Systematic review of the predictive effect of MSI status in colorectal cancer patients undergoing 5FU-based chemotherapy

por Webber, Elizabeth M, Kauffman, Tia L, O’Connor, Elizabeth, Goddard, Katrina AB
Publicado 2015

Identifying patients with Lynch syndrome using a universal tumor screening program in an integrated healthcare system

por Crain, Philip R., Zepp, Jamilyn M., Gille, Sara, Jenkins, Lindsay, Kauffman, Tia L., Shuster, Elizabeth, Goddard, Katrina A.B., Wilfond, Benjamin S., Hunter, Jessica Ezzell
Publicado 2022

Epidemiology of Upper Limb Complex Regional Pain Syndrome in a Retrospective Cohort of Persons Aged 9–30 Years, 2002–2017

por Naleway, Allison L, Henninger, Michelle L, Irving, Stephanie A, Bianca Salas, S, Kauffman, Tia L, Crane, Bradley, Mittendorf, Kathleen F, Harsh, Stacy, Elder, Charles, Gee, Julianne
Publicado 2023

Reliability of KRAS mutation testing in metastatic colorectal cancer patients across five laboratories

por Feigelson, Heather Spencer, Goddard, Katrina AB, Johnson, Monique A, Funk, Kellyan C, Rahm, Alanna Kulchak, Kauffman, Tia L, Chitale, Dhananjay A, Le Marchand, Loic, Richards, C Sue
Publicado 2012

The NextGen Study: patient motivation for participation in genome sequencing for carrier status

por Kauffman, Tia L., Irving, Stephanie A., Leo, Michael C., Gilmore, Marian J., Himes, Patricia, McMullen, Carmit K., Morris, Elissa, Schneider, Jennifer, Wilfond, Benjamin S., Goddard, Katrina A. B.
Publicado 2017

Assessment of willingness to pay for expanded carrier screening among women and couples undergoing preconception carrier screening

por Clarke, Elizabeth V., Schneider, Jennifer L., Lynch, Frances, Kauffman, Tia L., Leo, Michael C., Rosales, Ana G., Dickerson, John F., Shuster, Elizabeth, Wilfond, Benjamin S., Goddard, Katrina A. B.
Publicado 2018

“Is It Worth Knowing?” Focus Group Participants’ Perceived Utility of Genomic Preconception Carrier Screening

por Schneider, Jennifer L., Goddard, Katrina A. B., Davis, James, Wilfond, Benjamin, Kauffman, Tia L., Reiss, Jacob A., Gilmore, Marian, Himes, Patricia, Lynch, Frances L., Leo, Michael C., McMullen, Carmit
Publicado 2015

Oncologists' attitudes toward KRAS testing: a multisite study

por Harris, Julie N, Liljestrand, Petra, Alexander, Gwen L, Goddard, Katrina A B, Kauffman, Tia, Kolevska, Tatjana, McCarty, Catherine, O'Neill, Suzanne, Pawloski, Pamala, Rahm, Alanna, Williams, Andrew, Somkin, Carol P
Publicado 2013

Design of a randomized controlled trial for genomic carrier screening in healthy patients seeking preconception genetic testing

por Kauffman, Tia L., Wilfond, Benjamin S., Jarvik, Gail P., Leo, Michael C., Lynch, Frances L., Reiss, Jacob A., Richards, C. Sue, McMullen, Carmit, Nickerson, Deborah, Dorschner, Michael O., Goddard, Katrina A.B.
Publicado 2016

Factors associated with recruitment, surveillance participation, and retention in an observational study of pregnant women and influenza

por Thompson, Mark G., Li, De-Kun, Naleway, Allison L., Ferber, Jeannette R., Henninger, Michelle L., Shifflett, Pat, Sokolow, Leslie Z., Odouli, Roxana, Kauffman, Tia L., Fink, Rebecca V., Bulkley, Joanna, Cragan, Janet D., Bozeman, Sam
Publicado 2019

Retrospective assessment of barriers and access to genetic services for hereditary cancer syndromes in an integrated health care delivery system

por Muessig, Kristin R., Zepp, Jamilyn M., Keast, Erin, Shuster, Elizabeth E., Reyes, Ana A., Arnold, Briana, Ingphakorn, Chalinya, Gilmore, Marian J., Kauffman, Tia L., Hunter, Jessica Ezzell, Knerr, Sarah, Feigelson, Heather S., Goddard, Katrina A. B.
Publicado 2022

Evaluating cancer genetic services in a safety net system: overcoming barriers for a lasting impact beyond the CHARM research project

por Okuyama, Sonia, White, Larissa L., Anderson, Katherine P., Medina, Elizabeth, Deutsch, Sonia, Ransom, Chelese, Jackson, Paige, Kauffman, Tia L., Mittendorf, Kathleen F., Leo, Michael C., Bulkley, Joanna E., Wilfond, Benjamin S., Goddard, Katrina AB, Feigelson, Heather Spencer
Publicado 2023

