Janet C Lockman

Gene expression profiling of isogenic cells with different TP53 gene dosage reveals numerous genes that are affected by TP53 dosage and identifies CSPG2 as a direct target of p53

F. Wright, S. Liyanarachchi, A. de la Chapelle, 2002, Proceedings of the National Academy of Sciences of the United States of America.

Mismatch Repair Gene PMS2

Hidewaki Nakagawa, Heather Hampel, Wendy L Frankel, 2004, Cancer Research.

Long‐range PCR facilitates the identification of PMS2‐specific mutations

A. de la Chapelle, A. Lindblom, Janet C Lockman, 2006, Human mutation.

Screening for Lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patients.

W. Frankel, A. de la Chapelle, H. Nakagawa, 2006, Cancer research.

Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer).

W. Frankel, A. de la Chapelle, H. Nakagawa, 2005, The New England journal of medicine.

Comment on: Screening for Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer) among Endometrial Cancer Patients.

W. Frankel, A. de la Chapelle, H. Nakagawa, 2007, Cancer research.

Allele separation facilitates interpretation of potential splicing alterations and genomic rearrangements.

K. Kinzler, B. Vogelstein, Hai Yan, 2002, Cancer research.

Feasibility of screening for Lynch syndrome among patients with colorectal cancer.

Heather Hampel, Wendy L Frankel, W. Frankel, 2008, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Colorectal Cancer ) among Endometrial Cancer Patients Screening for Lynch Syndrome ( Hereditary Nonpolyposis

W. Frankel, H. Nakagawa, Janet C Lockman, 2006 .

Recurrent germline mutation in MSH2arises frequently de novo

R. Chadwick, A. de la Chapelle, D. Evans, 2000, Journal of medical genetics.