Variation among DNA banking consent forms: points for clinicians to bank on
Huang, Samuel J., Amendola, Laura M., Sternen, Darci L.
Published in Journal of community genetics (01.08.2022)
Published in Journal of community genetics (01.08.2022)
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Journal Article
Preventing Genetic Testing Order Errors With a Laboratory Utilization Management Program
Mathias, Patrick C., Conta, Jessie H., Konnick, Eric Q., Sternen, Darci L., Stasi, Shannon M., Cole, Bonnie L., Astion, Michael L., Dickerson, Jane A.
Published in American journal of clinical pathology (01.08.2016)
Published in American journal of clinical pathology (01.08.2016)
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Journal Article
A Report on Ten Asia Pacific Countries on Current Status and Future Directions of the Genetic Counseling Profession: The Establishment of the Professional Society of Genetic Counselors in Asia
Laurino, Mercy Y., Leppig, Kathleen A., Abad, Peter James, Cham, Breana, Chu, Yoyo Wing Yiu, Kejriwal, Saahil, Lee, Juliana M. H., Sternen, Darci L., Thompson, Jennifer K., Burgess, Matthew J., Chien, Shu, Elackatt, Niby, Lim, Jiin Ying, Sura, Thanyachai, Faradz, Sultana, Padilla, Carmencita, Paz, Eva Cutiongco de-la, Nauphar, Donny, Nguyen, Khanh Ngoc, Zayts, Olya, Vu, Dung Chi, Thong, Meow-Keong
Published in Journal of genetic counseling (01.02.2018)
Published in Journal of genetic counseling (01.02.2018)
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Journal Article
P438: Clinical RNA sequencing to clarify variants of uncertain significance and identify missing variants
Cech, Jennifer, Miller, Danny, Paschal, Cate, Dingmann, Bri, Scott, Anna, Thies, Jenny, Mills, Maria, Merritt, J. Lawrence, Mirzaa, Ghayda, Bennett, James, Glass, Ian, Sternen, Darci, Mefford, Heather
Published in Genetics in Medicine Open (2023)
Published in Genetics in Medicine Open (2023)
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Journal Article
Clinical RNA sequencing clarifies variants of uncertain significance identified by prior testing
Marquez, Jonathan, Cech, Jennifer N., Paschal, Cate R., Dingmann, Bri, Scott, Anna I., Thies, Jenny M., Mills, Maria R., Albert, Catherine M., Beck, Anita E., Beckman, Erika, Bonkowski, Emily S., Earl, Dawn L., Lam, Christina T., Mefford, Heather C., Merritt, J. Lawrence, Nelson, Zoe, Ohlsen, Timothy J.D., Taylor, Mallory R., Perlman, Seth J., Rudzinski, Erin R., Sikes, Megan C., Waligorski, Natalie, Wenger, Tara L., Adam, Margaret P., Mirzaa, Ghayda M., Bennett, James T., Glass, Ian A., Sternen, Darci L., Miller, Danny E.
Published in Genetics in Medicine Open (2024)
Published in Genetics in Medicine Open (2024)
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Journal Article
Fanconi anemia‐like presentation in an infant with constitutional deletion of 21q including the RUNX1 gene
Click, Eleanor S., Cox, Barbara, Olson, Susan B., Grompe, Markus, Akkari, Yassmine, Moreau, Lisa A., Shimamura, Akiko, Sternen, Darci L., Liu, Yajuan J., Leppig, Kathleen A., Matthews, Dana C., Parisi, Melissa A.
Published in American journal of medical genetics. Part A (01.07.2011)
Published in American journal of medical genetics. Part A (01.07.2011)
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Journal Article
EXT2-positive multiple hereditary osteochondromas with some features suggestive of metachondromatosis
Vining, Neil C., Done, Stephen, Glass, Ian A., Parnell, Shawn E., Sternen, Darci L., Leppig, Kathleen A., Mosca, Vincent S., Goldberg, Michael J.