Stakeholder perspectives on implementing a universal lynch syndrome screening program: A qualitative study of early barriers and facilitators

por Schneider, Jennifer L, Davis, James, Kauffman, Tia L, Reiss, Jacob A, McGinley, Cheryl, Arnold, Kathleen, Zepp, Jamilyn, Gilmore, Marian, Muessig, Kristin R., Syngal, Sapna, Acheson, Louise, Wiesner, Georgia L, Peterson, Susan K, Goddard, Katrina A.B.
Publicado 2015

1162. Influenza Vaccination Among Pregnant People in the Vaccine Safety Datalink, 2016-17 through 2022-23 Influenza Seasons

por Irving, Stephanie, Crane, Bradley, Weintraub, Eric, Kauffman, Tia L, Brooks, Neon, Patel, Suchita A, Razzaghi, Hilda, Belongia, Edward, Daley, Matthew F, Getahun, Darios, Glenn, Sungching C, Hambidge, Simon, Jackson, Lisa, Kharbanda, Elyse, Klein, Nicola P, Zerbo, Ousseny, Naleway, Allison L
Publicado 2023

Time Costs for Genetic Counseling in Preconception Carrier Screening with Genome Sequencing

por Lynch, Frances L., Himes, Patricia, Gilmore, Marian J., Morris, Elissa M., Schneider, Jennifer L., Kauffman, Tia L., Shuster, Elizabeth, Reiss, Jacob A., Dickerson, John F., Leo, Michael C., Davis, James V., McMullen, Carmit K., Wilfond, Benjamin S., Goddard, Katrina A.B.
Publicado 2018

Genome sequencing and carrier testing: decisions on categorization and whether to disclose results of carrier testing

por Himes, Patricia, Kauffman, Tia L., Muessig, Kristin R., Amendola, Laura M., Berg, Jonathan S., Dorschner, Michael O., Gilmore, Marian, Nickerson, Deborah A., Reiss, Jacob A., Richards, C. Sue, Rope, Alan F., Simpson, Dana K., Wilfond, Benjamin S., Jarvik, Gail P., Goddard, Katrina A.B.
Publicado 2017

Integrating stakeholder feedback in translational genomics research: An ethnographic analysis of a study protocol’s evolution

por Kraft, Stephanie A., McMullen, Carmit, Lindberg, Nangel M., Bui, David, Shipman, Kelly, Anderson, Katherine, Joseph, Galen, Duenas, Devan M., Porter, Kathryn M., Kauffman, Tia L., Koomas, Alyssa, Ransom, Chelese L., Jackson, Paige, Goddard, Katrina A.B., Wilfond, Benjamin S., Lee, Sandra Soo-Jin
Publicado 2020

Feasibility of a Traceback Approach for Using Pathology Specimens to Facilitate Genetic Testing in the Genetic Risk Analysis in Ovarian Cancer (GRACE) Study Protocol

por Kauffman, Tia L., Prado, Yolanda K., Reyes, Ana A., Zepp, Jamilyn M., Sawyer, Jennifer, White, Larissa Lee, Martucci, Jessica, Salas, Suzanne Bianca, Vertrees, Sarah, Rope, Alan F., Weinmann, Sheila, Henrikson, Nora B., Lee, Sandra Soo-Jin, Feigelson, Heather Spencer, Hunter, Jessica Ezzell
Publicado 2021

Literacy-adapted, electronic family history assessment for genetics referral in primary care: patient user insights from qualitative interviews

por Mittendorf, Kathleen F., Lewis, Hannah S., Duenas, Devan M., Eubanks, Donna J., Gilmore, Marian J., Goddard, Katrina A. B., Joseph, Galen, Kauffman, Tia L., Kraft, Stephanie A., Lindberg, Nangel M., Reyes, Ana A., Shuster, Elizabeth, Syngal, Sapna, Ukaegbu, Chinedu, Zepp, Jamilyn M., Wilfond, Benjamin S., Porter, Kathryn M.
Publicado 2022

A case for expanding carrier testing to include actionable X‐linked disorders

por Rope, Alan F., Kauffman, Tia L., Himes, Pat, Amendola, Laura M., Punj, Sumit, Akkari, Yassmine, Potter, Amiee, Davis, James V., Schneider, Jennifer L., Reiss, Jacob A., Gilmore, Mari J., McMullen, Carmit K., Nickerson, Deborah A., Richards, C. Sue, Jarvik, Gail P., Wilfond, Benjamin S., Goddard, Katrina A. B.
Publicado 2018