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.

Leukemia (14)
Nature Genetics (9)
Oncogene (5)
Nature Communications (4)
Nature Physics (4)

Choose more journals

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

Research (43)
Reviews (6)
Amendments and Corrections (5)
Correspondence (4)
News & Views (1)

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

Anatomy
Biochemistry
Biomarkers
Cancer
Cell biology
Computational biology and bioinformatics
Developmental biology
Diseases
Drug discovery
Genetics
Health care
Immunology
Medical research
Molecular biology
Neuroscience
Physics

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 1–50 of 59 results

Advanced filters: Author: C Finelli Clear advanced filters

Laryngeal Articular Reflexes

JOHN A. KIRCHNER
BARRY WYKE
Research09 May 1964
Nature

Volume: 202, P: 600
16p11.2–p12.2 duplication syndrome; a genomic condition differentiated from euchromatic variation of 16p11.2

John C K Barber
Victoria Hall
Helen White
Research25 Jul 2012
European Journal of Human Genetics

Volume: 21, P: 182-189
Mutations in the activin receptor–like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2

D.W. Johnson
J.N. Berg
D.A. Marchuk
Research01 Jun 1996
Nature Genetics

Volume: 13, P: 189-195
Multi-ancestry genome-wide association study of kidney cancer identifies 63 susceptibility regions

A multi-ancestry genome-wide association meta-analysis of kidney cancer identifies 63 regions associated with disease susceptibility including one locus that was associated with increased risk in individuals with African ancestry.

Mark P. Purdue
Diptavo Dutta
Stephen J. Chanock
Research26 Apr 2024
Nature Genetics

Volume: 56, P: 809-818
Transcription of plant defence genes in response to UV light or fungal elicitor

Joseph Chappell
Klaus Hahlbrock
Research06 Sept 1984
Nature

Volume: 311, P: 76-78
The role of low subcortical iron, white matter myelin, and oligodendrocytes in schizophrenia: a quantitative susceptibility mapping and diffusion tensor imaging study

Luke J. Vano
Robert A. McCutcheon
Oliver D. Howes
ResearchOpen Access05 Sept 2025
Molecular Psychiatry

P: 1-12
Padlock probes reveal single-nucleotide differences, parent of origin and in situ distribution of centromeric sequences in human chromosomes 13 and 21

Mats Nilsson
Katerina Krejci
Ulf Landegren
Research01 Jul 1997
Nature Genetics

Volume: 16, P: 252-255
A tRNA suppressor mutation in human mitochondria

Abdellatif El Meziane
Sanna K. Lehtinen
Howard T. Jacobs
Research01 Apr 1998
Nature Genetics

Volume: 18, P: 350-353
Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction

A meta-analysis of genome-wide association studies across different populations highlights new risk loci and provides a genetic risk score that can stratify prostate cancer risk across ancestries.

David V. Conti
Burcu F. Darst
Christopher A. Haiman
Research04 Jan 2021
Nature Genetics

Volume: 53, P: 65-75
Cl^- Permeabilities in Red Blood Cells and Peripheral Blood Lymphocytes from Cystic Fibrosis and Control Subjects

Richard C Boucher
Dennis W Ross
John C Parker
Research01 Dec 1984
Pediatric Research

Volume: 18, P: 1336-1339
Fine-mapping of prostate cancer susceptibility loci in a large meta-analysis identifies candidate causal variants

Prostate cancer (PrCa) involves a large heritable genetic component. Here, the authors perform multivariate fine-mapping of known PrCa GWAS loci, identifying variants enriched for biological function, explaining more familial relative risk, and with potential application in clinical risk profiling.

Tokhir Dadaev
Edward J. Saunders
Zsofia Kote-Jarai
ResearchOpen Access11 Jun 2018
Nature Communications

Volume: 9, P: 1-19
Observation of electroweak production of two jets and a Z-boson pair

The ATLAS Collaboration reports the observation of the electroweak production of two jets and a Z-boson pair. This process is related to vector-boson scattering and allows the nature of electroweak symmetry breaking to be probed.

