Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

Advertisement

Nature

View all journals
Search
Log in

nature
search

Search

Advanced search

Filter By:

Journal Check one or more journals to show results from those journals only.

Nature (13)
Nature Genetics (11)
Pediatric Research (8)
Nature Communications (8)
Oncogene (7)

Choose more journals

Article type Check one or more article types to show results from those article types only.

Research (77)
Reviews (6)
Correspondence (4)
Amendments and Corrections (1)
Books & Arts (1)
Comments & Opinion (1)
News & Views (1)
Protocols (1)

Subject Check one or more subjects to show results from those subjects only.

Biochemistry
Biological techniques
Biomarkers
Biotechnology
Cancer
Cell biology
Computational biology and bioinformatics
Developmental biology
Diseases
Evolution
Genetics
Health care
Immunology
Medical research
Microbiology
Molecular biology
Nephrology
Neuroscience
Pathogenesis
Scientific community

Date Choose a date option to show results from those dates only.

Today
Last 7 days
Last 30 days
Last 12 months
Last 2 years
Last 5 years

Custom date range

Clear all filters

Sort by:

Relevance

Date published (new to old)

Date published (old to new)

Showing 51–92 of 92 results

Advanced filters: Author: David C. Samuels Clear advanced filters

Mutations in PNPLA6 are linked to photoreceptor degeneration and various forms of childhood blindness

Blindness due to retinal degeneration affects millions of people worldwide, but many disease-causing mutations remain unknown. Here the authors link mutations in the gene PNPLA6 with childhood blindness in seven families with retinal degeneration and show that the gene plays a role in photoreceptor survival in Drosophila.

S. Kmoch
J. Majewski
R. K. Koenekoop
Research09 Jan 2015
Nature Communications

Volume: 6, P: 1-10
S 38093, a histamine H₃ antagonist/inverse agonist, promotes hippocampal neurogenesis and improves context discrimination task in aged mice

Jean-Philippe Guilloux
Benjamin A. Samuels
Denis J. David
ResearchOpen Access20 Feb 2017
Scientific Reports

Volume: 7, P: 1-13
Oculofaciocardiodental and Lenz microphthalmia syndromes result from distinct classes of mutations in BCOR

David Ng
Nalin Thakker
Leslie G Biesecker
Research07 Mar 2004
Nature Genetics

Volume: 36, P: 411-416
Mutations in STAMBP, encoding a deubiquitinating enzyme, cause microcephaly–capillary malformation syndrome

Kym Boycott, Mark O'Driscoll and colleagues report identification of mutations in STAMBP, a gene encoding the deubiquitinating isopeptidase STAMBP, in individuals with microcephaly–capillary malformation syndrome.

Laura M McDonell
Ghayda M Mirzaa
Kym M Boycott
Research31 Mar 2013
Nature Genetics

Volume: 45, P: 556-562
US immigration order strikes against biotech

Jeremy M Levin
Steven H Holtzman
Sandford (Sandy) Zweifach
Correspondence07 Mar 2017
Nature Biotechnology

Volume: 35, P: 204-206
Author Correction: FAM222A encodes a protein which accumulates in plaques in Alzheimer’s disease

Tingxiang Yan
Jingjing Liang
Xinglong Wang
Amendments and CorrectionsOpen Access11 Jul 2022
Nature Communications

Volume: 13, P: 1-2
Immunolocalization of Transforming Growth Factor-α, Epidermal Growth Factor (EGF), and EGF-Receptor in Normal and Injured Developing Human Lung

Thomas P Strandjord
Joan G Clark
David K Madtes
Research01 Dec 1995
Pediatric Research

Volume: 38, P: 851-856
A reduction of mitochondrial DNA molecules during embryogenesis explains the rapid segregation of genotypes

Lynsey M Cree
David C Samuels
Patrick F Chinnery
Research27 Jan 2008
Nature Genetics

Volume: 40, P: 249-254
Integrated multi-omics analyses reveal homology-directed repair pathway as a unique dependency in near-haploid leukemia

