Expanded Gene Panel Use for Women With Breast Cancer: Identification and Intervention Beyond Breast Cancer Risk

por O’Leary, Erin, Iacoboni, Daniela, Holle, Jennifer, Michalski, Scott T., Esplin, Edward D., Yang, Shan, Ouyang, Karen
Publicado 2017

The Impact of Proband Indication for Genetic Testing on the Uptake of Cascade Testing Among Relatives

por Schmidlen, Tara J., Bristow, Sara L., Hatchell, Kathryn E., Esplin, Edward D., Nussbaum, Robert L., Haverfield, Eden V.
Publicado 2022

Multigene Panel Testing Yields High Rates of Clinically Actionable Variants Among Patients With Colorectal Cancer

por Coughlin, Sarah E., Heald, Brandie, Clark, Dana Farengo, Nielsen, Sarah M., Hatchell, Kathryn E., Esplin, Edward D., Katona, Bryson W.
Publicado 2022

Underdiagnosis of Hereditary Colorectal Cancers Among Medicare Patients: Genetic Testing Criteria for Lynch Syndrome Miss the Mark

por Muller, Charles, Nielsen, Sarah M., Hatchell, Kathryn E., Yang, Shan, Michalski, Scott T., Hamlington, Barbara, Nussbaum, Robert L., Esplin, Edward D., Kupfer, Sonia S.
Publicado 2021

Ashkenazi Jewish and Other White APC I1307K Carriers Are at Higher Risk for Multiple Cancers

por Forkosh, Esther, Bergel, Michael, Hatchell, Kathryn E., Nielsen, Sarah M., Heald, Brandie, Benson, Ariel A., Friedman, Eitan, Esplin, Edward D., Katz, Lior H.
Publicado 2022

Yield and Utility of Germline Testing Following Tumor Sequencing in Patients With Cancer

por Lincoln, Stephen E., Nussbaum, Robert L., Kurian, Allison W., Nielsen, Sarah M., Das, Kingshuk, Michalski, Scott, Yang, Shan, Ngo, Nhu, Blanco, Amie, Esplin, Edward D.
Publicado 2020

Universal Germline-Genetic Testing for Breast Cancer: Implementation in a Rural Practice and Impact on Shared Decision-Making

por Shelton, Charles, Ruiz, Antonio, Shelton, Lauren, Montgomery, Hannah, Freas, Karen, Ellsworth, Rachel E., Poll, Sarah, Pineda-Alvarez, Daniel, Heald, Brandie, Esplin, Edward D., Nielsen, Sarah M.
Publicado 2023

Universal Germline Genetic Testing for Hereditary Cancer Syndromes in Patients With Solid Tumor Cancer

por Esplin, Edward D., Nielsen, Sarah M., Bristow, Sara L., Garber, Judy E., Hampel, Heather, Rana, Huma Q., Samadder, N. Jewel, Shore, Neal D., Nussbaum, Robert L.
Publicado 2022

Comprehensive Genetic Testing for Pediatric Hypertrophic Cardiomyopathy Reveals Clinical Management Opportunities and Syndromic Conditions

por Gal, Dana B., Morales, Ana, Rojahn, Susan, Callis, Tom, Garcia, John, Priest, James R., Truty, Rebecca, Vatta, Matteo, Nussbaum, Robert L., Esplin, Edward D., Hollander, Seth A.
Publicado 2021

Retrospective Cohort Study on the Limitations of Direct-to-Consumer Genetic Screening in Hereditary Breast and Ovarian Cancer

por Desai, Neelam V., Barrows, Elizabeth D., Nielsen, Sarah M., Hatchell, Kathryn E., Anderson, Michael J., Haverfield, Eden V., Herrera, Blanca, Esplin, Edward D., Lucassen, Anneke, Tung, Nadine M., Isaacs, Claudine
Publicado 2023

Limited-Variant Screening vs Comprehensive Genetic Testing for Familial Hypercholesterolemia Diagnosis

por Sturm, Amy C., Truty, Rebecca, Callis, Thomas E., Aguilar, Sienna, Esplin, Edward D., Garcia, Sarah, Haverfield, Eden V., Morales, Ana, Nussbaum, Robert L., Rojahn, Susan, Vatta, Matteo, Rader, Daniel J.
Publicado 2021

Rate of Pathogenic Germline Variants in Patients With Lung Cancer

por Sorscher, Steven, LoPiccolo, Jaclyn, Heald, Brandie, Chen, Elaine, Bristow, Sara L., Michalski, Scott T., Nielsen, Sarah M., Lacoste, Alix, Keyder, Emil, Lee, Hayan, Nussbaum, Robert L., Martins, Renato, Esplin, Edward D.
Publicado 2023