G. Aad
B. Abbott
L. Zwalinski
ResearchOpen Access09 Feb 2023
Nature Physics

Volume: 19, P: 237-253
Somatic driver mutation prevalence in 1844 prostate cancers identifies ZNRF3 loss as a predictor of metastatic relapse

Biomarkers of prostate cancer metastasis have been difficult to determine with confidence. Here the authors analyse mutation prevalence in 1844 prostate cancers and show that ZNRF3 loss is enriched in metastatic, castration-resistant prostate cancer and associated with metastasis of localized disease.

Michael Fraser
Julie Livingstone
Paul C. Boutros
ResearchOpen Access29 Oct 2021
Nature Communications

Volume: 12, P: 1-15
Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants

A multi-ancestry genome-wide association study of prostate cancer performed in 156,319 cases and 788,443 controls identifies 187 novel risk variants associated with the disease. Genetic risk scores associated with overall risk, and risk of aggressive disease in men of African ancestry.

Anqi Wang
Jiayi Shen
Christopher A. Haiman
Research09 Nov 2023
Nature Genetics

Volume: 55, P: 2065-2074
Overexpression of the HMGA2 gene in transgenic mice leads to the onset of pituitary adenomas

Monica Fedele
Sabrina Battista
Alfredo Fusco
Research07 May 2002
Oncogene

Volume: 21, P: 3190-3198
Transgenic mice overexpressing the wild-type form of the HMGA1 gene develop mixed growth hormone/prolactin cell pituitary adenomas and natural killer cell lymphomas

Monica Fedele
Francesca Pentimalli
Alfredo Fusco
Research28 Feb 2005
Oncogene

Volume: 24, P: 3427-3435
Test of the universality of τ and μ lepton couplings in W-boson decays with the ATLAS detector

The ATLAS Collaboration reports a measurement of the ratio of the decay rates of W bosons to τ leptons and muons, in agreement with universal lepton couplings as postulated in the standard model of particle physics.

G. Aad
B. Abbott
L. Zwalinski
ResearchOpen Access05 Jul 2021
Nature Physics

Volume: 17, P: 813-818
Search for charged-lepton-flavour violation in Z-boson decays with the ATLAS detector

The ATLAS experiment at the Large Hadron Collider reports a search for charged-lepton-flavour violation in decays of Z bosons into a τ lepton and an electron or muon of opposite charge.

G. Aad
B. Abbott
L. Zwalinski
ResearchOpen Access01 Jul 2021
Nature Physics

Volume: 17, P: 819-825
Emerging guidelines for managing small renal masses

The 2017 ASCO guidelines present six well-reasoned recommendations for the management of small renal masses. We expand these recommendations to contextualize the use of renal tumour biopsy, clarify when active surveillance could be more inclusive, and highlight nuances in surgical decision making for patients with anatomically complex tumours and a normal contralateral kidney.

Benjamin T. Ristau
Marc C. Smaldone
News & Views14 Mar 2017
Nature Reviews Urology

Volume: 14, P: 329-330
Evidence for light-by-light scattering in heavy-ion collisions with the ATLAS detector at the LHC

Quantum electrodynamics predicts a rare process in which light is scattered by light. The ATLAS Collaboration reports signs of this elusive effect in the collisions of ultra-relativistic lead ions.

M. Aaboud
G. Aad
L. Zwalinski
ResearchOpen Access14 Aug 2017
Nature Physics

Volume: 13, P: 852-858
Germline variation at 8q24 and prostate cancer risk in men of European ancestry

Chromosome 8q24 is known to be a major susceptibility region for prostate cancer risk. Here the authors analyze genetic data across the 8q24 region from 71,535 prostate cancer patients identifying 12 risk loci, three previously unreported, highlighting the contribution of germline variation at this locus.

Marco Matejcic
Edward J. Saunders
Christopher A. Haiman
ResearchOpen Access05 Nov 2018
Nature Communications

Volume: 9, P: 1-11
Nutritional deficiencies after bariatric surgery

Deficiencies in micronutrients, including trace elements, minerals, water-soluble and fat-soluble vitamins, are common before bariatric surgery and often persist postoperatively, despite universal recommendations on multivitamin and mineral supplements. This Review highlights follow-up and treatment options for bariatric patients who develop nutrient deficiencies.

