Stemming the Tide of Cancer for BRCA1/2 Mutation Carriers

Por Lynch, Henry T., Marcus, Joseph N., Rubinstein, Wendy S.
Publicado em 2008

Genome-wide analysis of antisense transcription with Affymetrix exon array

Por Jung Yong-chul, Rubinstein Wendy S, Ge Xijin, Wu Qingfa
Publicado em 2008-01-01

Genome-wide analysis of antisense transcription with Affymetrix exon array

Por Ge, Xijin, Rubinstein, Wendy S, Jung, Yong-chul, Wu, Qingfa
Publicado em 2008

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

Por Mangold, Kathy A., Wang, Vivien, Weissman, Scott M., Rubinstein, Wendy S., Kaul, Karen L.
Publicado em 2010

Elevated Levels of Somatic Mutation in a Manifesting BRCA1 Mutation Carrier

Por GRANT, Stephen G., DAS, Rubina, CERCEO, Christina M., RUBINSTEIN, Wendy S., LATIMER, Jean J.
Publicado no 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

Por Rubinstein, Wendy S, Latimer, Jean J, Sumkin, Jules H, Huerbin, Michelle, Grant, Stephen G, Vogel, Victor G
Publicado em 2006

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

Por Wang, Catharine, Sen, Ananda, Plegue, Melissa, Ruffin, Mack T., O'Neill, Suzanne M., Rubinstein, Wendy S., Acheson, Louise S.
Publicado no Prev Med (2015)

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

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

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

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

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

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

Family History Assessment: Impact on Disease Risk Perceptions

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

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

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

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

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

Comparison of risk perceptions and beliefs across common chronic diseases

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

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

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

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

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

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

Por 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.
Publicado em 2012

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

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

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

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

Family history and perceptions about risk and prevention for chronic diseases in primary care: A report from the Family Healthware™ Impact Trial

Por Acheson, Louise S., Wang, Catharine, Zyzanski, Stephen J., Lynn, Audrey, Ruffin, Mack T., Gramling, Robert, Rubinstein, Wendy S., O'Neill, Suzanne M., Nease, Donald E.
Publicado em 2010