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Author Details

Nabila Bouatia-Naji
2005
80
34
PMIDPaper TitleJournal TitlePublished Year
36873395Genetics and pathophysiology of mitral valve prolapse.2023
36655574Genomic, Transcriptomic, and Proteomic Depiction of Induced Pluripotent Stem Cells-Derived Smooth Muscle Cells As Emerging Cellular Models for Arterial Diseases.2023
36655558Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity.2023
35132965Computational estimates of annular diameter reveal genetic determinants of mitral valve function and disease.JCI Insight2022
36043395The complex genetic basis of fibromuscular dysplasia, a systemic arteriopathy associated with multiple forms of cardiovascular disease.Clinical Science2022
36448890[Fibromuscular dysplasia as a polygenic disease].Medecine/Sciences2022
36480975Research Opportunities in the Treatment of Mitral Valve Prolapse: JACC Expert Panel.J Am Coll Cardiol2022
35245370Genome-wide association study reveals novel genetic loci: a new polygenic risk score for mitral valve prolapse.Eur Heart J2022
34534607Plasma and genetic determinants of soluble TREM-1 and major adverse cardiovascular events in a prospective cohort of acute myocardial infarction patients. Results from the FAST-MI 2010 study.Int J Cardiol2021
33508947Chromatin Accessibility of Human Mitral Valves and Functional Assessment of MVP Risk Loci.Circulation Research2021
33558525Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.Nat Commun2021
32531060Rare loss-of-function mutations of PTGIR are enriched in fibromuscular dysplasia.Cardiovasc Res2021
33402679Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.Nat Commun2021
34461747Genome-Wide Association Meta-Analysis Supports Genes Involved in Valve and Cardiac Development to Associate With Mitral Valve Prolapse.Circulation. Genomic and precision medicine2021
34706548Recent Advances on the Genetics of Spontaneous Coronary Artery Dissection.Circulation. Genomic and precision medicine2021
31424497A plasma proteogenomic signature for fibromuscular dysplasia.Cardiovasc Res2020
31678991Transcriptome Analysis of lncRNAs in Pheochromocytomas and Paragangliomas.Journal of Clinical Endocrinology and Metabolism2020
32475314Genetic Study of and Fibromuscular Dysplasia, Meta-Analysis and Effects on Clinical Features of Patients: The ARCADIA-POL Study.Hypertension2020
33125268Spontaneous Coronary Artery Dissection: Insights on Rare Genetic Variation From Genome Sequencing.Circ Genom Precis Med2020
31532366[Genetics provides a link between cardiovascular diseases predominantly afflicting women].Medecine/Sciences2019
30448113Spontaneous coronary artery dissections and fibromuscular dysplasia: Current insights on pathophysiology, sex and gender.International Journal of Cardiology2019
30285053Fibromuscular Dysplasia and Its Neurologic Manifestations: A Systematic Review.JAMA Neurol2019
30621952Association of the PHACTR1/EDN1 Genetic Locus With Spontaneous Coronary Artery Dissection.J Am Coll Cardiol2019
31263163Genome-wide Association Study of Change in Fasting Glucose over time in 13,807 non-diabetic European Ancestry Individuals.Sci Rep2019
31112420Genome-Wide Association Study-Driven Gene-Set Analyses, Genetic, and Functional Follow-Up Suggest GLIS1 as a Susceptibility Gene for Mitral Valve Prolapse.Circ Genom Precis Med2019
31336484Genetic association study between T-786C NOS3 polymorphism and essential hypertension in an Algerian population of the Oran city.Diabetes and Metabolic Syndrome: Clinical Research and Reviews2019
27780089The relationship between MTHFR C677T gene polymorphism and essential hypertension in a sample of an Algerian population of Oran city.International Journal of Cardiology2016
27094201Top Advances in Functional Genomics and Translational Biology for 2015.Circ Cardiovasc Genet2016
26831199Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.Nat Commun2016
26830076Genetic risk of type 2 diabetes in populations of the African continent: A systematic review and meta-analyses.Diabetes Res Clin Pract2016
27618452The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals.Nat Genet2016
27792790PHACTR1 Is a Genetic Susceptibility Locus for Fibromuscular Dysplasia Supporting Its Complex Genetic Pattern of Inheritance.PLoS Genet2016
27680874The MITF, p.E318K Variant, as a Risk Factor for Pheochromocytoma and Paraganglioma.Journal of Clinical Endocrinology and Metabolism2016
26147384Exome sequencing in seven families and gene-based association studies indicate genetic heterogeneity and suggest possible candidates for fibromuscular dysplasia.J Hypertens2015
29371517Investigation of the Matrix Metalloproteinase-2 Gene in Patients with Non-Syndromic Mitral Valve Prolapse.Journal of Cardiovascular Development and Disease2015
26483167Mitral valve disease--morphology and mechanisms.Nat Rev Cardiol2015
26258302Mutations in DCHS1 cause mitral valve prolapse.Nature2015
26301497Genetic association analyses highlight biological pathways underlying mitral valve prolapse.Nat Genet2015
24699409A central role for GRB10 in regulation of islet function in man.PLoS Genet2014
24472454[New genetic determinants of glycemic traits: insights in biological pathways of glucose homeostasis].Medecine/Sciences2014
23508304Multiple functional polymorphisms in the G6PC2 gene contribute to the association with higher fasting plasma glucose levels.Diabetologia2013
23263486Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.Nat Genet2013
23583979Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.Nat Genet2013
22238593A genome-wide association search for type 2 diabetes genes in African Americans.PLoS One2012
22479202Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.PLoS Genet2012
22698912Impact of common variation in bone-related genes on type 2 diabetes and related traits.Diabetes2012
22844403Dietary factors impact on the association between CTSS variants and obesity related traits.PLoS ONE2012
22885924Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways.Nat Genet2012
22581228A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.Nat Genet2012
22421893Association between FTO variant and change in body weight and its interaction with dietary factors: the DiOGenes study.2012
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University of Oxford
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Stanford University School of Medicine
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University of Maryland School of Medicine
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William Harvey Research Institute, Queen Mary University of London
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National Institute on Aging, National Institutes of Health
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National Institute on Aging, National Institutes of Health
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