Bikram S. Bal
Frederick C. Finelli
Timothy R. Koch
Reviews24 Apr 2012
Nature Reviews Endocrinology

Volume: 8, P: 544-556
Cytogenetic and molecular evaluation of 241 small supernumerary marker chromosomes: Cooperative study of 19 Italian laboratories

Leda Dalprà
Daniela Giardino
Lidia Larizza
Research01 Nov 2005
Genetics in Medicine

Volume: 7, P: 620-625
Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci

A large meta-analysis combining genome-wide and custom high-density genotyping array data identifies 63 new susceptibility loci for prostate cancer, enhancing fine-mapping efforts and providing insights into the underlying biology.

Fredrick R. Schumacher
Ali Amin Al Olama
Rosalind A. Eeles
Research11 Jun 2018
Nature Genetics

Volume: 50, P: 928-936
Roles of HMGA proteins in cancer

High mobility group A (HMGA) proteins alter chromatin structure and therefore affect the transcription of large sets of genes. This can contribute to both benign and malignant disease in several ways.

Alfredo Fusco
Monica Fedele
Reviews01 Dec 2007
Nature Reviews Cancer

Volume: 7, P: 899-910
Author Correction: Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci

Fredrick R. Schumacher
Ali Amin Al Olama
Rosalind A. Eeles
Amendments and Corrections08 Jan 2019
Nature Genetics

Volume: 51, P: 363
Antipsychotics cause reversible structural brain changes within one week

Pierluigi Selvaggi
Martin Osugo
Oliver D. Howes
Research07 May 2025
Neuropsychopharmacology

Volume: 50, P: 1275-1283
The cognitive neuroscience of sleep: neuronal systems, consciousness and learning

J. Allan Hobson
Edward F. Pace-Schott
Reviews01 Sept 2002
Nature Reviews Neuroscience

Volume: 3, P: 679-693
Cancer-associated alteration of pericentromeric heterochromatin may contribute to chromosome instability

R B Slee
C M Steiner
B R Grimes
Research28 Nov 2011
Oncogene

Volume: 31, P: 3244-3253
Implications of TP53 allelic state for genome stability, clinical presentation and outcomes in myelodysplastic syndromes

Clinical sequencing across a large prospective cohort of patients with myelodysplasic syndrome uncovers distinct associations between the mono- and biallelic states of TP53 and clinical presentation

Elsa Bernard
Yasuhito Nannya
Elli Papaemmanuil
Research03 Aug 2020
Nature Medicine

Volume: 26, P: 1549-1556
Author Correction: Implications of TP53 allelic state for genome stability, clinical presentation and outcomes in myelodysplastic syndromes

Elsa Bernard
Yasuhito Nannya
Elli Papaemmanuil
Amendments and Corrections09 Feb 2021
Nature Medicine

Volume: 27, P: 562
Author Correction: Implications of TP53 allelic state for genome stability, clinical presentation and outcomes in myelodysplastic syndromes

Elsa Bernard
Yasuhito Nannya
Elli Papaemmanuil
Amendments and Corrections04 May 2021
Nature Medicine

Volume: 27, P: 927
hSmad5 gene, a human hSmad family member: its full length cDNA, genomic structure, promoter region and mutation analysis in human tumors

Akihiko Gemma
Koichi Hagiwara
Curtis C Harris
Research03 Mar 1998
Oncogene

Volume: 16, P: 951-956
Mapping of chromosome 20 for loss of heterozygosity in childhood ALL reveals a 1000-kb deletion in one patient

N Couque
C Chambon-Pautas
B Grandchamp
Research02 Dec 1999
Leukemia

Volume: 13, P: 1972-1974
MYEOV, a gene at 11q13, is coamplified with CCND1, but epigenetically inactivated in a subset of esophageal squamous cell carcinomas

J. W. G. Janssen
I. Imoto
J. Inazawa
Research01 Sept 2002
Journal of Human Genetics

Volume: 47, P: 460-464
Publisher Correction: Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction

David V. Conti
Burcu F. Darst
Christopher A. Haiman
Amendments and Corrections20 Jan 2021
Nature Genetics

Volume: 53, P: 413
Managing medical and surgical disorders after divided Roux-en-Y gastric bypass surgery

This Review provides an overview of the symptoms, complications, nutritional deficiencies and medical disorders associated with Roux-en-Y gastric bypass—the most frequently performed bariatric procedure in the USA and Canada. Although some symptoms are expected and predictable, some complications may require active medical or surgical intervention. Physicians should be able to predict and manage most postoperative medical and nutritional disorders and should be prepared to assess patients for potential referral for surgical intervention or revision.