Yunpeng Liu-Lupo
James Dongjoo Ham
Michael T. Hemann
ResearchOpen Access08 Jun 2023
Blood Cancer Journal

Volume: 13, P: 1-14
Deciphering the involvement of the Hippo pathway co-regulators, YAP/TAZ in invadopodia formation and matrix degradation

Jubina Balan Venghateri
Bareket Dassa
Benjamin Geiger
ResearchOpen Access25 Apr 2023
Cell Death & Disease

Volume: 14, P: 1-14
Mitochondrial aging is accelerated by anti-retroviral therapy through the clonal expansion of mtDNA mutations

Patrick Chinnery and colleagues analyze the effects on mitochondrial DNA of nucleoside analogue anti-retroviral (NRTIs) drugs in patients infected with HIV. The authors find that patients treated with commonly used NRTIs accumulate somatic mitochondrial DNA mutations in a process similar to normal aging.

Brendan A I Payne
Ian J Wilson
Patrick F Chinnery
Research26 Jun 2011
Nature Genetics

Volume: 43, P: 806-810
Role of PPARs in the regulation of obesity-related insulin sensitivity and inflammation

D E Moller
J P Berger
Research14 Nov 2003
International Journal of Obesity

Volume: 27, P: S17-S21
Reassessing evidence for a postnatal mitochondrial genetic bottleneck

David C Samuels
Passorn Wonnapinij
Patrick F Chinnery
Correspondence01 Jun 2010
Nature Genetics

Volume: 42, P: 471-472
Timed daily exercise remodels circadian rhythms in mice

Using mice with disrupted neuropeptide signaling, Hughes et al. show that daily scheduled voluntary exercise (SVE) promotes suprachiasmatic nuclei (SCN) clock cell synchrony and robust 24 h rhythms in behavior. This study suggests the potential utility of regular exercise as a non-invasive intervention for the elderly or mentally ill, where circadian rhythms can be poorly aligned to the external world.

Alun Thomas Lloyd Hughes
Rayna Eve Samuels
Hugh David Piggins
ResearchOpen Access18 Jun 2021
Communications Biology

Volume: 4, P: 1-17
A distinct transcriptional signature of antidepressant response in hippocampal dentate gyrus granule cells

David P. Herzog
Diego Pascual Cuadrado
Marianne B. Müller
ResearchOpen Access05 Jan 2021
Translational Psychiatry

Volume: 11, P: 1-12
Chinese scientists and US leadership in the life sciences

Steven H. Holtzman
Ron Cohen
Shuguang Zhang
Correspondence03 Oct 2019
Nature Biotechnology

Volume: 37, P: 1261-1263
De novo CCND2 mutations leading to stabilization of cyclin D2 cause megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome

Eamonn Sheridan, Elizabeth Ross and colleagues report discovery of a new megalencephaly syndrome caused by de novo missense mutations in CCND2. They show that these mutations lead to stabilization of cyclin D2, and they present evidence that cyclin D2 stabilization may be a common downstream mechanism in PI3K-AKT–associated megalencephaly syndromes.

Ghayda M Mirzaa
David A Parry
Eamonn G Sheridan
Research06 Apr 2014
Nature Genetics

Volume: 46, P: 510-515
Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration

Rui Chen and colleagues identify mutations in NMNAT1 as a new cause of Leber congenital amaurosis. They further show that all examined individuals with NMNAT1 mutations have macular colobomas, a condition marked by severe degeneration of the central retina.

