scispace - formally typeset
C

Claes Ladenvall

Researcher at Lund University

Publications -  47
Citations -  10809

Claes Ladenvall is an academic researcher from Lund University. The author has contributed to research in topics: Genome-wide association study & Type 2 diabetes. The author has an hindex of 30, co-authored 44 publications receiving 9142 citations. Previous affiliations of Claes Ladenvall include University of Helsinki & Science for Life Laboratory.

Papers
More filters
Journal ArticleDOI

Age-Related Clonal Hematopoiesis Associated with Adverse Outcomes

TL;DR: Age-related clonal hematopoiesis is a common condition that is associated with increases in the risk of hematologic cancer and in all-cause mortality, with the latter possibly due to an increased risk of cardiovascular disease.
Journal ArticleDOI

Genome-wide meta-analyses identify multiple loci associated with smoking behavior

Helena Furberg, +123 more
- 01 May 2010 - 
TL;DR: A meta-analyses of several smoking phenotypes within cohorts of the Tobacco and Genetics Consortium found the strongest association was a synonymous 15q25 SNP in the nicotinic receptor gene CHRNA3, and three loci associated with number of cigarettes smoked per day were identified.
Journal ArticleDOI

The genetic architecture of type 2 diabetes

Christian Fuchsberger, +349 more
- 11 Jul 2016 - 
TL;DR: In this paper, the authors performed whole-genome sequencing in 2,657 European individuals with and without diabetes, and exome sequencing for 12,940 individuals from five ancestry groups.
Journal ArticleDOI

A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.

Alisa K. Manning, +243 more
- 01 Jun 2012 - 
TL;DR: Six previously unknown loci associated with fasting insulin at P < 5 × 10−8 in combined discovery and follow-up analyses of 52 studies comprising up to 96,496 non-diabetic individuals are presented.

The genetic architecture of type 2 diabetes

Christian Fuchsberger, +300 more
TL;DR: Large-scale sequencing does not support the idea that lower-frequency variants have a major role in predisposition to type 2 diabetes, but most fell within regions previously identified by genome-wide association studies.