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Journal of the American College of Surgeons|February 22, 2003
A636P is associated with early-onset colon cancer in Ashkenazi JewsJosé G Guillem, Beth S Rapaport, Tomas Kirchhoff, et al.
BMC Medical Genetics|January 17, 2003
Frequency of CHEK2*1100delC in New York breast cancer cases and controlsKenneth Offit, Heather Pierce, Tomas Kirchhoff, et al.
Genetic Epidemiology|October 6, 2005
Localization of breast cancer susceptibility loci by genome-wide SNP linkage disequilibrium mappingNathan A Ellis, Tomas Kirchhoff, Nandita Mitra, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|September 17, 2008
Frequency and distinctive spectrum of KRAS mutations in never smokers with lung adenocarcinomaGregory J Riely, Mark G Kris, Daniel Rosenbaum, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|November 22, 2018
Diagnosis of known sarcoma fusions and novel fusion partners by targeted RNA sequencing with identification of a recurrent ACTB-FOSB fusion in pseudomyogenic hemangioendotheliomaGuo Zhu, Ryma Benayed, Caleb Ho, et al.
Carcinogenesis|June 16, 2006
Increased frequency of disease-causing MYH mutations in colon cancer familiesPaolo Peterlongo, Nandita Mitra, Ana Sanchez de Abajo, et al.
International Journal of Cancer|October 2, 2003
MSH6 germline mutations are rare in colorectal cancer familiesPaolo Peterlongo, Khedoudja Nafa, Gabriel S Lerman, et al.
Human Molecular Genetics|January 15, 2005
Functional and genomic approaches reveal an ancient CHEK2 allele associated with breast cancer in the Ashkenazi Jewish populationAvraham Shaag, Tom Walsh, Paul Renbaum, et al.
Genes, Chromosomes & Cancer|April 14, 2016
Genomic aberrations frequently alter chromatin regulatory genes in chordomaLu Wang, Ahmet Zehir, Khedoudja Nafa, et al.
The Journal of Molecular Diagnostics : JMD|April 17, 2022
Clinical Utility and Performance of an Ultrarapid Multiplex RNA-Based Assay for Detection of ALK, ROS1, RET, and NTRK1/2/3 Rearrangements and MET Exon 14 Skipping AlterationsYing-Hsia Chu, Jada Barbee, Soo-Ryum Yang, et al.
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