018
Scientific Reports

Volume: 8, P: 1-8
Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson’s disease

Integration of GWAS and single-cell transcriptomic data from the entire nervous system systematically identifies cell types underlying brain complex traits and provides insights into the etiology of Parkinson’s disease.

Julien Bryois
Nathan G. Skene
Patrick F. Sullivan
Research27 Apr 2020
Nature Genetics

Volume: 52, P: 482-493
Detection of low-level mosaicism and placental mosaicism by oligonucleotide array comparative genomic hybridization

Stuart A Scott
Ninette Cohen
Lisa Edelmann
Research15 Jan 2010
Genetics in Medicine

Volume: 12, P: 85-92
Inflammation and limited adaptive immunity predict worse outcomes on immunotherapy in head and neck cancer

Lisa Paschold
Christoph Schultheiss
Mascha Binder
ResearchOpen Access05 Aug 2025
npj Precision Oncology

Volume: 9, P: 1-10
3-Methylglutaconic Acidemia in Smith-Lemli-Opitz Syndrome

Richard I Kelley
Lisa Kratz
Research01 May 1995
Pediatric Research

Volume: 37, P: 671-674
In Vitro and In Vivo Effects of Granulocyte Colony-Stimulating Factor on Neutrophils in Glycogen Storage Disease Type IB: Granulocyte Colony-Stimulating Factor Therapy Corrects the Neutropenia and the Defects in Respiratory Burst Activity and Ca²⁺ Mobilization

Lisa J Mccawley
Helen M Korchak
Laurie Kilpatrick
Research01 Jan 1994
Pediatric Research

Volume: 35, P: 84-90
RAS–MAPK–MSK1 pathway modulates ataxin 1 protein levels and toxicity in SCA1

Cross-species genetic screens reveal that decreased mitogen-activated protein kinase signalling reduces polyglutamine-expanded ataxin 1 levels and toxicity in models of spinocerebellar ataxia type 1.

Jeehye Park
Ismael Al-Ramahi
Huda Y. Zoghbi
Research29 May 2013
Nature

Volume: 498, P: 325-331
Oncogenic activation of the PDGF β receptor by the transmembrane domain of p185^neu*

Lisa M Petti
Pablo M Irusta
Daniel DiMaio
Research03 Mar 1998
Oncogene

Volume: 16, P: 843-851
The Somatic Mosaicism across Human Tissues Network

The Somatic Mosaicism across Human Tissues Network aims to create a reference catalogue of somatic mosaicism across different tissues and cells within individuals.

Tim H. H. Coorens
Ji Won Oh
Yuqing Wang
Reviews02 Jul 2025
Nature

Volume: 643, P: 47-59
Analyses of allele-specific gene expression in highly divergent mouse crosses identifies pervasive allelic imbalance

Fernando Pardo-Manuel de Villena and colleagues generate a 3 × 3 diallel cross of three inbred mouse lines and examine gene expression in multiple tissues. They identify allelic imbalance favoring the expression of the paternal allele across the genome.

James J Crowley
Vasyl Zhabotynsky
Fernando Pardo-Manuel de Villena
Research02 Mar 2015
Nature Genetics

Volume: 47, P: 353-360
IBD risk loci are enriched in multigenic regulatory modules encompassing putative causative genes

Most of the more than 200 known genetic risk loci for inflammatory bowel disease (IBD) reside in regulatory regions. Here, the authors provide eQTL datasets for six circulating immune cell types and ileal, colonic and rectal biopsies to map regulatory modules and identify potential causative genes for IBD.

Yukihide Momozawa
Julia Dmitrieva
Michel Georges
ResearchOpen Access21 Jun 2018
Nature Communications

Volume: 9, P: 1-18
Leveraging transdiagnostic genetic liability to psychiatric disorders to dissect clinical outcomes of anorexia nervosa

Zheng-An Lu
Alexander Ploner
Sarah E. Bergen
ResearchOpen Access23 Sept 2025
Molecular Psychiatry

P: 1-10
SARS-CoV-2 RNA and antibody dynamics in a Dutch household study with dense sampling frame

Wanda G. H. Han
Arno Swart
Adam Meijer
ResearchOpen Access13 May 2022
Scientific Reports

Volume: 12, P: 1-12
Delineating immune variation between adult and children COVID-19 cases and associations with disease severity

Alper Cevirgel
Martijn Vos
Jelle de Wit
ResearchOpen Access01 Mar 2024
Scientific Reports

Volume: 14, P: 1-11
Functional and clinical studies reveal pathophysiological complexity of CLCN4-related neurodevelopmental condition

