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21.
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Variant interpretation is a component of clinical practice among genetic counselors in multiple specialties. [electronic resource] by
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- Johnson, Amy Knight
- Krautscheid, Patti
- Lepore, Brianna
- O'Daniel, Julianne M
- Ritter, Deborah
- Savatt, Juliann M
- Riggs, Erin Rooney
- Martin, Christa Lese
Producer: 20210427
In:
Genetics in medicine : official journal of the American College of Medical Genetics vol. 22
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22.
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Examining the Cascade of Participant Attrition in a Genomic Medicine Research Study: Barriers and Facilitators to Achieving Diversity. [electronic resource] by
- Moore, Elizabeth G
- Roche, Myra
- Rini, Christine
- Corty, Edward W
- Girnary, Zahra
- O'Daniel, Julianne M
- Lin, Feng-Chang
- Corbie-Smith, Giselle
- Evans, James P
- Henderson, Gail E
- Berg, Jonathan S
Publication details: Public health genomics 2017
In:
Public health genomics vol. 20
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23.
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Is "incidental finding" the best term?: a study of patients' preferences. [electronic resource] by
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- Boshe, Lacey
- Henderson, Gail E
- Rini, Christine
- Roche, Myra I
- Hisama, Fuki M
- Burke, Wylie
- Wilfond, Benjamin
- Jarvik, Gail P
Producer: 20171211
In:
Genetics in medicine : official journal of the American College of Medical Genetics vol. 19
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24.
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Operationalizing the Reciprocal Engagement Model of Genetic Counseling Practice: a Framework for the Scalable Delivery of Genomic Counseling and Testing. [electronic resource] by
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- Sturm, Amy C
- Hovick, Shelly
- Scheinfeldt, Laura
- Scott Roberts, J
- Morr, Lindsey
- McElroy, Joseph
- Toland, Amanda E
- Christman, Michael
- O'Daniel, Julianne M
- Gordon, Erynn S
- Bernhardt, Barbara A
- Ormond, Kelly E
- Sweet, Kevin
Producer: 20190911
In:
Journal of genetic counseling vol. 27
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25.
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The who, what, and why of research participants' intentions to request a broad range of secondary findings in a diagnostic genomic sequencing study. [electronic resource] by
- Rini, Christine
- Khan, Cynthia M
- Moore, Elizabeth
- Roche, Myra I
- Evans, James P
- Berg, Jonathan S
- Powell, Bradford C
- Corbie-Smith, Giselle
- Foreman, Ann Katherine M
- Griesemer, Ida
- Lee, Kristy
- O'Daniel, Julianne M
- Henderson, Gail E
Producer: 20181211
In:
Genetics in medicine : official journal of the American College of Medical Genetics vol. 20
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26.
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Factors influencing NCGENES research participants' requests for non-medically actionable secondary findings. [electronic resource] by
- Roche, Myra I
- Griesemer, Ida
- Khan, Cynthia M
- Moore, Elizabeth
- Lin, Feng-Chang
- O'Daniel, Julianne M
- Foreman, Ann Katherine M
- Lee, Kristy
- Powell, Bradford C
- Berg, Jonathan S
- Evans, James P
- Henderson, Gail E
- Rini, Christine
Producer: 20200213
In:
Genetics in medicine : official journal of the American College of Medical Genetics vol. 21
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27.
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CORRIGENDUM: ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing. [electronic resource] by
- Green, Robert C
- Berg, Jonathan S
- Grody, Wayne W
- Kalia, Sarah S
- Korf, Bruce R
- Martin, Christa L
- McGuire, Amy L
- Nussbaum, Robert L
- O'Daniel, Julianne M
- Ormond, Kelly E
- Rehm, Heidi L
- Watson, Michael S
- Williams, Marc S
- Biesecker, Leslie G
Publication details: Genetics in medicine : official journal of the American College of Medical Genetics 05 2017
In:
Genetics in medicine : official journal of the American College of Medical Genetics vol. 19
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28.
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ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing. [electronic resource] by
- Green, Robert C
- Berg, Jonathan S
- Grody, Wayne W
- Kalia, Sarah S
- Korf, Bruce R
- Martin, Christa L
- McGuire, Amy L
- Nussbaum, Robert L
- O'Daniel, Julianne M
- Ormond, Kelly E
- Rehm, Heidi L
- Watson, Michael S
- Williams, Marc S
- Biesecker, Leslie G
Producer: 20140508
In:
Genetics in medicine : official journal of the American College of Medical Genetics vol. 15
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29.
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Germline Analysis from Tumor-Germline Sequencing Dyads to Identify Clinically Actionable Secondary Findings. [electronic resource] by
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- O'Daniel, Julianne M
- Amin, Krunal
- Marchuk, Daniel S
- Patel, Nirali M
- Parker, Joel S
- Hoyle, Alan P
- Mose, Lisle E
- Marron, Andrew
- Hayward, Michele C
- Bizon, Christopher
- Wilhelmsen, Kirk C
- Evans, James P
- Earp, H Shelton
- Sharpless, Norman E
- Hayes, D Neil
- Berg, Jonathan S
Producer: 20180112
In:
Clinical cancer research : an official journal of the American Association for Cancer Research vol. 22
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30.
