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Nilesh J. Samani

Researcher at University of Leicester

Publications -  836
Citations -  127518

Nilesh J. Samani is an academic researcher from University of Leicester. The author has contributed to research in topics: Genome-wide association study & Population. The author has an hindex of 149, co-authored 779 publications receiving 113545 citations. Previous affiliations of Nilesh J. Samani include University Hospitals of Leicester NHS Trust & Glenfield Hospital.

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Circulating stromelysin-1 (MMP-3): a novel predictor of LV dysfunction, remodelling and all-cause mortality after acute myocardial infarction.

TL;DR: This work investigated the temporal profile of MMP‐3 and its relationship to LV dysfunction and prognosis following AMI and found that changes to cardiac matrix are central to ventricular remodelling after acute MI.
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Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci.

A. Mesut Erzurumluoglu, +206 more
- 01 Oct 2020 - 
TL;DR: The novel loci will facilitate understanding the genetic aetiology of smoking behaviour and may lead to the identification of potential drug targets for smoking prevention and/or cessation.
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Determinants and Functional Significance of Myocardial Perfusion Reserve in Severe Aortic Stenosis

TL;DR: LV remodeling appears to be a more important determinant of impaired MPR than stenosis severity per se, and CMR-quantified MPR is independently associated with aerobic exercise capacity in severe AS.
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Analysis of Quantitative Trait Loci for Blood Pressure on Rat Chromosomes 2 and 13 Age-Related Differences in Effect

TL;DR: The findings provide important information on QTLs influencing blood pressure on rat chromosomes 2 and 13 that will be useful in localizing and identifying the causative genes and emphasize the importance of age being taken into account when the effects of individualQTLs on a trait that shows significant age-related changes are being analyzed.
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Galactosylation of IgA1 Is Associated with Common Variation in C1GALT1

TL;DR: It is demonstrated that common variation at C1GALT1 influences Gd-IgA1 level in the population, which independently associates with risk of progressive IgAN, and that the pathogenic importance of changes in IgA1 O-glycosylation may vary between white and Chinese patients with IgAN.