Robert K Koenekoop
Hui Wang
Rui Chen
Research29 Jul 2012
Nature Genetics

Volume: 44, P: 1035-1039
A positive feedback mechanism in the transcriptional activation of Apaf-1 by p53 and the coactivator Zac-1

Galit Rozenfeld-Granot
Janakiraman Krishnamurthy
Gideon Rechavi
Research27 Feb 2002
Oncogene

Volume: 21, P: 1469-1476
Acquired MET expression confers resistance to EGFR inhibition in a mouse model of glioblastoma multiforme

H J Jun
J Acquaviva
A Charest
Research24 Oct 2011
Oncogene

Volume: 31, P: 3039-3050
Phospholipase D overcomes cell cycle arrest induced by high-intensity Raf signaling

Troy Joseph
Annika Bryant
David A Foster
Research21 May 2002
Oncogene

Volume: 21, P: 3651-3658
Biotech leaders call for free press

Ron Cohen
Steven Holtzman
Sanford Sandy Zweifach
Correspondence01 Oct 2018
Nature Biotechnology

Volume: 36, P: 920-922
Unnatural injuries

David Taylor
Reviews01 Mar 2000
Eye

Volume: 14, P: 123-150
A cross-species approach to disorders affecting brain and behaviour

Many disorders of brain and behaviour affect human and veterinary patients. In this Perspectives, Orrin Devinsky and colleagues outline a cross-species approach to understanding neurological and psychiatric conditions, including pain, cognitive decline, epilepsy, anxiety and CNS infections, and propose that collaborations between physicians and veterinarians will generate new insights for therapy development.

Orrin Devinsky
Jordyn M. Boesch
Barbara Natterson-Horowitz
Reviews04 Oct 2018
Nature Reviews Neurology

Volume: 14, P: 677-686
Automated and virus variant-programmable surrogate test qualitatively compares to the gold standard SARS-CoV-2 neutralization assay

Danielle W. Ali
Maggie L. Bartlett
Darci R. Smith
ResearchOpen Access30 Dec 2024
npj Viruses

Volume: 2, P: 1-8
Identifying healthy individuals with Alzheimer’s disease neuroimaging phenotypes in the UK Biobank

Azevedo et al. conduct a machine learning-based analysis of structural MRI data from multiple cohorts. The authors identify Alzheimer’s disease-like neuroimaging phenotypes associated with poorer cognitive performance in a healthy UK Biobank cohort, potentially highlighting a population at risk of Alzheimer’s disease.

Tiago Azevedo
Richard A. I. Bethlehem
Gail Li
ResearchOpen Access20 Jul 2023
Communications Medicine

Volume: 3, P: 1-15
Role of Cortisol in Menstrual Recovery in Adolescent Girls with Anorexia Nervosa

Madhusmita Misra
Rajani Prabhakaran
Anne Klibanski
Research01 Apr 2006
Pediatric Research

Volume: 59, P: 598-603
A predictive model using the mesoscopic architecture of the living brain to detect Alzheimer’s disease

Inglese et al. develop a predictive model that computes multi-regional statistical morpho-functional mesoscopic traits from T1-weighted magnetic resonance imaging scans. Their model reliably discriminates people with Alzheimer’s disease-related pathologies from those without.

Marianna Inglese
Neva Patel
Eric O. Aboagye
ResearchOpen Access20 Jun 2022
Communications Medicine

Volume: 2, P: 1-16
Plasma phosphorylated-tau181 as a predictive biomarker for Alzheimer’s amyloid, tau and FDG PET status

Xue-Ning Shen
Yu-Yuan Huang
Michelle Zmuda
ResearchOpen Access13 Nov 2021
Translational Psychiatry

Volume: 11, P: 1-10
Staging tau pathology with tau PET in Alzheimer’s disease: a longitudinal study

Shi-Dong Chen
Jia-Ying Lu
Michelle Zmuda
ResearchOpen Access18 Sept 2021
Translational Psychiatry

Volume: 11, P: 1-12
Revealing the complex genetic architecture of obsessive–compulsive disorder using meta-analysis

Paul D Arnold
Kathleen D Askland
Gwyneth Zai
Research01 Aug 2017
Molecular Psychiatry

Volume: 23, P: 1181-1188
Meier–Gorlin syndrome genotype–phenotype studies: 35 individuals with pre-replication complex gene mutations and 10 without molecular diagnosis

