Elizabeth Chao

Utilization of multigene panels in hereditary cancer predisposition testing: analysis of more than 2,000 patients

Tina Pesaran, C. Gau, S. Keiles, 2014, Genetics in Medicine.

Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline CDH1 sequence variants

Carla Oliveira, Rachid Karam, Chimene Kesserwan, 2018, Human mutation.

Combined genetic and splicing analysis of BRCA1 c.[594-2A>C; 641A>G] highlights the relevance of naturally occurring in-frame transcripts for developing disease gene variant classification algorithms.

Julian Peto, Kyriaki Michailidou, Kamila Czene, 2016, Human molecular genetics.