Daniela Macaya

James S Ware 2 collaborations

None None 2 collaborations

Rebecca Latimer 1 collaboration

Heather MacLeod 1 collaboration

Lisa Dellefave-Castillo 1 collaboration

Tara R Hart 1 collaboration

Ana Morales 1 collaboration

Alexander Ing 1 collaboration

Christian Antolik 1 collaboration

Christina Austin-Tse 1 collaboration

Linnea M Baudhuin 1 collaboration

Lucas Bronicki 1 collaboration

Allison Cirino 1 collaboration

Megan H Hawley 1 collaboration

Michael Fietz 1 collaboration

John Garcia 1 collaboration

Carolyn Ho 1 collaboration

Jodie Ingles 1 collaboration

Olga Jarinova 1 collaboration

Tami Johnston 1 collaboration

Melissa A Kelly 1 collaboration

C Lisa Kurtz 1 collaboration

Matt Lebo 1 collaboration

Lisa Mahanta 1 collaboration

Joseph Maleszewski 1 collaboration

Arjun K Manrai 1 collaboration

Mitzi Murray 1 collaboration

Gabriele Richard 1 collaboration

Chris Semsarian 1 collaboration

Kate L Thomson 1 collaboration

Tom Winder 1 collaboration

Ray E Hershberger 1 collaboration

Birgit H Funke 1 collaboration

Matteo Vatta 1 collaboration

Kathryn A McGurk 1 collaboration

Xiaolei Zhang 1 collaboration

Pantazis Theotokis 1 collaboration

Kate Thomson 1 collaboration

Andrew Harper 1 collaboration

Rachel J Buchan 1 collaboration

Erica Mazaika 1 collaboration

Elizabeth Ormondroyd 1 collaboration

William T Wright 1 collaboration

Chee Jian Pua 1 collaboration

Birgit Funke 1 collaboration

Daniel G MacArthur 1 collaboration

Sanjay K Prasad 1 collaboration

Stuart A Cook 1 collaboration

Mona Allouba 1 collaboration

Yasmine Aguib 1 collaboration

Magdi H Yacoub 1 collaboration

Declan P O'Regan 1 collaboration

Paul J R Barton 1 collaboration

Hugh Watkins 1 collaboration

Leonardo Bottolo 1 collaboration

Publications (3)

Postmortem Genetic Testing Is an Increasingly Utilized Tool in Death Investigation.

Harmonizing the Collection of Clinical Data on Genetic Testing Requisition Forms to Enhance Variant Interpretation in Hypertrophic Cardiomyopathy (HCM): A Study from the ClinGen Cardiomyopathy Variant Curation Expert Panel.

The penetrance of rare variants in cardiomyopathy-associated genes: A cross-sectional approach to estimating penetrance for secondary findings.

Réseau de co-auteurs