Author details

Full Name

Joban Sehmi

Affiliation

ORCID

Career Start Year

2006

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
38015442	A Placebo-Controlled Trial of Percutaneous Coronary Intervention for Stable Angina.		2023
35148997	CT multivessel aggregate stenosis score: A novel point-of-care tool for predicting major adverse cardiac events.		2022
33109707	Hypertension attenuates the prognostic value of coronary artery calcification scoring in low-risk patients.	Heart	2021
33998247	Automated Left Ventricular Dimension Assessment Using Artificial Intelligence Developed and Validated by a UK-Wide Collaborative.	Circulation: Cardiovascular Imaging	2021
34340523	Placebo-Controlled Efficacy of Percutaneous Coronary Intervention for Focal and Diffuse Patterns of Stable Coronary Artery Disease.	Circulation: Cardiovascular Interventions	2021
32586942	A 53-year-old man presenting with palpitations.	Heart	2020
31251381	Association of Titin-Truncating Genetic Variants With Life-threatening Cardiac Arrhythmias in Patients With Dilated Cardiomyopathy and Implanted Defibrillators.	JAMA network open	2019
31707827	Dobutamine Stress Echocardiography Ischemia as a Predictor of the Placebo-Controlled Efficacy of Percutaneous Coronary Intervention in Stable Coronary Artery Disease: The Stress Echocardiography-Stratified Analysis of ORBITA.	Circulation	2019
29789302	Fractional Flow Reserve and Instantaneous Wave-Free Ratio as Predictors of the Placebo-Controlled Response to Percutaneous Coronary Intervention in Stable Single-Vessel Coronary Artery Disease.	Circulation	2018
29116125	Erratum: Large meta-analysis of genome-wide association studies identifies five loci for lean body mass.	Nat Commun	2017
28341696	A Low-Frequency Inactivating <i>AKT2</i> Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk.	Diabetes	2017
28724990	Large meta-analysis of genome-wide association studies identifies five loci for lean body mass.	Nat Commun	2017
27659466	52 Genetic Loci Influencing MyocardialÂ Mass.	J Am Coll Cardiol	2016
26238113	The effects of angiotensin II signaling blockade on platelet activity in subjects with hypertension.	Current Hypertension Reviews	2015
26566451	Unsuspected large left ventricular pseudoaneurysm: rapid bedside diagnosis by contrast-enhanced echocardiography.	Oxford Medical Case Reports	2015
26459079	Mass Confusion: Defining Aortic Pathology With Ultrasound Contrast.	Circulation	2015
25054115	Coronary heart disease in Indian Asians.	Glob Cardiol Sci Pract	2014
25282103	Defining the role of common variation in the genomic and biological architecture of adult human height.	Nat Genet	2014
25115870	The South Asian genome.	PLoS One	2014
24509480	Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility.	Nat Genet	2014
23583979	Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.	Nat Genet	2013
23222517	Seventy-five genetic loci influencing the human red blood cell.	Nature	2012
21874001	Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci.	Nat Genet	2011
21233446	The CXCL16 A181V mutation selectively inhibits monocyte adhesion to CXCR6 but is not associated with human coronary heart disease.	Arterioscler Thromb Vasc Biol	2011
22001757	Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.	Nat Genet	2011
21909115	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Nature	2011
20661308	Genome-wide meta-analysis for serum calcium identifies significantly associated SNPs near the calcium-sensing receptor (CASR) gene.	PLoS Genet	2010
20383145	Genetic loci influencing kidney function and chronic kidney disease.	Nat Genet	2010
20062061	Genetic variation in SCN10A influences cardiac conduction.	Nat Genet	2010
19820698	Genome-wide association study identifies variants in TMPRSS6 associated with hemoglobin levels.	Nat Genet	2009
19651812	Common genetic variation near melatonin receptor MTNR1B contributes to raised plasma glucose and increased risk of type 2 diabetes among Indian Asians and European Caucasians.	Diabetes	2009
17080113	Impact of new dialysis solutions on peritonitis rates.	Kidney International, Supplement	2006