B. Hanna

Functional genomics and gene-environment interaction highlight the complexity of Congenital Heart Disease caused by Notch pathway variants.

S. Grieve, E. Giannoulatou, S. Dunwoodie, 2019, Human molecular genetics.

Ventricular Tachycardia in a Patient With Dilated Cardiomyopathy Caused by a Novel Mutation of Lamin A/C Gene: Insights From Features on Electroanatomic Mapping, Catheter Ablation and Tissue Pathology.

L. Yeates, Saurabh Kumar, R. Bennett, 2020, Heart, lung & circulation.

Standardized practices for RNA diagnostics using clinically accessible specimens reclassifies 75% of putative splicing variants.

Robert J. Weatheritt, Stephanie L. White, N. Brown, 2021, Genetics in medicine : official journal of the American College of Medical Genetics.

The spectrum of infantile myofibromatosis includes both non-penetrance and adult recurrence.

Philippe M. Campeau, N. Graf, A. Ronan, 2017, European journal of medical genetics.

A preliminary Genome Wide Association Study to identify candidate genes responsible for Spastic Syndrome in Holstein cattle

F. Schenkel, R. Ventura, J. Baird, 2012 .

A clinical scoring system for congenital contractural arachnodactyly

A. Green, Alison M. Male, F. McKenzie, 2019, Genetics in Medicine.