Published in Skeletal radiology (01.05.2012)
Published in Skeletal radiology (01.05.2012)
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Journal Article
eP349 - Five year trends in DNA bank utilization across two clinical institutions
Huang, Samuel, Cox, Hannah, Zaleski, Christina, Dorshorst, Donna, Paschal, Cate, Sternen, Darci
Published in Molecular genetics and metabolism (01.04.2021)
Published in Molecular genetics and metabolism (01.04.2021)
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Journal Article
Five year trends in DNA bank utilization across two clinical institutions
Huang, Samuel, Cox, Hannah, Zaleski, Christina, Dorshorst, Donna, Paschal, Cate, Sternen, Darci
Published in Molecular genetics and metabolism (01.04.2021)
Published in Molecular genetics and metabolism (01.04.2021)
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Journal Article
An Integrated Approach to Genetic Test Stewardship: The Role of Laboratory Genetic Counselors in Test Preauthorization and Ordering
Conta, Jessie, Sternen, Darci, Stasi, Shannon, Candadai, Sarah Clowes, Wellner, Monica, Dickerson, Jane
Published in American journal of clinical pathology (11.09.2019)
Published in American journal of clinical pathology (11.09.2019)
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Journal Article
32. Genetic testing for individuals with non-syndromic differences in sex development (DSD): collaborative approach yields results
Paschal, Cate Randall, Myers, Candace T., Gillentine, Madelyn, Sternen, Darci L., Squire, Audrey, Fechner, Patricia, Oelschlager, Anne-Marie Amies, Shnorhavorian, Margarett, Adam, Margaret
Published in Cancer genetics (01.06.2022)
Published in Cancer genetics (01.06.2022)
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Journal Article
42. Laboratory and clinician collaboration yields results: Development of a comprehensive craniosynostosis genetic testing panel with a high diagnostic rate
Paschal, Cate Randall, Myers, Candace, Sternen, Darci, Narayanan, Jaya, Gaulin, Becky, Wenger, Tara, Cunningham, Michael, Hing, Anne
Published in Cancer genetics (01.04.2021)
Published in Cancer genetics (01.04.2021)
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Journal Article
20. Diagnostic utility and lessons learned from deep sequencing vascular malformations
Myers, Candace, Bennett, James, Sternen, Darci, Rogge, Larissa, Emery, Louisa, Narayanan, Jaya, Brooks, Nicole, Nelson, Zoe, Jensen, Dana, Dmyterko, Victoria, Perkins, Jonathan, Paschal, Cate
Published in Cancer genetics (01.01.2022)
Published in Cancer genetics (01.01.2022)
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Journal Article
AB030. The evolving role of genetic counseling
Leppig, Kathleen, Sternen, Darci, Thompson, Jennifer, Laurino, Mercy
Published in Annals of translational medicine (01.09.2015)
Published in Annals of translational medicine (01.09.2015)
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Journal Article
Adverse Events in Genetic Testing: The Fourth Case Series
Farmer, Meagan B, Bonadies, Danielle C, Mahon, Suzanne M, Baker, Maria J, Ghate, Sumedha M, Munro, Christine, Nagaraj, Chinmayee B, Besser, Andria G, Bui, Kara, Csuy, Christen M, Kirkpatrick, Brianne, McCarty, Andrew J, McQuaid, Shelly Weiss, Sebastian, Jessica, Sternen, Darci L, Walsh, Leslie K, Matloff, Ellen T
Published in The cancer journal (Sudbury, Mass.) (01.07.2019)
Published in The cancer journal (Sudbury, Mass.) (01.07.2019)
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Journal Article
Fanconi anemia-like presentation in an infant with constitutional deletion of 21q including the RUNX1 gene
Click, Eleanor S., Cox, Barbara, Olson, Susan B., Grompe, Markus, Akkari, Yassmine, Moreau, Lisa A., Shimamura, Akiko, Sternen, Darci L., Liu, Yajuan J., Leppig, Kathleen A., Matthews, Dana C., Parisi, Melissa A.
Published in American Journal of Medical Genetics Part A (01.07.2011)
Published in American Journal of Medical Genetics Part A (01.07.2011)
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