Author details

Full Name

Seyedeh M Zekavat

Affiliation

ORCID

Career Start Year

2015

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37292770	Insights into human health from phenome- and genome-wide analyses of UK Biobank retinal optical coherence tomography phenotypes.	medRxiv	2023
36707304	Reply.		2023
36949957	<i>TP53-</i>mediated clonal hematopoiesis confers increased risk for incident atherosclerotic disease.	Nat Cardiovasc Res	2023
37498674	Genetic modification of inflammation- and clonal hematopoiesis-associated cardiovascular risk.	J Clin Invest	2023
35157520	Microvascular Outcomes in Women With a History of Hypertension in Pregnancy.	Circulation	2022
35771531	A <i>MUC5B</i> Gene Polymorphism, rs35705950-T, Confers Protective Effects Against COVID-19 Hospitalization but Not Severe Disease or Mortality.	Am J Respir Crit Care Med	2022
35452290	Genome-wide pleiotropy analysis of coronary artery disease and pneumonia identifies shared immune pathways.	Science advances	2022
35759254	Association of Kidney Comorbidities and Acute Kidney Failure With Unfavorable Outcomes After COVID-19 in Individuals With the Sickle Cell Trait.	JAMA Intern Med	2022
35508625	Genetics of smoking and risk of clonal hematopoiesis.	Sci Rep	2022
35385311	Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential.	Sci Adv	2022
35482673	A Phenome-Wide Association Study of genes associated with COVID-19 severity reveals shared genetics with complex diseases in the Million Veteran Program.	PLoS Genet	2022
34743536	Clonal Hematopoiesis Is Associated With Higher Risk of Stroke.	Stroke	2022
35234813	Fibrillar Collagen Variants in Spontaneous Coronary Artery Dissection.	JAMA Cardiol	2022
35149155	Photoreceptor Layer Thinning Is an Early Biomarker for Age-Related Macular Degeneration: Epidemiologic and Genetic Evidence from UK Biobank OCT Data.	Ophthalmology	2022
35086662	Genetic IL-6 Signaling Modifies Incident Coronary Artery Disease Risk in Chronic KidneyÂ Disease.	Journal of the American College of Cardiology	2022
35177190	Repeat Measures of Lipoprotein(a) Molar Concentration and Cardiovascular Risk.	Journal of the American College of Cardiology	2022
34663986	Distinction of lymphoid and myeloid clonal hematopoiesis.	Nat Med	2021
34015477	Cardiovascular and KidneyÂ Outcomes Across the GlycemicÂ Spectrum: Insights From the UK Biobank.	Journal of the American College of Cardiology	2021
33629108	Apolipoprotein B is an insufficient explanation for the risk of coronary disease associated with lipoprotein(a).	Cardiovascular Research	2021
34106216	Association of Diet Quality With Prevalence of Clonal Hematopoiesis and Adverse Cardiovascular Events.	JAMA Cardiology	2021
34210413	Supplemental Association of Clonal Hematopoiesis With Incident HeartÂ Failure.	J Am Coll Cardiol	2021
33283203	Elevated Blood Pressure Increases Pneumonia Risk: Epidemiological Association and Mendelian Randomization in the UK Biobank.	Med	2021
33161765	Premature Menopause, Clonal Hematopoiesis, and Coronary Artery Disease in Postmenopausal Women.	Circulation	2021
32511360	Androgen Regulates SARS-CoV-2 Receptor Levels and Is Associated with Severe COVID-19 Symptoms in Men.	bioRxiv	2020
33236004	Hematopoietic mosaic chromosomal alterations and risk for infection among 767,891 individuals without blood cancer.	Res Sq	2020
33232663	Androgen Signaling Regulates SARS-CoV-2 Receptor Levels and Is Associated with Severe COVID-19 Symptoms in Men.	Cell Stem Cell	2020
31211625	Genetic Link Between Arterial Stiffness and Atrial Fibrillation.	Circ Genom Precis Med	2019
31738818	Association of Premature Natural and Surgical Menopause With Incident Cardiovascular Disease.	JAMA	2019
31727424	Long-Term Cardiovascular Risk inÂ WomenÂ With Hypertension DuringÂ Pregnancy.	J Am Coll Cardiol	2019
31727422	Rare Genetic Variants Associated With Sudden Cardiac Death in Adults.	J Am Coll Cardiol	2019
30270359	Recall by genotype and cascade screening for familial hypercholesterolemia in a population-based biobank from Estonia.	Genet Med	2019
30586733	Whole-Genome Sequencing to Characterize Monogenic and Polygenic Contributions in Patients Hospitalized With Early-Onset Myocardial Infarction.	Circulation	2019
30389748	DNA Sequence Variation in <i>ACVR1C</i> Encoding the Activin Receptor-Like Kinase 7 Influences Body Fat Distribution and Protects Against Type 2 Diabetes.	Diabetes	2019
30804563	A statistical framework for cross-tissue transcriptome-wide association analysis.	Nat Genet	2019
31070453	Genetic Association of Finger Photoplethysmography-Derived Arterial Stiffness Index With Blood Pressure and Coronary Artery Disease.	Arterioscler Thromb Vasc Biol	2019
29691411	Analysis of predicted loss-of-function variants in UK Biobank identifies variants protective for disease.	Nat Commun	2018
28982690	Phenotypic Consequences of a Genetic Predisposition to Enhanced Nitric Oxide Signaling.	Circulation	2018
29973585	Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries.	Nat Commun	2018
30140049	Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries.	Nat Commun	2018
30140000	Deep-coverage whole genome sequences and blood lipids among 16,324 individuals.	Nat Commun	2018
29861106	Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum.	Am J Hum Genet	2018
28031487	Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms.	Proc Natl Acad Sci U S A	2017
28821595	A computational model of 1,5-AG dynamics during pregnancy.	Physiological Reports	2017
28506971	Protein-Truncating Variants at the Cholesteryl Ester Transfer Protein Gene and Risk for Coronary Heart Disease.	Circ Res	2017
28385496	ANGPTL3 Deficiency and Protection Against Coronary Artery Disease.	J Am Coll Cardiol	2017
28753427	A Genetic Variant Associated with Five Vascular Diseases Is a Distal Regulator of Endothelin-1 Gene Expression.	Cell	2017
28928999	Acquired Vitamin K Deficiency as Unusual Cause of Bleeding Tendency in Adults: A Case Report of a Nonhospitalized Student Presenting with Severe Menorrhagia.	Case Reports in Obstetrics and Gynecology	2017
28442497	An in silico model of retinal cholesterol dynamics (RCD model): insights into the pathophysiology of dry AMD.	Journal of Lipid Research	2017
28196256	Genetic Association of Waist-to-Hip Ratio With Cardiometabolic Traits, Type 2 Diabetes, and Coronary Heart Disease.	JAMA - Journal of the American Medical Association	2017
27694993	Ultra-rare disruptive and damaging mutations influence educational attainment in the general population.	Nat Neurosci	2016