Samuel A Lambert
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Explore the profile of Samuel A Lambert including associated specialties, affiliations and a list of published articles.
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26
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4033
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Recent Articles
1.
Tokolyi A, Persyn E, Nath A, Burnham K, Marten J, Vanderstichele T, et al.
Nat Genet
. 2025 Mar;
57(3):616-625.
PMID: 40038547
The biological mechanisms through which most nonprotein-coding genetic variants affect disease risk are unknown. To investigate gene-regulatory mechanisms, we mapped blood gene expression and splicing quantitative trait loci (QTLs) through...
2.
Ardissino M, Paraboschi E, Lambert S, Kim L, Kelemen M, Maglietta G, et al.
Circ Genom Precis Med
. 2024 Nov;
17(6):e004687.
PMID: 39611259
Background: Myocardial infarction (MI) is a complex disease caused by both lifestyle and genetic factors. This study aims to investigate the predictive value of genetic risk, in addition to traditional...
3.
Cerezo M, Sollis E, Ji Y, Lewis E, Abid A, Bircan K, et al.
Nucleic Acids Res
. 2024 Nov;
53(D1):D998-D1005.
PMID: 39530240
The NHGRI-EBI GWAS Catalog serves as a vital resource for the genetic research community, providing access to the most comprehensive database of human GWAS results. Currently, it contains close to...
4.
Cerezo M, Sollis E, Ji Y, Lewis E, Abid A, Bircan K, et al.
bioRxiv
. 2024 Nov;
PMID: 39484403
The NHGRI-EBI GWAS Catalog serves as a vital resource for the genetic research community, providing access to the most comprehensive database of human GWAS results. Currently, it contains close to...
5.
Lambert S, Wingfield B, Gibson J, Gil L, Ramachandran S, Yvon F, et al.
Nat Genet
. 2024 Sep;
56(10):1989-1994.
PMID: 39327485
No abstract available.
6.
Ritchie S, Taylor H, Liang Y, Manikpurage H, Pennells L, Foguet C, et al.
medRxiv
. 2024 Sep;
PMID: 39228710
Combining information from multiple GWASs for a disease and its risk factors has proven a powerful approach for development of polygenic risk scores (PRSs). This may be particularly useful for...
7.
Lambert S, Wingfield B, Gibson J, Gil L, Ramachandran S, Yvon F, et al.
medRxiv
. 2024 Jun;
PMID: 38853961
Polygenic scores (PGS) have transformed human genetic research and have multiple potential clinical applications, including risk stratification for disease prevention and prediction of treatment response. Here, we present a series...
8.
Xiang R, Liu Y, Ben-Eghan C, Ritchie S, Lambert S, Xu Y, et al.
medRxiv
. 2024 May;
PMID: 38699308
Blood cell phenotypes are routinely tested in healthcare to inform clinical decisions. Genetic variants influencing mean blood cell phenotypes have been used to understand disease aetiology and improve prediction; however,...
9.
Xiang R, Kelemen M, Xu Y, Harris L, Parkinson H, Inouye M, et al.
Genome Med
. 2024 Feb;
16(1):33.
PMID: 38373998
Polygenic scores (PGS) can be used for risk stratification by quantifying individuals' genetic predisposition to disease, and many potentially clinically useful applications have been proposed. Here, we review the latest...
10.
Xu Y, Ritchie S, Liang Y, Timmers P, Pietzner M, Lannelongue L, et al.
Nature
. 2023 Mar;
616(7955):123-131.
PMID: 36991119
The use of omic modalities to dissect the molecular underpinnings of common diseases and traits is becoming increasingly common. But multi-omic traits can be genetically predicted, which enables highly cost-effective...