Comparison of Germline Genetic Testing Before and After a Medical Policy Covering Universal Testing Among Patients With Colorectal Cancer

por Moretz, Chad, Byfield, Stacey DaCosta, Hatchell, Kathryn E., Dalton, Joline, Onglao, Peter Nicholas, Hang, Lillian, Hansen, Pamela, Radford, Cristi, Nielsen, Sarah M., Heald, Brandie, Munro, Sandra B., Nussbaum, Robert L., Esplin, Edward D.
Publicado 2022

Assessment of the Diagnostic Yield of Combined Cardiomyopathy and Arrhythmia Genetic Testing

por Dellefave-Castillo, Lisa M., Cirino, Allison L., Callis, Thomas E., Esplin, Edward D., Garcia, John, Hatchell, Kathryn E., Johnson, Britt, Morales, Ana, Regalado, Ellen, Rojahn, Susan, Vatta, Matteo, Nussbaum, Robert L., McNally, Elizabeth M.
Publicado 2022

Patterns of germline and somatic testing after universal tumor screening for Lynch syndrome: A clinical practice survey of active members of the Collaborative Group of the Americas...

por Hodan, Rachel, Rodgers‐Fouche, Linda, Arora, Sanjeevani, Dominguez‐Valentin, Mev, Kanth, Priyanka, Katona, Bryson W., Mraz, Kathryn A., Roberts, Maegan E., Vilar, Eduardo, Soto‐Azghani, Cynthia M., Brand, Randall E, Esplin, Edward D., Perez, Kimberly
Publicado 2022

Prevalence and clinical implications of germline mutations among Jordanian patients with ovarian cancer. The Jordanian exploratory cancer genetics (Jo‐ECAG) ovarian study

por Abdel‐Razeq, Hikmat, Al‐Azzam, Khansa, Elemian, Shatha, Abu‐Fares, Hala, Abu Sheikha, Areej, Bani Hani, Hira, Bater, Rayan, Sharaf, Baha’, Heald, Brandie, Esplin, Edward D., Nielsen, Sarah M., Alkyam, Mais, Abujamous, Lama, Al‐Attary, Areej
Publicado 2022

CDH1 germline variants are enriched in patients with colorectal cancer, gastric cancer, and breast cancer

por Adib, Elio, El Zarif, Talal, Nassar, Amin H., Akl, Elie W., Abou Alaiwi, Sarah, Mouhieddine, Tarek H., Esplin, Edward D., Hatchell, Kathryn, Nielsen, Sarah M., Rana, Huma Q., Choueiri, Toni K., Kwiatkowski, David J., Sonpavde, Guru
Publicado 2021

Segmentation of human functional tissue units in support of a Human Reference Atlas

por Jain, Yashvardhan, Godwin, Leah L., Ju, Yingnan, Sood, Naveksha, Quardokus, Ellen M., Bueckle, Andreas, Longacre, Teri, Horning, Aaron, Lin, Yiing, Esplin, Edward D., Hickey, John W., Snyder, Michael P., Patterson, Nathan Heath, Spraggins, Jeffrey M., Börner, Katy
Publicado 2023

Possible precision medicine implications from genetic testing using combined detection of sequence and intragenic copy number variants in a large cohort with childhood epilepsy

por Truty, Rebecca, Patil, Nila, Sankar, Raman, Sullivan, Joseph, Millichap, John, Carvill, Gemma, Entezam, Ali, Esplin, Edward D., Fuller, Amy, Hogue, Michelle, Johnson, Britt, Khouzam, Amirah, Kobayashi, Yuya, Lewis, Rachel, Nykamp, Keith, Riethmaier, Darlene, Westbrook, Jody, Zeman, Michelle, Nussbaum, Robert L., Aradhya, Swaroop
Publicado 2019

Clinical Impact of Pathogenic Germline Variants in Pancreatic Cancer: Results From a Multicenter, Prospective, Universal Genetic Testing Study

por Uson, Pedro L. S., Samadder, N. Jewel, Riegert-Johnson, Douglas, Boardman, Lisa, Borad, Mitesh J., Ahn, Daniel, Sonbol, Mohamad B., Faigel, Douglas O., Fukami, Norio, Pannala, Rahul, Kunze, Katie, Golafshar, Michael, Klint, Margaret, Esplin, Edward D., Nussbaum, Robert L., Stewart, A. Keith, Bekaii-Saab, Tanios
Publicado 2021