Sonja A de Munnik
Louise S Bicknell
Ernie M H F Bongers
Research15 Feb 2012
European Journal of Human Genetics

Volume: 20, P: 598-606
Whole-genome association analysis of treatment response in obsessive-compulsive disorder

H Qin
J F Samuels
Y Y Shugart
Research31 Mar 2015
Molecular Psychiatry

Volume: 21, P: 270-276
Illumina human exome genotyping array clustering and quality control

A protocol for processing exome genotyping array data that proceeds by targeting the exome plus rare SNPs and provides a feasible, cheaper alternative to exome sequencing when analyzing data from large genome-wide association studies.

Yan Guo
Jing He
Jirong Long
Protocols16 Oct 2014
Nature Protocols

Volume: 9, P: 2643-2662
Genome-wide association study of pediatric obsessive-compulsive traits: shared genetic risk between traits and disorder

Christie L. Burton
Mathieu Lemire
Paul D. Arnold
ResearchOpen Access02 Feb 2021
Translational Psychiatry

Volume: 11, P: 1-10
Global human frequencies of predicted nuclear pathogenic variants and the role played by protein hydrophobicity in pathogenicity potential

Luísa Pereira
Pedro Soares
David C. Samuels
ResearchOpen Access21 Nov 2014
Scientific Reports

Volume: 4, P: 1-8
Polygenic risk score-based phenome-wide association study identifies novel associations for Tourette syndrome

Pritesh Jain
Tyne Miller-Fleming
Peristera Paschou
ResearchOpen Access23 Feb 2023
Translational Psychiatry

Volume: 13, P: 1-10
Phasic vs Sustained Fear in Rats and Humans: Role of the Extended Amygdala in Fear vs Anxiety

Michael Davis
David L Walker
Christian Grillon
Reviews19 Aug 2009
Neuropsychopharmacology

Volume: 35, P: 105-135
A resource of lipidomics and metabolomics data from individuals with undiagnosed diseases

Jennifer E. Kyle
Kelly G. Stratton
Thomas O. Metz
ResearchOpen Access21 Apr 2021
Scientific Data

Volume: 8, P: 1-12
Application of rare variant transmission disequilibrium tests to epileptic encephalopathy trio sequence data

Andrew S Allen
Samuel F Berkovic
Melodie R Winawer
Research17 May 2017
European Journal of Human Genetics

Volume: 25, P: 894-899
Mutations in NGLY1 cause an inherited disorder of the endoplasmic reticulum–associated degradation pathway

Gregory M. Enns
Vandana Shashi
David B. Goldstein
Research20 Mar 2014
Genetics in Medicine

Volume: 16, P: 751-758
Mammography service screening and breast cancer mortality in New Zealand: a National Cohort Study 1999–2011

Stephen Morrell
Richard Taylor
Kirsty Craig
ResearchOpen Access09 Feb 2017
British Journal of Cancer

Volume: 116, P: 828-839

Previous page
page 1
page 2
Next page

Search

Search articles by subject, keyword or author

Show results from

Advanced search

Quick links

Explore articles by subject
Find a job
Guide to authors
Editorial policies

Nature.com

nature.com sitemap

About Nature Portfolio

About us
Press releases
Press office
Contact us

Discover content

Journals A-Z
Articles by subject
protocols.io
Nature Index

Publishing policies

Nature portfolio policies
Open access

Author & Researcher services

Reprints & permissions
Research data
Language editing
Scientific editing
Nature Masterclasses
Research Solutions

Libraries & institutions

Librarian service & tools
Librarian portal
Open research
Recommend to library

Advertising & partnerships

Advertising
Partnerships & Services
Media kits
Branded content

Professional development

Nature Awards
Nature Careers
Nature Conferences

Regional websites

Nature Africa
Nature China
Nature India
Nature Japan
Nature Middle East

Privacy Policy
Use of cookies
Legal notice
Accessibility statement
Terms & Conditions
Your US state privacy rights

© 2025 Springer Nature Limited