Bikram Bal
Timothy R. Koch
Michael G. Sarr
Reviews11 May 2010
Nature Reviews Gastroenterology & Hepatology

Volume: 7, P: 320-334
MTHFR, TS and XRCC1 genetic variants may affect survival in patients with myelodysplastic syndromes treated with supportive care or azacitidine

G Visani
F Loscocco
A Isidori
ResearchOpen Access05 Dec 2017
The Pharmacogenomics Journal

Volume: 18, P: 444-449
Epigenetic regulation of nuclear PI-PLCbeta1 signaling pathway in low-risk MDS patients during azacitidine treatment

M Y Follo
D Russo
L Cocco
Research28 Oct 2011
Leukemia

Volume: 26, P: 943-950
Identification of the critical region of 12p over-representation in testicular germ cell tumors of adolescents and adults

Marijke C Mostert
Annemieke JMH Verkerk
Leendert HJ Looijenga
Research02 Jun 1998
Oncogene

Volume: 16, P: 2617-2627
Metabolic syndrome and ADRB3 gene polymorphism in severely obese patients from South Italy

R Bracale
F Pasanisi
G Oriani
Research14 Feb 2007
European Journal of Clinical Nutrition

Volume: 61, P: 1213-1219
Developmental Differences in Catalase Activity and Hypoxic-Hyperoxic Effects on Fluid Balance in Isolated Lamb Lungs

C M Bonuccelli
S Permutt
J T Sylvester
Research01 May 1993
Pediatric Research

Volume: 33, P: 519-526
Noninvasive estimation of tumour viability in a xenograft model of human neuroblastoma with proton magnetic resonance spectroscopy (¹H MRS)

M Lindskog
P Kogner
C Spenger
ResearchOpen Access10 Feb 2003
British Journal of Cancer

Volume: 88, P: 478-485
Response of high-risk MDS to azacitidine and lenalidomide is impacted by baseline and acquired mutations in a cluster of three inositide-specific genes

Matilde Y. Follo
Andrea Pellagatti
Lucio Cocco
ResearchOpen Access20 Feb 2019
Leukemia

Volume: 33, P: 2276-2290
Hypocellular myelodysplastic syndromes (h-MDS): from clinical description to immunological characterization in the Italian multi-center experience

Giulia Calabretto
Enrico Attardi
Valeria Santini
ResearchOpen Access21 May 2022
Leukemia

Volume: 36, P: 1947-1950
Evaluation of models predicting insignificant prostate cancer to select men for active surveillance of prostate cancer

L-M Wong
D E Neal
N M Corcoran
Research10 Feb 2015
Prostate Cancer and Prostatic Diseases

Volume: 18, P: 137-143
Cancer stem cells are underestimated by standard experimental methods in clear cell renal cell carcinoma

Craig Gedye
Danylo Sirskyj
Laurie E. Ailles
ResearchOpen Access28 Apr 2016
Scientific Reports

Volume: 6, P: 1-13
Author Correction: Germline variation at 8q24 and prostate cancer risk in men of European ancestry

Marco Matejcic
Edward J. Saunders
Christopher A. Haiman
Amendments and CorrectionsOpen Access17 Jan 2019
Nature Communications

Volume: 10, P: 1-5
A phase II, multicentre trial of decitabine in higher-risk chronic myelomonocytic leukemia

V Santini
B Allione
A Levis
ResearchOpen Access13 Jun 2017
Leukemia

Volume: 32, P: 413-418
Clinical efficacy and antiangiogenic activity of thalidomide in myelofibrosis with myeloid metaplasia. A pilot study

PP Piccaluga
G Visani
S Tura
Research30 Aug 2002
Leukemia

Volume: 16, P: 1609-1614

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