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Sean J. Jurgens

Kardiologe

Name	Sean J. Jurgens
Place	Niederlande
Gender	männlich
Academic degree	MD MSc PhD
Profession	Kardiologe (characteristic profession)
Variant	Sean Joseph Jurgens Sean Jurgens
Source	https://www.linkedin.com/in/sean-joseph-jurgens-1a4330137/?originalSubdomain=nl (Stand: 10.04.2025)
Record type	Person
GND-Identifier	1362761753
Record ID	1362761753
Involved in show all Cardiac adaptation to endurance exercise training requires suppression of GDF15 via PGC-1α Coagulation factor XII haploinsufficiency is protective against venous thromboembolism in a population-scale multidimensional analysis Polygenic Risk Scores in Dilated Cardiomyopathy: Towards the Future Rare genetic variation in PTPRB is associated with central serous chorioretinopathy, varicose veins and glaucoma Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases Evaluation of polygenic scores for hypertrophic cardiomyopathy in the general population and across clinical settings Large-scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy The impact of common and rare genetic variants on bradyarrhythmia development Publisher Correction: Genome-wide association study reveals mechanisms underlying dilated cardiomyopathy and myocardial resilience Genome-wide association study reveals mechanisms underlying dilated cardiomyopathy and myocardial resilience Rare coding variant analysis for human diseases across biobanks and ancestries Deep learning of left atrial structure and function provides link to atrial fibrillation risk TAD boundary deletion causes PITX2-related cardiac electrical and structural defects Selenoprotein deficiency disorder predisposes to aortic aneurysm formation Exploring the complex spectrum of dominance and recessiveness in genetic cardiomyopathies Publisher Correction: Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genes Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genes Inherited basis of visceral, abdominal subcutaneous and gluteofemoral fat depots

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Sean J. Jurgens

Cardiac adaptation to endurance exercise training requires suppression of GDF15 via PGC-1α

Coagulation factor XII haploinsufficiency is protective against venous thromboembolism in a population-scale multidimensional analysis

Polygenic Risk Scores in Dilated Cardiomyopathy: Towards the Future

Rare genetic variation in PTPRB is associated with central serous chorioretinopathy, varicose veins and glaucoma

Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk

Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases

Evaluation of polygenic scores for hypertrophic cardiomyopathy in the general population and across clinical settings

Large-scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy

The impact of common and rare genetic variants on bradyarrhythmia development

Publisher Correction: Genome-wide association study reveals mechanisms underlying dilated cardiomyopathy and myocardial resilience

Genome-wide association study reveals mechanisms underlying dilated cardiomyopathy and myocardial resilience

Rare coding variant analysis for human diseases across biobanks and ancestries

Deep learning of left atrial structure and function provides link to atrial fibrillation risk

TAD boundary deletion causes PITX2-related cardiac electrical and structural defects

Selenoprotein deficiency disorder predisposes to aortic aneurysm formation

Exploring the complex spectrum of dominance and recessiveness in genetic cardiomyopathies

Publisher Correction: Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genes

Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genes

Inherited basis of visceral, abdominal subcutaneous and gluteofemoral fat depots