Elizabeth E. Palmer
Michael Pusch
Vera M. Kalscheuer
ResearchOpen Access16 Nov 2022
Molecular Psychiatry

Volume: 28, P: 668-697
Antifouling coatings can reduce algal growth while preserving coral settlement

Lisa K. Roepke
David Brefeld
Andreas Kunzmann
ResearchOpen Access24 Sept 2022
Scientific Reports

Volume: 12, P: 1-14
Correction: Adapting ACMG/AMP sequence variant classification guidelines for single-gene copy-number variants

Tracy Brandt
Laura M. Sack
Jeanne M. Meck
Amendments and Corrections17 Dec 2019
Genetics in Medicine

Volume: 22, P: 670-671
Author Correction: Repetitive transcranial magnetic stimulation reveals a causal role of the human precuneus in spatial updating

Notger G. Müller
Martin Riemer
Thomas Wolbers
Amendments and CorrectionsOpen Access07 Sept 2018
Scientific Reports

Volume: 8, P: 1-2
Predicting breast cancer response to neoadjuvant treatment using multi-feature MRI: results from the I-SPY 2 TRIAL

Wen Li
David C. Newitt
Nola M. Hylton
ResearchOpen Access27 Nov 2020
npj Breast Cancer

Volume: 6, P: 1-6
Adapting ACMG/AMP sequence variant classification guidelines for single-gene copy number variants

Tracy Brandt
Laura M. Sack
Jeanne M. Meck
Research19 Sept 2019
Genetics in Medicine

Volume: 22, P: 336-344
High quality of SARS-CoV-2 molecular diagnostics in a diverse laboratory landscape through supported benchmark testing and External Quality Assessment

John Sluimer
Willem M. R. van den Akker
Adam Meijer
ResearchOpen Access16 Jan 2024
Scientific Reports

Volume: 14, P: 1-12
Defining suicidality phenotypes for genetic studies: perspectives of the Psychiatric Genomics Consortium Suicide Working Group

Sarah M. C. Colbert
Eric T. Monson
Lea Zillich
ReviewsOpen Access25 Sept 2025
Molecular Psychiatry

Volume: 30, P: 6144-6154
Virulence from vesicles: Novel mechanisms of host cell injury by Escherichia coli O104:H4 outbreak strain

Lisa Kunsmann
Christian Rüter
Martina Bielaszewska
ResearchOpen Access18 Aug 2015
Scientific Reports

Volume: 5, P: 1-18
The Psychotomimetic Effects of Intravenous Delta-9-Tetrahydrocannabinol in Healthy Individuals: Implications for Psychosis

Deepak Cyril D'Souza
Edward Perry
John Harrison Krystal
Research02 Jun 2004
Neuropsychopharmacology

Volume: 29, P: 1558-1572
Respiratory syncytial, parainfluenza and influenza virus infection in young children with acute lower respiratory infection in rural Gambia

Grant A. Mackenzie
Aminata Vilane
Adam Meijer
ResearchOpen Access29 Nov 2019
Scientific Reports

Volume: 9, P: 1-10
An Ashkenazi Jewish SMN1 haplotype specific to duplication alleles improves pan-ethnic carrier screening for spinal muscular atrophy

Minjie Luo
Liu Liu
Lisa Edelmann
Research20 Jun 2013
Genetics in Medicine

Volume: 16, P: 149-156
Resting-state MRI functional connectivity as a neural correlate of multidomain lifestyle adherence in older adults at risk for Alzheimer’s disease

Meishan Ai
Timothy P. Morris
Seqian Wang
ResearchOpen Access09 May 2023
Scientific Reports

Volume: 13, P: 1-14
A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling

Dong Li
Xiao Chang
Hakon Hakonarson
ResearchOpen Access19 Jun 2017
Scientific Reports

Volume: 7, P: 1-8
Preferential induction of necrosis in human breast cancer cells by a p53 peptide derived from the MDM2 binding site

Tamara N Do
Ramon V Rosal
Paul W Brandt-Rauf
Research11 Mar 2003
Oncogene

Volume: 22, P: 1431-1444
Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index

A Hinney
M Kesselmeier
J Hebebrand
Research17 May 2016
Molecular Psychiatry

Volume: 22, P: 192-201
Test-retest resting-state fMRI in healthy elderly persons with a family history of Alzheimer’s disease

Pierre Orban
Cécile Madjar
Seqian Wang
ResearchOpen Access13 Oct 2015
Scientific Data

Volume: 2, P: 1-11
Erratum: A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling

Dong Li
Xiao Chang
Hakon Hakonarson
Amendments and CorrectionsOpen Access21 Aug 2017
Scientific Reports

Volume: 7, P: 1-4

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