Jinlian Chen

A clinical scoring system for selection of patients for PTEN mutation testing is proposed on the basis of a prospective study of 3042 probands.

Charis Eng, Jessica Mester, C. Eng, 2011, American journal of human genetics.

Germline PIK3CA and AKT1 mutations in Cowden and Cowden-like syndromes.

C. Eng, J. Mester, Charissa Peterson, 2013, American journal of human genetics.

Germline SDHx variants modify breast and thyroid cancer risks in Cowden and Cowden-like syndrome via FAD/NAD-dependant destabilization of p53

C. Eng, M. Ringel, J. Mester, 2011, Human molecular genetics.

Exome sequencing reveals germline gain-of-function EGFR mutation in an adult with Lhermitte–Duclos disease

Charis Eng, Samantha Colby, C. Eng, 2016, Cold Spring Harbor molecular case studies.

Exome Sequencing Reveals Germline SMAD9 Mutation That Reduces Phosphatase and Tensin Homolog Expression and Is Associated With Hamartomatous Polyposis and Gastrointestinal Ganglioneuromas.

L. Tucker-Kellogg, C. Eng, Haiwei Song, 2015, Gastroenterology.