Nature Search

Genomic risk model to implement precision prostate cancer screening in clinical care: the ProGRESS study

Vassy, Dornisch and colleagues developed a genomics-based prostate cancer risk model to support a randomized clinical trial of precision screening in a national healthcare system.

Jason L. Vassy
Anna M. Dornisch
Tyler M. Seibert
Research26 Jan 2026
Nature Cancer

Volume: 7, P: 352-367
An autosomal screen for genes that predispose to celiac disease in the western counties of Ireland

Fei Zhong
Candace C. McCombs
Joseph P. Michalski
Research01 Nov 1996
Nature Genetics

Volume: 14, P: 329-333
Multi-ancestry genome-wide gene–smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids

A multi-ancestry genome-wide gene–smoking interaction study identifies 13 new loci associated with serum lipids.

Amy R. Bentley
Yun J. Sung
L. Adrienne Cupples
Research29 Mar 2019
Nature Genetics

Volume: 51, P: 636-648
Post-COVID conditions following COVID-19 vaccination: a retrospective matched cohort study of patients with SARS-CoV-2 infection

The impact of COVID-19 vaccination on post-COVID conditions is not well understood. Here, the authors use electronic health record data from a network of eight integrated healthcare systems in the United States to compare rates of post-COVID conditions in those with and without vaccination.

Debbie E. Malden
In-Lu Amy Liu
Sara Y. Tartof
ResearchOpen Access22 May 2024
Nature Communications

Volume: 15, P: 1-10
Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data

Analysis of whole-genome sequences of 25,465 individuals of European ancestry shows that rare variants contribute substantially to the heritability of height and body mass index.

Pierrick Wainschtein
Deepti Jain
Peter M. Visscher
Research07 Mar 2022
Nature Genetics

Volume: 54, P: 263-273
Vitamin D signalling pathways in cancer: potential for anticancer therapeutics

Accumulating evidence indicates that the active metabolite of vitamin D, 1α,25(OH)₂D₃, or vitamin D analogues might have potential as anticancer agents because their administration has antiproliferative effects, can activate apoptotic pathways and inhibit angiogenesis. What are the possibilities for 1α,25(OH)₂D₃and vitamin D analogues as preventative and therapeutic anticancer agents?

Kristin K. Deeb
Donald L. Trump
Candace S. Johnson
Reviews01 Sept 2007
Nature Reviews Cancer

Volume: 7, P: 684-700
Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture

Fernando Rivadeneira and colleagues in the Genetic Factors for Osteoporosis Consortium report a large-scale meta-analysis identifying new loci associated with bone mineral density (BMD) and risk of fracture. Thirty-two new loci are found to be associated with BMD, and 6 loci confer higher risk for low-trauma bone fracture.

Karol Estrada
Unnur Styrkarsdottir
Fernando Rivadeneira
Research15 Apr 2012
Nature Genetics

Volume: 44, P: 491-501
Organization and Fine Structure of a Pacemaker Derived from Fetal Rat Myocardium

Wenning Qin
Candace G Woods
W T Woods Jr.
Research01 Mar 1995
Pediatric Research

Volume: 37, P: 283-288
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders

Genetic variants in ionotropic glutamate receptors have been implicated in neurodevelopmental disorders. Here, the authors report heterozygous de novo mutations in the GRIA2 gene in 28 individuals with intellectual disability and neurodevelopmental abnormalities associated with reduced Ca²⁺ transport and AMPAR currents.”

Vincenzo Salpietro
Christine L. Dixon
Henry Houlden
ResearchOpen Access12 Jul 2019
Nature Communications

Volume: 10, P: 1-16
Author Correction: Enhancing untargeted metabolomics using metadata-based source annotation

Julia M. Gauglitz
Kiana A. West
Pieter C. Dorrestein
Amendments and Corrections18 Oct 2023
Nature Biotechnology

Volume: 41, P: 1656
Enhancing untargeted metabolomics using metadata-based source annotation

Metabolomics is improved by using a reference library of both known and unknown molecules.

Julia M. Gauglitz
Kiana A. West
Pieter C. Dorrestein
Research07 Jul 2022
Nature Biotechnology

Volume: 40, P: 1774-1779
Brown bear skin-borne secretions display evidence of individuality and age-sex variation

Melanie Clapham
Abbey E. Wilson
Agnieszka Sergiel
ResearchOpen Access23 Feb 2023
Scientific Reports

Volume: 13, P: 1-13
Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error

Qiao Fan et al. report a genome-wide association analysis of corneal curvature—an important measurement for identifying vision problems, such as myopia—in more than 45,000 individuals of either European or Asian ancestry. They identify 47 loci, 26 of which are novel, with some showing population-specific effects and pleiotropic effects on eye elongation and myopia.

Qiao Fan
Alfred Pozarickij
Ching-Yu Cheng
ResearchOpen Access19 Mar 2020
Communications Biology

Volume: 3, P: 1-14
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants

The Myocardial Infarction Genetics Consortium reports results of a genome-wide association study of early-onset myocardial infarction. The study analyzed common SNPs, common CNVs and rare CNVs and identified SNP alleles at three new loci associated with disease risk.

Sekar Kathiresan
Benjamin F Voight
David Altshuler
Research08 Feb 2009
Nature Genetics

Volume: 41, P: 334-341
Rare variant analyses across multiethnic cohorts identify novel genes for refractive error

A multi-ethnic meta-analysis of exome array data from over 27,000 participants identifies several rare variants that could contribute to risk of ocular refractive error.

Anthony M. Musolf
Annechien E. G. Haarman
Joan E. Bailey-Wilson
ResearchOpen Access03 Jan 2023
Communications Biology

Volume: 6, P: 1-17

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