Zobrazeno 1 - 10
of 134
pro vyhledávání: '"Amy C, Sturm"'
Autor:
Laney K. Jones, PharmD, MPH, Gemme Campbell-Salome, PhD, Nicole L. Walters, BS, Andrew Brangan, BS, Kelly M. Morgan, MS, Eric P. Tricou, MS, Zoe T. Lindsey Mills, BS, Mary P. McGowan, MD, Samuel S. Gidding, MD, Alicia M. Johns, PhD, H. Lester Kirchner, PhD, Alanna Kulchak Rahm, PhD, Amy C. Sturm, MS
Publikováno v:
JACC: Advances, Vol 3, Iss 9, Pp 101198- (2024)
Background: Relatives of probands diagnosed with familial hypercholesterolemia (FH) should undergo cascade testing for FH. Objectives: The purpose of this study was to evaluate probands’ choices of innovative strategies to communicate their FH resu
Externí odkaz:
https://doaj.org/article/783b7d5f51a54c71b4cd5f9ef467d74a
Autor:
Katherine S. Josephs, Angharad M. Roberts, Pantazis Theotokis, Roddy Walsh, Philip J. Ostrowski, Matthew Edwards, Andrew Fleming, Courtney Thaxton, Jason D. Roberts, Melanie Care, Wojciech Zareba, Arnon Adler, Amy C. Sturm, Rafik Tadros, Valeria Novelli, Emma Owens, Lucas Bronicki, Olga Jarinova, Bert Callewaert, Stacey Peters, Tom Lumbers, Elizabeth Jordan, Babken Asatryan, Neesha Krishnan, Ray E. Hershberger, C. Anwar A. Chahal, Andrew P. Landstrom, Cynthia James, Elizabeth M. McNally, Daniel P. Judge, Peter van Tintelen, Arthur Wilde, Michael Gollob, Jodie Ingles, James S. Ware
Publikováno v:
Genome Medicine, Vol 15, Iss 1, Pp 1-15 (2023)
Abstract Background As the availability of genomic testing grows, variant interpretation will increasingly be performed by genomic generalists, rather than domain-specific experts. Demand is rising for laboratories to accurately classify variants in
Externí odkaz:
https://doaj.org/article/b19fec6981b54abc9f8f6edd48178160
Autor:
Nicole L. Walters, Zoe T. Lindsey-Mills, Andrew Brangan, Sarah K. Savage, Tara J. Schmidlen, Kelly M. Morgan, Eric P. Tricou, Megan M. Betts, Laney K. Jones, Amy C. Sturm, Gemme Campbell-Salome
Publikováno v:
PEC Innovation, Vol 2, Iss , Pp 100134- (2023)
Objective: To assess use of two web-based conversational agents, the Family Sharing Chatbot (FSC) and One Month Chatbot (OMC), by individuals with familial hypercholesterolemia (FH). Methods: FSC and OMC were sent using an opt-out methodology to a co
Externí odkaz:
https://doaj.org/article/4f5ef3314c2841cca458a381cb9d2e1f
Autor:
Gemme Campbell-Salome, Laney K. Jones, Nicole L. Walters, Kelly M. Morgan, Andrew Brangan, Ilene G. Ladd, Mary P. McGowan, Katherine Wilemon, Tara J. Schmidlen, Emilie Simmons, Marci L. B. Schwartz, Megan N. McMinn, Eric Tricou, Alanna K. Rahm, Catherine D. Ahmed, Amy C. Sturm
Publikováno v:
BMC Health Services Research, Vol 23, Iss 1, Pp 1-13 (2023)
Abstract Background This project aimed to optimize communication strategies to support family communication about familial hypercholesterolemia (FH) and improve cascade testing uptake among at-risk relatives. Individuals and families with FH provided
Externí odkaz:
https://doaj.org/article/f16fbdb1412c4e85adc34d625d531fdc
Autor:
Samuel S. Gidding, H. Lester Kirchner, Andrew Brangan, William Howard, Melissa A. Kelly, Kelly D. Myers, Kelly M. Morgan, Matthew T. Oetjens, Timothy C. Shuey, David Staszak, Natasha T. Strande, Nicole L. Walters, Kristen D. Yu, Katherine A. Wilemon, Marc S. Williams, Amy C. Sturm, Laney K. Jones
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 12, Iss 13 (2023)
