Suchergebnisse - "Zekavat, Seyedeh M"

PubPharm (27)

1

Rare Genetic Variants Associated With Sudden Cardiac Death in Adults

enthalten in: Journal of the American College of Cardiology | 2019

von Khera, A. | Mason-Suares, H. | Brockman, D. | +24

CommentIn: J Am Coll Cardiol. 2019 Nov 26;74(21):2635-2637. - PMID 31727423

2

Inherited Causes of Clonal Hematopoiesis of Indeterminate Potential in TOPMed Whole Genomes

enthalten in: bioRxiv.org | 2019

von Bick, A. | Weinstock, J. | Nandakumar, S. | +120

3

Genetic Link Between Arterial Stiffness and Atrial Fibrillation

enthalten in: Circulation. Genomic and precision medicine | 2019

von Zekavat, S. | Roselli, C. | Hindy, G. | +4

4

Genetic Association of Finger Photoplethysmography-Derived Arterial Stiffness Index With Blood Pressure and Coronary Artery Disease

enthalten in: Arteriosclerosis, thrombosis, and vascular biology | 2019

von Zekavat, S. | Aragam, K. | Emdin, C. | +4

5

Whole-Genome Sequencing to Characterize Monogenic and Polygenic Contributions in Patients Hospitalized With Early-Onset Myocardial Infarction

enthalten in: Circulation | 2019

von Khera, A. | Chaffin, M. | Zekavat, S. | +20

6

A statistical framework for cross-tissue transcriptome-wide association analysis

enthalten in: Nature genetics | 2019

von Hu, Y. | Li, M. | Lu, Q. | +18

7

DNA Sequence Variation in ACVR1C Encoding the Activin Receptor-Like Kinase 7 Influences Body Fat Distribution and Protects Against Type 2 Diabetes

enthalten in: Diabetes | 2019

von Emdin, C. | Khera, A. | Aragam, K. | +22

8

Publisher Correction : Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries

enthalten in: Nature communications | 2018

von Zekavat, S. | Ruotsalainen, S. | Handsaker, R. | +136

ErratumFor: Nat Commun. 2018 Jul 4;9(1):2606. - PMID 29973585

9

Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries

enthalten in: Nature communications | 2018

von Zekavat, S. | Ruotsalainen, S. | Handsaker, R. | +136

ErratumIn: Nat Commun. 2018 Aug 23;9(1):3493. - PMID 30140049

10

Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum

enthalten in: American journal of human genetics | 2018

von Ganna, A. | Satterstrom, F. | Zekavat, S. | +45