Stemming the Tide of Cancer for BRCA1/2 Mutation Carriers

di Lynch, Henry T., Marcus, Joseph N., Rubinstein, Wendy S.
Pubblicazione 2008

Genome-wide analysis of antisense transcription with Affymetrix exon array

di Jung Yong-chul, Rubinstein Wendy S, Ge Xijin, Wu Qingfa
Pubblicazione 2008-01-01

Genome-wide analysis of antisense transcription with Affymetrix exon array

di Ge, Xijin, Rubinstein, Wendy S, Jung, Yong-chul, Wu, Qingfa
Pubblicazione 2008

Next-Generation Sequencing and the Clinical Oncology Workflow: Data Challenges, Proposed Solutions, and a Call to Action

di Conway, Jake R., Warner, Jeremy L., Rubinstein, Wendy S., Miller, Robert S.
Pubblicato in JCO Precis Oncol (2019)

Detection of BRCA1 and BRCA2 Ashkenazi Jewish Founder Mutations in Formalin-Fixed Paraffin-Embedded Tissues Using Conventional PCR and Heteroduplex/Amplicon Size Differences

di Mangold, Kathy A., Wang, Vivien, Weissman, Scott M., Rubinstein, Wendy S., Kaul, Karen L.
Pubblicazione 2010

Elevated Levels of Somatic Mutation in a Manifesting BRCA1 Mutation Carrier

di GRANT, Stephen G., DAS, Rubina, CERCEO, Christina M., RUBINSTEIN, Wendy S., LATIMER, Jean J.
Pubblicato in Pathol Oncol Res (2007)

Prospective screening study of 0.5 Tesla dedicated magnetic resonance imaging for the detection of breast cancer in young, high-risk women

di Rubinstein, Wendy S, Latimer, Jean J, Sumkin, Jules H, Huerbin, Michelle, Grant, Stephen G, Vogel, Victor G
Pubblicazione 2006

Impact of Family History Assessment on Communication with Family Members and Health Care Providers: A report from the Family Healthware(™) Impact Trial (FHITr)

di Wang, Catharine, Sen, Ananda, Plegue, Melissa, Ruffin, Mack T., O'Neill, Suzanne M., Rubinstein, Wendy S., Acheson, Louise S.
Pubblicato in Prev Med (2015)

Haploinsufficiency for BRCA1 is associated with normal levels of DNA nucleotide excision repair in breast tissue and blood lymphocytes

di Latimer, Jean J, Rubinstein, Wendy S, Johnson, Jennifer M, Kanbour-Shakir, Amal, Vogel, Victor G, Grant, Stephen G
Pubblicazione 2005

Clinical utility of family history for cancer screening and referral in primary care: A report from the Family Healthware Impact Trial

di Rubinstein, Wendy S., Acheson, Louise S., O’Neill, Suzanne M., Ruffin, Mack T., Wang, Catharine, Beaumont, Jennifer L., Rothrock, Nan
Pubblicazione 2011

Effect of a Computer-Based Decision Aid on Knowledge, Perceptions, and Intentions About Genetic Testing for Breast Cancer Susceptibility: A Randomized Controlled Trial

di Green, Michael J., Peterson, Susan K., Baker, Maria Wagner, Harper, Gregory R., Friedman, Lois C., Rubinstein, Wendy S., Mauger, David T.
Pubblicazione 2004

Family History Assessment: Impact on Disease Risk Perceptions

di Wang, Catharine, Sen, Ananda, Ruffin, Mack T., Nease, Donald E., Gramling, Robert, Acheson, Louise S., O’Neill, Suzanne M., Rubinstein, Wendy S.
Pubblicazione 2012

ClinVar: public archive of relationships among sequence variation and human phenotype

di Landrum, Melissa J., Lee, Jennifer M., Riley, George R., Jang, Wonhee, Rubinstein, Wendy S., Church, Deanna M., Maglott, Donna R.
Pubblicazione 2014

Hereditary diffuse gastric cancer: diagnosis, genetic counseling, and prophylactic total gastrectomy

di Lynch, Henry T., Kaurah, Pardeep, Wirtzfeld, Debrah, Rubinstein, Wendy S., Weissman, Scott, Lynch, Jane F., Grady, William, Wiyrick, Sara, Senz, Janine, Huntsman, David
Pubblicazione 2008

Comparison of risk perceptions and beliefs across common chronic diseases

di Wang, Catharine, O'Neill, Suzanne M., Rothrock, Nan, Gramling, Robert, Sen, Ananda, Acheson, Louise S., Rubinstein, Wendy S., Nease, Donald E., Ruffin, Mack T.
Pubblicazione 2008

Effect of Preventive Messages Tailored to Family History on Health Behaviors: The Family Healthware Impact Trial

di Ruffin, Mack T., Nease, Donald E., Sen, Ananda, Pace, Wilson D., Wang, Catharine, Acheson, Louise S., Rubinstein, Wendy S., O’Neill, Suzanne, Gramling, Robert
Pubblicazione 2011

Genotype–Phenotype Correlations of Pheochromocytoma in Two Large von Hippel–Lindau (VHL) Type 2A Kindreds With Different Missense Mutations

di Nielsen, Sarah M., Rubinstein, Wendy S., Thull, Darcy L., Armstrong, Michaele J., Feingold, Eleanor, Stang, Michael T., Gnarra, James R., Carty, Sally E.
Pubblicazione 2011

Health beliefs among individuals at increased familial risk for type 2 diabetes: Implications for prevention(,)

di Dorman, Janice S., Valdez, Rodolfo, Liu, Tiebin, Wang, Catharine, Rubinstein, Wendy S., O'Neill, Suzanne M., Acheson, Louise S., Ruffin, Mack T., Khoury, Muin J.
Pubblicazione 2012

Use of an educational computer program before genetic counseling for breast cancer susceptibility: Effects on duration and content of counseling sessions

di Green, Michael J., Peterson, Susan K., Baker, Maria Wagner, Friedman, Lois C., Harper, Gregory R., Rubinstein, Wendy S., Peters, June A., Mauger, David T.
Pubblicazione 2005

Secondary Variants in Individuals Undergoing Exome Sequencing: Screening of 572 Individuals Identifies High-Penetrance Mutations in Cancer-Susceptibility Genes

di Johnston, Jennifer J., Rubinstein, Wendy S., Facio, Flavia M., Ng, David, Singh, Larry N., Teer, Jamie K., Mullikin, James C., Biesecker, Leslie G.
Pubblicazione 2012