Background Data mining of electronic health records to identify patients suspected of familial hypercholesterolemia (FH) has been limited by absence of both phenotypic and genomic data in the same cohort. Methods and Results Using the Geisinger MyCod
Externí odkaz:
https://doaj.org/article/05b8f792bfdd43bc923992cd079ffc47
Autor:
Juliann M. Savatt, Nicole M. Ortiz, Gretchen M. Thone, Whitney S. McDonald, Melissa A. Kelly, Alexander S. F. Berry, Madiha M. Alvi, Miranda L. G. Hallquist, Jennifer Malinowski, Nicholas C. Purdy, Marc S. Williams, Amy C. Sturm, Adam H. Buchanan
Publikováno v:
BMC Medicine, Vol 20, Iss 1, Pp 1-15 (2022)
Abstract Background In current care, patients’ personal and self-reported family histories are primarily used to determine whether genetic testing for hereditary endocrine tumor syndromes (ETS) is indicated. Population genomic screening for other c
Externí odkaz:
https://doaj.org/article/b1bdba2497124f9699e8abe03f4b831d
Autor:
Laney K. Jones, Stephanie Tilberry, Christina Gregor, Lauren H. Yaeger, Yirui Hu, Amy C. Sturm, Terry L. Seaton, Thomas J. Waltz, Alanna K. Rahm, Anne Goldberg, Ross C. Brownson, Samuel S. Gidding, Marc S. Williams, Michael R. Gionfriddo
Publikováno v:
Implementation Science, Vol 16, Iss 1, Pp 1-15 (2021)
Abstract Background Numerous implementation strategies to improve utilization of statins in patients with hypercholesterolemia have been utilized, with varying degrees of success. The aim of this systematic review is to determine the state of evidenc
Externí odkaz:
https://doaj.org/article/476ddb071f614dcea8d147ecc5b30808
Autor:
Laney K. Jones, Megan McMinn, David Kann, Michael Lesko, Amy C. Sturm, Nicole Walters, Nan Chen, Kerrianne Fry, Ross C. Brownson, Samuel S. Gidding, Marc S. Williams, Alanna Kulchak Rahm
Publikováno v:
Implementation Science Communications, Vol 2, Iss 1, Pp 1-10 (2021)
Abstract Background Individuals with complex dyslipidemia, or those with medication intolerance, are often difficult to manage in primary care. They require the additional attention, expertise, and adherence counseling that occurs in multidisciplinar
Externí odkaz:
https://doaj.org/article/30693c068a054d9880fcc8c2c46890c6
Autor:
Laney K. Jones, Nicole Walters, Andrew Brangan, Catherine D. Ahmed, Katherine A. Wilemon, Gemme Campbell-Salome, Alanna K. Rahm, Samuel S. Gidding, Amy C. Sturm
Publikováno v:
American Journal of Preventive Cardiology, Vol 10, Iss , Pp 100344- (2022)
Objective: To explore alignment of perspectives from individuals and families with familial hypercholesterolemia (FH) to the FH Global Call to Action recommendations. Methods: Interviews and focus groups were conducted with individuals and families w
Externí odkaz:
https://doaj.org/article/6c3b72930acc41f98f7de4cadd27b152
Autor:
Laney K. Jones, Natasha T. Strande, Evan M. Calvo, Jingheng Chen, Gabriela Rodriguez, Cara Z. McCormick, Miranda L. G. Hallquist, Juliann M. Savatt, Heather Rocha, Marc S. Williams, Amy C. Sturm, Adam H. Buchanan, Russell E. Glasgow, Christa L. Martin, Alanna Kulchak Rahm
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Introduction: DNA-based population screening has been proposed as a public health solution to identify individuals at risk for serious health conditions who otherwise may not present for medical care. The clinical utility and public health impact of
Externí odkaz:
https://doaj.org/article/522103d74d794e618ecf78894398352a