Publications by authors named "Janet Lockman"

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Feasibility of screening for Lynch syndrome among patients with colorectal cancer.
Heather Hampel, Wendy L Frankel, Edward Martin, Mark Arnold, Karamjit Khanduja, Janet Lockman

J Clin Oncol· December 2008

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Comment on: Screening for Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer) among Endometrial Cancer Patients.
Heather Hampel, Jenny Panescu, Janet Lockman, Kaisa Sotamaa, Daniel Fix

Cancer Res· October 2007

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Screening for Lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patients.
Heather Hampel, Wendy Frankel, Jenny Panescu, Janet Lockman, Kaisa Sotamaa

Cancer Res· August 2006

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Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer).
Heather Hampel, Wendy L Frankel, Edward Martin, Mark Arnold, Karamjit Khanduja, Janet Lockman

N Engl J Med· May 2005

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Mismatch repair gene PMS2: disease-causing germline mutations are frequent in patients whose tumors stain negative for PMS2 protein, but paralogous genes obscure mutation detection and interpretation.
Hidewaki Nakagawa, Janet C Lockman, Wendy L Frankel, Heather Hampel, Kelle Steenblock

Cancer Res· July 2004

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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.
Heejei Yoon, Sandya Liyanarachchi, Fred A Wright, Ramana Davuluri, Janet C Lockman

Proc Natl Acad Sci U S A· November 2002

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Allele separation facilitates interpretation of potential splicing alterations and genomic rearrangements.
Hidewaki Nakagawa, Hai Yan, Janet Lockman, Heather Hampel, Kenneth W Kinzler

Cancer Res· August 2002

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