A. Stuenkel

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.

The spectrum of FBN1, TGFβR1, TGFβR2 and ACTA2 variants in 594 individuals with suspected Marfan Syndrome, Loeys-Dietz Syndrome or Thoracic Aortic Aneurysms and Dissections (TAAD).

A. Stuenkel, M. Kelly, J. Lerner-Ellis, 2014, Molecular genetics and metabolism.

Diagnosing hereditary cancer predisposition in men with prostate cancer

Jianfeng Xu, B. Helfand, H. LaDuca, 2020, Genetics in Medicine.

Transition to the Clinical Doctorate: Attitudes of the Genetic Counseling Training Program Directors in North America

A. Stuenkel, H. Hampel, M. Campion, 2012, Journal of Genetic Counseling.

Breast cancer risk in neurofibromatosis type 1 is a function of the type of NF1 gene mutation: a new genotype-phenotype correlation

D. Baralle, P. Summerour, D. Eccles, 2018, Journal of Medical Genetics.

The Validation and Clinical Implementation of BRCAplus: A Comprehensive High-Risk Breast Cancer Diagnostic Assay

Elizabeth C. Chao, Tao Wang, S. Keiles, 2014, PloS one.

Diagnosing Hereditary Cancer Susceptibility Through Multigene Panel Testing

H. LaDuca, A. Stuenkel, V. Speare, 2017 .