Colorectal Cancer Molecular Biology Moves Into Clinical Practice

Por Pritchard, Colin C., Grady, William M.
Publicado em 2010

Molecular alterations and biomarkers in colorectal cancer

Por Grady, William M., Pritchard, Colin C.
Publicado em 2013

Germline, hematopoietic, mosaic, and somatic variation: interplay between inherited and acquired genetic alterations in disease assessment

Por Konnick, Eric Q., Pritchard, Colin C.
Publicado no Genome Med (2016)

MicroRNA profiling: approaches and considerations

Por Pritchard, Colin C., Cheng, Heather H., Tewari, Muneesh
Publicado no Nat Rev Genet (2012)

Family-Specific Variants and the Limits of Human Genetics

Por Shirts, Brian H., Pritchard, Colin C., Walsh, Tom
Publicado no Trends Mol Med (2016)

Project normal: Defining normal variance in mouse gene expression

Por Pritchard, Colin C., Hsu, Li, Delrow, Jeffrey, Nelson, Peter S.
Publicado em 2001

Design and Analysis for Studying microRNAs in Human Disease: A Primer on -Omic Technologies

Por Nair, Viswam S., Pritchard, Colin C., Tewari, Muneesh, Ioannidis, John P. A.
Publicado em 2014

BRCA2-Associated Prostate Cancer in a Patient With Spinal and Bulbar Muscular Atrophy

Por Conteduca, Vincenza, Sigouros, Michael, Sboner, Andrea, Pritchard, Colin C., Beltran, Himisha
Publicado no JCO Precis Oncol (2018)

Biallelic inactivation of BRCA2 in platinum sensitive, metastatic castration resistant prostate cancer

Por Cheng, Heather H., Pritchard, Colin C., Boyd, Thomas, Nelson, Peter S., Montgomery, Bruce
Publicado no Eur Urol (2015)

COLD-PCR enhanced melting curve analysis improves diagnostic accuracy for KRAS mutations in colorectal carcinoma

Por Pritchard, Colin C, Akagi, Laura, Reddy, Poluru L, Joseph, Loren, Tait, Jonathan F
Publicado em 2010

The effects of genomic germline variant reclassification on clinical cancer care

Por Slavin, Thomas P., Manjarrez, Sophia, Pritchard, Colin C., Gray, Stacy, Weitzel, Jeffrey N.
Publicado no Oncotarget (2019)

Polyclonal BRCA2 Reversion Mutations Detected in Circulating Tumor DNA After Platinum Chemotherapy in a Patient With Metastatic Prostate Cancer

Por Cheng, Heather H., Salipante, Stephen J., Nelson, Peter S., Montgomery, Bruce, Pritchard, Colin C.
Publicado no JCO Precis Oncol (2018)

Single molecule molecular inversion probes for targeted, high-accuracy detection of low-frequency variation

Por Hiatt, Joseph B., Pritchard, Colin C., Salipante, Stephen J., O'Roak, Brian J., Shendure, Jay
Publicado em 2013

DNA Damage Repair Alterations are Frequent in Prostatic Adenocarcinomas with Focal Pleomorphic Giant Cell Features

Por Lotan, Tamara L., Kaur, Harsimar B., Alharbi, Abdullah M., Pritchard, Colin C., Epstein, Jonathan I.
Publicado no Histopathology (2019)

Significance and implications of FDA approval of pembrolizumab for biomarker-defined disease

Por Boyiadzis, Michael M., Kirkwood, John M., Marshall, John L., Pritchard, Colin C., Azad, Nilofer S., Gulley, James L.
Publicado no J Immunother Cancer (2018)

Efficient Detection of Copy Number Mutations in PMS2 Exons with a Close Homolog

Por Herman, Daniel S., Smith, Christina, Liu, Chang, Vaughn, Cecily P., Palaniappan, Selvi, Pritchard, Colin C., Shirts, Brian H.
Publicado no J Mol Diagn (2018)

Colon and Endometrial Cancers with Mismatch Repair Deficiency can Arise from Somatic, Rather Than Germline, Mutations

Por Haraldsdottir, Sigurdis, Hampel, Heather, Tomsic, Jerneja, Frankel, Wendy L., Pearlman, Rachel, de la Chapelle, Albert, Pritchard, Colin C.
Publicado no Gastroenterology (2014)

MSH6 immunohistochemical heterogeneity in colorectal cancer: comparative sequencing from different tumor areas

Por Chen, Wei, Pearlman, Rachel, Hampel, Heather, Pritchard, Colin C., Markow, Michael, Arnold, Christina, Knight, Deborah, Frankel, Wendy L.
Publicado no Hum Pathol (2019)

CADD score has limited clinical validity for the identification of pathogenic variants in non-coding regions in a hereditary cancer panel

Por Mather, Cheryl A, Mooney, Sean D, Salipante, Stephen J, Scroggins, Sheena, Wu, David, Pritchard, Colin C, Shirts, Brian H
Publicado no Genet Med (2016)

Two-stain immunohistochemical screening for Lynch syndrome in colorectal cancer may fail to detect mismatch repair deficiency

Por Pearlman, Rachel, Markow, Michael, Knight, Deborah, Chen, Wei, Arnold, Christina A., Pritchard, Colin C., Hampel, Heather, Frankel, Wendy L.
Publicado no Mod Pathol (2018)