Zobrazeno 1 - 10
of 116
pro vyhledávání: '"Kurt A. Christensen"'
Publikováno v:
npj Genomic Medicine, Vol 9, Iss 1, Pp 1-9 (2024)
Abstract Panel germline testing allows for the efficient detection of deleterious variants for multiple conditions, but the benefits and harms of identifying these variants are not always well understood. We present a multi-gene, multi-disease aggreg
Externí odkaz:
https://doaj.org/article/a79574b0279e42fd94d37c221541cee8
Autor:
Kurt D. Christensen, Mengran Zhang, Lauren N. Galbraith, Einat Granot-Hershkovitz, Sarah C. Nelson, Sara Gonzalez, Maria Argos, Krista M. Perreira, Martha L. Daviglus, Carmen R. Isasi, Jianwen Cai, Gregory A. Talavera, Carrie L. Blout Zawatsky, Robert C. Green, Rosario Isasi, Robert Kaplan, Tamar Sofer
Publikováno v:
HGG Advances, Vol 4, Iss 1, Pp 100160- (2023)
Summary: We investigated the awareness, perceived usefulness, and use of genetic testing among Hispanic and Latino individuals. Annual follow-up surveys for the Hispanic Community Health Study/Study of Latinos (HCHS/SOL) from 2019 to April 2020 asses
Externí odkaz:
https://doaj.org/article/8ff2e6c54d70411d90040259888b69d3
Autor:
Kurt D. Christensen, Erica F. Schonman, Jill O. Robinson, J. Scott Roberts, Pamela M. Diamond, Kaitlyn B. Lee, Robert C. Green, Amy L. McGuire
Publikováno v:
npj Genomic Medicine, Vol 6, Iss 1, Pp 1-8 (2021)
Abstract Many expect genome sequencing (GS) to become routine in patient care and preventive medicine, but uncertainties remain about its ability to motivate participants to improve health behaviors and the psychological impact of disclosing results.
Externí odkaz:
https://doaj.org/article/b79ae75876f14fea94621325471eb616
Autor:
Brittan Armstrong, Kurt D. Christensen, Casie A. Genetti, Richard B. Parad, Jill Oliver Robinson, Carrie L. Blout Zawatsky, Bethany Zettler, Alan H. Beggs, Ingrid A. Holm, Robert C. Green, Amy L. McGuire, Hadley Stevens Smith, Stacey Pereira, The BabySeq Project Team
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Introduction: With increasing utility and decreasing cost of genomic sequencing, augmentation of standard newborn screening (NBS) programs with newborn genomic sequencing (nGS) has been proposed. Before nGS can be integrated into newborn screening, p
Externí odkaz:
https://doaj.org/article/a5e73206e51142deb82cd9b8ec557eff
Autor:
Kurt D. Christensen, Megan Bell, Carrie L. B. Zawatsky, Lauren N. Galbraith, Robert C. Green, Allison M. Hutchinson, Leila Jamal, Jessica L. LeBlanc, Jennifer R. Leonhard, Michelle Moore, Lisa Mullineaux, Natasha Petry, Dylan M. Platt, Sherin Shaaban, April Schultz, Bethany D. Tucker, Joel Van Heukelom, Elizabeth Wheeler, Emilie S. Zoltick, Catherine Hajek, on behalf of the Imagenetics Metrics Team, Baye Jordan, Bell Megan, Deberg Kristen, Forred Benjamin, Free Colette, Hajek Catherine, Heukelom Joel Van, Hopp Ashley, Hutchinson Allison, Lees Ryne, Leonhard Jennifer, Massmann Amanda, Moore Michelle, Mroch Amelia, Petry Natasha, Platt Dylan, Royer Erin, Schultz April, Sincan Murat, Tucker Bethany, Wheeler Elizabeth, Christensen Kurt, Galbraith Lauren, LeBlanc Jessica, Walsh Ryan, Zoltick Emilie, Green Robert, Preys Charlene, Zawatsky Carrie, Mullineaux Lisa, Jamal Leila
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Genetic testing has the potential to revolutionize primary care, but few health systems have developed the infrastructure to support precision population medicine applications or attempted to evaluate its impact on patient and provider outcomes. In 2
