Amy Curry Sturm
机构: Professor, Licensed Genetic Counselor, Geisinger
每年引用次数
引用次数
引用: 4,967
H-指数: 33
I10-指数 : 84
出版物: 172
Secondary Findings of Loss-of-function Variants in FLNC Are Associated With Arrhythmogenic Cardiomyopathy Phenotypes in a General Clinical Population
Christopher M Haggerty , Melissa Kelly , Crystal Tichnell , Brittney Murray
Circulation 142 ( Suppl_3) A13583 -A13583
2020
Initial Assessment of Diagnostic Yield of Arrhythmogenic Right Ventricular Cardiomyopathy in Patients Ascertained Through Secondary Genomic Findings
Dominik Beer , Marci Schwartz , Melissa Kelly , Megan McMinn
Circulation 140 ( Suppl_1) A12247 -A12247
2019
HF-566-02 PREDICTED RISK OF VENTRICULAR ARRHYTHMIA IN INDIVIDUALS WITH DESMOSOME GENE VARIANTS IDENTIFIED VIA POPULATION GENOMIC SCREENING
Eric Carruth , Amro Alsaid , Brittney Murray , Crystal Tichnell
Heart Rhythm 19 ( 5) S41 -S41
2022
Translating guidelines into practice via implementation science: an update in lipidology
Laney K Jones , Amy C Sturm , Michael R Gionfriddo
Current opinion in lipidology 33 ( 6) 336 -341
9
2022
Healthcare utilization and patients’ perspectives after receiving a positive genetic test for familial hypercholesterolemia: a pilot study
Laney K Jones , Alanna Kulchak Rahm , Kandamurugu Manickam , Loren Butry
Circulation: Genomic and Precision Medicine 11 ( 8) e002146 -e002146
28
2018
Facilitating family communication of familial hypercholesterolemia genetic risk: Assessing engagement with innovative chatbot technology from the IMPACT-FH study
Nicole L Walters , Zoe T Lindsey-Mills , Andrew Brangan , Sarah K Savage
PEC innovation 2 100134 -100134
4
2023
Optimizing communication strategies and designing a comprehensive program to facilitate cascade testing for familial hypercholesterolemia
Gemme Campbell-Salome , Laney K Jones , Nicole L Walters , Kelly M Morgan
BMC Health Services Research 23 ( 1) 340 -340
1
2023
Facilitating cascade testing by offering a range of strategies through the impact-FH trial: Feasibility and potential optimizations
Gemme Campbell-Salome , Kelly M Morgan , Jazmine Gabriel , Mary P McGowan
16 th Annual Conference on the Science of Dissemination and Implementation
2023
Direct Contact of At-Risk Relatives in the United States Identifies Familial Hypercholesterolemia Cases
Kelly M Morgan , Nicole L Walters , Gemme Campbell-Salome , Megan N Betts
Journal of Clinical Lipidology 17 ( 4) e23 -e24
2023
Motivating cascade testing for familial hypercholesterolemia: applying the extended parallel process model for clinician communication
Gemme Campbell-Salome , Nicole L Walters , Ilene G Ladd , Amanda Sheldon
Translational Behavioral Medicine 12 ( 7) 800 -809
7
2022
Acceptability and Feasibility of Novel Screening Models and Family Communication Methods for Familial Hypercholesterolemia
Laney K Jones , Nicole Walters , Andrew Brangan , Catherine D Ahmed
Circulation 142 ( Suppl_3) A13161 -A13161
1
2020
No one size fits all: The acceptability of multiple strategies to support cascade testing through the impact-FH trial
Gemme Campbell-Salome , Kelly M Morgan , Jazmine Gabriel , Mary P McGowan
16 th Annual Conference on the Science of Dissemination and Implementation
2023
Familial Hypercholesterolemia Patient Perspectives and their Alignment With the FH Global Call to Action
Laney K Jones , Amanda Sheldon , Nicole Walters , Andrew Brangan
Circulation 144 ( Suppl_1) A9584 -A9584
2021
Genetic testing for heritable cardiovascular diseases in pediatric patients: a scientific statement from the American Heart Association
Andrew P Landstrom , Jeffrey J Kim , Bruce D Gelb , Benjamin M Helm
Circulation: Genomic and Precision Medicine 14 ( 5) e000086 -e000086
48
2021
Genetic Testing for Inherited Cardiovascular Diseases: A Scientific Statement From the American Heart Association.
Kiran Musunuru , Ray E Hershberger , Sharlene M Day , N Jennifer Klinedinst
Circulation: Genomic and Precision Medicine 13 ( 4)
29
2020
Interpreting incidentally identified variants in genes associated with heritable cardiovascular disease: a scientific statement from the American Heart Association
Andrew P Landstrom , Anwar A Chahal , Michael J Ackerman , Sharon Cresci
Circulation: Genomic and Precision Medicine 16 ( 2) e000092 -e000092
13
2023
How online family history tool design and message content impact user perceptions: An examination of family HealthLink
Sarah N Thomas , Shelly R Hovick , Naomi Tan , Amy C Sturm
Public Health Genomics 21 ( 1-2) 53 -66
4
2019
Exome Sequencing-Based Screening for BRCA1/2 Expected Pathogenic Variants Among Adult Biobank Participants.
Kandamurugu Manickam , Adam H Buchanan , Marci LB Schwartz , Miranda LG Hallquist
JAMA Network Open 1 ( 5)
167
2018
Pediatric reporting of genomic results study (PROGRESS): a mixed-methods, longitudinal, observational cohort study protocol to explore disclosure of actionable adult- and pediatric-onset genomic variants to minors and their parents.
Juliann M Savatt , Jennifer K Wagner , Steven Joffe , Alanna Kulchak Rahm
BMC Pediatrics 20 ( 1) 1 -13
2
2020
Use of a chatbot to increase uptake of cascade genetic testing
Tara Schmidlen , Claire L Jones , Gemme Campbell‐Salome , Cara Z McCormick
Journal of genetic counseling 31 ( 5) 1219 -1230
26
2022
Alanna Kulchak Rahm Marc S. Williams Adam H. Buchanan Kandamurugu Manickam Michael F. Murray, MD David J Carey Shelly Hovick William Andrew Faucett Amanda Ewart Toland or Amanda Toland or Amanda Ewart Laura Scheinfeldt Peter J Mohler Albert de la Chapelle Lauren Frisbie Monica A. Giovanni, MS, CGC Matthew Lebo Ahmet Kilic Paul ML Janssen Thomas J. Hund Philip Binkley Vadim Fedorov