Kaitlin Sesock

Gene‐specific criteria for PTEN variant curation: Recommendations from the ClinGen PTEN Expert Panel

Robert Huether, Rachid Karam, Charis Eng, 2018, Human mutation.

Breast cancer risk and clinical implications for germline PTEN mutation carriers

C. Eng, J. Ngeow, Kaitlin Sesock, 2017, Breast Cancer Research and Treatment.

Unexpected cancer-predisposition gene variants in Cowden syndrome and Bannayan-Riley-Ruvalcaba syndrome patients without underlying germline PTEN mutations

T. LaFramboise, C. Eng, F. Niazi, 2018, PLoS genetics.

Clinical Implications for Germline PTEN Spectrum Disorders.

C. Eng, Kaitlin Sesock, J. Ngeow, 2017, Endocrinology and metabolism clinics of North America.

Characterization of cryptic splicing in germline PTEN intronic variants in Cowden syndrome

Charis Eng, C. Eng, T. Romigh, 2017, Human mutation.

The c.1364C>A (p.A455E) Mutation in the CFTR Pseudogene Results in an Incorrectly Assigned Carrier Status by a Commonly Used Screening Platform.

Junqing Shen, K. Deeb, Kaitlin Sesock, 2015, The Journal of molecular diagnostics : JMD.

Clinical Implications for Germline PTEN Spectrum Disorders.

C. Eng, Kaitlin Sesock, J. Ngeow, 2017, Endocrinology and metabolism clinics of North America.