J
Janet L. Williams
Researcher at Geisinger Health System
Publications - 71
Citations - 2602
Janet L. Williams is an academic researcher from Geisinger Health System. The author has contributed to research in topics: Palliative care & Biobank. The author has an hindex of 21, co-authored 63 publications receiving 1907 citations. Previous affiliations of Janet L. Williams include Gundersen Health System & Intermountain Healthcare.
Papers
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Journal ArticleDOI
A new definition of Genetic Counseling: National Society of Genetic Counselors' Task Force report.
Robert G. Resta,Barbara B. Biesecker,Robin L. Bennett,Sandra Blum,Susan E. Hahn,Michelle N. Strecker,Janet L. Williams +6 more
TL;DR: The Genetic Counseling Definition Task Force of the National Society of Genetic Counselors developed the following definition of genetic counseling that was approved by the NSGC Board of Directors: genetic counseling is the process of helping people understand and adapt to the medical, psychological and familial implications of genetic contributions to disease.
Journal ArticleDOI
Public Attitudes toward Consent and Data Sharing in Biobank Research: A Large Multi-site Experimental Survey in the US.
Saskia C. Sanderson,Saskia C. Sanderson,Saskia C. Sanderson,Nathaniel D. Mercaldo,Ellen Wright Clayton,Armand H. Matheny Antommaria,Sharon Aufox,Murray H. Brilliant,Diego Campos,David Carrell,John J. Connolly,Pat Conway,Stephanie M. Fullerton,Nanibaa’ A. Garrison,Nanibaa’ A. Garrison,Carol R. Horowitz,Gail P. Jarvik,David J. Kaufman,Terrie Kitchner,Rongling Li,Evette Ludman,Catherine A. McCarty,Jennifer B. McCormick,Valerie D. McManus,Melanie F. Myers,Aaron Scrol,Janet L. Williams,Martha J. Shrubsole,Jonathan S. Schildcrout,Maureen E. Smith,Ingrid A. Holm +30 more
TL;DR: Willingness to participate was associated with self-identified white race, higher educational attainment, lower religiosity, perceiving more research benefits, fewer concerns, and fewer information needs, and the concern that the use of broad consent and open data sharing could adversely affect participant recruitment is not supported.
Journal ArticleDOI
Financial Distress and Its Associations With Physical and Emotional Symptoms and Quality of Life Among Advanced Cancer Patients
Marvin Omar Delgado-Guay,Jeanette Ferrer,Alyssa G. Rieber,Wadih Rhondali,Supakarn Tayjasanant,Jewel Ochoa,Hilda Cantu,Gary B. Chisholm,Janet L. Williams,Susan Frisbee-Hume,Eduardo Bruera +10 more
TL;DR: FD was very frequent in both groups, but median intensity was double among GPH patients, and more research is needed to better characterize FD and its correlates in AdCa and possible interventions.
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Exome Sequencing-Based Screening for BRCA1/2 Expected Pathogenic Variants Among Adult Biobank Participants.
Kandamurugu Manickam,Adam H. Buchanan,Marci L.B. Schwartz,Miranda L.G. Hallquist,Janet L. Williams,Alanna Kulchak Rahm,Heather Rocha,Juliann M. Savatt,Alyson E. Evans,Loren Butry,Amanda L. Lazzeri,D’Andra M. Lindbuchler,Carroll N. Flansburg,Rosemary Leeming,Victor G. Vogel,Matthew S. Lebo,Heather Mason-Suares,Derick Hoskinson,Noura S. Abul-Husn,Frederick E. Dewey,John D. Overton,Jeffrey G. Reid,Aris Baras,Huntington F. Willard,Cara Zayac McCormick,Sarath B Krishnamurthy,Dustin N. Hartzel,Korey A. Kost,Daniel R. Lavage,Amy C. Sturm,Lauren R. Frisbie,T. Nate Person,Raghu Metpally,Monica A. Giovanni,Lacy E. Lowry,Joseph B. Leader,Marylyn D. Ritchie,David J. Carey,Anne E. Justice,H. Lester Kirchner,W. Andrew Faucett,Marc S. Williams,David H. Ledbetter,Michael F. Murray +43 more
TL;DR: Current methods to identify BRCA1/2 variant carriers may not be sufficient as a screening tool; population genomic screening for hereditary breast and ovarian cancer may better identify patients at high risk and provide an intervention opportunity to reduce mortality and morbidity.
Journal ArticleDOI
A Model for Genome-First Care: Returning Secondary Genomic Findings to Participants and Their Healthcare Providers in a Large Research Cohort
Marci L.B. Schwartz,Cara Zayac McCormick,Amanda L. Lazzeri,D’Andra M. Lindbuchler,Miranda L.G. Hallquist,Kandamurugu Manickam,Adam H. Buchanan,Alanna Kulchak Rahm,Monica A. Giovanni,Lauren R. Frisbie,Carroll N. Flansburg,F. Daniel Davis,Amy C. Sturm,Christine Nicastro,Matthew S. Lebo,Heather Mason-Suares,Lisa Mahanta,David J. Carey,Janet L. Williams,Marc S. Williams,David H. Ledbetter,W. Andrew Faucett,Michael F. Murray +22 more
TL;DR: An exportable model for delivery of clinical care through secondary use of research data is described and subject and provider participation data from the initial phase of these efforts can inform other institutions planning similar programs.