Stemming the Tide of Cancer for BRCA1/2 Mutation Carriers

Autor Lynch, Henry T., Marcus, Joseph N., Rubinstein, Wendy S.
Vydáno 2008

Genome-wide analysis of antisense transcription with Affymetrix exon array

Autor Jung Yong-chul, Rubinstein Wendy S, Ge Xijin, Wu Qingfa
Vydáno 2008-01-01

Genome-wide analysis of antisense transcription with Affymetrix exon array

Autor Ge, Xijin, Rubinstein, Wendy S, Jung, Yong-chul, Wu, Qingfa
Vydáno 2008

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

Autor Conway, Jake R., Warner, Jeremy L., Rubinstein, Wendy S., Miller, Robert S.
Vydáno v 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

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

Elevated Levels of Somatic Mutation in a Manifesting BRCA1 Mutation Carrier

Autor GRANT, Stephen G., DAS, Rubina, CERCEO, Christina M., RUBINSTEIN, Wendy S., LATIMER, Jean J.
Vydáno v 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

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

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

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

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

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

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

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

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

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

Family History Assessment: Impact on Disease Risk Perceptions

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

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

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

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

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

Comparison of risk perceptions and beliefs across common chronic diseases

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

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

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

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

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

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

Autor 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.
Vydáno 2012

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

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

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

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