Patrick Thomas Ellinor, M.D.,Ph.D.
This page shows the publications co-authored by Patrick Ellinor and Alan Hanley.
Mutation of a common amino acid in NKX2.5 results in dilated cardiomyopathy in two large families. BMC Med Genet. 2016 Nov 17; 17(1):83.
Improving Atrial Fibrillation Therapy: Is There a Gene for That? J Am Coll Cardiol. 2017 Apr 25; 69(16):2088-2095.
Gain-of-function mutations in GATA6 lead to atrial fibrillation. Heart Rhythm. 2017 02; 14(2):284-291.
Ibrutinib-Mediated Atrial Fibrillation Attributable to Inhibition of C-Terminal Src Kinase. Circulation. 2020 12 22; 142(25):2443-2455.
Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval. Circ Genom Precis Med. 2018 05; 11(5):e002037.
Macrophages Facilitate Electrical Conduction in the Heart. Cell. 2017 04 20; 169(3):510-522.e20.
The connection strength for co-authors is the sum of the scores for each of their shared publications.
Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.