Genetic Testing for Hereditary Colorectal Cancer

Por Hampel, Heather
Publicado em 2009

Clinical Relevance of Microsatellite Instability in Colorectal Cancer

Por de la Chapelle, Albert, Hampel, Heather
Publicado em 2010

The Search for Unaffected Individuals with Lynch Syndrome: Do the Ends Justify the Means?

Por Hampel, Heather, de la Chapelle, Albert
Publicado em 2011

How do we approach the goal of identifying everybody with Lynch Syndrome?

Por Hampel, Heather, de la Chapelle, Albert
Publicado no Fam Cancer (2013)

Identifying Lynch Syndrome

Por de la Chapelle, Albert, Palomaki, Glenn, Hampel, Heather
Publicado em 2009

Current and emerging trends in Lynch syndrome identification in women with endometrial cancer

Por Resnick, Kimberly E., Hampel, Heather, Fishel, Richard, Cohn, David E.
Publicado em 2009

The cost-effectiveness of routine testing for Lynch syndrome in newly diagnosed patients with colorectal cancer in the United States: corrected estimates

Por Grosse, Scott D., Palomaki, Glenn E., Mvundura, Mercy, Hampel, Heather
Publicado no Genet Med (2015)

Genotyping panel for assessing response to cancer chemotherapy

Por Dai, Zunyan, Papp, Audrey C, Wang, Danxin, Hampel, Heather, Sadee, Wolfgang
Publicado em 2008

Genetic counselors: translating genomic science into clinical practice

Por Bennett, Robin L., Hampel, Heather L., Mandell, Jessica B., Marks, Joan H.
Publicado em 2003

Epigenetic PTEN Silencing in Malignant Melanomas without PTEN Mutation

Por Zhou, Xiao-Ping, Gimm, Oliver, Hampel, Heather, Niemann, Theodore, Walker, Michael J., Eng, Charis
Publicado em 2000

A 39-bp Deletion Polymorphism in PTEN in African American Individuals: Implications for Molecular Diagnostic Testing

Por Zhou, Xiao-Ping, Hampel, Heather, Roggenbuck, Jennifer, Saba, Nabil, Prior, Thomas W., Eng, Charis
Publicado em 2002

Comparing Universal Lynch Syndrome Tumor Screening Programs to Evaluate Associations Between Implementation Strategies and Patient Follow-through

Por Cragun, Deborah, DeBate, Rita D., Vadaparampil, Susan T., Baldwin, Julie, Hampel, Heather, Pal, Tuya
Publicado em 2014

Qualitative Comparative Analysis: A Hybrid Method for Identifying Factors Associated with Program Effectiveness

Por Cragun, Deborah, Pal, Tuya, Vadaparampil, Susan T., Baldwin, Julie, Hampel, Heather, DeBate, Rita D.
Publicado no J Mix Methods Res (2015)

EGAPP supplementary evidence review: DNA testing strategies aimed at reducing morbidity and mortality from Lynch syndrome

Por Palomaki, Glenn E., McClain, Monica R., Melillo, Stephanie, Hampel, Heather L., Thibodeau, Stephen N.
Publicado em 2009

Mismatch Repair Analysis of Inherited MSH2 and/or MSH6 Variation Pairs Found in Cancer Patients

Por Kantelinen, Jukka, Kansikas, Minttu, Candelin, Satu, Hampel, Heather, Smith, Betsy, Holm, Liisa, Kariola, Reetta, Nyström, Minna
Publicado no Hum Mutat (2012)

Biallelic MUTYH mutations can mimic Lynch syndrome

Por Morak, Monika, Heidenreich, Barbara, Keller, Gisela, Hampel, Heather, Laner, Andreas, de la Chapelle, Albert, Holinski-Feder, Elke
Publicado em 2014

ACG Clinical Guideline: Genetic Testing and Management of Hereditary Gastrointestinal Cancer Syndromes

Por Syngal, Sapna, Brand, Randall E., Church, James M., Giardiello, Francis M., Hampel, Heather L., Burt, Randall W.
Publicado no Am J Gastroenterol (2015)

Reflex microsatellite instability & immunohistochemistry testing practices & follow-up of abnormal results at U.S. cancer programs

Por Beamer Laura C, Grant Marcia, MacDonald Deborah J, Hampel Heather, Blazer Kathleen, Huizenga Carin, Weitzel Jeffrey N
Publicado em 2011-03-01

Reflex microsatellite instability & immunohistochemistry testing practices & follow-up of abnormal results at U.S. cancer programs

Por Beamer, Laura C, Grant, Marcia, MacDonald, Deborah J, Hampel, Heather, Blazer, Kathleen, Huizenga, Carin, Weitzel, Jeffrey N
Publicado em 2011

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)