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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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A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure

Yun J. Sung, +329 more
TL;DR: The identified loci show strong evidence for regulatory features and support shared pathophysiology with cardiometabolic and addiction traits and highlight a role in BP regulation for biological candidates such as modulators of vascular structure and function.
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A saturated map of common genetic variants associated with human height

Loic Yengo, +617 more
- 10 Jan 2022 - 
TL;DR: In this article , the authors show that common single-nucleotide polymorphisms (SNPs) are predicted to collectively explain 40-50% of phenotypic variation in human height, but identifying the specific variants and associated regions requires huge sample sizes.
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Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility

Maria Teresa Landi, +183 more
- 27 Apr 2020 - 
TL;DR: Analysis of risk estimates across geographical regions and host factors suggests the acral melanoma subtype is uniquely unrelated to pigmentation, and analysis combining nevus count and hair color GWAS results provide insights into the genetic architecture of melanoma.
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Secretory Phospholipase A2-IIA and Cardiovascular Disease: A Mendelian Randomization Study

Michael V. Holmes, +119 more
TL;DR: In this paper, the role of secretory phospholipase A2 (sPLA2)-IIA in cardiovascular disease was investigated by using a Mendelian randomization meta-analysis of 19 general population studies and 10 acute coronary syndrome (ACS) cohorts.