Externí odkaz:
https://doaj.org/article/492eb908c6f04497b0fc91553705e6e8
Autor:
Kurt D. Christensen, Jason Karlawish, J. Scott Roberts, Wendy R. Uhlmann, Kristin Harkins, Elisabeth M. Wood, Thomas O. Obisesan, Lan Q. Le, L. Adrienne Cupples, Emilie S. Zoltick, Megan S. Johnson, Margaret K. Bradbury, Leo B. Waterston, Clara A. Chen, Sara Feldman, Denise L. Perry, Robert C. Green, for the REVEAL Study Group
Publikováno v:
Alzheimer’s & Dementia: Translational Research & Clinical Interventions, Vol 6, Iss 1, Pp n/a-n/a (2020)
Abstract Introduction The safety of predicting conversion from mild cognitive impairment (MCI) to Alzheimer's disease (AD) dementia using apolipoprotein E (APOE) genotyping is unknown. Methods We randomized 114 individuals with MCI to receive estimat
Externí odkaz:
https://doaj.org/article/70a3ee90dc4b4d9eb0f679eff74edb87
Autor:
Ingrid A. Holm, Pankaj B. Agrawal, Ozge Ceyhan-Birsoy, Kurt D. Christensen, Shawn Fayer, Leslie A. Frankel, Casie A. Genetti, Joel B. Krier, Rebecca C. LaMay, Harvey L. Levy, Amy L. McGuire, Richard B. Parad, Peter J. Park, Stacey Pereira, Heidi L. Rehm, Talia S. Schwartz, Susan E. Waisbren, Timothy W. Yu, The BabySeq Project Team, Robert C. Green, Alan H. Beggs
Publikováno v:
BMC Pediatrics, Vol 18, Iss 1, Pp 1-10 (2018)
Abstract Background The greatest opportunity for lifelong impact of genomic sequencing is during the newborn period. The “BabySeq Project” is a randomized trial that explores the medical, behavioral, and economic impacts of integrating genomic se
Externí odkaz:
https://doaj.org/article/ef710afcaf8e4d019d8c6869cf074068
Autor:
Amanda Massmann, Joel Van Heukelom, Robert C Green, Catherine Hajek, Madison R Hickingbotham, Eric A Larson, Christine Y Lu, Ann Chen Wu, Emilie S Zoltick, Kurt D Christensen, April Schultz
Publikováno v:
Pharmacogenomics.
Background: SLCO1B1 variants are known to be a strong predictor of statin-associated muscle symptoms (SAMS) risk with simvastatin. Methods: The authors conducted a retrospective chart review on 20,341 patients who had SLCO1B1 genotyping to quantify t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c458f716a00b585c020dc1d585211357
https://doi.org/10.2217/pgs-2023-0056
https://doi.org/10.2217/pgs-2023-0056
Publikováno v:
Journal of Genetic Counseling.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::edb51dae0cc5cfb0a5fa4868279cb742
https://doi.org/10.1002/jgc4.1708
https://doi.org/10.1002/jgc4.1708
Autor:
Catherine Hajek, Allison M. Hutchinson, Lauren N. Galbraith, Robert C. Green, Michael F. Murray, Natasha Petry, Charlene L. Preys, Carrie L.B. Zawatsky, Emilie S. Zoltick, Kurt D. Christensen, Jordan Baye, Megan Bell, Kristen Deberg, Benjamin Forred, Colette Free, Joel Van Heukelom, Ashley Hopp, Allison Hutchinson, Ryne Lees, Jennifer Leonhard, Amanda Massmann, Michelle Moore, Amelia Mroch, Dylan Platt, Erin Royer, April Schultz, Murat Sincan, Bethany Tucker, Elizabeth Wheeler, Kurt Christensen, Lauren Galbraith, Jessica LeBlanc, Ryan Walsh, Emilie Zoltick, Robert Green, Charlene Preys, Carrie Zawatsky, Lisa Mullineaux, Leila Jamal
Publikováno v:
Genetics in Medicine. 24:214-224
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b38f37a06132f88807c510f643e42a3
https://doi.org/10.1016/j.gim.2021.08.008
https://doi.org/10.1016/j.gim.2021.08.008