B. Keavney

发表

Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16

S. Heath, G. Lathrop, M. Farrall, 2013, Nature Genetics.

Genome-wide analysis identifies 12 loci influencing human reproductive behavior

M. P. Concas, N. Eriksson, M. Nalls, 2016, Nature Genetics.

The Mouseion at the JAXlibrary The Mouseion at the JAXlibrary

Ferhaan Ahmad, M. Rynkiewicz, A. Bais, 2022 .

Cardiovascular, obstetric and neonatal outcomes in women with previous fontan repair.

B. Keavney, O. Asghar, S. Bonner, 2017, European journal of obstetrics, gynecology, and reproductive biology.

Atrial fibrillation associated with ivabradine treatment: meta-analysis of randomised controlled trials

J. Bourke, B. Keavney, M. Teare, 2014, Heart.

Stroke following percutaneous coronary intervention: type-specific incidence, outcomes and determinants seen by the British Cardiovascular Intervention Society 2007-12.

A. Zaman, E. Kontopantelis, P. Myint, 2015, European heart journal.

Stroke Following Percutaneous Coronary Intervention: Type-specific incidence, outcomes and determinants seen by the British Cardiovascular Intervention Society 2007-2012

A. Zaman, E. Kontopantelis, P. Myint, 2015 .

Genetic variants associated with risk of atrial fibrillation regulate expression of PITX2, CAV1, MYOZ1, C9orf3 and FANCC.

B. Keavney, M. Choy, N. Yonan, 2015, Journal of molecular and cellular cardiology.

U.K. Prospective Diabetes Study. XV: Relationship of renin-angiotensin system gene polymorphisms with microalbuminuria in NIDDM.

I. Stratton, R. Turner, B. Keavney, 1995, Kidney international.

Stroke following percutaneous coronary intervention: type-specific incidence, outcomes and determinants seen by the British Cardiovascular Intervention Society 2007-12.

A. Zaman, E. Kontopantelis, P. Myint, 2015, European heart journal.