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Plaque erosion and acute coronary syndromes: phenotype, molecular characteristics and future directions

Nature reviews cardiology, 2021-10, Vol.18 (10), p.724-734

2021

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Clinical applications of polygenic risk score for coronary artery disease through the life course

Atherosclerosis, 2023-12, Vol.386, p.117356, Article 117356

2023

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Polygenic background modifies penetrance of monogenic variants for tier 1 genomic conditions

Nature communications, 2020-08, Vol.11 (1), p.3635-3635, Article 3635

2020

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The potential of polygenic scores to improve cost and efficiency of clinical trials

Nature communications, 2022-05, Vol.13 (1), p.2922-4, Article 2922

2022

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Translational Medicine in the Era of Big Data and Machine Learning

Circulation research, 2018-11, Vol.123 (11), p.1202-1204

2018

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MSGene: a multistate model using genetic risk and the electronic health record applied to lifetime risk of coronary artery disease

Nature communications, 2024-06, Vol.15 (1), p.4884-14

2024

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PET myocardial perfusion imaging of regadenoson-induced coronary vasospasm

Journal of nuclear cardiology, 2023-10, Vol.30 (5), p.2187-2190

2023

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Massive underrepresentation of Arabs in genomic studies of common disease

Genome medicine, 2023-11, Vol.15 (1), p.99-5, Article 99

2023

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Clinical utility of polygenic scores for cardiometabolic disease in Arabs

Nature communications, 2023-10, Vol.14 (1), p.6535-6535, Article 6535

2023

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Design and user experience testing of a polygenic score report: a qualitative study of prospective users

BMC medical genomics, 2021-10, Vol.14 (1), p.238-238, Article 238

2021

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Students' perceptions of peer-organized extra-curricular research course during medical school: a qualitative study

PloS one, 2015-03, Vol.10 (3), p.e0119375-e0119375

2015

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Familial hypercholesterolemia: the lipids or the genes?

Nutrition & metabolism, 2011-04, Vol.8 (1), p.23-23

2011

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UBQLN2 mutation causing heterogeneous X-linked dominant neurodegeneration

Annals of neurology, 2014-05, Vol.75 (5), p.793-798

2014

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Genetics of Congenital Heart Disease: The Glass Half Empty

Circulation research, 2013-02, Vol.112 (4), p.707-720

2013

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NKX2-5 Mutations in an Inbred Consanguineous Population: Genetic and Phenotypic Diversity

Scientific reports, 2015-03, Vol.5 (1), p.8848-8848, Article 8848

2015

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Ocular manifestations of severe familial hypercholesterolemia

Heliyon, 2024-05, Vol.10 (9), p.e30487, Article e30487

2024

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Machine Learning in Invasive and Noninvasive Coronary Angiography

Current atherosclerosis reports, 2023-12, Vol.25 (12), p.1025-1033

2023

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Degenerated hair follicle cells and partial loss of sebaceous and eccrine glands in a familial case of axenfeld-rieger syndrome: An emerging role for the FOXC1/NFATC1 genetic axis

Journal of dermatological science, 2018-12, Vol.92 (3), p.237-244

2018

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Association of genetic risk, lifestyle, and their interaction with obesity and obesity-related morbidities

Cell metabolism, 2024-07, Vol.36 (7), p.1494-1503.e3

2024

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The Role of Genetics in Advancing Cardiometabolic Drug Development

Current atherosclerosis reports, 2024-05, Vol.26 (5), p.153-162

2024

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A multi-ancestry polygenic risk score improves risk prediction for coronary artery disease

Nature medicine, 2023-07, Vol.29 (7), p.1793-1803

2023

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A Novel Role for CSRP1 in a Lebanese Family with Congenital Cardiac Defects

Frontiers in genetics, 2017-12, Vol.8, p.217-217

2017

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CYP2C19 Genotyping in Anticoagulated Patients After Percutaneous Coronary Intervention: Should It Be Routine?

Circulation (New York, N.Y.), 2022-03, Vol.145 (10), p.721-723

2022

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Diet, genetics, and disease : a focus on the middle east and North Africa region

Journal of nutrition and metabolism, 2012-01, Vol.2012 (2012), p.1-19

2012

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Multivariate genomic analysis of 5 million people elucidates the genetic architecture of shared components of the metabolic syndrome

Nature genetics, 2024-09, Vol.56 (11), p.2380-2391

2024

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Plaque erosion and acute coronary syndromes: phenotype, molecular characteristics and future directions

Clinical applications of polygenic risk score for coronary artery disease through the life course

Polygenic background modifies penetrance of monogenic variants for tier 1 genomic conditions

The potential of polygenic scores to improve cost and efficiency of clinical trials

Translational Medicine in the Era of Big Data and Machine Learning

MSGene: a multistate model using genetic risk and the electronic health record applied to lifetime risk of coronary artery disease

PET myocardial perfusion imaging of regadenoson-induced coronary vasospasm

Massive underrepresentation of Arabs in genomic studies of common disease

Clinical utility of polygenic scores for cardiometabolic disease in Arabs

Design and user experience testing of a polygenic score report: a qualitative study of prospective users

Students' perceptions of peer-organized extra-curricular research course during medical school: a qualitative study

Familial hypercholesterolemia: the lipids or the genes?

UBQLN2 mutation causing heterogeneous X-linked dominant neurodegeneration

Genetics of Congenital Heart Disease: The Glass Half Empty

NKX2-5 Mutations in an Inbred Consanguineous Population: Genetic and Phenotypic Diversity

Ocular manifestations of severe familial hypercholesterolemia

Machine Learning in Invasive and Noninvasive Coronary Angiography

Degenerated hair follicle cells and partial loss of sebaceous and eccrine glands in a familial case of axenfeld-rieger syndrome: An emerging role for the FOXC1/NFATC1 genetic axis

Association of genetic risk, lifestyle, and their interaction with obesity and obesity-related morbidities

The Role of Genetics in Advancing Cardiometabolic Drug Development

A multi-ancestry polygenic risk score improves risk prediction for coronary artery disease

A Novel Role for CSRP1 in a Lebanese Family with Congenital Cardiac Defects

CYP2C19 Genotyping in Anticoagulated Patients After Percutaneous Coronary Intervention: Should It Be Routine?

Diet, genetics, and disease : a focus on the middle east and North Africa region

Multivariate genomic analysis of 5 million people elucidates the genetic architecture of shared components of the metabolic syndrome

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