D. W. Benson

发表

Bacteremia in Patients with Heterotaxy: A Review and Implications for Management.

G. Geddes, Donald G Basel, N. Ghanayem, 2016, Congenital heart disease.

Mutations in SGOL1 cause a novel cohesinopathy affecting heart and gut rhythm

Steven J. M. Jones, D. Labuda, H. Dietz, 2014, Nature Genetics.

Platelet Function Changes during Neonatal Cardiopulmonary Bypass Surgery: Mechanistic Basis and Lack of Correlation with Excessive Bleeding

P. Simpson, P. Newman, D. Newman, 2019, Thrombosis and Haemostasis.

Impact of MYH6 variants in hypoplastic left heart syndrome

P. Simpson, J. Tweddell, J. Lough, 2016, Physiological genomics.

Common deletion variants causing protocadherin-α deficiency contribute to the complex genetics of BAV and left-sided congenital heart disease

Lisa J. Martin, Julie A. Phillippi, P. Kirshbom, 2021, HGG advances.

Rotational Thromboelastometry Rapidly Predicts Thrombocytopenia and Hypofibrinogenemia During Neonatal Cardiopulmonary Bypass

P. Simpson, J. Tweddell, D. Newman, 2018, World journal for pediatric & congenital heart surgery.

Classic and atypical Wenckebach periodicity in a late gestation fetus with maternal anti-Ro/SSA antibodies

B. Cuneo, J. V. von Alvensleben, M. R. Gropler, 2021, HeartRhythm case reports.

Highly sensitive noninvasive cardiac transplant rejection monitoring using targeted quantification of donor-specific cell-free deoxyribonucleic acid.

A. Oliphant, S. Berger, P. Simpson, 2014, Journal of the American College of Cardiology.

Highly sensitive noninvasive cardiac transplant rejection monitoring using targeted quantification of donor-specific cell-free deoxyribonucleic acid.

A. Oliphant, S. Berger, P. Simpson, 2014, Journal of the American College of Cardiology.

Impact of MYH6 variants in hypoplastic left heart syndrome

P. Simpson, J. Tweddell, J. Lough, 2016, Physiological genomics.