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An Age-Based Framework for Evaluating Genome-Scale Sequencing Results in Newborn Screening. [electronic resource] by
- Milko, Laura V
- O'Daniel, Julianne M
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- Crowley, Stephanie B
- Foreman, Ann Katherine M
- Wallace, Kathleen E
- Mollison, Lonna F
- Strande, Natasha T
- Girnary, Zahra S
- Boshe, Lacey J
- Aylsworth, Arthur S
- Gucsavas-Calikoglu, Muge
- Frazier, Dianne M
- Vora, Neeta L
- Roche, Myra I
- Powell, Bradford C
- Powell, Cynthia M
- Berg, Jonathan S
Producer: 20200415
In:
The Journal of pediatrics vol. 209
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31.
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A semiquantitative metric for evaluating clinical actionability of incidental or secondary findings from genome-scale sequencing. [electronic resource] by
- Berg, Jonathan S
- Foreman, Ann Katherine M
- O'Daniel, Julianne M
- Booker, Jessica K
- Boshe, Lacey
- Carey, Timothy
- Crooks, Kristy R
- Jensen, Brian C
- Juengst, Eric T
- Lee, Kristy
- Nelson, Daniel K
- Powell, Bradford C
- Powell, Cynthia M
- Roche, Myra I
- Skrzynia, Cecile
- Strande, Natasha T
- Weck, Karen E
- Wilhelmsen, Kirk C
- Evans, James P
Producer: 20170915
In:
Genetics in medicine : official journal of the American College of Medical Genetics vol. 18
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32.
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Evidence-based assessments of clinical actionability in the context of secondary findings: Updates from ClinGen's Actionability Working Group. [electronic resource] by
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- Hunter, Jessica Ezzell
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- Buchanan, Adam H
- Clarke, Elizabeth V
- Currey, Erin
- Dagan-Rosenfeld, Orit
- Lee, Kristy
- Lindor, Noralane M
- Martin, Christa Lese
- Milosavljevic, Aleksandar
- Mittendorf, Kathleen F
- Muessig, Kristin R
- O'Daniel, Julianne M
- Patel, Ronak Y
- Ramos, Erin M
- Rego, Shannon
- Slavotinek, Anne M
- Sobriera, Nara Lygia M
- Weaver, Meredith A
- Williams, Marc S
- Evans, James P
- Goddard, Katrina A B
Producer: 20190820
In:
Human mutation vol. 39
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33.
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Evaluating the Clinical Validity of Gene-Disease Associations: An Evidence-Based Framework Developed by the Clinical Genome Resource. [electronic resource] by
- Strande, Natasha T
- Riggs, Erin Rooney
- Buchanan, Adam H
- Ceyhan-Birsoy, Ozge
- DiStefano, Marina
- Dwight, Selina S
- Goldstein, Jenny
- Ghosh, Rajarshi
- Seifert, Bryce A
- Sneddon, Tam P
- Wright, Matt W
- Milko, Laura V
- Cherry, J Michael
- Giovanni, Monica A
- Murray, Michael F
- O'Daniel, Julianne M
- Ramos, Erin M
- Santani, Avni B
- Scott, Alan F
- Plon, Sharon E
- Rehm, Heidi L
- Martin, Christa L
- Berg, Jonathan S
Producer: 20170731
In:
American journal of human genetics vol. 100
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34.
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A survey of current practices for genomic sequencing test interpretation and reporting processes in US laboratories. [electronic resource] by
- O'Daniel, Julianne M
- McLaughlin, Heather M
- Amendola, Laura M
- Bale, Sherri J
- Berg, Jonathan S
- Bick, David
- Bowling, Kevin M
- Chao, Elizabeth C
- Chung, Wendy K
- Conlin, Laura K
- Cooper, Gregory M
- Das, Soma
- Deignan, Joshua L
- Dorschner, Michael O
- Evans, James P
- Ghazani, Arezou A
- Goddard, Katrina A
- Gornick, Michele
- Farwell Hagman, Kelly D
- Hambuch, Tina
- Hegde, Madhuri
- Hindorff, Lucia A
- Holm, Ingrid A
- Jarvik, Gail P
- Knight Johnson, Amy
- Mighion, Lindsey
- Morra, Massimo
- Plon, Sharon E
- Punj, Sumit
- Richards, C Sue
- Santani, Avni
- Shirts, Brian H
- Spinner, Nancy B
- Tang, Sha
- Weck, Karen E
- Wolf, Susan M
- Yang, Yaping
- Rehm, Heidi L
Producer: 20180116
In:
Genetics in medicine : official journal of the American College of Medical Genetics vol. 19
Availability: No items available.
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